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Mahtab Tavasoli

Showing results (21-30 of 25) with videos related to

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The Journal of Biological Chemistry|November 27, 2025
Neurodevelopmental disease-causing variants in choline kinase CHKA gene couple phosphatidylcholine synthesis to oxidative stress damage and disease etiologyMahtab Tavasoli, Mariam Alkandari, Gabriel Dorighello, et al.
The Journal of Biological Chemistry|February 13, 2022
A mouse model of inherited choline kinase β-deficiency presents with specific cardiac abnormalities and a predisposition to arrhythmiaMahtab Tavasoli, Tiam Feridooni, Hirad Feridooni, et al.
Nature Communications|September 27, 2024
Computer-aided drug design to generate a unique antibiotic familyChristopher J Barden, Fan Wu, J Pedro Fernandez-Murray, et al.
Nature Communications|March 24, 2022
Mechanism of action and therapeutic route for a muscular dystrophy caused by a genetic defect in lipid metabolismMahtab Tavasoli, Sarah Lahire, Stanislav Sokolenko, et al.
Brain : a Journal of Neurology|February 24, 2022
Bi-allelic variants in CHKA cause a neurodevelopmental disorder with epilepsy and microcephalyChiara Klöckner, J Pedro Fernández-Murray, Mahtab Tavasoli, et al.
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Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
The Journal of Biological Chemistry|November 27, 2025
Neurodevelopmental disease-causing variants in choline kinase CHKA gene couple phosphatidylcholine synthesis to oxidative stress damage and disease etiologyMahtab Tavasoli, Mariam Alkandari, Gabriel Dorighello, et al.
The Journal of Biological Chemistry|February 13, 2022
A mouse model of inherited choline kinase β-deficiency presents with specific cardiac abnormalities and a predisposition to arrhythmiaMahtab Tavasoli, Tiam Feridooni, Hirad Feridooni, et al.
Nature Communications|September 27, 2024
Computer-aided drug design to generate a unique antibiotic familyChristopher J Barden, Fan Wu, J Pedro Fernandez-Murray, et al.
Nature Communications|March 24, 2022
Mechanism of action and therapeutic route for a muscular dystrophy caused by a genetic defect in lipid metabolismMahtab Tavasoli, Sarah Lahire, Stanislav Sokolenko, et al.
Brain : a Journal of Neurology|February 24, 2022
Bi-allelic variants in CHKA cause a neurodevelopmental disorder with epilepsy and microcephalyChiara Klöckner, J Pedro Fernández-Murray, Mahtab Tavasoli, et al.
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