The Fas Death Factor

Lymphoproliferation disorder in mice explained by defects in Fas antigen that mediates apoptosis

Watanabe‐Fukunaga, R., Brannan, C., Copeland, N., Jenkins, N., & Nagata, S. (1992) · Nature · doi:10.1038/356314a0 · Cited by 3,153

The polypeptide encoded by the cDNA for human cell surface antigen Fas can mediate apoptosis

Itoh, N., Yonehara, S., Ishii, A., Yonehara, M., Mizushima, S.-I., Sameshima, M., Hase, A., Seto, Y., & Nagata, S. (1991) · Cell · doi:10.1016/0092-8674(91)90614-5 · Cited by 2,736

Social controls on cell survival and cell death

RAFF, M. C. (1992) · Nature · doi:10.1038/356397a0 · Cited by 2,591

Molecular cloning and expression of the fas ligand, a novel member of the tumor necrosis factor family

Suda, T., Takahashi, T., Golstein, P., & Nagata, S. (1993) · Cell · doi:10.1016/0092-8674(93)90326-l · Cited by 2,494

Site-restricted persistent cytomegalovirus infection after selective long-term depletion of CD4+ T lymphocytes.

Jonjić, S., Mutter, W., Weiland, F., Reddehase, M. J., & Koszinowski, U. H. (1989) · The Journal of Experimental Medicine · doi:10.1084/jem.169.4.1199 · Cited by 2,106

The TNF receptor superfamily of cellular and viral proteins: Activation, costimulation, and death

Smith, C. A., Farrah, T., & Goodwin, R. G. (1994) · Cell · doi:10.1016/0092-8674(94)90372-7 · Cited by 1,909

Lethal effect of the anti-Fas antibody in mice

Ogasawara, J., Watanabe-Fukunaga, R., Adachi, M., Matsuzawa, A., Kasugai, T., Kitamura, Y., Itoh, N., Suda, T., & Nagata, S. (1993) · Nature · doi:10.1038/364806a0 · Cited by 1,881

Autocrine T-cell suicide mediated by APO-1/(Fas/CD95)

Dhein, J., Walczak, H., Bäumler, C., Debatin, K., & Krammer, P. (1995) · Nature · doi:10.1038/373438a0 · Cited by 1,814

Cytotoxicity mediated by T cells and natural killer cells is greatly impaired in perforin-deficient mice

Kägi, D., Ledermann, B., Bürki, K., Seiler, P. J., Odermatt, B., Olsen, K. J., Podack, E. R., Zinkernagel, R. M., & Hengartner, H. (1994) · Nature · doi:10.1038/369031a0 · Cited by 1,758

Monoclonal Antibody-Mediated Tumor Regression by Induction of Apoptosis

Trauth, B. C., Klas, C., Peters, A. M. J., Matzku, S., Mӧller, P., Falk, W., Debatin, K., & Krammer, P. H. (1989) · Science · doi:10.1126/science.2787530 · Cited by 1,716

Activation-induced cell death in T cells and autoimmunity.

JianZhang, XuemeiXu, & YongLiu (2004) · PubMed · Cited by 95

Intracellular survival pathways in the liver

Luedde, T., & Trautwein, C. (2006) · Liver International · doi:10.1111/j.1478-3231.2006.01366.x · Cited by 95

Roles of Fas and Fas ligand during mammary gland remodeling

Song, J. H., Sapi, E., Brown, W., Nilsen, J., Tartaro, K. R., Kacinski, B. M., Craft, J. E., Naftolin, F. N., & Mor, G. (2000) · Journal of Clinical Investigation · doi:10.1172/jci10411 · Cited by 95

Mechanisms of Immune Regulation in the Peripheral Nervous System

Gold, R., Archelos, J. J., & Hartung, H. (1999) · Brain Pathology · doi:10.1111/j.1750-3639.1999.tb00231.x · Cited by 95

Shaping limbs by apoptosis>

Chen, Y., & Zhao, X. (1998) · Journal of Experimental Zoology · doi:10.1002/(sici)1097-010x(19981215)282:6 · Cited by 95

