Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Bohumila Jurkovičová-Tarabová"'
Autor:
Zuzana Bačová, Bohumila Jurkovičová-Tarabová, Tomáš Havránek, Denisa Mihalj, Veronika Borbélyová, Zdenko Pirnik, Boris Mravec, Daniela Ostatníková, Ján Bakoš
Publikováno v:
Molecular Brain, Vol 17, Iss 1, Pp 1-10 (2024)
Abstract Abnormalities in gamma-aminobutyric acid (GABA)ergic neurotransmission play a role in the pathogenesis of autism, although the mechanisms responsible for alterations in specific brain regions remain unclear. Deficits in social motivation and
Externí odkaz:
https://doaj.org/article/f13ea17d4655435b8646cc83a4e50af7
Autor:
Lubica, Lacinova, Robert Theodor, Mallmann, Bohumila, Jurkovičová-Tarabová, Norbert, Klugbauer
Publikováno v:
Channels
article-version (VoR) Version of Record
article-version (VoR) Version of Record
Voltage-gated Ca2+ channels are typically integrated in a complex network of protein-protein-interactions, also referred to as Ca2+ channel nanodomains. Amongst the neuronal CaV2 channel family, CaV2.2 is of particular importance due to its general r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fdc353c5d9a658475e1d60579bbde820
https://pubmed.ncbi.nlm.nih.gov/33006503
https://pubmed.ncbi.nlm.nih.gov/33006503
Autor:
Leos Cmarko, Robin N. Stringer, Bohumila Jurkovicova-Tarabova, Tomas Vacik, Lubica Lacinova, Norbert Weiss
Publikováno v:
Molecular Brain, Vol 15, Iss 1, Pp 1-5 (2022)
Abstract Low-voltage-activated T-type Ca2+ channels are key regulators of neuronal excitability both in the central and peripheral nervous systems. Therefore, their recruitment at the plasma membrane is critical in determining firing activity pattern
Externí odkaz:
https://doaj.org/article/8061933a66364f57af6eede9cdeef15d
Autor:
Robin N. Stringer, Bohumila Jurkovicova-Tarabova, Ivana A. Souza, Judy Ibrahim, Tomas Vacik, Waseem Mahmoud Fathalla, Jozef Hertecant, Gerald W. Zamponi, Lubica Lacinova, Norbert Weiss
Publikováno v:
Molecular Brain, Vol 14, Iss 1, Pp 1-5 (2021)
Abstract Developmental and epileptic encephalopathies (DEEs) are a group of severe epilepsies that are characterized by seizures and developmental delay. DEEs are primarily attributed to genetic causes and an increasing number of cases have been corr
Externí odkaz:
https://doaj.org/article/3f066df756e94d84ba7d997e8e58c750
Autor:
Robin N. Stringer, Bohumila Jurkovicova-Tarabova, Sun Huang, Omid Haji-Ghassemi, Romane Idoux, Anna Liashenko, Ivana A. Souza, Yuriy Rzhepetskyy, Lubica Lacinova, Filip Van Petegem, Gerald W. Zamponi, Roger Pamphlett, Norbert Weiss
Publikováno v:
Molecular Brain, Vol 13, Iss 1, Pp 1-11 (2020)
Abstract Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder characterized by the progressive loss of cortical, brain stem and spinal motor neurons that leads to muscle weakness and death. A previous study implicated CACNA1H encoding
Externí odkaz:
https://doaj.org/article/aa77ecf927be4dd78a092c2d4008c1cd
Autor:
Bohumila Jurkovicova-Tarabova, Leos Cmarko, Renata Rehak, Gerald W. Zamponi, Lubica Lacinova, Norbert Weiss
Publikováno v:
Molecular Brain, Vol 12, Iss 1, Pp 1-11 (2019)
Abstract The physiological functions controlled by T-type channels are intrinsically dependent on their gating properties, and alteration of T-type channel activity is linked to several human disorders. Therefore, it is essential to develop a clear u
Externí odkaz:
https://doaj.org/article/fd7ca55a414c49ea914616f16a36f01e