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المصدر: Leiherer, Andreas; Muendlein, Axel; Saely, Christoph H; Fraunberger, Peter; Drexel, Heinz (2019). Serotonin is elevated in risk-genotype carriers of TCF7L2-rs7903146. Scientific reports, 9(1), p. 12863. Springer Nature 10.1038/s41598-019-49347-y <http://dx.doi.org/10.1038/s41598-019-49347-yTest>
Scientific Reports, Vol 9, Iss 1, Pp 1-10 (2019)
Scientific Reportsمصطلحات موضوعية: Male, 0301 basic medicine, Linkage disequilibrium, endocrine system diseases, Metabolite, lcsh:Medicine, Type 2 diabetes, Linkage Disequilibrium, chemistry.chemical_compound, 0302 clinical medicine, Genotype, lcsh:Science, 610 Medicine & health, Multidisciplinary, Genomics, Middle Aged, Female, Transcription Factor 7-Like 2 Protein, Serotonin, medicine.medical_specialty, Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, Internal medicine, Diabetes mellitus, Transcription factors, medicine, Metabolomics, Humans, Allele, Alleles, Aged, business.industry, lcsh:R, nutritional and metabolic diseases, medicine.disease, 030104 developmental biology, Endocrinology, Risk factors, Diabetes Mellitus, Type 2, chemistry, lcsh:Q, business, TCF7L2, 030217 neurology & neurosurgery, Genome-Wide Association Study
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cf9e4e049bf2c1931ed1e2a3ba392b6Test
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المؤلفون: Takehiro Wakasugi, Hideyuki Ishiguro, Hiromitsu Takeyama, Nobuhiro Sakamoto, Hiroyuki Sagawa, Tatsuya Tanaka, Tomotaka Okubo, Yukio Terashita
المصدر: Cellular & Molecular Biology Letters
مصطلحات موضوعية: Male, 0301 basic medicine, medicine.medical_specialty, endocrine system, Esophageal Neoplasms, endocrine system diseases, Short Communication, Esophageal cancer, Wnt signal, Gastroenterology, Biochemistry, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, TCF4/TCF7L2, Humans, Clinicopathological factor, Medicine, Stage (cooking), Survival rate, Transcription factor, Molecular Biology, Aged, Cell Nucleus, business.industry, nutritional and metabolic diseases, TCF4, Cell Biology, Middle Aged, Prognosis, medicine.disease, Immunohistochemistry, Molecular medicine, Gene Expression Regulation, Neoplastic, 030104 developmental biology, 030220 oncology & carcinogenesis, Carcinoma, Squamous Cell, Cancer research, Female, Surgery, Esophageal Squamous Cell Carcinoma, business, Transcription Factor 7-Like 2 Protein, TCF7L2
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1525f77140abb6753ae8f9401f985c6Test
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3The TCF7L2rs7903146 polymorphism, dietary intakes and type 2 diabetes risk in an Algerian population
المؤلفون: Hadjira Ouhaibi-Djellouli, Leila Houti, Sarah Aïcha Lardjam-Hetraf, Xavier Hermant, Louisa Goumidi, Nadhira Saidi-Mehtar, Sounnia Mediene-Benchekor, Aline Meirhaeghe, I. Hamani-Medjaoui, Djabaria Naïma Meroufel, Houssam Boulenouar, Philippe Amouyel
المساهمون: Taibi, Nadia, Laboratoire de Génétique Moléculaire et Cellulaire, Université des sciences et de la Technologie d'Oran Mohamed Boudiaf [Oran] (USTO MB), Département de Biotechnologie, Faculté des Sciences de la Nature et de la Vie, Université d ’ Oran-Université d ’ Oran, Clinique Spécialisée en Orthopédie et Rééducation des Victimes des Accidents de Travail, Epidémiologie des maladies chroniques : impact des interactions gène environnement sur la santé des populations, Institut Pasteur de Lille, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille, Droit et Santé, Faculté de Médecine, Université Djilali Liabès [Sidi-Bel-Abbès], Laboratoire des Systèmes d ’Information en Santé, Université d ’ Oran, The ISOR project was funded through a collaboration agreement betweenthe Direction de la Post-Graduation et de la Recherche-Formation (DPGRF,Algeria) and the Institut National de la Santé et de la Recherche Médicale(INSERM, France). The work in France was also part-funded through otherINSERM programs. The work in Algeria was also part-funded by the AgenceThématique de Recherche en Sciences de la Santé (ATRSS) and a grant fromthe Projets Nationaux de Recherche (PNR) program, run by the AlgerianDirection Générale de la Recherche Scientifique et du DéveloppementTechnologique/Ministère de l’Enseignement Supérieur et de la RechercheScientifique (DGRSDT/MESRS).
