Works matching IS 10614036 AND DT 2000 AND VI 24 AND IP 4
Results: 31
Repair affairs.
- Published in:
- Nature Genetics, 2000, v. 24, n. 4, p. 325, doi. 10.1038/74122
- Publication type:
- Article
Fly meets shotgun: shotgun wins.
- Published in:
- Nature Genetics, 2000, v. 24, n. 4, p. 327, doi. 10.1038/74125
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- Article
Oct-4, Scene 1: the drama of mouse development.
- Published in:
- Nature Genetics, 2000, v. 24, n. 4, p. 328, doi. 10.1038/74129
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- Publication type:
- Article
ISIS, the intron information system, reveals the high frequency of alternative splicing in the human genome.
- Published in:
- Nature Genetics, 2000, v. 24, n. 4, p. 340, doi. 10.1038/74153
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- Article
Do all SINEs lead to LINEs?
- Published in:
- Nature Genetics, 2000, v. 24, n. 4, p. 332, doi. 10.1038/74135
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- Article
Getting a foothold in nephrotic syndrome.
- Published in:
- Nature Genetics, 2000, v. 24, n. 4, p. 333, doi. 10.1038/74139
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- Article
Touchingbase.
- Published in:
- Nature Genetics, 2000, v. 24, n. 4, p. 337
- Publication type:
- Article
A systematic, high-resolution linkage of the cytogenetic and physical maps of the human genome.
- Published in:
- Nature Genetics, 2000, v. 24, n. 4, p. 339, doi. 10.1038/74149
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- Publication type:
- Article
A hole in the head.
- Published in:
- Nature Genetics, 2000, v. 24, n. 4, p. 330, doi. 10.1038/74132
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- Article
MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans.
- Published in:
- Nature Genetics, 2000, v. 24, n. 4, p. 342, doi. 10.1038/74155
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- Publication type:
- Article
Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2.
- Published in:
- Nature Genetics, 2000, v. 24, n. 4, p. 343, doi. 10.1038/74159
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- Publication type:
- Article
Dolly part one: the end of the beginning in mammalian cloning?
- Published in:
- 2000
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- Publication type:
- Book Review
NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome.
- Published in:
- Nature Genetics, 2000, v. 24, n. 4, p. 349, doi. 10.1038/74166
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- Publication type:
- Article
Robustness against mutations in genetic networks of yeast.
- Published in:
- Nature Genetics, 2000, v. 24, n. 4, p. 355, doi. 10.1038/74174
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- Publication type:
- Article
Human LINE retrotransposons generate processed pseudogenes.
- Published in:
- Nature Genetics, 2000, v. 24, n. 4, p. 363, doi. 10.1038/74184
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- Publication type:
- Article
Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation.
- Published in:
- Nature Genetics, 2000, v. 24, n. 4, p. 368, doi. 10.1038/74191
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- Publication type:
- Article
Quantitative expression of Oct-3/4 defines differentiation, dedifferentiation or self-renewal of ES cells.
- Published in:
- Nature Genetics, 2000, v. 24, n. 4, p. 372, doi. 10.1038/74199
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- Publication type:
- Article
In vivo modulation of Hmgic reduces obesity.
- Published in:
- Nature Genetics, 2000, v. 24, n. 4, p. 377, doi. 10.1038/74207
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- Publication type:
- Article
Large-scale discovery and genotyping of single-nucleotide polymorphisms in the mouse.
- Published in:
- Nature Genetics, 2000, v. 24, n. 4, p. 381, doi. 10.1038/74215
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- Publication type:
- Article
Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification.
- Published in:
- Nature Genetics, 2000, v. 24, n. 4, p. 387, doi. 10.1038/74224
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- Publication type:
- Article
Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation.
- Published in:
- Nature Genetics, 2000, v. 24, n. 4, p. 391, doi. 10.1038/74231
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- Publication type:
- Article
The direction of microsatellite mutations is dependent upon allele length.
- Published in:
- Nature Genetics, 2000, v. 24, n. 4, p. 396, doi. 10.1038/74238
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- Publication type:
- Article
Heterogeneous mutation processes in human microsatellite DNA sequences.
- Published in:
- Nature Genetics, 2000, v. 24, n. 4, p. 400, doi. 10.1038/74249
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- Publication type:
- Article
Abnormal adaptations to stress and impaired cardiovascular function in mice lacking corticotropin-releasing hormone receptor-2.
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- Nature Genetics, 2000, v. 24, n. 4, p. 403, doi. 10.1038/74255
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- Publication type:
- Article
Mice deficient for corticotropin-releasing hormone receptor-2 display anxiety-like behaviour and are hypersensitive to stress.
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- Nature Genetics, 2000, v. 24, n. 4, p. 410, doi. 10.1038/74263
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- Publication type:
- Article
Deletion of Crhr2 reveals an anxiolytic role for corticotropin-releasing hormone receptor-2.
- Published in:
- Nature Genetics, 2000, v. 24, n. 4, p. 415, doi. 10.1038/74271
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- Publication type:
- Article
The SH2 tyrosine phosphatase Shp2 is required for mammalian limb development.
- Published in:
- Nature Genetics, 2000, v. 24, n. 4, p. 420, doi. 10.1038/74279
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- Publication type:
- Article
The homeobox gene mirror links EGF signalling to embryonic dorso-ventral axis formation through Notch activation.
- Published in:
- Nature Genetics, 2000, v. 24, n. 4, p. 429, doi. 10.1038/74294
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- Publication type:
- Article
Mutations in Sox18 underlie cardiovascular and hair follicle defects in ragged mice.
- Published in:
- Nature Genetics, 2000, v. 24, n. 4, p. 434, doi. 10.1038/74301
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- Publication type:
- Article
Mutations in the human Delta homologue, DLL3, cause axial skeletal defects in spondylocostal dysostosis.
- Published in:
- Nature Genetics, 2000, v. 24, n. 4, p. 438, doi. 10.1038/74307
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- Publication type:
- Article
Stereocilia defects in the sensory hair cells of the inner ear in mice deficient in integrin α8β1.
- Published in:
- Nature Genetics, 2000, v. 24, n. 4, p. 424, doi. 10.1038/74286
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- Publication type:
- Article