-
1
-
-
0030882270
-
Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23
-
Messina DN, Speer MC, Pericak-Vance MA, McNally EM,. Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23. Am J Hum Genet 1997; 61: 909-917. (Pubitemid 27418466)
-
(1997)
American Journal of Human Genetics
, vol.61
, Issue.4
, pp. 909-917
-
-
Messina, D.N.1
Speer, M.C.2
Pericak-Vance, M.A.3
McNally, E.M.4
-
2
-
-
77649298737
-
Interferon-stimulated gene 15 (ISG15) conjugates proteins in dermatomyositis muscle with perifascicular atrophy
-
Salajegheh M, Kong SW, Pinkus JL, et al. Interferon-stimulated gene 15 (ISG15) conjugates proteins in dermatomyositis muscle with perifascicular atrophy. Ann Neurol 2010; 67: 53-63.
-
(2010)
Ann Neurol
, vol.67
, pp. 53-63
-
-
Salajegheh, M.1
Kong, S.W.2
Pinkus, J.L.3
-
3
-
-
70349322489
-
Nature of "tau" immunoreactivity in normal myonuclei and inclusion body myositis
-
Salajegheh M, Pinkus JL, Nazareno R, et al. Nature of "Tau" immunoreactivity in normal myonuclei and inclusion body myositis. Muscle Nerve 2009; 40: 520-528.
-
(2009)
Muscle Nerve
, vol.40
, pp. 520-528
-
-
Salajegheh, M.1
Pinkus, J.L.2
Nazareno, R.3
-
4
-
-
67650354409
-
Characterization of human skeletal muscle biopsy samples using shotgun proteomics
-
Parker KC, Walsh RJ, Salajegheh M, et al. Characterization of human skeletal muscle biopsy samples using shotgun proteomics. J Proteome Res 2009; 8: 3265-3277.
-
(2009)
J Proteome Res
, vol.8
, pp. 3265-3277
-
-
Parker, K.C.1
Walsh, R.J.2
Salajegheh, M.3
-
5
-
-
67049165108
-
Fast-twitch sarcomeric and glycolytic enzyme protein loss in inclusion body myositis
-
Parker KC, Kong SW, Walsh RJ, et al. Fast-twitch sarcomeric and glycolytic enzyme protein loss in inclusion body myositis. Muscle Nerve 2009; 39: 739-753.
-
(2009)
Muscle Nerve
, vol.39
, pp. 739-753
-
-
Parker, K.C.1
Kong, S.W.2
Walsh, R.J.3
-
6
-
-
70350449457
-
When less can yield moreâcomputational preprocessing of MS/MS spectra for peptide identification
-
Renard BY, Kirchner M, Monigatti F, et al. When less can yield moreâcomputational preprocessing of MS/MS spectra for peptide identification. Proteomics 2009; 9: 4978-4984.
-
(2009)
Proteomics
, vol.9
, pp. 4978-4984
-
-
Renard, B.Y.1
Kirchner, M.2
Monigatti, F.3
-
7
-
-
40549108276
-
Proteomic identification of FHL1 as the protein mutated in human reducing body myopathy
-
DOI 10.1172/JCI34450
-
Schessl J, Zou Y, McGrath MJ, et al. Proteomic identification of FHL1 as the protein mutated in human reducing body myopathy. J Clin Invest 2008; 118: 904-912. (Pubitemid 351364598)
-
(2008)
Journal of Clinical Investigation
, vol.118
, Issue.3
, pp. 904-912
-
-
Schessl, J.1
Zou, Y.2
McGrath, M.J.3
Cowling, B.S.4
Maiti, B.5
Chin, S.S.6
Sewry, C.7
Battini, R.8
Hu, Y.9
Cottle, D.L.10
Rosenblatt, M.11
Spruce, L.12
Ganguly, A.13
Kirschner, J.14
Judkins, A.R.15
Golden, J.A.16
Goebel, H.-H.17
Muntoni, F.18
Flanigan, K.M.19
Mitchell, C.A.20
Bonnemann, C.G.21
more..
-
8
-
-
0033746702
-
Desmin splice variants causing cardiac and skeletal myopathy
-
Park KY, Dalakas MC, Goebel HH, et al. Desmin splice variants causing cardiac and skeletal myopathy. J Med Genet 2000; 37: 851-857.
-
(2000)
J Med Genet
, vol.37
, pp. 851-857
-
-
Park, K.Y.1
Dalakas, M.C.2
Goebel, H.H.3
-
9
-
-
33747180877
-
Desmin accumulation restrictive cardiomyopathy and atrioventricular block associated with desmin gene defects
-
DOI 10.1016/j.ejheart.2005.11.003, PII S1388984205003016
-
Arbustini E, Pasotti M, Pilotto A, et al. Desmin accumulation restrictive cardiomyopathy and atrioventricular block associated with desmin gene defects. Eur J Heart Fail 2006; 8: 477-483. (Pubitemid 44226451)
-
(2006)
European Journal of Heart Failure
, vol.8
, Issue.5
, pp. 477-483
-
-
Arbustini, E.1
Pasotti, M.2
Pilotto, A.3
Pellegrini, C.4
Grasso, M.5
Previtali, S.6
Repetto, A.7
Bellini, O.8
Azan, G.9
Scaffino, M.10
Campana, C.11
Piccolo, G.12
Vigano, M.13
Tavazzi, L.14
|