Sex hormones and skeletal muscle weakness

Frailty in Older Adults: Evidence for a Phenotype

Fried, L. P., Tangen, C. M., Walston, J., Newman, A. B., Hirsch, C., Gottdiener, J., Seeman, T., Tracy, R., Kop, W. J., Burke, G., et al. (2001) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/56.3.m146 · Cited by 24,907 · see citing works

Inflamm‐aging: An Evolutionary Perspective on Immunosenescence

FRANCESCHI, C., BONAFÈ, M., VALENSIN, S., OLIVIERI, F., DE LUCA, M., OTTAVIANI, E., & DE BENEDICTIS, G. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb06651.x · Cited by 5,358 · see citing works

Longitudinal Effects of Aging on Serum Total and Free Testosterone Levels in Healthy Men

Harman, S. M., Metter, E. J., Tobin, J. D., Pearson, J., & Blackman, M. R. (2001) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.86.2.7219 · Cited by 2,760 · see citing works

Age trends in the level of serum testosterone and other hormones in middle-aged men: longitudinal results from the Massachusetts Male Aging Study

Feldman, H. A., Longcope, C., Derby, C. A., Johannes, C. B., Araujo, A. B., Coviello, A. D., Bremner, W. J., & McKinlay, J. B. (2002) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.87.2.8201 · Cited by 1,861 · see citing works

The effects of supraphysiologic doses of testosterone on muscle size and strength in normal men

Bhasin, S., Storer, T. W., Berman, N., Callegari, C., Clevenger, B., Phillips, J., Bunnell, T. J., Tricker, R., Shirazi, A., & Casaburi, R. (1996) · New England Journal of Medicine · doi:10.1056/nejm199607043350101 · Cited by 1,659 · see citing works

Mediation of IGF-1-induced skeletal myotube hypertrophy by PI(3)K/Akt/mTOR and PI(3)K/Akt/GSK3 pathways

Rommel, C., Bodine, S. C., Clarke, B. A., Rossman, R., Nunez, L., Stitt, T. N., Yancopoulos, G. D., & Glass, D. J. (2001) · Nature Cell Biology · doi:10.1038/ncb1101-1009 · Cited by 1,583 · see citing works

Adverse Events Associated with Testosterone Administration

Basaria, S., Coviello, A. D., Travison, T. G., Storer, T. W., Farwell, W. R., Jette, A. M., Eder, R., Tennstedt, S., Ulloor, J., Zhang, A., et al. (2010) · New England Journal of Medicine · doi:10.1056/nejmoa1000485 · Cited by 1,494 · see citing works

Age, Disease, and Changing Sex Hormone Levels in Middle-Aged Men: Results of the Massachusetts Male Aging Study*

Gray, A., Feldman, H. A., McKinlay, J. B., & Longcope, C. (1991) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-73-5-1016 · Cited by 1,115 · see citing works

Cell Membrane and Nuclear Estrogen Receptors (ERs) Originate from a Single Transcript: Studies of ERα and ERβ Expressed in Chinese Hamster Ovary Cells

Razandi, M., Pedram, A., Greene, G. L., & Levin, E. R. (1999) · Molecular Endocrinology · doi:10.1210/mend.13.2.0239 · Cited by 1,046 · see citing works

Testosterone Replacement in Older Hypogonadal Men: A 12-Month Randomized Controlled Trial

Sih, R., Morley, J. E., Kaiser, F. E., Perry, H. M., Patrick, P., & Ross, C. (1997) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.82.6.3988 · Cited by 920 · see citing works

Changes in Proinflammatory Cytokine Activity after Menopause

Pfeilschifter, J., Köditz, R., Pfohl, M., & Schatz, H. (2002) · Endocrine Reviews · doi:10.1210/edrv.23.1.0456 · Cited by 911 · see citing works

Estrogen signaling: a subtle balance between ER alpha and ER beta.

Matthews, J., & Gustafsson, J. (2003) · Molecular Interventions · doi:10.1124/mi.3.5.281 · Cited by 844 · see citing works

Early skeletal muscle hypertrophy and architectural changes in response to high-intensity resistance training

Seynnes, O. R., de Boer, M., & Narici, M. V. (2007) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00789.2006 · Cited by 660 · cited 1× · see citing works

Effects of Testosterone on Muscle Strength, Physical Function, Body Composition, and Quality of Life in Intermediate-Frail and Frail Elderly Men: A Randomized, Double-Blind, Placebo-Controlled Study

Srinivas-Shankar, U., Roberts, S. A., Connolly, M. J., O'Connell, M. D. L., Adams, J. E., Oldham, J. A., & Wu, F. C. W. (2010) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2009-1251 · Cited by 629 · see citing works

Change in Muscle Strength Explains Accelerated Decline of Physical Function in Older Women With High Interleukin‐6 Serum Levels

Ferrucci, L., Penninx, B. W. J. H., Volpato, S., Harris, T. B., Bandeen‐Roche, K., Balfour, J., Leveille, S. G., Fried, L. P., & Md, J. M. G. (2002) · Journal of the American Geriatrics Society · doi:10.1046/j.1532-5415.2002.50605.x · Cited by 618 · see citing works

Older Men Are as Responsive as Young Men to the Anabolic Effects of Graded Doses of Testosterone on the Skeletal Muscle

Bhasin, S., Woodhouse, L., Casaburi, R., Singh, A. B., Mac, R. P., Lee, M., Yarasheski, K. E., Sinha-Hikim, I., Dzekov, C., Dzekov, J., et al. (2005) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2004-1184 · Cited by 544 · see citing works

Testosterone Replacement Increases Fat-Free Mass and Muscle Size in Hypogonadal Men 1

Bhasin, S., Storer, T. W., Berman, N., Yarasheski, K. E., Clevenger, B., Phillips, J., Lee, W. P., Bunnell, T. J., & Casaburi, R. H. (1997) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.82.2.3733 · Cited by 540 · see citing works

Testosterone administration to older men improves muscle function: molecular and physiological mechanisms

Ferrando, A. A., Sheffield-Moore, M., Yeckel, C. W., Gilkison, C., Jiang, J., Achacosa, A., Lieberman, S. A., Tipton, K., Wolfe, R. R., & Urban, R. J. (2002) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00362.2001 · Cited by 522 · see citing works

Muscle-fiber pennation angles are greater in hypertrophied than in normal muscles

Kawakami, Y., Abe, T., & Fukunaga, T. (1993) · Journal of Applied Physiology · doi:10.1152/jappl.1993.74.6.2740 · Cited by 518 · see citing works

Andropause: clinical implications of the decline in serum testosterone levels with aging in men

Matsumoto, A. M. (2002) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/57.2.m76 · Cited by 490 · see citing works

Testosterone-induced increase in muscle size in healthy young men is associated with muscle fiber hypertrophy

