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1دورية أكاديمية
المؤلفون: Tanja Grimminger, Katharina Pernhorst, Rainer Surges, Pitt Niehusmann, Lutz Priebe, Marec von Lehe, Per Hoffmann, Sven Cichon, Susanne Schoch, Albert J. Becker
المصدر: Neurobiology of Disease, Vol 60, Iss , Pp 115-125 (2013)
مصطلحات موضوعية: A priori non-responders, Luciferase, Promoter variants, PIGP, Presynapse, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: Stéphane Jamain, Sven Cichon, Bruno Etain, Thomas W Mühleisen, Alexander Georgi, Nora Zidane, Lucie Chevallier, Jasmine Deshommes, Aude Nicolas, Annabelle Henrion, Franziska Degenhardt, Manuel Mattheisen, Lutz Priebe, Flavie Mathieu, Jean-Pierre Kahn, Chantal Henry, Anne Boland, Diana Zelenika, Ivo Gut, Simon Heath, Mark Lathrop, Wolfgang Maier, Margot Albus, Marcella Rietschel, Thomas G Schulze, Francis J McMahon, John R Kelsoe, Marian Hamshere, Nicholas Craddock, Markus M Nöthen, Frank Bellivier, Marion Leboyer
المصدر: PLoS ONE, Vol 9, Iss 8, p e104326 (2014)
وصف الملف: electronic resource
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3دورية أكاديمية
المؤلفون: Johanna Hass, Esther Walton, Holger Kirsten, Jingyu Liu, Lutz Priebe, Christiane Wolf, Nazanin Karbalai, Randy Gollub, Tonya White, Veit Roessner, Kathrin U Müller, Tomas Paus, Michael N Smolka, Gunter Schumann, IMAGEN Consortium, Markus Scholz, Sven Cichon, Vince Calhoun, Stefan Ehrlich
المصدر: PLoS ONE, Vol 8, Iss 6, p e64872 (2013)
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1932-6203
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4دورية أكاديمية
المؤلفون: Lutz Priebe, Franziska Degenhardt, Jana Strohmaier, René Breuer, Stefan Herms, Stephanie H Witt, Per Hoffmann, Rebecca Kulbida, Manuel Mattheisen, Susanne Moebus, Andreas Meyer-Lindenberg, Henrik Walter, Rainald Mössner, Igor Nenadic, Heinrich Sauer, Dan Rujescu, Wolfgang Maier, Marcella Rietschel, Markus M Nöthen, Sven Cichon
المصدر: PLoS ONE, Vol 8, Iss 7, p e64035 (2013)
وصف الملف: electronic resource
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المؤلفون: Per Hoffmann, Lutz Priebe, Rainer Surges, Albert J. Becker, Tanja Grimminger, Katharina Pernhorst, Sven Cichon, Pitt Niehusmann, Marec von Lehe, Susanne Schoch
المصدر: Neurobiology of Disease, Vol 60, Iss, Pp 115-125 (2013)
مصطلحات موضوعية: Adult, Male, Levetiracetam, Adolescent, Drug Resistance, Presynaptic Terminals, Single-nucleotide polymorphism, Biology, Hippocampal formation, Bioinformatics, Hippocampus, Polymorphism, Single Nucleotide, Presynapse, lcsh:RC321-571, Transcriptome, Young Adult, A priori non-responders, medicine, Humans, Epilepsy surgery, Child, Promoter Regions, Genetic, PIGP, Transcription factor, lcsh:Neurosciences. Biological psychiatry. Neuropsychiatry, SV2A, Epilepsy, Infant, Membrane Proteins, Promoter variants, Middle Aged, Piracetam, Hexosyltransferases, Neurology, Child, Preschool, Anticonvulsants, Female, Luciferase, medicine.drug
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ae00b625dadfc4a05e3fd1974d50d41
http://www.sciencedirect.com/science/article/pii/S0969996113002362 -
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المؤلفون: Louise Frisén, Sara K. Olsson, Catharina Lavebratt, Lena Backlund, Pernilla Nikamo, Göran Engberg, Lil Träskman-Bendz, Mikael Landén, Carl M. Sellgren, Urban Ösby, Lutz Priebe, Martin Schalling, Sven Cichon, Marquis P. Vawter, Sophie Erhardt
المصدر: Molecular psychiatry
Molecular Psychiatry; 19(3), pp 334-341 (2014)مصطلحات موضوعية: Adult, Male, Psychosis, medicine.medical_specialty, Bipolar Disorder, Kynurenine pathway, Gene Expression, Prefrontal Cortex, Kynurenic Acid, Hippocampus, Article, Cell Line, Young Adult, Cellular and Molecular Neuroscience, chemistry.chemical_compound, Kynurenine 3-Monooxygenase, Kynurenic acid, kynurenic acid, Internal medicine, mental disorders, Gene expression, medicine, Humans, Genetic Predisposition to Disease, psychosis, Bipolar disorder, Allele, Molecular Biology, Alleles, Aged, Psychiatry, prefrontal cortex, Middle Aged, medicine.disease, Psychiatry and Mental health, Endocrinology, Psychotic Disorders, chemistry, Schizophrenia, Case-Control Studies, genetic variation, gene expression, Female, Psychology, Neuroscience, kynurenine pathway
