Detalhe da pesquisa
1.
Association of genetic variants in CHEK2 with oesophageal squamous cell carcinoma in the South African Black population.
Carcinogenesis;
40(4): 513-520, 2019 06 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30753320
2.
Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes.
PLoS Genet;
11(2): e1004955, 2015 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25671699
3.
Mutation detection in saliva from oral cancer patients.
Oral Oncol;
151: 106717, 2024 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38412584
4.
Conserved γδ T cell selection by BTNL proteins limits progression of human inflammatory bowel disease.
Science;
381(6663): eadh0301, 2023 09 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37708268
5.
Age acquired skewed X chromosome inactivation is associated with adverse health outcomes in humans.
Elife;
112022 11 22.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36412098
6.
Streptococcus Salivarius: A Potential Salivary Biomarker for Orofacial Granulomatosis and Crohn's Disease?
Inflamm Bowel Dis;
25(8): 1367-1374, 2019 07 17.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30796823
7.
Exome Sequencing and Genotyping Identify a Rare Variant in NLRP7 Gene Associated With Ulcerative Colitis.
J Crohns Colitis;
12(3): 321-326, 2018 Feb 28.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29211899
8.
Mutations in DONSON disrupt replication fork stability and cause microcephalic dwarfism.
Nat Genet;
49(4): 537-549, 2017 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28191891