Gallic Acid Induces Apoptosis in 3T3-L1 Pre-adipocytes via a Fas- and Mitochondrial-Mediated Pathway

Hsu, C., Lo, W.-H., & Yen, G. (2007) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf071223c · Cited by 94

High levels of osteopontin associated with polymorphisms in its gene are a risk factor for development of autoimmunity/lymphoproliferation

Chiocchetti, A. (2003) · Blood · doi:10.1182/blood-2003-05-1748 · Cited by 94

Repression of IFN Regulatory Factor 8 by DNA Methylation Is a Molecular Determinant of Apoptotic Resistance and Metastatic Phenotype in Metastatic Tumor Cells

Yang, D., Thangaraju, M., Greeneltch, K. M., Browning, D. D., Schoenlein, P. V., Tamura, T., Ozato, K., Ganapathy, V., Abrams, S. I., & Liu, K. (2007) · Cancer Research · doi:10.1158/0008-5472.can-06-4068 · Cited by 94

Necrosis Is an Active and Controlled Form of Programmed Cell Death

Proskuryakov, S. Y., Gabai, V. L., & Konoplyannikov, A. (2002) · Biochemistry (Moscow) · doi:10.1023/a:1015289521275 · Cited by 94

Localization of the Th2 Cytokines IL‐3, IL‐4, IL‐10 at the Fetomaternal Interface During Human and Murine Pregnancy and Lack of Requirement for Fas/Fas Ligand Interaction for a Successful Allogeneic Pregnancy

Chaouat, G., Cayol, V., Mairovitz, V., & Dubanchet, S. (1999) · American Journal of Reproductive Immunology · doi:10.1111/j.1600-0897.1999.tb00459.x · Cited by 94

Neutrophils induce apoptosis of lung epithelial cells via release of soluble Fas ligand

Serrao, K. L., Fortenberry, J. D., Owens, M. L., Harris, F. L., & Brown, L. A. S. (2001) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.2001.280.2.l298 · Cited by 94

Ionizing radiation sensitizes erythroleukemic cells but not normal erythroblasts to tumor necrosis factor–related apoptosis-inducing ligand (TRAIL)–mediated cytotoxicity by selective up-regulation of TRAIL-R1

Pietro, R. D., Secchiero, P., Rana, R., Gibellini, D., Visani, G., Bemis, K., Zamai, L., Miscia, S., & Zauli, G. (2001) · Blood · doi:10.1182/blood.v97.9.2596 · Cited by 94

Novel Fas (CD95/APO-1) mutations in infants with a lymphoproliferative disorder.

Kasahara, Y., Wada, T., Niida, Y., Yachie, A., Seki, H., Ishida, Y., Sakai, T., Koizumi, F., Koizumi, S., Miyawaki, T., et al. (1998) · International Immunology · doi:10.1093/intimm/10.2.195 · Cited by 94

Immunolocalization of the apoptosis regulating proteins Bcl-2 and Bax in human endometrium and isolated peritoneal fluid macrophages in endometriosis

McLaren, J. F., Prentice, A., Jones, D. S., Sharkey, A., & Smith, S. K. (1997) · Human Reproduction · doi:10.1093/humrep/12.1.146 · Cited by 94

Apoptosis in the rheumatic diseases

Vaishnaw, A. K., McNally, J., & Elkon, K. B. (1997) · Arthritis & Rheumatism · doi:10.1002/art.1780401102 · Cited by 94

Neutrophils in Tissue Injury and Repair: Molecular Mechanisms and Therapeutic Targets

Yang, L., Shi, F., Cao, F., Wang, L., She, J., He, B., Xu, X., Kong, L., & Cai, B. (2025) · MedComm · doi:10.1002/mco2.70184 · Cited by 100

Apoptosis of testicular germ cells induced by exogenous glucocorticoid in rats

Yazawa, H., Sasagawa, I., & Nakada, T. (2000) · Human Reproduction · doi:10.1093/humrep/15.9.1917 · Cited by 93

