User profiles for Riad Bayoumi
Riad BayoumiProfessor, Mohammed Bin Rashid University; Dubai Healthcare City, Dubai, UAE. Verified email at dhcc.ae Cited by 5144 |
Mutations in INPP5E, encoding inositol polyphosphate-5-phosphatase E, link phosphatidyl inositol signaling to the ciliopathies
…, MV Kisseleva, L Al-Gazali, L Sztriha, RA Bayoumi… - Nature …, 2009 - nature.com
Phosphotidylinositol (PtdIns) signaling is tightly regulated both spatially and temporally by
subcellularly localized PtdIns kinases and phosphatases that dynamically alter downstream …
subcellularly localized PtdIns kinases and phosphatases that dynamically alter downstream …
Resistance to antifolates in Plasmodium falciparum monitored by sequence analysis of dihydropteroate synthetase and dihydrofolate reductase alleles in a large …
Resistance of Plasmodium falciparum to antifolate chemotherapy is a significant problem
where combinations such as Fansidar (pyrimethamine–sulfadoxine; PYR–SDX) are used in …
where combinations such as Fansidar (pyrimethamine–sulfadoxine; PYR–SDX) are used in …
Evaluation of methods of coenzyme activation of erythrocyte enzymes for detection of deficiency of vitamins B1, B2, and B6.
RA Bayoumi, SB Rosalki - Clinical chemistry, 1976 - academic.oup.com
We describe optimized, ultraviolet spectrophotometric procedures for determination of
erythrocyte transketolase, glutathione reductase, and aspartate aminotransferase activity, and …
erythrocyte transketolase, glutathione reductase, and aspartate aminotransferase activity, and …
[PDF][PDF] Mutations in DDHD2, encoding an intracellular phospholipase A1, cause a recessive form of complex hereditary spastic paraplegia
…, S Tariq, T Pramathan, R Bayoumi… - The American Journal of …, 2012 - cell.com
We report on four families affected by a clinical presentation of complex hereditary spastic
paraplegia (HSP) due to recessive mutations in DDHD2, encoding one of the three …
paraplegia (HSP) due to recessive mutations in DDHD2, encoding one of the three …
Digital codes from hypervariable tandemly repeated DNA sequences in the Plasmodium falciparum circumsporozoite gene can genetically barcode isolates
DE Arnot, C Roper, RAL Bayoumi - Molecular and Biochemical …, 1993 - Elsevier
DNA typing systems currently used in parasitology involve either hybridising Southern blots
with repetitive sequence probes or amplifying genomic sequences using the polymerase …
with repetitive sequence probes or amplifying genomic sequences using the polymerase …
[HTML][HTML] Genetic loci associated with heart rate variability and their effects on cardiac disease risk
Reduced cardiac vagal control reflected in low heart rate variability (HRV) is associated with
greater risks for cardiac morbidity and mortality. In two-stage meta-analyses of genome-…
greater risks for cardiac morbidity and mortality. In two-stage meta-analyses of genome-…
[HTML][HTML] Epidemiology of Diabetes Mellitus in Oman: Results from two decades of research
…, HJ Al-Lawati, RA Bayoumi - Sultan Qaboos …, 2015 - ncbi.nlm.nih.gov
Objectives: This study aimed to describe the epidemiology of diabetes mellitus over the past
two decades in Oman, particularly in terms of its prevalence and incidence. In addition, the …
two decades in Oman, particularly in terms of its prevalence and incidence. In addition, the …
[PDF][PDF] Homozygosity mapping in families with Joubert syndrome identifies a locus on chromosome 9q34. 3 and evidence for genetic heterogeneity
…, M Nur-E-Kamal, A Reis, R Bayoumi - The American Journal of …, 1999 - cell.com
Joubert syndrome is a rare developmental defect of the cerebellar vermis, with autosomal
recessive inheritance. The phenotype is highly variable and may include episodic hyperpnea, …
recessive inheritance. The phenotype is highly variable and may include episodic hyperpnea, …
Heritability of determinants of the metabolic syndrome among healthy Arabs of the Oman family study
RA Bayoumi, SAS Al‐Yahyaee, SA Albarwani… - …, 2007 - Wiley Online Library
The metabolic syndrome, as defined by the International Diabetes Federation, was investigated
in five large, extended, highly consanguineous, healthy Omani Arab families of a total of …
in five large, extended, highly consanguineous, healthy Omani Arab families of a total of …
[HTML][HTML] Association of gene variants with susceptibility to type 2 diabetes among Omanis
AIM: To investigate the association of 10 known common gene variants with susceptibility to
type 2 diabetes mellitus (T2D) among Omanis. METHODS: Using case-control design, a …
type 2 diabetes mellitus (T2D) among Omanis. METHODS: Using case-control design, a …