Works matching IS 09646906 AND DT 2009 AND VI 18 AND IP 17
Results: 22
Discrimination of common and unique RNA-binding activities among Fragile X mental retardation protein paralogs.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 17, p. 3164, doi. 10.1093/hmg/ddp255
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- Article
Subscription Page.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 17, p. NP, doi. 10.1093/hmg/ddp343
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- Article
Cover Page.
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- Human Molecular Genetics, 2009, v. 18, n. 17, p. NP, doi. 10.1093/hmg/ddp341
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- Article
Mitochondrial abnormalities, energy deficit and oxidative stress are features of calpain 3 deficiency in skeletal muscle.
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- Human Molecular Genetics, 2009, v. 18, n. 17, p. 3194, doi. 10.1093/hmg/ddp257
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- Article
Inhibition of myostatin does not ameliorate disease features of severe spinal muscular atrophy mice.
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- Human Molecular Genetics, 2009, v. 18, n. 17, p. 3145, doi. 10.1093/hmg/ddp253
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- Article
Disc1 regulates granule cell migration in the developing hippocampus.
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- Human Molecular Genetics, 2009, v. 18, n. 17, p. 3286, doi. 10.1093/hmg/ddp266
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- Article
CK2-dependent phosphorylation determines cellular localization and stability of ataxin-3.
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- Human Molecular Genetics, 2009, v. 18, n. 17, p. 3334, doi. 10.1093/hmg/ddp274
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- Article
Variation in aggregation propensities among ALS-associated variants of SOD1: Correlation to human disease.
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- Human Molecular Genetics, 2009, v. 18, n. 17, p. 3217, doi. 10.1093/hmg/ddp260
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- Article
Functional interaction of mammalian target of rapamycin complexes in regulating mammalian cell size and cell cycle.
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- Human Molecular Genetics, 2009, v. 18, n. 17, p. 3298, doi. 10.1093/hmg/ddp271
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- Article
Partial loss of GATA factor Pannier impairs adult heart function in Drosophila.
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- Human Molecular Genetics, 2009, v. 18, n. 17, p. 3153, doi. 10.1093/hmg/ddp254
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- Article
Golgi function and dysfunction in the first COG4-deficient CDG type II patient.
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- Human Molecular Genetics, 2009, v. 18, n. 17, p. 3244, doi. 10.1093/hmg/ddp262
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- Article
Contents Page.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 17, p. NP, doi. 10.1093/hmg/ddp340
- Publication type:
- Article
Editorial Board.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 17, p. NP, doi. 10.1093/hmg/ddp342
- Publication type:
- Article
Ciliary and centrosomal defects associated with mutation and depletion of the Meckel syndrome genes MKS1 and MKS3.
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- Human Molecular Genetics, 2009, v. 18, n. 17, p. 3311, doi. 10.1093/hmg/ddp272
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- Article
Expansion of the Parkinson disease-associated SNCA-Rep1 allele upregulates human α-synuclein in transgenic mouse brain.
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- Human Molecular Genetics, 2009, v. 18, n. 17, p. 3274, doi. 10.1093/hmg/ddp265
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- Article
A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism.
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- Human Molecular Genetics, 2009, v. 18, n. 17, p. 3257, doi. 10.1093/hmg/ddp263
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- Publication type:
- Article
DNMT3B interacts with constitutive centromere protein CENP-C to modulate DNA methylation and the histone code at centromeric regions.
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- Human Molecular Genetics, 2009, v. 18, n. 17, p. 3178, doi. 10.1093/hmg/ddp256
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- Article
Parkin promotes intracellular Aβ1–42 clearance.
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- Human Molecular Genetics, 2009, v. 18, n. 17, p. 3206, doi. 10.1093/hmg/ddp258
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- Article
Serine racemase is associated with schizophrenia susceptibility in humans and in a mouse model.
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- Human Molecular Genetics, 2009, v. 18, n. 17, p. 3227, doi. 10.1093/hmg/ddp261
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- Article
Vascular endothelial growth factor gene polymorphisms as prognostic markers for ocular manifestations in pseudoxanthoma elasticum.
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- Human Molecular Genetics, 2009, v. 18, n. 17, p. 3344, doi. 10.1093/hmg/ddp259
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- Article
Towards a functional classification of pathogenic FOXL2 mutations using transactivation reporter systems.
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- Human Molecular Genetics, 2009, v. 18, n. 17, p. 3324, doi. 10.1093/hmg/ddp273
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- Publication type:
- Article
Correction of tau mis-splicing caused by FTDP-17 MAPT mutations by spliceosome-mediated RNA trans-splicing.
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- Human Molecular Genetics, 2009, v. 18, n. 17, p. 3266, doi. 10.1093/hmg/ddp264
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- Article