Works matching IS 09646906 AND DT 2009 AND VI 18 AND IP 15
Results: 23
Vascular defects in a mouse model of hypotrichosis-lymphedema-telangiectasia syndrome indicate a role for SOX18 in blood vessel maturation.
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- Human Molecular Genetics, 2009, v. 18, n. 15, p. 2839, doi. 10.1093/hmg/ddp219
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- Article
Subscription Page.
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- Human Molecular Genetics, 2009, v. 18, n. 15, p. NP, doi. 10.1093/hmg/ddp270
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- Article
Linkage and linkage disequilibrium scan for autism loci in an extended pedigree from Finland.
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- Human Molecular Genetics, 2009, v. 18, n. 15, p. 2912, doi. 10.1093/hmg/ddp229
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Functional complementation studies identify candidate genes and common genetic variants associated with ovarian cancer survival.
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- Human Molecular Genetics, 2009, v. 18, n. 15, p. 2928, doi. 10.1093/hmg/ddp234
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Loss of connexin43-mediated gap junctional coupling in the mesenchyme of limb buds leads to altered expression of morphogens in mice.
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- Human Molecular Genetics, 2009, v. 18, n. 15, p. 2899, doi. 10.1093/hmg/ddp227
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PDK1 signaling in oocytes controls reproductive aging and lifespan by manipulating the survival of primordial follicles.
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- Human Molecular Genetics, 2009, v. 18, n. 15, p. 2813, doi. 10.1093/hmg/ddp217
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Functional interaction of DYX1C1 with estrogen receptors suggests involvement of hormonal pathways in dyslexia.
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- Human Molecular Genetics, 2009, v. 18, n. 15, p. 2802, doi. 10.1093/hmg/ddp215
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- Article
Cover Page.
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- Human Molecular Genetics, 2009, v. 18, n. 15, p. NP, doi. 10.1093/hmg/ddp268
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- Article
Unravelling the genetic basis of variable clinical expression in neurofibromatosis 1.
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- Human Molecular Genetics, 2009, v. 18, n. 15, p. 2768, doi. 10.1093/hmg/ddp212
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- Article
Defective pulmonary vascular remodeling in Smad8 mutant mice.
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- Human Molecular Genetics, 2009, v. 18, n. 15, p. 2791, doi. 10.1093/hmg/ddp214
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Promoter and intron 1 polymorphisms of COL1A1 interact to regulate transcription and susceptibility to osteoporosis.
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- Human Molecular Genetics, 2009, v. 18, n. 15, p. 2729, doi. 10.1093/hmg/ddp205
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- Article
DNA hypomethylation restricted to the murine forebrain induces cortical degeneration and impairs postnatal neuronal maturation.
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- Human Molecular Genetics, 2009, v. 18, n. 15, p. 2875, doi. 10.1093/hmg/ddp222
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CADASIL mutations enhance spontaneous multimerization of NOTCH3.
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- Human Molecular Genetics, 2009, v. 18, n. 15, p. 2761, doi. 10.1093/hmg/ddp211
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Editorial Board.
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- Human Molecular Genetics, 2009, v. 18, n. 15, p. NP, doi. 10.1093/hmg/ddp269
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- Article
Positional identification of variants of Adamts16 linked to inherited hypertension.
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- Human Molecular Genetics, 2009, v. 18, n. 15, p. 2825, doi. 10.1093/hmg/ddp218
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Contents Page.
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- Human Molecular Genetics, 2009, v. 18, n. 15, p. NP, doi. 10.1093/hmg/ddp267
- Publication type:
- Article
A common genetic variant in the 15q24 nicotinic acetylcholine receptor gene cluster (CHRNA5–CHRNA3–CHRNB4) is associated with a reduced ability of women to quit smoking in pregnancy.
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- Human Molecular Genetics, 2009, v. 18, n. 15, p. 2922, doi. 10.1093/hmg/ddp216
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Usher syndrome IIIA gene clarin-1 is essential for hair cell function and associated neural activation†.
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- Human Molecular Genetics, 2009, v. 18, n. 15, p. 2748, doi. 10.1093/hmg/ddp210
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Pathogenic mechanisms of tooth agenesis linked to paired domain mutations in human PAX9.
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- Human Molecular Genetics, 2009, v. 18, n. 15, p. 2863, doi. 10.1093/hmg/ddp221
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- Article
AIP-1 ameliorates β-amyloid peptide toxicity in a Caenorhabditis elegans Alzheimer's disease model.
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- Human Molecular Genetics, 2009, v. 18, n. 15, p. 2739, doi. 10.1093/hmg/ddp209
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Otoferlin interacts with myosin VI: implications for maintenance of the basolateral synaptic structure of the inner hair cell.
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- Human Molecular Genetics, 2009, v. 18, n. 15, p. 2779, doi. 10.1093/hmg/ddp213
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Germline and somatic cancer-associated mutations in the ATP-binding motifs of PTEN influence its subcellular localization and tumor suppressive function.
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- Human Molecular Genetics, 2009, v. 18, n. 15, p. 2851, doi. 10.1093/hmg/ddp220
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Introducing the human Leigh syndrome mutation T9176G into Saccharomyces cerevisiae mitochondrial DNA leads to severe defects in the incorporation of Atp6p into the ATP synthase and in the mitochondrial morphology.
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- Human Molecular Genetics, 2009, v. 18, n. 15, p. 2889, doi. 10.1093/hmg/ddp226
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- Article