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Bassam R Ali

Showing results (71-80 of 173) with videos related to

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Genes|March 28, 2024
Novel Pathogenic Variants Leading to Sporadic Amyotrophic Lateral Sclerosis in Greek PatientsOuliana Ivantsik, Anne John, Kyriaki Kydonopoulou, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|June 22, 2022
Congenital Teratocarcinosarcoma With <i>CTNNB1</i> Gene Mutation Presenting as an Ocular MassSaeeda Almarzooqi, Miguel Reyes-Múgica, Bassam R Ali, et al.
Human Genome Variation|April 16, 2016
Mutation spectrum of Joubert syndrome and related disorders among ArabsSalma Ben-Salem, Aisha M Al-Shamsi, Joseph G Gleeson, et al.
Human Genome Variation|April 16, 2016
Erratum: Mutation spectrum of Joubert syndrome and related disorders among ArabsSalma Ben-Salem, Aisha M Al-Shamsi, Joseph G Gleeson, et al.
Orphanet Journal of Rare Diseases|June 19, 2013
LINS, a modulator of the WNT signaling pathway, is involved in human cognitionNadia A Akawi, Fatma Al-Jasmi, Aisha M Al-Shamsi, et al.
Bone|December 2, 2015
FGF23-S129F mutant bypasses ER/Golgi to the circulation of hyperphosphatemic familial tumoral calcinosis patientsSaid M Shawar, Ahmad R Ramadan, Bassam R Ali, et al.
Gene|August 13, 2013
Determination of the CCR5∆32 frequency in Emiratis and Tunisians and the screening of the CCR5 gene for novel alleles in EmiratisSara A Al-Jaberi, Salma Ben-Salem, Meriam Messedi, et al.
Public Health Genomics|March 17, 2021
Stakeholders' Interest and Attitudes toward Genomic Medicine and Pharmacogenomics Implementation in the United Arab Emirates: A Qualitative StudyAzhar T Rahma, Iffat Elbarazi, Bassam R Ali, et al.
Journal of Personalized Medicine|September 23, 2020
Genomics and Pharmacogenomics Knowledge, Attitude and Practice of Pharmacists Working in United Arab Emirates: Findings from Focus Group Discussions-A Qualitative StudyAzhar T Rahma, Iffat Elbarazi, Bassam R Ali, et al.
Annals of Human Genetics|June 28, 2017
Studies on N-Acetyltransferase (NAT2) Genotype Relationships in Emiratis: Confirmation of the Existence of Phenotype Variation among Slow AcetylatorsMohammad M Al-Ahmad, Naheed Amir, Subramanian Dhanasekaran, et al.
Pageof 18

Showing results (71-80 of 173) with videos related to

Sort By:
Pageof 18
Genes|March 28, 2024
Novel Pathogenic Variants Leading to Sporadic Amyotrophic Lateral Sclerosis in Greek PatientsOuliana Ivantsik, Anne John, Kyriaki Kydonopoulou, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|June 22, 2022
Congenital Teratocarcinosarcoma With <i>CTNNB1</i> Gene Mutation Presenting as an Ocular MassSaeeda Almarzooqi, Miguel Reyes-Múgica, Bassam R Ali, et al.
Human Genome Variation|April 16, 2016
Mutation spectrum of Joubert syndrome and related disorders among ArabsSalma Ben-Salem, Aisha M Al-Shamsi, Joseph G Gleeson, et al.
Human Genome Variation|April 16, 2016
Erratum: Mutation spectrum of Joubert syndrome and related disorders among ArabsSalma Ben-Salem, Aisha M Al-Shamsi, Joseph G Gleeson, et al.
Orphanet Journal of Rare Diseases|June 19, 2013
LINS, a modulator of the WNT signaling pathway, is involved in human cognitionNadia A Akawi, Fatma Al-Jasmi, Aisha M Al-Shamsi, et al.
Bone|December 2, 2015
FGF23-S129F mutant bypasses ER/Golgi to the circulation of hyperphosphatemic familial tumoral calcinosis patientsSaid M Shawar, Ahmad R Ramadan, Bassam R Ali, et al.
Gene|August 13, 2013
Determination of the CCR5∆32 frequency in Emiratis and Tunisians and the screening of the CCR5 gene for novel alleles in EmiratisSara A Al-Jaberi, Salma Ben-Salem, Meriam Messedi, et al.
Public Health Genomics|March 17, 2021
Stakeholders' Interest and Attitudes toward Genomic Medicine and Pharmacogenomics Implementation in the United Arab Emirates: A Qualitative StudyAzhar T Rahma, Iffat Elbarazi, Bassam R Ali, et al.
Journal of Personalized Medicine|September 23, 2020
Genomics and Pharmacogenomics Knowledge, Attitude and Practice of Pharmacists Working in United Arab Emirates: Findings from Focus Group Discussions-A Qualitative StudyAzhar T Rahma, Iffat Elbarazi, Bassam R Ali, et al.
Annals of Human Genetics|June 28, 2017
Studies on N-Acetyltransferase (NAT2) Genotype Relationships in Emiratis: Confirmation of the Existence of Phenotype Variation among Slow AcetylatorsMohammad M Al-Ahmad, Naheed Amir, Subramanian Dhanasekaran, et al.
Pageof 18