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Nuha Alrayes

Showing results (11-20 of 18) with videos related to

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Endocrinology, Diabetes & Metabolism|September 12, 2023
Association of a single nucleotide polymorphism in SOD2 with susceptibility for the development of diabetic nephropathy in patients with type 2 diabetes: A Saudi population studySamar Sultan, Meshari Alharbi, Nuha Alrayes, et al.
Journal of the Neurological Sciences|March 23, 2016
The alkylglycerol monooxygenase (AGMO) gene previously involved in autism also causes a novel syndromic form of primary microcephaly in a consanguineous Saudi familyNuha Alrayes, Hussein Sheikh Ali Mohamoud, Saleem Ahmed, et al.
Journal of the Neurological Sciences|May 10, 2015
Exome analysis identified a novel missense mutation in the CLPP gene in a consanguineous Saudi family expanding the clinical spectrum of Perrault Syndrome type-3Saleem Ahmed, Musharraf Jelani, Nuha Alrayes, et al.
Bioinformatics and Biology Insights|May 8, 2023
Potential Biomarkers for Parkinson Disease from Functional Enrichment and Bioinformatic Analysis of Global Gene Expression Patterns of Blood and Substantia Nigra TissuesRamu Elango, Babajan Banaganapalli, Abdulrahman Mujalli, et al.
Cureus|July 3, 2023
The Association of Sociodemographic Factors, Postictal Symptoms, and Medical History With Seizure Type in Patients With Epilepsy: A Cross-Sectional StudyReem Alyoubi, Summayah A Kobeisy, Mazen Basheikh, et al.
Molecular Genetics & Genomic Medicine|December 14, 2023
Quality of life in children with Down syndrome and its association with parent and child demographic characteristics: Parent-reported measuresNuha Alrayes, Noha M Issa, Omar Y Alghubayshi, et al.
Gene|September 26, 2022
Identification of a de novo LRP1 mutation in a Saudi family with Tetralogy of FallotNuha Alrayes, Bayan A Mallah, Noha M Issa, et al.
Frontiers in Medicine|May 22, 2023
Rare variant burden analysis from exomes of three consanguineous families reveals <i>LILRB1</i> and <i>PRSS3</i> as potential key proteins in inflammatory bowel disease pathogenesisRana Mohammed Jan, Huda Husain Al-Numan, Nada Hassan Al-Twaty, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Endocrinology, Diabetes & Metabolism|September 12, 2023
Association of a single nucleotide polymorphism in SOD2 with susceptibility for the development of diabetic nephropathy in patients with type 2 diabetes: A Saudi population studySamar Sultan, Meshari Alharbi, Nuha Alrayes, et al.
Journal of the Neurological Sciences|March 23, 2016
The alkylglycerol monooxygenase (AGMO) gene previously involved in autism also causes a novel syndromic form of primary microcephaly in a consanguineous Saudi familyNuha Alrayes, Hussein Sheikh Ali Mohamoud, Saleem Ahmed, et al.
Journal of the Neurological Sciences|May 10, 2015
Exome analysis identified a novel missense mutation in the CLPP gene in a consanguineous Saudi family expanding the clinical spectrum of Perrault Syndrome type-3Saleem Ahmed, Musharraf Jelani, Nuha Alrayes, et al.
Bioinformatics and Biology Insights|May 8, 2023
Potential Biomarkers for Parkinson Disease from Functional Enrichment and Bioinformatic Analysis of Global Gene Expression Patterns of Blood and Substantia Nigra TissuesRamu Elango, Babajan Banaganapalli, Abdulrahman Mujalli, et al.
Cureus|July 3, 2023
The Association of Sociodemographic Factors, Postictal Symptoms, and Medical History With Seizure Type in Patients With Epilepsy: A Cross-Sectional StudyReem Alyoubi, Summayah A Kobeisy, Mazen Basheikh, et al.
Molecular Genetics & Genomic Medicine|December 14, 2023
Quality of life in children with Down syndrome and its association with parent and child demographic characteristics: Parent-reported measuresNuha Alrayes, Noha M Issa, Omar Y Alghubayshi, et al.
Gene|September 26, 2022
Identification of a de novo LRP1 mutation in a Saudi family with Tetralogy of FallotNuha Alrayes, Bayan A Mallah, Noha M Issa, et al.
Frontiers in Medicine|May 22, 2023
Rare variant burden analysis from exomes of three consanguineous families reveals <i>LILRB1</i> and <i>PRSS3</i> as potential key proteins in inflammatory bowel disease pathogenesisRana Mohammed Jan, Huda Husain Al-Numan, Nada Hassan Al-Twaty, et al.
Pageof 2