Elizabeth M. McNally
Elizabeth M. McNally
Zweryfikowany adres z northwestern.edu - Strona główna
Cytowane przez
Cytowane przez
The ubiquitin-modifying enzyme A20 is required for termination of Toll-like receptor responses
DL Boone, EE Turer, EG Lee, RC Ahmad, MT Wheeler, C Tsui, P Hurley, ...
Nature immunology 5 (10), 1052-1060, 2004
Myosin subfragment-1 is sufficient to move actin filaments in vitro
YY Toyoshima, SJ Kron, EM McNally, KR Niebling, C Toyoshima, ...
Nature 328 (6130), 536-539, 1987
Mutations in the dystrophin-associated protein γ-sarcoglycan in chromosome 13 muscular dystrophy
S Noguchi, EM McNally, KB Othmane, Y Hagiwara, Y Mizuno, M Yoshida, ...
Science 270 (5237), 819-822, 1995
The dystrophin glycoprotein complex: signaling strength and integrity for the sarcolemma
KA Lapidos, R Kakkar, EM McNally
Circulation research 94 (8), 1023-1031, 2004
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
Genetic mutations and mechanisms in dilated cardiomyopathy
EM McNally, JR Golbus, MJ Puckelwartz
The Journal of clinical investigation 123 (1), 19-26, 2013
γ-Sarcoglycan deficiency leads to muscle membrane defects and apoptosis independent of dystrophin
AA Hack, CT Ly, F Jiang, CJ Clendenin, KS Sigrist, RL Wollmann, ...
The Journal of cell biology 142 (5), 1279-1287, 1998
Nesprin-1α self-associates and binds directly to emerin and lamin A in vitro
JMK Mislow, JM Holaska, MS Kim, KK Lee, M Segura-Totten, KL Wilson, ...
FEBS letters 525 (1-3), 135-140, 2002
Filamin 2 (FLN2): A muscle-specific sarcoglycan interacting protein
TG Thompson, YM Chan, AA Hack, M Brosius, M Rajala, HGW Lidov, ...
The Journal of cell biology 148 (1), 115-126, 2000
Dilated cardiomyopathy: genetic determinants and mechanisms
EM McNally, L Mestroni
Circulation research 121 (7), 731-748, 2017
Mechanisms of muscle degeneration, regeneration, and repair in the muscular dystrophies
GQ Wallace, EM McNally
Annual review of physiology 71, 37-57, 2009
Episodic coronary artery vasospasm and hypertension develop in the absence of Sur2 KATP channels
WA Chutkow, J Pu, MT Wheeler, T Wada, JC Makielski, CF Burant, ...
The Journal of clinical investigation 110 (2), 203-208, 2002
Dominant negative myostatin produces hypertrophy without hyperplasia in muscle
X Zhu, M Hadhazy, M Wehling, JG Tidball, EM McNally
FEBS letters 474 (1), 71-75, 2000
Caveolin-3 in muscular dystrophy
EM McNally, E de Sá Moreira, DJ Duggan, CG Bönnemann, MP Lisanti, ...
Human molecular genetics 7 (5), 871-877, 1998
Hormonal modulation of a gene injected into rat heart in vivo.
RN Kitsis, PM Buttrick, EM McNally, ML Kaplan, LA Leinwand
Proceedings of the National Academy of Sciences 88 (10), 4138-4142, 1991
Differential requirement for individual sarcoglycans and dystrophin in the assembly and function of the dystrophin-glycoprotein complex
AA Hack, MY Lam, L Cordier, DI Shoturma, CT Ly, MA Hadhazy, ...
Journal of cell science 113 (14), 2535-2544, 2000
Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23
DN Messina, MC Speer, MA Pericak-Vance, EM McNally
The American Journal of Human Genetics 61 (4), 909-917, 1997
The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies
M Vainzof, MR Passos-Bueno, M Canovas, ES Moreira, RCM Pavanello, ...
Human molecular genetics 5 (12), 1963-1969, 1996
Calcium-sensitive phospholipid binding properties of normal and mutant ferlin C2 domains
DB Davis, KR Doherty, AJ Delmonte, EM McNally
Journal of Biological Chemistry 277 (25), 22883-22888, 2002
Normal myoblast fusion requires myoferlin
KR Doherty, A Cave, DB Davis, AJ Delmonte, A Posey, JU Earley, ...
Development 132 (24), 5565-5575, 2005
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