Found: 14
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Four new polymorphisms in the human dystrophin gene from an Argentinian population.
- Published in:
- 1997
- By:
- Publication type:
- journal article
Antisense oligonucleotides and short interfering RNAs silencing the cyclin-dependent kinase inhibitor p21 improve proliferation of Duchenne muscular dystrophy patients’ primary skeletal myoblasts.
- Published in:
- Journal of Molecular Medicine, 2005, v. 83, n. 1, p. 64, doi. 10.1007/s00109-004-0607-3
- By:
- Publication type:
- Article
Transfection of normal primary human skeletal myoblasts with p21 and p57 antisense oligonucleotides to improve their proliferation: a first step towards an alternative molecular therapy approach of Duchenne muscular dystrophy.
- Published in:
- Journal of Molecular Medicine, 2003, v. 81, n. 6, p. 355, doi. 10.1007/s00109-003-0439-6
- By:
- Publication type:
- Article
Elevated p21 mRNA level in skeletal muscle of DMD patients and mdx mice indicates either an exhausted satellite cell pool or a higher p21 expression in dystrophin-deficient cells per se.
- Published in:
- Journal of Molecular Medicine, 2000, v. 78, n. 10, p. 569, doi. 10.1007/s001090000153
- By:
- Publication type:
- Article
β<sub>1</sub>-Adrenoceptor gene variations: a role in idiopathic dilated cardiomyopathy?
- Published in:
- Journal of Molecular Medicine, 2000, v. 78, n. 2, p. 87, doi. 10.1007/s001090000080
- By:
- Publication type:
- Article
Identification of transcripts from a subtraction library which might be responsible for the mild phenotype in an intrafamilially variable course of Duchenne muscular dystrophy.
- Published in:
- Human Genetics, 2004, v. 114, n. 2, p. 149, doi. 10.1007/s00439-003-1041-2
- By:
- Publication type:
- Article
Modularization of biochemical networks based on classification of Petri net t-invariants.
- Published in:
- BMC Bioinformatics, 2008, v. 9, p. 1, doi. 10.1186/1471-2105-9-90
- By:
- Publication type:
- Article
Apoptotic neurodegeneration following trauma is markedly enhanced in the immature brain.
- Published in:
- 1999
- By:
- Publication type:
- journal article
The glial glutamate transporter complementary DNA in patients with amyotrophic lateral sclerosis.
- Published in:
- 1996
- By:
- Publication type:
- journal article
A small in-frame deletion within the protease domain of muscle-specific calpain, p94 causes early-onset limb-girdle muscular dystrophy 2A.
- Published in:
- Human Mutation, 1998, v. 11, p. S298, doi. 10.1002/humu.1380110193
- By:
- Publication type:
- Article
A common base change in the promoter region of the human endothelial NO-synthase ( NQS3) gene.
- Published in:
- Human Mutation, 1996, v. 8, n. 4, p. 394, doi. 10.1002/(SICI)1098-1004(1996)8:4<394::AID-HUMU22>3.0.CO;2-X
- By:
- Publication type:
- Article
A Cysteine 3340 Substitution in the Dystroglycan-Binding Domain of Dystrophin Associated with Duchenne Muscular Dystrophy, Mental Retardation and Absence of the ERG b-Wave.
- Published in:
- Human Molecular Genetics, 1996, v. 5, n. 7, p. 973, doi. 10.1093/hmg/5.7.973
- By:
- Publication type:
- Article
E-selectin polymorphism and atherosclerosis: an association study.
- Published in:
- Human Molecular Genetics, 1994, v. 3, n. 11, p. 1935
- By:
- Publication type:
- Article
Point mutations at the carboxy terminus of the human dystrophin gene: implications for an association with mental retardation in DMD patients.
- Published in:
- Human Molecular Genetics, 1993, v. 2, n. 11, p. 1877
- By:
- Publication type:
- Article