Cancer-associated cachexia

Acute-Phase Proteins and Other Systemic Responses to Inflammation

Gabay, C., & Kushner, I. (1999) · New England Journal of Medicine · doi:10.1056/nejm199902113400607 · Cited by 6,734 · see citing works

Definition and classification of cancer cachexia: an international consensus

Fearon, K., Strasser, F., Anker, S. D., Bosaeus, I. G., Bruera, E. D., Fainsinger, R. L., Jatoi, A., Loprinzi, C. L., Macdonald, N., Mantovani, G., et al. (2011) · The Lancet Oncology · doi:10.1016/s1470-2045(10)70218-7 · Cited by 5,800 · see citing works

Epidemiology of Sarcopenia among the Elderly in New Mexico

Baumgartner, R. N., Koehler, K. M., Gallagher, D., Romero, L., Heymsfield, S. B., Ross, R. R., Garry, P. J., & Lindeman, R. D. (1998) · American Journal of Epidemiology · doi:10.1093/oxfordjournals.aje.a009520 · Cited by 4,004 · see citing works

Identification of ubiquitin ligases required for skeletal muscle atrophy.

Bodine, S. C., Latres, E., Baumhueter, S., Lai, V. K.-M., Nunez, L., Clarke, B. A., Poueymirou, W. T., Panaro, F. J., Na, E., Dharmarajan, K., et al. (2001) · Science · doi:10.1126/science.1065874 · Cited by 3,521 · see citing works

Prevalence and clinical implications of sarcopenic obesity in patients with solid tumours of the respiratory and gastrointestinal tracts: A population-based study

Prado, C. M., Lieffers, J. R., McCargar, L. J., Reiman, T., Sawyer, M. B., Martin, L., & Baracos, V. E. (2008) · The Lancet Oncology · doi:10.1016/s1470-2045(08)70153-0 · Cited by 3,238 · see citing works

ESPEN guidelines on nutrition in cancer patients

Arends, J., Bachmann, P., Baracos, V., Barthelemy, N., Bertz, H., Bozzetti, F., Fearon, K., Hütterer, E., Isenring, E., Kaasa, S., et al. (2017) · Clinical Nutrition · doi:10.1016/j.clnu.2016.07.015 · Cited by 3,114 · see citing works

Nutritional risk screening (NRS 2002): a new method based on an analysis of controlled clinical trials

KONDRUP, J. (2003) · Clinical Nutrition · doi:10.1016/s0261-5614(02)00214-5 · Cited by 3,063 · see citing works

Foxo transcription factors induce the atrophy-related ubiquitin ligase atrogin-1 and cause skeletal muscle atrophy.

Sandri, M., Sandri, C., Gilbert, A., Skurk, C., Calabria, E., Picard, A., Walsh, K., Schiaffino, S., Lecker, S. H., & Goldberg, A. L. (2004) · Cell · doi:10.1016/s0092-8674(04)00400-3 · Cited by 3,012 · see citing works

Screening for Undernutrition in Geriatric Practice: Developing the Short-Form Mini-Nutritional Assessment (MNA-SF)

Rubenstein, L. Z., Harker, J. O., Salva, A., Guigoz, Y., & Vellas, B. (2001) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/56.6.m366 · Cited by 2,751 · see citing works

Cancer Cachexia in the Age of Obesity: Skeletal Muscle Depletion Is a Powerful Prognostic Factor, Independent of Body Mass Index

Martin, L., Birdsell, L., Macdonald, N., Reiman, T., Clandinin, M. T., McCargar, L. J., Murphy, R. A., Ghosh, S., Sawyer, M. B., & Baracos, V. E. (2013) · Journal of Clinical Oncology · doi:10.1200/jco.2012.45.2722 · Cited by 2,698 · see citing works

Prognostic effect of weight loss prior tochemotherapy in cancer patients

DeWys, W. D., Begg, C. B., Lavin, P. T., Band, P. R., Bennett, J. M., Bertino, J. R., Cohen, M. H., Douglass, H. O., Engstrom, P. F., Ezdinli, E. Z., et al. (1980) · The American Journal of Medicine · doi:10.1016/s0149-2918(05)80001-3 · Cited by 2,350 · see citing works

Pax7 Is Required for the Specification of Myogenic Satellite Cells

Seale, P., Sabourin, L. A., Girgis-Gabardo, A., Mansouri, A., Gruß, P., & Rudnicki, M. A. (2000) · Cell · doi:10.1016/s0092-8674(00)00066-0 · Cited by 2,345 · see citing works

Fat Mobilization in Adipose Tissue Is Promoted by Adipose Triglyceride Lipase

Zimmermann, R., Bogner‐Strauß, J. G., Haemmerle, G., Schoiswohl, G., Birner‐Gruenberger, R., Riederer, M., Lass, A., Neuberger, G., Eisenhaber, F., Hermetter, A., et al. (2004) · Science · doi:10.1126/science.1100747 · Cited by 2,121 · see citing works

The IGF-1/PI3K/Akt pathway prevents expression of muscle atrophy-induced ubiquitin ligases by inhibiting FOXO transcription factors.

Stitt, T. N., Drujan, D., Clarke, B. A., Panaro, F., Timofeyva, Y., Kline, W. O., Gonzalez, M., Yancopoulos, G. D., & Glass, D. J. (2004) · Molecular Cell · doi:10.1016/s1097-2765(04)00211-4 · Cited by 1,964 · see citing works

Oxford Textbook of Palliative Medicine

(2009) · Oxford University Press eBooks · doi:10.1093/med/9780198570295.001.0001 · Cited by 1,921 · see citing works

Atrogin-1, a muscle-specific F-box protein highly expressed during muscle atrophy

Gomes, M. D., Lecker, S. H., Jagoe, R. T., Navon, A., & Goldberg, A. L. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.251541198 · Cited by 1,774 · see citing works

Multiple types of skeletal muscle atrophy involve a common program of changes in gene expression

Lecker, S. H., Jagoe, R. T., Gilbert, A., Gomes, M., Baracos, V., Bailey, J., Price, S. R., Mitch, W. E., & Goldberg, A. L. (2004) · The FASEB Journal · doi:10.1096/fj.03-0610com · Cited by 1,539 · see citing works

Nutritional and metabolic assessment of the hospitalized patient

Blackburn, G. L., Bistrian, B. R., Maini, B. S., Schlamm, H. T., & Smith, M. F. (1977) · Journal of Parenteral and Enteral Nutrition · doi:10.1177/014860717700100101 · Cited by 1,426 · see citing works

IKKβ/NF-κB Activation Causes Severe Muscle Wasting in Mice

Cai, D., Frantz, J. D., Tawa, N. E., Melendez, P. A., Oh, B.-C., Lidov, H. G. W., Hasselgren, P.-O., Frontera, W. R., Lee, J., Glass, D. J., et al. (2004) · Cell · doi:10.1016/j.cell.2004.09.027 · Cited by 1,367 · see citing works

American Society of Clinical Oncology Provisional Clinical Opinion: The Integration of Palliative Care Into Standard Oncology Care

Smith, T. J., Temin, S., Alesi, E. R., Abernethy, A. P., Balboni, T. A., Basch, E., FERRELL, B. R., Loscalzo, M., Meier, D. E., Paice, J. A., et al. (2012) · Journal of Clinical Oncology · doi:10.1200/jco.2011.38.5161 · Cited by 1,319 · see citing works

Malnutrition in hospital outpatients and inpatients: prevalence, concurrent validity and ease of use of the ‘malnutrition universal screening tool’ (‘MUST’) for adults

Stratton, R. J., Hackston, A., Longmore, D., Dixon, R., Price, S., Stroud, M. A., King, C. L., & Elia, M. (2004) · British Journal Of Nutrition · doi:10.1079/bjn20041258 · Cited by 1,247 · see citing works

Cancer Cachexia: Mediators, Signaling, and Metabolic Pathways

Fearon, K. C. H., Glass, D. J., & D, D. C. G. (2012) · Cell Metabolism · doi:10.1016/j.cmet.2012.06.011 · Cited by 1,203 · see citing works

Skeletal Muscle Cutpoints Associated with Elevated Physical Disability Risk in Older Men and Women

Janssen, I. (2004) · American Journal of Epidemiology · doi:10.1093/aje/kwh058 · Cited by 1,190 · see citing works

Targeting RAS–ERK signalling in cancer: promises and challenges

Samatar, A. A., & Poulikakos, P. I. (2014) · Nature Reviews Drug Discovery · doi:10.1038/nrd4281 · Cited by 1,163 · see citing works

Body Composition in Healthy Aging

BAUMGARTNER, R. N. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb06498.x · Cited by 1,078 · see citing works

Antiemetics: American Society of Clinical Oncology Clinical Practice Guideline Update

Basch, E., Prestrud, A. A., Hesketh, P. J., Kris, M. G., Feyer, P., Somerfield, M. R., Chesney, M., Clark-Snow, R. A., Flaherty, A. M. C., Freundlich, B., et al. (2011) · Journal of Clinical Oncology · doi:10.1200/jco.2010.34.4614 · Cited by 1,057 · see citing works

