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1.
Novel EXOSC9 variants cause pontocerebellar hypoplasia type 1D with spinal motor neuronopathy and cerebellar atrophy.
J Hum Genet
; 66(4): 401-407, 2021 Apr.
Article
in English
| MEDLINE | ID: mdl-33040083
2.
RPE65 and retinal dystrophy: Report of new and recurrent mutations.
J Gene Med
; 22(3): e3154, 2020 03.
Article
in English
| MEDLINE | ID: mdl-31957135
3.
Investigation of promoter methylation of FSCN1 gene and FSCN1 protein expression in differentiated thyroid carcinomas.
Mol Biol Rep
; 47(3): 2161-2169, 2020 Mar.
Article
in English
| MEDLINE | ID: mdl-32072403
4.
The first cohort of Iranian patients with hyper immunoglobulin E syndrome: A long-term follow-up and genetic analysis.
Pediatr Allergy Immunol
; 30(4): 469-478, 2019 06.
Article
in English
| MEDLINE | ID: mdl-30801830
5.
Clinical, immunologic, and genetic spectrum of 696 patients with combined immunodeficiency.
J Allergy Clin Immunol
; 141(4): 1450-1458, 2018 04.
Article
in English
| MEDLINE | ID: mdl-28916186
6.
Mutations in the histamine N-methyltransferase gene, HNMT, are associated with nonsyndromic autosomal recessive intellectual disability.
Hum Mol Genet
; 24(20): 5697-710, 2015 Oct 15.
Article
in English
| MEDLINE | ID: mdl-26206890
7.
Demethylation and alterations in the expression level of the cell cycle-related genes as possible mechanisms in arsenic trioxide-induced cell cycle arrest in human breast cancer cells.
Tumour Biol
; 39(2): 1010428317692255, 2017 Feb.
Article
in English
| MEDLINE | ID: mdl-28218039
8.
A SNP in the ABCC11 gene is the determinant of human earwax type.
Nat Genet
; 38(3): 324-30, 2006 Mar.
Article
in English
| MEDLINE | ID: mdl-16444273
9.
MicroRNA biosensors for detection of glioblastoma.
Clin Chim Acta
; 556: 117829, 2024 Mar 15.
Article
in English
| MEDLINE | ID: mdl-38355000
10.
Comparison of Plasma Levels of MicroRNA-155-5p, MicroRNA-210-3p, and MicroRNA-16-5p in Rheumatoid Arthritis Patients with Healthy Controls in a Case-control Study.
Iran J Allergy Asthma Immunol
; 22(4): 354-365, 2023 Sep 03.
Article
in English
| MEDLINE | ID: mdl-37767678
11.
The Clinical and Molecular Assessment of Iranian Families with Severe Congenital Neutropenia, Identification of HYOU1 and SHOC2 as Potential Novel Gene Defects.
Iran J Allergy Asthma Immunol
; 21(3): 344-354, 2022 Jun 18.
Article
in English
| MEDLINE | ID: mdl-35822684
12.
Plasma Levels of MicroRNA-146a-5p, MicroRNA-24-3p, and MicroRNA-125a-5p as Potential Diagnostic Biomarkers for Rheumatoid Arthris.
Iran J Allergy Asthma Immunol
; 20(3): 326-337, 2021 Jun 06.
Article
in English
| MEDLINE | ID: mdl-34134454
13.
RET Proto-Oncogene Mutational Analysis in 45 Iranian Patients Affected with Medullary Thyroid Carcinoma: Report of a New Variant.
J Thyroid Res
; 2021: 7250870, 2021.
Article
in English
| MEDLINE | ID: mdl-34777782
14.
Familial ankyloglossia (tongue-tie): a case report.
Acta Med Iran
; 48(2): 123-4, 2010.
Article
in English
| MEDLINE | ID: mdl-21133006
15.
Variable Clinical Manifestations of COVID-19: Viral and Human Genomes Talk.
Iran J Allergy Asthma Immunol
; 19(5): 456-470, 2020 Oct 18.
Article
in English
| MEDLINE | ID: mdl-33463113
16.
Cell Free Tumoral DNA Versus Paraffin Block Epidermal Growth Factor Receptor Mutation Detection in Patients with Non-Small Cell Lung Cancer.
Asian Pac J Cancer Prev
; 20(12): 3591-3596, 2019 Dec 01.
Article
in English
| MEDLINE | ID: mdl-31870098
17.
Evaluation of the Prevalence of Exons 1 And 10 Polymorphisms of LHCGR Gene and Its Relationship with IVF Success.
J Reprod Infertil
; 20(4): 218-224, 2019.
Article
in English
| MEDLINE | ID: mdl-31897388
18.
Circulating free DNA concentration as a marker of disease recurrence and metastatic potential in lung cancer.
Clin Transl Med
; 8(1): 14, 2019 Apr 18.
Article
in English
| MEDLINE | ID: mdl-31001798
19.
Association of SP-B gene 9306 A/G polymorphism (rs7316) and risk of RDS.
J Matern Fetal Neonatal Med
; 31(22): 2965-2970, 2018 Nov.
Article
in English
| MEDLINE | ID: mdl-28738720
20.
Association of SP-C gene codon 186 polymorphism (rs1124) and risk of RDS.
J Matern Fetal Neonatal Med
; 30(21): 2585-2589, 2017 Nov.
Article
in English
| MEDLINE | ID: mdl-27884070