Detalhe da pesquisa
1.
A narrow repertoire of transcriptional modules responsive to pyogenic bacteria is impaired in patients carrying loss-of-function mutations in MYD88 or IRAK4.
Nat Immunol
; 15(12): 1134-42, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25344726
2.
Association of DRD2, DRD4 and COMT genes variants and their gene-gene interactions with antipsychotic treatment response in patients with schizophrenia.
BMC Psychiatry
; 23(1): 781, 2023 10 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-37880658
3.
Identification of Cytochrome b-245, beta-chain gene mutations, and clinical presentations in Iranian patients with X-linked chronic granulomatous disease.
J Clin Lab Anal
; 35(2): e23637, 2021 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-33098164
4.
The first report of two homozygous sequence variants in FKRP and SELENON genes associated with syndromic congenital muscular dystrophy in Iran: Further expansion of the clinical phenotypes.
J Gene Med
; 22(12): e3265, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32864802
5.
A novel homozygous variant in an Iranian pedigree with cerebellar ataxia, mental retardation, and dysequilibrium syndrome type 4.
J Clin Lab Anal
; 34(11): e23484, 2020 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-33079427
6.
Association of vascular endothelial growth factor A polymorphisms and aberrant expression of connexin 43 and VEGFA with idiopathic recurrent spontaneous miscarriage.
J Obstet Gynaecol Res
; 46(3): 369-375, 2020 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-32003128
7.
Identification of the PRM1 gene mutations in oligoasthenoteratozoospermic men.
Andrologia
; 52(11): e13872, 2020 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-33118225
8.
Mechanism of dysfunction of human variants of the IRAK4 kinase and a role for its kinase activity in interleukin-1 receptor signaling.
J Biol Chem
; 293(39): 15208-15220, 2018 09 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-30115681
9.
Association study between two polymorphisms of tumor necrosis factor ligand superfamily member 15 (TNFSF15) gene and ulcerative colitis in south-west of Iran.
J Cell Biochem
; 120(5): 8784-8791, 2019 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-30556168
10.
Effect of herbal antioxidant-rich formula on improvement of antioxidant defense system and heat shock protein-70 expression in recreational female athletes: A randomized controlled trial.
J Res Med Sci
; 24: 37, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31143238
11.
Association between HLA-G 14bp Gene Polymorphism and Serum sHLA-G Protein Concentrations in Preeclamptic Patients and Normal Pregnant Women.
Immunol Invest
; 47(6): 558-568, 2018 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-29952661
12.
Folate gene polymorphisms CBS 844ins68 and RFC1 A80G and risk of Down syndrome offspring in young Iranian women: A cross-sectional study.
Int J Reprod Biomed
; 22(2): 127-138, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38628775
13.
Genetic features of patients with MPS type IIIB: Description of five pathogenic gene variations.
Gene
; 913: 148354, 2024 Jun 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38492611
14.
Association of rs1570360 and rs2010963 in VEGF and rs2279744 in the MDM2 gene with Recurrent Implantation Failure in Iranian Women.
JBRA Assist Reprod
; 27(3): 342-347, 2023 09 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37257061
15.
Clinical and Molecular Spectrum of Muscular Dystrophies (MDs) with Intellectual Disability (ID): a Comprehensive Overview.
J Mol Neurosci
; 72(1): 9-23, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34727324
16.
Effects of epigallocatechin gallate on total antioxidant capacity, biomarkers of systemic low-grade inflammation and metabolic risk factors in patients with type 2 diabetes mellitus: the role of FTO-rs9939609 polymorphism.
Arch Med Sci
; 17(6): 1722-1729, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34900054
17.
Utilization of Whole Exome Sequencing in Non-Syndromic Premature Ovarian Failure: Ficolin-3 Gene Mutation in an Iranian Family
Iran Biomed J
; 25(6): 441-6, 2021 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34641644
18.
Molecular diagnosis of maturity onset diabetes of the young in Iranian patients: improving management.
J Diabetes Metab Disord
; 20(2): 1369-1374, 2021 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-34900788
19.
Genetic association study of CTLA4 and FCεRIα polymorphisms in asthmatic patients in the southwestern region of Iran.
Nucleosides Nucleotides Nucleic Acids
; 40(9): 914-925, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34420484
20.
Clinical features and tubulin folding cofactor E gene analysis in Iranian patients with Sanjad-Sakati syndrome.
J Pediatr (Rio J)
; 96(1): 60-65, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-30080992