Следене
Eric P Hoffman
Eric P Hoffman
Professor, Department of Pharmaceutical Sciences, Binghamton University
Потвърден имейл адрес: binghamton.edu - Начална страница
Заглавие
Позовавания
Позовавания
Година
Dystrophin: the protein product of the Duchenne muscular dystrophy locus
EP Hoffman, RH Brown Jr, LM Kunkel
Cell 51 (6), 919-928, 1987
56871987
Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals
M Koenig, EP Hoffman, CJ Bertelson, AP Monaco, C Feener, LM Kunkel
Cell 50 (3), 509-517, 1987
31001987
Conversion of mdx myofibres from dystrophin-negative to-positive by injection of normal myoblasts
TA Partridge, JE Morgan, GR Coulton, EP Hoffman, LM Kunkel
Nature 337 (6203), 176-179, 1989
11121989
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
10831988
Multiple-laboratory comparison of microarray platforms
RA Irizarry, D Warren, F Spencer, IF Kim, S Biswal, BC Frank, ...
Nature methods 2 (5), 345-350, 2005
10742005
Glucose restriction inhibits skeletal myoblast differentiation by activating SIRT1 through AMPK-mediated regulation of Nampt
M Fulco, Y Cen, P Zhao, EP Hoffman, MW McBurney, AA Sauve, ...
Developmental cell 14 (5), 661-673, 2008
9232008
Duchenne muscular dystrophy: deficiency of dystrophin at the muscle cell surface
E Bonilla, CE Samitt, AF Miranda, AP Hays, G Salviati, S DiMauro, ...
Cell 54 (4), 447-452, 1988
7701988
Sir2 regulates skeletal muscle differentiation as a potential sensor of the redox state
M Fulco, RL Schiltz, S Iezzi, MT King, P Zhao, Y Kashiwaya, E Hoffman, ...
Molecular cell 12 (1), 51-62, 2003
7452003
Variability in muscle size and strength gain after unilateral resistance training
MJ Hubal, H Gordish-Dressman, PD Thompson, TB Price, EP Hoffman, ...
Medicine & science in sports & exercise 37 (6), 964-972, 2005
6892005
Expression profiling in the muscular dystrophies: identification of novel aspects of molecular pathophysiology
YW Chen, P Zhao, R Borup, EP Hoffman
The Journal of cell biology 151 (6), 1321-1336, 2000
5842000
Molecular cloning, structure, and chromosomal localization of the human inducible nitric oxide synthase gene.
NA Chartrain, DA Geller, PP Koty, NF Sitrin, AK Nussler, EP Hoffman, ...
Journal of biological chemistry 269 (9), 6765-6772, 1994
5711994
β–sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex
CG Bönnemann, R Modi, S Noguchi, Y Mizuno, M Yoshida, E Gussoni, ...
Nature genetics 11 (3), 266-273, 1995
5541995
Immunoelectron microscopic localization of dystrophin in myofibres
SC Watkins, EP Hoffman, HS Slayter, LM Kunkel
Nature 333 (6176), 863-866, 1988
5421988
Exploring the molecular basis for variability among patients with Becker muscular dystrophy: dystrophin gene and protein studies.
AH Beggs, EP Hoffman, JR Snyder, K Arahata, L Specht, F Shapiro, ...
American journal of human genetics 49 (1), 54, 1991
5351991
The homologue of the Duchenne locus is defective in X-linked muscular dystrophy of dogs
BJ Cooper, NJ Winand, H Stedman, BA Valentine, EP Hoffman, ...
Nature 334 (6178), 154-156, 1988
5301988
Genomics, intellectual disability, and autism
HC Mefford, ML Batshaw, EP Hoffman
New England Journal of Medicine 366 (8), 733-743, 2012
4982012
Efficacy of systemic morpholino exon‐skipping in Duchenne dystrophy dogs
T Yokota, Q Lu, T Partridge, M Kobayashi, A Nakamura, S Takeda, ...
Annals of Neurology: Official Journal of the American Neurological …, 2009
4872009
Long-term effects of glucocorticoids on function, quality of life, and survival in patients with Duchenne muscular dystrophy: a prospective cohort study
CM McDonald, EK Henricson, RT Abresch, T Duong, NC Joyce, F Hu, ...
The Lancet 391 (10119), 451-461, 2018
4732018
Dystrophin abnormalities in Duchenne/Becker muscular dystrophy
EP Hoffman, LM Kunkel
Neuron 2 (1), 1019-1029, 1989
4721989
Mutations in the integrin α7 gene cause congenital myopathy
YK Hayashi, FL Chou, E Engvall, M Ogawa, C Matsuda, S Hirabayashi, ...
Nature genetics 19 (1), 94-97, 1998
4621998
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