Works in Human Molecular Genetics, 2017, Vol 26, Issue 7
Results: 15
GWAS of self-reported mosquito bite size, itch intensity and attractiveness to mosquitoes implicates immune-related predisposition loci.
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- Human Molecular Genetics, 2017, v. 26, n. 7, p. 1391, doi. 10.1093/hmg/ddx036
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- Article
Gclc deficiency in mouse CNS causes mitochondrial damage and neurodegeneration.
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- Human Molecular Genetics, 2017, v. 26, n. 7, p. 1376, doi. 10.1093/hmg/ddx040
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- Article
Cowden syndrome-associated germline succinate dehydrogenase complex subunit D (SDHD) variants cause PTEN-mediated down-regulation of autophagy in thyroid cancer cells.
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- Human Molecular Genetics, 2017, v. 26, n. 7, p. 1365, doi. 10.1093/hmg/ddx037
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- Article
AAV9 delivered bispecific nanobody attenuates amyloid burden in the gelsolin amyloidosis mouse model.
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- Human Molecular Genetics, 2017, v. 26, n. 7, p. 1353, doi. 10.1093/hmg/ddx056
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- Article
Fragile X related protein 1 (FXR1P) regulates proliferation of adult neural stem cells.
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- Human Molecular Genetics, 2017, v. 26, n. 7, p. 1340, doi. 10.1093/hmg/ddx034
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- Article
Mitochondrial complex II regulates a distinct oxygen sensing mechanism in monocytes.
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- Human Molecular Genetics, 2017, v. 26, n. 7, p. 1328, doi. 10.1093/hmg/ddx041
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- Article
Sex specific activation of the ERα axis of the mitochondrial UPR (UPR<sup>mt</sup>) in the G93A-SOD1 mouse model of familial ALS.
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- Human Molecular Genetics, 2017, v. 26, n. 7, p. 1318, doi. 10.1093/hmg/ddx049
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- Article
Inhibiting sphingosine kinase 2 mitigates mutant Huntingtin-induced neurodegeneration in neuron models of Huntington disease.
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- Human Molecular Genetics, 2017, v. 26, n. 7, p. 1305, doi. 10.1093/hmg/ddx046
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- Article
Opposing FlnA and FlnB interactions regulate RhoA activation in guiding dynamic actin stress fiber formation and cell spreading.
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- Human Molecular Genetics, 2017, v. 26, n. 7, p. 1294, doi. 10.1093/hmg/ddx047
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- Article
A point mutation in Fgf9 impedes joint interzone formation leading to multiple synostoses syndrome.
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- Human Molecular Genetics, 2017, v. 26, n. 7, p. 1280, doi. 10.1093/hmg/ddx029
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- Article
Rdh10 loss-of-function and perturbed retinoid signaling underlies the etiology of choanal atresia.
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- Human Molecular Genetics, 2017, v. 26, n. 7, p. 1268, doi. 10.1093/hmg/ddx031
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- Article
Novel allele-specific quantification methods reveal no effects of adult onset CAG repeats on HTT mRNA and protein levels.
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- Human Molecular Genetics, 2017, v. 26, n. 7, p. 1258, doi. 10.1093/hmg/ddx033
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- Article
LRRK2(I2020T) functional genetic interactors that modify eye degeneration and dopaminergic cell loss in Drosophila.
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- Human Molecular Genetics, 2017, v. 26, n. 7, p. 1247, doi. 10.1093/hmg/ddx030
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- Article
Therapeutic potential of AAV-mediated MMP-3 secretion from corneal endothelium in treating glaucoma.
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- Human Molecular Genetics, 2017, v. 26, n. 7, p. 1230, doi. 10.1093/hmg/ddx028
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- Article
Klinefelter syndrome comorbidities linked to increased X chromosome gene dosage and altered protein interactome activity.
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- Human Molecular Genetics, 2017, v. 26, n. 7, p. 1219, doi. 10.1093/hmg/ddx014
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- Article