المؤلفون: Maria, Grigoroiu-Serbanescu, Stefan, Herms, Thomas W, Mühleisen, Alexander, Georgi, Carmen C, Diaconu, Jana, Strohmaier, Piotr, Czerski, Joanna, Hauser, Anna, Leszczynska-Rodziewicz, Rami Abou, Jamra, Gulia, Babadjanova, A, Tiganov, V, Krasnov, Sofia, Kapiletti, Ana Iulia, Neagu, Jennifer, Vollmer, René, Breuer, Marcella, Rietschel, Markus M, Nöthen, Sven, Cichon, Peter, Propping

المصدر: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. (7)

مصطلحات موضوعية: Adult, Male, Candidate gene, Bipolar I disorder, Bipolar Disorder, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, Genetic determinism, White People, Cellular and Molecular Neuroscience, Gene Frequency, mental disorders, Genetic variation, medicine, SNP, Humans, Genetic Predisposition to Disease, Bipolar disorder, Allele, Genetics (clinical), Alleles, Genetics, Depressive Disorder, Receptors, Purinergic P2, medicine.disease, Psychiatry and Mental health, Case-Control Studies, Female, Receptors, Purinergic P2X7

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc86920a337092260d7754cac898b5f7
https://pubmed.ncbi.nlm.nih.gov/19330776

المؤلفون: A. Karpushova, Manuel Mattheisen, Johannes Schumacher, Jan Haavik, Ann Van Den Bogaert, Gulia Babadjanova, Marcella Rietschel, Sven Cichon, Lilia I. Abramova, Markus M. Nöthen, Rami Abou Jamra, Alexander Georgi, Jeffrey A. McKinney, Sofia Kapiletti, Wolfgang Maier, Thomas G. Schulze, Yun Freudenberg-Hua, Ingeborg Winge, Peter Propping, Jan Freudenberg, Per M. Knappskog

المصدر: Cichon, S, Winge, I, Mattheisen, M, Georgi, A, Karpushova, A, Freudenberg, J, Freudenberg-Hua, Y, Babadjanova, G, Van Den Bogaert, A, Abramova, L I, Kapiletti, S, Knappskog, P M, McKinney, J, Maier, W, Jamra, R A, Schulze, T G, Schumacher, J, Propping, P, Rietschel, M, Haavik, J & Nöthen, M M 2008, ' Brain-specific tryptophan hydroxylase 2 (TPH2) : a functional Pro206Ser substitution and variation in the 5'-region are associated with bipolar affective disorder ' Human Molecular Genetics, vol. 17, no. 1, pp. 87-97 . https://doi.org/10.1093/hmg/ddm286
Human molecular genetics

مصطلحات موضوعية: Adult, Male, Models, Molecular, Heterozygote, Bipolar Disorder, Single-nucleotide polymorphism, Biology, In Vitro Techniques, Tryptophan Hydroxylase, Polymorphism, Single Nucleotide, Protein Structure, Secondary, Genetic variation, Enzyme Stability, Genetics, medicine, Animals, Humans, Bipolar disorder, Allele, Molecular Biology, Genetics (clinical), DNA Primers, TPH2, Base Sequence, Haplotype, Homozygote, Brain, Genetic Variation, General Medicine, Tryptophan hydroxylase, Middle Aged, medicine.disease, Recombinant Proteins, Pedigree, Minor allele frequency, Phenotype, Amino Acid Substitution, Haplotypes, Case-Control Studies, Female, Rabbits

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f78df3f7f775f4e620065024be22e071
https://pubmed.ncbi.nlm.nih.gov/17905754