Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Lutz Priebe"'
Autor:
Tanja Grimminger, Katharina Pernhorst, Rainer Surges, Pitt Niehusmann, Lutz Priebe, Marec von Lehe, Per Hoffmann, Sven Cichon, Susanne Schoch, Albert J. Becker
Publikováno v:
Neurobiology of Disease, Vol 60, Iss , Pp 115-125 (2013)
Pharmacoresistance to antiepileptic drugs (AEDs) is a major clinical problem in patients with mesial temporal lobe epilepsy (mTLE). Levetiracetam (LEV) represents a unique type of AED as its high-affinity binding site, the synaptic vesicle protein SV
Externí odkaz:
https://doaj.org/article/9c6829355a2d4c9690c003f4ee91a966
Autor:
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
Publikováno v:
PLoS ONE, Vol 9, Iss 8, p e104326 (2014)
Bipolar disorder is one of the most common and devastating psychiatric disorders whose mechanisms remain largely unknown. Despite a strong genetic contribution demonstrated by twin and adoption studies, a polygenic background influences this multifac
Externí odkaz:
https://doaj.org/article/a0a21a9615324b178e8eea2ec3cbbf88
Autor:
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
Publikováno v:
PLoS ONE, Vol 8, Iss 6, p e64872 (2013)
Patients with schizophrenia and their siblings typically show subtle changes of brain structures, such as a reduction of hippocampal volume. Hippocampal volume is heritable, may explain a variety of cognitive symptoms of schizophrenia and is thus con
Externí odkaz:
https://doaj.org/article/84aee48741c3419396749009aa0d271d
Autor:
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
Publikováno v:
PLoS ONE, Vol 8, Iss 7, p e64035 (2013)
Large rare copy number variants (CNVs) have been recognized as significant genetic risk factors for the development of schizophrenia (SCZ). However, due to their low frequency (1∶150 to 1∶1000) among patients, large sample sizes are needed to det
Externí odkaz:
https://doaj.org/article/aa40682df3914b2a8a019f4252c725a5
Autor:
Per Hoffmann, Lutz Priebe, Rainer Surges, Albert J. Becker, Tanja Grimminger, Katharina Pernhorst, Sven Cichon, Pitt Niehusmann, Marec von Lehe, Susanne Schoch
Publikováno v:
Neurobiology of Disease, Vol 60, Iss, Pp 115-125 (2013)
Pharmacoresistance to antiepileptic drugs (AEDs) is a major clinical problem in patients with mesial temporal lobe epilepsy (mTLE). Levetiracetam (LEV) represents a unique type of AED as its high-affinity binding site, the synaptic vesicle protein SV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ae00b625dadfc4a05e3fd1974d50d41
http://www.sciencedirect.com/science/article/pii/S0969996113002362
http://www.sciencedirect.com/science/article/pii/S0969996113002362
Autor:
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
Publikováno v:
Molecular psychiatry
Molecular Psychiatry; 19(3), pp 334-341 (2014)
Molecular Psychiatry; 19(3), pp 334-341 (2014)
The kynurenine pathway metabolite kynurenic acid (KYNA), modulating glutamatergic and cholinergic neurotransmission, is increased in cerebrospinal fluid (CSF) of patients with schizophrenia or bipolar disorder type 1 with psychotic features. KYNA pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5b1b228fdf34e79b9bc99c79af4210b
https://doi.org/10.1038/mp.2013.11
https://doi.org/10.1038/mp.2013.11
Autor:
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
Publikováno v:
British Journal of Dermatology. 165:1293-1302
Summary Background Male-pattern baldness (androgenetic alopecia, AGA) is the most common form of hair loss among humans. Research has shown that it is caused by genetic factors. Numerous studies have unequivocally identified two major genetic risk lo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24c2fa5834824c125d19875eaaa1d8f2
https://doi.org/10.1111/j.1365-2133.2011.10708.x
https://doi.org/10.1111/j.1365-2133.2011.10708.x
Autor:
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
Publikováno v:
Biological Psychiatry. 70:35-42
Background Patients with schizophrenia often suffer from cognitive dysfunction, including impaired learning and memory. We recently demonstrated that long-term potentiation in rat hippocampus, a mechanistic model of learning and memory, is linked to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d4e7452f5b3cc102384d6093f941b94
https://doi.org/10.1016/j.biopsych.2011.01.030
https://doi.org/10.1016/j.biopsych.2011.01.030
Autor:
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
Publikováno v:
European Journal of Human Genetics. 19:1161-1166
Non-specific intellectual disability of autosomal recessive inheritance (NS-ARID) represents an important fraction of severe cognitive dysfunction disorders. To date, only 10 genes have been identified, and further 24 linked-ARID loci have been repor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2118baeb89244f4ec35cc0f452a7a6c7
https://doi.org/10.1038/ejhg.2011.98
https://doi.org/10.1038/ejhg.2011.98
Autor:
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
Publikováno v:
Schizophrenia Research. 127:35-40
Large rare deletions in NRXN1 increase the risk for schizophrenia. The aim of the present study was to determine whether small rare sequence changes in exons and splice sites contribute to the development of schizophrenia in a high-penetrance manner.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fa42d125dceb3a1275d3fa35b638a96
https://doi.org/10.1016/j.schres.2011.01.001
https://doi.org/10.1016/j.schres.2011.01.001