Detalhe da pesquisa
1.
Contribution of ADD3 and the HLA Genes to Biliary Atresia Risk in Chinese.
Int J Mol Sci
; 24(19)2023 Sep 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-37834180
2.
Common variation of the NSD1 gene is associated with susceptibility to Hirschsprung's disease in Chinese Han population.
Pediatr Res
; 89(3): 694-700, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32380506
3.
Fine mapping MHC associations in Graves' disease and its clinical subtypes in Han Chinese.
J Med Genet
; 55(10): 685-692, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-29987165
4.
Clinical characteristics and prognosis of serous body cavity effusions in patients with sepsis: a retrospective observational study.
BMC Anesthesiol
; 18(1): 169, 2018 11 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-30428838
5.
Association of 4p14 and 6q27 variation with Graves disease: a case-control study and a meta-analysis of available evidence.
BMC Med Genet
; 18(1): 56, 2017 05 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-28521825
6.
Diagnostic and prognostic utility of tissue factor for severe sepsis and sepsis-induced acute lung injury.
J Transl Med
; 13: 172, 2015 May 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-26025445
7.
An X chromosome-wide association analysis identifies variants in GPR174 as a risk factor for Graves' disease.
J Med Genet
; 50(7): 479-85, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23667180
8.
An SNP of the ZBTB38 gene is associated with idiopathic short stature in the Chinese Han population.
Clin Endocrinol (Oxf)
; 79(3): 402-8, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23302005
9.
Association analysis and functional follow-up identified common variants of JAG1 accounting for risk to biliary atresia.
Front Genet
; 14: 1186882, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37255715
10.
Functional SNPs in the SCGB3A2 promoter are associated with susceptibility to Graves' disease.
Hum Mol Genet
; 18(6): 1156-70, 2009 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19126779
11.
A novel locus for disseminated superficial actinic porokeratosis maps to chromosome 16q24.1-24.3.
Hum Genet
; 129(3): 329-34, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21161278
12.
Saltmarsh resilience controlled by patch size and plant density of habitat-forming species that trap shells.
Sci Total Environ
; 778: 146119, 2021 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-33725609
13.
Association Analysis of Variants of DSCAM and BACE2 With Hirschsprung Disease Susceptibility in Han Chinese and Functional Evaluation in Zebrafish.
Front Cell Dev Biol
; 9: 641152, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34136475
14.
Common polymorphisms in ITGA2, PON1 and THBS2 are associated with coronary atherosclerosis in a candidate gene association study of the Chinese Han population.
J Hum Genet
; 55(8): 490-4, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20485444
15.
Common variants of NRG1 and ITGB4 confer risk of Hirschsprung disease in Han Chinese population.
J Pediatr Surg
; 55(12): 2758-2765, 2020 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-32418639
16.
The increased marginal zone B cells attenuates early inflammatory responses during sepsis in Gpr174 deficient mice.
Int Immunopharmacol
; 81: 106034, 2020 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-31786099
17.
Association of common variation in ADD3 and GPC1 with biliary atresia susceptibility.
Aging (Albany NY)
; 12(8): 7163-7182, 2020 04 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-32315284
18.
Association of Variants in PLD1, 3p24.1, and 10q11.21 Regions With Hirschsprung's Disease in Han Chinese Population.
Front Genet
; 11: 738, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32765588
19.
Polymorphisms in the ADRB2 gene and Graves disease: a case-control study and a meta-analysis of available evidence.
BMC Med Genet
; 10: 26, 2009 Mar 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-19284637
20.
Gpr174-deficient regulatory T cells decrease cytokine storm in septic mice.
Cell Death Dis
; 10(3): 233, 2019 03 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30850582