Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Nina Miljanovic"'
Autor:
Hannah King, Maria Reiber, Vanessa Philippi, Helen Stirling, Katharina Aulehner, Marion Bankstahl, André Bleich, Verena Buchecker, Aylina Glasenapp, Paulin Jirkof, Nina Miljanovic, Katharina Schönhoff, Lara von Schumann, Cathalijn Leenaars, Heidrun Potschka
Publikováno v:
Frontiers in Neuroscience, Vol 17 (2023)
Experimental craniotomies are a common surgical procedure in neuroscience. Because inadequate analgesia appears to be a problem in animal-based research, we conducted this review and collected information on management of craniotomy-associated pain i
Externí odkaz:
https://doaj.org/article/801a5678ce2f410fa2eae9361acd21f2
Autor:
Nina Miljanovic, Stefanie M. Hauck, R. Maarten van Dijk, Valentina Di Liberto, Ali Rezaei, Heidrun Potschka
Publikováno v:
Neurobiology of Disease, Vol 157, Iss , Pp 105423- (2021)
Background: Dravet syndrome is a rare, severe pediatric epileptic encephalopathy associated with intellectual and motor disabilities. Proteomic profiling in a mouse model of Dravet syndrome can provide information about the molecular consequences of
Externí odkaz:
https://doaj.org/article/cbb84c3f0ac14bdeba164ee825eecaf2
Autor:
Christine Henke, Kathrin Töllner, R. Maarten van Dijk, Nina Miljanovic, Thekla Cordes, Friederike Twele, Sonja Bröer, Vanessa Ziesak, Marco Rohde, Stefanie M. Hauck, Charlotte Vogel, Lisa Welzel, Tina Schumann, Diana M. Willmes, Anica Kurzbach, Nermeen N. El-Agroudy, Stefan R. Bornstein, Susanne A. Schneider, Jens Jordan, Heidrun Potschka, Christian M. Metallo, Rüdiger Köhling, Andreas L. Birkenfeld, Wolfgang Löscher
Publikováno v:
Neurobiology of Disease, Vol 143, Iss , Pp 105018- (2020)
In addition to tissues such as liver, the plasma membrane sodium-dependent citrate transporter, NaCT (SLC13A5), is highly expressed in brain neurons, but its function is not understood. Loss-of-function mutations in the human SLC13A5 gene have been a
Externí odkaz:
https://doaj.org/article/df9b3f253ba04e89ae8d4ee2953dca43
Publikováno v:
Epilepsybehavior : EB. 136
Dravet syndrome is a rare, severe, infancy-onset epileptic encephalopathy associated with a high premature mortality. In most patients, Dravet syndrome is caused by a heterozygous loss-of-function mutation in the SCN1A gene encoding the alpha 1 subun
Autor:
Nina Miljanovic, Heidrun Potschka
Publikováno v:
Epilepsy research. 178
Purpose The gut-brain axis has been discussed as a possible factor contributing to ictogenesis and epilepsy. While recent preclinical studies have proposed a link between the antiseizure effect of a ketogenic diet (KD) and alterations to the gut micr
Publikováno v:
EpilepsiaREFERENCES. 62(8)
Objective Alterations in metabolic homeostasis can contribute to neuronal hyperexcitability and seizure susceptibility. Although the pivotal role of impaired bioenergetics is obvious in metabolic epilepsies, there is a gap of knowledge regarding seco
Autor:
Ali Rezaei, Nina Miljanovic, Valentina Di Liberto, Stefanie M. Hauck, R. Maarten van Dijk, Heidrun Potschka
BackgroundDravet syndrome is a rare, severe pediatric epileptic encephalopathy associated with intellectual and motor disabilities. Proteomic profiling in a mouse model of Dravet syndrome can provide information about the molecular consequences of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d65a1633f2c98f242ea1684d337b30d
https://doi.org/10.1101/2021.04.27.441099
https://doi.org/10.1101/2021.04.27.441099
Autor:
Valentina Di Liberto, Ali Rezaei, Heidrun Potschka, Nina Miljanovic, R. Maarten van Dijk, Stefanie M. Hauck
Publikováno v:
Neurobiol. Dis. 157:105423 (2021)
Neurobiology of Disease, Vol 157, Iss, Pp 105423-(2021)
Neurobiology of Disease, Vol 157, Iss, Pp 105423-(2021)
Background Dravet syndrome is a rare, severe pediatric epileptic encephalopathy associated with intellectual and motor disabilities. Proteomic profiling in a mouse model of Dravet syndrome can provide information about the molecular consequences of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a83b87483ab00ea1c173931eabe59222
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=62322
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=62322
Autor:
Rupert Palme, Heidrun Potschka, R. Maarten van Dijk, Ines Koska, Steven R. Talbot, André Bleich, Nina Miljanovic, Lena Boldt
Publikováno v:
Epilepsybehavior : EB. 115
Objective Ethical decisions about an allowance for animal experiments need to be based on scientifically sound information about the burden and distress associated with the experimental procedure and models. Thereby, species differences need to be co
Autor:
Steven R. Talbot, Leonie Zieglowski, Dietmar Zechner, Kerstin Schwabe, Simeon O. A. Helgers, Brigitte Vollmar, Tjark Wölk, Christine Häger, Nora Weegh, Andreas Wree, Franz-Tassilo Müller-Graff, Nina Miljanovic, Roelof Maarten van Dijk, Ines Koska, André Bleich, Fabio Wolf, Heidrun Potschka, Angela Kuhla, Lisa Ernst, Babette Koegel, Rene Tolba, Svenja Biernot
Publikováno v:
Laboratory animals. 54(1)
In many animal experiments scientists and local authorities define a body-weight reduction of 20% or more as severe suffering and thereby as a potential parameter for humane endpoint decisions. In this study, we evaluated distinct animal experiments