| Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification JS Chamberlain, RA Gibbs, JE Rainer, PN Nguyen, C Thomas Nucleic acids research 16 (23), 11141-11156, 1988 | 2012 | 1988 |
| Pericytes of human skeletal muscle are myogenic precursors distinct from satellite cells A Dellavalle, M Sampaolesi, R Tonlorenzi, E Tagliafico, B Sacchetti, ... Nature cell biology 9 (3), 255-267, 2007 | 1150 | 2007 |
| Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscular dystrophy EP Hoffman, KH Fischbeck, RH Brown, M Johnson, R Medori, JD Loire, ... New England Journal of Medicine 318 (21), 1363-1368, 1988 | 1062 | 1988 |
| Systemic delivery of genes to striated muscles using adeno-associated viral vectors P Gregorevic, MJ Blankinship, JM Allen, RW Crawford, L Meuse, ... Nature medicine 10 (8), 828-834, 2004 | 734 | 2004 |
| Modular flexibility of dystrophin: implications for gene therapy of Duchenne muscular dystrophy SQ Harper, MA Hauser, C DelloRusso, D Duan, RW Crawford, SF Phelps, ... Nature medicine 8 (3), 253-261, 2002 | 679 | 2002 |
| X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus. JA Towbin, JF Hejtmancik, P Brink, B Gelb, XM Zhu, JS Chamberlain, ... Circulation 87 (6), 1854-1865, 1993 | 626 | 1993 |
| Animal models for muscular dystrophy show different patterns of sarcolemmal disruption V Straub, JA Rafael, JS Chamberlain, KP Campbell The Journal of cell biology 139 (2), 375-385, 1997 | 588 | 1997 |
| Identification and characterization of the dystrophin anchoring site on β-dystroglycan D Jung, B Yang, J Meyer, JS Chamberlain, KP Campbell Journal of Biological Chemistry 270 (45), 27305-27310, 1995 | 436 | 1995 |
| Muscle-specific CRISPR/Cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for Duchenne muscular dystrophy NE Bengtsson, JK Hall, GL Odom, MP Phelps, CR Andrus, RD Hawkins, ... Nature communications 8 (1), 14454, 2017 | 435 | 2017 |
| Dystrophins carrying spectrin-like repeats 16 and 17 anchor nNOS to the sarcolemma and enhance exercise performance in a mouse model of muscular dystrophy Y Lai, GD Thomas, Y Yue, HT Yang, D Li, C Long, L Judge, B Bostick, ... The Journal of clinical investigation 119 (3), 624-635, 2009 | 421 | 2009 |
| Dystrophindeficient mdx mice display a reduced life span and are susceptible to spontaneous rhabdomyosarcoma JS Chamberlain, J Metzger, M Reyes, DW Townsend, JA Faulkner Federation of American Societies for Experimental Biology, 2007 | 381 | 2007 |
| Overexpression of dystrophin in transgenic mdx mice eliminates dystrophic symptoms without toxicity GA Cox, NM Cole, K Matsumura, SF Phelps, SD Hauschka, KP Campbell, ... Nature 364 (6439), 725-729, 1993 | 376 | 1993 |
| rAAV6-microdystrophin preserves muscle function and extends lifespan in severely dystrophic mice P Gregorevic, JM Allen, E Minami, MJ Blankinship, M Haraguchi, L Meuse, ... Nature medicine 12 (7), 787-789, 2006 | 361 | 2006 |
| Multiple PCR for the diagnosis of Duchenne muscular dystrophy. JS Chamberlain PCR protocols: a guide to methods and applicationsl., 272-281, 1990 | 359 | 1990 |
| Production and characterization of improved adenovirus vectors with the E1, E2b, and E3 genes deleted A Amalfitano, MA Hauser, H Hu, D Serra, CR Begy, JS Chamberlain Journal of virology 72 (2), 926-933, 1998 | 355 | 1998 |
| Expression of full-length and truncated dystrophin mini-genes in transgenic mdx mice SF Phelps, MA Hauser, NM Cole, JA Rafael, RT Hinkle, JA Faulkner, ... Human molecular genetics 4 (8), 1251-1258, 1995 | 355 | 1995 |
| Force and power output of fast and slow skeletal muscles from mdx mice 628 months old GS Lynch, RT Hinkle, JS Chamberlain, SV Brooks, JA Faulkner The Journal of physiology 535 (2), 591-600, 2001 | 354 | 2001 |
| Sarcolemma-localized nNOS is required to maintain activity after mild exercise YM Kobayashi, EP Rader, RW Crawford, NK Iyengar, DR Thedens, ... Nature 456 (7221), 511-515, 2008 | 330 | 2008 |
| Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphisms. PR Clemens, RG Fenwick, JS Chamberlain, RA Gibbs, M De Andrade, ... American journal of human genetics 49 (5), 951, 1991 | 326 | 1991 |
| High levels of AAV vector integration into CRISPR-induced DNA breaks KS Hanlon, BP Kleinstiver, SP Garcia, MP Zaborowski, A Volak, SE Spirig, ... Nature communications 10 (1), 4439, 2019 | 315 | 2019 |
