Detalhe da pesquisa
1.
Distinct physiological states of Plasmodium falciparum in malaria-infected patients.
Nature
; 450(7172): 1091-5, 2007 Dec 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-18046333
2.
Analysing complex genetic traits with chromosome substitution strains.
Nat Genet
; 24(3): 221-5, 2000 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-10700173
3.
Renal disease susceptibility and hypertension are under independent genetic control in the fawn-hooded rat.
Nat Genet
; 12(1): 44-51, 1996 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-8528250
4.
Genetic dissection of autoimmune type I diabetes in the BB rat.
Nat Genet
; 2(1): 56-60, 1992 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-1303251
5.
CLN5, a novel gene encoding a putative transmembrane protein mutated in Finnish variant late infantile neuronal ceroid lipofuscinosis.
Nat Genet
; 19(3): 286-8, 1998 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-9662406
6.
High-resolution haplotype structure in the human genome.
Nat Genet
; 29(2): 229-32, 2001 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-11586305
7.
Genetic analysis of non-insulin dependent diabetes mellitus in the GK rat.
Nat Genet
; 12(1): 31-7, 1996 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-8528247
8.
Quantitative locus analysis of airway hyperresponsiveness in A/J and C57BL/6J mice.
Nat Genet
; 11(2): 150-4, 1995 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-7550342
9.
Secretory phospholipase Pla2g2a confers resistance to intestinal tumorigenesis.
Nat Genet
; 17(1): 88-91, 1997 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-9288104
10.
A novel member of the F-box/WD40 gene family, encoding dactylin, is disrupted in the mouse dactylaplasia mutant.
Nat Genet
; 23(1): 104-7, 1999 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-10471509
11.
Direct isolation of polymorphic markers linked to a trait by genetically directed representational difference analysis.
Nat Genet
; 6(1): 57-63, 1994 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-8136836
12.
ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF.
Nat Genet
; 24(2): 120-5, 2000 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-10655055
13.
Mutations in the human delta homologue, DLL3, cause axial skeletal defects in spondylocostal dysostosis.
Nat Genet
; 24(4): 438-41, 2000 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-10742114
14.
Radiation hybrid map of the mouse genome.
Nat Genet
; 22(4): 384-7, 1999 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-10431245
15.
The mouse pudgy mutation disrupts Delta homologue Dll3 and initiation of early somite boundaries.
Nat Genet
; 19(3): 274-8, 1998 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-9662403
16.
A susceptibility locus for asthma-related traits on chromosome 7 revealed by genome-wide scan in a founder population.
Nat Genet
; 28(1): 87-91, 2001 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-11326283
17.
Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish families.
Nat Genet
; 14(1): 90-4, 1996 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-8782826
18.
Large-scale discovery and genotyping of single-nucleotide polymorphisms in the mouse.
Nat Genet
; 24(4): 381-6, 2000 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-10742102
19.
The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes.
Nat Genet
; 26(1): 76-80, 2000 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-10973253
20.
Determination of ancestral alleles for human single-nucleotide polymorphisms using high-density oligonucleotide arrays.
Nat Genet
; 22(2): 164-7, 1999 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-10369258