The DOI matches its Crossref record; 83 of the 83 references it cites were found in a registry or an index.
Inhibition of myostatin with emphasis on follistatin as a therapy for muscle disease
Open accessAbstract
In most cases, pharmacologic strategies to treat genetic muscle disorders and certain acquired disorders, such as sporadic inclusion body myositis, have produced modest clinical benefits. In these conditions, inhibition of the myostatin pathway represents an alternative strategy to improve functional outcomes. Preclinical data that support this approach clearly demonstrate the potential for blocking the myostatin pathway. Follistatin has emerged as a powerful antagonist of myostatin that can increase muscle mass and strength. Follistatin was first isolated from the ovary and is known to suppress follicle-stimulating hormone. This raises concerns for potential adverse effects on the hypothalamic-pituitary-gonadal axis and possible reproductive capabilities. In this review we demonstrate a strategy to bypass off-target effects using an alternatively spliced cDNA of follistatin (FS344) delivered by adeno-associated virus (AAV) to muscle. The transgene product is a peptide of 315 amino acids that is secreted from the muscle and circulates in the serum, thus avoiding cell-surface binding sites. Using this approach our translational studies show increased muscle size and strength in species ranging from mice to monkeys. Adverse effects are avoided, and no organ system pathology or change in reproductive capabilities has been seen. These findings provide the impetus to move toward gene therapy clinical trials with delivery of AAV-FS344 to increase size and function of muscle in patients with neuromuscular disease.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“FST acts as a multi-faceted hepatokine that is involved in reproduction [181], muscle growth [182], cancer development [183], and metabolism [184].”
From Hepatokines and metabolism: Deciphering communication from the liver (2021) · cites this paper as [182]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Regulation of skeletal muscle mass in mice by a new TGF-p superfamily member
McPherron, A. C., Lawler, A. M., & Lee, S.-J. (1997) · Nature · doi:10.1038/387083a0 · Cited by 4,013
Safety and Efficacy of Gene Transfer for Leber's Congenital Amaurosis
Maguire, A. M., Simonelli, F., Pierce, E. A., Pugh, E. N., Mingozzi, F., Bennicelli, J., Banfi, S., Marshall, K. A., Testa, F., Surace, E. M., et al. (2008) · New England Journal of Medicine · doi:10.1056/nejmoa0802315 · Cited by 2,145
Transcriptional control by the TGF‐β/Smad signaling system
Massagué, J., & Wotton, D. (2000) · The EMBO Journal · doi:10.1093/emboj/19.8.1745 · Cited by 1,990
Regulation of myostatin activity and muscle growth
Lee, S.-J., & McPherron, A. C. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.151270098 · Cited by 1,616
Myostatin, a Negative Regulator of Muscle Growth, Functions by Inhibiting Myoblast Proliferation
Thomas, M., Langley, B., Berry, C., Sharma, M., Kirk, S., Bass, J., & Kambadur, R. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m004356200 · Cited by 1,014
Myostatin Inhibits Myoblast Differentiation by Down-regulating MyoD Expression
