Works matching IS 09646906 AND DT 2006 AND VI 15 AND IP 10
Results: 18
New susceptibility locus for hypertension on chromosome 8q by efficient pedigree-breaking in an Italian isolate.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 10, p. 1735, doi. 10.1093/hmg/ddl097
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A haplotype spanning two genes, ELN and LIMK1, decreases their transcripts and confers susceptibility to intracranial aneurysms.
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- Human Molecular Genetics, 2006, v. 15, n. 10, p. 1722, doi. 10.1093/hmg/ddl096
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- Article
Progressive alterations in the hypothalamic-pituitary-adrenal axis in the R6/2 transgenic mouse model of Huntington's disease.
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- Human Molecular Genetics, 2006, v. 15, n. 10, p. 1713
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- Article
E-cadherin missense mutations, associated with hereditary diffuse gastric cancer (HDGC) syndrome, display distinct invasive behaviors and genetic interactions with the Wnt and Notch pathways in Drosophila epithelia.
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- Human Molecular Genetics, 2006, v. 15, n. 10, p. 1704, doi. 10.1093/hmg/ddl093
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- Article
Early development of aberrant synaptic plasticity in a mouse model of Huntington's disease.
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- Human Molecular Genetics, 2006, v. 15, n. 10, p. 1690, doi. 10.1093/hmg/ddl092
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- Article
Disease mechanisms in late-onset retinal macular degeneration associated with mutation in C1QTNF5.
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- Human Molecular Genetics, 2006, v. 15, n. 10, p. 1680, doi. 10.1093/hmg/ddl091
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- Article
Neuropeptide S and G protein-coupled receptor 154 modulate macrophage immune responses.
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- Human Molecular Genetics, 2006, v. 15, n. 10, p. 1667, doi. 10.1093/hmg/ddl090
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- Article
The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration.
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- Human Molecular Genetics, 2006, v. 15, n. 10, p. 1659, doi. 10.1093/hmg/ddl089
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- Article
Genetic linkage of hyperglycemia, body weight and serum amyloid-P in an intercross between C57BL/6 and C3H apolipoprotein E-deficient mice.
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- Human Molecular Genetics, 2006, v. 15, n. 10, p. 1650, doi. 10.1093/hmg/ddl088
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- Article
Genetic variation in soluble epoxide hydrolase (EPHX2) and risk of coronary heart disease: The Atherosclerosis Risk in Communities (ARIC) study.
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- Human Molecular Genetics, 2006, v. 15, n. 10, p. 1640, doi. 10.1093/hmg/ddl085
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- Article
Tissue-specific roles of Tbx1 in the development of the outer, middle and inner ear, defective in 22q11DS patients.
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- Human Molecular Genetics, 2006, v. 15, n. 10, p. 1629, doi. 10.1093/hmg/ddl084
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- Article
Naturally occurring utrophin correlates with disease severity in Duchenne muscular dystrophy.
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- Human Molecular Genetics, 2006, v. 15, n. 10, p. 1623, doi. 10.1093/hmg/ddl083
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- Article
A highly functional mini-dystrophin/GFP fusion gene for cell and gene therapy studies of Duchenne muscular dystrophy.
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- Human Molecular Genetics, 2006, v. 15, n. 10, p. 1610, doi. 10.1093/hmg/ddl082
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- Article
WFS1-deficiency increases endoplasmic reticulum stress, impairs cell cycle progression and triggers the apoptotic pathway specifically in pancreatic β-cells.
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- Human Molecular Genetics, 2006, v. 15, n. 10, p. 1600, doi. 10.1093/hmg/ddl081
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- Article
C-termini of P/Q-type Ca2+ channel α1A subunits translocate to nuclei and promote polyglutamine-mediated toxicity.
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- Human Molecular Genetics, 2006, v. 15, n. 10, p. 1587, doi. 10.1093/hmg/ddl080
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- Article
Palmitoyl-protein thioesterase-1 deficiency leads to the activation of caspase-9 and contributes to rapid neurodegeneration in INCL.
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- Human Molecular Genetics, 2006, v. 15, n. 10, p. 1580, doi. 10.1093/hmg/ddl078
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- Article
A quantitative trait locus (QTL) on chromosome 6q influences birth weight in two independent family studies.
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- Human Molecular Genetics, 2006, v. 15, n. 10, p. 1569, doi. 10.1093/hmg/ddl076
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- Article
Genetic variation in DTNBP1 influences general cognitive ability.
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- Human Molecular Genetics, 2006, v. 15, n. 10, p. 1563, doi. 10.1093/hmg/ddi481
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- Article