Cryptosporidium parvuminduces apoptosis in biliary epithelia by a Fas/Fas ligand-dependent mechanism

Chen, X., Gores, G. J., Payá, C. V., & LaRusso, N. F. (1999) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1999.277.3.g599 · Cited by 93

Modulation of Human Neutrophil Apoptosis by Immune Complexes

Gamberale, R., Giordano, M., Trevani, A. S., Andonegui, G., & Geffner, J. R. (1998) · The Journal of Immunology · doi:10.4049/jimmunol.161.7.3666 · Cited by 93

Genetic basis of systemic lupus erythematosus

Vyse, T. J., & Kotzin, B. L. (1996) · Current Opinion in Immunology · doi:10.1016/s0952-7915(96)80014-8 · Cited by 93

Does innate immune privilege exist?

Streilein, J. W., & Stein‐Streilein, J. (2000) · Journal of Leukocyte Biology · doi:10.1002/jlb.67.4.479 · Cited by 93

Fas ligand, Fas antigen and Bcl-2 expression in human endometrium during the menstrual cycle

Yamashita, H. (1999) · Molecular Human Reproduction · doi:10.1093/molehr/5.4.358 · Cited by 93

Immunochemotherapy of malignant glioma: synergistic activity of CD95 ligand and chemotherapeutics

Roth, W., Fontana, A., Trepel, M., Reed, J. C., DICHGANS, J., & Weller, M. (1997) · Cancer Immunology Immunotherapy · doi:10.1007/s002620050355 · Cited by 93

True

Das, H., Koizumi, T., Sugimoto, T., Chakraborty, S., Nishimura, R., Ichimura, T., & Hasegawa, K. (2000) · British Journal of Cancer · doi:10.1054/bjoc.2000.1118 · Cited by 92

Expression of Fas Receptor on Disc Cells in Herniated Lumbar Disc Tissue

Park, J., Kim, K.-W., Han, C. W., & Chang, H. (2001) · Spine · doi:10.1097/00007632-200101150-00006 · Cited by 92

An introduction to death receptors in apoptosis

Kumar, R., Herbert, P. E., & Warrens, A. Ν. (2005) · International Journal of Surgery · doi:10.1016/j.ijsu.2005.05.002 · Cited by 92

Roles of IL-1 in the development of rheumatoid arthritis: consideration from mouse models

Iwakura, Y. (2002) · Cytokine & Growth Factor Reviews · doi:10.1016/s1359-6101(02)00021-7 · Cited by 95

Augmented Intracellular Glutathione Inhibits Fas-Triggered Apoptosis of Activated Human Neutrophils

Watson, R. W. G., Rotstein, O. D., Jimenez, M. F., Parodo, J. C., & Marshall, J. C. (1997) · Blood · doi:10.1182/blood.v89.11.4175 · Cited by 93

Apoptosis in liver disease

Galle, P. R. (1997) · Journal of Hepatology · doi:10.1016/s0168-8278(97)80189-4 · Cited by 92

Fas and Fas Ligand are associated with neuritic degeneration in the AD brain and participate in β-amyloid-induced neuronal death

Su, J. H., Anderson, A. J., Cribbs, D. H., Tu, C. H., Tong, L., Kesslak, P. J., & Cotman, C. W. (2003) · Neurobiology of Disease · doi:10.1016/s0969-9961(02)00019-0 · Cited by 91

Extracellular matrix interacts with soluble CD95L: Retention and enhancement of cytotoxicity

Aoki, K., Kurooka, M., Chen, J., Petryniak, J., Nabel, E. G., & Nabel, G. J. (2001) · Nature Immunology · doi:10.1038/86336 · Cited by 91

Apoptosis and the cell cycle

Fotedar, R., Diederich, L., & Fotedar, A. (1996) · Springer eBooks · doi:10.1007/978-1-4615-5873-6_15 · Cited by 91