Langley, B. C., Thomas, M., Bishop, A., Sharma, M., Gilmour, S., & Kambadur, R. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m204291200 · Cited by 910
Activin-Binding Protein from Rat Ovary Is Follistatin
Nakamura, T., Takio, K., Eto, Y., Shibai, H., Titani, K., & Sugino, H. (1990) · Science · doi:10.1126/science.2106159 · Cited by 883
Functional improvement of dystrophic muscle by myostatin blockade
Bogdanovich, S., Krag, T. O. B., Barton, E. R., Morris, L. D., Whittemore, L.-A., Ahima, R. S., & Khurana, T. S. (2002) · Nature · doi:10.1038/nature01154 · Cited by 831
REGULATION OF MUSCLE MASS BY MYOSTATIN
Lee, S.-J. (2004) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.20.012103.135836 · Cited by 819
Mesoangioblast stem cells ameliorate muscle function in dystrophic dogs
Sampaolesi, M., Blot, S., D’Antona, G., Granger, N. P., Tonlorenzi, R., Innocenzi, A., Mognol, P., Thibaud, J. L., Gálvez, B. G., Barthélémy, I., et al. (2006) · Nature · doi:10.1038/nature05282 · Cited by 768
Systemic delivery of genes to striated muscles using adeno-associated viral vectors
Gregorevic, P., Blankinship, M. J., Allen, J. M., Crawford, R. W., Meuse, L., Miller, D. G., Russell, D. W., & Chamberlain, J. S. (2004) · Nature Medicine · doi:10.1038/nm1085 · Cited by 620
Psychiatric and Medical Effects of Anabolic-Androgenic Steroid Use
Pope, H. G. (1994) · Archives of General Psychiatry · doi:10.1001/archpsyc.1994.03950050035004 · Cited by 606
Multiple defects and perinatal death in mice deficient in follistatin
Matzuk, M. M., Lu, N., Vogel, H. S., Sellheyer, K., Roop, D. R., & Bradley, A. (1995) · Nature · doi:10.1038/374360a0 · Cited by 584
Aminoglycoside antibiotics restore dystrophin function to skeletal muscles of mdx mice
Barton-Davis, E. R., Cordier, L., Shoturma, D. I., Leland, S. E., & Sweeney, H. L. (1999) · Journal of Clinical Investigation · doi:10.1172/jci7866 · Cited by 579
Rebbapragada, A., Benchabane, H., Wrana, J. L., Celeste, A. J., & Attisano, L. (2003) · Molecular and Cellular Biology · doi:10.1128/mcb.23.20.7230-7242.2003 · Cited by 573
Emerging Themes in Lipid Rafts and Caveolae
Galbiati, F., Razani, B., & Lisanti, M. P. (2001) · Cell · doi:10.1016/s0092-8674(01)00472-x · Cited by 567
Randomized, Double-Blind Six-Month Trial of Prednisone in Duchenne's Muscular Dystrophy
Mendell, J. R., Moxley, R. T., Griggs, R. C., Brooke, M. H., Fenichel, G. M., Miller, J. P., King, W. M., Signore, L., Pandya, S., Florence, J. M., et al. (1989) · New England Journal of Medicine · doi:10.1056/nejm198906153202405 · Cited by 520
Regulation of muscle growth by multiple ligands signaling through activin type II receptors
Lee, S.-J., Reed, L. A., Davies, M. V., Girgenrath, S., Goad, M. E. P., Tomkinson, K. N., Wright, J. F., Barker, C., Ehrmantraut, G., Holmstrom, J., et al. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0505996102 · Cited by 501
A phase I/IItrial of MYO‐029 in adult subjects with muscular dystrophy
Wagner, K. R., Fleckenstein, J. L., Amato, A. A., Barohn, R. J., Bushby, K., Escolar, D. M., Flanigan, K. M., Pestronk, A., Tawil, R., Wolfe, G. I., et al. (2008) · Annals of Neurology · doi:10.1002/ana.21338 · Cited by 481
Self-citationUeno, N., LING, N. C., Ying, S. Y., Esch, F. S., Shimasaki, S., & Guillemin, R. (1987) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.84.23.8282 · Cited by 445
