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Kudryashova Elena
Kudryashova Elena
Research Scientist, The Ohio State University
在 osu.edu 的电子邮件经过验证 - 首页
标题
引用次数
引用次数
年份
Osteopontin promotes fibrosis in dystrophic mouse muscle by modulating immune cell subsets and intramuscular TGF-β
SA Vetrone, E Montecino-Rodriguez, E Kudryashova, I Kramerova, ...
The Journal of clinical investigation 119 (6), 1583-1594, 2009
3402009
Trim32 is a ubiquitin ligase mutated in limb girdle muscular dystrophy type 2H that binds to skeletal muscle myosin and ubiquitinates actin
E Kudryashova, D Kudryashov, I Kramerova, MJ Spencer
Journal of molecular biology 354 (2), 413-424, 2005
2542005
Null mutation of calpain 3 (p94) in mice causes abnormal sarcomere formation in vivo and in vitro
I Kramerova, E Kudryashova, JG Tidball, MJ Spencer
Human molecular genetics 13 (13), 1373-1388, 2004
2402004
Opposing activities of IFITM proteins in SARS‐CoV‐2 infection
G Shi, AD Kenney, E Kudryashova, A Zani, L Zhang, KK Lai, ...
The EMBO journal 40 (3), e106501, 2021
2122021
Calpain 3 participates in sarcomere remodeling by acting upstream of the ubiquitin–proteasome pathway
I Kramerova, E Kudryashova, G Venkatraman, MJ Spencer
Human molecular genetics 14 (15), 2125-2134, 2005
1932005
Satellite cell senescence underlies myopathy in a mouse model of limb-girdle muscular dystrophy 2H
E Kudryashova, I Kramerova, MJ Spencer
The Journal of clinical investigation 122 (5), 1764-1776, 2012
1512012
Deficiency of the E3 ubiquitin ligase TRIM32 in mice leads to a myopathy with a neurogenic component
E Kudryashova, J Wu, LA Havton, MJ Spencer
Human molecular genetics 18 (7), 1353-1367, 2009
1382009
Novel role of calpain-3 in the triad-associated protein complex regulating calcium release in skeletal muscle
I Kramerova, E Kudryashova, B Wu, C Ottenheijm, H Granzier, ...
Human molecular genetics 17 (21), 3271-3280, 2008
1232008
Calpain 3 cleaves filamin C and regulates its ability to interact with γ‐and δ‐sarcoglycans
JR Guyon, E Kudryashova, A Potts, I Dalkilic, MA Brosius, TG Thompson, ...
Muscle & Nerve: Official Journal of the American Association of …, 2003
1212003
Expression of adhesion molecule T-cadherin is increased during neointima formation in experimental restenosis
E Kudrjashova, P Bashtrikov, V Bochkov, Y Parfyonova, V Tkachuk, ...
Histochemistry and cell biology 118, 281-290, 2002
1092002
Human Defensins Facilitate Local Unfolding of Thermodynamically Unstable Regions of Bacterial Protein Toxins
E Kudryashova, R Quintyn, S Seveau, W Lu, VH Wysocki, DS Kudryashov
Immunity 41 (5), 709-721, 2014
922014
Mitochondrial abnormalities, energy deficit and oxidative stress are features of calpain 3 deficiency in skeletal muscle
I Kramerova, E Kudryashova, B Wu, S Germain, K Vandenborne, ...
Human molecular genetics 18 (17), 3194-3205, 2009
812009
Mdm muscular dystrophy: interactions with calpain 3 and a novel functional role for titin's N2A domain
KA Huebsch, E Kudryashova, CM Wooley, RB Sher, KL Seburn, ...
Human molecular genetics 14 (19), 2801-2811, 2005
742005
Regulation of the M-cadherin-β-catenin complex by calpain 3 during terminal stages of myogenic differentiation
I Kramerova, E Kudryashova, B Wu, MJ Spencer
Molecular and Cellular Biology 26 (22), 8437-8447, 2006
722006
Impaired calcium calmodulin kinase signaling and muscle adaptation response in the absence of calpain 3
I Kramerova, E Kudryashova, N Ermolova, A Saenz, O Jaka, ...
Human molecular genetics 21 (14), 3193-3204, 2012
642012
Identification of putative in vivo substrates of calpain 3 by comparative proteomics of overexpressing transgenic and nontransgenic mice
N Cohen, E Kudryashova, I Kramerova, LVB Anderson, JS Beckmann, ...
Proteomics 6 (22), 6075-6084, 2006
632006
Calcium binding is essential for plastin 3 function in Smn-deficient motoneurons
AN Lyon, RH Pineda, E Kudryashova, DS Kudryashov, CE Beattie
Human molecular genetics 23 (8), 1990-2004, 2013
582013
ACD toxin–produced actin oligomers poison formin-controlled actin polymerization
DB Heisler, E Kudryashova, DO Grinevich, C Suarez, JD Winkelman, ...
Science 349 (6247), 535-539, 2015
562015
The common missense mutation D489N in TRIM32 causing limb girdle muscular dystrophy 2H leads to loss of the mutated protein in knock-in mice resulting in a Trim32-null phenotype
E Kudryashova, A Struyk, E Mokhonova, SC Cannon, MJ Spencer
Human molecular genetics 20 (20), 3925-3932, 2011
552011
Pathogenity of some limb girdle muscular dystrophy mutations can result from reduced anchorage to myofibrils and altered stability of calpain 3
N Ermolova, E Kudryashova, M DiFranco, J Vergara, I Kramerova, ...
Human molecular genetics 20 (17), 3331-3345, 2011
542011
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