Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Aet O'Leary"'
Autor:
I. Hyun Ruisch, Joanna Widomska, Ward De Witte, Nina R. Mota, Giuseppe Fanelli, Veerle Van Gils, Willemijn J. Jansen, Stephanie J. B. Vos, Abel Fóthi, Csaba Barta, Simone Berkel, Kazi A. Alam, Aurora Martinez, Jan Haavik, Aet O’Leary, David Slattery, Mairéad Sullivan, Jeffrey Glennon, Jan K. Buitelaar, Janita Bralten, Barbara Franke, Geert Poelmans
Publikováno v:
Alzheimer’s Research & Therapy, Vol 16, Iss 1, Pp 1-16 (2024)
Abstract Alzheimer’s disease (AD) is a multifactorial disease with both genetic and environmental factors contributing to its etiology. Previous evidence has implicated disturbed insulin signaling as a key mechanism that plays a role in both neurod
Externí odkaz:
https://doaj.org/article/ec15a71192f24d8aaffafb95a2cae7a1
Autor:
Sharif Jabra, Michael Rietsche, Julia Muellerleile, Aet O’Leary, David A. Slattery, Thomas Deller, Meike Fellenz
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-10 (2024)
Abstract Sex hormones affect structural and functional plasticity in the rodent hippocampus. However, hormone levels not only differ between males and females, but also fluctuate across the female estrous cycle. While sex- and cycle-dependent differe
Externí odkaz:
https://doaj.org/article/a00f61bd05ab439c90ea83286867f95e
Autor:
Ilya M. Veer, Antje Riepenhausen, Matthias Zerban, Carolin Wackerhagen, Lara M. C. Puhlmann, Haakon Engen, Göran Köber, Sophie A. Bögemann, Jeroen Weermeijer, Aleksandra Uściłko, Netali Mor, Marta A. Marciniak, Adrian Dahl Askelund, Abbas Al-Kamel, Sarah Ayash, Giulia Barsuola, Vaida Bartkute-Norkuniene, Simone Battaglia, Yaryna Bobko, Sven Bölte, Paolo Cardone, Edita Chvojková, Kaja Damnjanović, Joana De Calheiros Velozo, Lena de Thurah, Yacila I. Deza-Araujo, Annika Dimitrov, Kinga Farkas, Clémence Feller, Mary Gazea, Donya Gilan, Vedrana Gnjidić, Michal Hajduk, Anu P. Hiekkaranta, Live S. Hofgaard, Laura Ilen, Zuzana Kasanova, Mohsen Khanpour, Bobo Hi Po Lau, Dionne B. Lenferink, Thomas B. Lindhardt, Dávid Á. Magas, Julian Mituniewicz, Laura Moreno-López, Sofiia Muzychka, Maria Ntafouli, Aet O’Leary, Ilenia Paparella, Nele Põldver, Aki Rintala, Natalia Robak, Anna M. Rosická, Espen Røysamb, Siavash Sadeghi, Maude Schneider, Roma Siugzdaite, Mirta Stantić, Ana Teixeira, Ana Todorovic, Wendy W. N. Wan, Rolf van Dick, Klaus Lieb, Birgit Kleim, Erno J. Hermans, Dorota Kobylińska, Talma Hendler, Harald Binder, Inez Myin-Germeys, Judith M. C. van Leeuwen, Oliver Tüscher, Kenneth S. L. Yuen, Henrik Walter, Raffael Kalisch
Publikováno v:
Translational Psychiatry, Vol 11, Iss 1, Pp 1-11 (2021)
Abstract The SARS-CoV-2 pandemic is not only a threat to physical health but is also having severe impacts on mental health. Although increases in stress-related symptomatology and other adverse psycho-social outcomes, as well as their most important
Externí odkaz:
https://doaj.org/article/4e12843f37be4cbc84aa71973320b0ee
Autor:
Susanne Knorr, Lisa Rauschenberger, Uri Ramirez Pasos, Maximilian U. Friedrich, Robert L. Peach, Kathrin Grundmann-Hauser, Thomas Ott, Aet O'Leary, Andreas Reif, Philip Tovote, Jens Volkmann, Chi Wang Ip
Publikováno v:
Neurobiology of Disease, Vol 154, Iss , Pp 105337- (2021)
TOR1A is the most common inherited form of dystonia with still unclear pathophysiology and reduced penetrance of 30–40%. ∆ETorA rats mimic the TOR1A disease by expression of the human TOR1A mutation without presenting a dystonic phenotype. We aim
Externí odkaz:
https://doaj.org/article/8c06d0bbd2204284a3bf0ac22fbea2a6
Autor:
Benedikt Grünewald, Maren D Lange, Christian Werner, Aet O'Leary, Andreas Weishaupt, Sandy Popp, David A Pearce, Heinz Wiendl, Andreas Reif, Hans C Pape, Klaus V Toyka, Claudia Sommer, Christian Geis
