Detalhe da pesquisa
1.
Heterozygous mutations in the C-terminal domain of COPA underlie a complex autoinï¬ammatory syndrome.
J Clin Invest;
134(4)2024 Jan 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38175705
2.
Clinical application of multigene panel testing for bleeding, thrombotic, and platelet disorders: a 3-year Belgian experience.
J Thromb Haemost;
21(4): 887-895, 2023 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36696193
3.
Common variable immunodeficiency in two kindreds with heterogeneous phenotypes caused by novel heterozygous NFKB1 mutations.
Front Immunol;
13: 973543, 2022.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36203612
4.
Respiratory viral infections in otherwise healthy humans with inherited IRF7 deficiency.
J Exp Med;
219(7)2022 07 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35670811
5.
Combined inhibition of CDK and HDAC as a promising therapeutic strategy for both cutaneous and uveal metastatic melanoma.
Oncotarget;
9(5): 6174-6187, 2018 Jan 19.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29464063
6.
Amplification of 1q32.1 Refines the Molecular Classification of Endometrial Carcinoma.
Clin Cancer Res;
23(23): 7232-7241, 2017 Dec 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28939739
7.
Correction: Respiratory viral infections in otherwise healthy humans with inherited IRF7 deficiency.
J Exp Med;
219(12)2022 Dec 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36342405
8.
Antisense oligonucleotide-mediated MDM4 exon 6 skipping impairs tumor growth.
J Clin Invest;
126(1): 68-84, 2016 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26595814
9.
Different levels of Twist1 regulate skin tumor initiation, stemness, and progression.
Cell Stem Cell;
16(1): 67-79, 2015 Jan 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25575080