Cachexia in cancer patients

Tisdale, M. J. (2002) · Nature reviews. Cancer · doi:10.1038/nrc927 · Cited by 983 · see citing works

Development of a valid and reliable malnutrition screening tool for adult acute hospital patients

Ferguson, M. L., Capra, S. M., Bauer, J. D., & Banks, M. (1999) · Nutrition · doi:10.1016/s0899-9007(99)00084-2 · Cited by 967 · see citing works

Reversal of Cancer Cachexia and Muscle Wasting by ActRIIB Antagonism Leads to Prolonged Survival

Zhou, X., Wang, J. L., Lu, J., Song, Y., Kwak, K. S., Jiao, Q., Rosenfeld, R., Chen, Q., Boone, T. C., Simonet, W. S., et al. (2010) · Cell · doi:10.1016/j.cell.2010.07.011 · Cited by 941 · see citing works

Understanding the mechanisms and treatment options in cancer cachexia

Fearon, K. C. H., Arends, J., & Baracos, V. E. (2012) · Nature Reviews Clinical Oncology · doi:10.1038/nrclinonc.2012.209 · Cited by 937 · see citing works

Sarcopenic Obesity Predicts Instrumental Activities of Daily Living Disability in the Elderly

Baumgartner, R. N., Wayne, S. J., Waters, D. L., Janssen, I., Gallagher, D., & Morley, J. E. (2004) · Obesity Research · doi:10.1038/oby.2004.250 · Cited by 937 · see citing works

NF-κB-Induced Loss of MyoD Messenger RNA: Possible Role in Muscle Decay and Cachexia

D, D. C. G., Mayo, M. W., Madrid, L. V., Wang, C., & Baldwin, A. S. (2000) · Science · doi:10.1126/science.289.5488.2363 · Cited by 922 · see citing works

Overview of the MNA--Its history and challenges.

Vellas, B. J., Villars, H., van Kan, G. A., Soto, M. E., Rolland, Y., Guigoz, Y., Morley, J. E., Chumlea, W. M. C., Salvà, A., Rubenstein, L. Z., et al. (2006) · PubMed · Cited by 910 · see citing works

Prevalence of Malnutrition and Current Use of Nutrition Support in Patients With Cancer

Hébuterne, X., Lemarié, É., Michallet, M., de Montreuil, C. B., Schneider, S. M., & Goldwasser, F. (2014) · Journal of Parenteral and Enteral Nutrition · doi:10.1177/0148607113502674 · Cited by 826 · see citing works

Body composition and mortality in chronic obstructive pulmonary disease

Schols, A. M. W. J., Broekhuizen, R., Weling-Scheepers, C. A., & Wouters, E. F. �. (2005) · American Journal of Clinical Nutrition · doi:10.1093/ajcn.82.1.53 · Cited by 808 · see citing works

Diagnostic Criteria for the Classification of Cancer-Associated Weight Loss

Martin, L., Sénesse, P., Gioulbasanis, I., Antoun, S., Bozzetti, F., Deans, C., Strasser, F., Thoresen, L., Jagoe, R. T., Chasen, M. R., et al. (2014) · Journal of Clinical Oncology · doi:10.1200/jco.2014.56.1894 · Cited by 799 · see citing works

A Switch from White to Brown Fat Increases Energy Expenditure in Cancer-Associated Cachexia

Petruzzelli, M., Schweiger, M., Schreiber, R., Campos‐Olivas, R., Tsoli, M., Allen, J., Swarbrick, M. M., Rose‐John, S., Rincón, M., Robertson, G. R., et al. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2014.06.011 · Cited by 752 · see citing works

Energy balance and its components: implications for body weight regulation

Hall, K. D., Heymsfield, S. B., Kemnitz, J. W., Klein, S., Schoeller, D. A., & Speakman, J. R. (2012) · The American Journal of Clinical Nutrition · doi:10.3945/ajcn.112.036350 · Cited by 721 · see citing works

Regulation of autophagy and the ubiquitin-proteasome system by the FoxO transcriptional network during muscle atrophy

Milan, G., Romanello, V., Pescatore, F., Armani, A., Paik, J.-H., Frasson, L., Seydel, A., Zhao, J., Abraham, R., Goldberg, A. L., et al. (2015) · Nature Communications · doi:10.1038/ncomms7670 · Cited by 709 · see citing works

Sarcopenia, intramuscular fat deposition, and visceral adiposity independently predict the outcomes of hepatocellular carcinoma

Fujiwara, N., Nakagawa, H., Kudo, Y., Tateishi, R., Taguri, M., Watadani, T., Nakagomi, R., Kondo, M., Nakatsuka, T., Minami, T., et al. (2015) · Journal of Hepatology · doi:10.1016/j.jhep.2015.02.031 · Cited by 707 · see citing works

Protein breakdown in muscle wasting: Role of autophagy-lysosome and ubiquitin-proteasome

Sandri, M. (2013) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2013.04.023 · Cited by 689 · see citing works

Stimulation of Muscle Protein Degradation and Prostaglandin E2Release by Leukocytic Pyrogen (Interleukin-1)

Baracos, V. E., Rodemann, H. P., Dinarello, C. A., & Goldberg, A. L. (1983) · New England Journal of Medicine · doi:10.1056/nejm198303103081002 · Cited by 687 · see citing works

The E3 Ligase MuRF1 Degrades Myosin Heavy Chain Protein in Dexamethasone-Treated Skeletal Muscle

Clarke, B. A., Drujan, D., Willis, M. S., Murphy, L. O., Corpina, R. A., Burova, E., Rakhilin, S. V., Stitt, T. N., Patterson, C., Latres, E., et al. (2007) · Cell Metabolism · doi:10.1016/j.cmet.2007.09.009 · Cited by 683 · see citing works

Tumour-derived PTH-related protein triggers adipose tissue browning and cancer cachexia

Kır, S., White, J. P., Kleiner, S., Kazak, L., Cohen, P., Baracos, V. E., & Spiegelman, B. M. (2014) · Nature · doi:10.1038/nature13528 · Cited by 673 · see citing works

Prevalence, risk factors and clinical implications of malnutrition in French Comprehensive Cancer Centres

Pressoir, M., Desné, S., Berchery, D., Rossignol, G., Poirée, B., Meslier, M., Traversier, S., Vittot, M., Simon, M., Gékière, J.-P., et al. (2010) · British Journal of Cancer · doi:10.1038/sj.bjc.6605578 · Cited by 669 · see citing works

Prognostic Factors in Advanced Cancer Patients: Evidence-Based Clinical Recommendations—A Study by the Steering Committee of the European Association for Palliative Care

Maltoni, M. C., Caraceni, A. T., Brunelli, C., Broeckaert, B., Christakis, N. A., Eychmueller, S., Glare, P. A., Nabal, M., Vigano, A. A. L., Larkin, P. J., et al. (2005) · Journal of Clinical Oncology · doi:10.1200/jco.2005.06.866 · Cited by 666 · see citing works

Anamorelin in patients with non-small-cell lung cancer and cachexia (ROMANA 1 and ROMANA 2): results from two randomised, double-blind, phase 3 trials

Temel, J. S., Abernethy, A. P., Currow, D. C., Friend, J., Duus, E. M., Yan, Y., & Fearon, K. C. (2016) · The Lancet Oncology · doi:10.1016/s1470-2045(15)00558-6 · Cited by 639 · see citing works

Antiemetics: American Society of Clinical Oncology Clinical Practice Guideline Update

Hesketh, P. J., Kris, M. G., Basch, E., Bohlke, K., Barbour, S. Y., Clark-Snow, R. A., Danso, M. A., Dennis, K. E. B., Dupuis, L. L., Dusetzina, S. B., et al. (2017) · Journal of Clinical Oncology · doi:10.1200/jco.2017.74.4789 · Cited by 634 · see citing works

Development and validation of a hospital screening tool for malnutrition: the short nutritional assessment questionnaire (SNAQ©)

Kruizenga, H. M., Seidell, J. C., de Vet, H. C. W., Wierdsma, N., & de van der Schueren, M. A. E. (2004) · Clinical Nutrition · doi:10.1016/j.clnu.2004.07.015 · Cited by 604 · see citing works

Effect of a protein and energy dense n-3 fatty acid enriched oral supplement on loss of weight and lean tissue in cancer cachexia: a randomised double blind trial

Fearon, K. C. H. (2003) · Gut · doi:10.1136/gut.52.10.1479 · Cited by 603 · see citing works

Adipose Triglyceride Lipase Contributes to Cancer-Associated Cachexia

Das, S. K., Eder, S., Schauer, S., Diwoky, C., Temmel, H., Guertl, B., Gorkiewicz, G., Tamilarasan, K. P., Kumari, P., Trauner, M. A., et al. (2011) · Science · doi:10.1126/science.1198973 · Cited by 586 · see citing works

Cancer cachexia is regulated by selective targeting of skeletal muscle gene products

Acharyya, S., Ladner, K. J., Nelsen, L., Damrauer, J. S., Reiser, P. J., Swoap, S. J., & D, D. C. G. (2004) · Journal of Clinical Investigation · doi:10.1172/jci20174 · Cited by 541 · see citing works

