Search Results - "Anoop, Emil"

Single nucleotide polymorphisms in vitamin D binding protein and 25-hydroxylase genes affect vitamin D levels in adolescents of Arab ethnicity in Kuwait by Rahman, Abdur, Abu-Farha, Mohamed, Channanath, Arshad, Hammad, Maha M., Anoop, Emil, Chandy, Betty, Melhem, Motasem, Al-Mulla, Fahd, Thanaraj, Thangavel Alphonse, Abubaker, Jehad

“…Vitamin D deficiency (VDD) is widespread in the Arab world despite ample sunshine throughout the year. In our previous study, lifestyle and socio-demographic…”
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The miR-668 binding site variant rs1046322 on WFS1 is associated with obesity in Southeast Asians by Hammad, Maha M., Abu-Farha, Mohamed, Hebbar, Prashantha, Anoop, Emil, Chandy, Betty, Melhem, Motasem, Channanath, Arshad, Al-Mulla, Fahd, Thanaraj, Thangavel Alphonse, Abubaker, Jehad

“…The Wolfram syndrome 1 gene ( WFS1) is the main causative locus for Wolfram syndrome, an inherited condition characterized by childhood-onset diabetes…”
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ANGPTL3 Variants Associate with Lower Levels of Irisin and C-Peptide in a Cohort of Arab Individuals by Alanbaei, Muath, Abu-Farha, Mohamed, Hebbar, Prashantha, Melhem, Motasem, Chandy, Betty S., Anoop, Emil, Cherian, Preethi, Al-Khairi, Irina, Alkayal, Fadi, Al-Mulla, Fahd, Abubaker, Jehad, Thanaraj, Thangavel Alphonse

“…ANGPTL3 is an important regulator of lipid metabolism. Its inhibition in people with hypercholesteremia reduces plasma lipid levels dramatically. Genome-wide…”
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