Works matching IS 09646906 AND DT 2012 AND VI 21 AND IP 5
Results: 25
Cover Page.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 5, p. NP, doi. 10.1093/hmg/dds042
- Publication type:
- Article
Cellular prion protein is essential for oligomeric amyloid-β-induced neuronal cell death.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 5, p. 1138, doi. 10.1093/hmg/ddr542
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- Publication type:
- Article
A glial origin for periventricular nodular heterotopia caused by impaired expression of Filamin-A.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 5, p. 1004, doi. 10.1093/hmg/ddr531
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- Publication type:
- Article
BLM helicase facilitates RNA polymerase I-mediated ribosomal RNA transcription.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 5, p. 1172, doi. 10.1093/hmg/ddr545
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- Publication type:
- Article
Tuberin and PRAS40 are anti-apoptotic gatekeepers during early human amniotic fluid stem-cell differentiation.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 5, p. 1049, doi. 10.1093/hmg/ddr535
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- Publication type:
- Article
Mitochondrial autophagy in cells with mtDNA mutations results from synergistic loss of transmembrane potential and mTORC1 inhibition.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 5, p. 978, doi. 10.1093/hmg/ddr529
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- Publication type:
- Article
The chromosome 2p21 region harbors a complex genetic architecture for association with risk for renal cell carcinoma.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 5, p. 1190, doi. 10.1093/hmg/ddr551
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- Publication type:
- Article
Genetic polymorphism of cytochrome P450 2D6 determines oestrogen receptor activity of the major infertility drug clomiphene via its active metabolites.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 5, p. 1145, doi. 10.1093/hmg/ddr543
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- Publication type:
- Article
Differential effects of a polyalanine tract expansion in Arx on neural development and gene expression.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 5, p. 1090, doi. 10.1093/hmg/ddr538
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- Publication type:
- Article
Contents Page.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 5, p. NP, doi. 10.1093/hmg/dds041
- Publication type:
- Article
Functional genomic analysis unravels a metabolic-inflammatory interplay in adrenoleukodystrophy.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 5, p. 1062, doi. 10.1093/hmg/ddr536
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- Publication type:
- Article
Knockdown of the psychosis susceptibility gene ZNF804A alters expression of genes involved in cell adhesion.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 5, p. 1018, doi. 10.1093/hmg/ddr532
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- Publication type:
- Article
Subscription Page.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 5, p. NP, doi. 10.1093/hmg/dds044
- Publication type:
- Article
Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 5, p. 1184, doi. 10.1093/hmg/ddr550
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- Publication type:
- Article
Editorial Board.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 5, p. NP, doi. 10.1093/hmg/dds043
- Publication type:
- Article
DelK32-lamin A/C has abnormal location and induces incomplete tissue maturation and severe metabolic defects leading to premature death.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 5, p. 1037, doi. 10.1093/hmg/ddr534
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- Publication type:
- Article
The homocysteine-inducible endoplasmic reticulum (ER) stress protein Herp counteracts mutant α-synuclein-induced ER stress via the homeostatic regulation of ER-resident calcium release channel proteins.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 5, p. 963, doi. 10.1093/hmg/ddr502
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- Publication type:
- Article
Pharmacologic activation of mitochondrial biogenesis exerts widespread beneficial effects in a transgenic mouse model of Huntington's disease.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 5, p. 1124, doi. 10.1093/hmg/ddr541
- By:
- Publication type:
- Article
The Nek8 protein kinase, mutated in the human cystic kidney disease nephronophthisis, is both activated and degraded during ciliogenesis.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 5, p. 1155, doi. 10.1093/hmg/ddr544
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- Publication type:
- Article
C/EBPβ and RUNX2 cooperate to degrade cartilage with MMP-13 as the target and HIF-2α as the inducer in chondrocytes.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 5, p. 1111, doi. 10.1093/hmg/ddr540
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- Publication type:
- Article
The early-onset torsion dystonia-associated protein, torsinA, is a homeostatic regulator of endoplasmic reticulum stress response.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 5, p. 1201, doi. 10.1093/hmg/ddr571
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- Publication type:
- Article
Targeted mutation of SLC4A5 induces arterial hypertension and renal metabolic acidosis.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 5, p. 1025, doi. 10.1093/hmg/ddr533
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- Publication type:
- Article
Parkin interacts with Klokin1 for mitochondrial import and maintenance of membrane potential.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 5, p. 991, doi. 10.1093/hmg/ddr530
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- Publication type:
- Article
Ataxin-7 associates with microtubules and stabilizes the cytoskeletal network.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 5, p. 1099, doi. 10.1093/hmg/ddr539
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- Publication type:
- Article
Altered dopamine metabolism and increased vulnerability to MPTP in mice with partial deficiency of mitochondrial complex I in dopamine neurons.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 5, p. 1078, doi. 10.1093/hmg/ddr537
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- Publication type:
- Article