BMP signaling controls muscle mass

Sartori, R., Schirwis, E., Blaauw, B., Bortolanza, S., Zhao, J., Enzo, E., Stantzou, A., Mouisel, E., Toniolo, L., Ferry, A., et al. (2013) · Nature Genetics · doi:10.1038/ng.2772 · Cited by 467 · see citing works

Physiologic Effects of Nutritional Support and Anabolic Steroids in Patients With Chronic Obstructive Pulmonary Disease. A Placebo-Controlled Randomized Trial

Schols, A. M. W. J., Soeters, P. B., Mostert, R., Pluymers, R. J., & Wouters, E. F. �. (1995) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/ajrccm.152.4.7551381 · Cited by 461 · see citing works

Ghrelin Increases Energy Intake in Cancer Patients with Impaired Appetite: Acute, Randomized, Placebo-Controlled Trial

Neary, N. M., Small, C. J., Wren, A., Lee, J. L., Druce, M. R., Palmieri, C., Frost, G. S., Ghatei, M. A., Coombes, R. C., & Bloom, S. R. (2004) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2003-031768 · Cited by 456 · see citing works

Cancer cachexia: Developing multimodal therapy for a multidimensional problem

Fearon, K. C. H. (2008) · European Journal of Cancer · doi:10.1016/j.ejca.2008.02.033 · Cited by 444 · see citing works

Taste and Smell in Disease

Epstein, F. H., & Schiffman, S. S. (1983) · New England Journal of Medicine · doi:10.1056/nejm198305263082107 · Cited by 443 · see citing works

Raised CRP levels mark metabolic and functional impairment in advanced COPD

Broekhuizen, R. (2005) · Thorax · doi:10.1136/thx.2005.041996 · Cited by 441 · see citing works

Characterization of a cancer cachectic factor

Todorov, P., Cariuk, P., McDevitt, T., Coles, B., Fearon, K. C. H., & Tisdale, M. J. (1996) · Nature · doi:10.1038/379739a0 · Cited by 437 · see citing works

Tumor Necrosis Factor α Produces Insulin Resistance in Skeletal Muscle by Activation of Inhibitor κB Kinase in a p38 MAPK-dependent Manner

de Álvaro, C., Teruel, T., Hernández, R., & Lorenzo, M. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m312021200 · Cited by 430 · see citing works

Nutritional support of the cancer patient: issues and dilemmas

Nitenberg, G., & Raynard, B. (2000) · Critical Reviews in Oncology/Hematology · doi:10.1016/s1040-8428(00)00048-2 · Cited by 421 · see citing works

Assessing nutritional status in cancer

Jager‐Wittenaar, H., & Ottery, F. D. (2017) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0000000000000389 · Cited by 420 · see citing works

Comparison of Orally Administered Cannabis Extract and Delta-9-Tetrahydrocannabinol in Treating Patients With Cancer-Related Anorexia-Cachexia Syndrome: A Multicenter, Phase III, Randomized, Double-Blind, Placebo-Controlled Clinical Trial From the Cannabis-In-Cachexia-Study-Group

Strasser, F., Luftner, D., Possinger, K., Ernst, G., Ruhstaller, T., Meissner, W., Ko, Y.-D., Schnelle, M., Reif, M., & Cerny, T. (2006) · Journal of Clinical Oncology · doi:10.1200/jco.2005.05.1847 · Cited by 413 · see citing works

What do we really know about the ubiquitin-proteasome pathway in muscle atrophy?

Jagoe, R. T., & Goldberg, A. L. (2001) · Current Opinion in Clinical Nutrition and Metabolic Care · doi:10.1097/00075197-200105000-00003 · Cited by 399 · see citing works

Excess TGF-β mediates muscle weakness associated with bone metastases in mice

Waning, D. L., Mohammad, K. S., Reiken, S. R., Xie, W., Andersson, D. C., John, S. K., Chiechi, A., Wright, L. E., Umanskaya, A., Niewolna, M., et al. (2015) · Nature Medicine · doi:10.1038/nm.3961 · Cited by 380 · see citing works

NF-κB–mediated Pax7 dysregulation in the muscle microenvironment promotes cancer cachexia

He, W. A., Berardi, E., Cardillo, V. M., Acharyya, S., Aulino, P., Thomas-Ahner, J., Wang, J., Bloomston, M., Muscarella, P., Nau, P., et al. (2013) · Journal of Clinical Investigation · doi:10.1172/jci68523 · Cited by 357 · see citing works

A proposed hypothalamic–thalamic–striatal axis for the integration of energy balance, arousal, and food reward

Kelley, A. E., Baldo, B. A., & Pratt, W. E. (2005) · Journal of Comparative Neurology · doi:10.1002/cne.20769 · Cited by 352 · see citing works

The role of the systemic inflammatory response in predicting outcomes in patients with advanced inoperable cancer: Systematic review and meta -analysis

Dolan, R. D., McSorley, S. T., Horgan, P. G., Laird, B. J. A., & McMillan, D. C. (2017) · Critical Reviews in Oncology/Hematology · doi:10.1016/j.critrevonc.2017.06.002 · Cited by 352 · see citing works

Ingestion of Casein and Whey Proteins Result in Muscle Anabolism after Resistance Exercise

Tipton, K. D., Elliott, T. A., Cree‐Green, M., Wolf, S. E., Sanford, A. P., & Wolfe, R. R. (2004) · Medicine & Science in Sports & Exercise · doi:10.1249/01.mss.0000147582.99810.c5 · Cited by 349 · see citing works

Muscle-specific expression of IGF-1 blocks angiotensin II–induced skeletal muscle wasting

Song, Y., Li, Y., Du, J., Mitch, W. E., Rosenthal, N. A., & Delafontaine, P. (2005) · Journal of Clinical Investigation · doi:10.1172/jci22324 · Cited by 347 · see citing works

Thalidomide in the treatment of cancer cachexia: a randomised placebo controlled trial

Gordon, J., Trebble, T. M., Ellis, R. D., Duncan, H. D., Johns, T., & Goggin, P. M. (2005) · Gut · doi:10.1136/gut.2004.047563 · Cited by 322 · see citing works

Body composition and time course changes in regional distribution of fat and lean tissue in unselected cancer patients on palliative care—Correlations with food intake, metabolism, exercise capacity, and hormones

Fouladiun, M., Körner, U., Bosaeus, I. G., Daneryd, P., Hyltander, A. G., & Lundholm, K. (2005) · Cancer · doi:10.1002/cncr.21013 · Cited by 322 · see citing works

Dystrophin glycoprotein complex dysfunction: A regulatory link between muscular dystrophy and cancer cachexia

Acharyya, S., Butchbach, M. E. R., Sahenk, Z., Wang, H., Saji, M., Carathers, M., Ringel, M. D., Skipworth, R. J. E., Fearon, K. C. H., Hollingsworth, M. A., et al. (2005) · Cancer Cell · doi:10.1016/j.ccr.2005.10.004 · Cited by 316 · see citing works

Targeted ablation of IKK2 improves skeletal muscle strength, maintains mass, and promotes regeneration

Mourkioti, F., Kratsios, P., Luedde, T., Song, Y.-H., Delafontaine, P., Adami, R., Parente, V., Bottinelli, R., Pasparakis, M., & Rosenthal, N. A. (2006) · Journal of Clinical Investigation · doi:10.1172/jci28721 · Cited by 315 · see citing works

Computed tomography-defined muscle and fat wasting are associated with cancer clinical outcomes

Kazemi‐Bajestani, S. M. R., Mazurak, V. C., & Baracos, V. E. (2015) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2015.09.001 · Cited by 314 · see citing works

Clinical-practice recommendations for the management of bowel obstruction in patients with end-stage cancer

Ripamonti, C. I., Twycross, R., Baines, M., Bozzetti, F., Capri, S., Conno, F. D., Gemlo, B. T., Hunt, T., Hans-B., K., Mercadante, S., et al. (2001) · Supportive Care in Cancer · doi:10.1007/s005200000198 · Cited by 313 · see citing works

Mechanism of Increased Lipolysis in Cancer Cachexia

Agustsson, T., Rydén, M., Hoffstedt, J., van Harmelen, V., Dicker, A., Laurencikiene, J., Isaksson, B., Permert, J., & Arner, P. (2007) · Cancer Research · doi:10.1158/0008-5472.can-06-4585 · Cited by 308 · see citing works

Early recognition of malnutrition and cachexia in the cancer patient: a position paper of a European School of Oncology Task Force

Aapro, M., Arends, J., Bozzetti, F., Fearon, K. C. H., Grunberg, S. M., Herrstedt, J., Hopkinson, J. B., Jacquelin-Ravel, N., Jatoi, A., Kaasa, S., et al. (2014) · Annals of Oncology · doi:10.1093/annonc/mdu085 · Cited by 308 · see citing works

A literature synthesis of symptom prevalence and severity in persons receiving active cancer treatment

Reilly, C. M., Bruner, D. W., Mitchell, S. A., Minasian, L. M., Basch, E., Dueck, A. C., Cella, D. F., & Reeve, B. B. (2013) · Supportive Care in Cancer · doi:10.1007/s00520-012-1688-0 · Cited by 299 · see citing works