Sinha-Hikim, I., Artaza, J., Woodhouse, L., Gonzalez-Cadavid, N., Singh, A. B., Lee, M. I., Storer, T. W., Casaburi, R., Shen, R., & Bhasin, S. (2002) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00502.2001 · Cited by 464 · see citing works

Testosterone action on skeletal muscle

Herbst, K. L., & Bhasin, S. (2004) · Current Opinion in Clinical Nutrition and Metabolic Care · doi:10.1097/00075197-200405000-00006 · Cited by 457 · cited 2× · see citing works

Influence of some biological indexes on sex hormone-binding globulin and androgen levels in aging or obese males

Vermeulen, A. (1996) · Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.81.5.1821 · Cited by 455 · see citing works

Cell Membrane and Nuclear Estrogen Receptors (ERs) Originate from a Single Transcript: Studies of ER and ER Expressed in Chinese Hamster Ovary Cells

Razandi, M. (1999) · Molecular Endocrinology · doi:10.1210/me.13.2.307 · Cited by 385 · see citing works

Theories of biological aging: Genes, proteins, and free radicals

Rattan, S. I. S. (2006) · Free Radical Research · doi:10.1080/10715760600911303 · Cited by 364 · see citing works

The unfolding stories of GPR30, a new membrane-bound estrogen receptor

Maggiolini, M., & Picard, D. (2010) · Journal of Endocrinology · doi:10.1677/joe-09-0242 · Cited by 360 · see citing works

Transdermal Testosterone Gel Improves Sexual Function, Mood, Muscle Strength, and Body Composition Parameters in Hypogonadal Men

Wang, C. (2000) · Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.85.8.2839 · Cited by 359 · see citing works

“Reprint of” A longitudinal study of the perimenopausal transition: altered profiles of steroid and pituitary hormones, SHBG and bone mineral density

Rannevik, G., Jeppsson, S., Johnell, O., Bjerre, B., Laurell-Borulf, Y., & Svanberg, L. (2008) · Maturitas · doi:10.1016/j.maturitas.2008.09.010 · Cited by 349 · see citing works

DHEA and the intracrine formation of androgens and estrogens in peripheral target tissues: its role during aging

Labrie, F., Bélanger, A., Luu-The, V., Labrie, C., Simard, J., Cusan, L., Gomez, J.-L., & Candas, B. (1998) · Steroids · doi:10.1016/s0039-128x(98)00007-5 · Cited by 347 · see citing works

Testosterone-induced muscle hypertrophy is associated with an increase in satellite cell number in healthy, young men

Sinha-Hikim, I., Roth, S. M., Lee, M. I., & Bhasin, S. (2003) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00370.2002 · Cited by 344 · see citing works

Long-Term Pharmacokinetics of Transdermal Testosterone Gel in Hypogonadal Men 1

Swerdloff, R. S., Wang, C., Cunningham, G. R., Dobs, A. S., Iranmanesh, A., Matsumoto, A. M., Snyder, P. J., Weber, T. J., Longstreth, J. A., & Berman, N. (2000) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.85.12.7045 · Cited by 343 · see citing works

Testosterone Replacement Increases Fat-Free Mass and Muscle Size in Hypogonadal Men

Bhasin, S. (1997) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.82.2.407 · Cited by 318 · see citing works

Androgen Receptor in Human Skeletal Muscle and Cultured Muscle Satellite Cells: Up-Regulation by Androgen Treatment

Sinha‐Hikim, I., Taylor, W. E., González-Cadavid, N. F., Zheng, W. D., & Bhasin, S. (2004) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2004-0084 · Cited by 312 · see citing works

Role of MCP-1 in cardiovascular disease: molecular mechanisms and clinical implications

Niu, J., & Kolattukudy, P. E. (2009) · Clinical Science · doi:10.1042/cs20080581 · Cited by 292 · see citing works

Long-Term Pharmacokinetics of Transdermal Testosterone Gel in Hypogonadal Men

Swerdloff, R. S. (2000) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.85.12.4500 · Cited by 262 · see citing works

Testosterone injection stimulates net protein synthesis but not tissue amino acid transport

Ferrando, A. A., Tipton, K. D., Doyle, D., Phillips, S. M., Cortiella, J., & Wolfe, R. R. (1998) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1998.275.5.e864 · Cited by 256 · see citing works

Hormone Therapy and Skeletal Muscle Strength: A Meta-Analysis

Greising, S. M., Baltgalvis, K. A., Lowe, D. A., & Warren, G. L. (2009) · The Journals of Gerontology Series A · doi:10.1093/gerona/glp082 · Cited by 240 · see citing works

Influence of 90-day simulated microgravity on human tendon mechanical properties and the effect of resistive countermeasures

Reeves, N. D., Maganaris, C. N., Ferretti, G., & Narici, M. V. (2005) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01266.2004 · Cited by 236 · see citing works

Effects of hormone replacement therapy and high-impact physical exercise on skeletal muscle in post-menopausal women: a randomized placebo-controlled study

SIPILÄ, S., TAAFFE, D. R., CHENG, S., PUOLAKKA, J., TOIVANEN, J., & SUOMINEN, H. (2001) · Clinical Science · doi:10.1042/cs1010147 · Cited by 230 · see citing works

Regulation of protein synthesis associated with skeletal muscle hypertrophy by insulin-, amino acid- and exercise-induced signalling

Bolster, D. R., Jefferson, L. S., & Kimball, S. R. (2004) · Proceedings of The Nutrition Society · doi:10.1079/pns2004355 · Cited by 223 · see citing works

Growth hormone stimulates the collagen synthesis in human tendon and skeletal muscle without affecting myofibrillar protein synthesis

Doessing, S., Heinemeier, K. M., Holm, L., Mackey, A. L., Schjerling, P., Rennie, M. J., Smith, K., Reitelseder, S., Kappelgaard, A., Rasmussen, M. H., et al. (2009) · The Journal of Physiology · doi:10.1113/jphysiol.2009.179325 · Cited by 207 · see citing works

Nonsteroidal Selective Androgen Receptor Modulators (SARMs): Dissociating the Anabolic and Androgenic Activities of the Androgen Receptor for Therapeutic Benefit

Mohler, M. L., Bohl, C. E., Jones, A. J., Coss, C. C., Narayanan, R., He, Y., Hwang, D., Dalton, J. T., & Miller, D. D. (2009) · Journal of Medicinal Chemistry · doi:10.1021/jm900280m · Cited by 206 · see citing works

Immunological functions of leptin and adiponectin

Carbone, F., Rocca, C. L., & Matarese, G. (2012) · Biochimie · doi:10.1016/j.biochi.2012.05.018 · Cited by 204 · see citing works

