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Jeffrey Chamberlain
Jeffrey Chamberlain
University of Washington School of Medicine
Verified email at uw.edu - Homepage
Title
Cited by
Cited by
Year
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
20111988
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
11482007
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
10611988
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
7342004
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
6782002
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
6261993
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
5881997
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
4361995
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
4342017
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
4212009
Dystrophin‐deficient 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
3802007
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
3761993
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
3602006
Multiple PCR for the diagnosis of Duchenne muscular dystrophy.
JS Chamberlain
PCR protocols: a guide to methods and applicationsl., 272-281, 1990
3591990
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
3551998
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
3551995
Force and power output of fast and slow skeletal muscles from mdx mice 6‐28 months old
GS Lynch, RT Hinkle, JS Chamberlain, SV Brooks, JA Faulkner
The Journal of physiology 535 (2), 591-600, 2001
3542001
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
3302008
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
3261991
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
3122019
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