| 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 |