Detalhe da pesquisa
1.
CTNND1 is involved in germline predisposition to early-onset gastric cancer by affecting cell-to-cell interactions.
Gastric Cancer;
2024 May 25.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38796558
2.
Germline mutations in WNK2 could be associated with serrated polyposis syndrome.
J Med Genet;
60(6): 557-567, 2023 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36270769
3.
Germline Mutations in FAF1 Are Associated With Hereditary Colorectal Cancer.
Gastroenterology;
159(1): 227-240.e7, 2020 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32179092
4.
Colorectal cancer genetic variants are also associated with serrated polyposis syndrome susceptibility.
J Med Genet;
57(10): 677-682, 2020 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32170005
5.
Identification of New Genes Involved in Germline Predisposition to Early-Onset Gastric Cancer.
Int J Mol Sci;
22(3)2021 Jan 28.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33525650
6.
Using linkage studies combined with whole-exome sequencing to identify novel candidate genes for familial colorectal cancer.
Int J Cancer;
146(6): 1568-1577, 2020 03 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31525256
7.
The Effects of Paracoccidioides brasiliensis Infection on GM-CSF- and M-CSF-Induced Mouse Bone Marrow-Derived Macrophage from Resistant and Susceptible Mice Strains.
Mediators Inflamm;
2015: 605450, 2015.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26543326
8.
Unraveling the impact of a germline heterozygous POLD1 frameshift variant in serrated polyposis syndrome.
Front Mol Biosci;
10: 1119900, 2023.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36756361
9.
Germline and Somatic Whole-Exome Sequencing Identifies New Candidate Genes Involved in Familial Predisposition to Serrated Polyposis Syndrome.
Cancers (Basel);
13(4)2021 Feb 23.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33672345
10.
Identification of a Novel Candidate Gene for Serrated Polyposis Syndrome Germline Predisposition by Performing Linkage Analysis Combined With Whole-Exome Sequencing.
Clin Transl Gastroenterol;
10(10): e00100, 2019 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31663907
11.
Syndromic hearing loss molecular diagnosis: Application of massive parallel sequencing.
Hear Res;
370: 181-188, 2018 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30390570