Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Eneko Pina‐Fernandez"'
Autor:
Carolina Montenegro‐Venegas, Debarpan Guhathakurta, Eneko Pina‐Fernandez, Maria Andres‐Alonso, Florian Plattner, Eckart D Gundelfinger, Anna Fejtova
Publikováno v:
EMBO reports, 23(8):e53659
Neuronal presynaptic terminals contain hundreds of neurotransmitter-filled synaptic vesicles (SVs). The morphologically uniform SVs differ in their release competence segregating into functional pools that differentially contribute to neurotransmissi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5dd7dbad444ce6b885aeb819177b94d
https://repository.publisso.de/resource/frl:6434807
https://repository.publisso.de/resource/frl:6434807
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
Abstract The sense of familiarity for events is crucial for successful recognition memory. However, the neural substrate and mechanisms supporting familiarity remain unclear. A major controversy in memory research is whether the parahippocampal areas
Externí odkaz:
https://doaj.org/article/140504ea2ab243f68d310ee4bdc4d3ed
Autor:
Franziska Altmüller, Santosh Pothula, Anil Annamneedi, Saeideh Nakhaei-Rad, Carolina Montenegro-Venegas, Eneko Pina-Fernández, Claudia Marini, Monica Santos, Denny Schanze, Dirk Montag, Mohammad R Ahmadian, Oliver Stork, Martin Zenker, Anna Fejtova
Publikováno v:
PLoS Genetics, Vol 13, Iss 6, p e1006843 (2017)
[This corrects the article DOI: 10.1371/journal.pgen.1006684.].
Externí odkaz:
https://doaj.org/article/9f508d33e6cd48faa1a9521ab6557376
Autor:
Franziska Altmüller, Santosh Pothula, Anil Annamneedi, Saeideh Nakhaei-Rad, Carolina Montenegro-Venegas, Eneko Pina-Fernández, Claudia Marini, Monica Santos, Denny Schanze, Dirk Montag, Mohammad R Ahmadian, Oliver Stork, Martin Zenker, Anna Fejtova
Publikováno v:
PLoS Genetics, Vol 13, Iss 3, p e1006684 (2017)
Noonan syndrome (NS) is characterized by reduced growth, craniofacial abnormalities, congenital heart defects, and variable cognitive deficits. NS belongs to the RASopathies, genetic conditions linked to mutations in components and regulators of the
Externí odkaz:
https://doaj.org/article/4d79c075e1a8490e85b7c3fa7893b496