Hill, J. J., Davies, M. V., Pearson, A. A., Wang, J. H., Hewick, R. M., Wolfman, N. M., & Qiu, Y. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m206379200 · Cited by 444
Loss of myostatin attenuates severity of muscular dystrophy in mdx mice
Wagner, K. R., McPherron, A. C., Winik, N., & Lee, S. (2002) · Annals of Neurology · doi:10.1002/ana.10385 · Cited by 378
Use of doping agents, particularly anabolic steroids, in sports and society
Sjöqvist, F., Garle, M., & Rane, A. (2008) · The Lancet · doi:10.1016/s0140-6736(08)60801-6 · Cited by 349
Robertson, D. M., Klein, R., de Vos, F. L., McLachlan, R. I., Wettenhall, R. E. H., Hearn, M. T. W., Burger, H., & de Kretser, D. M. (1987) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(87)90430-x · Cited by 345
Minetti, G., Colussi, C., Adami, R., Serra, C., Mozzetta, C., Parente, V., Fortuni, S., Straino, S., Sampaolesi, M., Padova, M. D., et al. (2006) · Nature Medicine · doi:10.1038/nm1479 · Cited by 343
Lower skeletal muscle mass in male transgenic mice with muscle-specific overexpression of myostatin
Reisz‐Porszasz, S., Bhasin, S., Artaza, J. N., Shen, R., Sinha‐Hikim, I., Hogue, A., Fielder, T. J., & González-Cadavid, N. F. (2003) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00107.2003 · Cited by 333
Immune Responses to AAV in Clinical Trials
Mingozzi, F., & A. High, K. (2011) · Current Gene Therapy · doi:10.2174/156652311796150354 · Cited by 324
Quadrupling Muscle Mass in Mice by Targeting TGF-ß Signaling Pathways
Lee, S.-J. (2007) · PLoS ONE · doi:10.1371/journal.pone.0000789 · Cited by 316
Clinical gene therapy using recombinant adeno-associated virus vectors
Mueller, C., & Flotte, T. R. (2008) · Gene Therapy · doi:10.1038/gt.2008.68 · Cited by 312
rAAV6-microdystrophin preserves muscle function and extends lifespan in severely dystrophic mice
Gregorevic, P., Allen, J. M., Minami, E., Blankinship, M. J., Haraguchi, M., Meuse, L., Finn, E. E., Adams, M. E., Froehner, S. C., Murry, C. E., et al. (2006) · Nature Medicine · doi:10.1038/nm1439 · Cited by 309
Practice Parameter: Corticosteroid treatment of Duchenne dystrophy [RETIRED]
Moxley, R. T., Ashwal, S., Pandya, S., Connolly, A. M., Florence, J. M., Mathews, K. D., Baumbach, L. L., McDonald, C. M., Sussman, M. D., & Wade, C. (2005) · Neurology · doi:10.1212/01.wnl.0000148485.00049.b7 · Cited by 301
Jones, K. L., Mansell, A. S., Patella, S., Scott, B. J., Hedger, M. P., de Kretser, D., & Phillips, D. J. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0705971104 · Cited by 284
Follistatin: A Multifunctional Regulatory Protein
Phillips, D. J., & de Kretser, D. M. (1998) · Frontiers in Neuroendocrinology · doi:10.1006/frne.1998.0169 · Cited by 274
Haidet, A. M., Rizo, L., Handy, C. R., Umapathi, P., Eagle, A., Shilling, C., Boué, D. R., Martin, P. T., Sahenk, Z., Mendell, J. R., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0709144105 · Cited by 274
Myostatin Directly Regulates Skeletal Muscle Fibrosis
Li, Z. B., Kollias, H. D., & Wagner, K. R. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m802585200 · Cited by 267
Comparative Genome Map of Human and Cattle
Solinas‐Toldo, S., Lengauer, C., & Fries, R. (1995) · Genomics · doi:10.1006/geno.1995.1081 · Cited by 266
Myostatin propeptide‐mediated amelioration of dystrophic pathophysiology
