Zobrazeno 1 - 10 of 12 pro vyhledávání: '"D B, Wildenauer"'
1
Characterization of serotonin transporter gene (SLC6A4) polymorphisms and its association with drug dependence in a Jordanian Arab population
Autor: Gary K. Hulse, Saied A. Jaradat, Dieter B. Wildenauer, Wenwen Qin, Laith N. AL-Eitan, D. B. Wildenauer, Guan K. Tay
Publikováno v: Toxicology and Industrial Health. 30:598-610
Drug dependence is a pattern of repeated self-administration of a drug, which can result in tolerance, withdrawal and compulsive drug-taking behaviour. It has been recently suggested that 5-HTTLPR ( LL/ LS/ SS) variants and rs25531 (A/G) polymorphism
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb22f188e751bba6858502a407320308
https://doi.org/10.1177/0748233712462446
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2
A transmission disequilibrium and linkage analysis of D22S278 marker alleles in 574 families: further support for a susceptibility locus for schizophrenia at 22q12
Autor: Derek J. Nancarrow, G Kalsi, Dermot Walsh, Hugh Gurling, J Brynjolfsson, Hannes Petursson, Jeremy M. Silverman, Kenneth S. Kendler, Robin M. Murray, T. d'Amato, Lynn R. Goldin, Hiroshi Kunugi, Robert B. Freedman, M. Jay, T. Sigmundson, W. Muri, Wolfgang Maier, William Byerley, J. Mallet, L. Yang, A. E. Pulver, C J MacLean, P. C. Sham, L. He, Raymond R. Crowe, R. E. Straub, Margot Albus, Dominique Campion, Michael John Owen, Richard P. Ebstein, Elliot S. Gershon, H. Donis-Keller, Hans W. Moises, Gerald Nestadt, D. H. R. Blackwood, Haig H. Kazazian, D. StClair, Claudine Laurent, Joachim Hallmayer, Claudia Wiese, D. B. Wildenauer, Stylianos E. Antonarakis, Bryan J. Mowry, Michael Gill, Homero Vallada, David E. Housman, H. Kristbjarnarson, R. Lofthouse, C. M. Read, Shinichiro Nanko, Mihael H. Polymeropoulos, P. McGuffin, Nicholas K. Hayward, H-G Hwu, S. Bodeau-Pean, Manfred Ackenheil, B. Lerer, David A. Collier, Douglas F. Levinson, Hilary Coon, Lynn E. DeLisi, J. H. Zhao, David Curtis, S. Maguire
Publikováno v: Schizophrenia Research. 32:115-121
Patients with schizophrenia rarely develop rheumatoid arthritis, an autoimmune disease that exhibits genetic association with the HLA DRB1*04 gene. We previously investigated the hypothesis that schizophrenia is negatively associated with DRB1*04, an
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ff34745dccce4cde02a71de82c7cf9e3
https://doi.org/10.1016/s0920-9964(98)00048-6
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3
GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia
Autor: D. St Clair, Edward M. Scolnick, Michael Conlon O'Donovan, Ayman H. Fanous, Markus M. Noethen, Aiden Corvin, G. Lee, Daniel R. Weinberger, Andrew McQuillin, António Macedo, Hugh Gurling, Todd Lencz, Jianxin Shi, Brion S. Maher, M. T. Pato, Zhongming Zhao, Marcella Rietschel, Ina Giegling, Pablo V. Gejman, Francis A. O'Neill, Thomas Werge, Rita M. Cantor, Ariel Darvasi, Christina M. Hultman, Pamela Sklar, Paul Lichtenstein, Janet Blackman, Kenneth S. Kendler, Michal Bronstein, Michael Gill, Douglas F. Levinson, Xiangning Chen, Sven Cichon, Anil K. Malhotra, Srdjan Djurovic, Sibylle G. Schwab, Douglas Blackwood, W. Qin, Shaun Purcell, Carlos N. Pato, Nicholas John Craddock, Patrick F. Sullivan, D. Lewis, Andrés Ingason, D. B. Wildenauer, Derek W. Morris, Dan Rujescu, An-Yuan Guo, Ole A. Andreassen, Jonathan Pimm, E J C G van den Oord, Michael John Owen, Jubao Duan, Vishwajit L. Nimgaonkar, George Kirov, Richard E. Straub, Roel A. Ophoff, Declan Walsh, Thomas Hansen, Jingchun Chen, Alan R. Sanders, Kodavali V. Chowdari
Publikováno v: Molecular psychiatry, 16(11), 1117-1129. Nature Publishing Group
Molecular Psychiatry, 16(11), 1117-1129. Nature Publishing Group
