Works matching IS 09646906 AND DT 2011 AND VI 20 AND IP 22
Results: 22
Temporal and cell-specific deletion establishes that neuronal Npc1 deficiency is sufficient to mediate neurodegeneration.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 22, p. 4440, doi. 10.1093/hmg/ddr372
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- Article
Subscription Page.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 22, p. NP, doi. 10.1093/hmg/ddr486
- Publication type:
- Article
DNA methylation directly silences genes with non-CpG island promoters and establishes a nucleosome occupied promoter.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 22, p. 4299, doi. 10.1093/hmg/ddr356
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- Article
Editorial Board.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 22, p. NP, doi. 10.1093/hmg/ddr485
- Publication type:
- Article
15q11.2–13.3 chromatin analysis reveals epigenetic regulation of CHRNA7 with deficiencies in Rett and autism brain.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 22, p. 4311, doi. 10.1093/hmg/ddr357
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- Article
Exploring the genomic basis of pharmacoresistance in epilepsy: an integrative analysis of large-scale gene expression profiling studies on brain tissue from epilepsy surgery.
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- Human Molecular Genetics, 2011, v. 20, n. 22, p. 4381, doi. 10.1093/hmg/ddr365
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- Article
Contents Page.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 22, p. NP, doi. 10.1093/hmg/ddr483
- Publication type:
- Article
Fine-mapping of breast cancer susceptibility loci characterizes genetic risk in African Americans.
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- Human Molecular Genetics, 2011, v. 20, n. 22, p. 4491, doi. 10.1093/hmg/ddr367
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- Article
Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE.
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- Human Molecular Genetics, 2011, v. 20, n. 22, p. 4360, doi. 10.1093/hmg/ddr363
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- Article
Additional genomic duplications in AZFc underlie the b2/b3 deletion-associated risk of spermatogenic impairment in Han Chinese population.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 22, p. 4411, doi. 10.1093/hmg/ddr369
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- Article
Cover Page.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 22, p. NP, doi. 10.1093/hmg/ddr484
- Publication type:
- Article
GWAS of butyrylcholinesterase activity identifies four novel loci, independent effects within BCHE and secondary associations with metabolic risk factors.
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- Human Molecular Genetics, 2011, v. 20, n. 22, p. 4504, doi. 10.1093/hmg/ddr375
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- Article
The selective footprints of viral pressures at the human RIG-I-like receptor family.
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- Human Molecular Genetics, 2011, v. 20, n. 22, p. 4462, doi. 10.1093/hmg/ddr377
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- Article
Generation of a novel mouse model that recapitulates early and adult onset glycogenosis type IV.
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- Human Molecular Genetics, 2011, v. 20, n. 22, p. 4430, doi. 10.1093/hmg/ddr371
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- Article
Genomic imprinting at a boundary element flanking the SDHD locus.
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- Human Molecular Genetics, 2011, v. 20, n. 22, p. 4452, doi. 10.1093/hmg/ddr376
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- Article
Impaired motoneuronal retrograde transport in two models of SBMA implicates two sites of androgen action.
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- Human Molecular Genetics, 2011, v. 20, n. 22, p. 4475, doi. 10.1093/hmg/ddr380
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- Article
Mutations in the planar cell polarity gene, Fuzzy, are associated with neural tube defects in humans.
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- Human Molecular Genetics, 2011, v. 20, n. 22, p. 4324, doi. 10.1093/hmg/ddr359
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- Article
Adeno-associated virus-mediated expression of β-hexosaminidase prevents neuronal loss in the Sandhoff mouse brain.
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- Human Molecular Genetics, 2011, v. 20, n. 22, p. 4371, doi. 10.1093/hmg/ddr364
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- Article
Increased levels of noisy splicing in cancers, but not for oncogene-derived transcripts.
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- Human Molecular Genetics, 2011, v. 20, n. 22, p. 4422, doi. 10.1093/hmg/ddr370
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- Article
Reversible molecular pathology of skeletal muscle in spinal muscular atrophy.
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- Human Molecular Genetics, 2011, v. 20, n. 22, p. 4334, doi. 10.1093/hmg/ddr360
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- Article
Elevated levels of active matrix metalloproteinase-9 cause hypertrophy in skeletal muscle of normal and dystrophin-deficient mdx mice.
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- Human Molecular Genetics, 2011, v. 20, n. 22, p. 4345, doi. 10.1093/hmg/ddr362
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Functional and physical interaction between the mismatch repair and FA-BRCA pathways.
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- Human Molecular Genetics, 2011, v. 20, n. 22, p. 4395, doi. 10.1093/hmg/ddr366
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- Article