Bogdanovich, S., Perkins, K. J., Krag, T. O. B., Whittemore, L.-A., & Khurana, T. S. (2005) · The FASEB Journal · doi:10.1096/fj.04-2796com · Cited by 244
Immune Responses to AAV in Clinical Trials
Mingozzi, F., & High, K. A. (2007) · Current Gene Therapy · doi:10.2174/156652307782151425 · Cited by 241
Primary structure of the human follistatin precursor and its genomic organization
Shimasaki, S., Koga, M., Esch, F., Cooksey, K., Mercado, M., Koba, A., Ueno, N., Ying, S. Y., Ling, N., & Guillemin, R. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.12.4218 · Cited by 232
Sugino, K., Kurosawa, N., Nakamura, T., Takio, K., Shimasaki, S., LING, N. C., Titani, K., & Sugino, H. (1993) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)82296-7 · Cited by 228
Hill, J. J., Qiu, Y., Hewick, R. M., & Wolfman, N. M. (2003) · Molecular Endocrinology · doi:10.1210/me.2002-0366 · Cited by 225
Overexpression of Mouse Follistatin Causes Reproductive Defects in Transgenic Mice
Guo, Q., Kumar, T. R., Woodruff, T. K., Hadsell, L. A., DeMayo, F. J., & Matzuk, M. M. (1998) · Molecular Endocrinology · doi:10.1210/mend.12.1.0053 · Cited by 209
McClorey, G., Moulton, H. M., Iversen, P. L., Fletcher, S., & Wilton, S. D. (2006) · Gene Therapy · doi:10.1038/sj.gt.3302800 · Cited by 208
Tsuchida, K., Arai, K. Y., Kuramoto, Y., Yamakawa, N., Hasegawa, Y., & Sugino, H. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m006114200 · Cited by 192
Hashimoto, O., Nakamura, T., Shoji, H., Shimasaki, S., Hayashi, Y., & Sugino, H. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.21.13835 · Cited by 186
Liu, M., Yue, Y., Harper, S. Q., Grange, R. W., Chamberlain, J. S., & Duan, D. (2005) · Molecular Therapy · doi:10.1016/j.ymthe.2004.09.013 · Cited by 178
Esch, F. S., Shimasaki, S., Mercado, M., Cooksey, K., LING, N. C., Ying, S., Ueno, N., & Guillemin, R. (1987) · Molecular Endocrinology · doi:10.1210/mend-1-11-849 · Cited by 175
Qiao, C., Li, J., Jiang, J., Zhu, X., Wang, B., Li, J., & Xiao, X. (2008) · Human Gene Therapy · doi:10.1089/hum.2007.159 · Cited by 161
Caveolae — from ultrastructure to molecular mechanisms
Parton, R. G. (2003) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1017 · Cited by 151
Amthor, H., Huang, R., McKinnell, I. W., Christ, B., Kambadur, R., Sharma, M., & Patel, K. (2002) · Developmental Biology · doi:10.1006/dbio.2002.0812 · Cited by 138
Lenders, J. W. M., Demacker, P. N. M., Vos, J., Jansen, P. L. M., Hoitsma, A. J., Laar, A. V. '., & Thien, T. A. (1988) · International Journal of Sports Medicine · doi:10.1055/s-2007-1024972 · Cited by 126
Cerletti, M., Negri, T., Cozzi, F., Colpo, R., Andreetta, F., Croci, D., Davies, K. E., Cornelio, F., Pozza, O., Karpati, G., et al. (2003) · Gene Therapy · doi:10.1038/sj.gt.3301941 · Cited by 126
Muscular atrophy of caveolin-3–deficient mice is rescued by myostatin inhibition
Ohsawa, Y., Hagiwara, H., Nakatani, M., Yasue, A., Moriyama, K., Murakami, T., Tsuchida, K., Noji, S., & Sunada, Y. (2006) · Journal of Clinical Investigation · doi:10.1172/jci28520 · Cited by 122
Shimasaki, S., Koga, M., Esch, F. S., Mercado, M., Cooksey, K., Koba, A., & LING, N. C. (1988) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(88)80097-4 · Cited by 115
The androgen receptor A mediator of diverse responses
