Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
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.
Journal of Genetics|February 24, 2023
Identification of a novel mutation in the <i>HACD1</i> gene in an Iranian family with autosomal recessive congenital myopathy, with fibre-type disproportionNeda Jabbarpour, Bita Poorshiri, Hassan Saei, et al.
Ophthalmic Genetics|June 21, 2022
Identification of novel cis-mutations in the <i>GJA8</i> gene in a 3-generation Iranian family with autosomal dominant congenital nuclear cataractNeda Jabbarpour, Hassan Saei, Mohammad Hossein Jabbarpoor Bonyadi, 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.
Clinical Journal of the American Society of Nephrology : CJASN|December 4, 2025
Exome Sequencing in a Large Cohort with Ciliopathy-Related Kidney DiseaseFriederike Petzold, Cécile Jeanpierre, Xiaoyi Chen, et al.
Frontiers in Genetics|January 28, 2021
Whole-Exome Sequencing Uncovers Novel Causative Variants and Additional Findings in Three Patients Affected by Glycogen Storage Disease Type VI and Fanconi-Bickel SyndromeMaryam Eghbali, Kiyana Sadat Fatemi, Shadab Salehpour, et al.
Molecular Plant-Microbe Interactions : MPMI|April 9, 2021
Rapid Methodologies for Assessing <i>Pseudomonas syringae</i> pv. <i>actinidiae</i> Colonization and Effector-Mediated Hypersensitive Response in KiwifruitJay Jayaraman, Abhishek Chatterjee, Shannon Hunter, et al.
JCI Insight|December 18, 2025
Splice modulation of COL4A5 reinstates collagen IV assembly in an organoid model of Alport syndromeHassan Saei, Bruno Estebe, Nicolas Goudin, et al.
Frontiers in Cell and Developmental Biology|June 24, 2026
Co-trimoxazole-induced reproductive toxicity and placental-barrier disruption: impact on cell-cell junctions and ERK signaling pathwayMehrdad Azarmi, Hassan Saei, I A C van Vugt, et al.
Iscience|July 17, 2023
VNtyper enables accurate alignment-free genotyping of <i>MUC1</i> coding VNTR using short-read sequencing data in autosomal dominant tubulointerstitial kidney diseaseHassan Saei, Vincent Morinière, Laurence Heidet, et al.
Pageof 2