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N Mohammed

Showing results (241-250 of 255) with videos related to

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Nature|June 26, 1997
Congenital leptin deficiency is associated with severe early-onset obesity in humansC T Montague, I S Farooqi, J P Whitehead, et al.
Heliyon|May 22, 2024
Establishment of reference values based on influential characteristics of hematopoietic stem cells and immune cell subsets in the bone marrowRebar N Mohammed, Najmaddin S H Khoshnaw, Vian Faeq Mohammed, et al.
Annals of Neurology|December 26, 2015
A Novel Nonsense Mutation in DNAJC6 Expands the Phenotype of Autosomal-Recessive Juvenile-Onset Parkinson's DiseaseLiena Elbaghir Omer Elsayed, Valérie Drouet, Tatiana Usenko, et al.
Journal of Human Genetics|September 10, 2021
Novel variants causing megalencephalic leukodystrophy in Sudanese familiesMutaz Amin, Cedric Vignal, Ahlam A A Hamed, et al.
Frontiers in Genetics|June 20, 2022
Case Report: A New Family With Pontocerebellar Hypoplasia 10 From SudanMutaz Amin, Cedric Vignal, Ahlam A A Hamed, et al.
Annals of Human Genetics|June 10, 2021
An identical-by-descent novel splice-donor variant in PRUNE1 causes a neurodevelopmental syndrome with prominent dystonia in two consanguineous Sudanese familiesMahmoud Koko, Ashraf Yahia, Liena E Elsayed, et al.
Scientific Reports|April 4, 2019
ADAM17-dependent proteolysis of L-selectin promotes early clonal expansion of cytotoxic T cellsRebar N Mohammed, Sophie C Wehenkel, Elena V Galkina, et al.
Annals of Human Genetics|February 4, 2022
Genetic diagnosis in Sudanese and Tunisian families with syndromic intellectual disability through exome sequencingAshraf Yahia, Ikhlas Ben Ayed, Ahlam A Hamed, et al.
American Journal of Medical Genetics. Part A|October 13, 2006
Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformationNathaniel H Robin, Clare J Taylor, Donna M McDonald-McGinn, et al.
Nature Genetics|January 29, 2013
Reduced dosage of ERF causes complex craniosynostosis in humans and mice and links ERK1/2 signaling to regulation of osteogenesisStephen R F Twigg, Elena Vorgia, Simon J McGowan, et al.
Pageof 26

Showing results (241-250 of 255) with videos related to

Sort By:
Pageof 26
Nature|June 26, 1997
Congenital leptin deficiency is associated with severe early-onset obesity in humansC T Montague, I S Farooqi, J P Whitehead, et al.
Heliyon|May 22, 2024
Establishment of reference values based on influential characteristics of hematopoietic stem cells and immune cell subsets in the bone marrowRebar N Mohammed, Najmaddin S H Khoshnaw, Vian Faeq Mohammed, et al.
Annals of Neurology|December 26, 2015
A Novel Nonsense Mutation in DNAJC6 Expands the Phenotype of Autosomal-Recessive Juvenile-Onset Parkinson's DiseaseLiena Elbaghir Omer Elsayed, Valérie Drouet, Tatiana Usenko, et al.
Journal of Human Genetics|September 10, 2021
Novel variants causing megalencephalic leukodystrophy in Sudanese familiesMutaz Amin, Cedric Vignal, Ahlam A A Hamed, et al.
Frontiers in Genetics|June 20, 2022
Case Report: A New Family With Pontocerebellar Hypoplasia 10 From SudanMutaz Amin, Cedric Vignal, Ahlam A A Hamed, et al.
Annals of Human Genetics|June 10, 2021
An identical-by-descent novel splice-donor variant in PRUNE1 causes a neurodevelopmental syndrome with prominent dystonia in two consanguineous Sudanese familiesMahmoud Koko, Ashraf Yahia, Liena E Elsayed, et al.
Scientific Reports|April 4, 2019
ADAM17-dependent proteolysis of L-selectin promotes early clonal expansion of cytotoxic T cellsRebar N Mohammed, Sophie C Wehenkel, Elena V Galkina, et al.
Annals of Human Genetics|February 4, 2022
Genetic diagnosis in Sudanese and Tunisian families with syndromic intellectual disability through exome sequencingAshraf Yahia, Ikhlas Ben Ayed, Ahlam A Hamed, et al.
American Journal of Medical Genetics. Part A|October 13, 2006
Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformationNathaniel H Robin, Clare J Taylor, Donna M McDonald-McGinn, et al.
Nature Genetics|January 29, 2013
Reduced dosage of ERF causes complex craniosynostosis in humans and mice and links ERK1/2 signaling to regulation of osteogenesisStephen R F Twigg, Elena Vorgia, Simon J McGowan, et al.
Pageof 26