Treatment of Cachexia With Ghrelin in Patients With COPD

Nagaya, N., Itoh, T., Murakami, S., Oya, H., Uematsu, M., Miyatake, K., & Kangawa, K. (2005) · CHEST Journal · doi:10.1378/chest.128.3.1187 · Cited by 295 · see citing works

Dietary intake and resting energy expenditure in relation to weight loss in unselected cancer patients

Bosaeus, I. G., Daneryd, P., Svanberg, E., & Lundholm, K. (2001) · International Journal of Cancer · doi:10.1002/ijc.1332 · Cited by 292 · see citing works

Effect of Fish Oil on Appetite and Other Symptoms in Patients With Advanced Cancer and Anorexia/Cachexia: A Double-Blind, Placebo-Controlled Study

Bruera, E. D., Strasser, F., Palmer, J. L., Willey, J. S., Calder, K., Amyotte, G., & Baracos, V. E. (2002) · Journal of Clinical Oncology · doi:10.1200/jco.2003.01.101 · Cited by 287 · see citing works

Double-Blind, Placebo-Controlled, Randomized Study of Eicosapentaenoic Acid Diester in Patients With Cancer Cachexia

Fearon, K. C. H., Barber, M. D., Moses, A. G. W., Ahmedzai, S. H., Taylor, G. S., Tisdale, M. J., & Murray, G. D. (2006) · Journal of Clinical Oncology · doi:10.1200/jco.2005.04.5724 · Cited by 282 · see citing works

Association of Skeletal Muscle Wasting With Treatment With Sorafenib in Patients With Advanced Renal Cell Carcinoma: Results From a Placebo-Controlled Study

Antoun, S., Birdsell, L., Sawyer, M. B., Venner, P. M., Escudier, B. J., & Baracos, V. E. (2010) · Journal of Clinical Oncology · doi:10.1200/jco.2009.24.9730 · Cited by 280 · see citing works

Agreement between patient-reported symptoms and their documentation in the medical record.

Pakhomov, S., Jacobsen, S. J., Chute, C. G., & Roger, V. L. (2008) · PubMed · Cited by 273 · see citing works

Anti-inflammatory treatment may prolong survival in undernourished patients with metastatic solid tumors.

Lundholm, K., Gélin, J., Hyltander, A. G., Lönnroth, C., Sandström, R., Svaninger, G., Körner, U., Gulich, M. P., Kärrefors, I., & Norli, B. (1994) · PubMed · Cited by 269 · see citing works

Marked changes in body composition following neoadjuvant chemotherapy for oesophagogastric cancer

Awad, S., Tan, B. H. L., Cui, H. W., Bhalla, A., Fearon, K. C. H., Parsons, S. L., Catton, J. A., & Lobo, D. N. (2011) · Clinical Nutrition · doi:10.1016/j.clnu.2011.08.008 · Cited by 269 · see citing works

Active Ghrelin Levels and Active to Total Ghrelin Ratio in Cancer-Induced Cachexia

Garcia, J. M., Garcia‐Touza, M., Hijazi, R. A., Taffet, G. E., Epner, D. E., Mann, D. L., Smith, R. G., Cunningham, G. R., & Marcelli, M. (2005) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2004-1788 · Cited by 261 · see citing works

Screening the nutritional status in oncology: a preliminary report on 1,000 outpatients

Bozzetti, F., & on behalf of the SCRINIO Working Group (2008) · Supportive Care in Cancer · doi:10.1007/s00520-008-0476-3 · Cited by 258 · see citing works

Local and Systemic Inflammation in Chronic Obstructive Pulmonary Disease

Wouters, E. F. �. (2005) · Proceedings of the American Thoracic Society · doi:10.1513/pats.200408-039ms · Cited by 253 · see citing works

A viscerally driven cachexia syndrome in patients with advanced colorectal cancer: contributions of organ and tumor mass to whole-body energy demands

Lieffers, J. R. L., Mourtzakis, M., Hall, K. D., McCargar, L. J., Prado, C. M. M., & Baracos, V. E. (2009) · American Journal of Clinical Nutrition · doi:10.3945/ajcn.2008.27273 · Cited by 251 · see citing works

Microvesicles containing miRNAs promote muscle cell death in cancer cachexia via TLR7

He, W. A., Calore, F., Londhe, P., Canella, A., D, D. C. G., & Croce, C. M. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1402714111 · Cited by 251 · see citing works

The TWEAK–Fn14 system is a critical regulator of denervation-induced skeletal muscle atrophy in mice

Mittal, A., Bhatnagar, S., Kumar, A., Lach-Trifilieff, E., Wauters, S., Li, H., Makonchuk, D. Y., Glass, D. J., & Kumar, A. (2010) · Journal of Cell Biology · doi:10.1083/jcb.200909117 · Cited by 250 · see citing works

Tumor induces muscle wasting in mice through releasing extracellular Hsp70 and Hsp90

Zhang, G., Liu, Z., Ding, H., Zhou, Y., Doan, H. A., Sin, K. W. T., Zhu, Z. J., Flores, R., Wen, Y., Gong, X., et al. (2017) · Nature Communications · doi:10.1038/s41467-017-00726-x · Cited by 248 · see citing works

Pathogenesis of pancreatic cancer exosome-induced lipolysis in adipose tissue

Sagar, G., Sah, R. P., Javeed, N., Dutta, S. K., Smyrk, T. C., Lau, J. S., Giorgadze, N., Tchkonia, T., Kirkland, J. L., Chari, S. T., et al. (2015) · Gut · doi:10.1136/gutjnl-2014-308350 · Cited by 247 · see citing works

An epidemiological evaluation of the prevalence of malnutrition in Spanish patients with locally advanced or metastatic cancer

Segura, Á., Pardo, J. M., Jara, C., Olabarria, L. Z., Carulla, J., Peñas, R. D. L., García-Cabrera, E., Azuara, M. L., Casadó, J., & Gómez‐Candela, C. (2005) · Clinical Nutrition · doi:10.1016/j.clnu.2005.05.001 · Cited by 244 · see citing works

Effects of an oral nutritional supplement containing eicosapentaenoic acid on nutritional and clinical outcomes in patients with advanced non-small cell lung cancer: Randomised trial

Sánchez-Lara, K., Turcott, J. G., Juárez-Hernández, E., Núñez-Valencia, C., Villanueva, G., Guevara‐Ramírez, P., la Torre-Vallejo, M. D., Mohar, A., & Arrieta, O. G. (2014) · Clinical Nutrition · doi:10.1016/j.clnu.2014.03.006 · Cited by 243 · see citing works

TNF‐α increases ubiquitin‐conjugating activity in skeletal muscle by up‐regulating UbcH2/E2 20k

LI, Y.-P., Lecker, S. H., Chen, Y., Waddell, I. D., Goldberg, A. L., & Reid, M. B. (2003) · The FASEB Journal · doi:10.1096/fj.02-0759com · Cited by 243 · see citing works

Pulmonary Rehabilitation Exercise Prescription in Chronic Obstructive Pulmonary Disease

Garvey, C., Bayles, M. P., Hamm, L. F., Hill, K., Holland, A. E., Limberg, T. M., & Spruit, M. A. (2016) · Journal of Cardiopulmonary Rehabilitation and Prevention · doi:10.1097/hcr.0000000000000171 · Cited by 243 · see citing works

Changes in body mass, energy balance, physical function, and inflammatory state in patients with locally advanced head and neck cancer treated with concurrent chemoradiation after low‐dose induction chemotherapy

Silver, H. J., Dietrich, M. S., & Murphy, B. A. (2007) · Head & Neck · doi:10.1002/hed.20607 · Cited by 232 · see citing works

Body-composition changes in patients who gain weight while receiving megestrol acetate.

Loprinzi, C. L., Schaid, D. J., Dose, A. M., Burnham, N. L., & Jensen, M. D. (1993) · Journal of Clinical Oncology · doi:10.1200/jco.1993.11.1.152 · Cited by 230 · see citing works

Inhibition of Stat3 Activation Suppresses Caspase-3 and the Ubiquitin-Proteasome System, Leading to Preservation of Muscle Mass in Cancer Cachexia

Silva, K. A. S., Dong, J., Dong, Y., Dong, Y., Schor, N., Tweardy, D. J., Zhang, L., & Mitch, W. E. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.641514 · Cited by 229 · see citing works

Central tenet of cancer cachexia therapy: do patients with advanced cancer have exploitable anabolic potential?