Estrogen Receptor Alpha mRNA in Human Skeletal Muscles

LEMOINE, S., GRANIER, P., TIFFOCHE, C., RANNOU-BEKONO, F., THIEULANT, M.-L., & DELAMARCHE, P. (2003) · Medicine & Science in Sports & Exercise · doi:10.1249/01.mss.0000053654.14410.78 · Cited by 201 · see citing works

Short-Term Oxandrolone Administration Stimulates Net Muscle Protein Synthesis in Young Men1

Sheffield-Moore, M., Urban, R. J., Wolf, S. E., Jiang, J., Catlin, D. H., Herndon, D. N., Wolfe, R. R., & Ferrando, A. A. (1999) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.84.8.5923 · Cited by 199 · see citing works

Androgens and skeletal muscle: cellular and molecular action mechanisms underlying the anabolic actions

Dubois, V., Laurent, M., Boonen, S., Vanderschueren, D., & Claessens, F. (2012) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-011-0883-3 · Cited by 197 · see citing works

Estrogen Regulates Estrogen Receptors and Antioxidant Gene Expression in Mouse Skeletal Muscle

Baltgalvis, K. A., Greising, S. M., Warren, G. L., & Lowe, D. A. (2010) · PLoS ONE · doi:10.1371/journal.pone.0010164 · Cited by 192 · see citing works

Expression of Both Oestrogen Receptor Alpha and Beta in Human Skeletal Muscle Tissue

Wiik, A., Ekman, M., Johansson, O., Jansson, E., & Esbjörnsson, M. (2009) · Histochemistry and Cell Biology · doi:10.1007/s00418-008-0512-x · Cited by 190 · see citing works

Expression Pattern of G Protein-Coupled Receptor 30 in LacZ Reporter Mice

Isensee, J., Meoli, L., Zazzu, V., Nabzdyk, C. S., Witt, H., Soewarto, D., Effertz, K., Fuchs, H., Gailus‐Durner, V., Busch, D. H., et al. (2008) · Endocrinology · doi:10.1210/en.2008-1488 · Cited by 189 · see citing works

Changes in Proinflammatory Cytokine Activity after Menopause

Pfeilschifter, J. (2002) · Endocrine Reviews · doi:10.1210/er.23.1.90 · Cited by 182 · see citing works

Androgen Treatment and Muscle Strength in Elderly Men: A Meta‐Analysis

Ottenbacher, K. J., Ottenbacher, M. E., Ottenbacher, A. J., Acha, A. A., & Ostir, G. V. (2006) · Journal of the American Geriatrics Society · doi:10.1111/j.1532-5415.2006.00938.x · Cited by 173 · see citing works

Postmenopausal hormone replacement therapy modifies skeletal muscle composition and function: a study with monozygotic twin pairs

Ronkainen, P. H. A., Kovanen, V., Alén, M., Pöllänen, E., Palonen, E.-M., Ankarberg-Lindgren, C., Hämäläinen, E., Turpeinen, U., Kujala, U. M., Puolakka, J., et al. (2009) · Journal of Applied Physiology · doi:10.1152/japplphysiol.91518.2008 · Cited by 168 · see citing works

Effect of estrogen on tendon collagen synthesis, tendon structural characteristics, and biomechanical properties in postmenopausal women

Hansen, M., Kongsgaard, M., Holm, L., Skovgaard, D. C., Magnusson, S. P., Qvortrup, K., Larsen, J. O., Aagaard, P., Dahl, M., Serup, A. K., et al. (2008) · Journal of Applied Physiology · doi:10.1152/japplphysiol.90935.2008 · Cited by 166 · see citing works

The expression of androgen receptors in human neck and limb muscles: effects of training and self-administration of androgenic-anabolic steroids

Kadi, F., Bonnerud, P., Eriksson, A., & Thornell, L. (2000) · Histochemistry and Cell Biology · doi:10.1007/s004180050003 · Cited by 164 · see citing works

Impact of menopause on collagen subtypes in the arcus tendineous fasciae pelvis

Moalli, P., Talarico, L. C., Sung, V. W., Klingensmith, W. L., Shand, S. H., Meyn, L. A., & Watkins, S. C. (2004) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2003.08.040 · Cited by 158 · see citing works

Effects of oral versus transdermal estrogen on the growth hormone/insulin-like growth factor I axis in younger and older postmenopausal women: a clinical research center study

Bellantoni, M. F., Vittone, J. L., Campfield, A., Bass, K. M., Harman, S. M., & Blackman, M. R. (1996) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.81.8.8768841 · Cited by 145 · see citing works

Increased molecular damage and heterogeneity as the basis of aging

Rattan, S. I. S. (2008) · Biological Chemistry · doi:10.1515/bc.2008.030 · Cited by 139 · see citing works

Midlife women

Greenblum, C. A., Rowe, M. A., Neff, D. F., & Greenblum, J. S. (2012) · Menopause The Journal of The North American Menopause Society · doi:10.1097/gme.0b013e31825a2a91 · Cited by 136 · see citing works

The effect of hormone replacement therapy and/or exercise on skeletal muscle attenuation in postmenopausal women: a yearlong intervention

Taaffe, D. R., Sipilä, S., Cheng, S., Puolakka, J. O., Toivanen, J., & Suominen, H. (2005) · Clinical Physiology and Functional Imaging · doi:10.1111/j.1475-097x.2005.00628.x · Cited by 127 · see citing works

Differential influence of peripheral and systemic sex steroids on skeletal muscle quality in pre‐ and postmenopausal women

Pöllänen, E., Sipilä, S., Alén, M., Ronkainen, P. H. A., Ankarberg‐Lindgren, C., Puolakka, J. O., Suominen, H., Hämäläinen, E. K., Turpeinen, U., Konttinen, Y. T., et al. (2011) · Aging Cell · doi:10.1111/j.1474-9726.2011.00701.x · Cited by 121 · see citing works

Differential effects of oral conjugated estrogens and transdermal estradiol on insulin-like growth factor 1, growth hormone and sex hormone binding globulin serum levels

Campagnoli, C., Biglia, N., Altare, F., Lanza, M., Lesca, L., Cantamessa, C., Peris, C., Fiorucci, G. C., & Sismondi, P. (1993) · Gynecological Endocrinology · doi:10.3109/09513599309152509 · Cited by 116 · see citing works

Local administration of insulin‐like growth factor‐ I ( IGF‐I ) stimulates tendon collagen synthesis in humans

Hansen, M., Boesen, A., Holm, L., Flyvbjerg, A., Langberg, H., & Kjær, M. (2012) · Scandinavian Journal of Medicine and Science in Sports · doi:10.1111/j.1600-0838.2011.01431.x · Cited by 115 · see citing works

Androgen receptor immunoreactivity in skeletal muscle: Enrichment at the neuromuscular junction

Monks, D. A., O’Bryant, E. L., & Jordan, C. L. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20088 · Cited by 102 · see citing works

Expression of steroidogenic enzymes and synthesis of sex steroid hormones from DHEA in skeletal muscle of rats

