Found: 34
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Chopping and changing.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 1, doi. 10.1038/83655
- Publication type:
- Article
Corrections.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 125, doi. 10.1038/83691
- Publication type:
- Article
Methylation meets genomics.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 9, doi. 10.1038/83825
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- Article
Cytoskeletal catastrophe causes brain degeneration.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 10, doi. 10.1038/83657
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- Article
SGS1, the Saccharomyces cerevisiae homologue of BLM and WRN, suppresses genome instability and homeologous recombination.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 113, doi. 10.1038/83673
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- Article
Lipodystrophy in the fld mouse results from mutation of a new gene encoding a nuclear protein, lipin.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 121
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- Article
Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 103, doi. 10.1038/83660
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- Article
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 108, doi. 10.1038/83667
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- Article
Erratum.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 125, doi. 10.1038/83693
- Publication type:
- Article
Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 117, doi. 10.1038/83679
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- Article
Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 17, doi. 10.1038/83703
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- Article
X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy.
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- Nature Genetics, 2001, v. 27, n. 1, p. 18, doi. 10.1038/83707
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- Article
TOUCHINGbase.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 13
- Publication type:
- Article
Cloning reality into fiction.
- Published in:
- 2001
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- Publication type:
- Book Review
The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 20, doi. 10.1038/83713
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- Publication type:
- Article
Dominant effector genetics in mammalian cells.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 23, doi. 10.1038/83717
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- Article
You say tomato, I say tomato.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 2, doi. 10.1038/83711
- Publication type:
- Article
Transcriptional regulation and function during the human cell cycle.
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- Nature Genetics, 2001, v. 27, n. 1, p. 48, doi. 10.1038/83751
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- Article
Loss of genomic methylation causes p53-dependent apoptosis and epigenetic deregulation.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 31, doi. 10.1038/83730
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- Publication type:
- Article
Arabidopsis arrives.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 3, doi. 10.1038/83726
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- Article
A biochemical function for attractin in agouti-induced pigmentation and obesity.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 40, doi. 10.1038/83741
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- Article
Insertion of β-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 59, doi. 10.1038/83768
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- Article
A mechanism for exon skipping caused by nonsense or missense mutations in BRCA1 and other genes.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 55, doi. 10.1038/83762
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- Article
The power of point mutations.
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- Nature Genetics, 2001, v. 27, n. 1, p. 5, doi. 10.1038/83759
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- Article
A peptide needle in a signaling haystack.
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- Nature Genetics, 2001, v. 27, n. 1, p. 6, doi. 10.1038/83775
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- Article
Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse.
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- Nature Genetics, 2001, v. 27, n. 1, p. 68, doi. 10.1038/83784
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- Article
The function of a stem-loop in telomerase RNA is linked to the DNA repair protein Ku.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 64, doi. 10.1038/83778
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- Publication type:
- Article
Vitamin A controls epithelial/mesenchymal interactions through Ret expression.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 74, doi. 10.1038/83792
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- Article
Fish × 3.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 8, doi. 10.1038/83807
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- Article
Identification of a gene, ABCG5, important in the regulation of dietary cholesterol absorption.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 79, doi. 10.1038/83799
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- Article
Bone morphogenetic protein-3 is a negative regulator of bone density.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 84, doi. 10.1038/83810
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- Publication type:
- Article
A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 89, doi. 10.1038/83817
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- Article
A thyroid hormone receptor that is required for the development of green cone photoreceptors.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 94, doi. 10.1038/83829
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- Article
The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 99, doi. 10.1038/83837
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- Article