Detalhe da pesquisa
1.
Pseudouridylation defect due to DKC1 and NOP10 mutations causes nephrotic syndrome with cataracts, hearing impairment, and enterocolitis.
Proc Natl Acad Sci U S A
; 117(26): 15137-15147, 2020 06 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-32554502
2.
Sequencing of Chromosomal Locus 6q25.1 Revealed Two Significant SNPs rs2046210 and rs2046211 Associated with Breast Cancer: A Case-Control Study in Egyptian Women.
Asian Pac J Cancer Prev
; 23(4): 1359-1364, 2022 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35485697
3.
Mutations in LAMB2 Are Associated With Albuminuria and Optic Nerve Hypoplasia With Hypopituitarism.
J Clin Endocrinol Metab
; 105(3)2020 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31769495
4.
Role of the von Willebrand factor and the VITRO score as predictors for variceal bleeding in patients with hepatitis C-related cirrhosis.
Eur J Gastroenterol Hepatol
; 31(2): 241-247, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30281535
5.
Cardiac matrix remodelling in congestive heart failure: the role of matrix metalloproteinases.
Clin Invest Med
; 27(2): 93-100, 2004 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-15202828