Pathogenity of some limb girdle muscular dystrophy mutations can result from reduced anchorage to myofibrils and altered stability of calpain 3ERMOLOVA, Natalia; KUDRYASHOVA, Elena; DIFRANCO, Marino et al.Human molecular genetics (Print). 2011, Vol 20, Num 17, pp 3331-3345, issn 0964-6906, 15 p.Article

Deficiency of the E3 ubiquitin ligase TRIM32 in mice leads to a myopathy with a neurogenic componentKUDRYASHOVA, Elena; JUN WU; HAVTON, Leif A et al.Human molecular genetics (Print). 2009, Vol 18, Num 7, pp 1353-1367, issn 0964-6906, 15 p.Article

Calpain 3 participates in sarcomere remodeling by acting upstream of the ubiquitin-proteasome pathwayKRAMEROVA, Irina; KUDRYASHOVA, Elena; VENKATRAMAN, Gayathri et al.Human molecular genetics (Print). 2005, Vol 14, Num 15, pp 2125-2134, issn 0964-6906, 10 p.Article

Calpain 3 cleaves filamin C and regulates its ability to interact with γ- and δ-sarcoglycansGUYON, Jeffrey R; KUDRYASHOVA, Elena; POTTS, Alexandra et al.Muscle & nerve. 2003, Vol 28, Num 4, pp 472-483, issn 0148-639X, 12 p.Article

Ventilatory dysfunction in mdx mice: Impact of tumor necrosis factor-alpha deletionGOSSELIN, Luc E; BARKLEY, Jacob E; SPENCER, Melissa J et al.Muscle & nerve. 2003, Vol 28, Num 3, pp 336-343, issn 0148-639X, 8 p.Article

Myogenic Akt signaling attenuates muscular degeneration, promotes myofiber regeneration and improves muscle function in dystrophin-deficient mdx miceKIM, Michelle H; KAY, Danielle I; CROSBIE, Rachelle H et al.Human molecular genetics (Print). 2011, Vol 20, Num 7, pp 1324-1338, issn 0964-6906, 15 p.Article

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 phenotypeKUDRYASHOVA, Elena; STRUYK, Arie; MOKHONOVA, Ekaterina et al.Human molecular genetics (Print). 2011, Vol 20, Num 20, pp 3925-3932, issn 0964-6906, 8 p.Article

Novel role of calpain-3 in the triad-associated protein complex regulating calcium release in skeletal muscleKRAMEROVA, Irina; KUDRYASHOVA, Elena; WU, Benjamin et al.Human molecular genetics (Print). 2008, Vol 17, Num 21, pp 3271-3280, issn 0964-6906, 10 p.Article

Identification of putative in vivo substrates of calpain 3 by comparative proteomics of overexpressing transgenic and nontransgenic miceCOHEN, Niaz; KUDRYASHOVA, Elena; KRAMEROVA, Irina et al.Proteomics (Weinheim. Print). 2006, Vol 6, Num 22, pp 6075-6084, issn 1615-9853, 10 p.Article

Mdm muscular dystrophy : interactions with calpain 3 and a novel functional role for titin's N2A domainHUEBSCH, Kimberly A; KUDRYASHOVA, Elena; WOOLEY, Christine M et al.Human molecular genetics (Print). 2005, Vol 14, Num 19, pp 2801-2811, issn 0964-6906, 11 p.Article

Helper (CD4⁺) and cytotoxic (CD8⁺) T cells promote the pathology of dystrophin-deficient muscleSPENCER, Melissa J; MONTECINO-RODRIGUEZ, Encarnacion; DORSHKIND, Kenneth et al.Clinical immunology (Orlando, Fla. Print). 2001, Vol 98, Num 2, pp 235-243, issn 1521-6616Article