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Mohammad Keramatipour

Showing results (1-10 of 76) with videos related to

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Iranian Journal of Child Neurology|January 31, 2018
Effect of Whole Exome Sequencing in Diagnosis of Inborn Errors of Metabolism and Neurogenetic DisordersMarjan Shakiba, Mohammad Keramatipour
Avicenna Journal of Medical Biotechnology|February 15, 2013
Producing a Mammalian GFP Expression Vector Containing Neomycin Resistance GeneManizheh Izadi, Maryam Abiri, Mohammad Keramatipour
Cell Journal|May 24, 2013
Effect of embryonic cerebrospinal fluid on proliferation and differentiation of neuroprogenitor cellsSiamak Yari, Kazem Parivar, Mohammad Nabiuni, et al.
Iranian Journal of Child Neurology|November 16, 2020
Succinate Dehydrogenase Deficiency: A Treatable Neurometabolic DisorderParvaneh Karimzadeh, Mohammad Keramatipour, Arezou Karamzade, et al.
Iranian Journal of Public Health|April 29, 2017
Comparison of Two Different PCR-based Methods for Detection of GAA Expansions in Frataxin GeneMona Entezam, Akbar Amirfiroozi, Mansoureh Togha, et al.
International Journal of Pediatric Otorhinolaryngology|December 31, 2017
Targeted next generation sequencing identified a novel mutation in MYO7A causing Usher syndrome type 1 in an Iranian consanguineous pedigreeDaniz Kooshavar, Masoumeh Razipour, Morteza Movasat, et al.
Iranian Journal of Allergy, Asthma, and Immunology|December 17, 2013
Lack of association between single nucleotide polymorphism rs10818488 in TRAF1/C5 region and rheumatoid arthritis in iranian populationSomayeh Ahmadlou, Mohsen Akhiani, Ahmad Salimzadeh, et al.
International Journal of Endocrinology and Metabolism|January 27, 2017
A Case Series: Congenital HyperinsulinismMohammad Reza Alaei, Susan Akbaroghli, Mohammad Keramatipour, et al.
BMC Neurology|January 16, 2021
SPOAN syndrome: a novel mutation and new ocular findings; a case reportFatemeh Bazvand, Mohammad Keramatipour, Hamid Riazi-Esfahani, et al.
Iranian Journal of Allergy, Asthma, and Immunology|November 9, 2015
Single Nucleotide Polymorphism rs 2476601 of PTPN22 Gene and Susceptibility to Rheumatoid Arthritis in Iranian PopulationSomayeh Ahmadloo, Mohsen Taghizadeh, Mohsen Akhiani, et al.
Pageof 8

Showing results (1-10 of 76) with videos related to

Sort By:
Pageof 8
Iranian Journal of Child Neurology|January 31, 2018
Effect of Whole Exome Sequencing in Diagnosis of Inborn Errors of Metabolism and Neurogenetic DisordersMarjan Shakiba, Mohammad Keramatipour
Avicenna Journal of Medical Biotechnology|February 15, 2013
Producing a Mammalian GFP Expression Vector Containing Neomycin Resistance GeneManizheh Izadi, Maryam Abiri, Mohammad Keramatipour
Cell Journal|May 24, 2013
Effect of embryonic cerebrospinal fluid on proliferation and differentiation of neuroprogenitor cellsSiamak Yari, Kazem Parivar, Mohammad Nabiuni, et al.
Iranian Journal of Child Neurology|November 16, 2020
Succinate Dehydrogenase Deficiency: A Treatable Neurometabolic DisorderParvaneh Karimzadeh, Mohammad Keramatipour, Arezou Karamzade, et al.
Iranian Journal of Public Health|April 29, 2017
Comparison of Two Different PCR-based Methods for Detection of GAA Expansions in Frataxin GeneMona Entezam, Akbar Amirfiroozi, Mansoureh Togha, et al.
International Journal of Pediatric Otorhinolaryngology|December 31, 2017
Targeted next generation sequencing identified a novel mutation in MYO7A causing Usher syndrome type 1 in an Iranian consanguineous pedigreeDaniz Kooshavar, Masoumeh Razipour, Morteza Movasat, et al.
Iranian Journal of Allergy, Asthma, and Immunology|December 17, 2013
Lack of association between single nucleotide polymorphism rs10818488 in TRAF1/C5 region and rheumatoid arthritis in iranian populationSomayeh Ahmadlou, Mohsen Akhiani, Ahmad Salimzadeh, et al.
International Journal of Endocrinology and Metabolism|January 27, 2017
A Case Series: Congenital HyperinsulinismMohammad Reza Alaei, Susan Akbaroghli, Mohammad Keramatipour, et al.
BMC Neurology|January 16, 2021
SPOAN syndrome: a novel mutation and new ocular findings; a case reportFatemeh Bazvand, Mohammad Keramatipour, Hamid Riazi-Esfahani, et al.
Iranian Journal of Allergy, Asthma, and Immunology|November 9, 2015
Single Nucleotide Polymorphism rs 2476601 of PTPN22 Gene and Susceptibility to Rheumatoid Arthritis in Iranian PopulationSomayeh Ahmadloo, Mohsen Taghizadeh, Mohsen Akhiani, et al.
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