Publikováno v:
eLife, Vol 6 (2017)
Juvenile neuronal ceroid lipofuscinosis (JNCL or Batten disease) caused by mutations in the CLN3 gene is the most prevalent inherited neurodegenerative disease in childhood resulting in widespread central nervous system dysfunction and premature deat
Externí odkaz:
https://doaj.org/article/73ff6f4c6ad249a0ae51af6071b9bb4c
Autor:
Judit Cabana-Domínguez, Ester Antón-Galindo, Noèlia Fernàndez-Castillo, Euginia L. Singgih, Aet O’Leary, William HG Norton, Tatyana Strekalova, Annette Schenck, Andreas Reif, Klaus-Peter Lesch, David Slattery, Bru Cormand
Publikováno v:
Neuroscience and Biobehavioral Reviews, 144
Neuroscience and Biobehavioural Review
Neuroscience and Biobehavioural Review
Contains fulltext : 290890.pdf (Publisher’s version ) (Open Access) Attention-deficit/hyperactivity disorder (ADHD) is a highly prevalent neurodevelopmental disorder resulting from the interaction between genetic and environmental risk factors. It
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dedcf2359e5a4b67b9a8967eb567c9d8
https://doi.org/10.1016/j.neubiorev.2022.104949
https://doi.org/10.1016/j.neubiorev.2022.104949
Autor:
Mairéad Sullivan, Fernando Fernandez-Aranda, Lucía Camacho-Barcia, Andrew Harkin, Simone Macrì, Bernat Mora-Maltas, Susana Jiménez-Murcia, Aet O'Leary, Angela Maria Ottomana, Martina Presta, David Slattery, Samantha Scholtz, Jeffrey C. Glennon
Publikováno v:
Neuroscience & Biobehavioral Reviews. 150:105169
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eef0d95c4145b5ff09175dfdfca1e0e4
https://doi.org/10.1016/j.neubiorev.2023.105169
https://doi.org/10.1016/j.neubiorev.2023.105169
Autor:
Mariliis Vaht, Toomas Veidebaum, Andreas Reif, Jaanus Harro, Kariina Laas, Evelyn Kiive, Aet O'Leary
Publikováno v:
European Neuropsychopharmacology. 30:56-65
Nitric oxide signalling has been implicated in impulsive and aggressive traits and behaviours in both animals and humans. In the present study, we investigated the effects of a functional variable number of tandem repeats (VNTR) polymorphism in exon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f3f6bf6fa10a6ff4f7f55ea89ae5e2c
https://doi.org/10.1016/j.euroneuro.2019.07.241
https://doi.org/10.1016/j.euroneuro.2019.07.241
Autor:
Jaanus Harro, Aet O’Leary
Publikováno v:
Handbook of Substance Misuse and Addictions ISBN: 9783030679286
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47cd3cbbe4d6ddcdb6a4362c8ccb15fe
https://doi.org/10.1007/978-3-030-92392-1_108
https://doi.org/10.1007/978-3-030-92392-1_108
Autor:
Aet O’Leary, Noèlia Fernàndez-Castillo, Gabriela Gan, Yunbo Yang, Anna Y. Yotova, Thorsten M. Kranz, Lena Grünewald, Florian Freudenberg, Ester Antón-Galindo, Judit Cabana-Domínguez, Anais Harneit, Janina I. Schweiger, Kristina Schwarz, Ren Ma, Junfang Chen, Emanuel Schwarz, Marcella Rietschel, Heike Tost, Andreas Meyer-Lindenberg, Christiane A. Pané-Farré, Tilo Kircher, Alfons O. Hamm, Demian Burguera, Nina Roth Mota, Barbara Franke, Susann Schweiger, Jennifer Winter, Andreas Heinz, Susanne Erk, Nina Romanczuk-Seiferth, Henrik Walter, Andreas Ströhle, Lydia Fehm, Thomas Fydrich, Ulrike Lueken, Heike Weber, Thomas Lang, Alexander L. Gerlach, Markus M. Nöthen, Georg W. Alpers, Volker Arolt, Stephanie Witt, Jan Richter, Benjamin Straube, Bru Cormand, David A. Slattery, Andreas Reif
Publikováno v:
Mol Psychiatry
Common variation in the gene encoding the neuron-specific RNA splicing factor RNA Binding Fox-1 Homolog 1 (RBFOX1) has been identified as a risk factor for several psychiatric conditions, and rare genetic variants have been found causal for autism sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97658d2ed857991b8db598d104859a1a