Samir S. Deeb mainly investigates Internal medicine, Endocrinology, Genetics, Gene and Molecular biology. His study in Internal medicine is interdisciplinary in nature, drawing from both Diabetes mellitus and Type 2 diabetes. His Endocrinology research is multidisciplinary, relying on both Peroxisome proliferator-activated receptor and Polymorphism.
His Genetics study integrates concerns from other disciplines, such as Color Vision Defects, Opsin and Photopigment. His Gene research entails a greater understanding of Biochemistry. His studies in Molecular biology integrate themes in fields like Lipoprotein lipase, Cellular differentiation, Messenger RNA, Exon and Regulation of gene expression.
His main research concerns Genetics, Internal medicine, Endocrinology, Gene and Molecular biology. The various areas that Samir S. Deeb examines in his Genetics study include Color vision and Color Vision Defects. His Internal medicine research integrates issues from Diabetes mellitus, Promoter and Polymorphism.
His Endocrinology study frequently intersects with other fields, such as Genotype. Samir S. Deeb has included themes like Hexokinase and DNA in his Gene study. His Molecular biology research incorporates elements of Enhancer, Gene expression, Lipoprotein lipase, Cellular differentiation and Complementary DNA.
Samir S. Deeb mostly deals with Gene, Genetics, Internal medicine, Endocrinology and Artificial intelligence. His Gene study frequently draws connections to adjacent fields such as Molecular biology. His Molecular biology research incorporates themes from Oxidative stress, Cell and Phospholipid.
His Gene duplication, Mutation, Allele and Compound heterozygosity study in the realm of Genetics interacts with subjects such as Platypus. He usually deals with Internal medicine and limits it to topics linked to Type 1 diabetes and Risk factor, Glycated hemoglobin and Randomized controlled trial. Samir S. Deeb performs multidisciplinary study in Endocrinology and Lipodystrophy in his work.
His primary areas of study are Genetics, Gene, Internal medicine, Hepatic lipase and Single-nucleotide polymorphism. His work on Exon, Compound heterozygosity and Mutation as part of general Genetics research is frequently linked to Thyroid hormone receptor beta, thereby connecting diverse disciplines of science. When carried out as part of a general Gene research project, his work on Microarray is frequently linked to work in ARR3, therefore connecting diverse disciplines of study.
His research on Internal medicine often connects related areas such as Endocrinology. His Hepatic lipase research is multidisciplinary, incorporating perspectives in Hypertriglyceridemia, Glycerol, Chromatography and Reverse cholesterol transport. He has researched Single-nucleotide polymorphism in several fields, including Age of onset, Allele, Locus and Heritability.
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A Pro12Ala substitution in PPARgamma2 associated with decreased receptor activity, lower body mass index and improved insulin sensitivity.
Samir S. Deeb;Lluis Fajas;Masami Nemoto;Jussi Pihlajamäki.
Nature Genetics (1998)
The organization, promoter analysis, and expression of the human PPARgamma gene.
Lluis Fajas;Didier Auboeuf;Eric Raspé;Kristina Schoonjans.
Journal of Biological Chemistry (1997)
Impaired expression of peroxisome proliferator-activated receptor γ in ulcerative colitis
Laurent Dubuquoy;Emmelie Å Jansson;Samir Deeb;Sabine Rakotobe.
Prolonged effect of intensive therapy on the risk of retinopathy complications in patients with type 1 diabetes mellitus: 10 years after the diabetes control and complications trial
Neil H. White;Wanjie Sun;Patricia A. Cleary;Ronald P. Danis.
Archives of Ophthalmology (2008)
Two polymorphisms in the peroxisome proliferator-activated receptor-gamma gene are associated with severe overweight among obese women.
R. Valve;K. Sivenius;R. Miettinen;J. Pihlajamäki.
The Journal of Clinical Endocrinology and Metabolism (1999)
Absence of linkage of chromosome 21q21 markers to familial Alzheimer's disease
Gerard D. Schellenberg;Thomas D. Bird;Ellen M. Wijsman;Deborah K. Moore.
Elimination of Cholesterol in Macrophages and Endothelial Cells by the Sterol 27-Hydroxylase Mechanism COMPARISON WITH HIGH DENSITY LIPOPROTEIN-MEDIATED REVERSE CHOLESTEROL TRANSPORT
Amir Babiker;Olof Andersson;Erik Lund;Rui-Juan Xiu.
Journal of Biological Chemistry (1997)
Polymorphism in red photopigment underlies variation in colour matching
Joris Winderickx;Delwin T. Lindsey;Elizabeth Sanocki;Davida Y. Teller.
Structure of the human lipoprotein lipase gene.
Samir S. Deeb;Reiling Peng.
Common Variants in the Promoter of the Hepatic Lipase Gene Are Associated With Lower Levels of Hepatic Lipase Activity, Buoyant LDL, and Higher HDL2 Cholesterol
Zambon A;Deeb Ss;Hokanson Je;Brown Bg.
Arteriosclerosis, Thrombosis, and Vascular Biology (1998)
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