المصدر: BMC Genetics
BMC Genetics, BioMed Central, 2014, 15 (1), pp.134. ⟨10.1186/s12863-014-0134-3⟩مصطلحات موضوعية: Adult, Male, ISOR study, Waist, endocrine system diseases, Population, 030209 endocrinology & metabolism, Single-nucleotide polymorphism, Type 2 diabetes, [SDV.GEN] Life Sciences [q-bio]/Genetics, Biology, Polymorphism, Single Nucleotide, 03 medical and health sciences, Food Preferences, 0302 clinical medicine, Polymorphism (computer science), Risk Factors, Gene-diet interaction, medicine, Genetics, Humans, Genetic Predisposition to Disease, Genetics(clinical), Polymorphism, education, Genetics (clinical), Genetic Association Studies, 030304 developmental biology, 0303 health sciences, education.field_of_study, [SDV.GEN]Life Sciences [q-bio]/Genetics, Diabetes, nutritional and metabolic diseases, Odds ratio, Middle Aged, medicine.disease, Confidence interval, TCF7L2, Cross-Sectional Studies, Diabetes Mellitus, Type 2, Algeria, Female, Transcription Factor 7-Like 2 Protein, Research Article
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::797940c3fa37f0916b57a6222f1f6e2aTest
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المؤلفون: Laurence N. Kolonel, Lynne R. Wilkens, James B. Meigs, Fredrick R. Schumacher, Kristine R. Monroe, Barbara V. Howard, Ulrike Peters, JoAnn E. Manson, Nora Franceschini, Jose C. Florez, James S. Pankow, Dana C. Crawford, Peggy Wan, Petra Bůžková, Steven Buyske, Andrew Nato, Robert Goodloe, Kari E. North, Lucia A. Hindorff, Christopher A. Haiman, José Luis Ambite, Jeff Haessler, Venkata Saroja Voruganti, Holli H. Dilks, Loic Le Marchand, Kylee L. Spencer, Megan D. Fesinmeyer, Sarah A. Pendergrass, Rebecca D. Jackson, Kenneth J. Mukamal, Simin Liu
المصدر: Fesinmeyer, Megan D; Meigs, James B; North, Kari E; Schumacher, Fredrick R; Bůžková, Petra; Franceschini, Nora; et al.(2013). Genetic variants associated with fasting glucose and insulin concentrations in an ethnically diverse population: results from the Population Architecture using Genomics and Epidemiology (PAGE) study. BMC Medical Genetics, 14(1), 98. doi: http://dx.doi.org/10.1186/1471-2350-14-98Test. Retrieved from: http://www.escholarship.org/uc/item/3bm037rsTest
BMC Medical Geneticsمصطلحات موضوعية: Adult, Blood Glucose, Male, medicine.medical_treatment, Population, 030209 endocrinology & metabolism, Genome-wide association study, Type 2 diabetes, Biology, Polymorphism, Single Nucleotide, White People, 03 medical and health sciences, 0302 clinical medicine, Asian People, Gene Frequency, medicine, Genetics, Glucose homeostasis, Humans, Insulin, Genetics(clinical), education, Allele frequency, Genetics (clinical), Alleles, 030304 developmental biology, Genetic association, Adaptor Proteins, Signal Transducing, Aged, 0303 health sciences, education.field_of_study, Genomics, Hispanic or Latino, Middle Aged, medicine.disease, Human genetics, Black or African American, Diabetes Mellitus, Type 2, Genetic Loci, Indians, North American, Female, Transcription Factor 7-Like 2 Protein, Research Article, Genome-Wide Association Study
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6a93dd1aca1ab711e1a3c37bd6c6c48Test
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المؤلفون: Whady Hueb, Andre Gustavo P. Sousa, Alexandre C. Pereira, José Geraldo Mill, Guilherme Figueiredo Marquezine, José Eduardo Krieger
