Works matching IS 10614036 AND DT 2007 AND VI 39 AND IP 1
Results: 27
Lessons in the genomic diversity of malaria.
- Published in:
- 2007
- Publication type:
- Editorial
Chaotic license for genetic instability and cancer.
- Published in:
- Nature Genetics, 2007, v. 39, n. 1, p. 10, doi. 10.1038/ng0107-10
- By:
- Publication type:
- Article
Telomeres, p21 and the cancer-aging hypothesis.
- Published in:
- Nature Genetics, 2007, v. 39, n. 1, p. 11, doi. 10.1038/ng0107-11
- By:
- Publication type:
- Article
Touching base.
- Published in:
- Nature Genetics, 2007, v. 39, n. 1, p. 13, doi. 10.1038/ng0107-13
- Publication type:
- Article
Corrigendum: Cxorf6 is a causative gene for hypospadias.
- Published in:
- 2007
- By:
- Publication type:
- Correction Notice
Research highlights.
- Published in:
- Nature Genetics, 2007, v. 39, n. 1, p. 15, doi. 10.1038/ng0107-15
- Publication type:
- Article
Awesome, in brief.
- Published in:
- 2007
- By:
- Publication type:
- Book Review
Toward a malaria haplotype map.
- Published in:
- Nature Genetics, 2007, v. 39, n. 1, p. 5, doi. 10.1038/ng0107-5
- By:
- Publication type:
- Article
Following the herd.
- Published in:
- Nature Genetics, 2007, v. 39, n. 1, p. 7, doi. 10.1038/ng0107-7
- By:
- Publication type:
- Article
Sending out an SOS.
- Published in:
- Nature Genetics, 2007, v. 39, n. 1, p. 8, doi. 10.1038/ng0107-8
- By:
- Publication type:
- Article
PDGF signaling specificity is mediated through multiple immediate early genes.
- Published in:
- Nature Genetics, 2007, v. 39, n. 1, p. 52, doi. 10.1038/ng1922
- By:
- Publication type:
- Article
Genome-wide variation and identification of vaccine targets in the Plasmodium falciparum genome.
- Published in:
- Nature Genetics, 2007, v. 39, n. 1, p. 126, doi. 10.1038/ng1924
- By:
- Publication type:
- Article
Germline gain-of-function mutations in SOS1 cause Noonan syndrome.
- Published in:
- Nature Genetics, 2007, v. 39, n. 1, p. 70, doi. 10.1038/ng1926
- By:
- Publication type:
- Article
Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxia.
- Published in:
- Nature Genetics, 2007, v. 39, n. 1, p. 80, doi. 10.1038/ng1927
- By:
- Publication type:
- Article
Genome-wide analysis of Arabidopsis thaliana DNA methylation uncovers an interdependence between methylation and transcription.
- Published in:
- Nature Genetics, 2007, v. 39, n. 1, p. 61, doi. 10.1038/ng1929
- By:
- Publication type:
- Article
A genome-wide map of diversity in Plasmodium falciparum.
- Published in:
- Nature Genetics, 2007, v. 39, n. 1, p. 113, doi. 10.1038/ng1930
- By:
- Publication type:
- Article
A viable allele of Mcm4 causes chromosome instability and mammary adenocarcinomas in mice.
- Published in:
- Nature Genetics, 2007, v. 39, n. 1, p. 93, doi. 10.1038/ng1936
- By:
- Publication type:
- Article
Wnt-β-catenin signaling initiates taste papilla development.
- Published in:
- Nature Genetics, 2007, v. 39, n. 1, p. 106, doi. 10.1038/ng1932
- By:
- Publication type:
- Article
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders.
- Published in:
- Nature Genetics, 2007, v. 39, n. 1, p. 25, doi. 10.1038/ng1933
- By:
- Publication type:
- Article
Systematic meta-analyses of Alzheimer disease genetic association studies: the AlzGene database.
- Published in:
- Nature Genetics, 2007, v. 39, n. 1, p. 17, doi. 10.1038/ng1934
- By:
- Publication type:
- Article
Integrative molecular concept modeling of prostate cancer progression.
- Published in:
- Nature Genetics, 2007, v. 39, n. 1, p. 41, doi. 10.1038/ng1935
- By:
- Publication type:
- Article
Genome variation and evolution of the malaria parasite Plasmodium falciparum.
- Published in:
- Nature Genetics, 2007, v. 39, n. 1, p. 120, doi. 10.1038/ng1931
- By:
- Publication type:
- Article
Cdkn1a deletion improves stem cell function and lifespan of mice with dysfunctional telomeres without accelerating cancer formation.
- Published in:
- Nature Genetics, 2007, v. 39, n. 1, p. 99, doi. 10.1038/ng1937
- By:
- Publication type:
- Article
Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome.
- Published in:
- Nature Genetics, 2007, v. 39, n. 1, p. 75, doi. 10.1038/ng1939
- By:
- Publication type:
- Article
HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease).
- Published in:
- Nature Genetics, 2007, v. 39, n. 1, p. 86, doi. 10.1038/ng1940
- By:
- Publication type:
- Article
Convergent adaptation of human lactase persistence in Africa and Europe.
- Published in:
- Nature Genetics, 2007, v. 39, n. 1, p. 31, doi. 10.1038/ng1946
- By:
- Publication type:
- Article
The gene encoding adipose triglyceride lipase (PNPLA2) is mutated in neutral lipid storage disease with myopathy.
- Published in:
- Nature Genetics, 2007, v. 39, n. 1, p. 28, doi. 10.1038/ng1951
- By:
- Publication type:
- Article