Prado, C. M. M., Sawyer, M. B., Ghosh, S., Lieffers, J. R. L., Esfandiari, N., Antoun, S., & Baracos, V. E. (2013) · American Journal of Clinical Nutrition · doi:10.3945/ajcn.113.060228 · Cited by 227 · see citing works

Overexpression of interleukin-15 induces skeletal muscle hypertrophy in vitro: implications for treatment of muscle wasting disorders

Quinn, L. S., Anderson, B. G., Drivdahl, R. H., Alvarez, B., & Argilés, J. M. (2002) · Experimental Cell Research · doi:10.1006/excr.2002.5624 · Cited by 226 · see citing works

Anabolic-Androgenic Steroid Therapy in the Treatment of Chronic Diseases

Basaria, S. S. (2001) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.86.11.5108 · Cited by 223 · see citing works

Geriatric cachexia: the role of cytokines

Yeh, S., & Schuster, M. W. (1999) · American Journal of Clinical Nutrition · doi:10.1093/ajcn.70.2.183 · Cited by 220 · see citing works

Weight management and its role in breast cancer rehabilitation

Demark‐Wahnefried, W., Campbell, K. L., & Hayes, S. C. (2012) · QUT ePrints (Queensland University of Technology) · Cited by 219 · see citing works

STAT3 in the Systemic Inflammation of Cancer Cachexia

Zimmers, T., Fishel, M., & Bonetto, A. (2016) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2016.02.009 · Cited by 216 · see citing works

Central nervous system inflammation induces muscle atrophy via activation of the hypothalamic–pituitary–adrenal axis

Braun, T. P., Zhu, X., Szumowski, M., Scott, G. D., Grossberg, A. J., Levasseur, P. R., Graham, K., Khan, S., Damaraju, S., Colmers, W. F., et al. (2011) · Journal of Experimental Medicine · doi:10.1084/jem.20111020 · Cited by 213 · see citing works

Role of Activin A and Myostatin in Human Cancer Cachexia

Loumaye, A., de Barsy, M., Nachit, M., Lause, P., Frateur, L., Maanen, A. G. V., Tréfois, P., Gruson, D., & Thissen, J. (2015) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2014-4318 · Cited by 212 · see citing works

Effect of physical exercise on muscle mass and strength in cancer patients during treatment—a systematic review

Stene, G. B., Helbostad, J. L., Balstad, T. R., Riphagen, I. I., Kaasa, S., & Oldervoll, L. M. (2013) · Critical Reviews in Oncology/Hematology · doi:10.1016/j.critrevonc.2013.07.001 · Cited by 210 · see citing works

Increased length of hospital stay in underweight and overweight patients at hospital admission: a controlled population study

Kyle, U. G., Pirlich, M., Lochs, H. H., Schuetz, T., & Pichard, C. (2005) · Clinical Nutrition · doi:10.1016/j.clnu.2004.08.012 · Cited by 210 · see citing works

Plasma growth differentiation factor 15 is associated with weight loss and mortality in cancer patients: GDF15 in cancer-related weight loss

Lerner, L., Hayes, T. G., Tao, N., Krieger, B., Feng, B., Wu, Z., Nicoletti, R., Chiu, M. I., Gyuris, J., & Garcia, J. M. (2015) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12033 · Cited by 208 · see citing works

Understanding and Managing Cancer Cachexia

Macdonald, N., Easson, A. M., Mazurak, V. C., Dunn, G. P., & Baracos, V. E. (2003) · Journal of the American College of Surgeons · doi:10.1016/s1072-7515(03)00382-x · Cited by 207 · see citing works

Long-term efficacy and safety of dronabinol for acquired immunodeficiency syndrome-associated anorexia

Beal, J. E., OLSON, R. R., Lefkowitz, L. B., Laubenstein, L. J., Bellman, P., Yangco, B. G., Morales, J. O., Murphy, R. L., Powderly, W. G., Plasse, T. F., et al. (1997) · Journal of Pain and Symptom Management · doi:10.1016/s0885-3924(97)00038-9 · Cited by 207 · see citing works

Implementation of Enhanced Recovery After Surgery (ERAS) Across a Provincial Healthcare System: The ERAS Alberta Colorectal Surgery Experience

Nelson, G., Kiyang, L., Crumley, E., Chuck, A., Nguyen, T., Faris, P., Wasylak, T., Basualdo-Hammond, C., McKay, S., Ljungqvist, O., et al. (2016) · World Journal of Surgery · doi:10.1007/s00268-016-3472-7 · Cited by 203 · see citing works

Experimental cancer cachexia induced by transplantable colon 26 adenocarcinoma in mice.

Tanaka, Y., Eda, H., Tanaka, T., Udagawa, T., Ishikawa, T., Horii, I., Ishitsuka, H., KATAOKA, T., & Taguchi, T. (1990) · PubMed · Cited by 198 · see citing works

Cancer anorexia-cachexia syndrome: cytokines and neuropeptides

Ramos, E. J., Suzuki, S., Marks, D. L., Inui, A., Asakawa, A., & Meguid, M. M. (2004) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/01.mco.0000134363.53782.cb · Cited by 196 · see citing works

Taste changes experienced by patients receiving chemotherapy.

Wickham, R. S., Rehwaldt, M., Kefer, C., et al. (1999) · PubMed · Cited by 193 · see citing works

Nutritional enhancement of exercise performance in chronic obstructive pulmonary disease: a randomised controlled trial

STEINER, M. C. (2003) · Thorax · doi:10.1136/thorax.58.9.745 · Cited by 193 · see citing works

Brain regulation of food intake and appetite: molecules and networks

Roberger, C. B. (2005) · Cited by 191 · see citing works

Increased Muscle Proteasome Activity Correlates With Disease Severity in Gastric Cancer Patients

Bossola, M., Muscaritoli, M., Costelli, P., Grieco, G., Bonelli, G., Pacelli, F., Fanelli, F., Doglietto, G., & Baccino, F. (2003) · Annals of Surgery · doi:10.1097/01.sla.0000055225.96357.71 · Cited by 189 · see citing works

The impact of body composition parameters on ipilimumab toxicity and survival in patients with metastatic melanoma

Daly, L. E., Power, D. G., O’Reilly, A., Donnellan, P. P., Cushen, S. J., O’Sullivan, K., Twomey, ‎., Woodlock, D. P., Redmond, H. P., & Ryan, A. M. (2017) · British Journal of Cancer · doi:10.1038/bjc.2016.431 · Cited by 185 · see citing works

Disrupted Skeletal Muscle Mitochondrial Dynamics, Mitophagy, and Biogenesis during Cancer Cachexia: A Role for Inflammation

VanderVeen, B. N., Fix, D. K., & Carson, J. A. (2017) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2017/3292087 · Cited by 182 · see citing works

Study Design and Rationale for the Phase 3 Clinical Development Program of Enobosarm, a Selective Androgen Receptor Modulator, for the Prevention and Treatment of Muscle Wasting in Cancer Patients (POWER Trials)

Crawford, J., Prado, C. M. M., Johnston, M. A., Gralla, R. J., Taylor, R. P., Hancock, M. L., & Dalton, J. T. (2016) · Current Oncology Reports · doi:10.1007/s11912-016-0522-0 · Cited by 178 · see citing works

Cytokines modulate glucose transport in skeletal muscle by inducing the expression of inducible nitric oxide synthase

BÉDARD, S., Marcotte, B., & Marette, A. (1997) · Biochemical Journal · doi:10.1042/bj3250487 · Cited by 175 · see citing works

Pancreatic Cancer as a Model: Inflammatory Mediators, Acute‐phase Response, and Cancer Cachexia

Fearon, K. C. H., Barber, M. D., Falconer, J. S., McMillan, D. C., Ross, J. A., & Preston, T. (1999) · World Journal of Surgery · doi:10.1007/pl00012351 · Cited by 175 · see citing works

Review Article: Exercise, Aging, and Muscle Protein Metabolism

Yarasheski, K. E. (2003) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/58.10.m918 · Cited by 173 · see citing works

Taste and Smell in Disease

Epstein, F. H., & Schiffman, S. S. (1983) · New England Journal of Medicine · doi:10.1056/nejm198306023082207 · Cited by 173 · see citing works

Anticachectic Effects of Formoterol

Busquets, S., Figueras, M. T., Fuster, G., Almendro, V., Moore‐Carrasco, R., Ametller, E., Argilés, J. M. A., & López-Soriano, F. J. (2004) · Cancer Research · doi:10.1158/0008-5472.can-04-0425 · Cited by 167 · see citing works

Dietary evaluation of patients with smell and/or taste disorders

Mattes, R., Cowart, B., Schiavo, M., Arnold, C. D., Garrison, B. S., Kare, M. R., & Lowry, L. (1990) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/51.2.233 · Cited by 166 · see citing works

Nutrition intervention improves outcomes in patients with cancer cachexia receiving chemotherapy?a pilot study

Bauer, J. D., & Capra, S. M. (2004) · Supportive Care in Cancer · doi:10.1007/s00520-004-0746-7 · Cited by 166 · see citing works

Increased muscle ubiquitin mRNA levels in gastric cancer patients.

