All Relations between Muscular Diseases and dmd

Reference Sentence Publish Date Extraction Date Species
M L Bianchi, A Mazzanti, E Galbiati, S Saraifoger, A Dubini, F Cornelio, L Morand. Bone mineral density and bone metabolism in Duchenne muscular dystrophy. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA vol 14 issue 9 2003 12897980 dmd is a severe, progressive muscular disease resulting in death at a young age. 2003-12-16 2023-01-24 human
M C Mariol, L S\\xc3\\xa9gala. Muscular degeneration in the absence of dystrophin is a calcium-dependent process. Current biology : CB vol 11 issue 21 2002 11696327 duchenne muscular dystrophy (dmd) is a progressive degenerative muscular disease that is due to mutations in the dystrophin gene. 2002-01-22 2023-01-24 caenorhabditis_elegans
Y Takeshima, M Matsu. [Molecular genetics and problems found in genetic diagnosis of Duchenne Becker muscular dystrophy]. Nihon rinsho. Japanese journal of clinical medicine vol 55 issue 12 1998 9436421 duchenne and becker muscular dystrophies (dmd and bmd, respectively) are the most common inherited muscular diseases and caused by mutations in the dystrophin gene. 1998-03-24 2023-01-24 Not clear
P Gallano, A Lasa, M Baige. [Dystrophinopathies]. Neurologia (Barcelona, Spain) vol 10 Suppl 1 issue 1996 8838554 in 1987 a new concept in the x-linked muscular dystrophies was born with the identification of dystrophin, a cytoskeletal protein responsible for several muscular diseases previously grouped as duchenne's or becker's muscular dystrophies (dmd and bmd, respectively). 1996-12-05 2023-01-24 Not clear
K Hamano, T Takeya, N Iwasaki, N Okoshi, T Fukubayashi, M Kirinoki, Y Yao, T Hirabayashi, H Takit. Analysis of dystrophin in muscular diseases by two-dimensional gel electrophoresis using agarose gels in the first dimension. Acta neurologica Belgica vol 96 issue 2 1996 8711982 we analyzed dystrophin in case of normal control, duchenne muscular dystrophy (dmd), becker muscular dystrophy (bmd) and infectious muscular disease using two-dimensional gel electrophoresis and immunoblotting with 3 monoclonal dystrophin antibodies: dys 1, a mid-rod-domain antibody; dys 2, a c-terminal-domain antibody; and dys 3, an n-terminal-domain antibody. 1996-09-12 2023-01-24 Not clear
N Yasuda, K Kond\\xc3\\xb. No sex difference in mutations rates of Duchenne muscular dystrophy. Journal of medical genetics vol 17 issue 2 1980 7381863 it was based on 514 males with duchenne type muscular dystrophy (dmd) from five of nineteen hospitals for muscular disease in japan. 1980-08-15 2023-01-24 Not clear