JMM--past and present. Invited commentary on A. Blaschko: alopecia areata and trichorrhexis.
- Published in:
- Journal of Molecular Medicine, 2002, v. 80, n. 7, p. 387, doi. 10.1007/s00109-002-0361-3
- Publication type:
- Article
Works matching IS 09462716 AND DT 2002 AND VI 80 AND IP 7
Results: 10
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Familial glucocorticoid deficiency syndromes.
- Published in:
- Journal of Molecular Medicine, 2002, v. 80, n. 7, p. 385, doi. 10.1007/s00109-002-0347-1
- Publication type:
- Article
3
Functional relationships between three novel homozygous mutations in the ACTH receptor gene and familial glucocorticoid deficiency.
- Published in:
- Journal of Molecular Medicine, 2002, v. 80, n. 7, p. 406, doi. 10.1007/s00109-002-0333-7
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- Article
4
Mutations in hepatocyte nuclear factor 4α (HNF4α) gene associated with diabetes result in greater loss of HNF4α function in pancreatic β-cells than in nonpancreatic β-cells and in reduced activation of the apolipoprotein CIII promoter in hepatic cells
- Published in:
- Journal of Molecular Medicine, 2002, v. 80, n. 7, p. 423, doi. 10.1007/s00109-002-0340-8
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- Publication type:
- Article
5
CD4<sup>+</sup> T helper cells and the role they play in viral control.
- Published in:
- Journal of Molecular Medicine, 2002, v. 80, n. 7, p. 397, doi. 10.1007/s00109-002-0337-3
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- Publication type:
- Article
6
Stimulation of human natural interferon-α response via paramyxovirus hemagglutinin lectin-cell interaction.
- Published in:
- Journal of Molecular Medicine, 2002, v. 80, n. 7, p. 443, doi. 10.1007/s00109-002-0339-1
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- Publication type:
- Article
7
Expression and mutation analysis of BRUNOL3, a candidate gene for heart and thymus developmental defects associated with partial monosomy 10p.
- Published in:
- Journal of Molecular Medicine, 2002, v. 80, n. 7, p. 431, doi. 10.1007/s00109-002-0331-9
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- Publication type:
- Article
8
Mutations in the cardiac myosin-binding protein C gene are the predominant cause of familial hypertrophic cardiomyopathy in eastern Finland.
- Published in:
- Journal of Molecular Medicine, 2002, v. 80, n. 7, p. 412, doi. 10.1007/s00109-002-0323-9
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- Publication type:
- Article
9
Depletion of the other genome-mitochondrial DNA depletion syndromes in humans.
- Published in:
- Journal of Molecular Medicine, 2002, v. 80, n. 7, p. 389, doi. 10.1007/s00109-002-0343-5
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- Publication type:
- Article
10
Association of polymorphisms of the estrogen receptor α gene with bone mineral density of the femoral neck in elderly Japanese women.
- Published in:
- Journal of Molecular Medicine, 2002, v. 80, n. 7, p. 452, doi. 10.1007/s00109-002-0348-0
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- Publication type:
- Article