Aizawa, K., Iemitsu, M., Maeda, S., Jesmin, S., Otsuki, T., Mowa, C. N., Miyauchi, T., & Mesaki, N. (2006) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00367.2006 · Cited by 95 · see citing works

Hormone therapy is associated with smaller Achilles tendon diameter in active post‐menopausal women

Cook, J. L., Bass, S. L., & Black, J. (2006) · Scandinavian Journal of Medicine and Science in Sports · doi:10.1111/j.1600-0838.2006.00543.x · Cited by 90 · see citing works

Effects of Testosterone on Skeletal Muscle Architecture in Intermediate-Frail and Frail Elderly Men

Atkinson, R. A., Srinivas-Shankar, U., Roberts, S. A., Connolly, M. J., Adams, J. E., Oldham, J. A., Wu, F. C. W., Seynnes, O., Stewart, C. E., Maganaris, C. N., et al. (2010) · The Journals of Gerontology Series A · doi:10.1093/gerona/glq118 · Cited by 79 · see citing works

Effects of Estrogen Replacement and Lower Androgen Status on Skeletal Muscle Collagen and Myofibrillar Protein Synthesis in Postmenopausal Women

Hansen, M., Skovgaard, D. C., Reitelseder, S., Holm, L., Langberg, H., & Kjær, M. (2012) · The Journals of Gerontology Series A · doi:10.1093/gerona/gls007 · Cited by 78 · see citing works

Short-Term Oxandrolone Administration Stimulates Net Muscle Protein Synthesis in Young Men

Sheffield‐Moore, M. (1999) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.84.8.2705 · Cited by 74 · see citing works

Biogerontology: from here to where? The Lord Cohen Medal Lecture-2011

Rattan, S. I. S. (2011) · Biogerontology · doi:10.1007/s10522-011-9354-3 · Cited by 72 · see citing works

Effects of hormone replacement therapy and high-impact physical exercise on skeletal muscle in post-menopausal women: a randomized placebo-controlled study

Sipilä, S., Taaffe, D. R., Cheng, S., et al. (2001) · Clinical Science · doi:10.1042/cs20000271 · Cited by 62 · see citing works

Aromatase in skeletal muscle

Larionov, A. A., Vasyliev, D. A., Mason, J. I., Howie, A. F., Berstein, L. M., & Miller, W. R. (2003) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/s0960-0760(03)00059-1 · Cited by 58 · see citing works

Age- and Gender-Related Changes in Ligament Components

Osakabe, T., Hayashi, M., Hasegawa, K., Okuaki, T., Ritty, T. M., Mecham, R. P., Wachi, H., & Seyama, Y. (2001) · Annals of Clinical Biochemistry International Journal of Laboratory Medicine · doi:10.1177/000456320103800510 · Cited by 57 · see citing works

Effects of combined hormone replacement therapy or its effective agents on the IGF-1 pathway in skeletal muscle

Pöllänen, E., Ronkainen, P. H. A., Horttanainen, M., Takala, T., Puolakka, J., Suominen, H., Sipilä, S., & Kovanen, V. (2010) · Growth Hormone & IGF Research · doi:10.1016/j.ghir.2010.07.003 · Cited by 54 · see citing works

Effect of resistance exercise on muscle steroidogenesis

Vingren, J. L., Kraemer, W. J., Hatfield, D. L., Anderson, J. M., Volek, J. S., Ratamess, N. A., Thomas, G. A., Ho, J., Fragala, M. S., & Maresh, C. M. (2008) · Journal of Applied Physiology · doi:10.1152/japplphysiol.91235.2008 · Cited by 51 · see citing works

Effects of transdermal estrogen on collagen turnover at rest and in response to exercise in postmenopausal women

Pingel, J., Langberg, H., Skovgård, D., Koskinen, S., Flyvbjerg, A., Frystyk, J., Kjær, M., & Hansen, M. (2012) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01463.2011 · Cited by 44 · see citing works

Muscular Transcriptome in Postmenopausal Women With or Without Hormone Replacement

Pöllänen, E., Ronkainen, P. H. A., Suominen, H., Takala, T., Koskinen, S. O. A., Puolakka, J. O., Sipilä, S., & Kovanen, V. (2007) · Rejuvenation Research · doi:10.1089/rej.2007.0536 · Cited by 41 · see citing works

Age and estrogen-based hormone therapy affect systemic and local IL-6 and IGF-1 pathways in women

Ahtiainen, M., Pöllänen, E., Ronkainen, P. H. A., Alén, M., Puolakka, J. O., Kaprio, J. A., Sipilä, S., & Kovanen, V. (2011) · AGE · doi:10.1007/s11357-011-9298-1 · Cited by 41 · see citing works

Global gene expression profiles in skeletal muscle of monozygotic female twins discordant for hormone replacement therapy

Ronkainen, P. H. A., Pöllänen, E., Alén, M., Pitkänen, R., Puolakka, J. O., Kujala, U. M., Kaprio, J. A., Sipilä, S., & Kovanen, V. (2010) · Aging Cell · doi:10.1111/j.1474-9726.2010.00636.x · Cited by 37 · see citing works

Power training and postmenopausal hormone therapy affect transcriptional control of specific co-regulated gene clusters in skeletal muscle

Pöllänen, E., Fey, V., Törmäkangas, T., Ronkainen, P. H. A., Taaffe, D. R., Takala, T., Koskinen, S., Cheng, S., Puolakka, J. O., Kujala, U. M., et al. (2010) · AGE · doi:10.1007/s11357-010-9140-1 · Cited by 35 · see citing works

Muscle function in monozygotic female twin pairs discordant for hormone replacement therapy

Finni, T. J., Noorkõiv, M., Pöllänen, E., Ronkainen, P. H. A., Alén, M., Kaprio, J. A., Kovanen, V., & Sipilä, S. (2011) · Muscle & Nerve · doi:10.1002/mus.22162 · Cited by 28 · see citing works

Hormone therapy is associated with better body composition and adipokine/glucose profiles

Ahtiainen, M., Alén, M., Pöllänen, E., Pulkkinen, S., Ronkainen, P. H. A., Kujala, U. M., Kaprio, J. A., Sipilä, S., & Kovanen, V. (2012) · Menopause The Journal of The North American Menopause Society · doi:10.1097/gme.0b013e31825a3344 · Cited by 27 · see citing works

Testosterone Replacement Therapy for Male Aging: ASA Position Statement

(2006) · Journal of Andrology · doi:10.1002/j.1939-4640.2006.tb01177.x · Cited by 23 · see citing works

Age- and gender-related changes in ligament components

Osakabe, T., Hayashi, M., Hasegawa, K., et al. (2001) · Annals of Clinical Biochemistry International Journal of Laboratory Medicine · doi:10.1258/0004563011901118 · Cited by 12 · see citing works