وصف الملف: application/pdf
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7
المؤلفون: Lutz Priebe, Margrieta A. Alblas, Rami Abou Jamra, Nadine Kluck, Sibylle Eigelshoven, Susanne Moebus, Felix F. Brockschmidt, Stefanie Heilmann, Raimund Erbel, Tim Becker, Christine Herold, Holger Fröhlich, Stephen B. Harrap, Axel M. Hillmer, Christian Meesters, Karl-Heinz Jöckel, Rudolf Kruse, B. Lippke, Justine A. Ellis, Franziska Degenhardt, Sandra Hanneken, Markus M. Nöthen, Johannes Schumacher
المصدر: British Journal of Dermatology. 165:1293-1302
مصطلحات موضوعية: Genetics, Candidate gene, Hair cycle, HDAC9, medicine, Male-pattern baldness, Genome-wide association study, Single-nucleotide polymorphism, Locus (genetics), Dermatology, Biology, medicine.disease, Gene
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المؤلفون: Ingrid Melle, Vidar M. Steen, Thomas G. Schulze, Markus M. Nöthen, Srdjan Djurovic, Lutz Priebe, Thomas Hansen, Helle Lybæk, Marcella Rietschel, Ole A. Andreassen, Sven Cichon, Thomas Werge, René Breuer, Bjarte Håvik, Beth Stevens, Clive R. Bramham, Thomas W. Mühleisen, Franziska Degenhardt, Wolfgang Maier, Stephanie Le Hellard, Manuel Mattheisen, Ingrid Agartz
المصدر: Biological Psychiatry. 70:35-42
مصطلحات موضوعية: Adult, Male, Psychosis, Genotype, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, Genetic determinism, Major Histocompatibility Complex, 03 medical and health sciences, 0302 clinical medicine, medicine, Genetic predisposition, Humans, SNP, Genetic Association Studies, Biological Psychiatry, Genetic association, Genetics, CD46, Tumor Suppressor Proteins, Membrane Proteins, Complement System Proteins, medicine.disease, 3. Good health, 030227 psychiatry, Schizophrenia, Case-Control Studies, Female, 030217 neurology & neurosurgery
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المؤلفون: R Abou Jamra, Johannes Schumacher, Mohammed Ayman Al Khateeb, Steffen Uebe, Markus M. Nöthen, Lutz Priebe, Mahmoud Fakher, André Reis, Sigrun Wohlfart, Susanne Giesebrecht, Markus Zweier, Safia Muhammad, Arif B. Ekici, Saber Hamdan, Ahmad Abboud, Amina Ismael
المصدر: European Journal of Human Genetics. 19:1161-1166
مصطلحات موضوعية: Adult, Male, Microcephaly, Adolescent, Consanguinity, Biology, Article, Genetic Heterogeneity, Young Adult, Intellectual Disability, Intellectual disability, Genetics, medicine, Humans, Child, Genetics (clinical), Family Health, Linkage (software), Syria, Genetic heterogeneity, Homozygote, Chromosome Mapping, Chromosome, Disease gene identification, medicine.disease, Pedigree, Genetic Loci, Child, Preschool, Mutation, Mutation (genetic algorithm), Intercellular Signaling Peptides and Proteins, Female, Carrier Proteins
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المؤلفون: Stefan Herms, Dan Rujescu, Marcella Rietschel, Markus M. Nöthen, Heinrich Sauer, Michael Ludwig, Susanne Moebus, Igor Nenadic, F. Buket Basmanav, Wolfgang Maier, Thomas W. Mühleisen, Andreas J. Forstner, Rainald Mössner, René Breuer, Sven Cichon, Lutz Priebe, Manuel Mattheisen
المصدر: Schizophrenia Research. 127:35-40
مصطلحات موضوعية: Adult, Male, Models, Molecular, Psychosis, Genotype, Cell Adhesion Molecules, Neuronal, Medizin, Mutation, Missense, Nerve Tissue Proteins, Genome-wide association study, Biology, Genetic determinism, Gene Frequency, medicine, Humans, Missense mutation, Genetic Predisposition to Disease, splice, Neural Cell Adhesion Molecules, Genotyping, Allele frequency, Biological Psychiatry, Genetics, Calcium-Binding Proteins, Computational Biology, Exons, Middle Aged, medicine.disease, Psychiatry and Mental health, Schizophrenia, Female, Follow-Up Studies, Genome-Wide Association Study