Chang, C. (1996) · Frontiers in bioscience · doi:10.2741/a116 · Cited by 104
Parsons, S. A., Millay, D. P., Sargent, M. A., McNally, E. M., & Molkentin, J. D. (2006) · American Journal Of Pathology · doi:10.2353/ajpath.2006.051316 · Cited by 102
Therapeutic potential of follistatin for colonic inflammation in mice
Dohi, T., Ejima, C., Kato, R., Kawamura, Y. I., Kawashima, R., Mizutani, N., Tabuchi, Y., & Kojima, I. (2005) · Gastroenterology · doi:10.1053/j.gastro.2004.11.063 · Cited by 95
Bartoli, M., Poupiot, J., Vulin, A., Fougerousse, F., Arandel, L., Danièle, N., Roudaut, C., Noulet, F., Garcı́a, L., Danos, O., et al. (2007) · Gene Therapy · doi:10.1038/sj.gt.3302928 · Cited by 85
A CAV3 microdeletion differentially affects skeletal muscle and myocardium
Cagliani, R., Bresolin, N., Prelle, A. C., Gallanti, A., Fortunato, F., Sironi, M., Ciscato, P., Fagiolari, G., Bonato, S., Galbiati, S., et al. (2003) · Neurology · doi:10.1212/01.wnl.0000097320.35982.03 · Cited by 84
Aartsma-Rus, A. M., Kaman, W. E., Weij, R., den Dunnen, J. T., van Ommen, G. B., & van Deutekom, J. C. T. (2006) · Molecular Therapy · doi:10.1016/j.ymthe.2006.02.022 · Cited by 79
Bogdanovich, S., McNally, E. M., & Khurana, T. S. (2007) · Muscle & Nerve · doi:10.1002/mus.20920 · Cited by 77
Evans, L., Muttukrishna, S., & Groome, N. (1998) · Journal of Endocrinology · doi:10.1677/joe.0.1560275 · Cited by 77
Transcriptional activation of the gonadotropin-releasing hormone receptor gene by activin A
Fernández‐Vázquez, G., Kaiser, U. B., Albarracin, C. T., & Chin, W. W. (1996) · Molecular Endocrinology · doi:10.1210/mend.10.4.8721981 · Cited by 75
Abmayr, S., Gregorevic, P., Allen, J. M., & Chamberlain, J. S. (2005) · Molecular Therapy · doi:10.1016/j.ymthe.2005.04.001 · Cited by 73
Hartgens, F., Cheriex, E. C., & Kuipers, H. (2003) · International Journal of Sports Medicine · doi:10.1055/s-2003-40705 · Cited by 71
Differential distribution of follistatin isoforms: application of a new FS315-specific immunoassay
Schneyer, A. L., Wang, Q., Sidis, Y., & Sluss, P. M. (2004) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2004-0162 · Cited by 71
The Congenital Muscular Dystrophies: Recent Advances and Molecular Insights
Mendell, J. R., Boué, D. R., & Martin, P. T. (2006) · Pediatric and Developmental Pathology · doi:10.2350/06-07-0127.1 · Cited by 69
Kuang, W., Xu, H. M., Vilquin, J., & Engvall, E. (1999) · PubMed · Cited by 69
Li, Z., Shelton, G. D., & Engvall, E. (2005) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)62271-7 · Cited by 67
Serum follistatin levels in women: evidence against an endocrine function of ovarian follistatin
Khoury, R. H., Wang, Q. F., Crowley, W. F., Hall, J. E., Schneyer, A. L., Toth, T. L., MIDGLEY, A. R., & Sluss, P. M. (1995) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.80.4.7714112 · Cited by 63
WAKATSUKI, M., Shintani, Y., Abe, M., Liu, Z. H., Shitsukawa, K., & Saito, S. (1996) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.81.2.8636280 · Cited by 52
Activin A and follistatin are dynamically regulated during human pregnancy
Woodruff, T. K., Sluss, P., Wang, E., Janssen, I., & Mersol-Barg, M. S. (1997) · Journal of Endocrinology · doi:10.1677/joe.0.1520167 · Cited by 50
Drug evaluation: PTC-124--a potential treatment of cystic fibrosis and Duchenne muscular dystrophy.
