Evolution and population genetics of the H-ras minisatellite and cancer predisposition.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 8, p. 891, doi. 10.1093/hmg/ddg105
- By:
- Publication type:
- Article
Works matching IS 09646906 AND DT 2003 AND VI 12 AND IP 8
Results: 15
1
2
Sox10 and Pax3 physically interact to mediate activation of a conserved c-RET enhancer.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 8, p. 937, doi. 10.1093/hmg/ddg107
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- Publication type:
- Article
3
Neurons but not glial cells show reciprocal imprinting of sense and antisense transcripts of Ube3a.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 8, p. 837, doi. 10.1093/hmg/ddg106
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- Publication type:
- Article
4
Interleukin 10 haplotype associated with increased risk of hepatocellular carcinoma.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 8, p. 901, doi. 10.1093/hmg/ddg104
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- Publication type:
- Article
5
A naturally occurring mutation in an ATP-binding domain of the recombination repair gene XRCC3 ablates its function without causing cancer susceptibility.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 8, p. 915, doi. 10.1093/hmg/ddg102
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- Publication type:
- Article
6
Genomic inversions of human chromosome 15q11–q13 in mothers of Angelman syndrome patients with class II (BP2/3) deletions.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 8, p. 849, doi. 10.1093/hmg/ddg101
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- Publication type:
- Article
7
Therapeutic antisense-induced exon skipping in cultured muscle cells from six different DMD patients.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 8, p. 907, doi. 10.1093/hmg/ddg100
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- Publication type:
- Article
8
Alzheimer-associated C allele of the promoter polymorphism −22C>T causes a critical neuron-specific decrease of presenilin 1 expression.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 8, p. 869, doi. 10.1093/hmg/ddg098
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- Publication type:
- Article
9
Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 8, p. 925, doi. 10.1093/hmg/ddg097
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- Publication type:
- Article
10
Iron use for haeme synthesis is under control of the yeast frataxin homologue (Yfh1).
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 8, p. 879, doi. 10.1093/hmg/ddg096
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- Publication type:
- Article
11
Pattern recognition in gene expression profiling using DNA array: a comparative study of different statistical methods applied to cancer classification.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 8, p. 823, doi. 10.1093/hmg/ddg093
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- Publication type:
- Article
12
Intermediate filament aggregation in fibroblasts of giant axonal neuropathy patients is aggravated in non dividing cells and by microtubule destabilization.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 8, p. 813, doi. 10.1093/hmg/ddg092
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- Publication type:
- Article
13
Differential binding of transcription factor E2F-2 to the endothelin-converting enzyme-1b promoter affects blood pressure regulation.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 8, p. 947, doi. 10.1093/hmg/ddg091
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- Publication type:
- Article
14
Mutations in the gene for connexin 26 (GJB2) that cause hearing loss have a dominant negative effect on connexin 30.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 8, p. 805, doi. 10.1093/hmg/ddg076
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- Publication type:
- Article
15
Haplotypes extending across ACE are associated with Alzheimer's disease.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 8, p. 859, doi. 10.1093/hmg/ddg094
- By:
- Publication type:
- Article