Bossola, M., Muscaritoli, M., Costelli, P., Bellantone, R., Pacelli, F., Busquets, S., Argilès, J., López-Soriano, F., Civello, I. M., Baccino, F., et al. (2001) · American Journal of Physiology. Regulatory Integrative and Comparative Physiology · doi:10.1152/ajpregu.2001.280.5.r1518 · Cited by 164 · see citing works

Quality of Life in Patients With Advanced Cancer: Differential Association With Performance Status and Systemic Inflammatory Response

Laird, B. J. A., Fallon, M., Hjermstad, M. J., Tuck, S., Kaasa, S., Klepstad, P., & McMillan, D. C. (2016) · Journal of Clinical Oncology · doi:10.1200/jco.2015.65.7742 · Cited by 162 · see citing works

Systematic review of the efficacy of antiemetics in the treatment of nausea in patients with far-advanced cancer

Glare, P. A., Pereira, G., Kristjanson, L. J., Tattersall, M., & Stockler, M. R. (2004) · Supportive Care in Cancer · doi:10.1007/s00520-004-0629-y · Cited by 157 · see citing works

Anti-cachectic effect of ghrelin in nude mice bearing human melanoma cells

Hanada, T., Toshinai, K., Kajimura, N., Nara, N., Tsukada, T., Hayashi, Y., Osuye, K., Kangawa, K., Matsukura, S., & Nakazato, M. (2003) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(02)03028-0 · Cited by 156 · see citing works

The central role of hypothalamic inflammation in the acute illness response and cachexia

Burfeind, K. G., Michaelis, K. A., & Marks, D. L. (2016) · Seminars in Cell & Developmental Biology · doi:10.1016/j.semcdb.2015.10.038 · Cited by 156 · see citing works

An AMP-activated protein kinase–stabilizing peptide ameliorates adipose tissue wasting in cancer cachexia in mice

Rohm, M., Schäfer, M., Laurent, V., Üstünel, B. E., Niopek, K., Algire, C., Hautzinger, O., Sijmonsma, T., Zota, A., Medříková, D., et al. (2016) · Nature Medicine · doi:10.1038/nm.4171 · Cited by 153 · see citing works

Targeting of Fn14 Prevents Cancer-Induced Cachexia and Prolongs Survival

Johnston, A. J., Murphy, K. T., Jenkinson, L., Laine, D., Emmrich, K., Faou, P., Weston, R. T., Jayatilleke, K. M., Schloegel, J., Talbo, G. H., et al. (2015) · Cell · doi:10.1016/j.cell.2015.08.031 · Cited by 152 · see citing works

The neutrophil lymphocyte ratio is associated with breast cancer prognosis: an updated systematic review and meta-analysis

Wei, B., Yao, M., Xing, C., Wang, W., Yao, J., Hong, Y. S., Liu, Y., & Fu, P. (2016) · OncoTargets and Therapy · doi:10.2147/ott.s108419 · Cited by 152 · see citing works

Towards a simple objective framework for the investigation and treatment of cancer cachexia: The Glasgow Prognostic Score

Douglas, E., & McMillan, D. C. (2013) · Cancer Treatment Reviews · doi:10.1016/j.ctrv.2013.11.007 · Cited by 150 · see citing works

Increased expression of proteasome subunits in skeletal muscle of cancer patients with weight loss.

Khal, J., Hine, A., Fearon, K., Dejong, C., & Tisdale, M. (2005) · International Journal of Biochemistry and Cell Biology · doi:10.1016/j.biocel.2004.10.017 · Cited by 150 · see citing works

Why cachexia kills: examining the causality of poor outcomes in wasting conditions

Kalantar‐Zadeh, K., Rhee, C. M., Sim, J. J., Stenvinkel, P., Anker, S. D., & Kovesdy, C. P. (2013) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1007/s13539-013-0111-0 · Cited by 149 · see citing works

Intertwining of Activin A and TGFβ Signaling: Dual Roles in Cancer Progression and Cancer Cell Invasion

Loomans-Kropp, H. A., & Andl, C. D. (2014) · Cancers · doi:10.3390/cancers7010070 · Cited by 148 · see citing works

Establishment and characterization of a novel murine model of pancreatic cancer cachexia

Michaelis, K. A., Zhu, X., Burfeind, K. G., Krasnow, S. M., Levasseur, P. R., Morgan, T. K., & Marks, D. L. (2017) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12225 · Cited by 148 · see citing works

A phase II trial of olanzapine for the prevention of chemotherapy-induced nausea and vomiting: A Hoosier Oncology Group study

Navari, R. M., Einhorn, L. H., Passik, S. D., Loehrer, P. J., Johnson, C. S., Mayer, M. L., McClean, J., Vinson, J., & Pletcher, W. (2005) · Supportive Care in Cancer · doi:10.1007/s00520-004-0755-6 · Cited by 146 · see citing works

Accuracy of survival prediction by palliative radiation oncologists

Chow, E., Davis, L., Panzarella, T., Hayter, C. R. R., Szumacher, E., Loblaw, A., Wong, R. K. S., & Danjoux, C. E. (2005) · International Journal of Radiation Oncology*Biology*Physics · doi:10.1016/j.ijrobp.2004.07.697 · Cited by 145 · see citing works

A multicenter, phase II study of infliximab plus gemcitabine in pancreatic cancer cachexia.

Wiedenmann, B., Malfertheiner, P., Friess, H., Ritch, P. S., Arseneau, J. C., Mantovani, G., Caprioni, F., Cutsem, E. V., Richel, D. J., DeWitte, M., et al. (2008) · PubMed · Cited by 144 · see citing works

A randomized phase III clinical trial of a combined treatment for cachexia in patients with gynecological cancers: Evaluating the impact on metabolic and inflammatory profiles and quality of life

Macciò, A., Madeddu, C., Gramignano, G., Mulas, C., Floris, C., Sanna, E., Cau, M. C., Panzone, F., & Mantovani, G. (2011) · Gynecologic Oncology · doi:10.1016/j.ygyno.2011.12.435 · Cited by 144 · see citing works

Randomized phase III clinical trial of a combined treatment with carnitine + celecoxib ± megestrol acetate for patients with cancer-related anorexia/cachexia syndrome

Madeddu, C., Dessì, M., Panzone, F., Serpe, R., Antoni, G., Cau, M. C., Montaldo, L., Mela, Q., Mura, M., Astara, G., et al. (2011) · Clinical Nutrition · doi:10.1016/j.clnu.2011.10.005 · Cited by 144 · see citing works

The pivotal role of cytokines in muscle wasting during cancer

Argilés, J. M. A., Busquets, S., & López-Soriano, F. J. (2005) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2005.03.014 · Cited by 142 · see citing works

Mechanism of muscle protein degradation induced by a cancer cachectic factor

Lorite, M., Thompson, M., Drake, J. L., et al. (1998) · British Journal of Cancer · doi:10.1038/bjc.1998.592 · Cited by 142 · see citing works

Neuropeptide Y, α-melanocyte–stimulating hormone, and monoamines in food intake regulation

Ramos, E. J. B., Meguid, M. M., Campos, A. C. L., & Coelho, J. C. U. (2005) · Nutrition · doi:10.1016/j.nut.2004.06.021 · Cited by 142 · see citing works

Nutritional Assessment in Cancer: Comparing the Mini-Nutritional Assessment (MNA) With the Scored Patient-Generated Subjective Global Assessment (PGSGA)

Read, J. A., Crockett, N., Volker, D. H., MacLennan, P., Choy, S. T. B., Beale, P. J., & Clarke, S. J. (2005) · Nutrition and Cancer · doi:10.1207/s15327914nc5301_6 · Cited by 141 · see citing works

Body Composition as a Prognostic Factor of Neoadjuvant Chemotherapy Toxicity and Outcome in Patients with Locally Advanced Gastric Cancer

Palmela, C., Velho, S., Agostinho, L., Branco, F., Santos, M., Santos, M. P. C., Oliveira, M. H., Strecht, J., Maio, R., Cravo, M. L., et al. (2017) · Journal of the Korean Gastric Cancer Association · doi:10.5230/jgc.2017.17.e8 · Cited by 141 · see citing works

STAT3 promotes IFNγ/TNFα‐induced muscle wasting in an NF‐κB‐dependent and IL‐6‐independent manner

Ma, J. F., Sánchez, B. J., Hall, D. T., Tremblay, A. K., Marco, S. D., & Gallouzi, I. (2017) · EMBO Molecular Medicine · doi:10.15252/emmm.201607052 · Cited by 135 · see citing works

Protein breakdown in cancer cachexia

Sandri, M. (2016) · Seminars in Cell & Developmental Biology · doi:10.1016/j.semcdb.2015.11.002 · Cited by 134 · see citing works

Reversal of COPD-Associated Weight Loss Using the Anabolic Agent Oxandrolone

Yeh, S., DeGuzman, B., & Kramer, T. (2002) · CHEST Journal · doi:10.1378/chest.122.2.421 · Cited by 131 · see citing works

Key determinants of energy expenditure in cancer and implications for clinical practice

Purcell, S. A., Elliott, S. A., Baracos, V. E., Chu, Q. S.-C., & Prado, C. M. M. (2016) · European Journal of Clinical Nutrition · doi:10.1038/ejcn.2016.96 · Cited by 131 · see citing works

Nutritional Advice in Older Patients at Risk of Malnutrition during Treatment for Chemotherapy: A Two-Year Randomized Controlled Trial

Bourdel‐Marchasson, I., Blanc-Bisson, C., Doussau, A., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0108687 · Cited by 129 · see citing works

Body Mass index and Colon Cancer in a National Sample of Adult US Men and Women

Ford, E. S. (1999) · American Journal of Epidemiology · doi:10.1093/oxfordjournals.aje.a010018 · Cited by 125 · see citing works

Induction of cachexia in mice by a product isolated from the urine of cachectic cancer patients

Cariuk, P., Lorite, M., Todorov, P. T., et al. (1997) · British Journal of Cancer · doi:10.1038/bjc.1997.433 · Cited by 125 · see citing works