Hamed, S. A. (2006) · PubMed · Cited by 48
The Heparin Binding Site of Follistatin Is Involved in Its Interaction with Activin
Sumitomo, S., Inouye, S., Liu, X. J., LING, N. C., & Shimasaki, S. (1995) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1995.1297 · Cited by 43
Administration of myostatin does not alter fat mass in adult mice
Stolz, L. E., Li, D., Qadri, A., Jalenak, M., Klaman, L. D., & Tobin, J. F. (2006) · Diabetes Obesity and Metabolism · doi:10.1111/j.1463-1326.2006.00672.x · Cited by 40
Transcriptional activation of the gonadotropin-releasing hormone receptor gene by activin A
Fernandez-Vazquez, G. (1996) · Molecular Endocrinology · doi:10.1210/me.10.4.356 · Cited by 39
Balagopal, P., Olney, R. C., Darmaun, D., Mougey, E. B., Dokler, M., Sieck, G. C., & Hammond, D. (2005) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00412.2005 · Cited by 38
Alén, M., & Rahkila, P. (1984) · International Journal of Sports Medicine · doi:10.1055/s-2008-1025929 · Cited by 36
A CAV3 microdeletion differentially affects skeletal muscle and myocardium
Finsterer, J., & Stoellberger, C. (2004) · Neurology · doi:10.1212/wnl.63.1.195 · Cited by 33
Development and validation of a radioimmunoassay for follistatin in human serum
Gilfillan, C. P., & Robertson, D. M. (1994) · Clinical Endocrinology · doi:10.1111/j.1365-2265.1994.tb02576.x · Cited by 27
WANG, Q. F., Farnworth, P. G., Findlay, J. K., & Burger, H. (1990) · Endocrinology · doi:10.1210/endo-127-3-1385 · Cited by 24
Wang, Q. F., Farnworth, P. G., Burger, H., & Findlay, J. K. (1990) · Molecular and Cellular Endocrinology · doi:10.1016/0303-7207(90)90237-3 · Cited by 12
Left Ventricular Dimensions and Function in Strength Athletes
Kindermann, W., & Urhausen, A. J. P. (2004) · International Journal of Sports Medicine · doi:10.1055/s-2004-817850 · Cited by 7
Flagged first, then by citations
Cited by
Sorted by citations
Diamanti-Kandarakis, E., & Dunaif, A. (2012) · Endocrine Reviews · doi:10.1210/er.2011-1034 · Cited by 1,947
Aberrant repair and fibrosis development in skeletal muscle
Mann, C. J., Perdiguero, E., Kharraz, Y., Aguilar, S., Pessina, P., Serrano, A. L., & Muñoz-Cánoves, P. (2011) · Skeletal Muscle · doi:10.1186/2044-5040-1-21 · Cited by 853
“Normal myostatin signaling can be counter-regulated by the extracellular protein follistatin [95].”
BackgroundAnimal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapy
McGreevy, J. W., Hakim, C. H., McIntosh, M. A., & Duan, D. (2015) · Disease Models & Mechanisms · doi:10.1242/dmm.018424 · Cited by 534
Skeletal muscle fibrosis: an overview
Mahdy, M. A. A. (2018) · Cell and Tissue Research · doi:10.1007/s00441-018-2955-2 · Cited by 320
Regulation of Muscle Mass by Follistatin and Activins
Lee, S.-J., Lee, Y.-S., Zimmers, T. A., Soleimani, A., Matzuk, M. M., Tsuchida, K., Cohn, R. D., & Barton, E. R. (2010) · Molecular Endocrinology · doi:10.1210/me.2010-0127 · Cited by 273
Metadata
- Authors
- Rodino‐Klapac, L. R., Haidet, A. M., Kota, J., Handy, C., Kaspar, B. K., & Mendell, J. R.
- Affiliations
- Nationwide Children's Hospital (US)
- Corresponding author
- Mendell, Jerry R.
- Venue
- Muscle & Nerve
- Publisher
- Wiley
- Published
- 2009-02-10
- Volume
- 39
- Issue
- 3
- Pages
- 283-296
- ISSN
- 0148-639X (ISSN-L)
- 1097-4598
- PMC
- PMC2717722
- OpenAlex
- W2108645449
- Cited by
- 194
- References
- 83
- Citations by year
- 2026: 6 · 2025: 5 · 2024: 4 · 2023: 8 · 2022: 8 · 2021: 9 · 2020: 13 · 2019: 12 · 2018: 14 · 2017: 7 · 2016: 14 · 2015: 10 · 2014: 10 · 2013: 10 · 2012: 21
- FWCI
- 1.63
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Muscle & Nerve (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Neurological Disorders and Stroke (F31NS058224)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Health Sciences › Medicine › Genetics (clinical) › Neurogenetic and Muscular Disorders Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Virus-based gene therapy research
- Keywords
- myostatin inhibition, follistatin, adeno-associated virus gene therapy, myopathy, neuromuscular disorders, sporadic inclusion body myositis, muscle mass and strength, hypothalamic-pituitary-gonadal axis, reproductive safety, alternative splicing
- MeSH terms
- Dependovirus, Animals, Humans, Mice, Mutant Strains, Muscles, Muscular Diseases, Genetic Therapy, Alternative Splicing, DNA, Complementary, Follistatin, Mice, Myostatin
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review