Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Mireia Moreno-Estelles"'
Autor:
Begüm Aydin, Michael Sierk, Mireia Moreno-Estelles, Link Tejavibulya, Nikathan Kumar, Nuria Flames, Shaun Mahony, Esteban O. Mazzoni
Publikováno v:
Frontiers in Neuroscience, Vol 16 (2022)
Neuronal programming by forced expression of transcription factors (TFs) holds promise for clinical applications of regenerative medicine. However, the mechanisms by which TFs coordinate their activities on the genome and control distinct neuronal fa
Externí odkaz:
https://doaj.org/article/7f1cb8a0d28b411c88f0b01e3a7958e8
Autor:
Alessandra Zappulo, David van den Bruck, Camilla Ciolli Mattioli, Vedran Franke, Koshi Imami, Erik McShane, Mireia Moreno-Estelles, Lorenzo Calviello, Andrei Filipchyk, Esteban Peguero-Sanchez, Thomas Müller, Andrew Woehler, Carmen Birchmeier, Enrique Merino, Nikolaus Rajewsky, Uwe Ohler, Esteban O. Mazzoni, Matthias Selbach, Altuna Akalin, Marina Chekulaeva
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-13 (2017)
Subcellular localization of RNAs and proteins is important for polarized cells such as neurons. Here the authors differentiate mouse embryonic stem cells into neurons, and analyze the local transcriptome, proteome, and translated transcriptome in the
Externí odkaz:
https://doaj.org/article/78855abe544f4175b8a66cdc42637e8a
Publikováno v:
Neurobiology of Disease, Vol 176, Iss , Pp 105964- (2023)
Lafora disease (LD; OMIM#254780) is a rare form of progressive myoclonus epilepsy (prevalence
Externí odkaz:
https://doaj.org/article/8b995996921a47c5abe54c94aa491382
Autor:
Mireia Moreno-Estellés, Ángela Campos-Rodríguez, Carla Rubio-Villena, Lorena Kumarasinghe, Maria Adelaida Garcia-Gimeno, Pascual Sanz
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 7, p 6020 (2023)
Lafora disease (LD) is a neurological disorder characterized by progressive myoclonus epilepsy. The hallmark of the disease is the presence of insoluble forms of glycogen (polyglucosan bodies, or PGBs) in the brain. The accumulation of PGBs is causat
Externí odkaz:
https://doaj.org/article/2a61872d58184cbd8a01148435d07684
Autor:
Carlos Romá-Mateo, Sheila Lorente-Pozo, Lucía Márquez-Thibaut, Mireia Moreno-Estellés, Concepción Garcés, Daymé González, Marcos Lahuerta, Carmen Aguado, José Luis García-Giménez, Pascual Sanz, Federico V. Pallardó
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 2, p 1089 (2023)
Lafora disease is a rare, fatal form of progressive myoclonus epilepsy characterized by continuous neurodegeneration with epileptic seizures, characterized by the intracellular accumulation of aberrant polyglucosan granules called Lafora bodies. Seve
Externí odkaz:
https://doaj.org/article/5a79290cd58b40259fafb3296af69246