Works matching IS 09646906 AND DT 2010 AND VI 19 AND IP 15
Results: 21
Tbx22null mice have a submucous cleft palate due to reduced palatal bone formation and also display ankyloglossia and choanal atresia phenotypes.
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- Human Molecular Genetics, 2010, v. 19, n. 15, p. 3103, doi. 10.1093/hmg/ddq223
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- Article
Evolution of alternative splicing in primate brain transcriptomes.
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- Human Molecular Genetics, 2010, v. 19, n. 15, p. 2958, doi. 10.1093/hmg/ddq201
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Tau Ser262 phosphorylation is critical for Aβ42-induced tau toxicity in a transgenic Drosophila model of Alzheimer's disease.
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- Human Molecular Genetics, 2010, v. 19, n. 15, p. 2947, doi. 10.1093/hmg/ddq200
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ALS-linked mutant SOD1 damages mitochondria by promoting conformational changes in Bcl-2.
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- Human Molecular Genetics, 2010, v. 19, n. 15, p. 2974, doi. 10.1093/hmg/ddq202
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- Article
Editorial Board.
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- Human Molecular Genetics, 2010, v. 19, n. 15, p. NP, doi. 10.1093/hmg/ddq243
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- Article
Fragile X protein controls neural stem cell proliferation in the Drosophila brain.
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- Human Molecular Genetics, 2010, v. 19, n. 15, p. 3068, doi. 10.1093/hmg/ddq213
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OPA1 mutations cause cytochrome c oxidase deficiency due to loss of wild-type mtDNA molecules.
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- Human Molecular Genetics, 2010, v. 19, n. 15, p. 3043, doi. 10.1093/hmg/ddq209
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- Article
A comprehensive analysis of common IGF1, IGFBP1 and IGFBP3 genetic variation with prospective IGF-I and IGFBP-3 blood levels and prostate cancer risk among Caucasians†.
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- Human Molecular Genetics, 2010, v. 19, n. 15, p. 3089, doi. 10.1093/hmg/ddq210
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- Article
Methylation profile of TP53 regulatory pathway and mtDNA alterations in breast cancer patients lacking TP53 mutations.
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- Human Molecular Genetics, 2010, v. 19, n. 15, p. 2936, doi. 10.1093/hmg/ddq199
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- Article
BMP antagonism protects Nodal signaling in the gastrula to promote the tissue interactions underlying mammalian forebrain and craniofacial patterning.
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- Human Molecular Genetics, 2010, v. 19, n. 15, p. 3030, doi. 10.1093/hmg/ddq208
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Subscription Page.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 15, p. NP, doi. 10.1093/hmg/ddq245
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- Article
Refining the association of MHC with multiple sclerosis in African Americans.
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- Human Molecular Genetics, 2010, v. 19, n. 15, p. 3080, doi. 10.1093/hmg/ddq197
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Contents Page.
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- Human Molecular Genetics, 2010, v. 19, n. 15, p. NP, doi. 10.1093/hmg/ddq239
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- Article
In vivo expression of polyglutamine-expanded huntingtin by mouse striatal astrocytes impairs glutamate transport: a correlation with Huntington's disease subjects.
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- Human Molecular Genetics, 2010, v. 19, n. 15, p. 3053, doi. 10.1093/hmg/ddq212
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- Article
Inactivation of Palb2 gene leads to mesoderm differentiation defect and early embryonic lethality in mice.
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- Human Molecular Genetics, 2010, v. 19, n. 15, p. 3021, doi. 10.1093/hmg/ddq207
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A transgenic mouse model for uromodulin-associated kidney diseases shows specific tubulo-interstitial damage, urinary concentrating defect and renal failure.
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- Human Molecular Genetics, 2010, v. 19, n. 15, p. 2998, doi. 10.1093/hmg/ddq205
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- Article
Saposin C mutations in Gaucher disease patients resulting in lysosomal lipid accumulation, saposin C deficiency, but normal prosaposin processing and sorting.
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- Human Molecular Genetics, 2010, v. 19, n. 15, p. 2987, doi. 10.1093/hmg/ddq204
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- Article
SDHA is a tumor suppressor gene causing paraganglioma.
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- Human Molecular Genetics, 2010, v. 19, n. 15, p. 3011, doi. 10.1093/hmg/ddq206
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- Article
Gain and loss of function of ALS-related mutations of TARDBP (TDP-43) cause motor deficits in vivo.
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- Human Molecular Genetics, 2010, v. 19, n. 15, p. 3102, doi. 10.1093/hmg/ddq203
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- Article
Genomic and geographic distribution of SNP-defined runs of homozygosity in Europeans.
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- Human Molecular Genetics, 2010, v. 19, n. 15, p. 2927, doi. 10.1093/hmg/ddq198
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- Article
Cover Page.
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- Human Molecular Genetics, 2010, v. 19, n. 15, p. NP, doi. 10.1093/hmg/ddq241
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- Article