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N Mohammed

Showing results (231-240 of 255) with videos related to

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Cell Communication and Signaling : CCS|April 8, 2022
Tumor immunotherapies by immune checkpoint inhibitors (ICIs); the pros and consAdel Naimi, Rebar N Mohammed, Ahmed Raji, et al.
Biotechnology and Applied Biochemistry|March 31, 2021
Under hypoxic conditions, MSCs affect the expression and methylation level of survival-related genes in ALL independent of apoptosis pathways in vitroFaroogh Marofi, Navid Shomali, Laith A Younus, et al.
IJTLD Open|July 11, 2024
Non-communicable airway disease and air pollution in three African Countries: Benin, Cameroon and The GambiaB Awokola, H Lawin, O Johnson, et al.
Biorxiv : the Preprint Server for Biology|January 7, 2025
A gated hydrophobic funnel within BAX binds long-chain alkenals to potentiate pro-apoptotic functionJesse D Gelles, Yiyang Chen, Mark P A Luna-Vargas, et al.
Infection and Drug Resistance|February 19, 2021
Detection of gyrA and parC Mutations and Prevalence of Plasmid-Mediated Quinolone Resistance Genes in <i>Klebsiella pneumoniae</i>Sawsan Mohammed Kareem, Israa M S Al-Kadmy, Saba S Kazaal, et al.
Nature Communications|February 25, 2026
A gated hydrophobic funnel within BAX binds bioactive lipids to potentiate pro-apoptotic functionJesse D Gelles, Yiyang Chen, Mark P A Luna-Vargas, et al.
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.
Molecular Cell|March 19, 2019
MDM2 Integrates Cellular Respiration and Apoptotic Signaling through NDUFS1 and the Mitochondrial NetworkRana Elkholi, Ioana Abraham-Enachescu, Andrew P Trotta, 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.
Pageof 26

Showing results (231-240 of 255) with videos related to

Sort By:
Pageof 26
Cell Communication and Signaling : CCS|April 8, 2022
Tumor immunotherapies by immune checkpoint inhibitors (ICIs); the pros and consAdel Naimi, Rebar N Mohammed, Ahmed Raji, et al.
Biotechnology and Applied Biochemistry|March 31, 2021
Under hypoxic conditions, MSCs affect the expression and methylation level of survival-related genes in ALL independent of apoptosis pathways in vitroFaroogh Marofi, Navid Shomali, Laith A Younus, et al.
IJTLD Open|July 11, 2024
Non-communicable airway disease and air pollution in three African Countries: Benin, Cameroon and The GambiaB Awokola, H Lawin, O Johnson, et al.
Biorxiv : the Preprint Server for Biology|January 7, 2025
A gated hydrophobic funnel within BAX binds long-chain alkenals to potentiate pro-apoptotic functionJesse D Gelles, Yiyang Chen, Mark P A Luna-Vargas, et al.
Infection and Drug Resistance|February 19, 2021
Detection of gyrA and parC Mutations and Prevalence of Plasmid-Mediated Quinolone Resistance Genes in <i>Klebsiella pneumoniae</i>Sawsan Mohammed Kareem, Israa M S Al-Kadmy, Saba S Kazaal, et al.
Nature Communications|February 25, 2026
A gated hydrophobic funnel within BAX binds bioactive lipids to potentiate pro-apoptotic functionJesse D Gelles, Yiyang Chen, Mark P A Luna-Vargas, et al.
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.
Molecular Cell|March 19, 2019
MDM2 Integrates Cellular Respiration and Apoptotic Signaling through NDUFS1 and the Mitochondrial NetworkRana Elkholi, Ioana Abraham-Enachescu, Andrew P Trotta, 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.
Pageof 26