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Mutation Research|October 18, 2012
Cytogenetic analysis in lymphocytes from radiation workers exposed to low level of ionizing radiation in radiotherapy, CT-scan and angiocardiography unitsAlihossein Saberi, Elahe Salari, Sayyed Mahmood Latifi
Molecular Genetics & Genomic Medicine|May 21, 2024
Identification of a new mutation in the ACTL9 gene in men with unexplained infertilityRoya Sinaei, Maryam Eslami, Mohammadreza Dadfar, et al.
Vascular Health and Risk Management|July 2, 2020
The Effect of CYP2C9 Genotype Variants in Type 2 Diabetes on the Pharmacological Effectiveness of Sulfonylureas, Diabetic Retinopathy, and NephropathyMeisam Saberi, Zahra Ramazani, Homeira Rashidi, et al.
Indian Journal of Clinical Biochemistry : IJCB|September 12, 2025
Upregulation of SLC25A32 in Tumorous Tissues of Patients with Non-Metastatic Colorectal Cancer: A Pilot StudyMehdi Hashemi, Maryam Tahmasebi-Birgani, Abdolhassan Talaiezadeh, et al.
Journal of Diabetes and Metabolic Disorders|June 8, 2022
KCNQ1 rs2237895 polymorphism is associated with the therapeutic response to sulfonylureas in Iranian type 2 diabetes mellitus patientsSiavash Shakerian, Homeira Rashidi, Maryam Tahmasebi Birgani, et al.
Annals of Human Genetics|August 30, 2018
Genotype-phenotype correlation and the size of microdeletion or microduplication of 7q11.23 region in patients with Williams-Beuren syndromeMahsa Ghaffari, Maryam Tahmasebi Birgani, Roxana Kariminejad, et al.
Advances in Clinical and Experimental Medicine : Official Organ Wroclaw Medical University|November 10, 2018
Adipose tissue miRNA level variation through conjugated linoleic acid supplementation in diet-induced obese ratsMaryam Nazari, Alihossein Saberi, Majid Karandish, et al.
Clinical Genitourinary Cancer|September 13, 2024
Quantitative Investigation of MicroRNA-32 in the Urine of Prostate Cancer Patients and Its Relationship With Clinicopathological CharacteristicsAmir Hossein Mahdizade, Meysam Yousefi, Mohsen Sarkarian, et al.
The Journal of Obstetrics and Gynaecology Research|February 1, 2020
Association of vascular endothelial growth factor A polymorphisms and aberrant expression of connexin 43 and VEGFA with idiopathic recurrent spontaneous miscarriageMaryam S Sajjadi, Pegah Ghandil, Nahid Shahbazian, et al.
DNA Repair|June 30, 2006
Differential usage of non-homologous end-joining and homologous recombination in double strand break repairEiichiro Sonoda, Helfrid Hochegger, Alihossein Saberi, et al.
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