Sarcopenia: Aging-Related Loss of Muscle Mass and Function

Larsson, L., Degens, H., Li, M., Salviati, L., Lee, Y. I., Thompson, W., Kirkland, J. L., & Sandri, M. (2019) · Physiological Reviews · doi:10.1152/physrev.00061.2017 · Cited by 1,797 · see citing works

The Sick and the Weak: Neuropathies/Myopathies in the Critically Ill

Friedrich, O., Reid, M. B., den Berghe, G. V., Vanhorebeek, I., Hermans, G., Rich, M. M., & Larsson, L. (2015) · Physiological Reviews · doi:10.1152/physrev.00028.2014 · Cited by 394 · see citing works

Osteoporosis and Sarcopenia Increase Frailty Syndrome in the Elderly

Greco, E. A., Pietschmann, P., & Migliaccio, S. (2019) · Frontiers in Endocrinology · doi:10.3389/fendo.2019.00255 · Cited by 338 · see citing works

Pathophysiology and mechanisms of primary sarcopenia (Review)

Nishikawa, H., Fukunishi, S., Asai, A., Yokohama, K., Nishiguchi, S., & Higuchi, K. (2021) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2021.4989 · Cited by 235 · see citing works

Diabetes and Sarcopenic Obesity: Pathogenesis, Diagnosis, and Treatments

Wang, M., Tan, Y., Shi, Y., Wang, X., Liao, Z., & Wei, P. (2020) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.00568 · Cited by 231 · see citing works

Sex Differences in Muscle Wasting

Anderson, L. J., Liu, H. M., & Garcia, J. M. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-70178-3_9 · Cited by 222 · see citing works

A positive association of vitamin D deficiency and sarcopenia in 50 year old women, but not men

Park, S., Ham, J.-O., & Lee, B.-K. (2013) · Clinical Nutrition · doi:10.1016/j.clnu.2013.09.016 · Cited by 103 · see citing works

Aging of the endocrine system and its potential impact on sarcopenia

Vitale, G., Cesari, M., & Mari, D. (2016) · European Journal of Internal Medicine · doi:10.1016/j.ejim.2016.07.017 · Cited by 106 · see citing works

Prevalence of Undernutrition, Frailty and Sarcopenia in Community-Dwelling People Aged 50 Years and Above: Systematic Review and Meta-Analysis

AlMohaisen, N., Gittins, M., Todd, C. J., Sremanakova, J., Sowerbutts, A. M., Aldossari, A., Almutairi, A. S., Jones, D. J., & Burden, S. T. (2022) · Nutrients · doi:10.3390/nu14081537 · Cited by 105 · see citing works

Managing Sarcopenia and Its Related-Fractures to Improve Quality of Life in Geriatric Populations

Hida, T. (2014) · Aging and Disease · doi:10.14336/ad.2014.0500226 · Cited by 75 · see citing works

Hormones and Muscle Atrophy.

Martín, A., Priego, T., & López-Calderón, A. (2018) · Advances in Experimental Medicine and Biology · doi:10.1007/978-981-13-1435-3_9 · Cited by 68 · see citing works

Sarcopenia in post-menopausal women: Is there any role for vitamin D?

Anagnostis, P. G., Dimopoulou, C., Karras, S. Ν., Lambrinoudaki, I. V., & Goulis, D. G. (2015) · Maturitas · doi:10.1016/j.maturitas.2015.03.014 · Cited by 69 · see citing works

Design and protocol of Estrogenic Regulation of Muscle Apoptosis (ERMA) study with 47 to 55-year-old women's cohort: novel results show menopause-related differences in blood count

Kovanen, V., Aukee, P., Kokko, K., Finni, T. J., Tarkka, I. M., Tammelin, T., Kujala, U. M., Sipilä, S., & Laakkonen, E. K. (2018) · Menopause The Journal of The North American Menopause Society · doi:10.1097/gme.0000000000001117 · Cited by 68 · see citing works

Intramuscular sex steroid hormones are associated with skeletal muscle strength and power in women with different hormonal status

Pöllänen, E., Kangas, R., Horttanainen, M., Niskala, P., Kaprio, J. A., Butler-Browne, G. S., Mouly, V., Sipilä, S., & Kovanen, V. (2015) · Aging Cell · doi:10.1111/acel.12309 · Cited by 62 · see citing works

Assessing the influence of age and gender on the phenotype of myotonic dystrophy type 2

Montagnese, F., Mondello, S., Wenninger, S., Kreß, W., & Schoser, B. G. H. (2017) · Journal of Neurology · doi:10.1007/s00415-017-8653-2 · Cited by 57 · see citing works

The Therapeutic Intervention of Sex Steroid Hormones for Sarcopenia

Huang, L., & Wang, J. (2021) · Frontiers in Medicine · doi:10.3389/fmed.2021.739251 · Cited by 59 · see citing works

Biomarkers Profile of People With Sarcopenia: A Cross-sectional Analysis From UK Biobank

Petermann-Rocha, F. E., Gray, S. R., Pell, J. P., Celis-Morales, C. A., & Ho, F. K. W. (2020) · Journal of the American Medical Directors Association · doi:10.1016/j.jamda.2020.05.005 · Cited by 56 · see citing works

Type 2 diabetes mellitus related sarcopenia: a type of muscle loss distinct from sarcopenia and disuse muscle atrophy

Liu, Z., Guo, Y., & Zheng, C. (2024) · Frontiers in Endocrinology · doi:10.3389/fendo.2024.1375610 · Cited by 62 · see citing works

Influence of sex on the age‐related adaptations of neuromuscular function and motor unit properties in elite masters athletes

Piasecki, J., Inns, T. B., Bass, J. J., Scott, R., Stashuk, D. W., Phillips, B. E., Atherton, P. J., & Piasecki, M. (2020) · The Journal of Physiology · doi:10.1113/jp280679 · Cited by 49 · see citing works

Menopause and frailty: a scoping review

Ruan, H., Hu, J., Zhao, J., Tao, H., Chi, J., Niu, X., Zhang, J., & Wang, Y. (2020) · Menopause The Journal of The North American Menopause Society · doi:10.1097/gme.0000000000001612 · Cited by 51 · see citing works

Physical activity and fat-free mass during growth and in later life

Westerterp, K. R., Yamada, Y., Sagayama, H., Ainslie, P. N., Andersen, L. F., Anderson, L. J., Arab, L., Baddou, I., Bedu-Addo, K., Blaak, E. E., et al. (2021) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/nqab260 · Cited by 50 · see citing works

Regenerative Medicine Approaches for Age-Related Muscle Loss and Sarcopenia: A Mini-Review

Naranjo, J. D., Dziki, J. L., & Badylak, S. F. (2017) · Gerontology · doi:10.1159/000479278 · Cited by 49 · see citing works

