Works matching IS 09646906 AND DT 2012 AND VI 21 AND IP 14
Results: 22
Hnf1b and Pax2 cooperate to control different pathways in kidney and ureter morphogenesis.
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- Human Molecular Genetics, 2012, v. 21, n. 14, p. 3143, doi. 10.1093/hmg/dds141
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- Article
Trisomy for Synaptojanin1 in Down syndrome is functionally linked to the enlargement of early endosomes.
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- Human Molecular Genetics, 2012, v. 21, n. 14, p. 3156, doi. 10.1093/hmg/dds142
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- Article
α-Synuclein expression and Nrf2 deficiency cooperate to aggravate protein aggregation, neuronal death and inflammation in early-stage Parkinson's disease.
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- Human Molecular Genetics, 2012, v. 21, n. 14, p. 3173, doi. 10.1093/hmg/dds143
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- Article
Contents Page.
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- Human Molecular Genetics, 2012, v. 21, n. 14, p. NP, doi. 10.1093/hmg/dds249
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- Article
Impaired calcium calmodulin kinase signaling and muscle adaptation response in the absence of calpain 3.
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- Human Molecular Genetics, 2012, v. 21, n. 14, p. 3193, doi. 10.1093/hmg/dds144
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- Article
Cover Page.
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- Human Molecular Genetics, 2012, v. 21, n. 14, p. NP, doi. 10.1093/hmg/dds252
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- Article
Ryanodine receptor antagonists adapt NPC1 proteostasis to ameliorate lipid storage in Niemann–Pick type C disease fibroblasts.
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- Human Molecular Genetics, 2012, v. 21, n. 14, p. 3205, doi. 10.1093/hmg/dds145
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- Article
Evidence for FHL1 as a novel disease gene for isolated hypertrophic cardiomyopathy.
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- Human Molecular Genetics, 2012, v. 21, n. 14, p. 3237, doi. 10.1093/hmg/dds157
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- Article
Identification of a novel percent mammographic density locus at 12q24.
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- Human Molecular Genetics, 2012, v. 21, n. 14, p. 3299, doi. 10.1093/hmg/dds158
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- Article
Meta-analysis of two genome-wide association studies identifies four genetic loci associated with thyroid function.
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- Human Molecular Genetics, 2012, v. 21, n. 14, p. 3275, doi. 10.1093/hmg/dds136
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- Article
Caffeine intake and CYP1A2 variants associated with high caffeine intake protect non-smokers from hypertension.
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- Human Molecular Genetics, 2012, v. 21, n. 14, p. 3283, doi. 10.1093/hmg/dds137
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- Article
Discovery of novel protein partners of the transcription factor FOXL2 provides insights into its physiopathological roles.
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- Human Molecular Genetics, 2012, v. 21, n. 14, p. 3264, doi. 10.1093/hmg/dds170
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- Article
Validated SNPs for eGFR and their associations with albuminuria.
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- Human Molecular Genetics, 2012, v. 21, n. 14, p. 3293
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- Article
Editorial Board.
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- Human Molecular Genetics, 2012, v. 21, n. 14, p. NP, doi. 10.1093/hmg/dds255
- Publication type:
- Article
Forkhead box protein p1 is a transcriptional repressor of immune signaling in the CNS: implications for transcriptional dysregulation in Huntington disease.
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- Human Molecular Genetics, 2012, v. 21, n. 14, p. 3097, doi. 10.1093/hmg/dds132
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- Article
Enriched rearing improves behavioral responses of an animal model for CNV-based autistic-like traits.
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- Human Molecular Genetics, 2012, v. 21, n. 14, p. 3083, doi. 10.1093/hmg/dds124
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- Article
The GTPase ARFRP1 controls the lipidation of chylomicrons in the Golgi of the intestinal epithelium.
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- Human Molecular Genetics, 2012, v. 21, n. 14, p. 3128, doi. 10.1093/hmg/dds140
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- Article
The differential effects of prenatal and/or postnatal rapamycin on neurodevelopmental defects and cognition in a neuroglial mouse model of tuberous sclerosis complex.
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- Human Molecular Genetics, 2012, v. 21, n. 14, p. 3226, doi. 10.1093/hmg/dds156
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- Article
Subscription Page.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 14, p. NP, doi. 10.1093/hmg/dds258
- Publication type:
- Article
Androgen-regulated processing of the oncomir MiR-27a, which targets Prohibitin in prostate cancer.
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- Human Molecular Genetics, 2012, v. 21, n. 14, p. 3112, doi. 10.1093/hmg/dds139
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- Article
Human DJ-1 and its homologs are novel glyoxalases.
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- Human Molecular Genetics, 2012, v. 21, n. 14, p. 3215, doi. 10.1093/hmg/dds155
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- Article
Regulatory variation in a TBX5 enhancer leads to isolated congenital heart disease.
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- Human Molecular Genetics, 2012, v. 21, n. 14, p. 3255, doi. 10.1093/hmg/dds165
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- Article