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Journal of Enzyme Inhibition and Medicinal Chemistry
|
October 22, 2016
Diethylalkylsulfonamido(4-methoxyphenyl)methyl)phosphonate/phosphonic acid derivatives act as acid phosphatase inhibitors: synthesis accompanied by experimental and molecular modeling assessments
Nahid Alimoradi, Mohammad Reza Ashrafi-Kooshk, Mohsen Shahlaei, et al.
International Journal of Biological Macromolecules
|
February 7, 2024
Crosstalk between tau protein autoproteolysis and amyloid fibril formation
Mohammad Reza Ashrafi-Kooshk, Fatemeh Norouzi, Ashkan Zare Karizak, et al.
Cells
|
December 24, 2021
Cannabidiol Inhibits Tau Aggregation In Vitro
Soha Alali, Gholamhossein Riazi, Mohammad Reza Ashrafi-Kooshk, et al.
Iranian Journal of Child Neurology
|
March 14, 2015
Comparative efficacy of zonisamide and pregabalin as an adjunctive therapy in children with refractory epilepsy
Mohammad Mahdi Taghdiri, Mohammad Kazem Bakhshandeh Bali, Parvaneh Karimzadeh, et al.
Mitochondrion
|
April 3, 2021
Crystallographic modeling of the PNPT1:c.1453A>G variant as a cause of mitochondrial dysfunction and autosomal recessive deafness; expanding the neuroimaging and clinical features
Ali Hosseini Bereshneh, Zahra Rezaei, Ehsan Jafarinia, et al.
Iranian Journal of Pharmaceutical Research : IJPR
|
February 23, 2022
Astaxanthin Decreases Spatial Memory and Glutamate Transport Impairment Induced by Fluoride
Farzaneh Mirsaeed-Ghazi, Mohammad Sharifzadeh, Mohammad Reza Ashrafi-Kooshk, et al.
Optics Express
|
July 21, 2015
Time-delay to intensity mapping based on a second-order optical integrator: application to optical arbitrary waveform generation
Reza Ashrafi, Mohammad Rezagholipour Dizaji, Luis Romero Cortés, et al.
Muscle & Nerve
|
September 21, 2016
Late-onset pompe disease in Iran: A clinical and genetic report
Ferdos Nazari, Farnaz Sinaei, Yalda Nilipour, et al.
Mitochondrion
|
July 12, 2021
Defective complex III mitochondrial respiratory chain due to a novel variant in CYC1 gene masquerades acute demyelinating syndrome or Leber hereditary optic neuropathy
Erfan Heidari, Maryam Rasoulinezhad, Neda Pak, et al.
Italian Journal of Pediatrics
|
June 6, 2023
Spinal Muscular Atrophy with Progressive Myoclonic Epilepsy (SMA-PME): three new cases and review of the mutational spectrum
Ali Najafi, Behnoosh Tasharrofi, Farshid Zandsalimi, et al.
Page
of 23
Search research articles
Search
Showing results (101-110 of 222) with videos related to
Sort By:
Page
of 23
Journal of Enzyme Inhibition and Medicinal Chemistry
|
October 22, 2016
Diethylalkylsulfonamido(4-methoxyphenyl)methyl)phosphonate/phosphonic acid derivatives act as acid phosphatase inhibitors: synthesis accompanied by experimental and molecular modeling assessments
Nahid Alimoradi, Mohammad Reza Ashrafi-Kooshk, Mohsen Shahlaei, et al.
International Journal of Biological Macromolecules
|
February 7, 2024
Crosstalk between tau protein autoproteolysis and amyloid fibril formation
Mohammad Reza Ashrafi-Kooshk, Fatemeh Norouzi, Ashkan Zare Karizak, et al.
Cells
|
December 24, 2021
Cannabidiol Inhibits Tau Aggregation In Vitro
Soha Alali, Gholamhossein Riazi, Mohammad Reza Ashrafi-Kooshk, et al.
Iranian Journal of Child Neurology
|
March 14, 2015
Comparative efficacy of zonisamide and pregabalin as an adjunctive therapy in children with refractory epilepsy
Mohammad Mahdi Taghdiri, Mohammad Kazem Bakhshandeh Bali, Parvaneh Karimzadeh, et al.
Mitochondrion
|
April 3, 2021
Crystallographic modeling of the PNPT1:c.1453A>G variant as a cause of mitochondrial dysfunction and autosomal recessive deafness; expanding the neuroimaging and clinical features
Ali Hosseini Bereshneh, Zahra Rezaei, Ehsan Jafarinia, et al.
Iranian Journal of Pharmaceutical Research : IJPR
|
February 23, 2022
Astaxanthin Decreases Spatial Memory and Glutamate Transport Impairment Induced by Fluoride
Farzaneh Mirsaeed-Ghazi, Mohammad Sharifzadeh, Mohammad Reza Ashrafi-Kooshk, et al.
Optics Express
|
July 21, 2015
Time-delay to intensity mapping based on a second-order optical integrator: application to optical arbitrary waveform generation
Reza Ashrafi, Mohammad Rezagholipour Dizaji, Luis Romero Cortés, et al.
Muscle & Nerve
|
September 21, 2016
Late-onset pompe disease in Iran: A clinical and genetic report
Ferdos Nazari, Farnaz Sinaei, Yalda Nilipour, et al.
Mitochondrion
|
July 12, 2021
Defective complex III mitochondrial respiratory chain due to a novel variant in CYC1 gene masquerades acute demyelinating syndrome or Leber hereditary optic neuropathy
Erfan Heidari, Maryam Rasoulinezhad, Neda Pak, et al.
Italian Journal of Pediatrics
|
June 6, 2023
Spinal Muscular Atrophy with Progressive Myoclonic Epilepsy (SMA-PME): three new cases and review of the mutational spectrum
Ali Najafi, Behnoosh Tasharrofi, Farshid Zandsalimi, et al.
Page
of 23