Found: 31
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Genes, drugs and race.
- Published in:
- 2001
- Publication type:
- Editorial
A fever gene comes in from the cold.
- Published in:
- Nature Genetics, 2001, v. 29, n. 3, p. 241, doi. 10.1038/ng1101-241
- By:
- Publication type:
- Article
The fragility of fertility.
- Published in:
- Nature Genetics, 2001, v. 29, n. 3, p. 243, doi. 10.1038/ng1101-243
- By:
- Publication type:
- Article
The replication requirement.
- Published in:
- Nature Genetics, 2001, v. 29, n. 3, p. 244, doi. 10.1038/ng1101-244
- By:
- Publication type:
- Article
High Oct-ane fuel powers the stem cell.
- Published in:
- Nature Genetics, 2001, v. 29, n. 3, p. 246, doi. 10.1038/ng1101-246
- By:
- Publication type:
- Article
Pharmacogenetics: more than skin deep.
- Published in:
- Nature Genetics, 2001, v. 29, n. 3, p. 247, doi. 10.1038/ng1101-247
- By:
- Publication type:
- Article
TOUCHINGbase.
- Published in:
- Nature Genetics, 2001, v. 29, n. 3, p. 249
- Publication type:
- Article
The Church of Charles Darwin (without Darwin).
- Published in:
- 2001
- By:
- Publication type:
- Book Review
An Flp indicator mouse expressing alkaline phosphatase from the ROSA26 locus.
- Published in:
- Nature Genetics, 2001, v. 29, n. 3, p. 257, doi. 10.1038/ng1101-257
- By:
- Publication type:
- Article
Erratum: TGF-β signaling in tumor suppression and cancer progression.
- Published in:
- 2001
- By:
- Publication type:
- Correction Notice
Erratum: A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2.
- Published in:
- 2001
- By:
- Publication type:
- Erratum
Erratum: The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis.
- Published in:
- 2001
- By:
- Publication type:
- Erratum
Erratum: A radiation hybrid transcript map of the mouse genome.
- Published in:
- 2001
- By:
- Publication type:
- Correction Notice
Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus.
- Published in:
- Nature Genetics, 2001, v. 29, n. 3, p. 345, doi. 10.1038/ng726
- By:
- Publication type:
- Article
Homozygous mutations in ARIX(PHOX2A) result in congenital fibrosis of the extraocular muscles type 2.
- Published in:
- Nature Genetics, 2001, v. 29, n. 3, p. 315, doi. 10.1038/ng744
- By:
- Publication type:
- Article
Mutant protein in Huntington disease is resistant to proteolysis in affected brain.
- Published in:
- Nature Genetics, 2001, v. 29, n. 3, p. 270, doi. 10.1038/ng745
- By:
- Publication type:
- Article
The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA.
- Published in:
- Nature Genetics, 2001, v. 29, n. 3, p. 337, doi. 10.1038/ng746
- By:
- Publication type:
- Article
Replication validity of genetic association studies.
- Published in:
- Nature Genetics, 2001, v. 29, n. 3, p. 306, doi. 10.1038/ng749
- By:
- Publication type:
- Article
Epigenetic silencing of CD4 in T cells committed to the cytotoxic lineage.
- Published in:
- Nature Genetics, 2001, v. 29, n. 3, p. 332, doi. 10.1038/ng750
- By:
- Publication type:
- Article
The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men.
- Published in:
- Nature Genetics, 2001, v. 29, n. 3, p. 279, doi. 10.1038/ng757
- By:
- Publication type:
- Article
Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy.
- Published in:
- Nature Genetics, 2001, v. 29, n. 3, p. 342, doi. 10.1038/ng751
- By:
- Publication type:
- Article
Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia.
- Published in:
- Nature Genetics, 2001, v. 29, n. 3, p. 326, doi. 10.1038/ng758
- By:
- Publication type:
- Article
Assembly of microarrays for genome-wide measurement of DNA copy number.
- Published in:
- Nature Genetics, 2001, v. 29, n. 3, p. 263, doi. 10.1038/ng754
- By:
- Publication type:
- Article
Bioinformatic identification of potential autocrine signaling loops in cancers from gene expression profiles.
- Published in:
- Nature Genetics, 2001, v. 29, n. 3, p. 295, doi. 10.1038/ng755
- By:
- Publication type:
- Article
Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle?Wells syndrome.
- Published in:
- Nature Genetics, 2001, v. 29, n. 3, p. 301, doi. 10.1038/ng756
- By:
- Publication type:
- Article
Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure.
- Published in:
- Nature Genetics, 2001, v. 29, n. 3, p. 310
- By:
- Publication type:
- Article
A 1.5 million?base pair inversion polymorphism in families with Williams-Beuren syndrome.
- Published in:
- Nature Genetics, 2001, v. 29, n. 3, p. 321, doi. 10.1038/ng753
- By:
- Publication type:
- Article
MID1, mutated in Opitz syndrome, encodes an ubiquitin ligase that targets phosphatase 2A for degradation.
- Published in:
- Nature Genetics, 2001, v. 29, n. 3, p. 287, doi. 10.1038/ng762
- By:
- Publication type:
- Article
Genomics and future biological weapons: the need for preventive action by the biomedical community.
- Published in:
- Nature Genetics, 2001, v. 29, n. 3, p. 253, doi. 10.1038/ng763
- By:
- Publication type:
- Article
Mutations at the mitochondrial DNA polymerase (POLG) locus associated with male infertility.
- Published in:
- Nature Genetics, 2001, v. 29, n. 3, p. 261, doi. 10.1038/ng759
- By:
- Publication type:
- Article
Population genetic structure of variable drug response.
- Published in:
- Nature Genetics, 2001, v. 29, n. 3, p. 265, doi. 10.1038/ng761
- By:
- Publication type:
- Article