Works matching IS 09646906 AND DT 2010 AND VI 19 AND IP 17
Results: 22
Increased energy metabolism rescues glia-induced pathology in a Drosophila model of Huntington's disease.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 17, p. 3372, doi. 10.1093/hmg/ddq249
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- Article
A mutation in the 3′-UTR of the HDAC6 gene abolishing the post-transcriptional regulation mediated by hsa-miR-433 is linked to a new form of dominant X-linked chondrodysplasia.
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- Human Molecular Genetics, 2010, v. 19, n. 17, p. 3489, doi. 10.1093/hmg/ddq256
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- Article
Maternal high-fat diet interacts with embryonic Cited2 genotype to reduce Pitx2c expression and enhance penetrance of left–right patterning defects.
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- Human Molecular Genetics, 2010, v. 19, n. 17, p. 3394, doi. 10.1093/hmg/ddq251
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- Article
Large inverted repeats within Xp11.2 are present at the breakpoints of isodicentric X chromosomes in Turner syndrome.
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- Human Molecular Genetics, 2010, v. 19, n. 17, p. 3383, doi. 10.1093/hmg/ddq250
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- Article
Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease.
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- Human Molecular Genetics, 2010, v. 19, n. 17, p. 3468
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- Article
Analysis of SNPs with an effect on gene expression identifies UBE2L3 and BCL3 as potential new risk genes for Crohn's disease.
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- Human Molecular Genetics, 2010, v. 19, n. 17, p. 3482, doi. 10.1093/hmg/ddq264
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- Article
Editorial Board.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 17, p. NP, doi. 10.1093/hmg/ddq296
- Publication type:
- Article
Mitochondrial calcium uptake capacity as a therapeutic target in the R6/2 mouse model of Huntington's disease.
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- Human Molecular Genetics, 2010, v. 19, n. 17, p. 3354, doi. 10.1093/hmg/ddq247
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- Publication type:
- Article
Gli3Xt−J/Xt−J mice exhibit lambdoid suture craniosynostosis which results from altered osteoprogenitor proliferation and differentiation.
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- Human Molecular Genetics, 2010, v. 19, n. 17, p. 3457, doi. 10.1093/hmg/ddq258
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- Article
Penetrance for copy number variants associated with schizophrenia.
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- Human Molecular Genetics, 2010, v. 19, n. 17, p. 3477, doi. 10.1093/hmg/ddq259
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- Article
Clorgyline-mediated reversal of neurological deficits in a Complexin 2 knockout mouse.
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- Human Molecular Genetics, 2010, v. 19, n. 17, p. 3402, doi. 10.1093/hmg/ddq252
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- Article
Cover Page.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 17, p. NP, doi. 10.1093/hmg/ddq295
- Publication type:
- Article
Reduced expression of Pax6 in lens and cornea of mutant mice leads to failure of chamber angle development and juvenile glaucoma.
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- Human Molecular Genetics, 2010, v. 19, n. 17, p. 3332, doi. 10.1093/hmg/ddq237
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- Publication type:
- Article
Unmasking the causes of multifactorial disorders: OXPHOS differences between mitochondrial haplogroups.
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- Human Molecular Genetics, 2010, v. 19, n. 17, p. 3343
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- Article
Contribution of human amniotic fluid stem cells to renal tissue formation depends on mTOR.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 17, p. 3320, doi. 10.1093/hmg/ddq236
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- Publication type:
- Article
Contents Page.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 17, p. NP, doi. 10.1093/hmg/ddq294
- Publication type:
- Article
Polycystic kidney disease protein fibrocystin localizes to the mitotic spindle and regulates spindle bipolarity.
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- Human Molecular Genetics, 2010, v. 19, n. 17, p. 3306, doi. 10.1093/hmg/ddq233
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- Article
The small heat shock protein B8 (HspB8) promotes autophagic removal of misfolded proteins involved in amyotrophic lateral sclerosis (ALS).
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 17, p. 3440, doi. 10.1093/hmg/ddq257
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- Article
Mitochondrial ATP synthase deficiency due to a mutation in the ATP5E gene for the F1 ε subunit.
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- Human Molecular Genetics, 2010, v. 19, n. 17, p. 3430, doi. 10.1093/hmg/ddq254
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- Publication type:
- Article
Antioxidants can inhibit basal autophagy and enhance neurodegeneration in models of polyglutamine disease.
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- Human Molecular Genetics, 2010, v. 19, n. 17, p. 3413, doi. 10.1093/hmg/ddq253
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- Article
Subscription Page.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 17, p. NP, doi. 10.1093/hmg/ddq297
- Publication type:
- Article
Leena Peltonen-Palotie: the human side of genetics.
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- Human Molecular Genetics, 2010, v. 19, n. 17, p. 3303, doi. 10.1093/hmg/ddq255
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- Article