Works matching IS 09646906 AND DT 2013 AND VI 22 AND IP 9
Results: 24
Hypoxia-inducible factor 1a is a Tsc1-regulated survival factor in newborn neurons in tuberous sclerosis complex.
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- Human Molecular Genetics, 2013, v. 22, n. 9, p. 1725, doi. 10.1093/hmg/ddt018
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- Article
Contents Page.
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- Human Molecular Genetics, 2013, v. 22, n. 9, p. NP, doi. 10.1093/hmg/ddt151
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- Article
Low p14ARF expression in neuroblastoma cells is associated with repressed histone mark status, and enforced expression induces growth arrest and apoptosis.
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- Human Molecular Genetics, 2013, v. 22, n. 9, p. 1735, doi. 10.1093/hmg/ddt020
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Motor and sensory neuropathy due to myelin infolding and paranodal damage in a transgenic mouse model of Charcot–Marie–Tooth disease type 1C.
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- Human Molecular Genetics, 2013, v. 22, n. 9, p. 1755, doi. 10.1093/hmg/ddt022
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- Article
A critical role of astrocyte-mediated nuclear factor-κB-dependent inflammation in Huntington's disease.
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- Human Molecular Genetics, 2013, v. 22, n. 9, p. 1826, doi. 10.1093/hmg/ddt036
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- Article
Multiple postnatal craniofacial anomalies are characterized by conditional loss of polycystic kidney disease 2 (Pkd2).
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- Human Molecular Genetics, 2013, v. 22, n. 9, p. 1873, doi. 10.1093/hmg/ddt041
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- Article
Susceptibility-associated genetic variation at IL12B enhances Th1 polarization in psoriasis.
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- Human Molecular Genetics, 2013, v. 22, n. 9, p. 1807, doi. 10.1093/hmg/ddt034
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- Article
Site-specific Mtm1 mutagenesis by an AAV-Cre vector reveals that myotubularin is essential in adult muscle.
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- Human Molecular Genetics, 2013, v. 22, n. 9, p. 1856, doi. 10.1093/hmg/ddt038
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- Article
Contribution of copy number variants involving nonsense-mediated mRNA decay pathway genes to neuro-developmental disorders.
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- Human Molecular Genetics, 2013, v. 22, n. 9, p. 1816, doi. 10.1093/hmg/ddt035
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- Article
Protein profiles in Tc1 mice implicate novel pathway perturbations in the Down syndrome brain.
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- Human Molecular Genetics, 2013, v. 22, n. 9, p. 1709, doi. 10.1093/hmg/ddt017
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- Article
Development and characterization of an SMN2-based intermediate mouse model of Spinal Muscular Atrophy.
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- Human Molecular Genetics, 2013, v. 22, n. 9, p. 1843, doi. 10.1093/hmg/ddt037
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- Article
NAD+ salvage pathway proteins suppress proteotoxicity in yeast models of neurodegeneration by promoting the clearance of misfolded/oligomerized proteins.
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- Human Molecular Genetics, 2013, v. 22, n. 9, p. 1699, doi. 10.1093/hmg/ddt016
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- Article
The genome-defence gene Tex19.1 suppresses LINE-1 retrotransposons in the placenta and prevents intra-uterine growth retardation in mice.
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- Human Molecular Genetics, 2013, v. 22, n. 9, p. 1791, doi. 10.1093/hmg/ddt029
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- Article
Mutation dependance of the mitochondrial DNA copy number in the first stages of human embryogenesis.
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- Human Molecular Genetics, 2013, v. 22, n. 9, p. 1867, doi. 10.1093/hmg/ddt040
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- Article
Missense mutations in β-1,3-N-acetylglucosaminyltransferase 1 (B3GNT1) cause Walker–Warburg syndrome.
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- Human Molecular Genetics, 2013, v. 22, n. 9, p. 1746, doi. 10.1093/hmg/ddt021
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Editorial Board.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 9, p. NP, doi. 10.1093/hmg/ddt153
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- Article
A functional copy number variation in the WWOX gene is associated with lung cancer risk in Chinese.
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- Human Molecular Genetics, 2013, v. 22, n. 9, p. 1886, doi. 10.1093/hmg/ddt019
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- Article
A genome-wide association study of resistance to HIV infection in highly exposed uninfected individuals with hemophilia A.
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- Human Molecular Genetics, 2013, v. 22, n. 9, p. 1903
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Subscription Page.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 9, p. NP, doi. 10.1093/hmg/ddt154
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- Article
Cystic fibrosis in an era of genomically guided therapy.
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- Human Molecular Genetics, 2013, v. 22, n. 9, p. 1911, doi. 10.1093/hmg/ddt045
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- Article
Cover Page.
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- Human Molecular Genetics, 2013, v. 22, n. 9, p. NP, doi. 10.1093/hmg/ddt152
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- Article
Role of WT1–ZNF224 interaction in the expression of apoptosis-regulating genes.
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- Human Molecular Genetics, 2013, v. 22, n. 9, p. 1771, doi. 10.1093/hmg/ddt027
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- Article
Novel locus including FGF21 is associated with dietary macronutrient intake.
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- Human Molecular Genetics, 2013, v. 22, n. 9, p. 1895, doi. 10.1093/hmg/ddt032
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Hdac6 deletion delays disease progression in the SOD1G93A mouse model of ALS.
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- Human Molecular Genetics, 2013, v. 22, n. 9, p. 1783, doi. 10.1093/hmg/ddt028
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- Article