The Effect of Exercise on Glucoregulatory Hormones: A Countermeasure to Human Aging: Insights from a Comprehensive Review of the Literature

Sellami, M., Bragazzi, N. L., Slimani, M., Hayes, L. D., Jabbour, G., Giorgio, A. D., & Dugué, B. (2019) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph16101709 · Cited by 45 · see citing works

Impact of oestrogen deficiency and aging on tendon: concise review

Frizziero, A., Vittadini, F., Gasparre, G., & Masiero, S. (2019) · Muscles Ligaments and Tendons Journal · doi:10.32098/mltj.03.2014.11 · Cited by 44 · see citing works

Gender associated muscle-tendon adaptations to resistance training

McMahon, G. E., Morse, C. I., Winwood, K. L., Burden, A., & Onambélé-Pearson, G. L. (2018) · PLoS ONE · doi:10.1371/journal.pone.0197852 · Cited by 39 · see citing works

Hormones, Hypertrophy, and Hype: An Evidence-Guided Primer on Endogenous Endocrine Influences on Exercise-Induced Muscle Hypertrophy

Every, D. W. V., D’Souza, A. C., & Phillips, S. M. (2024) · Exercise and Sport Sciences Reviews · doi:10.1249/jes.0000000000000346 · Cited by 38 · see citing works

Impact of oestrogen deficiency and aging on tendon: concise review

Frizziero, A. (2014) · Muscles Ligaments and Tendons Journal · doi:10.11138/mltj/2014.4.3.324 · Cited by 38 · see citing works

Early menopause and premature ovarian insufficiency may increase the risk of sarcopenia: A systematic review and meta-analysis

Divaris, E., Anagnostis, P. G., Gkekas, N. K., Kouidi, E. J., & Goulis, D. G. (2023) · Maturitas · doi:10.1016/j.maturitas.2023.05.006 · Cited by 35 · see citing works

Hormonal Influences on Skeletal Muscle Function in Women across Life Stages: A Systematic Review

Kodete, C. S., Thuraka, B., Pasupuleti, V., & Malisetty, S. (2024) · Muscles · doi:10.3390/muscles3030024 · Cited by 29 · see citing works

The association between sex hormones and periodontitis among American adults: A cross-sectional study

Su, X., Jin, K., Zhou, X. J., Zhang, Z., Zhang, C., Li, Y., Yang, M., Huang, X., Xu, S., Wei, Q., et al. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1125819 · Cited by 27 · see citing works

Paeoniflorin Alleviates Skeletal Muscle Atrophy in Ovariectomized Mice through the ERα/NRF1 Mitochondrial Biogenesis Pathway

Park, K.-S., Kim, H., Kim, H. J., Lee, K.-I., Lee, S., & Kim, J. (2022) · Pharmaceuticals · doi:10.3390/ph15040390 · Cited by 24 · see citing works

Lumican, an Exerkine, Protects against Skeletal Muscle Loss

Cho, H. J., Lee, Y., Kim, D. A., Moon, S. A., Lee, S. E., Lee, S. H., & Koh, J. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231710031 · Cited by 24 · see citing works

Androgenic and estrogenic regulation of Atrogin-1, MuRF1 and myostatin expression in different muscle types of male mice

Naeyer, H. D., Lamon, S., Russell, A. P., Everaert, I., Spaey, A. D., Vanheel, B., Taes, Y., & Derave, W. (2014) · European Journal of Applied Physiology · doi:10.1007/s00421-013-2800-y · Cited by 24 · see citing works

Muscular Strength Adaptations and Hormonal Responses After Two Different Multiple-Set Protocols of Resistance Training in Postmenopausal Women

Nunes, P. R. P., Barcelos, L. C., de Oliveira, A. A., Júnior, R. F., Martins, F. M., Resende, E. A. M. R., & Orsatti, F. L. (2017) · The Journal of Strength and Conditioning Research · doi:10.1519/jsc.0000000000001788 · Cited by 23 · see citing works

Combined sprint and resistance training abrogates age differences in somatotropic hormones

Sellami, M., Dhahbi, W., Hayes, L. D., Padulo, J., Rhibi, F., Djemail, H., & Chaouachi, A. (2017) · PLoS ONE · doi:10.1371/journal.pone.0183184 · Cited by 23 · see citing works

Novel individualized power training protocol preserves physical function in adult and older mice

Graber, T. G., Fandrey, K. R., & Thompson, L. V. (2019) · GeroScience · doi:10.1007/s11357-019-00069-z · Cited by 22 · see citing works

Maintenance of type 2 glycolytic myofibers with age by Mib1-Actn3 axis

Seo, J., Kang, J., Kim, Y. L., Jo, Y., Kim, J.-H., Hann, S., Park, J., Park, I., Park, H., Yoo, K., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-21621-6 · Cited by 20 · see citing works

Age and sex differences in the biomechanical and viscoelastic properties of upper limb muscles in middle-aged and older adults: A pilot study

Lee, M.-T., Wu, C., Chen, C.-W., Cheng, H.-L., Chen, C.-C., & Hsieh, Y. (2022) · Journal of Biomechanics · doi:10.1016/j.jbiomech.2022.111002 · Cited by 20 · see citing works

Targeting muscle signaling pathways to minimize adverse effects of androgen deprivation

de Rooy, C., Grossmann, M., Zajac, J. D., & Cheung, A. S. (2015) · Endocrine Related Cancer · doi:10.1530/erc-15-0232 · Cited by 16 · see citing works

Menopause Transition: A Cross-Sectional Evaluation on Muscle Size and Quality

Smith‐Ryan, A. E., Hirsch, K. R., Cabre, H. E., Gould, L. M., Gordon, A. N., & Ferrando, A. A. (2023) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000003150 · Cited by 16 · see citing works

Potential Cellular and Biochemical Mechanisms of Exercise and Physical Activity on the Ageing Process

Ross, M., Lithgow, H., Hayes, L. D., & Florida-James, G. D. (2019) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-981-13-3681-2_12 · Cited by 16 · see citing works

Testosterone improves muscle function of the extensor digitorum longus in rats with sepsis

Wang, J., & Wu, T. (2020) · Bioscience Reports · doi:10.1042/bsr20193342 · Cited by 16 · see citing works

Perimenopausal women show modulation of excitatory and inhibitory neuromuscular mechanisms

Pesonen, H., Laakkonen, E. K., Hautasaari, P., Aukee, P., Kovanen, V., Sipilä, S., Finni, T. J., & Tarkka, I. M. (2021) · BMC Women s Health · doi:10.1186/s12905-021-01275-8 · Cited by 15 · see citing works

Association between serum copper levels and muscle mass: results from NHANES 2011–2016

Chen, Z., Hu, D., Wu, D., Song, C., Sun, J., & Liu, W. (2023) · Environmental Science and Pollution Research · doi:10.1007/s11356-023-31599-x · Cited by 15 · see citing works

