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Journal of Cancer Research and Therapeutics|June 14, 2021
<i>In vivo</i> study of interferon-γ, transforming growth factor-β, and interleukin-4 gene expression induced by radioadaptive responseMohammad-Taghi Bahreyni-Toossi, Mojtaba Sankian, Hosein Azimian, et al.
Iranian Journal of Basic Medical Sciences|June 4, 2020
PHA stimulation may be useful for FDXR gene expression-based biodosimetryHabibeh Vosoughi, Hosein Azimian, Sara Khademi, et al.
Nutrition and Health|June 3, 2022
Association between plant and animal proteins intake with lipid profile and anthropometric indices: A cross-sectional studyAtefeh Kohansal, Ali Zangene, Abduladheem Turki Jalil, et al.
Comparative Immunology, Microbiology and Infectious Diseases|December 23, 2025
Molecular detection of Coxiella burnetii in long-eared hedgehogs (Hemiechinus auritus) and related ticks, IraqPeyman Khademi, Amin Jaydari, Nemat Shams, et al.
Orphanet Journal of Rare Diseases|February 15, 2019
Mimicry and well known genetic friends: molecular diagnosis in an Iranian cohort of suspected Bartter syndrome and proposition of an algorithm for clinical differential diagnosisMaryam Najafi, Dor Mohammad Kordi-Tamandani, Farkhondeh Behjati, et al.
European Journal of Nutrition|March 22, 2017
Greater adherence to the dietary approaches to stop hypertension (DASH) dietary pattern is associated with lower blood pressure in healthy Iranian primary school childrenAida Najafi, Shiva Faghih, Abdollah Hojhabrimanesh, et al.
Journal of Medical Genetics|May 24, 2025
<i>RNU4-2</i> monoallelic variants as a leading cause of syndromic neurodevelopmental disorder, including in patients with parental consanguinityAida M Bertoli-Avella, Christian A Ganoza, Mariana Ferreira, et al.
Frontiers in Pediatrics|April 6, 2019
A 57 kB Genomic Deletion Causing CTNS Loss of Function Contributes to the <i>CTNS</i> Mutational Spectrum in the Middle EastMaryam Najafi, Dor Mohammad Kordi Tamandani, Anoush Azarfar, et al.
Archives of Endocrinology and Metabolism|October 18, 2024
Association of <i>IRS1</i> gene Pro512Ala polymorphism with nonalcoholic fatty liver diseaseAsadollah Asadi, Mitra Rostami, Radmehr Shafiee, et al.
Orphanet Journal of Rare Diseases|March 4, 2022
Identification of three novel homozygous variants in COL9A3 causing autosomal recessive Stickler syndromeAboulfazl Rad, Maryam Najafi, Fatemeh Suri, et al.
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