Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Lidia Babiec"'
Publikováno v:
Folia Neuropathologica, Vol 60, Iss 4, Pp 390-402 (2022)
Purinergic signalling is involved in the control of several processes related to brain development, such as neurogenesis and gliogenesis, migration and differentiation of neuronal precursors, synaptogenesis and synaptic elimination to achieve a fully
Externí odkaz:
https://doaj.org/article/218e33e0003e4630a2adc54eb9ae7308
Autor:
Lidia Babiec, Anna Wilkaniec, Marta Matuszewska, Ewelina Pałasz, Magdalena Cieślik, Agata Adamczyk
Publikováno v:
Brain Sciences, Vol 14, Iss 3, p 233 (2024)
In the original publication [...]
Externí odkaz:
https://doaj.org/article/47fac4998ad34dc899677fe043cdf6bb
Autor:
Lidia Babiec, Anna Wilkaniec, Marta Matuszewska, Ewelina Pałasz, Magdalena Cieślik, Agata Adamczyk
Publikováno v:
Brain Sciences, Vol 13, Iss 7, p 1088 (2023)
Recent data suggest that defects in purinergic signalling are a common denominator of autism spectrum disorders (ASDs), though nothing is known about whether the disorder-related imbalance occurs at the receptor level. In this study, we investigated
Externí odkaz:
https://doaj.org/article/6dfce820fc0a4df4b900bbd19f52170d
Autor:
Anna Wilkaniec, Anna M. Lenkiewicz, Lidia Babiec, Emilia Murawska, Henryk M. Jęśko, Magdalena Cieślik, Carsten Culmsee, Agata Adamczyk
Publikováno v:
Frontiers in Aging Neuroscience, Vol 13 (2021)
Aberrant secretion and accumulation of α-synuclein (α-Syn) as well as the loss of parkin function are associated with the pathogenesis of Parkinson’s disease (PD). Our previous study suggested a functional interaction between those two proteins,
Externí odkaz:
https://doaj.org/article/7c827104395b46819f287f33340f635d
Autor:
Magdalena Gąssowska-Dobrowolska, Grzegorz A. Czapski, Magdalena Cieślik, Karolina Zajdel, Małgorzata Frontczak-Baniewicz, Lidia Babiec, Agata Adamczyk
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 8; Pages: 7303
Tuberous sclerosis complex (TSC) is a rare genetic multisystem disorder caused by loss-of-function mutations in the tumour suppressors TSC1/TSC2, both of which are negative regulators of the mammalian target of rapamycin (mTOR) kinase. Importantly, m
Autor:
Grzegorz A. Czapski, Magdalena Gąssowska-Dobrowolska, Henryk Jęśko, Marta Matuszewska, Lidia Babiec, Karolina Zajdel, Małgorzata Frontczak-Baniewicz, Agata Adamczyk, Magdalena Cieślik
Publikováno v:
International Journal of Molecular Sciences
Volume 22
Issue 18
International Journal of Molecular Sciences, Vol 22, Iss 10058, p 10058 (2021)
Volume 22
Issue 18
International Journal of Molecular Sciences, Vol 22, Iss 10058, p 10058 (2021)
Tuberous sclerosis complex (TSC) is a rare, multi-system genetic disease with serious neurological and mental symptoms, including autism. Mutations in the TSC1/TSC2 genes lead to the overactivation of mTOR signalling, which is also linked to nonsyndr
Autor:
Emilia Murawska, Henryk Jęśko, Carsten Culmsee, Magdalena Cieślik, Anna Wilkaniec, Agata Adamczyk, Anna M. Lenkiewicz, Lidia Babiec
Publikováno v:
Frontiers in Aging Neuroscience
Frontiers in Aging Neuroscience, Vol 13 (2021)
Frontiers in Aging Neuroscience, Vol 13 (2021)
Aberrant secretion and accumulation of α-synuclein (α-Syn) as well as the loss of parkin function are associated with the pathogenesis of Parkinson’s disease (PD). Our previous study suggested a functional interaction between those two proteins,
Autor:
Magdalena Gewartowska, Lidia Babiec, Grzegorz A. Czapski, Agnieszka Dominiak, Agata Adamczyk, Rafał Polowy, Robert K. Filipkowski, Magdalena Gąssowska-Dobrowolska, Małgorzata Frontczak-Baniewicz, Henryk Jęśko, Magdalena Cieślik
Publikováno v:
International Journal of Molecular Sciences
Volume 21
Issue 10
International Journal of Molecular Sciences, Vol 21, Iss 3576, p 3576 (2020)
Volume 21
Issue 10
International Journal of Molecular Sciences, Vol 21, Iss 3576, p 3576 (2020)
Autism spectrum disorders (ASD) are a heterogeneous group of neurodevelopmental conditions categorized as synaptopathies. Environmental risk factors contribute to ASD aetiology. In particular, prenatal exposure to the anti-epileptic drug valproic aci
Autor:
Magdalena Gąssowska-Dobrowolska, Henryk Jęśko, Agata Adamczyk, Magdalena Cieślik, Anna Wilkaniec, Emilia Murawska, Ewelina Palasz, Lidia Babiec
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 3959, p 3959 (2020)
International Journal of Molecular Sciences
Volume 21
Issue 11
International Journal of Molecular Sciences
Volume 21
Issue 11
The purinergic P2X7 receptor (P2X7R) belongs to a family of trimeric ion channels that are gated by extracellular adenosine 5&prime
triphosphate (ATP). Several studies have pointed to a role of P2X7R-dependent signalling in Parkinson's disease (
triphosphate (ATP). Several studies have pointed to a role of P2X7R-dependent signalling in Parkinson's disease (