Resistance to Fas-Mediated T Cell Apoptosis in Asthma

Jayaraman, S., Castro, M., O’Sullivan, M. P., Bragdon, M. J., & Holtzman, M. J. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.162.3.1717 · Cited by 91

Essential role of active nuclear transport in apoptosis

Yasuhara, N., Eguchi, Y., Tachibana, T., Imamoto, N., Yoneda, Y., & Tsujimoto, Y. (1997) · Genes to Cells · doi:10.1046/j.1365-2443.1997.1010302.x · Cited by 91

Empirical identification and validation of tumor-targeting T cell receptors from circulation using autologous pancreatic tumor organoids

Meng, Q., Xie, S., Gray, G. K., Dezfulian, M. H., Gandarilla, O., Li, W., Huang, L., Akshinthala, D., Ferrer, E., Conahan, C., et al. (2021) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2021-003213 · Cited by 90

A Pathogenic Role of IL-12 in Blood-Stage Murine Malaria Lethal Strain Plasmodium berghei NK65 Infection

Yoshimoto, T., Takahama, Y., Wang, C., Yoneto, T., Waki, S., & Nariuchi, H. (1998) · The Journal of Immunology · doi:10.4049/jimmunol.160.11.5500 · Cited by 90

Activation of the Fas pathway independently of Fas ligand during apoptosis induced by camptothecin in p53 mutant human colon carcinoma cells

Shao, R., Cao, C.-X., Nieves‐Neira, W., Dimanche‐Boitrel, M., Solary, É., & Pommier, Y. G. (2001) · Oncogene · doi:10.1038/sj.onc.1204264 · Cited by 90

Frequent loss of Fas expression and function in human lung tumours with overexpression of FasL in small cell lung carcinoma

Viard, I., Veyrenc, S., French, L. E., Brambilla, C., & Brambilla, E. M. (2003) · The Journal of Pathology · doi:10.1002/path.1428 · Cited by 90

Morphine promotes Jurkat cell apoptosis through pro-apoptotic FADD/P53 and anti-apoptotic PI3K/Akt/NF-κB pathways

Yin, D., Woodruff, M. L., Zhang, Y., Whaley, S., Miao, J., Ferslew, K. E., Zhao, J., & Stuart, C. (2006) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2006.02.001 · Cited by 90

Pacing-induced heart failure: a model to study the mechanism of disease progression and novel therapy in heart failure

Moe, G. W. P. L. (1999) · Cardiovascular Research · doi:10.1016/s0008-6363(99)00032-2 · Cited by 90

Regulation of Fas Ligand Expression by Estradiol and Progesterone in Human Endometrium1

Selam, B., Kayisli, U. A., Mülayim, N., & Arici, A. M. (2001) · Biology of Reproduction · doi:10.1095/biolreprod65.4.979 · Cited by 90

The IFN Regulatory Factor Family Participates in Regulation of Fas Ligand Gene Expression in T Cells

Chow, W. A., Fang, J., & Yee, J. (2000) · The Journal of Immunology · doi:10.4049/jimmunol.164.7.3512 · Cited by 90

Radiation-Induced Apoptosis in Human Lymphocytes and Lymphoma Cells Critically Relies on the Up-Regulation of CD95/Fas/APO-1 Ligand

Belka, C., Marini, P., Budach, W., Schulze‐Osthoff, K., Lang, F. J. W., Gulbins, E., & BAMBERG, M. (1998) · Radiation Research · doi:10.2307/3579905 · Cited by 90

Elevated levels of biologically active soluble CD40 ligand in the serum of patients with chronic lymphocytic leukaemia

Younes, A., Snell, V., Consoli, U., Clodi, K., Zhao, S., Palmer, J. L., Thomas, E. K., Armitage, R. J., & Andreeff, M. (1998) · British Journal of Haematology · doi:10.1046/j.1365-2141.1998.00522.x · Cited by 90

Increased apoptosis of bone marrow CD34+ cells and impaired function of bone marrow stromal cells in patients with systemic lupus erythematosus

