Works matching IS 10614036 AND DT 2006 AND VI 38 AND IP 10
Results: 27
Many hypotheses but no replication for the association between PDE4D and stroke.
- Published in:
- 2006
- By:
- Publication type:
- Letter
Reply to “Many hypotheses but no replication for the association between PDE4D and stroke”.
- Published in:
- 2006
- By:
- Publication type:
- Letter
Minimum compliance for a microarray experiment?
- Published in:
- 2006
- Publication type:
- Editorial
The genetics of health.
- Published in:
- Nature Genetics, 2006, v. 38, n. 10, p. 1095, doi. 10.1038/ng1006-1095
- By:
- Publication type:
- Article
A weed for one year.
- Published in:
- 2006
- By:
- Publication type:
- Book Review
Tiling DNA microarrays for fly genome cartography.
- Published in:
- Nature Genetics, 2006, v. 38, n. 10, p. 1101, doi. 10.1038/ng1006-1101
- By:
- Publication type:
- Article
(Re)modeling the transcriptional enhancer.
- Published in:
- Nature Genetics, 2006, v. 38, n. 10, p. 1102, doi. 10.1038/ng1006-1102
- By:
- Publication type:
- Article
New evidence that DNA encodes its packaging.
- Published in:
- Nature Genetics, 2006, v. 38, n. 10, p. 1104, doi. 10.1038/ng1006-1104
- By:
- Publication type:
- Article
A WNK in the kidney controls blood pressure.
- Published in:
- Nature Genetics, 2006, v. 38, n. 10, p. 1105, doi. 10.1038/ng1006-1105
- By:
- Publication type:
- Article
Touching base.
- Published in:
- Nature Genetics, 2006, v. 38, n. 10, p. 1107, doi. 10.1038/ng1006-1107
- Publication type:
- Article
Research highlights.
- Published in:
- Nature Genetics, 2006, v. 38, n. 10, p. 1109, doi. 10.1038/ng1006-1109
- Publication type:
- Article
Heritable germline epimutation of MSH2 in a family with hereditary nonpolyposis colorectal cancer.
- Published in:
- 2006
- By:
- Publication type:
- Letter
Deficiency of hyccin, a newly identified membrane protein, causes hypomyelination and congenital cataract.
- Published in:
- Nature Genetics, 2006, v. 38, n. 10, p. 1111, doi. 10.1038/ng1870
- By:
- Publication type:
- Article
Lamin B1 duplications cause autosomal dominant leukodystrophy.
- Published in:
- Nature Genetics, 2006, v. 38, n. 10, p. 1114, doi. 10.1038/ng1872
- By:
- Publication type:
- Article
Indian hedgehog is a major mediator of progesterone signaling in the mouse uterus.
- Published in:
- 2006
- By:
- Publication type:
- Letter
Biological function of unannotated transcription during the early development of Drosophila melanogaster.
- Published in:
- Nature Genetics, 2006, v. 38, n. 10, p. 1151, doi. 10.1038/ng1875
- By:
- Publication type:
- Article
Cranio-lenticulo-sutural dysplasia is caused by a SEC23A mutation leading to abnormal endoplasmic-reticulum-to-Golgi trafficking.
- Published in:
- 2006
- By:
- Publication type:
- Letter
Wnk4 controls blood pressure and potassium homeostasis via regulation of mass and activity of the distal convoluted tubule.
- Published in:
- Nature Genetics, 2006, v. 38, n. 10, p. 1124, doi. 10.1038/ng1877
- By:
- Publication type:
- Article
Nucleosome positions predicted through comparative genomics.
- Published in:
- 2006
- By:
- Publication type:
- Letter
iASPP preferentially binds p53 proline-rich region and modulates apoptotic function of codon 72–polymorphic p53.
- Published in:
- Nature Genetics, 2006, v. 38, n. 10, p. 1133, doi. 10.1038/ng1879
- By:
- Publication type:
- Article
Secretory COPII coat component Sec23a is essential for craniofacial chondrocyte maturation.
- Published in:
- 2006
- By:
- Publication type:
- Letter
Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase.
- Published in:
- 2006
- By:
- Publication type:
- Letter
A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC.
- Published in:
- 2006
- By:
- Publication type:
- Letter
Quantitative and predictive model of transcriptional control of the Drosophila melanogaster even skipped gene.
- Published in:
- Nature Genetics, 2006, v. 38, n. 10, p. 1159, doi. 10.1038/ng1886
- By:
- Publication type:
- Article
Delineation of a Fat tumor suppressor pathway.
- Published in:
- Nature Genetics, 2006, v. 38, n. 10, p. 1142, doi. 10.1038/ng1887
- By:
- Publication type:
- Article
Mammalian ultraconserved elements are strongly depleted among segmental duplications and copy number variants.
- Published in:
- Nature Genetics, 2006, v. 38, n. 10, p. 1216, doi. 10.1038/ng1888
- By:
- Publication type:
- Article
A common CFH haplotype, with deletion of CFHR1 and CFHR3, is associated with lower risk of age-related macular degeneration.
- Published in:
- Nature Genetics, 2006, v. 38, n. 10, p. 1173, doi. 10.1038/ng1890
- By:
- Publication type:
- Article