Works matching IS 10614036 AND DT 1999 AND VI 23 AND IP 3
Results: 36
Connecting the dots.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 249, doi. 10.1038/15410
- Publication type:
- Article
A bumper crop of cancer genes.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 253, doi. 10.1038/15423
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- Article
Agouti germ line gets acquisitive.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 254, doi. 10.1038/15425
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- Article
The dynamics of dystroglycan.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 256, doi. 10.1038/15428
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- Publication type:
- Article
Modelling multiple sclerosis.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 258, doi. 10.1038/15430
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- Publication type:
- Article
TOUCHINGbase.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 261
- Publication type:
- Article
Colour-changing karyotyping: an alternative to M-FISH/SKY.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 263, doi. 10.1038/15437
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- Publication type:
- Article
Mutations in SLC4A4 cause permanent isolated proximal renal tubular acidosis with ocular abnormalities.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 264, doi. 10.1038/15440
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- Publication type:
- Article
The DNA repair gene MBD4 (MED1) is mutated in human carcinomas with microsatellite instability.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 266, doi. 10.1038/15443
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- Publication type:
- Article
Scd1 is expressed in sebaceous glands and is disrupted in the asebia mouse.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 268, doi. 10.1038/15446
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- Publication type:
- Article
Fine-mapping of an ancestral recombination breakpoint in DCP1.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 270, doi. 10.1038/15449
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- Publication type:
- Article
Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 271, doi. 10.1038/15452
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- Publication type:
- Article
Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 271, doi. 10.1038/15722
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- Publication type:
- Article
Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 272, doi. 10.1038/15723
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- Publication type:
- Article
A point of entry into genomics.
- Published in:
- 1999
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- Publication type:
- Book Review
Protecting communities in research: current guidelines and limits of extrapolation.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 275, doi. 10.1038/15455
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- Publication type:
- Article
Diverse and dynamic functions of the Sir silencing complex.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 281, doi. 10.1038/15458
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- Publication type:
- Article
A RA-dependent, tumour-growth suppressive transcription complex is the target of the PML-RARα and T18 oncoproteins.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 287, doi. 10.1038/15463
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- Publication type:
- Article
Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 296, doi. 10.1038/15472
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- Publication type:
- Article
Differential methylation of genes and retrotransposons facilitates shotgun sequencing of the maize genome.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 305, doi. 10.1038/15479
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- Publication type:
- Article
A shotgun optical map of the entire Plasmodium falciparum genome.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 309, doi. 10.1038/15484
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- Publication type:
- Article
Epigenetic inheritance at the agouti locus in the mouse.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 314, doi. 10.1038/15490
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- Publication type:
- Article
CACP, encoding a secreted proteoglycan, is mutated in camptodactyly-arthropathy-coxa vara-pericarditis syndrome.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 319, doi. 10.1038/15496
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- Publication type:
- Article
Mutations in NEUROD1 are associated with the development of type 2 diabetes mellitus.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 323, doi. 10.1038/15500
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- Publication type:
- Article
The pallid gene encodes a novel, syntaxin 13-interacting protein involved in platelet storage pool deficiency.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 329, doi. 10.1038/15507
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- Publication type:
- Article
Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 333, doi. 10.1038/15513
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- Publication type:
- Article
Chimaeric mice deficient in dystroglycans develop muscular dystrophy and have disrupted myoneural synapses.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 338
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- Publication type:
- Article
A humanized model for multiple sclerosis using HLA-DR2 and a human T-cell receptor.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 343, doi. 10.1038/15525
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- Publication type:
- Article
Leukaemia disease genes: large-scale cloning and pathway predictions.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 348, doi. 10.1038/15531
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- Publication type:
- Article
Perlecan is essential for cartilage and cephalic development.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 354, doi. 10.1038/15537
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- Publication type:
- Article
HNPCC-like cancer predisposition in mice through simultaneous loss of Msh3 and Msh6 mismatch-repair protein functions.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 359, doi. 10.1038/15544
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- Publication type:
- Article
Mammalian (cytosine-5) methyltransferases cause genomic DNA methylation and lethality in Drosophila.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 363, doi. 10.1038/15551
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- Publication type:
- Article
Meiotic instability of human minisatellite CEB1 in yeast requires DNA double-strand breaks.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 367
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- Publication type:
- Article
Characterization of single-nucleotide polymorphisms in coding regions of human genes.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 373, doi. 10.1038/15564
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- Publication type:
- Article
Griscelli disease maps to chromocome 15q and is associated with mutations in the Myosin-Va gene.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 373, doi. 10.1038/15565
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- Publication type:
- Article
Suppression of the novel growth inhibitor p33<sup>ING1</sup> promotes neoplastic transformation.
- Published in:
- 1999
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- Publication type:
- Erratum