Impact of estrogen deficiency on diaphragm and leg muscle contractile function in female mdx mice

Vang, P., Baumann, C. W., Barok, R., Larson, A. A., Dougherty, B. J., & Lowe, D. A. (2021) · PLoS ONE · doi:10.1371/journal.pone.0249472 · Cited by 15 · see citing works

Load-induced human skeletal muscle hypertrophy: Mechanisms, myths, and misconceptions

Every, D. W. V., Lees, M. J., Wilson, B., Nippard, J., & Phillips, S. M. (2025) · Journal of sport and health science/Journal of Sport and Health Science · doi:10.1016/j.jshs.2025.101104 · Cited by 14 · see citing works

Effect of Yijinjing combined with elastic band exercise on muscle mass and function in middle-aged and elderly patients with prediabetes: A randomized controlled trial

Huang, Y., Han, J., Gu, Q., Cai, Y., Li, J., Wang, S., Wang, S., Wang, R., & Liu, X. (2022) · Frontiers in Medicine · doi:10.3389/fmed.2022.990100 · Cited by 14 · see citing works

Feasibility of using chest computed tomography (CT) imaging at the first lumbar vertebra (L1) level to assess skeletal muscle mass: a retrospective study

Liu, S., Han, X., Li, J., Xie, X., Yang, Y., Jiang, W., Liu, L., & Liu, Z. (2023) · PeerJ · doi:10.7717/peerj.16652 · Cited by 13 · see citing works

Association between exposure to organophosphate esters metabolites and sarcopenia prevalence: A cross-sectional study using NHANES data

Nan, W., Peng, Z., Yi, T., Ouyang, M., & Hu, J. (2024) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2024.117041 · Cited by 13 · see citing works

Predictors of presarcopenia in community-dwelling older adults: A 5-year longitudinal study

Kobayashi, K., Ando, K., Tsushima, M., Machino, M., Ota, K., Morozumi, M., Tanaka, S. A., Kanbara, S., Ishiguro, N., Hasegawa, Y., et al. (2018) · Modern Rheumatology · doi:10.1080/14397595.2018.1551171 · Cited by 13 · see citing works

Cushing, acromegaly, GH deficiency and tendons

Galdiero, M. (2014) · Muscles Ligaments and Tendons Journal · doi:10.11138/mltj/2014.4.3.329 · Cited by 11 · see citing works

Maternal protein malnutrition: effects on prostate development and adult disease

Rinaldi, J. D. C., dos Santos, S. A. A., Colombelli, K. T., Birch, L. A., Prins, G. S., Justulin, L. A., & Felisbino, S. L. (2018) · Journal of Developmental Origins of Health and Disease · doi:10.1017/s2040174418000168 · Cited by 11 · see citing works

Gender specific association of parathyroid hormone and vitamin D with metabolic syndrome in population with preserved renal function

Kim, M., Lee, J., Ha, J., Jo, K., Lim, D.-J., Lee, J.-M., Chang, S., Kang, M.-I., & Cha, B. Y. (2018) · Scientific Reports · doi:10.1038/s41598-017-17397-9 · Cited by 10 · see citing works

The impact of sarcopenia on the efficacy of PD-1 inhibitors in non-small cell lung cancer and potential strategies to overcome resistance

Liu, Z., Lei, T., Guo, Y., & Zheng, C. (2024) · Frontiers in Pharmacology · doi:10.3389/fphar.2024.1377666 · Cited by 8 · see citing works

Estrogen in skeletal muscle: metabolism, mechanisms, and exercise-induced changes

Feng, Y., & Shi, R. (2025) · Journal of Endocrinological Investigation · doi:10.1007/s40618-025-02726-x · Cited by 8 · see citing works

Interaction of estradiol and vitamin D with low skeletal muscle mass among middle-aged and elderly women

Zhang, J., Cheng, Y., Chen, C., Wang, Q., Yang, C., Qiu, J., Li, J., Liu, X., Zhang, Y., Liu, L., et al. (2023) · BMC Women s Health · doi:10.1186/s12905-023-02646-z · Cited by 8 · see citing works

Dynapenia and Sarcopenia During Female Midlife

Pérez-López, F. R. (2017) · Springer eBooks · doi:10.1007/978-3-319-59318-0_20 · Cited by 8 · see citing works

Association Between Serum Follicle-Stimulating Hormone and Sarcopenia and Physical Disability Among Older Chinese Men: Evidence From a Cross-Sectional Study

Ke, Y., Xu, J., Zhang, X., Guo, Q., & Zhu, Y. (2022) · Frontiers in Medicine · doi:10.3389/fmed.2021.724649 · Cited by 7 · see citing works

A pro-inflammatory diet increases the risk of sarcopenia components and inflammatory biomarkers in postmenopausal women

Jin, M., Bok, M., Rho, H., Chon, J., & Lim, H. (2022) · Nutrition Research · doi:10.1016/j.nutres.2022.09.008 · Cited by 7 · see citing works

Estrogen regulates muscle bioenergetic signaling

Laakkonen, E. K., Soliymani, R., & Lalowski, M. M. (2018) · Aging · doi:10.18632/aging.101380 · Cited by 7 · see citing works

Identification of Target Body Composition Parameters by Dual-Energy X-Ray Absorptiometry, Bioelectrical Impedance, and Ultrasonography to Detect Older Adults With Frailty and Prefrailty Status Using a Mobile App in Primary Care Services: Descriptive Cross-Sectional Study

Ortiz-Navarro, B., Losa‐Reyna, J., Mihaiescu-Ion, V., García-Romero, J., de Albornoz-Gil, M. C., & Galán-Mercant, A. (2025) · JMIR Aging · doi:10.2196/67982 · Cited by 6 · see citing works

Physical Activity and Nutrition INfluences in Ageing: Current Findings from the PANINI Project

Whittaker, A. C., Asamane, E. A., Aunger, J. A., Bondarev, D., Cabbia, A., Doody, P., Gensous, N., Iadarola, B., Ramsey, K. A., Rodrigues, B., et al. (2019) · Advances in Geriatric Medicine and Research · doi:10.20900/agmr20190005 · Cited by 6 · see citing works

In vivo potentiation of muscle torque is enhanced in female mice through estradiol-estrogen receptor signaling

Le, G., Baumann, C. W., Warren, G. L., & Lowe, D. A. (2023) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00731.2022 · Cited by 6 · see citing works

Sarcopenia and Sarcopenic Obesity and Their Association with Cardiovascular Disease Risk in Postmenopausal Women: Results for the 2008-2011 Korea National Health and Nutrition Examination Survey

Kim, M., & Sohn, C. (2016) · 대한지역사회영양학회지 · doi:10.5720/kjcn.2016.21.4.378 · Cited by 6 · see citing works

