Detalhe da pesquisa
1.
Identification and bioinformatics analysis of a novel variant in the HERC2 gene in a patient with intellectual developmental disorder.
J Neurogenet
; : 1-7, 2024 Jun 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-38884635
2.
A novel loss of function mutation in the PHD domain of the RAG2 gene, affecting zinc-binding affinity.
Mol Biol Rep
; 50(10): 8771-8775, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37573280
3.
Identification of Two Novel Pathogenic Variants of the ATM Gene in the Iranian-Azeri Turkish Ethnic Group by Applying Whole Exome Sequencing.
Curr Genomics
; 24(6): 345-353, 2023 Dec 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-38327652
4.
Role of complement factor B rs4151667 (L9H) polymorphisms and its interactional role with CFH Y402H and C3 rs2230199 (R102G) risk variants in age-related macular degeneration: a case control study.
BMC Ophthalmol
; 20(1): 323, 2020 Aug 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32762675
5.
Thromboxane A synthase 1 gene expression and promotor haplotypes are associated with risk of large artery-atherosclerosis stroke in Iranian population.
J Cell Biochem
; 120(9): 15222-15232, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31026093
6.
Comparison of ARMS2/LOC387715 A69S and CFH Y402H risk effect in wet-type age-related macular degeneration: a meta-analysis.
Int Ophthalmol
; 39(4): 949-956, 2019 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-29423786
7.
Association of polymorphisms of complement factor I rs141853578 (G119R) with age-related macular degeneration in Iranian population.
Int Ophthalmol
; 39(3): 551-556, 2019 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-29392637
8.
Polymorphisms of Promoter Region of TNF-α Gene in Iranian Azeri Turkish Patients with Behçet's Disease.
J Korean Med Sci
; 32(1): 33-37, 2017 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-27914129
9.
Association of ARMS2/LOC387715 A69S, CFH Y402H, and CFH I62V polymorphisms with retinal angiomatous proliferation compared with typical age-related macular degeneration: a meta-analysis.
Int Ophthalmol
; 37(6): 1397-1409, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-28005184
10.
Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort.
Genet Med
; 18(4): 364-71, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26226137
11.
Extracellular signal-regulated kinase 1 and 2 in cancer therapy: a focus on hepatocellular carcinoma.
Mol Biol Rep
; 43(2): 107-16, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26767647
12.
Identification of a novel mutation in the HACD1 gene in an Iranian family with autosomal recessive congenital myopathy, with fibre-type disproportion.
J Genet
; 1022023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36823680
13.
Identification of a de novo, Novel Pathogenic Variant in the Splice Region of the SOX10 Gene in an Iranian Azeri Turkish Family with Waardenburg Syndrome.
Mol Syndromol
; 14(6): 516-522, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-38058752
14.
Identification of novel cis-mutations in the GJA8 gene in a 3-generation Iranian family with autosomal dominant congenital nuclear cataract.
Ophthalmic Genet
; 43(5): 609-614, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35726576
15.
Role of CFH Y402H and ARMS2 A69S polymorphisms in susceptibility to post rhegmatogenous retinal detachment macular complications.
Ophthalmic Genet
; 43(4): 446-449, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35236246
16.
Lack of Association between Monocyte Chemoattractant Protein-1 (MCP-1) Gene Promoter Polymorphism and Behcet's Disease with and without Ocular Involvement in Iranian Population: A Case-Control Study.
Curr Eye Res
; 47(2): 312-316, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34459335
17.
Plasma lncRNA profiling identified BC200 and NEAT1 lncRNAs as potential blood-based biomarkers for late-onset Alzheimer's disease.
EXCLI J
; 21: 772-785, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35949493
18.
Genotypes of ANKK1 and DRD2 genes and risk of metabolic syndrome and its components: A cross-sectional study on Iranian women.
Obes Res Clin Pract
; 15(5): 449-454, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34420901
19.
The Contribution of VKORC1 and CYP2C9 Genetic Polymorphisms and Patients' Demographic Characteristics with Warfarin Maintenance Doses: A Suggested Warfarin Dosing Algorithm.
Iran J Pharm Res
; 19(3): 77-85, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33680011
20.
Association of Saitohin gene rs62063857 polymorphism with dry type age-related macular degeneration.
Ophthalmic Genet
; 41(5): 505-506, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32615840