Detalhe da pesquisa
1.
Association of variants in HTRA1 and NOTCH3 with MRI-defined extremes of cerebral small vessel disease in older subjects.
Brain
; 142(4): 1009-1023, 2019 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30859180
2.
Genomic binding of Pol III transcription machinery and relationship with TFIIS transcription factor distribution in mouse embryonic stem cells.
Nucleic Acids Res
; 40(1): 270-83, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21911356
3.
Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4.
PLoS Genet
; 3(4): e58, 2007 Apr 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-17447842
4.
Genetic analysis of an F(2) intercross between two chicken lines divergently selected for body-weight.
BMC Genomics
; 10: 248, 2009 May 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-19473501
5.
Genetic and haplotypic structure in 14 European and African cattle breeds.
Genetics
; 177(2): 1059-70, 2007 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-17720924
6.
Exploration of associations between phospholipase A2 gene family polymorphisms and AIDS progression using the SNPlex method.
Biomed Pharmacother
; 62(1): 31-40, 2008 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-18096355
7.
Targeted disruption of Aldh1a1 (Raldh1) provides evidence for a complex mechanism of retinoic acid synthesis in the developing retina.
Mol Cell Biol
; 23(13): 4637-48, 2003 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-12808103
8.
Variation in genomic landscape of clear cell renal cell carcinoma across Europe.
Nat Commun
; 5: 5135, 2014 Oct 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-25351205
9.
Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma.
Nat Genet
; 46(5): 482-6, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24686846
10.
A role for non-coding Tsix transcription in partitioning chromatin domains within the mouse X-inactivation centre.
Epigenetics Chromatin
; 2(1): 8, 2009 Jul 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-19615107
11.
An autosomal-recessive form of cutis laxa is due to homozygous elastin mutations, and the phenotype may be modified by a heterozygous fibulin 5 polymorphism.
J Invest Dermatol
; 129(7): 1650-5, 2009 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-19194475
12.
An association study of 22 candidate genes in psoriasis families reveals shared genetic factors with other autoimmune and skin disorders.
J Invest Dermatol
; 129(11): 2637-45, 2009 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-19554025
13.
A high-density SNP-based linkage map of the chicken genome reveals sequence features correlated with recombination rate.
Genome Res
; 19(3): 510-9, 2009 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19088305
14.
SNP and haplotype mapping for genetic analysis in the rat.
Nat Genet
; 40(5): 560-6, 2008 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-18443594
15.
ADAM33, a new candidate for psoriasis susceptibility.
PLoS One
; 2(9): e906, 2007 Sep 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-17878941
16.
A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15.
Nat Genet
; 39(10): 1197-9, 2007 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-17767159
17.
Distinct retinoid metabolic functions for alcohol dehydrogenase genes Adh1 and Adh4 in protection against vitamin A toxicity or deficiency revealed in double null mutant mice.
J Biol Chem
; 277(16): 13804-11, 2002 Apr 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-11836246
18.
Stimulation of retinoic acid production and growth by ubiquitously expressed alcohol dehydrogenase Adh3.
Proc Natl Acad Sci U S A
; 99(8): 5337-42, 2002 Apr 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-11959987
19.
Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2.
Hum Mol Genet
; 12(18): 2369-78, 2003 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-12915478