المؤلفون: Hansen, Tue H, Vestergaard, Henrik, Jørgensen, Torben, Jørgensen, Marit Eika, Lauritzen, Torsten, Brandslund, Ivan, Christensen, Cramer, Pedersen, Oluf, Hansen, Torben, Gjesing, Anette P

المصدر: Hansen , T H , Vestergaard , H , Jørgensen , T , Jørgensen , M E , Lauritzen , T , Brandslund , I , Christensen , C , Pedersen , O , Hansen , T & Gjesing , A P 2015 , ' Impact of PTBP1 rs11085226 on glucose-stimulated insulin release in adult Danes ' , BMC Medical Genetics , vol. 16 , 17 , pp. 9-17 . https://doi.org/10.1186/s12881-015-0160-7Test

مصطلحات موضوعية: Adult, Alleles, Case-Control Studies, Denmark, Diabetes Mellitus, Type 2, Fasting, Female, Glucose, Glucose Tolerance Test, Heterogeneous-Nuclear Ribonucleoproteins, Humans, Insulin, Insulin-Secreting Cells, Male, Phenotype, Polymorphism, Single Nucleotide, Polypyrimidine Tract-Binding Protein, Type 2 diabetes, Insulin release, Polypyrimidine tract binding protein 1, Beta-cell function, Genetics

وصف الملف: application/pdf

العلاقة: https://portal.findresearcher.sdu.dk/da/publications/f730972f-ae6d-47d6-bb0c-5cb15ee3e7cdTest

الإتاحة: https://doi.org/10.1186/s12881-015-0160-7Test
https://portal.findresearcher.sdu.dk/da/publications/f730972f-ae6d-47d6-bb0c-5cb15ee3e7cdTest
https://findresearcher.sdu.dk/ws/files/134109513/Impact_of_PTBP1_rs11085226_on_glucose_stimulated_insulin_release_in_adult_Danes.pdfTest

المؤلفون: Vlaskamp, Danique R.M., Rump, Patrick, Callenbach, Petra M.C., Vos, Yvonne J., Sikkema-Raddatz, Birgit, van Ravenswaaij-Arts, Conny M.A., Brouwer, Oebele F.

المصدر: Vlaskamp , D R M , Rump , P , Callenbach , P M C , Vos , Y J , Sikkema-Raddatz , B , van Ravenswaaij-Arts , C M A & Brouwer , O F 2016 , ' Haploinsufficiency of the STX1B gene is associated with myoclonic astatic epilepsy ' , European Journal of Paediatric Neurology , vol. 20 , no. 3 , pp. 489-492 . https://doi.org/10.1016/j.ejpn.2015.12.014Test

مصطلحات موضوعية: Aetiology, Doose syndrome, Genetics, Myoclonic astatic epilepsy, STX1B, adult, case report, chromosome 16p, diagnosis, febrile convulsion, fever, gene deletion, genetic predisposition, haploinsufficiency, human, infantile spasm, intellectual impairment, male, missense mutation, problem behavior, severe myoclonic epilepsy in infancy, synaptic transmission, neurotransmitter, syntaxin 1, syntaxin 1A

العلاقة: https://research.rug.nl/en/publications/f13cc52b-9208-49b7-a3fb-363b521ca0b8Test

الإتاحة: https://doi.org/10.1016/j.ejpn.2015.12.014Test
https://hdl.handle.net/11370/f13cc52b-9208-49b7-a3fb-363b521ca0b8Test
https://research.rug.nl/en/publications/f13cc52b-9208-49b7-a3fb-363b521ca0b8Test

المؤلفون: Acuña-Alonzo, Víctor, Flores-Dorantes, Teresa, Kruit, Janine K, Villarreal-Molina, Teresa, Arellano-Campos, Olimpia, Hünemeier, Tábita, Moreno-Estrada, Andrés, Ortiz-López, Ma Guadalupe, Villamil-Ramírez, Hugo, León-Mimila, Paola, Villalobos-Comparan, Marisela, Jacobo-Albavera, Leonor, Ramírez-Jiménez, Salvador, Sikora, Martin, Zhang, Lin-Hua, Pape, Terry D, Granados-Silvestre, Ma de Angeles, Montufar-Robles, Isela, Tito-Alvarez, Ana M, Zurita-Salinas, Camilo, Bustos-Arriaga, José, Cedillo-Barrón, Leticia, Gómez-Trejo, Celta, Barquera-Lozano, Rodrigo, Vieira-Filho, Joao P, Granados, Julio, Romero-Hidalgo, Sandra, Huertas-Vázquez, Adriana, González-Martín, Antonio, Gorostiza, Amaya, Bonatto, Sandro L, Rodríguez-Cruz, Maricela, Wang, Li, Tusié-Luna, Teresa, Aguilar-Salinas, Carlos A, Lisker, Ruben, Moises, Regina S, Menjivar, Marta, Salzano, Francisco M, Knowler, William C, Bortolini, M Cátira, Hayden, Michael R, Baier, Leslie J, Canizales-Quinteros, Samuel

المصدر: Acuña-Alonzo , V , Flores-Dorantes , T , Kruit , J K , Villarreal-Molina , T , Arellano-Campos , O , Hünemeier , T , Moreno-Estrada , A , Ortiz-López , M G , Villamil-Ramírez , H , León-Mimila , P , Villalobos-Comparan , M , Jacobo-Albavera , L , Ramírez-Jiménez , S , Sikora , M , Zhang , L-H , Pape , T D , Granados-Silvestre , M D A , Montufar-Robles , I , Tito-Alvarez , A M , Zurita-Salinas , C , Bustos-Arriaga , J , Cedillo-Barrón , L , Gómez-Trejo , C , Barquera-Lozano ....

مصطلحات موضوعية: ATP Binding Cassette Transporter 1, ATP-Binding Cassette Transporters, Adult, Alleles, Cholesterol, HDL, Female, Gene Frequency, Genetics, Population, Genome-Wide Association Study, Geography, Haplotypes, Humans, Indians, North American, Linkage Disequilibrium, Male, Selection, Genetic

العلاقة: https://research.rug.nl/en/publications/70d79b2e-90d1-405e-a6b6-389dd572eff5Test

الإتاحة: https://doi.org/10.1093/hmg/ddq173Test
https://hdl.handle.net/11370/70d79b2e-90d1-405e-a6b6-389dd572eff5Test
https://research.rug.nl/en/publications/70d79b2e-90d1-405e-a6b6-389dd572eff5Test