Works matching IS 10614036 AND DT 2000 AND VI 25 AND IP 2
Results: 32
The nature of the number.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 127, doi. 10.1038/75946
- Publication type:
- Article
How to count…human genes.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 129, doi. 10.1038/75949
- By:
- Publication type:
- Article
Better taste through chemistry.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 130, doi. 10.1038/75952
- By:
- Publication type:
- Article
A radical solution to death.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 132, doi. 10.1038/75957
- By:
- Publication type:
- Article
Panning for pancreatic stem cells.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 134, doi. 10.1038/75960
- By:
- Publication type:
- Article
Lupus, DNase and defective disposal of cellular debris.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 135, doi. 10.1038/75963
- By:
- Publication type:
- Article
Touching base.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 137, doi. 10.1038/75968
- By:
- Publication type:
- Article
High-efficiency deleter mice show that FLPe is an alternative to Cre-loxP.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 139, doi. 10.1038/75973
- By:
- Publication type:
- Article
Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 141, doi. 10.1038/75977
- By:
- Publication type:
- Article
Mutations of PKD1 in ADPKD2 cysts suggest a pathogenic effect of trans-heterozygous mutations.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 143, doi. 10.1038/75981
- By:
- Publication type:
- Article
Quantitative mapping of amplicon structure by array CGH identifies CYP24 as a candidate oncogene.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 144, doi. 10.1038/75985
- By:
- Publication type:
- Article
Computer-based three-dimensional visualization of developmental gene expression.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 147, doi. 10.1038/75989
- By:
- Publication type:
- Article
Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 153, doi. 10.1038/75997
- By:
- Publication type:
- Article
Identification of the familial cylindromatosis tumour-suppressor gene.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 160, doi. 10.1038/76006
- By:
- Publication type:
- Article
Plzf regulates limb and axial skeletal patterning.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 166, doi. 10.1038/76014
- By:
- Publication type:
- Article
Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 173, doi. 10.1038/76024
- By:
- Publication type:
- Article
Features of systemic lupus erythematosus in Dnase1-deficient mice.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 177, doi. 10.1038/76032
- By:
- Publication type:
- Article
Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 182, doi. 10.1038/76041
- By:
- Publication type:
- Article
TLR4 mutations are associated with endotoxin hyporesponsiveness in humans.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 187, doi. 10.1038/76048
- By:
- Publication type:
- Article
Homologous recombination is responsible for cell death in the absence of the Sgs1 and Srs2 helicases.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 192, doi. 10.1038/76055
- By:
- Publication type:
- Article
Gene transfer by lentiviral vectors is limited by nuclear translocation and rescued by HIV-1 pol sequences.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 217, doi. 10.1038/76095
- By:
- Publication type:
- Article
More than 1,000 putative new human signalling proteins revealed by EST data mining.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 201, doi. 10.1038/76069
- By:
- Publication type:
- Article
Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 205, doi. 10.1038/76074
- By:
- Publication type:
- Article
Gata3 loss leads to embryonic lethality due to noradrenaline deficiency of the sympathetic nervous system.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 209, doi. 10.1038/76080
- By:
- Publication type:
- Article
Mutations in the gene encoding the serine protease inhibitor, Kazal type 1 are associated with chronic pancreatitis.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 213, doi. 10.1038/76088
- By:
- Publication type:
- Article
Mice deficient for δ- and μ-opioid receptors exhibit opposing alterations of emotional responses.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 195, doi. 10.1038/76061
- By:
- Publication type:
- Article
Mutations in a gene encoding an ABC transporter cause pseudoxanthoma elasticum.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 223, doi. 10.1038/76102
- By:
- Publication type:
- Article
Mutations in ABCC6 cause pseudoxanthoma elasticum.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 228, doi. 10.1038/76109
- By:
- Publication type:
- Article
Analysis of expressed sequence tags indicates 35,000 human genes.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 232, doi. 10.1038/76115
- By:
- Publication type:
- Article
Estimate of human gene number provided by genome-wide analysis using Tetraodon nigroviridis DNA sequence.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 235, doi. 10.1038/76118
- By:
- Publication type:
- Article
Gene Index analysis of the human genome estimates approximately 120,000 genes.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 239, doi. 10.1038/76126
- By:
- Publication type:
- Article
De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch.
- Published in:
- Nature Genetics, 2000, v. 25, n. 2, p. 241, doi. 10.1038/76128
- By:
- Publication type:
- Article