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Davood Zare

Showing results (41-50 of 56) with videos related to

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Dalton Transactions (Cambridge, England : 2003)|June 28, 2017
Cr<sup>III</sup> as an alternative to Ru<sup>II</sup> in metallo-supramolecular chemistryDavood Zare, Benjamin Doistau, Homayoun Nozary, et al.
Journal of Assisted Reproduction and Genetics|January 10, 2020
The second mutation of SYCE1 gene associated with autosomal recessive nonobstructive azoospermiaMahdieh Pashaei, Mohammad Masoud Rahimi Bidgoli, Davood Zare-Abdollahi, et al.
Current Journal of Neurology|November 27, 2023
Giant axonal neuropathy: The first Iranian case with a variation in the gigaxonin gene and a glance to the other casesMohammad Vafaee-Shahi, Saeideh Ghasemi, Masood Ghahvechi-Akbar, et al.
Inorganic Chemistry|May 21, 2016
Taming Lanthanide-Centered Upconversion at the Molecular LevelYan Suffren, Bahman Golesorkhi, Davood Zare, et al.
Molecular Genetics and Genomics : MGG|April 8, 2020
Mutation in ALOX12B likely cause of POI and also ichthyosis in a large Iranian pedigreeAfagh Alavi, Faezeh Darki, Mohammad Masoud Rahimi Bidgoli, et al.
The Journal of Gene Medicine|January 21, 2020
RPE65 and retinal dystrophy: Report of new and recurrent mutationsShamsi Safari, Davood Zare-Abdollahi, Ata Bushehri, et al.
Dalton Transactions (Cambridge, England : 2003)|October 31, 2014
Smaller than a nanoparticle with the design of discrete polynuclear molecular complexes displaying near-infrared to visible upconversionDavood Zare, Yan Suffren, Laure Guénée, et al.
International Journal of Molecular and Cellular Medicine|September 5, 2017
Prenatal Diagnosis of Mosaic Tetrasomy 18p in a Case without Sonographic AbnormalitiesJavad Karimzad Hagh, Thomas Liehr, Hamid Ghaedi, et al.
American Journal of Medical Genetics. Part A|November 20, 2020
Clinical spectrum in multiple families with primary COQ<sub>10</sub> deficiencySeyyed S Hashemi, Davood Zare-Abdollahi, Mohammad K Bakhshandeh, et al.
Hematology (Amsterdam, Netherlands)|January 17, 2015
A mutational and expressional analysis of DNMT3A in acute myeloid leukemia cytogenetic subgroupsDavood Zare-Abdollahi, Shamsi Safari, Abolfazl Movafagh, et al.
Pageof 6

Showing results (41-50 of 56) with videos related to

Sort By:
Pageof 6
Dalton Transactions (Cambridge, England : 2003)|June 28, 2017
Cr<sup>III</sup> as an alternative to Ru<sup>II</sup> in metallo-supramolecular chemistryDavood Zare, Benjamin Doistau, Homayoun Nozary, et al.
Journal of Assisted Reproduction and Genetics|January 10, 2020
The second mutation of SYCE1 gene associated with autosomal recessive nonobstructive azoospermiaMahdieh Pashaei, Mohammad Masoud Rahimi Bidgoli, Davood Zare-Abdollahi, et al.
Current Journal of Neurology|November 27, 2023
Giant axonal neuropathy: The first Iranian case with a variation in the gigaxonin gene and a glance to the other casesMohammad Vafaee-Shahi, Saeideh Ghasemi, Masood Ghahvechi-Akbar, et al.
Inorganic Chemistry|May 21, 2016
Taming Lanthanide-Centered Upconversion at the Molecular LevelYan Suffren, Bahman Golesorkhi, Davood Zare, et al.
Molecular Genetics and Genomics : MGG|April 8, 2020
Mutation in ALOX12B likely cause of POI and also ichthyosis in a large Iranian pedigreeAfagh Alavi, Faezeh Darki, Mohammad Masoud Rahimi Bidgoli, et al.
The Journal of Gene Medicine|January 21, 2020
RPE65 and retinal dystrophy: Report of new and recurrent mutationsShamsi Safari, Davood Zare-Abdollahi, Ata Bushehri, et al.
Dalton Transactions (Cambridge, England : 2003)|October 31, 2014
Smaller than a nanoparticle with the design of discrete polynuclear molecular complexes displaying near-infrared to visible upconversionDavood Zare, Yan Suffren, Laure Guénée, et al.
International Journal of Molecular and Cellular Medicine|September 5, 2017
Prenatal Diagnosis of Mosaic Tetrasomy 18p in a Case without Sonographic AbnormalitiesJavad Karimzad Hagh, Thomas Liehr, Hamid Ghaedi, et al.
American Journal of Medical Genetics. Part A|November 20, 2020
Clinical spectrum in multiple families with primary COQ<sub>10</sub> deficiencySeyyed S Hashemi, Davood Zare-Abdollahi, Mohammad K Bakhshandeh, et al.
Hematology (Amsterdam, Netherlands)|January 17, 2015
A mutational and expressional analysis of DNMT3A in acute myeloid leukemia cytogenetic subgroupsDavood Zare-Abdollahi, Shamsi Safari, Abolfazl Movafagh, et al.
Pageof 6