Works matching IS 10614036 AND DT 2000 AND VI 24 AND IP 2
Results: 27
A bird's eye view of global methylation.
- Published in:
- Nature Genetics, 2000, v. 24, n. 2, p. 101, doi. 10.1038/72730
- By:
- Publication type:
- Article
Pushing the envelope on lipodystrophy.
- Published in:
- Nature Genetics, 2000, v. 24, n. 2, p. 103, doi. 10.1038/72734
- By:
- Publication type:
- Article
A take on the tectorial membrane.
- Published in:
- Nature Genetics, 2000, v. 24, n. 2, p. 104, doi. 10.1038/72737
- By:
- Publication type:
- Article
TOUCHINGbase.
- Published in:
- Nature Genetics, 2000, v. 24, n. 2, p. 105
- Publication type:
- Article
The ethical challenges of in utero gene therapy.
- Published in:
- Nature Genetics, 2000, v. 24, n. 2, p. 107, doi. 10.1038/72747
- By:
- Publication type:
- Article
Nuclear transfer into mouse zygotes.
- Published in:
- Nature Genetics, 2000, v. 24, n. 2, p. 108, doi. 10.1038/72749
- By:
- Publication type:
- Article
Generation of mice from wild-type and targeted ES cells by nuclear cloning.
- Published in:
- Nature Genetics, 2000, v. 24, n. 2, p. 109, doi. 10.1038/72753
- By:
- Publication type:
- Article
Flu times two.
- Published in:
- 2000
- By:
- Publication type:
- Book Review
Gene-target recognition among members of the Myc superfamily and implications for oncogenesis.
- Published in:
- Nature Genetics, 2000, v. 24, n. 2, p. 113, doi. 10.1038/72761
- By:
- Publication type:
- Article
ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF.
- Published in:
- Nature Genetics, 2000, v. 24, n. 2, p. 120, doi. 10.1038/72769
- By:
- Publication type:
- Article
Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate.
- Published in:
- Nature Genetics, 2000, v. 24, n. 2, p. 127, doi. 10.1038/72777
- By:
- Publication type:
- Article
Aberrant CpG-island methylation has non-random and tumour-type?specific patterns.
- Published in:
- Nature Genetics, 2000, v. 24, n. 2, p. 132, doi. 10.1038/72785
- By:
- Publication type:
- Article
Targeted disruption of Otog results in deafness and severe imbalance.
- Published in:
- Nature Genetics, 2000, v. 24, n. 2, p. 139, doi. 10.1038/72793
- By:
- Publication type:
- Article
A genome-wide survey of RAS transformation targets.
- Published in:
- Nature Genetics, 2000, v. 24, n. 2, p. 144, doi. 10.1038/72799
- By:
- Publication type:
- Article
LMNA, encoding lamin A/C, is mutated in partial lipodystrophy.
- Published in:
- Nature Genetics, 2000, v. 24, n. 2, p. 153, doi. 10.1038/72807
- By:
- Publication type:
- Article
Kit/stem cell factor receptor-induced activation of phosphatidylinositol 3′-kinase is essential for male fertility.
- Published in:
- Nature Genetics, 2000, v. 24, n. 2, p. 157, doi. 10.1038/72814
- By:
- Publication type:
- Article
Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin.
- Published in:
- Nature Genetics, 2000, v. 24, n. 2, p. 163, doi. 10.1038/72822
- By:
- Publication type:
- Article
A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation.
- Published in:
- Nature Genetics, 2000, v. 24, n. 2, p. 167, doi. 10.1038/72829
- By:
- Publication type:
- Article
A role for Smad6 in development and homeostasis of the cardiovascular system.
- Published in:
- Nature Genetics, 2000, v. 24, n. 2, p. 171, doi. 10.1038/72835
- By:
- Publication type:
- Article
Fus deficiency in mice results in defective B-lymphocyte development and activation, high levels of chromosomal instability and perinatal death.
- Published in:
- Nature Genetics, 2000, v. 24, n. 2, p. 175, doi. 10.1038/72842
- By:
- Publication type:
- Article
Heritable and inducible genetic interference by double-stranded RNA encoded by transgenes.
- Published in:
- Nature Genetics, 2000, v. 24, n. 2, p. 180, doi. 10.1038/72850
- By:
- Publication type:
- Article
Giving in to the blues.
- Published in:
- Nature Genetics, 2000, v. 24, n. 2, p. 99, doi. 10.1038/72887
- By:
- Publication type:
- Article
Mutations in the gene encoding peroxisomal α-methylacyl-CoA racemase cause adult-onset sensory motor neuropathy.
- Published in:
- Nature Genetics, 2000, v. 24, n. 2, p. 188, doi. 10.1038/72861
- By:
- Publication type:
- Article
Transport of lipids from Golgi to plasma membrane is defective in Tangier disease patients and Abc1-deficient mice.
- Published in:
- Nature Genetics, 2000, v. 24, n. 2, p. 192, doi. 10.1038/72869
- By:
- Publication type:
- Article
Localization to Xq27 of a susceptibility gene for testicular germ-cell tumours.
- Published in:
- Nature Genetics, 2000, v. 24, n. 2, p. 197, doi. 10.1038/72877
- By:
- Publication type:
- Article
Census, race and science.
- Published in:
- Nature Genetics, 2000, v. 24, n. 2, p. 97, doi. 10.1038/72884
- Publication type:
- Article
Fosl1 is a transcriptional target of c-Fos during osteoclast differentiation.
- Published in:
- Nature Genetics, 2000, v. 24, n. 2, p. 184, doi. 10.1038/72855
- By:
- Publication type:
- Article