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Frontiers in Genetics|July 5, 2021
Hints From the Cellular Functions to the Practical Outlook of Circular RNAsLiora Yesharim, Marzieh Mojbafan, Maryam AbiriAvicenna Journal of Medical Biotechnology|February 15, 2013
Producing a Mammalian GFP Expression Vector Containing Neomycin Resistance GeneManizheh Izadi, Maryam Abiri, Mohammad KeramatipourInternational Journal of Reproductive Biomedicine|February 23, 2023
Prenatal diagnosis of citrullinemia type 1; seven families with c.1168G A mutation of Argininosuccinate synthetase 1 gene in Southwest Iran: A case seriesMaryam Hassanlou, Maryam Abiri, Sirous ZeinaliPlacenta|August 9, 2024
Comprehensive microarray analysis of severe preeclampsia placenta to identify differentially expressed genes, biological pathways, hub genes, and their related non-coding RNAsMaedeh Shabani, Maryam Eghbali, Ameneh Abiri, et al.Metabolic Brain Disease|June 26, 2019
Genetic testing of Mucopolysaccharidoses disease using multiplex PCR- based panels of STR markers: in silico analysis of novel mutationsMehdi Shafaat, Mehrdad Hashemi, Ahmad Majd, et al.Journal of Family & Reproductive Health|March 28, 2022
An Infertile Azoospermic Male With 45, X T(Yp;15) KaryotypeMaryam Abiri, Maryam Hassanlou, Nima Narimani, et al.Pregnancy Hypertension|June 7, 2021
Comprehensive transcriptome mining identified the gene expression signature and differentially regulated pathways of the late-onset preeclampsiaHassan Saei, Ali Govahi, Ameneh Abiri, et al.Metabolic Brain Disease|May 24, 2019
Maple syrup urine disease mutation spectrum in a cohort of 40 consanguineous patients and insilico analysis of novel mutationsMaryam Abiri, Hassan Saei, Maryam Eghbali, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|September 30, 2016
Co-existence of phenylketonuria either with maple syrup urine disease or Sandhoff disease in two patients from Iran: emphasizing the role of consanguinityMaryam Abiri, Saeed Talebi, Jouni Uitto, et al.Clinical and Experimental Reproductive Medicine|November 24, 2025
A highly rare female phenotype with complex chromosomal mosaicism: 46,XY/45,X/46,X,r(Y)Zohreh Maghsoomi, Maryam Abiri, Fatemeh Golgiri, et al.Pageof 3