| 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 | 340 | 2009 |
| 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 | 254 | 2005 |
| 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 | 240 | 2004 |
| 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 | 212 | 2021 |
| 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 | 193 | 2005 |
| 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 | 151 | 2012 |
| 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 | 138 | 2009 |
| 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 | 123 | 2008 |
| 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 | 121 | 2003 |
| 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 | 109 | 2002 |
| 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 | 92 | 2014 |
| 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 | 81 | 2009 |
| 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 | 74 | 2005 |
| 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 | 72 | 2006 |
| 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 | 64 | 2012 |
| 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 | 63 | 2006 |
| 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 | 58 | 2013 |
| 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 | 56 | 2015 |
| 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 | 55 | 2011 |
| 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 | 54 | 2011 |
Dmitri KudryashovDepartment of Chemistry and Biochemistry, Ohio State University在 osu.edu 的电子邮件经过验证
