Found: 33
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A radiation hybrid map of the rat genome containing 5,255 markers.
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- Nature Genetics, 1999, v. 22, n. 1, p. 27, doi. 10.1038/8737
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- Article
Conditional mutation of Brca1 in mammary epithelial cells results in blunted ductal morphogenesis and tumour formation.
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- Nature Genetics, 1999, v. 22, n. 1, p. 37, doi. 10.1038/8743
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Alymphoplasia is caused by a point mutation in the mouse gene encoding Nf-κb-inducing kinase.
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- Nature Genetics, 1999, v. 22, n. 1, p. 74, doi. 10.1038/8780
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DNA sequence variation in a non-coding region of low recombination on the human X chromosome.
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- Nature Genetics, 1999, v. 22, n. 1, p. 78, doi. 10.1038/8785
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Freely associating.
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- Nature Genetics, 1999, v. 22, n. 1, p. 1, doi. 10.1038/8702
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- Article
Branching out with BRCA1.
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- Nature Genetics, 1999, v. 22, n. 1, p. 10, doi. 10.1038/8714
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c-MYC interacts with INI1/hSNF5 and requires the SWI/SNF complex for transactivation function.
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- Nature Genetics, 1999, v. 22, n. 1, p. 102, doi. 10.1038/8811
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Evolution of neoplastic cell lineages in Barrett oesophagus.
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- Nature Genetics, 1999, v. 22, n. 1, p. 106, doi. 10.1038/8816
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TOUCHINGbase.
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- Nature Genetics, 1999, v. 22, n. 1, p. 11
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- Article
Synphilin-1 associates with α-synuclein and promotes the formation of cytosolic inclusions.
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- Nature Genetics, 1999, v. 22, n. 1, p. 110, doi. 10.1038/8820
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PML induces a novel caspase-independent cell death process.
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- Nature Genetics, 1999, v. 22, n. 1, p. 115, doi. 10.1038/8706
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A missense mutation in RPS6KA3 (RSK2) responsible for non-specific mental retardation.
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- Nature Genetics, 1999, v. 22, n. 1, p. 13, doi. 10.1038/8719
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Necdin-deficient mice do not show lethality or the obesity and infertility of Prader-Willi syndrome.
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- Nature Genetics, 1999, v. 22, n. 1, p. 15, doi. 10.1038/8722
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α-2 macroglobulin polymorphism and Alzheimer disease risk in the UK.
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- Nature Genetics, 1999, v. 22, n. 1, p. 16, doi. 10.1038/8724
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α-2 macroglobulin gene and Alzheimer disease.
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- Nature Genetics, 1999, v. 22, n. 1, p. 17, doi. 10.1038/8726
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- Article
An α-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease.
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- Nature Genetics, 1999, v. 22, n. 1, p. 19, doi. 10.1038/8729
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In reply.
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- Nature Genetics, 1999, v. 22, n. 1, p. 21, doi. 10.1038/8732
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Distribution and early development of microarray technology in Europe.
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- Nature Genetics, 1999, v. 22, n. 1, p. 22, doi. 10.1038/8734
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Status, sale and patenting of human genetic material: an international survey.
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- Nature Genetics, 1999, v. 22, n. 1, p. 23, doi. 10.1038/8735
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Rattus norvegicus and the Industrial Revolution.
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- Nature Genetics, 1999, v. 22, n. 1, p. 3, doi. 10.1038/8703
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Loss of Cdk4 expression causes insulin-deficient diabetes and Cdk4 activation results in β-islet cell hyperplasia.
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- Nature Genetics, 1999, v. 22, n. 1, p. 44, doi. 10.1038/8751
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The shuffling of a mortal coil.
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- Nature Genetics, 1999, v. 22, n. 1, p. 4, doi. 10.1038/8705
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Action of BTN1, the yeast orthologue of the gene mutated in Batten disease.
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- Nature Genetics, 1999, v. 22, n. 1, p. 55, doi. 10.1038/8861
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Sequence variation in the human angiotensin converting enzyme.
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- Nature Genetics, 1999, v. 22, n. 1, p. 59, doi. 10.1038/8760
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The House & Garden guide to chromatin remodelling.
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- Nature Genetics, 1999, v. 22, n. 1, p. 6, doi. 10.1038/8708
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Epidermal growth factor receptor function is necessary for normal craniofacial development and palate closure.
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- Nature Genetics, 1999, v. 22, n. 1, p. 69, doi. 10.1038/8773
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Inactivating mutations and overexpression of BCL10, a caspase recruitment domain-containing gene, in MALT lymphoma with t(1;14)(p22;q32).
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- Nature Genetics, 1999, v. 22, n. 1, p. 63, doi. 10.1038/8767
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Position of a 'green-red' hybrid gene in the visual pigment array determines colour-vision phenotype.
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- Nature Genetics, 1999, v. 22, n. 1, p. 90, doi. 10.1038/8798
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Transmutation of tRNA over time.
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- Nature Genetics, 1999, v. 22, n. 1, p. 8, doi. 10.1038/8711
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Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells.
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- Nature Genetics, 1999, v. 22, n. 1, p. 98, doi. 10.1038/8807
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Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome.
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- Nature Genetics, 1999, v. 22, n. 1, p. 82, doi. 10.1038/8788
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Sox9 is required for cartilage formation.
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- Nature Genetics, 1999, v. 22, n. 1, p. 85, doi. 10.1038/8792
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Maintenance of genomic methylation requires a SWI2/SNF2-like protein.
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- Nature Genetics, 1999, v. 22, n. 1, p. 94, doi. 10.1038/8803
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