Papadaki, H. Α., Boumpas, D. T., Gibson, F. M., Jayne, D. R. W., Axford, J. S., Gordon‐Smith, E. C., Marsh, J. C. W., & Eliopoulos, G. D. (2001) · British Journal of Haematology · doi:10.1046/j.1365-2141.2001.03076.x · Cited by 90

The tumor microenvironment: focus on myeloma

Dalton, W. J. (2003) · Cancer Treatment Reviews · doi:10.1016/s0305-7372(03)00077-x · Cited by 91

Lack of both Fas Ligand and Perforin Protects from Flavivirus-Mediated Encephalitis in Mice

Luna, R. M. L., Lee, E., Müllbacher, A., Blanden, R. V., Langman, R., & Lobigs, M. (2002) · Journal of Virology · doi:10.1128/jvi.76.7.3202-3211.2002 · Cited by 90

Death by any other name.

Schwartz, S. M., & Bennett, M. R. (1995) · Europe PMC (PubMed Central) · Cited by 90

Lack of cell surface Fas/APO-1 expression in pulmonary adenocarcinomas.

Nambu, Y., Hughes, S. J., Rehemtulla, A., Hamstra, D. A., Orringer, M. B., & Beer, D. G. (1998) · Journal of Clinical Investigation · doi:10.1172/jci1692 · Cited by 90

Release of preformed Fas ligand in soluble form is the major factor for activation‐induced death of Jurkat T cells

Martínez‐Lorenzo, M. J., Álava, M. A., Anel, A., Piñeiro, A., & Naval, J. (1996) · Immunology · doi:10.1046/j.1365-2567.1996.d01-782.x · Cited by 90

Molecular alterations in the aging immune system.

Hodes, R. J. (1995) · The Journal of Experimental Medicine · doi:10.1084/jem.182.1.1 · Cited by 90

Controlling programmed cell death with a cyclophilincyclosporin-based chemical inducer of dimerization

Belshawl, P. J., Spencer, D. M., Crabtree, G. R., & Schreiber, S. L. (1996) · Chemistry & Biology · doi:10.1016/s1074-5521(96)90249-5 · Cited by 89

The Fas/Fas‐ligand system: a mechanism for immune evasion in human breast carcinomas

Gutierrez, L. S., Eliza, M., Niven‐Fairchild, T., Naftolin, F. N., & Mor, G. (1999) · Breast Cancer Research and Treatment · doi:10.1023/a:1006102601215 · Cited by 89

Bax membrane insertion during Fas(CD95)-induced apoptosis precedes cytochrome c release and is inhibited by Bcl-2

Murphy, K. M., Streips, U. N., & Lock, R. B. (1999) · Oncogene · doi:10.1038/sj.onc.1203001 · Cited by 89

GD2 or HER2 targeting T cell engaging bispecific antibodies to treat osteosarcoma

Park, J. A., & Cheung, N.-K. V. (2020) · Journal of Hematology & Oncology · doi:10.1186/s13045-020-01012-y · Cited by 88

Apoptotic effects of mahanine on human leukemic cells are mediated through crosstalk between Apo-1/Fas signaling and the Bid protein and via mitochondrial pathways

Bhattacharya, K., Samanta, S. K., Tripathi, R. P., Mallick, A., Chandra, S., Pal, B. C., Shaha, C., & Mandal, C. (2009) · Biochemical Pharmacology · doi:10.1016/j.bcp.2009.09.007 · Cited by 89

Concerted Action of the FasL/Fas and Perforin/Granzyme A and B Pathways Is Mandatory for the Development of Early Viral Hepatitis but Not for Recovery from Viral Infection

Balkow, S., Kersten, A., Tran, T. T. T., Stehlé, T., Grosse, P., Muşeţeanu, C., Utermöhlen, O., Pircher, H., von Weizsäcker, F., Wallich, R., et al. (2001) · Journal of Virology · doi:10.1128/jvi.75.18.8781-8791.2001 · Cited by 88

