| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Janusz G Zimowski, Elzbieta Fidzianska, Mariola Holding, Jacek Zaremb. [Carrier detection in Duchenne/Becker muscular dystrophy in the families in which the DNA of the affected person is not available]. Medycyna wieku rozwojowego. vol 10. issue 1 Pt 2. 2007-03-21. PMID:17028400. |
duchenne muscular dystrophy (dmd) is a severe, progressive, x-linked muscular disease, which affects 1 in 3500 male newborns. |
2007-03-21 |
2023-08-12 |
human |
| Boaz Weisz, Anna L David, Lisa G Gregory, Dany Perocheau, Ali Ruthe, Simon N Waddington, Mike Themis, Terry Cook, Charles Coutelle, Charles H Rodeck, Donald M Peeble. Targeting the respiratory muscles of fetal sheep for prenatal gene therapy for Duchenne muscular dystrophy. American journal of obstetrics and gynecology. vol 193. issue 3 Pt 2. 2005-10-26. PMID:16157120. |
duchenne muscular dystrophy (dmd) is a lethal degenerative muscular disease. |
2005-10-26 |
2023-08-12 |
Not clear |
| Kiichiro Matsumura, Di Zhong, Fumiaki Saito, Ken Arai, Katsuhito Adachi, Hisaomi Kawai, Itsuro Higuchi, Ichizo Nishino, Teruo Shimiz. Proteolysis of beta-dystroglycan in muscular diseases. Neuromuscular disorders : NMD. vol 15. issue 5. 2005-06-17. PMID:15833425. |
in this study, we investigated the proteolysis of beta-dystroglycan in the biopsied skeletal muscles of various human muscular diseases, including sarcoglycanopathy, duchenne muscular dystrophy (dmd), becker muscular dystrophy, fukuyama congenital muscular dystrophy, miyoshi myopathy, lgmd2a, facioscapulohumeral muscular dystrophy, myotonic dystrophy and dermatomyositis/polymyositis. |
2005-06-17 |
2023-08-12 |
human |
| 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. 2003-12-16. PMID:12897980. |
dmd is a severe, progressive muscular disease resulting in death at a young age. |
2003-12-16 |
2023-08-12 |
human |
| M C Mariol, L Ségala. Muscular degeneration in the absence of dystrophin is a calcium-dependent process. Current biology : CB. vol 11. issue 21. 2002-01-22. PMID:11696327. |
duchenne muscular dystrophy (dmd) is a progressive degenerative muscular disease that is due to mutations in the dystrophin gene. |
2002-01-22 |
2023-08-12 |
mouse |
| 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. 1998-03-24. PMID: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 |
2023-08-12 |
Not clear |
| P Gallano, A Lasa, M Baige. [Dystrophinopathies]. Neurologia (Barcelona, Spain). vol 10 Suppl 1. 1996-12-05. PMID: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 |
2023-08-12 |
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. 1996-09-12. PMID: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 |
2023-08-12 |
Not clear |
| b' N Yasuda, K Kond\\xc3\\xb. No sex difference in mutations rates of Duchenne muscular dystrophy. Journal of medical genetics. vol 17. issue 2. 1980-08-15. PMID: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 |
2023-08-12 |
Not clear |