Works matching IS 10614036 AND DT 2000 AND VI 26 AND IP 1
Results: 36
Private matters, public affairs.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 1, doi. 10.1038/79061
- Publication type:
- Article
Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 103, doi. 10.1038/79063
- Publication type:
- Article
Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomaly.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 106, doi. 10.1038/79069
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- Publication type:
- Article
Nf1;Trp53 mutant mice develop glioblastoma with evidence of strain-specific effects.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 109, doi. 10.1038/79075
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- Publication type:
- Article
Touchingbase.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 11
- Publication type:
- Article
Telomerase-deficient mice with short telomeres are resistant to skin tumorigenesis.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 114, doi. 10.1038/79089
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- Publication type:
- Article
Identification of the gene causing mucolipidosis type IV.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 118, doi. 10.1038/79095
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- Publication type:
- Article
Pidd, a new death-domain?containing protein, is induced by p53 and promotes apoptosis.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 122, doi. 10.1038/79102
- By:
- Publication type:
- Article
Neurofibrillary tangles, amyotrophy and progressive motor disturbance in mice expressing mutant (P301L) tau protein.
- Published in:
- 2000
- Publication type:
- Erratum
Failure of adipocyte differentiation causes type II diabetes mellitus?
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 13, doi. 10.1038/79111
- By:
- Publication type:
- Article
Sampling SNPs.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 13, doi. 10.1038/79113
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- Publication type:
- Article
Mutations in MKKS cause Bardet-Biedl syndrome.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 15, doi. 10.1038/79116
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- Publication type:
- Article
Methylation of the CDH1 promoter as the second genetic hit in hereditary diffuse gastric cancer.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 16, doi. 10.1038/79120
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- Publication type:
- Article
A putative pheromone receptor gene expressed in human olfactory mucosa.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 18, doi. 10.1038/79124
- By:
- Publication type:
- Article
Domain-specific mutations in TGFB1 result in Camurati-Engelmann disease.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 19, doi. 10.1038/79128
- By:
- Publication type:
- Article
The humane genome project.
- Published in:
- 2000
- By:
- Publication type:
- Book Review
Circadian rhythm genetics: from flies to mice to humans.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 23, doi. 10.1038/79134
- By:
- Publication type:
- Article
Expanded polyglutamine stretches interact with TAF<sub>II</sub>130, interfering with CREB-dependent transcription.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 29, doi. 10.1038/79139
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- Publication type:
- Article
Pulling apart pulmonary hypertension.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 3, doi. 10.1038/79148
- By:
- Publication type:
- Article
A transactivation-deficient mouse model provides insights into Trp53 regulation and function.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 37, doi. 10.1038/79152
- By:
- Publication type:
- Article
Of microarrays and meandering data points.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 4, doi. 10.1038/79159
- By:
- Publication type:
- Article
Nuclear localization or inclusion body formation of ataxin-2 are not necessary for SCA2 pathogenesis in mouse or human.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 44, doi. 10.1038/79162
- By:
- Publication type:
- Article
A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 51, doi. 10.1038/79171
- By:
- Publication type:
- Article
A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 56, doi. 10.1038/79178
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- Publication type:
- Article
A PDZ protein ushers in new links.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 6, doi. 10.1038/79186
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- Publication type:
- Article
Large-scale human promoter mapping using CpG islands.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 61, doi. 10.1038/79189
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- Publication type:
- Article
In vivo selection using a cell-growth switch.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 64, doi. 10.1038/79194
- By:
- Publication type:
- Article
Mutations in MKKS cause obesity, retinal dystrophy and renal malformations associated with Bardet-Biedl syndrome.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 67, doi. 10.1038/79201
- By:
- Publication type:
- Article
Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 71, doi. 10.1038/79208
- By:
- Publication type:
- Article
The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 76, doi. 10.1038/79216
- By:
- Publication type:
- Article
Melanocortins and body weight: a tale of two receptors.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 8, doi. 10.1038/79223
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- Publication type:
- Article
Heterozygous germline mutations in BMPR2, encoding a TGF-β receptor, cause familial primary pulmonary hypertension.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 81, doi. 10.1038/79226
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- Publication type:
- Article
Telomere dysfunction impairs DNA repair and enhances sensitivity to ionizing radiation.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 85, doi. 10.1038/79232
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- Publication type:
- Article
Mutations of the gene encoding the protein kinase A type I-α regulatory subunit in patients with the Carney complex.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 89, doi. 10.1038/79238
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- Publication type:
- Article
Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 93, doi. 10.1038/79246
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- Publication type:
- Article
Inactivation of the mouse melanocortin-3 receptor results in increased fat mass and reduced lean body mass.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 97, doi. 10.1038/79254
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- Publication type:
- Article