Found: 23
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Zic3 is required in the extra-cardiac perinodal region of the lateral plate mesoderm for left–right patterning and heart development.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 5, p. 879, doi. 10.1093/hmg/dds494
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- Article
Contents Page.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 5, p. NP, doi. 10.1093/hmg/ddt047
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- Article
Cover Page.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 5, p. NP, doi. 10.1093/hmg/ddt048
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- Article
FTO, obesity and the adolescent brain.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 5, p. 1050, doi. 10.1093/hmg/dds504
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- Article
Identification of germline mutations in the cancer predisposing gene CDH1 in patients with orofacial clefts.
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- Human Molecular Genetics, 2013, v. 22, n. 5, p. 919, doi. 10.1093/hmg/dds497
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- Article
Interleukin-1 alpha blockade prevents hyperkeratosis in an in vitro model of lamellar ichthyosis.
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- Human Molecular Genetics, 2013, v. 22, n. 5, p. 1059, doi. 10.1093/hmg/dds511
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- Article
Loss of cIAP1 attenuates soleus muscle pathology and improves diaphragm function in mdx mice.
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- Human Molecular Genetics, 2013, v. 22, n. 5, p. 867, doi. 10.1093/hmg/dds493
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- Article
Epigenome-wide association study in the European Prospective Investigation into Cancer and Nutrition (EPIC-Turin) identifies novel genetic loci associated with smoking.
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- Human Molecular Genetics, 2013, v. 22, n. 5, p. 843, doi. 10.1093/hmg/dds488
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- Article
Reduction of mutant ataxin-7 expression restores motor function and prevents cerebellar synaptic reorganization in a conditional mouse model of SCA7.
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- Human Molecular Genetics, 2013, v. 22, n. 5, p. 890, doi. 10.1093/hmg/dds495
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- Article
Hedgehog regulates Norrie disease protein to drive neural progenitor self-renewal.
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- Human Molecular Genetics, 2013, v. 22, n. 5, p. 1005, doi. 10.1093/hmg/dds505
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- Article
Polg2 is essential for mammalian embryogenesis and is required for mtDNA maintenance.
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- Human Molecular Genetics, 2013, v. 22, n. 5, p. 1017, doi. 10.1093/hmg/dds506
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- Article
GLRB is the third major gene of effect in hyperekplexia.
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- Human Molecular Genetics, 2013, v. 22, n. 5, p. 927, doi. 10.1093/hmg/dds498
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- Article
Editorial Board.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 5, p. NP, doi. 10.1093/hmg/ddt049
- Publication type:
- Article
Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice.
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- Human Molecular Genetics, 2013, v. 22, n. 5, p. 1026, doi. 10.1093/hmg/dds507
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- Article
Subscription Page.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 5, p. NP, doi. 10.1093/hmg/ddt050
- Publication type:
- Article
Functional characterization of Klippel–Trenaunay syndrome gene AGGF1 identifies a novel angiogenic signaling pathway for specification of vein differentiation and angiogenesis during embryogenesis.
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- Human Molecular Genetics, 2013, v. 22, n. 5, p. 963, doi. 10.1093/hmg/dds501
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- Article
X-linked dystonia parkinsonism syndrome (XDP, lubag): disease-specific sequence change DSC3 in TAF1/DYT3 affects genes in vesicular transport and dopamine metabolism.
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- Human Molecular Genetics, 2013, v. 22, n. 5, p. 941, doi. 10.1093/hmg/dds499
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- Article
A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease.
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- Human Molecular Genetics, 2013, v. 22, n. 5, p. 1039
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- Article
LKB1-regulated adaptive mechanisms are essential for neuronal survival following mitochondrial dysfunction.
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- Human Molecular Genetics, 2013, v. 22, n. 5, p. 952, doi. 10.1093/hmg/dds500
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- Article
MicroRNA-21 silencing enhances the cytotoxic effect of the antiangiogenic drug sunitinib in glioblastoma.
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- Human Molecular Genetics, 2013, v. 22, n. 5, p. 904, doi. 10.1093/hmg/dds496
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- Article
Hippocampal dysfunction in the Euchromatin histone methyltransferase 1 heterozygous knockout mouse model for Kleefstra syndrome.
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- Human Molecular Genetics, 2013, v. 22, n. 5, p. 852, doi. 10.1093/hmg/dds490
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- Article
Defective mitochondrial disulfide relay system, altered mitochondrial morphology and function in Huntington's disease.
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- Human Molecular Genetics, 2013, v. 22, n. 5, p. 989, doi. 10.1093/hmg/dds503
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- Publication type:
- Article
Heterozygous inactivation of the Nf1 gene in myeloid cells enhances neointima formation via a rosuvastatin-sensitive cellular pathway.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 5, p. 977, doi. 10.1093/hmg/dds502
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- Article