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Bassam R Ali

Showing results (51-60 of 173) with videos related to

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The Journal of Biological Chemistry|November 23, 2006
Rab GTPases containing a CAAX motif are processed post-geranylgeranylation by proteolysis and methylationKa Fai Leung, Rudi Baron, Bassam R Ali, et al.
Annals of Human Genetics|October 24, 2008
R58fs mutation in the HGD gene in a family with alkaptonuria in the UAEYousef M Abdulrazzaq, Ahmed Ibrahim, Abdullah I Al-Khayat, et al.
Meta Gene|June 23, 2016
A novel de novo mutation in DYNC1H1 gene underlying malformation of cortical development and cataractJozef Hertecant, Makanko Komara, Aslam Nagi, et al.
American Journal of Medical Genetics. Part A|May 7, 2011
Is autosomal recessive Silver-Russel syndrome a separate entity or is it part of the 3-M syndrome spectrum?Nadia A Akawi, Bassam R Ali, Hanan Hamamy, et al.
Current Vascular Pharmacology|January 29, 2024
Utilizing Pharmacogenomic Data for a Safer Use of Statins among the Emirati PopulationMais N Alqasrawi, Zeina N Al-Mahayri, Hiba Alblooshi, et al.
FEBS Open Bio|October 7, 2019
Endoplasmic reticulum quality control of LDLR variants associated with familial hypercholesterolemiaPraseetha Kizhakkedath, Anne John, Buthaina K Al-Sawafi, et al.
Biochemical and Biophysical Research Communications|May 18, 2010
A novel statin-mediated "prenylation block-and-release" assay provides insight into the membrane targeting mechanisms of small GTPasesBassam R Ali, Ian Nouvel, Ka Fai Leung, et al.
Human Molecular Genetics|July 29, 2005
ER-associated protein degradation is a common mechanism underpinning numerous monogenic diseases including Robinow syndromeYing Chen, William P Bellamy, Miguel C Seabra, et al.
Child Neurology Open|November 26, 2019
A Novel SLC1A4 Mutation (p.Y191*) Causes Spastic Tetraplegia, Thin Corpus Callosum, and Progressive Microcephaly (SPATCCM) With Seizure DisorderHanadi A Abdelrahman, Aisha Al-Shamsi, Anne John, et al.
Orphanet Journal of Rare Diseases|May 17, 2012
A mutation in KIF7 is responsible for the autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia and distinctive facial appearanceBassam R Ali, Jennifer L Silhavy, Nadia A Akawi, et al.
Pageof 18

Showing results (51-60 of 173) with videos related to

Sort By:
Pageof 18
The Journal of Biological Chemistry|November 23, 2006
Rab GTPases containing a CAAX motif are processed post-geranylgeranylation by proteolysis and methylationKa Fai Leung, Rudi Baron, Bassam R Ali, et al.
Annals of Human Genetics|October 24, 2008
R58fs mutation in the HGD gene in a family with alkaptonuria in the UAEYousef M Abdulrazzaq, Ahmed Ibrahim, Abdullah I Al-Khayat, et al.
Meta Gene|June 23, 2016
A novel de novo mutation in DYNC1H1 gene underlying malformation of cortical development and cataractJozef Hertecant, Makanko Komara, Aslam Nagi, et al.
American Journal of Medical Genetics. Part A|May 7, 2011
Is autosomal recessive Silver-Russel syndrome a separate entity or is it part of the 3-M syndrome spectrum?Nadia A Akawi, Bassam R Ali, Hanan Hamamy, et al.
Current Vascular Pharmacology|January 29, 2024
Utilizing Pharmacogenomic Data for a Safer Use of Statins among the Emirati PopulationMais N Alqasrawi, Zeina N Al-Mahayri, Hiba Alblooshi, et al.
FEBS Open Bio|October 7, 2019
Endoplasmic reticulum quality control of LDLR variants associated with familial hypercholesterolemiaPraseetha Kizhakkedath, Anne John, Buthaina K Al-Sawafi, et al.
Biochemical and Biophysical Research Communications|May 18, 2010
A novel statin-mediated "prenylation block-and-release" assay provides insight into the membrane targeting mechanisms of small GTPasesBassam R Ali, Ian Nouvel, Ka Fai Leung, et al.
Human Molecular Genetics|July 29, 2005
ER-associated protein degradation is a common mechanism underpinning numerous monogenic diseases including Robinow syndromeYing Chen, William P Bellamy, Miguel C Seabra, et al.
Child Neurology Open|November 26, 2019
A Novel SLC1A4 Mutation (p.Y191*) Causes Spastic Tetraplegia, Thin Corpus Callosum, and Progressive Microcephaly (SPATCCM) With Seizure DisorderHanadi A Abdelrahman, Aisha Al-Shamsi, Anne John, et al.
Orphanet Journal of Rare Diseases|May 17, 2012
A mutation in KIF7 is responsible for the autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia and distinctive facial appearanceBassam R Ali, Jennifer L Silhavy, Nadia A Akawi, et al.
Pageof 18