Works matching IS 10614036 AND DT 2001 AND VI 27 AND IP 3
Results: 32
Harvesting the fruits of the human genome.
- Published in:
- 2001
- Publication type:
- Editorial
The end of all human DNA maps?
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 229, doi. 10.1038/85766
- By:
- Publication type:
- Article
BACking up the promises.
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 230, doi. 10.1038/85769
- By:
- Publication type:
- Article
Chipping away at the transcriptome.
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 232, doi. 10.1038/85772
- By:
- Publication type:
- Article
Variation is the spice of life.
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 234, doi. 10.1038/85776
- By:
- Publication type:
- Article
γ-H2AX illuminates meiosis.
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 236, doi. 10.1038/85781
- By:
- Publication type:
- Article
Deconstructing DiGeorge syndrome.
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 238, doi. 10.1038/85784
- By:
- Publication type:
- Article
Chipping away at chromatin.
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 240, doi. 10.1038/85787
- By:
- Publication type:
- Article
TOUCHINGbase.
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 243
- Publication type:
- Article
Alzheimer genetics, part I.
- Published in:
- 2001
- By:
- Publication type:
- Book Review
DNA double-strand breaks: signaling, repair and the cancer connection.
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 247, doi. 10.1038/85798
- By:
- Publication type:
- Article
Evolution of imprinting mechanisms: the battle of the sexes begins in the zygote.
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 255, doi. 10.1038/85804
- By:
- Publication type:
- Article
Selection for transgene homozygosity in embryonic stem cells results in extensive loss of heterozygosity.
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 257, doi. 10.1038/85808
- By:
- Publication type:
- Article
Multigenic control of Listeria monocytogenes susceptibility in mice.
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 259, doi. 10.1038/85812
- By:
- Publication type:
- Article
SPTLC1 is mutated in hereditary sensory neuropathy, type 1.
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 261, doi. 10.1038/85817
- By:
- Publication type:
- Article
A temperature-sensitive disorder in basal transcription and DNA repair in humans.
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 299, doi. 10.1038/85864
- By:
- Publication type:
- Article
Recombinational DNA double-strand breaks in mice precede synapsis.
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 271, doi. 10.1038/85830
- By:
- Publication type:
- Article
X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-κB signaling.
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 277
- By:
- Publication type:
- Article
DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1.
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 286, doi. 10.1038/85845
- By:
- Publication type:
- Article
Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome.
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 293, doi. 10.1038/85855
- By:
- Publication type:
- Article
Dominant-negative mutations of CEBPA, encoding CCAAT/enhancer binding protein-α (C/EBPα), in acute myeloid leukemia.
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 263, doi. 10.1038/85820
- By:
- Publication type:
- Article
Chromatin profiling using targeted DNA adenine methyltransferase.
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 304, doi. 10.1038/85871
- By:
- Publication type:
- Article
Mutations in SPTLC1, encoding serine palmitoyltransferase, long chain base subunit-1, cause hereditary sensory neuropathy type I.
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 309, doi. 10.1038/85879
- By:
- Publication type:
- Article
Maternal methylation imprints on human chromosome 15 are established during or after fertilization.
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 341, doi. 10.1038/85927
- By:
- Publication type:
- Article
Constitutively activating mutation in WASP causes X-linked severe congenital neutropenia.
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 313, doi. 10.1038/85886
- By:
- Publication type:
- Article
A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome.
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 322, doi. 10.1038/85899
- By:
- Publication type:
- Article
Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice.
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 327, doi. 10.1038/85906
- By:
- Publication type:
- Article
Homology-based annotation yields 1,042 new candidate genes in the Drosophila melanogaster genome.
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 337, doi. 10.1038/85922
- By:
- Publication type:
- Article
Episodic evolution of pyrin in primates: human mutations recapitulate ancestral amino acid states.
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 318, doi. 10.1038/85893
- By:
- Publication type:
- Article
Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP.
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 345
- Publication type:
- Article
Linkage disequilibrium of a type 1 diabetes susceptibility gene with regulatory IL12B alleles.
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 346
- Publication type:
- Article
Open-reading-frame sequence tags (OSTs) support the existence of at least 17,300 genes in C. elegans.
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 332, doi. 10.1038/85913
- By:
- Publication type:
- Article