Relationship of monocyte to high-density lipoprotein ratio (MHR) and other inflammatory biomarkers with sarcopenia: a population-based study

Xue, Z., Cao, J., Mou, J., Wang, R., & Liu, P. (2025) · Lipids in Health and Disease · doi:10.1186/s12944-025-02464-2 · Cited by 5 · see citing works

Dermal Advanced Glycation End-Product Accumulation is Associated with Sarcopenia-Related Measures in Middle-Aged and Older Men

Matsumoto, S., Ochi, M., Akechi, Y., Takei, S., Senzaki, K., Okada, Y., Miura, S., Ochi, H., Igase, M., & Ohyagi, Y. (2022) · Archives of Gerontology and Geriatrics · doi:10.1016/j.archger.2022.104704 · Cited by 5 · see citing works

Sex Differences in the Relationship of Muscle Strength, Proprioception, and Postural Stability in Older Adults

Gao, H., Hu, S., Hou, S., Song, Q., Shen, P., Liu, Y., & Ding, L. (2025) · Motor Control · doi:10.1123/mc.2024-0133 · Cited by 4 · see citing works

Associations Between Blood Concentrations of Sex Hormones and Physical Function in Community-Dwelling Older Women: A Prospective Cohort Study

Wang, Y., Islam, R. M., Hussain, S. M., McNeil, J. J., & Davis, S. R. (2023) · The Journals of Gerontology Series A · doi:10.1093/gerona/glad287 · Cited by 5 · see citing works

Role of Sarcopenia in Diabetes Mellitus

Rhee, S. Y. (2013) · Journal of Korean Diabetes · doi:10.4093/jkd.2013.14.4.178 · Cited by 4 · see citing works

A review of the status of sarcopenia in elderly hospitalized patients

Xian, X., Zhang, J., & Yang, H. (2025) · Medicine · doi:10.1097/md.0000000000043365 · Cited by 3 · see citing works

Explaining higher functional disability in women compared to men among older adults – the Singapore Chinese Health Study

Tan, L. F., Jin, A., Ying, A. F., Pan, A., Teng, G. G., & Koh, W. (2025) · BMC Geriatrics · doi:10.1186/s12877-025-06595-0 · Cited by 3 · see citing works

Sex hormones regulate neuromuscular junction structure, plasticity, and disease vulnerability

Qaisar, R., Ahmad, F., & Karim, A. (2026) · Discover Neuroscience · doi:10.1186/s13064-026-00241-0 · Cited by 3 · see citing works

Sex Differences in the Long-Term Consequences of Stroke

Stewart, C. E., Branyan, T. E., Sampath, D., & Sohrabji, F. (2022) · Current topics in behavioral neurosciences · doi:10.1007/7854_2022_311 · Cited by 3 · see citing works

Associated factors of low muscle mass in community-dwelling patients with type 2 diabetes

Lin, C., Yu, N., Wu, H., Liu, Y.-C., Chiu, I.-Y., Lin, W.-C., & Chien, W. (2024) · Medicine · doi:10.1097/md.0000000000038629 · Cited by 3 · see citing works

Strengths and Weaknesses of Two Theories for Explaining 15 Universal Sex Differences in Cognition and Behavior

Ellis, L. (2025) · Cambridge University Press eBooks · doi:10.1017/9781009581028 · Cited by 2 · see citing works

Impact of First 10 Years of Post Menopause on Muscle Function, Muscle Mass and Bone Mineral Density in Adult Women

Kochi, M. N., Marques, N. R., da, G. D. C., & Julia, C. (2015) · Journal of Osteoporosis and Physical Activity · doi:10.4172/2329-9509.1000151 · Cited by 3 · see citing works

Effects of exercise on circulating levels of sex hormones in overweight and obese postmenopausal women: A systematic review

Encabo, P. G., Valadés, D., de Cos, A. I., García‐Honduvilla, N., & Pérez‐López, A. (2019) · Science & Sports · doi:10.1016/j.scispo.2018.09.012 · Cited by 3 · see citing works

Sex-dependent and muscle-specific progression of the MYBPC1 E248K Myotrem myopathy in response to aging

Mariano, J. M., Joca, H. C., Kallenbach, J. G., Ranu, N., Ochala, J., Ward, C. W., & Kontrogianni‐Konstantopoulos, A. (2025) · JCI Insight · doi:10.1172/jci.insight.182471 · Cited by 2 · see citing works

Preventive Strategies to Reduce Sarcopenia Risk During GLP-1-Based Anti-Obesity Therapy

Belančić, A., Skroče, K., Gkrinia, E. M. M., Glavić, M. M., & Kwok, M. K. (2026) · Journal of Clinical Medicine · doi:10.3390/jcm15155870 · Cited by 2 · see citing works

Relevant Factors for Sarcopenia in Hyperthyroidism Patients

Liu, Z., Xia, F.-F., Zhao, X., & Zhou, D. (2018) · OALib · doi:10.4236/oalib.1104620 · Cited by 1 · see citing works

Cross-sectional and longitudinal associations between glycaemic measures and grip strength in people without diabetes in the UK Biobank cohort study

Granic, A., Cooper, R., Hurst, C., Hillman, S. J., Dodds, R. M., Witham, M. D., & Sayer, A. A. (2024) · European Geriatric Medicine · doi:10.1007/s41999-024-01119-2 · Cited by 2 · see citing works

Асоціація саркопенії й артеріальної гіпертензії, шляхи взаємного впливу на клінічний перебіг в осіб старших вікових груп (огляд літератури)

Masik, N. P., & Kalandey, K. Y. (2019) · PAIN JOINTS SPINE · doi:10.22141/2224-1507.9.2.2019.172123 · Cited by 2 · see citing works

The Role of Ultrasound Imaging of Musculotendinous Structures in the Elderly Population

Carrão, L., Santos, R. M., Espanha, M., Armada-da-Silva, P. A. S., Amaral, A. P., Amado, S., Almeida, H. A., Pascoal‐Faria, P., & Veloso, A. (2018) · Lecture notes in computational vision and biomechanics · doi:10.1007/978-3-319-71574-2_3 · Cited by 2 · see citing works

Hormone therapy and sarcopenia: implications for the prevention of frailty as women age

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Cross-bridge mechanisms of skeletal muscle fatigue: Effects of hydrogen ion, inorganic phosphate, and age

Nelson, C. R. (2014) · e-Publications@Marquette (Marquette University)

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Myllyaho, M. M. (2016) · Jyväskylä University Digital Archive (University of Jyväskylä)

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Trautman, K. A. (2020) · NDSU Repository (North Dakota State University)

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Lee, C. E., McArdle, A., & Griffiths, R. D. (2007) · Clinical Nutrition · doi:10.1016/j.clnu.2007.05.005 · Cited by 138 · see citing works

Global gene expression profiles in skeletal muscle of monozygotic female twins discordant for hormone replacement therapy

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