Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Matthieu Hammer"'
Autor:
Olga Babaev, Hugo Cruces-Solis, Carolina Piletti Chatain, Matthieu Hammer, Sally Wenger, Heba Ali, Nikolaos Karalis, Livia de Hoz, Oliver M. Schlüter, Yuchio Yanagawa, Hannelore Ehrenreich, Holger Taschenberger, Nils Brose, Dilja Krueger-Burg
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-16 (2018)
IgSF9b is a synaptic adhesion protein that has been linked to psychiatric disorders. Here the authors show that deletion of IgSF9b regulates anxiety-like behaviour in mice by increasing inhibitory synaptic transmission in the centromedial amygdala.
Externí odkaz:
https://doaj.org/article/362f3b269d1245b2923fe26c721003ee
Autor:
Matthieu Hammer, Dilja Krueger-Burg, Liam Patrick Tuffy, Benjamin Hillman Cooper, Holger Taschenberger, Sarit Pati Goswami, Hannelore Ehrenreich, Peter Jonas, Frederique Varoqueaux, Jeong-Seop Rhee, Nils Brose
Publikováno v:
Cell Reports, Vol 13, Iss 3, Pp 516-523 (2015)
Loss-of-function mutations in the synaptic adhesion protein Neuroligin-4 are among the most common genetic abnormalities associated with autism spectrum disorders, but little is known about the function of Neuroligin-4 and the consequences of its los
Externí odkaz:
https://doaj.org/article/667388ddc3cc4c2a98b9a39a1297d127
Autor:
Silvia Ripamonti, Mateusz C Ambrozkiewicz, Francesca Guzzi, Marta Gravati, Gerardo Biella, Ingo Bormuth, Matthieu Hammer, Liam P Tuffy, Albrecht Sigler, Hiroshi Kawabe, Katsuhiko Nishimori, Mauro Toselli, Nils Brose, Marco Parenti, JeongSeop Rhee
Publikováno v:
eLife, Vol 6 (2017)
Beyond its role in parturition and lactation, oxytocin influences higher brain processes that control social behavior of mammals, and perturbed oxytocin signaling has been linked to the pathogenesis of several psychiatric disorders. However, it is st
Externí odkaz:
https://doaj.org/article/74bbc3c9e85040aabd40e4e160d2ca42
Autor:
Bekir Altas, Liam P. Tuffy, Annarita Patrizi, Kalina Dimova, Tolga Soykan, Andrea J. Romanowski, Colin D. Robertson, Saovleak N. Khim, Garrett W. Bunce, Mateusz C. Ambrozkiewicz, Oleksandr Yagensky, Dilja Krueger-Burg, Matthieu Hammer, He-Hsuan Hsiao, Pawel R. Laskowski, Lydia Dyck, Marco Sassoè-Pognetto, John J.E. Chua, Henning Urlaub, Olaf Jahn, Nils Brose, Alexandros Poulopoulos
Neuroligin-3 is a postsynaptic adhesion molecule involved in development, function, and pathologies of synapses in the brain. It is a genetic cause of autism and a potent component of the tumor microenvironment in gliomas. There are four Neuroligins
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e76691efe7cb44aad12171d782def37
https://doi.org/10.1101/2022.07.23.501257
https://doi.org/10.1101/2022.07.23.501257
Autor:
Jenq-Wei Yang, Heiko J. Luhmann, Matthieu Hammer, Dilja Krueger-Burg, Sergei Kirischuk, Petr Unichenko, Werner Kilb, Nils Brose, Sergei N. Kolbaev
Publikováno v:
Cerebral Cortex. 28:2873-2886
Neuroligin-4 (Nlgn4) is a cell adhesion protein that regulates synapse organization and function. Mutations in human NLGN4 are among the causes of autism spectrum disorders. In mouse, Nlgn4 knockout (KO) perturbs GABAergic synaptic transmission and o
Autor:
Nils Brose, Holger Taschenberger, Olga Babaev, Carolina Piletti Chatain, Livia de Hoz, Sally Wenger, Heba Ali, Nikolaos Karalis, Yuchio Yanagawa, Oliver M. Schlüter, Dilja Krueger-Burg, Matthieu Hammer, Hugo Cruces-Solis, Hannelore Ehrenreich
Publikováno v:
Nature Communications
Nature Communications, Vol 9, Iss 1, Pp 1-16 (2018)
Nature Communications, Vol 9, Iss 1, Pp 1-16 (2018)
Abnormalities in synaptic inhibition play a critical role in psychiatric disorders, and accordingly, it is essential to understand the molecular mechanisms linking components of the inhibitory postsynapse to psychiatrically relevant neural circuits a
Autor:
Liam P. Tuffy, Holger Taschenberger, Nils Brose, Hannelore Ehrenreich, Matthieu Hammer, Sarit Pati Goswami, Frederique Varoqueaux, Jeong-Seop Rhee, Peter Jonas, Dilja Krueger-Burg, Benjamin H. Cooper
Publikováno v:
Cell reports
Cell Reports
Cell Reports, Vol 13, Iss 3, Pp 516-523 (2015)
Cell Reports
Cell Reports, Vol 13, Iss 3, Pp 516-523 (2015)
Summary Loss-of-function mutations in the synaptic adhesion protein Neuroligin-4 are among the most common genetic abnormalities associated with autism spectrum disorders, but little is known about the function of Neuroligin-4 and the consequences of
Autor:
Mauro Toselli, Francesca Guzzi, Ingo Bormuth, Matthieu Hammer, Katsuhiko Nishimori, Silvia Ripamonti, Gerardo Biella, Hiroshi Kawabe, Mateusz C. Ambrozkiewicz, Liam P. Tuffy, Jeong-Seop Rhee, Marta Gravati, Marco Parenti, Nils Brose, Albrecht Sigler
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::858310cc68a8863ada3528b1997f53cf
https://doi.org/10.7554/elife.22466.027
https://doi.org/10.7554/elife.22466.027
Autor:
Rémy Schlichter, Antoine G. Godin, Stéphane Gaillard, Bruce Mesnage, Matthieu Hammer, Jakob von Engelhardt, Yves De Koninck, Paul W. Wiseman, Matilde Cordero-Erausquin, Jean-Luc Rodeau
Publikováno v:
The Journal of Comparative Neurology. 519:3139-3158
Endogenous acetylcholine is an important modulator of sensory processing, especially at the spinal level, where nociceptive (pain-related) stimuli enter the central nervous system and are integrated before being relayed to the brain. To decipher the
Autor:
Siegrid Löwel, Tolga Soykan, Björn H. Falkenburger, Annarita Patrizi, Nils Brose, Frederique Varoqueaux, Tobias Moser, Marco Sassoè-Pognetto, Mrinalini Hoon, Holger Taschenberger, Matthieu Hammer, Karl-Friedrich Schmidt
Publikováno v:
Proceedings of the National Academy of Sciences; Vol 108
Proceedings of the National Academy of Sciences
Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences
Proceedings of the National Academy of Sciences of the United States of America
Neuroligins (NL1–NL4) are postsynaptic adhesion proteins that control the maturation and function of synapses in the central nervous system (CNS). Loss-of-function mutations in NL4 are linked to rare forms of monogenic heritable autism, but its loc