Detalhe da pesquisa
1.
A Comprehensive Study of Disease-Causing Variants in PAH, QDPR, PTS, and PCD Genes in Iranian Patients with Hyperphenylalaninemia: A Systematic Review.
Hum Hered
; 88(1): 8-17, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36646061
2.
Association of Genotypes of ANGPTL3 with Vitamin D and Calcium Concentration in Cardiovascular Disease.
Biochem Genet
; 2023 Nov 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-37955843
3.
MicroRNAs as the critical regulators of epithelial mesenchymal transition in pancreatic tumor cells.
Heliyon
; 10(9): e30599, 2024 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38726188
4.
An Update on the Application of CRISPR Technology in Clinical Practice.
Mol Biotechnol
; 66(2): 179-197, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37269466
5.
Inconsistency in the expression pattern of a five-lncRNA signature as a potential diagnostic biomarker for gastric cancer patients in bioinformatics and in vitro.
Iran J Basic Med Sci
; 25(6): 704-714, 2022 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-35949302
6.
Genetic evaluation of hyperphenylalaninemia patients with tetrahydrobiopterin deficiency in Iranian population: Identification of four novel disease-causing variants.
Mol Genet Genomic Med
; 10(12): e2081, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36382472
7.
A novel mutation in the cathepsin C (CTSC) gene in Iranian family with Papillon-Lefevre syndrome.
Clin Exp Dent Res
; 7(4): 568-573, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33586345
8.
Current insights into the metastasis of epithelial ovarian cancer - hopes and hurdles.
Cell Oncol (Dordr)
; 43(4): 515-538, 2020 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-32418122