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A Hamed

Showing results (511-520 of 637) with videos related to

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BMC Medical Genetics|May 10, 2018
Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese familyLiena E O Elsayed, Inaam N Mohammed, Ahlam A A Hamed, et al.
BMC Medical Genomics|November 9, 2022
A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disabilityMutaz Amin, Cedric Vignal, Esraa Eltaraifee, et al.
Plants (Basel, Switzerland)|July 27, 2022
LC/MS Profiling and Gold Nanoparticle Formulation of Major Metabolites from <i>Origanum majorana</i> as Antibacterial and Antioxidant PotentialitiesAhmed H El-Ghorab, Fathy A Behery, Mohamed A Abdelgawad, et al.
Plants (Basel, Switzerland)|December 11, 2022
Anticholinesterase Activity of Budmunchiamine Alkaloids Revealed by Comparative Chemical Profiling of Two <i>Albizia</i> spp., Molecular Docking and Dynamic StudiesMai E Hussein, Osama G Mohamed, Ahlam M El-Fishawy, et al.
Neuropsychiatric Disease and Treatment|June 8, 2013
Door-to-door survey of major neurological disorders (project) in Al Quseir City, Red Sea Governorate, EgyptHamdy Na El Tallawy, Wafaa Ma Farghaly, Tarek A Rageh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 29, 2020
A genomics approach to male infertilityNaif Alhathal, Sateesh Maddirevula, Serdar Coskun, et al.
Frontiers in Neurology|November 16, 2020
Novel Homozygous Missense Mutation in the <i>ARG1</i> Gene in a Large Sudanese FamilyLiena E O Elsayed, Inaam N Mohammed, Ahlam A A Hamed, et al.
Neurogenetics|July 27, 2024
A novel missense variant in the ATPase domain of ATP8A2 and review of phenotypic variability of ATP8A2-related disorders caused by missense changesKyle P Flannery, Sylvia Safwat, Eli Matsell, et al.
Archiv Der Pharmazie|November 20, 2022
Discovery of oxindole-based FLT3 inhibitors as a promising therapeutic lead for acute myeloid leukemia carrying the oncogenic ITD mutationOnur Bender, Mai E Shoman, Taha F S Ali, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|March 5, 2022
Glutamine restores testicular glutathione-dependent antioxidant defense and upregulates NO/cGMP signaling in sleep deprivation-induced reproductive dysfunction in ratsM A Hamed, T M Akhigbe, R E Akhigbe, et al.
Pageof 64

Showing results (511-520 of 637) with videos related to

Sort By:
Pageof 64
BMC Medical Genetics|May 10, 2018
Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese familyLiena E O Elsayed, Inaam N Mohammed, Ahlam A A Hamed, et al.
BMC Medical Genomics|November 9, 2022
A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disabilityMutaz Amin, Cedric Vignal, Esraa Eltaraifee, et al.
Plants (Basel, Switzerland)|July 27, 2022
LC/MS Profiling and Gold Nanoparticle Formulation of Major Metabolites from <i>Origanum majorana</i> as Antibacterial and Antioxidant PotentialitiesAhmed H El-Ghorab, Fathy A Behery, Mohamed A Abdelgawad, et al.
Plants (Basel, Switzerland)|December 11, 2022
Anticholinesterase Activity of Budmunchiamine Alkaloids Revealed by Comparative Chemical Profiling of Two <i>Albizia</i> spp., Molecular Docking and Dynamic StudiesMai E Hussein, Osama G Mohamed, Ahlam M El-Fishawy, et al.
Neuropsychiatric Disease and Treatment|June 8, 2013
Door-to-door survey of major neurological disorders (project) in Al Quseir City, Red Sea Governorate, EgyptHamdy Na El Tallawy, Wafaa Ma Farghaly, Tarek A Rageh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 29, 2020
A genomics approach to male infertilityNaif Alhathal, Sateesh Maddirevula, Serdar Coskun, et al.
Frontiers in Neurology|November 16, 2020
Novel Homozygous Missense Mutation in the <i>ARG1</i> Gene in a Large Sudanese FamilyLiena E O Elsayed, Inaam N Mohammed, Ahlam A A Hamed, et al.
Neurogenetics|July 27, 2024
A novel missense variant in the ATPase domain of ATP8A2 and review of phenotypic variability of ATP8A2-related disorders caused by missense changesKyle P Flannery, Sylvia Safwat, Eli Matsell, et al.
Archiv Der Pharmazie|November 20, 2022
Discovery of oxindole-based FLT3 inhibitors as a promising therapeutic lead for acute myeloid leukemia carrying the oncogenic ITD mutationOnur Bender, Mai E Shoman, Taha F S Ali, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|March 5, 2022
Glutamine restores testicular glutathione-dependent antioxidant defense and upregulates NO/cGMP signaling in sleep deprivation-induced reproductive dysfunction in ratsM A Hamed, T M Akhigbe, R E Akhigbe, et al.
Pageof 64