Works matching IS 10614036 AND DT 2006 AND VI 38 AND IP 5
Results: 27
Animal research and the search for understanding.
- Published in:
- 2006
- Publication type:
- Editorial
PTPN22 and invasive bacterial disease.
- Published in:
- Nature Genetics, 2006, v. 38, n. 5, p. 499, doi. 10.1038/ng0506-499
- By:
- Publication type:
- Article
GenePattern 2.0.
- Published in:
- Nature Genetics, 2006, v. 38, n. 5, p. 500, doi. 10.1038/ng0506-500
- By:
- Publication type:
- Article
Iron metabolism meets signal transduction.
- Published in:
- Nature Genetics, 2006, v. 38, n. 5, p. 503, doi. 10.1038/ng0506-503
- By:
- Publication type:
- Article
A broad band of silence.
- Published in:
- Nature Genetics, 2006, v. 38, n. 5, p. 504, doi. 10.1038/ng0506-504
- By:
- Publication type:
- Article
An adaptive path through jungle DNA.
- Published in:
- Nature Genetics, 2006, v. 38, n. 5, p. 506, doi. 10.1038/ng0506-506
- By:
- Publication type:
- Article
mtDNA clock runs out for dopaminergic neurons.
- Published in:
- Nature Genetics, 2006, v. 38, n. 5, p. 507, doi. 10.1038/ng0506-507
- By:
- Publication type:
- Article
Touching base.
- Published in:
- Nature Genetics, 2006, v. 38, n. 5, p. 509, doi. 10.1038/ng0506-509
- By:
- Publication type:
- Article
Research Highlights.
- Published in:
- Nature Genetics, 2006, v. 38, n. 5, p. 511, doi. 10.1038/ng0506-511
- By:
- Publication type:
- Article
Integrating genomics against infectious disease.
- Published in:
- Nature Genetics, 2006, v. 38, n. 5, p. 513, doi. 10.1038/ng0506-513
- By:
- Publication type:
- Article
Corrigendum: Germline KRAS mutations cause Noonan syndrome.
- Published in:
- 2006
- By:
- Publication type:
- Correction Notice
MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA depletion.
- Published in:
- Nature Genetics, 2006, v. 38, n. 5, p. 570, doi. 10.1038/ng1765
- By:
- Publication type:
- Article
High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease.
- Published in:
- Nature Genetics, 2006, v. 38, n. 5, p. 515, doi. 10.1038/ng1769
- By:
- Publication type:
- Article
Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies.
- Published in:
- Nature Genetics, 2006, v. 38, n. 5, p. 556, doi. 10.1038/ng1770
- By:
- Publication type:
- Article
BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locus.
- Published in:
- Nature Genetics, 2006, v. 38, n. 5, p. 521, doi. 10.1038/ng1771
- By:
- Publication type:
- Article
A truncating mutation of HDAC2 in human cancers confers resistance to histone deacetylase inhibition.
- Published in:
- Nature Genetics, 2006, v. 38, n. 5, p. 566, doi. 10.1038/ng1773
- By:
- Publication type:
- Article
Ablation of PDK1 in pancreatic β cells induces diabetes as a result of loss of β cell mass.
- Published in:
- Nature Genetics, 2006, v. 38, n. 5, p. 589, doi. 10.1038/ng1774
- By:
- Publication type:
- Article
Mutations in embryonic myosin heavy chain (MYH3) cause Freeman-Sheldon syndrome and Sheldon-Hall syndrome.
- Published in:
- Nature Genetics, 2006, v. 38, n. 5, p. 561, doi. 10.1038/ng1775
- By:
- Publication type:
- Article
Systematic identification of human mitochondrial disease genes through integrative genomics.
- Published in:
- Nature Genetics, 2006, v. 38, n. 5, p. 576, doi. 10.1038/ng1776
- By:
- Publication type:
- Article
Bone morphogenetic protein signaling by hemojuvelin regulates hepcidin expression.
- Published in:
- Nature Genetics, 2006, v. 38, n. 5, p. 531, doi. 10.1038/ng1777
- By:
- Publication type:
- Article
Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neurons.
- Published in:
- Nature Genetics, 2006, v. 38, n. 5, p. 518, doi. 10.1038/ng1778
- By:
- Publication type:
- Article
X-linked Cornelia de Lange syndrome owing to SMC1L1 mutations.
- Published in:
- Nature Genetics, 2006, v. 38, n. 5, p. 528, doi. 10.1038/ng1779
- By:
- Publication type:
- Article
Epigenetic remodeling in colorectal cancer results in coordinate gene suppression across an entire chromosome band.
- Published in:
- Nature Genetics, 2006, v. 38, n. 5, p. 540, doi. 10.1038/ng1781
- By:
- Publication type:
- Article
A common haplotype of interferon regulatory factor 5 (IRF5) regulates splicing and expression and is associated with increased risk of systemic lupus erythematosus.
- Published in:
- Nature Genetics, 2006, v. 38, n. 5, p. 550, doi. 10.1038/ng1782
- By:
- Publication type:
- Article
A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva.
- Published in:
- Nature Genetics, 2006, v. 38, n. 5, p. 525, doi. 10.1038/ng1783
- By:
- Publication type:
- Article
A distant upstream enhancer at the maize domestication gene tb1 has pleiotropic effects on plant and inflorescent architecture.
- Published in:
- Nature Genetics, 2006, v. 38, n. 5, p. 594, doi. 10.1038/ng1784
- By:
- Publication type:
- Article
Total insulin and IGF-I resistance in pancreatic β cells causes overt diabetes.
- Published in:
- Nature Genetics, 2006, v. 38, n. 5, p. 583, doi. 10.1038/ng1787
- By:
- Publication type:
- Article