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Hossein Jafari Khamirani

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Metabolic Syndrome and Related Disorders|November 1, 2022
Analysis of DYRK1B, PPARG, and CEBPB Expression Patterns in Adipose-Derived Stem Cells from Patients Carrying DYRK1B R102C and Healthy Individuals During AdipogenesisAzam Armanmehr, Hossein Jafari Khamirani, Sina Zoghi, et al.
Gene|March 10, 2023
NRXN3 mutations cause developmental delay, movement disorder, and behavioral problems: CRISPR edited cells based WES resultsNeda Kamal, Hossein Jafari Khamirani, Mahintaj Dara, et al.
Archives of Iranian Medicine|August 6, 2023
A Form of Metabolic-Associated Fatty Liver Disease Associated with a Novel LIPA VariantAmir Anushiravani, Hossein Jafari Khamirani, Ashraf Mohamadkhani, et al.
Journal of Medical Case Reports|January 4, 2026
A novel pathogenic mutation in TSPEAR associated with sensorineural hearing loss: a case report and review of the literatureAlireza Ahmadkhani, Erfan Taherifard, Sina Zoghi, et al.
European Journal of Medical Genetics|October 4, 2021
A novel non-sense mutation in TDP2 causes spinocerebellar ataxia autosomal recessive 23 accompanied by bilateral upward gaze; report of a case and review of the literatureSina Zoghi, Hossein Jafari Khamirani, Hamidreza Hassanipour, et al.
Human Genome Variation|July 22, 2021
A single-amino-acid in-frame deletion in CYP17A1 results in combined 17-hydroxylase and 17,20-lyase deficiency in an Iranian family despite the protein mutation siteAshkan Habib, Alireza Shojazadeh, Mohadeseh Molayemat, et al.
European Journal of Medical Genetics|May 26, 2022
ZNF142 mutation causes neurodevelopmental disorder with speech impairment and seizures: Novel variants and literature reviewNeda Kamal, Hossein Jafari Khamirani, Sanaz Mohammadi, et al.
Human Genome Variation|January 12, 2023
EPS8 variant causes deafness, autosomal recessive 102 (DFNB102) and literature reviewZahra Abbasi, Hossein Jafari Khamirani, Seyed Mohammad Bagher Tabei, et al.
European Journal of Medical Genetics|January 29, 2023
The third patient of ACACA-related acetyl-CoA carboxylase deficiency with seizure and literature reviewNegin Shafieipour, Hossein Jafari Khamirani, Neda Kamal, et al.
Human Genome Variation|June 11, 2021
A novel PTRH2 missense mutation causing IMNEPD: a case reportHossein Jafari Khamirani, Sina Zoghi, Mehdi Dianatpour, et al.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
Metabolic Syndrome and Related Disorders|November 1, 2022
Analysis of DYRK1B, PPARG, and CEBPB Expression Patterns in Adipose-Derived Stem Cells from Patients Carrying DYRK1B R102C and Healthy Individuals During AdipogenesisAzam Armanmehr, Hossein Jafari Khamirani, Sina Zoghi, et al.
Gene|March 10, 2023
NRXN3 mutations cause developmental delay, movement disorder, and behavioral problems: CRISPR edited cells based WES resultsNeda Kamal, Hossein Jafari Khamirani, Mahintaj Dara, et al.
Archives of Iranian Medicine|August 6, 2023
A Form of Metabolic-Associated Fatty Liver Disease Associated with a Novel LIPA VariantAmir Anushiravani, Hossein Jafari Khamirani, Ashraf Mohamadkhani, et al.
Journal of Medical Case Reports|January 4, 2026
A novel pathogenic mutation in TSPEAR associated with sensorineural hearing loss: a case report and review of the literatureAlireza Ahmadkhani, Erfan Taherifard, Sina Zoghi, et al.
European Journal of Medical Genetics|October 4, 2021
A novel non-sense mutation in TDP2 causes spinocerebellar ataxia autosomal recessive 23 accompanied by bilateral upward gaze; report of a case and review of the literatureSina Zoghi, Hossein Jafari Khamirani, Hamidreza Hassanipour, et al.
Human Genome Variation|July 22, 2021
A single-amino-acid in-frame deletion in CYP17A1 results in combined 17-hydroxylase and 17,20-lyase deficiency in an Iranian family despite the protein mutation siteAshkan Habib, Alireza Shojazadeh, Mohadeseh Molayemat, et al.
European Journal of Medical Genetics|May 26, 2022
ZNF142 mutation causes neurodevelopmental disorder with speech impairment and seizures: Novel variants and literature reviewNeda Kamal, Hossein Jafari Khamirani, Sanaz Mohammadi, et al.
Human Genome Variation|January 12, 2023
EPS8 variant causes deafness, autosomal recessive 102 (DFNB102) and literature reviewZahra Abbasi, Hossein Jafari Khamirani, Seyed Mohammad Bagher Tabei, et al.
European Journal of Medical Genetics|January 29, 2023
The third patient of ACACA-related acetyl-CoA carboxylase deficiency with seizure and literature reviewNegin Shafieipour, Hossein Jafari Khamirani, Neda Kamal, et al.
Human Genome Variation|June 11, 2021
A novel PTRH2 missense mutation causing IMNEPD: a case reportHossein Jafari Khamirani, Sina Zoghi, Mehdi Dianatpour, et al.
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