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Sina Narrei

Showing results (1-10 of 9) with videos related to

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Advances in Experimental Medicine and Biology|August 9, 2019
Epigenetics and Common Non Communicable DiseaseMohammad Amin Tabatabaiefar, Roshanak S Sajjadi, Sina Narrei
Iranian Journal of Medical Sciences|July 17, 2023
A Novel Germline Pathogenic Variant of <i>RECQL4</i> Gene in an Iranian Pedigree with Familial Squamous Cell Carcinoma: A Brief ReportMina Amin, Elaheh Mahmoodi-Khaledi, Sina Narrei, et al.
Neuromuscular Disorders : NMD|August 21, 2022
Whole exome sequencing identified a novel LAMA2 frameshift variant causing merosin-deficient congenital muscular dystrophy in a patient with cardiomyopathy, and autism-like behaviorZahra Nouri, Akram Sarmadi, Sina Narrei, et al.
Journal of Research in Medical Sciences : the Official Journal of Isfahan University of Medical Sciences|November 3, 2021
Trends of human brucellosis in Central Iran (2010-2018)Mohammad-Sadegh Khalilian, Javad Ramazanpour, Sayed Mohsen Hosseini, et al.
Molecular Biology Reports|July 6, 2020
Whole exome sequencing identifies novel compound heterozygous pathogenic variants in the MYO15A gene leading to autosomal recessive non-syndromic hearing lossAkram Sarmadi, Samane Nasrniya, Sina Narrei, et al.
BMC Medical Genomics|July 3, 2024
Clinical characterizations and molecular genetic study of two co-segregating variants in PDZD7 and PDE6C genes leading simultaneously to non-syndromic hearing loss and achromatopsiaZahra Nouri, Akram Sarmadi, Sina Narrei, et al.
Plos One|February 27, 2023
Novel in-frame duplication variant characterization in late infantile metachromatic leukodystrophy using whole-exome sequencing and molecular dynamics simulationZahra Ataei, Zahra Nouri, Farial Tavakoli, et al.
Laboratory Medicine|August 13, 2021
Whole-Exome Sequencing Identifies a Recurrent Small In-Frame Deletion in MYO15A Causing Autosomal Recessive Nonsyndromic Hearing Loss in 3 Iranian PedigreesSamane Nasrniya, Paniz Miar, Sina Narrei, et al.
BMC Medical Genetics|June 11, 2020
A novel pathogenic variant in the LRTOMT gene causes autosomal recessive non-syndromic hearing loss in an Iranian familyAkram Sarmadi, Samane Nasrniya, Maryam Soleimani Farsani, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Advances in Experimental Medicine and Biology|August 9, 2019
Epigenetics and Common Non Communicable DiseaseMohammad Amin Tabatabaiefar, Roshanak S Sajjadi, Sina Narrei
Iranian Journal of Medical Sciences|July 17, 2023
A Novel Germline Pathogenic Variant of <i>RECQL4</i> Gene in an Iranian Pedigree with Familial Squamous Cell Carcinoma: A Brief ReportMina Amin, Elaheh Mahmoodi-Khaledi, Sina Narrei, et al.
Neuromuscular Disorders : NMD|August 21, 2022
Whole exome sequencing identified a novel LAMA2 frameshift variant causing merosin-deficient congenital muscular dystrophy in a patient with cardiomyopathy, and autism-like behaviorZahra Nouri, Akram Sarmadi, Sina Narrei, et al.
Journal of Research in Medical Sciences : the Official Journal of Isfahan University of Medical Sciences|November 3, 2021
Trends of human brucellosis in Central Iran (2010-2018)Mohammad-Sadegh Khalilian, Javad Ramazanpour, Sayed Mohsen Hosseini, et al.
Molecular Biology Reports|July 6, 2020
Whole exome sequencing identifies novel compound heterozygous pathogenic variants in the MYO15A gene leading to autosomal recessive non-syndromic hearing lossAkram Sarmadi, Samane Nasrniya, Sina Narrei, et al.
BMC Medical Genomics|July 3, 2024
Clinical characterizations and molecular genetic study of two co-segregating variants in PDZD7 and PDE6C genes leading simultaneously to non-syndromic hearing loss and achromatopsiaZahra Nouri, Akram Sarmadi, Sina Narrei, et al.
Plos One|February 27, 2023
Novel in-frame duplication variant characterization in late infantile metachromatic leukodystrophy using whole-exome sequencing and molecular dynamics simulationZahra Ataei, Zahra Nouri, Farial Tavakoli, et al.
Laboratory Medicine|August 13, 2021
Whole-Exome Sequencing Identifies a Recurrent Small In-Frame Deletion in MYO15A Causing Autosomal Recessive Nonsyndromic Hearing Loss in 3 Iranian PedigreesSamane Nasrniya, Paniz Miar, Sina Narrei, et al.
BMC Medical Genetics|June 11, 2020
A novel pathogenic variant in the LRTOMT gene causes autosomal recessive non-syndromic hearing loss in an Iranian familyAkram Sarmadi, Samane Nasrniya, Maryam Soleimani Farsani, et al.
Pageof 1