Works matching IS 09646906 AND DT 2013 AND VI 22 AND IP 15
Results: 21
Cover Page.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 15, p. NP, doi. 10.1093/hmg/ddt322
- Publication type:
- Article
Evolutionarily conserved long intergenic non-coding RNAs in the eye.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 15, p. 2992, doi. 10.1093/hmg/ddt156
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- Publication type:
- Article
Impaired viability of muscle precursor cells in muscular dystrophy with glycosylation defects and amelioration of its severe phenotype by limited gene expression.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 15, p. 3003, doi. 10.1093/hmg/ddt157
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- Publication type:
- Article
Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 15, p. 3174, doi. 10.1093/hmg/ddt169
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- Publication type:
- Article
Heterozygous LmnadelK32 mice develop dilated cardiomyopathy through a combined pathomechanism of haploinsufficiency and peptide toxicity.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 15, p. 3152, doi. 10.1093/hmg/ddt172
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- Publication type:
- Article
Genetic regulation of human adipose microRNA expression and its consequences for metabolic traits.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 15, p. 3023, doi. 10.1093/hmg/ddt159
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- Publication type:
- Article
De-repression of FOXO3a death axis by microRNA-132 and -212 causes neuronal apoptosis in Alzheimer's disease.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 15, p. 3077, doi. 10.1093/hmg/ddt164
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- Publication type:
- Article
Deficiency of the E3 ubiquitin ligase TRIM2 in early-onset axonal neuropathy.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 15, p. 2975, doi. 10.1093/hmg/ddt149
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- Publication type:
- Article
The dual functions of the extreme N-terminus of TDP-43 in regulating its biological activity and inclusion formation.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 15, p. 3112, doi. 10.1093/hmg/ddt166
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- Publication type:
- Article
CEP89 is required for mitochondrial metabolism and neuronal function in man and fly.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 15, p. 3138, doi. 10.1093/hmg/ddt170
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- Publication type:
- Article
Comparative transgenic analysis of enhancers from the human SHOX and mouse Shox2 genomic regions.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 15, p. 3063, doi. 10.1093/hmg/ddt163
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- Publication type:
- Article
The Ras-GTPase activity of neurofibromin restrains ERK-dependent FGFR signaling during endochondral bone formation.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 15, p. 3048, doi. 10.1093/hmg/ddt162
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- Publication type:
- Article
Epigenome-wide ovarian cancer analysis identifies a methylation profile differentiating clear-cell histology with epigenetic silencing of the HERG K+ channel.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 15, p. 3038, doi. 10.1093/hmg/ddt160
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- Publication type:
- Article
Contents Page.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 15, p. NP, doi. 10.1093/hmg/ddt321
- Publication type:
- Article
Genome-wide association study in a Chinese population with diabetic retinopathy.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 15, p. 3165, doi. 10.1093/hmg/ddt161
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- Publication type:
- Article
Editorial Board.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 15, p. NP, doi. 10.1093/hmg/ddt323
- Publication type:
- Article
DNA co-methylation analysis suggests novel functional associations between gene pairs in breast cancer samples.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 15, p. 3016, doi. 10.1093/hmg/ddt158
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- Publication type:
- Article
Smooth muscle hyperplasia due to loss of smooth muscle α-actin is driven by activation of focal adhesion kinase, altered p53 localization and increased levels of platelet-derived growth factor receptor-β.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 15, p. 3123, doi. 10.1093/hmg/ddt167
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- Publication type:
- Article
Activation of p38 signaling increases utrophin A expression in skeletal muscle via the RNA-binding protein KSRP and inhibition of AU-rich element-mediated mRNA decay: implications for novel DMD therapeutics.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 15, p. 3093, doi. 10.1093/hmg/ddt165
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- Publication type:
- Article
Loss of FMR2 further emphasizes the link between deregulation of immediate early response genes FOS and JUN and intellectual disability.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 15, p. 2984, doi. 10.1093/hmg/ddt155
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- Publication type:
- Article
Subscription Page.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 15, p. NP, doi. 10.1093/hmg/ddt324
- Publication type:
- Article