Cancer cell sensitization to Fas-mediated apoptosis by sodium butyrate

Bonnotte, B., Favre, N., Reveneau, S., Micheau, O., Droin, N. M., Garrido, C., Fontana, A., Chauffert, B., Solary, É., & Martin, F. (1998) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4400371 · Cited by 88

Expression of Fas (CD95) and FasL (CD95L) in Human Airway Epithelium

Hamann, K. J., Dorscheid, D. R., Ko, F. D., Conforti, A. E., Sperling, A. I., Rabe, K. F., & White, S. R. (1998) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/ajrcmb.19.4.3100 · Cited by 88

Ineffective haemopoiesis and apoptosis in myelodysplastic syndromes

Parker, & Mufti (1998) · British Journal of Haematology · doi:10.1046/j.1365-2141.1998.00708.x · Cited by 88

Dissecting Fas signaling with an altered-specificity death-domain mutant: Requirement of FADD binding for apoptosis but not Jun N-terminal kinase activation

Chang, H. Y., Yang, X., & Baltimore, D. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.4.1252 · Cited by 88

Endogenous Control Mechanisms of FAK and PYK2 and Their Relevance to Cancer Development

Naser, R., Aldehaiman, A., Díaz‐Galicia, E., & Arold, S. T. (2018) · Cancers · doi:10.3390/cancers10060196 · Cited by 90

Inhibition of Fas-Mediated Apoptosis through Administration of Soluble Fas Receptor Improves Functional Outcome and Reduces Posttraumatic Axonal Degeneration after Acute Spinal Cord Injury

Ackery, A., Robins, S. L., & Fehlings, M. G. (2006) · Journal of Neurotrauma · doi:10.1089/neu.2006.23.604 · Cited by 88

Distinct effects of human glioblastoma immunoregulatory molecules programmed cell death ligand-1 (PDL-1) and indoleamine 2,3-dioxygenase (IDO) on tumour-specific T cell functions

Avril, T., Saïkali, S., Vauléon, É., Jary, A., Hamlat, A., de Tayrac, M., Mosser, J., & Quillien, V. (2010) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2010.04.003 · Cited by 87

TNF Superfamily: A Growing Saga of Kidney Injury Modulators

Sánchez-Niño, M. D., Benito‐Martín, A., Gonçalves, S., Sanz, A. B., Ucero, A. C., Izquierdo, M. C., Ramos, A. M., Berzal, S., Selgas, R., Ruiz‐Ortega, M., et al. (2010) · Mediators of Inflammation · doi:10.1155/2010/182958 · Cited by 89

Glutathione Peroxidase-1 Protects from CD95-induced Apoptosis

Gouazé‐Andersson, V., Andrieu‐Abadie, N., Cuvillier, O., Malagarie‐Cazenave, S., Frisach, M., Mirault, M.-É., & Levade, T. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m203067200 · Cited by 88

Survival of Virulent Mycobacterium tuberculosis Involves Preventing Apoptosis Induced by Bcl‐2 Upregulation and Release Resulting from Necrosis in J774 Macrophages

Zhang, J., Jiang, R., Takayama, H., & Tanaka, Y. (2005) · Microbiology and Immunology · doi:10.1111/j.1348-0421.2005.tb03673.x · Cited by 87

The tumor microenvironment as a determinant of drug response and resistance

Dalton, W. S. (1999) · Drug Resistance Updates · doi:10.1054/drup.1999.0097 · Cited by 92

Caspase activation in human spermatozoa in response to physiological and pathological stimuli

Grunewald, S., Paasch, U., Said, T. M., Sharma, R. K., Glander, H., & Agarwal, A. K. (2005) · Fertility and Sterility · doi:10.1016/j.fertnstert.2004.12.011 · Cited by 87

Molecular pathogenesis of thyroid cancer

Segev, D. L., Umbricht, C. B., & Zeiger, M. A. (2003) · Surgical Oncology · doi:10.1016/s0960-7404(03)00037-9 · Cited by 87

Secretory Lysosome Biogenesis in Cytotoxic T Lymphocytes from Normal and Chediak Higashi Syndrome Patients

