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Your search keyword '"Motasem, Melhem"' showing total 43 results

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1. The miR-668 binding site variant rs1046322 on WFS1 is associated with obesity in Southeast Asians

2. Single nucleotide polymorphisms in vitamin D binding protein and 25-hydroxylase genes affect vitamin D levels in adolescents of Arab ethnicity in Kuwait

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3. ONECUT1 variants beyond type 1 and type 2 diabetes: exploring clinical diversity and epigenetic associations in Arab cohorts

4. Caveolin-1 rs1997623 variant and adult metabolic syndrome—Assessing the association in three ethnic cohorts of Arabs, South Asians and South East Asians

5. Identification of Maturity-Onset-Diabetes of the Young (MODY) mutations in a country where diabetes is endemic

6. Ceramide kinase regulates TNF-α-induced immune responses in human monocytic cells

7. Delineation of Mitochondrial DNA Variants From Exome Sequencing Data and Association of Haplogroups With Obesity in Kuwait

8. MC4R Variant rs17782313 Associates With Increased Levels of DNAJC27, Ghrelin, and Visfatin and Correlates With Obesity and Hypertension in a Kuwaiti Cohort

9. Genome-wide association study identifies novel recessive genetic variants for high TGs in an Arab population

10. Investigation of genetic variation and lifestyle determinants in vitamin D levels in Arab individuals

11. FTO Variant rs1421085 Associates With Increased Body Weight, Soft Lean Mass, and Total Body Water Through Interaction With Ghrelin and Apolipoproteins in Arab Population

12. Increased Plasma Levels of Adenylate Cyclase 8 and cAMP Are Associated with Obesity and Type 2 Diabetes: Results from a Cross-Sectional Study

13. Increased Expression of Meteorin-Like Hormone in Type 2 Diabetes and Obesity and Its Association with Irisin

14. Neutral sphingomyelinase 2 regulates inflammatory responses in monocytes/macrophages induced by TNF-α

15. Ketogenic diet attenuates cerebellar atrophy progression in a subject with a biallelic variant at the ATAD3A locus

16. Mitochondrial DNA D-loop sequencing reveals obesity variants in an Arab population

17. ANGPTL3 Variants Associate with Lower Levels of Irisin and C-Peptide in a Cohort of Arab Individuals

18. GALNT2 rs4846914 SNP Is Associated with Obesity, Atherogenic Lipid Traits, and ANGPTL3 Plasma Level

19. Vitamin D insufficiency in Arabs and South Asians positively associates with polymorphisms in GC and CYP2R1 genes.

20. Interaction of osteopontin with IL-18 in obese individuals: implications for insulin resistance.

21. Delineation of Mitochondrial DNA Variants From Exome Sequencing Data and Association of Haplogroups With Obesity in Kuwait

22. Comparative Proteomic Analysis Identifies EphA2 as a Specific Cell Surface Marker for Wharton’s Jelly-Derived Mesenchymal Stem Cells

23. Increased Plasma Levels of Adenylate Cyclase 8 and cAMP Are Associated with Obesity and Type 2 Diabetes: Results from a Cross-Sectional Study

25. TheTCN2variant of rs9606756 [Ile23Val] acts as risk loci for obesity-related traits and mediates by interacting with Apo-A1

26. Genome-wide association study identifies novel risk variants from RPS6KA1, CADPS, VARS, and DHX58 for fasting plasma glucose in Arab population

27. Ketogenic diet attenuates cerebellar atrophy progression in a subject with a biallelic variant at the ATAD3A locus [Response to Letter]

28. Novel G6B gene variant causes familial autosomal recessive thrombocytopenia and anemia

29. Hereditary angioedema in a Jordanian family with a novel missense mutation in the C1-inhibitor N-terminal domain

30. Neutral sphingomyelinase 2 regulates inflammatory responses in monocytes/macrophages induced by TNF-α

31. Mitochondrial DNA D-loop sequencing reveals obesity variants in an Arab population

33. Investigation of genetic variation and lifestyle determinants in vitamin D levels in Arab individuals

34. Genome-wide association study identifies novel recessive genetic variants for high TGs in an Arab population

35. ND4L gene concurrent 10609T>C and 10663T>C mutations are associated with Leber's hereditary optic neuropathy in a large pedigree from Kuwait

36. Exome sequencing for the differential diagnosis of ciliary chondrodysplasias: Example of a WDR35 mutation case and review of the literature

37. Major Histocompatibility Complex Class II Deficiency in Kuwait: Clinical Manifestations, Immunological Findings and Molecular Profile

38. ANGPTL8/Betatrophin R59W variant is associated with higher glucose level in non-diabetic Arabs living in Kuwaits

39. Leptin in association with common variants of MC3R mediates hypertension

40. Interaction of osteopontin with IL-18 in obese individuals: implications for insulin resistance

41. Abstract # P-29: Gwa Study from Kuwait Highlights Junk DNA as a Potential Hotspot in Hypertension Research

42. Abstract # OR-12: Unraveling Kuwait-Specific Metabolic Gene Regulatory and Coding Variants: A Step Towards Bilding a National Exome Database

43. Response to Leptin and Nitric Oxide in Blood Pressure Regulation in Humans