We conducted data-mining analyses using the Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) and molecular genetics of schizophrenia genome-wide association study supported by the genetic association information network (MGS-GAIN)
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f58102a33596d2112644eac7e076d4c
https://pure.amc.nl/en/publications/gwa-study-data-mining-and-independent-replication-identify-cardiomyopathyassociated-5-cmya5-as-a-risk-gene-for-schizophrenia(aee54083-4726-43ba-8903-79a98f679dc9).html
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4
Dissecting the Molecular Causes of Schizophrenia
Autor: Sibylle G. Schwab, D. B. Wildenauer, Dieter B. Wildenauer
Publikováno v: Molecular Biology of Neuropsychiatric Disorders ISBN: 9783540853824
Schizophrenia is a complex genetic disorder with largely unknown aetiology. The search for molecular causes has been the focus for many years studying biochemistry, neurobiology, molecular biology, and molecular genetics of the disorder. Our intentio
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::19c36f88ba833b8bf2815cb2fbf3e908
https://doi.org/10.1007/978-3-540-85383-1_2
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5
Disturbed copper transport in humans. Part 2: mutations of the ATP7B gene lead to Wilson disease (WD)
Autor: J, Seidel, K, Caca, S G, Schwab, F, Berr, D B, Wildenauer, H J, Mentzel, N, Horn, E, Kauf
Publikováno v: Cellular and molecular biology (Noisy-le-Grand, France).
Mutations in the Wilson disease gene ATP7B, a P-type ATPase, are responsible for copper accumulation in the liver and other organs leading to Wilson disease (WD, OMIM 277900). Clinical manifestations of Wilson disease (WD) include chronic liver disea
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::3f3f0887786e7aba43f02a606b2c92ac
https://pubmed.ncbi.nlm.nih.gov/11936861
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7
Copper genes are not implicated in the pathogenesis of focal dystonia
Autor: D. B. Wildenauer, D. Sibbing, Friedrich Asmus, Werner Poewe, M. Grundmann, T. Gasser, W. H. Oertel, S. G. Schwab, J. Müller, Oliver Bandmann
Publikováno v: Scopus-Elsevier
A number of recently published studies provide evidence for disturbed copper metabolism in focal dystonia. Postmortem studies have identified significantly elevated copper and manganese levels in the globus pallidus and putamen of two patients with f
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fe8b17d8d3a49a51dc3bdc8ff73b3a9
https://doi.org/10.1212/wnl.59.5.782
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8
Interaction of cyclophosphamide metabolites with membrane proteins: an in vitro study with rabbit liver microsomes and human red blood cells. Effect of thiols
Autor: D B, Wildenauer, C E, Oehlmann
Publikováno v: Biochemical pharmacology. 31(22)
Cyclophosphamide metabolites have been generated in vitro by microsomal oxidation of cyclophosphamide and their binding to rabbit liver microsomes and to intact human red blood cells has been investigated. Reactions with proteins of membrane and cyto
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::a3c1c85897eaf9e685aea34fce738cec
https://pubmed.ncbi.nlm.nih.gov/7181935
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10
The interactions of mesna and dimesna with the sulfate exchange in human red blood cells
Autor: H, Reuther, M, Kohl, D B, Wildenauer
Publikováno v: Arzneimittel-Forschung. 36(4)
The influence of disodium 2-mercaptoethane sulfonate disulfide (mesna, Uromitexan) and sodium 2-mercaptoethane sulfonate (dimesna) on the carrier mediated exchange of 35S-sulfate in human red blood cells was investigated in vitro in order to contribu
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f442b6142cf5bb6c380798f0afdb4282
https://pubmed.ncbi.nlm.nih.gov/3087373
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