Stinchcombe, J. C., Page, L. J., & Griffiths, G. M. (2000) · Traffic · doi:10.1034/j.1600-0854.2000.010508.x · Cited by 87

Fas—Beyond Death: A regenerative role for Fas in the nervous system

Lambert, C., Landau, A. M., & Desbarats, J. (2003) · APOPTOSIS · doi:10.1023/a:1026113222478 · Cited by 88

The human melanoma cell line MelJuSo secretes bioactive FasL and APO2L/TRAIL on the surface of microvesicles. Possible contribution to tumor counterattack

Martínez‐Lorenzo, M. J., Anel, A., Álava, M. A., Piñeiro, A., Naval, J., Lasierra, P., & Larrad, L. (2004) · Experimental Cell Research · doi:10.1016/j.yexcr.2003.12.024 · Cited by 86

Addressing the “Fas Counterattack” Controversy: Blocking Fas Ligand Expression Suppresses Tumor Immune Evasion of Colon CancerIn vivo

Ryan, A. E., Shanahan, F., O’Connell, J., & Houston, A. M. (2005) · Cancer Research · doi:10.1158/0008-5472.can-05-1462 · Cited by 86

Cardioprotective effects and underlying mechanisms of oxymatrine against Ischemic myocardial injuries of rats

Sun, H.-L., Lei, L., Lei, S., Zhao, D., De‐li, D., Qiao, G., Liu, Y., Chu, W., & Yang, B. (2008) · Phytotherapy Research · doi:10.1002/ptr.2452 · Cited by 86

Diabetes Activates Cell Death Pathway After Transient Focal Cerebral Ischemia

Murányi, M., Fujioka, M., He, Q., Han, A. X., Yong, G., Csiszár, K., & Li, P. (2003) · Diabetes · doi:10.2337/diabetes.52.2.481 · Cited by 86

Cytotoxic T Lymphocyte Responses to Human Immunodeficiency Virus: Control and Escape

Sewell, A. K., Price, D. A., Oxenius, A., Kelleher, A. D., & Phillips, R. E. (2000) · Stem Cells · doi:10.1634/stemcells.18-4-230 · Cited by 87

Selectins mediate macrophage infiltration in obstructive nephropathy in newborn mice11See Editorial by Kipari and Hughes, p. 760.

Lange-Sperandio, B., Cachat, F., Thornhill, B. A., & Chevalier, R. L. (2002) · Kidney International · doi:10.1046/j.1523-1755.2002.00162.x · Cited by 86

FADD-deficient T Cells Exhibit a Disaccord in Regulation of the Cell Cycle Machinery

Zhang, J., Kabra, N. H., Cado, D., Kang, C., & Winoto, A. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m103838200 · Cited by 86

Assessment of stability, toxicity and immunogenicity of new polymeric nanoreactors for use in enzyme replacement therapy of MNGIE

Vocht, C. D., Ranquin, A., Willaert, R., Ginderachter, J. A. V., Vanhaecke, T., Rogiers, V., Versées, W., Gelder, P. V., & Steyaert, J. (2009) · Journal of Controlled Release · doi:10.1016/j.jconrel.2009.03.020 · Cited by 85

The presence of abnormal spermatozoa in the ejaculate: Did apoptosis fail?

Sakkas, D., Seli, E. U., Manicardi, G. C., Nijs, M., Ombelet, W., & Bizzaro, D. (2004) · Human Fertility · doi:10.1080/14647270410001720464 · Cited by 85

ISOLIQUIRITIGENIN INHIBITS THE PROLIFERATION AND INDUCES THE APOPTOSIS OF HUMAN NON‐SMALL CELL LUNG CANCER A549 CELLS

Hsu, Y., Kuo, P., Chiang, L., & Lin, C. (2004) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/j.1440-1681.2004.04016.x · Cited by 85

Ca2+ Signaling Modulates Cytolytic T Lymphocyte Effector Functions

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Suppression of Tumor Growth Following Intralesional Therapy with TRAIL Recombinant Adenovirus

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