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Mehdi Totonchi

Showing results (131-140 of 139) with videos related to

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Stem Cell Reports|September 19, 2017
Blockage of the Epithelial-to-Mesenchymal Transition Is Required for Embryonic Stem Cell DerivationMehdi Totonchi, Seyedeh-Nafiseh Hassani, Ali Sharifi-Zarchi, et al.
Pulmonary Pharmacology & Therapeutics|August 14, 2021
Evaluation of the prophylactic effect of hydroxychloroquine on people in close-contact with patients with COVID-19Minoosh Shabani, Mehdi Totonchi, Omidvar Rezaeimirghaed, et al.
Molecular Human Reproduction|February 12, 2022
Direct visualization of pre-protamine 2 detects protamine assembly failures and predicts ICSI successMaryam Rezaei-Gazik, Alexandra Vargas, Amir Amiri-Yekta, et al.
Journal of Human Genetics|July 20, 2019
Identification of a missense variant in CLDN2 in obstructive azoospermiaMasomeh Askari, Razieh Karamzadeh, Naser Ansari-Pour, et al.
Journal of Medical Genetics|September 17, 2020
Biallelic variant in cyclin B3 is associated with failure of maternal meiosis II and recurrent digynic triploidyNayeralsadat Fatemi, Najmeh Salehi, Laura Pignata, et al.
The Journal of Clinical Investigation|March 10, 2020
Claudin-2 deficiency associates with hypercalciuria in mice and human kidney stone diseaseJoshua N Curry, Matthew Saurette, Masomeh Askari, et al.
Stem Cell Reviews and Reports|September 17, 2013
Inhibition of TGFβ signaling promotes ground state pluripotencySeyedeh-Nafiseh Hassani, Mehdi Totonchi, Ali Sharifi-Zarchi, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|July 22, 2021
Expanding DSD Phenotypes Associated with Variants in the DEAH-Box RNA Helicase DHX37Housna Zidoune, Laetitia Martinerie, Daisylyn S Tan, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 5, 2020
Testis formation in XX individuals resulting from novel pathogenic variants in Wilms' tumor 1 (<i>WT1</i>) geneCaroline Eozenou, Nitzan Gonen, Maria Sol Touzon, et al.
Pageof 14

Showing results (131-140 of 139) with videos related to

Sort By:
Pageof 14
You have reached the last page of results.This site can display upto 139 results.
Stem Cell Reports|September 19, 2017
Blockage of the Epithelial-to-Mesenchymal Transition Is Required for Embryonic Stem Cell DerivationMehdi Totonchi, Seyedeh-Nafiseh Hassani, Ali Sharifi-Zarchi, et al.
Pulmonary Pharmacology & Therapeutics|August 14, 2021
Evaluation of the prophylactic effect of hydroxychloroquine on people in close-contact with patients with COVID-19Minoosh Shabani, Mehdi Totonchi, Omidvar Rezaeimirghaed, et al.
Molecular Human Reproduction|February 12, 2022
Direct visualization of pre-protamine 2 detects protamine assembly failures and predicts ICSI successMaryam Rezaei-Gazik, Alexandra Vargas, Amir Amiri-Yekta, et al.
Journal of Human Genetics|July 20, 2019
Identification of a missense variant in CLDN2 in obstructive azoospermiaMasomeh Askari, Razieh Karamzadeh, Naser Ansari-Pour, et al.
Journal of Medical Genetics|September 17, 2020
Biallelic variant in cyclin B3 is associated with failure of maternal meiosis II and recurrent digynic triploidyNayeralsadat Fatemi, Najmeh Salehi, Laura Pignata, et al.
The Journal of Clinical Investigation|March 10, 2020
Claudin-2 deficiency associates with hypercalciuria in mice and human kidney stone diseaseJoshua N Curry, Matthew Saurette, Masomeh Askari, et al.
Stem Cell Reviews and Reports|September 17, 2013
Inhibition of TGFβ signaling promotes ground state pluripotencySeyedeh-Nafiseh Hassani, Mehdi Totonchi, Ali Sharifi-Zarchi, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|July 22, 2021
Expanding DSD Phenotypes Associated with Variants in the DEAH-Box RNA Helicase DHX37Housna Zidoune, Laetitia Martinerie, Daisylyn S Tan, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 5, 2020
Testis formation in XX individuals resulting from novel pathogenic variants in Wilms' tumor 1 (<i>WT1</i>) geneCaroline Eozenou, Nitzan Gonen, Maria Sol Touzon, et al.
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