Works matching IS 09646906 AND DT 2011 AND VI 20 AND IP 16
Results: 22
Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 16, p. 3289, doi. 10.1093/hmg/ddr228
- By:
- Publication type:
- Article
Nephrocystin-4 is required for pronephric duct-dependent cloaca formation in zebrafish.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 16, p. 3119, doi. 10.1093/hmg/ddr214
- By:
- Publication type:
- Article
Subscription Page.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 16, p. NP, doi. 10.1093/hmg/ddr279
- Publication type:
- Article
Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 16, p. 3304
- By:
- Publication type:
- Article
The PINK1/Parkin pathway regulates mitochondrial dynamics and function in mammalian hippocampal and dopaminergic neurons.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 16, p. 3227, doi. 10.1093/hmg/ddr235
- By:
- Publication type:
- Article
RAD51C is a susceptibility gene for ovarian cancer.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 16, p. 3278, doi. 10.1093/hmg/ddr229
- By:
- Publication type:
- Article
Functional analysis of the RNF114 psoriasis susceptibility gene implicates innate immune responses to double-stranded RNA in disease pathogenesis.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 16, p. 3129, doi. 10.1093/hmg/ddr215
- By:
- Publication type:
- Article
DNMT1 deficiency triggers mismatch repair defects in human cells through depletion of repair protein levels in a process involving the DNA damage response.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 16, p. 3241, doi. 10.1093/hmg/ddr236
- By:
- Publication type:
- Article
Molecular mechanisms of MLC1 and GLIALCAM mutations in megalencephalic leukoencephalopathy with subcortical cysts.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 16, p. 3266
- By:
- Publication type:
- Article
Editorial Board.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 16, p. NP, doi. 10.1093/hmg/ddr278
- Publication type:
- Article
Methylation screening of reciprocal genome-wide UPDs identifies novel human-specific imprinted genes†.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 16, p. 3188, doi. 10.1093/hmg/ddr224
- By:
- Publication type:
- Article
Conditional deletion of Ccm2 causes hemorrhage in the adult brain: a mouse model of human cerebral cavernous malformations.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 16, p. 3198, doi. 10.1093/hmg/ddr225
- By:
- Publication type:
- Article
Grhl2 deficiency impairs otic development and hearing ability in a zebrafish model of the progressive dominant hearing loss DFNA28.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 16, p. 3213, doi. 10.1093/hmg/ddr234
- By:
- Publication type:
- Article
Reproductive dysfunction and decreased GnRH neurogenesis in a mouse model of CHARGE syndrome.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 16, p. 3138, doi. 10.1093/hmg/ddr216
- By:
- Publication type:
- Article
Contents Page.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 16, p. NP, doi. 10.1093/hmg/ddr276
- Publication type:
- Article
Co-aggregate formation of CADASIL-mutant NOTCH3: a single-particle analysis.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 16, p. 3256, doi. 10.1093/hmg/ddr237
- By:
- Publication type:
- Article
Large-scale fine mapping of the HNF1B locus and prostate cancer risk.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 16, p. 3322, doi. 10.1093/hmg/ddr213
- By:
- Publication type:
- Article
Cover Page.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 16, p. NP, doi. 10.1093/hmg/ddr277
- Publication type:
- Article
Long-term and age-dependent restoration of visual function in a mouse model of CNGB3-associated achromatopsia following gene therapy.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 16, p. 3161, doi. 10.1093/hmg/ddr218
- By:
- Publication type:
- Article
Rescue of ATP7B function in hepatocyte-like cells from Wilson's disease induced pluripotent stem cells using gene therapy or the chaperone drug curcumin.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 16, p. 3176, doi. 10.1093/hmg/ddr223
- By:
- Publication type:
- Article
Arginine-rich cell-penetrating peptide dramatically enhances AMO-mediated ATM aberrant splicing correction and enables delivery to brain and cerebellum.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 16, p. 3151, doi. 10.1093/hmg/ddr217
- By:
- Publication type:
- Article
Ataxin-2 repeat-length variation and neurodegeneration.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 16, p. 3207, doi. 10.1093/hmg/ddr227
- By:
- Publication type:
- Article