Works matching IS 10614036 AND DT 2007 AND VI 39 AND IP 2
Results: 35
GINA, aGAIN.
- Published in:
- Nature Genetics, 2007, v. 39, n. 2, p. 133, doi. 10.1038/ng0207-133
- Publication type:
- Article
Open-access database of candidate associations from a genome-wide SNP scan of the Framingham Heart Study.
- Published in:
- 2007
- By:
- Publication type:
- Letter
On the cloning of animals from terminally differentiated cells.
- Published in:
- 2007
- By:
- Publication type:
- Letter
Reply to “On the cloning of animals from terminally differentiated cells”.
- Published in:
- 2007
- By:
- Publication type:
- Letter
Cipher sleuth.
- Published in:
- 2007
- By:
- Publication type:
- Book Review
Latexin is a newly discovered regulator of hematopoietic stem cells.
- Published in:
- Nature Genetics, 2007, v. 39, n. 2, p. 141, doi. 10.1038/ng0207-141
- By:
- Publication type:
- Article
Fanconi anemia and breast cancer susceptibility.
- Published in:
- Nature Genetics, 2007, v. 39, n. 2, p. 142, doi. 10.1038/ng0207-142
- By:
- Publication type:
- Article
Personalized medicine and quantitative trait transcripts.
- Published in:
- Nature Genetics, 2007, v. 39, n. 2, p. 144, doi. 10.1038/ng0207-144
- By:
- Publication type:
- Article
Micromanaging the response to Hedgehog.
- Published in:
- Nature Genetics, 2007, v. 39, n. 2, p. 145, doi. 10.1038/ng0207-145
- By:
- Publication type:
- Article
A DNA methylation–based switch generates bistable gene expression.
- Published in:
- Nature Genetics, 2007, v. 39, n. 2, p. 146, doi. 10.1038/ng0207-146
- By:
- Publication type:
- Article
Touching base.
- Published in:
- Nature Genetics, 2007, v. 39, n. 2, p. 149, doi. 10.1038/ng0207-149
- By:
- Publication type:
- Article
Research highlights.
- Published in:
- Nature Genetics, 2007, v. 39, n. 2, p. 151, doi. 10.1038/ng0207-151
- By:
- Publication type:
- Article
Human Genome Variation 2006: emerging views on structural variation and large-scale SNP analysis.
- Published in:
- Nature Genetics, 2007, v. 39, n. 2, p. 153, doi. 10.1038/ng0207-153
- By:
- Publication type:
- Article
Corrigendum: Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome.
- Published in:
- 2007
- By:
- Publication type:
- Correction Notice
Corrigendum: A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva.
- Published in:
- 2007
- By:
- Publication type:
- Correction Notice
Corrigendum: Lamin B1 duplications cause autosomal dominant leukodystrophy.
- Published in:
- 2007
- By:
- Publication type:
- Correction Notice
PTEN-deficient intestinal stem cells initiate intestinal polyposis.
- Published in:
- Nature Genetics, 2007, v. 39, n. 2, p. 189, doi. 10.1038/ng1928
- By:
- Publication type:
- Article
The quantitative trait gene latexin influences the size of the hematopoietic stem cell population in mice.
- Published in:
- Nature Genetics, 2007, v. 39, n. 2, p. 178, doi. 10.1038/ng1938
- By:
- Publication type:
- Article
Epigenetic stem cell signature in cancer.
- Published in:
- Nature Genetics, 2007, v. 39, n. 2, p. 157, doi. 10.1038/ng1941
- By:
- Publication type:
- Article
Fanconi anemia is associated with a defect in the BRCA2 partner PALB2.
- Published in:
- Nature Genetics, 2007, v. 39, n. 2, p. 159, doi. 10.1038/ng1942
- By:
- Publication type:
- Article
The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease.
- Published in:
- Nature Genetics, 2007, v. 39, n. 2, p. 168, doi. 10.1038/ng1943
- By:
- Publication type:
- Article
Quantitative trait transcripts for nicotine resistance in Drosophila melanogaster.
- Published in:
- Nature Genetics, 2007, v. 39, n. 2, p. 264, doi. 10.1038/ng1944
- By:
- Publication type:
- Article
A nonsynonymous SNP in PRKCH (protein kinase C η) increases the risk of cerebral infarction.
- Published in:
- Nature Genetics, 2007, v. 39, n. 2, p. 212, doi. 10.1038/ng1945
- By:
- Publication type:
- Article
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer.
- Published in:
- Nature Genetics, 2007, v. 39, n. 2, p. 162, doi. 10.1038/ng1947
- By:
- Publication type:
- Article
Systematic pathway analysis using high-resolution fitness profiling of combinatorial gene deletions.
- Published in:
- Nature Genetics, 2007, v. 39, n. 2, p. 199, doi. 10.1038/ng1948
- By:
- Publication type:
- Article
Chromosome-wide nucleosome replacement and H3.3 incorporation during mammalian meiotic sex chromosome inactivation.
- Published in:
- Nature Genetics, 2007, v. 39, n. 2, p. 251, doi. 10.1038/ng1949
- By:
- Publication type:
- Article
Polycomb-mediated methylation on Lys27 of histone H3 pre-marks genes for de novo methylation in cancer.
- Published in:
- Nature Genetics, 2007, v. 39, n. 2, p. 232, doi. 10.1038/ng1950
- By:
- Publication type:
- Article
Telomere length regulates the epigenetic status of mammalian telomeres and subtelomeres.
- Published in:
- Nature Genetics, 2007, v. 39, n. 2, p. 243, doi. 10.1038/ng1952
- By:
- Publication type:
- Article
Zebrafish miR-214 modulates Hedgehog signaling to specify muscle cell fate.
- Published in:
- Nature Genetics, 2007, v. 39, n. 2, p. 259, doi. 10.1038/ng1953
- By:
- Publication type:
- Article
A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1.
- Published in:
- Nature Genetics, 2007, v. 39, n. 2, p. 207, doi. 10.1038/ng1954
- By:
- Publication type:
- Article
Common genetic variants account for differences in gene expression among ethnic groups.
- Published in:
- Nature Genetics, 2007, v. 39, n. 2, p. 226, doi. 10.1038/ng1955
- By:
- Publication type:
- Article
A multistep epigenetic switch enables the stable inheritance of DNA methylation states.
- Published in:
- Nature Genetics, 2007, v. 39, n. 2, p. 269, doi. 10.1038/ng1956
- By:
- Publication type:
- Article
PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene.
- Published in:
- Nature Genetics, 2007, v. 39, n. 2, p. 165, doi. 10.1038/ng1959
- By:
- Publication type:
- Article
Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution.
- Published in:
- Nature Genetics, 2007, v. 39, n. 2, p. 218, doi. 10.1038/ng1960
- By:
- Publication type:
- Article
A stem cell–like chromatin pattern may predispose tumor suppressor genes to DNA hypermethylation and heritable silencing.
- Published in:
- Nature Genetics, 2007, v. 39, n. 2, p. 237, doi. 10.1038/ng1972
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- Publication type:
- Article