Detalhe da pesquisa
1.
Overexpression of the Cytokine BAFF and Autoimmunity Risk.
N Engl J Med
; 376(17): 1615-1626, 2017 04 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-28445677
2.
Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa.
Am J Hum Genet
; 99(1): 236-45, 2016 Jul 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27392078
3.
Novel action of FOXL2 as mediator of Col1a2 gene autoregulation.
Dev Biol
; 416(1): 200-211, 2016 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27212026
4.
Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa.
Am J Hum Genet
; 102(4): 713, 2018 04 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29625027
5.
FOXL2 modulates cartilage, skeletal development and IGF1-dependent growth in mice.
BMC Dev Biol
; 15: 27, 2015 Jul 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-26134413
6.
Transcriptome organization of white blood cells through gene co-expression network analysis in a large RNA-seq dataset.
Front Immunol
; 15: 1350111, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38629067
7.
Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia.
Hum Mol Genet
; 18(14): 2711-8, 2009 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19419973
8.
Author Correction: Complex genetic signatures in immune cells underlie autoimmunity and inform therapy.
Nat Genet
; 52(11): 1266, 2020 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-32948852
9.
Complex genetic signatures in immune cells underlie autoimmunity and inform therapy.
Nat Genet
; 52(10): 1036-1045, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32929287
10.
Editorial: Female Infertility: Genetics of Reproductive Ageing, Menopause and Primary Ovarian Insufficiency.
Front Genet
; 13: 839758, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35368681
11.
Population- and individual-specific regulatory variation in Sardinia.
Nat Genet
; 49(5): 700-707, 2017 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-28394350
12.
SUMOylation of the Forkhead transcription factor FOXL2 promotes its stabilization/activation through transient recruitment to PML bodies.
PLoS One
; 6(10): e25463, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-22022399
13.
Differential secretion of the mutated protein is a major component affecting phenotypic severity in CRLF1-associated disorders.
Eur J Hum Genet
; 19(5): 525-33, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21326283
14.
The forkhead transcription factor Foxl2 is sumoylated in both human and mouse: sumoylation affects its stability, localization, and activity.
PLoS One
; 5(3): e9477, 2010 Mar 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-20209145
15.
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.
Nat Genet
; 42(12): 1077-85, 2010 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-21102462
16.
Withania somnifera prevents morphine withdrawal-induced decrease in spine density in nucleus accumbens shell of rats: a confocal laser scanning microscopy study.
Neurotox Res
; 16(4): 343-55, 2009 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-19551457
17.
Crisponi syndrome is caused by mutations in the CRLF1 gene and is allelic to cold-induced sweating syndrome type 1.
Am J Hum Genet
; 80(5): 971-81, 2007 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-17436252