المصدر: BMC Medical Genetics, Vol 9, Iss 1, p 106 (2008)
BMC Medical Geneticsمصطلحات موضوعية: Male, lcsh:Internal medicine, Diabetes risk, Genotype, lcsh:QH426-470, Population, Single-nucleotide polymorphism, Genome-wide association study, Coronary Artery Disease, Type 2 diabetes, Biology, Polymorphism, Single Nucleotide, Risk Assessment, Cohort Studies, medicine, Genetics, Humans, Genetic Predisposition to Disease, Genetics(clinical), education, lcsh:RC31-1245, Genetics (clinical), Aged, education.field_of_study, Middle Aged, medicine.disease, lcsh:Genetics, Cross-Sectional Studies, Logistic Models, Diabetes Mellitus, Type 2, ROC Curve, Genetic marker, Female, TCF Transcription Factors, Risk assessment, Transcription Factor 7-Like 2 Protein, TCF7L2, Brazil, Genome-Wide Association Study, Research Article, Demography
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2b8c6f4676f57bf5cc71ecd7359c77fTest
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المؤلفون: Daniela Tenório Furgeri, Antonio Fernando Ribeiro, Carmen Silvia Bertuzzo, Fernando Augusto Lima Marson
المصدر: BMC Research Notes
BMC Research Notes, Vol 5, Iss 1, p 561 (2012)مصطلحات موضوعية: Male, medicine.medical_specialty, Cystic Fibrosis, Genotype, Short Report, lcsh:Medicine, Cystic Fibrosis Transmembrane Conductance Regulator, IVS4G > T, Comorbidity, Polymorphism, Single Nucleotide, Gastroenterology, Cystic fibrosis, General Biochemistry, Genetics and Molecular Biology, Gene Frequency, Diabetes mellitus, Internal medicine, Diabetes Mellitus, Humans, Medicine, Genetic Predisposition to Disease, lcsh:Science (General), Child, lcsh:QH301-705.5, Allele frequency, Medicine(all), biology, business.industry, Biochemistry, Genetics and Molecular Biology(all), lcsh:R, Diabetes, General Medicine, medicine.disease, Cystic fibrosis transmembrane conductance regulator, TCF7L2, rs12255372, Endocrinology, lcsh:Biology (General), Mutation, Mutation (genetic algorithm), biology.protein, Female, business, Complication, Transcription Factor 7-Like 2 Protein, Brazil, lcsh:Q1-390
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a81ff4d5aea148b4faa9c815e54ce714Test
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7Carriers of a novel frame-shift insertion in WNT16a possess elevated pancreatic expression of TCF7L2
المؤلفون: Dharambir K. Sanghera, Latonya F. Been, Daniel J. Brackett, Megan R. Lerner, Elizabeth C. Bullen, Stan Lightfoot, Eric W. Howard
المصدر: BMC Genetics
مصطلحات موضوعية: Adult, Male, Exome sequencing, endocrine system, endocrine system diseases, Biology, medicine.disease_cause, Polymerase Chain Reaction, Frameshift mutation, 03 medical and health sciences, 0302 clinical medicine, Gene expression, medicine, Genetics, Humans, TCF7L2 gene variants, Genetics(clinical), Allele, Frameshift Mutation, Pancreas, Gene, Genetics (clinical), Aged, DNA Primers, 030304 developmental biology, 0303 health sciences, Mutation, Base Sequence, Genetic Carrier Screening, Wnt signaling pathway, nutritional and metabolic diseases, Type 2 diabetes, Middle Aged, β-cat /TCF7L2 signaling, Pancreatic β-cells, Wnt Proteins, Diabetes Mellitus, Type 2, Case-Control Studies, 030220 oncology & carcinogenesis, Wnt16a, Female, Signal transduction, Transcription Factor 7-Like 2 Protein, TCF7L2, Research Article, Insertion polymorphism
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49dd6de93e2b84575ed7ff4f729e8401Test