Plasma Concentration of Total Leptin and Human Lung-Cancer-Associated Cachexia

Simons, J., Schols, A. M. W. J., Campfield, L. A., Wouters, E. F. �., & Saris, W. H. M. (1997) · Clinical Science · doi:10.1042/cs0930273 · Cited by 123 · see citing works

Skeletal Muscle Inflammation and Nitric Oxide in Patients with COPD

Montes de Oca, M., Torres, S. H., De Sanctis, J., Mata, A., Hernández, N., & Tálamo, C. (2005) · European Respiratory Journal · doi:10.1183/09031936.05.00107404 · Cited by 123 · see citing works

A Double-Blind, Crossover Study of Controlled-Release Metoclopramide and Placebo for the Chronic Nausea and Dyspepsia of Advanced Cancer

Bruera, E. D., Belzile, M., Neumann, C. M., Harsanyi, Z., Babul, N., & Darke, A. C. (2000) · Journal of Pain and Symptom Management · doi:10.1016/s0885-3924(00)00138-x · Cited by 123 · see citing works

Role of TNF receptor 1 in protein turnover during cancer cachexia using gene knockout mice

Llovera, M., Garcia‐Martínez, C., López‐Soriano, J., Carbó, N., Agell, N., López-Soriano, F. J., & Argilés, J. M. A. (1998) · Molecular and Cellular Endocrinology · doi:10.1016/s0303-7207(98)00105-1 · Cited by 120 · see citing works

Evidence that long-term COX-treatment improves energy homeostasis and body composition in cancer patients with progressive cachexia

Lundholm, K., Daneryd, P., Körner, U., Hyltander, A. G., & Bosaeus, I. G. (2004) · International Journal of Oncology · doi:10.3892/ijo.24.3.505 · Cited by 119 · see citing works

The pathogenesis and treatment of cardiac atrophy in cancer cachexia

Murphy, K. T. (2015) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00720.2015 · Cited by 115 · see citing works

Psychosocial Effects of Cancer Cachexia: A Systematic Literature Search and Qualitative Analysis

Oberholzer, R., Hopkinson, J. B., Baumann, K., Omlin, A. G., Kaasa, S., Fearon, K. C. H., & Strasser, F. (2012) · Journal of Pain and Symptom Management · doi:10.1016/j.jpainsymman.2012.06.020 · Cited by 114 · see citing works

Muscle atrophy in experimental cancer cachexia: Is the IGF‐1 signaling pathway involved?

Penna, F., Bonetto, A., Muscaritoli, M., Costamagna, D., Minero, V. G., Bonelli, G., Fanelli, F., Baccino, F., & Costelli, P. (2010) · International Journal of Cancer · doi:10.1002/ijc.25146 · Cited by 111 · see citing works

Regulation of Protein Catabolism by Muscle-Specific and Cytokine-Inducible Ubiquitin Ligase E3α-II during Cancer Cachexia

Kwak, K. S., Zhou, X., Solomon, V., Baracos, V. E., Davis, J. G., Bannon, A. W., Boyle, W. J., Lacey, D. L., & Han, H. Q. (2004) · Cancer Research · doi:10.1158/0008-5472.can-04-2102 · Cited by 111 · see citing works

Increased frequency ofATM mutations in breast carcinoma patients with early onset disease and positive family history

Teraoka, S. N., Malone, K. E., Doody, D. R., Suter, N. M., Ostrander, E. A., Daling, J. R., & CONCANNON, P. J. (2001) · Cancer · doi:10.1002/1097-0142(20010801)92:3 · Cited by 111 · see citing works

Aggressive pharmacological treatment for reversing malignant bowel obstruction

Mercadante, S., Ferrera, P., Villari, P., et al. (2004) · Journal of Pain and Symptom Management · doi:10.1016/j.jpainsymman.2004.01.007 · Cited by 111 · see citing works

Interleukin‐15 is able to suppress the increased DNA fragmentation associated with muscle wasting in tumour‐bearing rats

Figueras, M., Busquets, S., Carbó, N., Barreiro, E., Almendro, V., Argilés, J. M. A., & López-Soriano, F. J. (2004) · FEBS Letters · doi:10.1016/j.febslet.2004.05.066 · Cited by 108 · see citing works

Compliance with nutrition prescription improves outcomes in patients with unresectable pancreatic cancer

Bauer, J. D., Capra, S. M., Battistutta, D., DAVIDSON, W., & Ash, S. (2005) · Clinical Nutrition · doi:10.1016/j.clnu.2005.07.002 · Cited by 106 · see citing works

Cognitive and mood disturbance as causes and symptoms of fatigue in cancer patients

Valentine, A. D., & Meyers, C. A. (2001) · Cancer · doi:10.1002/1097-0142(20010915)92:6+ · Cited by 106 · see citing works

Skeletal muscle anabolism is a side effect of therapy with the MEK inhibitor: selumetinib in patients with cholangiocarcinoma

Prado, C. M. M., Bekaii‐Saab, T., Doyle, L. A., Shrestha, S., Ghosh, S., Baracos, V. E., & Sawyer, M. B. (2012) · British Journal of Cancer · doi:10.1038/bjc.2012.144 · Cited by 105 · see citing works

Update on anorexia and cachexia

Strasser, F., & Bruera, E. D. (2002) · Hematology/Oncology Clinics of North America · doi:10.1016/s0889-8588(02)00011-4 · Cited by 105 · see citing works

Psychosocial impact of cancer cachexia

Hopkinson, J. B. (2014) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1007/s13539-014-0142-1 · Cited by 105 · see citing works

Request for regulatory guidance for cancer cachexia intervention trials

Fearon, K. C. H., Argilés, J. M. A., Baracos, V., Bernabei, R., Coats, A., Crawford, J., Deutz, N. E. P., Doehner, W., Evans, W. J., Ferrucci, L., et al. (2015) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12083 · Cited by 105 · see citing works

Pulmonary cachexia, systemic inflammatory profile, and the interleukin 1β −511 single nucleotide polymorphism

Broekhuizen, R., Grimble, R. F., Howell, W. M., Shale, D. J., Creutzberg, E. C., Wouters, E. F. �., & Schols, A. M. W. J. (2005) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/82.5.1059 · Cited by 104 · see citing works

Chronic heart failure: an example of a systemic chronic inflammatory disease resulting in cachexia

Conraads, V. M., Bosmans, J. M., & Vrints, C. J. (2002) · International Journal of Cardiology · doi:10.1016/s0167-5273(02)00232-2 · Cited by 103 · see citing works

Mediation of anorexia by human recombinant tumor necrosis factor through a peripheral action in the rat.

Bodnar, R. J., Pasternak, G. W., Mann, P. E., Paúl, D., Warren, R. S., & Donner, D. B. (1989) · PubMed · Cited by 102 · see citing works

Relation between hypermetabolism, cachexia, and survival in cancer patients: a prospective study in 390 cancer patients before initiation of anticancer therapy ,

Vazeille, C., Jouinot, A., Durand, J.-P., Neveux, N., Boudou, P., Huillard, O., Alexandre, J., Cynober, L., & Goldwasser, F. (2017) · American Journal of Clinical Nutrition · doi:10.3945/ajcn.116.140434 · Cited by 102 · see citing works

Dexamethasone in addition to metoclopramide for chronic nausea in patients with advanced cancer: a randomized controlled trial.

Bruera, E., Moyano, J. R., Sala, R., Rico, M. A., Bosnjak, S., Bertolino, M., Willey, J., Strasser, F., & Palmer, J. L. (2004) · Journal of Pain and Symptom Management · doi:10.1016/j.jpainsymman.2004.01.009 · Cited by 101 · see citing works

The Regulation of Feeding and Metabolic Rate and the Prevention of Murine Cancer Cachexia with a Small-Molecule Melanocortin-4 Receptor Antagonist

Markison, S., Foster, A. C., Chen, C., Brookhart, G., Hesse, A., Hoare, S. R. J., Fleck, B. A., Brown, B. T., & Marks, D. L. (2005) · Endocrinology · doi:10.1210/en.2005-0142 · Cited by 100 · see citing works

Systemic inflammation in COPD visualised by gene profiling in peripheral blood neutrophils

Oudijk, E. D. (2005) · Thorax · doi:10.1136/thx.2004.034009 · Cited by 95 · see citing works

Molecular pathways leading to loss of skeletal muscle mass in cancer cachexia – can findings from animal models be translated to humans?

Mueller, T. C., Bachmann, J., Prokopchuk, O., Friess, H., & Martignoni, M. E. (2016) · BMC Cancer · doi:10.1186/s12885-016-2121-8 · Cited by 95 · see citing works

High anabolic potential of essential amino acid mixtures in advanced nonsmall cell lung cancer

ENGELEN, M. P. K. J., Safar, A. M., Bartter, T., Koeman, F., & Deutz, N. E. P. (2015) · Annals of Oncology · doi:10.1093/annonc/mdv271 · Cited by 95 · see citing works

Pathophysiology of cancer cachexia: current understanding and areas for future research.

