المؤلفون: Axel Muendlein, Andreas Leiherer, Christoph H. Saely, Peter Fraunberger, Heinz Drexel

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 Reports

مصطلحات 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

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

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 Genetics

مصطلحات 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

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 Genetics

مصطلحات 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

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