Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Stefka Mincheva"'
Autor:
Stefka Mincheva-Tasheva, Chandran Pfitzner, Raman Kumar, Idha Kurtsdotter, Michaela Scherer, Tarin Ritchie, Jonas Muhr, Jozef Gecz, Paul Q. Thomas
Publikováno v:
Open Biology, Vol 14, Iss 4 (2024)
Non-clustered protocadherins (ncPcdhs) are adhesive molecules with spatio-temporally regulated overlapping expression in the developing nervous system. Although their unique role in neurogenesis has been widely studied, their combinatorial role in br
Externí odkaz:
https://doaj.org/article/1be471afb0de4b3196a50568149a88fa
Autor:
Ana Garcera, Stefka Mincheva, Myriam Gou-Fabregas, Víctor Caraballo-Miralles, Jerònia Lladó, Joan X. Comella, Rosa M. Soler
Publikováno v:
Neurobiology of Disease, Vol 42, Iss 3, Pp 415-426 (2011)
Spinal muscular atrophy (SMA) is a motoneuron disorder characterized by deletions or specific mutations in the Survival Motor Neuron gene (SMN). SMN is ubiquitously expressed and has a general role in the assembly of small nuclear ribonucleoprotein (
Externí odkaz:
https://doaj.org/article/cca0e6b8c4a44401a071870815f597f3
Publikováno v:
Molecular Neurobiology. 58:2005-2018
PCDH19-Clustering Epilepsy (PCDH19-CE) is an infantile onset disorder caused by mutation of the X-linked PCDH19 gene. Intriguingly, heterozygous females are affected while hemizygous males are not. While there is compelling evidence that this disorde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8cdf130faf6db0903814af8aeba3ccc
https://doi.org/10.1007/s12035-020-02242-4
https://doi.org/10.1007/s12035-020-02242-4
Autor:
Marta Medina-Carbonero, Rosa Purroy, Marta Llovera, Joaquim Ros, Stefka Mincheva-Tasheva, A. Sanz-Alcázar, Elena Britti, Fabien Delaspre, Jordi Tamarit
Publikováno v:
Repositorio Abierto de la UdL
Universitad de Lleida
Universitad de Lleida
Friedreich Ataxia (FA) is a neurodegenerative disease caused by the deficiency of frataxin, a mitochondrial protein. In primary cultures of dorsl root ganglia neurons, we showed that frataxin depletion resulted in decreased levels of the mitochondria
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8f40f77c23e61c953a14898c20f3a30
https://hdl.handle.net/10459.1/72921
https://hdl.handle.net/10459.1/72921
Publikováno v:
Molecular neurobiology. 58(5)
PCDH19-Clustering Epilepsy (PCDH19-CE) is an infantile onset disorder caused by mutation of the X-linked PCDH19 gene. Intriguingly, heterozygous females are affected while hemizygous males are not. While there is compelling evidence that this disorde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3a77c65239aefd7899cb7aa639e06638
https://pubmed.ncbi.nlm.nih.gov/33411240
https://pubmed.ncbi.nlm.nih.gov/33411240
Autor:
Stefka Mincheva-Tasheva, Jordi Tamarit, Rosa Purroy, Arabela Sanz, Marta Medina-Carbonero, Fabien Delaspre, Marta Llovera, Joaquim Ros, Elena Britti
Friedreich Ataxia (FA) is a neurodegenerative disease caused by the deficiency of frataxin, a mitochondrial protein. In primary cultures of dorsal root ganglia neurons, we showed that frataxin depletion resulted in decreased levels of the mitochondri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c4afe629d851236e9025d9602afafa4
Autor:
Ambika Periyakaruppiah, Ana Garcera, Stefka Mincheva-Tasheva, Saravanan Arumugam, Sandra de la Fuente, Rosa M. Soler
Publikováno v:
Recercat. Dipósit de la Recerca de Catalunya
instname
Repositorio Abierto de la UdL
Universitad de Lleida
instname
Repositorio Abierto de la UdL
Universitad de Lleida
Survival motor neuron (SMN) protein deficiency causes the genetic neuromuscular disorder spinal muscular atrophy (SMA), characterized by spinal cord motoneuron degeneration. Since SMN protein level is critical to disease onset and severity, analysis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf0fad0da9482a31ba26709fd46351e1
https://pubmed.ncbi.nlm.nih.gov/28808928
https://pubmed.ncbi.nlm.nih.gov/28808928
Autor:
Rosa M. Soler, Xavier Dolcet, Ana Garcera, Mario Encinas, Stefka Mincheva, Myriam Gou-Fabregas
Publikováno v:
The Journal of Neuroscience. 31:6493-6503
In vivoandin vitromotoneuron survival depends on the support of neurotrophic factors. These factors activate signaling pathways related to cell survival or inactivate proteins involved in neuronal death. In the present work, we analyzed the involveme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24740db2d0a4307a96d67ff5162caf9e
https://doi.org/10.1523/jneurosci.0206-11.2011
https://doi.org/10.1523/jneurosci.0206-11.2011
Publikováno v:
Human molecular genetics. 23(7)
Friedreich ataxia (FRDA) is a neurodegenerative disease characterized by a decreased expression of the mitochondrial protein frataxin. Major neurological symptoms of the disease are due to degeneration of dorsal root ganglion (DRG) sensory neurons. I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3364b52a2a054e94d1aa62b52e15b1a
https://pubmed.ncbi.nlm.nih.gov/24242291
https://pubmed.ncbi.nlm.nih.gov/24242291
Autor:
Stefka Mincheva-Tasheva, Rosa M. Soler
Publikováno v:
Repositorio Abierto de la UdL
Universitad de Lleida
Recercat. Dipósit de la Recerca de Catalunya
instname
Universitad de Lleida
Recercat. Dipósit de la Recerca de Catalunya
instname
Intracellular pathways related to cell survival regulate neuronal physiology during development and neurodegenerative disorders. One of the pathways that have recently emerged with an important role in these processes is nuclear factor- κB (NF-κB).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::651bd4baf7d45082e20739202e43c461
https://hdl.handle.net/10459.1/62850
https://hdl.handle.net/10459.1/62850