Site-specific strand bias in gene correction using single-stranded oligonucleotides.
- Published in:
- Journal of Molecular Medicine, 2005, v. 83, n. 1, p. 39, doi. 10.1007/s00109-004-0592-6
- By:
- Publication type:
- Article
Works matching IS 09462716 AND DT 2005 AND VI 83 AND IP 1
Results: 11
1
2
-717A>G polymorphism of human C-reactive protein gene associated with coronary heart disease in ethnic Han Chinese: the Beijing atherosclerosis study.
- Published in:
- Journal of Molecular Medicine, 2005, v. 83, n. 1, p. 72, doi. 10.1007/s00109-004-0585-5
- By:
- Publication type:
- Article
3
Functional analysis of a mutant form of the receptor tyrosine kinase Tie2 causing venous malformations.
- Published in:
- Journal of Molecular Medicine, 2005, v. 83, n. 1, p. 58, doi. 10.1007/s00109-004-0601-9
- By:
- Publication type:
- Article
4
Association of polymorphisms of the androgen receptor and klotho genes with bone mineral density in Japanese women.
- Published in:
- Journal of Molecular Medicine, 2005, v. 83, n. 1, p. 50, doi. 10.1007/s00109-004-0578-4
- By:
- Publication type:
- Article
5
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
6
Cellular prion protein neuroprotective function: implications in prion diseases.
- Published in:
- Journal of Molecular Medicine, 2005, v. 83, n. 1, p. 3, doi. 10.1007/s00109-004-0605-5
- By:
- Publication type:
- Article
7
Meta-analysis of clinical characteristics of 299 carriers ofLMNAgene mutations: do lamin A/C mutations portend a high risk of sudden death?
- Published in:
- Journal of Molecular Medicine, 2005, v. 83, n. 1, p. 79, doi. 10.1007/s00109-004-0589-1
- By:
- Publication type:
- Article
8
Role of endogenous antisense RNA in cardiac gene regulation.
- Published in:
- Journal of Molecular Medicine, 2005, v. 83, n. 1, p. 26, doi. 10.1007/s00109-004-0613-5
- By:
- Publication type:
- Article
9
Phosphate’s fate made easier.
- Published in:
- 2005
- By:
- Publication type:
- Editorial
10
Autoantigen complementarity: a new theory implicating complementary proteins as initiators of autoimmune disease.
- Published in:
- Journal of Molecular Medicine, 2005, v. 83, n. 1, p. 12, doi. 10.1007/s00109-004-0615-3
- By:
- Publication type:
- Article
11
Identification of a recurrent mutation inGALNT3demonstrates that hyperostosis-hyperphosphatemia syndrome and familial tumoral calcinosis are allelic disorders.
- Published in:
- Journal of Molecular Medicine, 2005, v. 83, n. 1, p. 33, doi. 10.1007/s00109-004-0610-8
- By:
- Publication type:
- Article