DeWys, W. D. (1982) · PubMed · Cited by 94 · see citing works

Effects of Muscle Strength Training and Testosterone in Frail Elderly Males

Sullivan, D. H., Roberson, P. K., Johnson, L. E., Bishara, O., Evans, W. J., Smith, E. S., & PRICE, J. A. (2005) · Medicine & Science in Sports & Exercise · doi:10.1249/01.mss.0000181840.54860.8b · Cited by 94 · see citing works

Clinical Classification of Cancer Cachexia: Phenotypic Correlates in Human Skeletal Muscle

Johns, N., Hatakeyama, S., Stephens, N. A., Degen, M., Degen, S., Frieauff, W., Lambert, C., Ross, J. A., Roubenoff, R., Glass, D. J., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0083618 · Cited by 94 · see citing works

Lipolysis and lipid oxidation in weight-losing cancer patients and healthy subjects

Leeuwen, S. D. Z.-V., van den Berg, J. W. O., Wattimena, J. L. D., et al. (2000) · Metabolism · doi:10.1053/meta.2000.6740 · Cited by 94 · see citing works

Preclinical Investigation of the Novel Histone Deacetylase Inhibitor AR-42 in the Treatment of Cancer-Induced Cachexia

Tseng, Y., Kulp, S. K., Lai, I., Hsu, E., He, W., Frankhouser, D. E., Yan, P. S., Mo, X. M., Bloomston, M., Lesinski, G. B., et al. (2015) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/djv274 · Cited by 94 · see citing works

Cytokines and endotoxin induce cytokine receptors in skeletal muscle

Zhang, Y., Pilon, G., Marette, A., & Baracos, V. E. (2000) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.2000.279.1.e196 · Cited by 94 · see citing works

Clinical determinants of weight loss in patients receiving radiation and chemoirradiation for head and neck cancer: A prospective longitudinal view

Kubrak, C., Olson, K. L., Jha, N., Scrimger, R. A., Parliament, M. B., McCargar, L. J., Koski, S. L., & Baracos, V. E. (2012) · Head & Neck · doi:10.1002/hed.23023 · Cited by 93 · see citing works

Suppression of Skeletal Muscle Turnover in Cancer Cachexia: Evidence from the Transcriptome in Sequential Human Muscle Biopsies

Gallagher, I. J., Stephens, N. A., MacDonald, A. J., Skipworth, R. J. E., Husi, H., Greig, C. A., Ross, J. A., Timmons, J. A., & Fearon, K. C. H. (2012) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-11-2133 · Cited by 93 · see citing works

Abnormalities of chromosome 1 in myeloproliferative disorders

Rowley, J. D. (1975) · Cancer · doi:10.1002/1097-0142(197511)36:5 · Cited by 92 · see citing works

Small RNAome profiling from human skeletal muscle: novel miRNAs and their targets associated with cancer cachexia

Narasimhan, A., Ghosh, S., Stretch, C., Greiner, R., Bathe, O. F., Baracos, V. E., & Damaraju, S. (2017) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12168 · Cited by 92 · see citing works

Sarcopenia

Cruz-Jentoft, A. J., & Sayer, A. A. (2019) · The Lancet · doi:10.1016/s0140-6736(19)31138-9 · Cited by 3,905 · see citing works

Exercise Guidelines for Cancer Survivors: Consensus Statement from International Multidisciplinary Roundtable

CAMPBELL, K. L., WINTERS-STONE, K. M., WISKEMANN, J., MAY, A. M., SCHWARTZ, A. L., COURNEYA, K. S., ZUCKER, D. S., MATTHEWS, C. E., LIGIBEL, J. A., GERBER, L. H., et al. (2019) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000002116 · Cited by 2,988 · see citing works

GDF15: a hormone conveying somatic distress to the brain

Lockhart, S. M., Saudek, V., & O’Rahilly, S. (2020) · Endocrine Reviews · doi:10.1210/endrev/bnaa007 · Cited by 256 · see citing works

Metastatic cancers promote cachexia through ZIP14 upregulation in skeletal muscle

Wang, G., Biswas, A. K., Ma, W., Kandpal, M., Coker, C., Grandgenett, P. M., Hollingsworth, M. A., Jain, R., Tanji, K., Lόpez-Pintado, S., et al. (2018) · Nature Medicine · doi:10.1038/s41591-018-0054-2 · Cited by 188 · see citing works

Klebsiella oxytoca expands in cancer cachexia and acts as a gut pathobiont contributing to intestinal dysfunction

Pötgens, S. A., Brossel, H., Sboarina, M., Catry, E., Cani, P. D., Neyrinck, A. M., Delzenne, N. M., & Bindels, L. B. (2018) · Scientific Reports · doi:10.1038/s41598-018-30569-5 · Cited by 114 · see citing works

PPARβ/δ: linking metabolism to regeneration

Magadum, A., & Engel, F. B. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19072013 · Cited by 110 · see citing works

DNA Double-Strand Break Accumulation in Alzheimer’s Disease: Evidence from Experimental Models and Postmortem Human Brains

Thadathil, N., Delotterie, D. F., Xiao, J., Hori, R., McDonald, M. P., & Khan, M. M. (2021) · Molecular Neurobiology · doi:10.1007/s12035-020-02109-8 · Cited by 94 · see citing works

Skeletal muscle fibrosis in pancreatic Cancer patients with respect to survival

Judge, S. M., Nosacka, R. L., Delitto, D., Gerber, M. H., Cameron, M. E., Trevino, J. G., & Judge, A. R. (2018) · JNCI Cancer Spectrum · doi:10.1093/jncics/pky043 · Cited by 91 · see citing works

Skeletal muscle atrogenes: From rodent models to human pathologies

Taillandier, D., & Polge, C. (2019) · Biochimie · doi:10.1016/j.biochi.2019.07.014 · Cited by 66 · see citing works

The Toll-Like Receptor/MyD88/XBP1 Signaling Axis Mediates Skeletal Muscle Wasting during Cancer Cachexia

Bohnert, K. R., Goli, P., Roy, A., Sharma, A. K., Xiong, G., Gallot, Y. S., & Kumar, A. (2019) · Molecular and Cellular Biology · doi:10.1128/mcb.00184-19 · Cited by 52 · see citing works

Interleukin-17 as a key player in neuroimmunometabolism

Douglas, A., Stevens, B., & Lynch, L. (2023) · Nature Metabolism · doi:10.1038/s42255-023-00846-3 · Cited by 49 · see citing works

Cryptotanshinone Prevents Muscle Wasting in CT26-Induced Cancer Cachexia through Inhibiting Stat3 Signaling Pathway

Chen, L., Yang, Q., Zhang, H., Wan, L., Xin, B., Cao, Y., Zhang, J., & Guo, C. (2020) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2020.113066 · Cited by 39 · see citing works

Virtual reality-empowered deep-learning analysis of brain cells

Kaltenecker, D., Al-Maskari, R., Negwer, M., Hoeher, L., Kofler, F., Zhao, S., Todorov, M., Rong, Z., Paetzold, J. C., Wiestler, B., et al. (2024) · Nature Methods · doi:10.1038/s41592-024-02245-2 · Cited by 38 · see citing works

The Extract of Arctium lappa L. Fruit (Arctii Fructus) Improves Cancer-Induced Cachexia by Inhibiting Weight Loss of Skeletal Muscle and Adipose Tissue

Han, Y.-H., Mun, J.-G., Jeon, H. D., Yoon, D. H., Choi, B.-M., Kee, J.-Y., & Hong, S.-H. (2020) · Nutrients · doi:10.3390/nu12103195 · Cited by 24 · see citing works

Skeletal Muscle–Adipose Tissue–Tumor Axis: Molecular Mechanisms Linking Exercise Training in Prostate Cancer

Rocha-Rodrigues, S., Matos, A., Afonso, J., Mendes-Ferreira, M., Abade, E., Teixeira, E., Silva, B., Murawska-Ciałowicz, E., Oliveira, M. J., & Ribeiro, R. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22094469 · Cited by 17 · see citing works

Differential effects of adrenocorticotropic hormone on human and mouse adipose tissue

Kiwaki, K., & Levine, J. A. (2003) · Journal of Comparative Physiology B · doi:10.1007/s00360-003-0377-1 · Cited by 28 · see citing works

[Pathophysiology of lipolysis in human adipose tissue (author's transl)].

Lisch, H. ‐. (1977) · PubMed

LIPOLYSIS:Contribution from Regional Fat

Jensen, M. D. (1997) · Annual Review of Nutrition · doi:10.1146/annurev.nutr.17.1.127 · Cited by 157 · see citing works

The Lipolytic Responsiveness to Endotoxin in Subcutaneous Adipose Tissue is Greater than Mesenteric Adipose Tissue

Sugawara, K., Miyata, G., Shineha, R., & Satomi, S. (2003) · The Tohoku Journal of Experimental Medicine · doi:10.1620/tjem.199.171 · Cited by 10 · see citing works

Effect of the hypophyseal preparation adiposin on the lipolytic activity of adipose tissue and on the serum concentration of free higher fatty acids

Leites, S., & Davtyan, N. K. (1964) · Bulletin of Experimental Biology and Medicine · doi:10.1007/bf00784410 · Cited by 1 · see citing works