Works matching IS 09646906 AND DT 2012 AND VI 21 AND IP 22
Results: 22
Neil1 is a genetic modifier of somatic and germline CAG trinucleotide repeat instability in R6/1 mice.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 22, p. 4939, doi. 10.1093/hmg/dds337
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- Article
High-content RNAi screening identifies the Type 1 inositol triphosphate receptor as a modifier of TDP-43 localization and neurotoxicity.
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- Human Molecular Genetics, 2012, v. 21, n. 22, p. 4845, doi. 10.1093/hmg/dds321
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- Article
LRRK2 functions as a Wnt signaling scaffold, bridging cytosolic proteins and membrane-localized LRP6.
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- Human Molecular Genetics, 2012, v. 21, n. 22, p. 4966, doi. 10.1093/hmg/dds342
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- Article
ROS-dependent regulation of Parkin and DJ-1 localization during oxidative stress in neurons.
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- Human Molecular Genetics, 2012, v. 21, n. 22, p. 4888, doi. 10.1093/hmg/dds325
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- Article
Dkk3 is a component of the genetic circuitry regulating aldosterone biosynthesis in the adrenal cortex.
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- Human Molecular Genetics, 2012, v. 21, n. 22, p. 4922, doi. 10.1093/hmg/dds333
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- Article
Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls.
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- Human Molecular Genetics, 2012, v. 21, n. 22, p. 4980, doi. 10.1093/hmg/dds334
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- Article
Using genome-wide complex trait analysis to quantify ‘missing heritability’ in Parkinson's disease.
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- Human Molecular Genetics, 2012, v. 21, n. 22, p. 4996
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- Article
Contents Page.
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- Human Molecular Genetics, 2012, v. 21, n. 22, p. NP, doi. 10.1093/hmg/dds452
- Publication type:
- Article
Converging evidence that sequence variations in the novel candidate gene MAP2K7 (MKK7) are functionally associated with schizophrenia.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 22, p. 4910, doi. 10.1093/hmg/dds331
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- Article
Subscription Page.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 22, p. NP, doi. 10.1093/hmg/dds461
- Publication type:
- Article
Editorial Board.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 22, p. NP, doi. 10.1093/hmg/dds458
- Publication type:
- Article
Impaired proteolysis underlies autophagic dysfunction in Niemann–Pick type C disease.
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- Human Molecular Genetics, 2012, v. 21, n. 22, p. 4876, doi. 10.1093/hmg/dds324
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- Article
Opa3, a novel regulator of mitochondrial function, controls thermogenesis and abdominal fat mass in a mouse model for Costeff syndrome.
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- Human Molecular Genetics, 2012, v. 21, n. 22, p. 4836, doi. 10.1093/hmg/dds315
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- Article
Comparative analysis of somatic copy-number alterations across different human cancer types reveals two distinct classes of breakpoint hotspots.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 22, p. 4957, doi. 10.1093/hmg/dds340
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- Publication type:
- Article
Cover Page.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 22, p. NP, doi. 10.1093/hmg/dds455
- Publication type:
- Article
The nuclease hSNM1B/Apollo is linked to the Fanconi anemia pathway via its interaction with FANCP/SLX4.
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- Human Molecular Genetics, 2012, v. 21, n. 22, p. 4948, doi. 10.1093/hmg/dds338
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- Publication type:
- Article
Functional characterization of tissue-specific enhancers in the DLX5/6 locus.
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- Human Molecular Genetics, 2012, v. 21, n. 22, p. 4930, doi. 10.1093/hmg/dds336
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- Publication type:
- Article
Loss of Mfn2 results in progressive, retrograde degeneration of dopaminergic neurons in the nigrostriatal circuit.
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- Human Molecular Genetics, 2012, v. 21, n. 22, p. 4817, doi. 10.1093/hmg/dds311
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- Publication type:
- Article
Mutant human APP exacerbates pathology in a mouse model of NPC and its reversal by a β-cyclodextrin.
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- Human Molecular Genetics, 2012, v. 21, n. 22, p. 4857, doi. 10.1093/hmg/dds322
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- Publication type:
- Article
Pancreatic beta-cell function and type 2 diabetes risk: quantify the causal effect using a Mendelian randomization approach based on meta-analyses.
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- Human Molecular Genetics, 2012, v. 21, n. 22, p. 5010, doi. 10.1093/hmg/dds339
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- Publication type:
- Article
Mitofusin 2 is necessary for striatal axonal projections of midbrain dopamine neurons.
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- Human Molecular Genetics, 2012, v. 21, n. 22, p. 4827, doi. 10.1093/hmg/dds352
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- Article
Whole-exome sequencing identifies mutations in the nucleoside transporter gene SLC29A3 in dysosteosclerosis, a form of osteopetrosis.
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- Human Molecular Genetics, 2012, v. 21, n. 22, p. 4904, doi. 10.1093/hmg/dds326
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- Publication type:
- Article