Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Sergi Verdés"'
Autor:
Joan Roig-Soriano, Cristina Sánchez-de-Diego, Jon Esandi-Jauregui, Sergi Verdés, Carmela R. Abraham, Assumpció Bosch, Francesc Ventura, Miguel Chillón
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-10 (2023)
Abstract The aging-protective gene α-Klotho (KL) produces two main transcripts. The full-length mRNA generates a transmembrane protein that after proteolytic ectodomain shedding can be detected in serum as processed Klotho (p-KL), and a shorter tran
Externí odkaz:
https://doaj.org/article/6d0e213469a84004ae0d9ef85a56bf58
Autor:
Marc Leal-Julià, Jorge J. Vilches, Andrea Onieva, Sergi Verdés, Ángela Sánchez, Miguel Chillón, Xavier Navarro, Assumpció Bosch
Publikováno v:
Molecular Metabolism, Vol 55, Iss , Pp 101408- (2022)
Objective: Peripheral neuropathy is the most common and debilitating complication of type 2 diabetes, leading to sensory loss, dysautonomia, hyperalgesia, and spontaneous noxious sensations. Despite the clinical and economic burden of diabetic neurop
Externí odkaz:
https://doaj.org/article/affdf19c56474612aa5aab5b0da3ff60
Autor:
Guillem Mòdol-Caballero, Mireia Herrando-Grabulosa, Sergi Verdés, Belén García-Lareu, Neus Hernández, Isaac Francos-Quijorna, Rubén López-Vales, Assumpció Bosch, Xavier Navarro
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease affecting the neuromuscular system for which currently there is no effective therapy. Motoneuron (MN) degeneration involves several complex mechanisms, including surrounding gli
Externí odkaz:
https://doaj.org/article/de3aa861366a46a9a56f3e37e6182c97
Autor:
Guillem Mòdol-Caballero, Mireia Herrando-Grabulosa, Belén García-Lareu, Neus Solanes, Sergi Verdés, Rosario Osta, Isaac Francos-Quijorna, Rubèn López-Vales, Ana Cristina Calvo, Assumpció Bosch, Xavier Navarro
Publikováno v:
Neurobiology of Disease, Vol 137, Iss , Pp 104793- (2020)
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder affecting motoneurons (MNs), with no effective treatment currently available. The molecular mechanisms that are involved in MN death are complex and not fully understood, with partia
Externí odkaz:
https://doaj.org/article/b575c34266b74f7da9212ad1f511120c
Autor:
Mireia Herrando-Grabulosa, Xavier Navarro, Assumpció Bosch, Guillem Mòdol-Caballero, Lorena Ariza, Frédéric Brocard, Irene Sanchez-Brualla, Belén García-Lareu, Sergi Verdés
Publikováno v:
Neurotherapeutics
Neurotherapeutics, 2020, 17 (3), pp.1048-1060. ⟨10.1007/s13311-019-00811-7⟩
Neurotherapeutics, Springer Verlag, 2020, 17 (3), pp.1048-1060. ⟨10.1007/s13311-019-00811-7⟩
Neurotherapeutics, 2020, 17 (3), pp.1048-1060. ⟨10.1007/s13311-019-00811-7⟩
Neurotherapeutics, Springer Verlag, 2020, 17 (3), pp.1048-1060. ⟨10.1007/s13311-019-00811-7⟩
Amyotrophic lateral sclerosis (ALS) is a devastating motoneuron (Mn) disease without effective cure currently available. Death of MNs in ALS is preceded by failure of neuromuscular junctions and axonal retraction. Neuregulin 1 (NRG1) is a neurotrophi
Autor:
Joan Roig-Soriano, Cristina Sánchez-de-Diego, Jon Esandi-Jauregui, Sergi Verdés, Assumpció Bosch, Francesc Ventura, Miguel Chillón
Publikováno v:
SSRN Electronic Journal.
Autor:
Belén García-Lareu, Assumpció Bosch, Rubèn López-Vales, Xavier Navarro, Sergi Verdés, Miguel Chillón, Gemma Pagès, Mireia Herrando-Grabulosa, Guillem Mòdol-Caballero
Publikováno v:
Neurotherapeutics
Glial cell line–derived neurotrophic factor (GDNF) is a powerful neuroprotective growth factor. However, systemic or intrathecal administration of GDNF is associated with side effects. Here, we aimed to avoid this by restricting the transgene expre
Autor:
Assumpció Bosch, Xavier Navarro, Sergi Verdés, Andrea Onieva, Marc Leal-Julià, Miguel Chillón, Ángela María Muñoz Sánchez, Jorge J. Vilches
Publikováno v:
Molecular Metabolism
Molecular Metabolism, Vol 55, Iss, Pp 101408-(2022)
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Scientia
Molecular Metabolism, Vol 55, Iss, Pp 101408-(2022)
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Scientia
Objective Peripheral neuropathy is the most common and debilitating complication of type 2 diabetes, leading to sensory loss, dysautonomia, hyperalgesia, and spontaneous noxious sensations. Despite the clinical and economic burden of diabetic neuropa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::efbcd1d8134e46e35d8154e356de60d2
https://ddd.uab.cat/record/250533
https://ddd.uab.cat/record/250533
Autor:
Guillem Mòdol-Caballero, Mireia Herrando-Grabulosa, Sergi Verdés, Belén García-Lareu, Neus Hernández, Isaac Francos-Quijorna, Rubén López-Vales, Assumpció Bosch, Xavier Navarro
Publikováno v:
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Scientia
Frontiers in Neurology, Vol 12 (2021)
Frontiers in Neurology
Universitat Autònoma de Barcelona
Scientia
Frontiers in Neurology, Vol 12 (2021)
Frontiers in Neurology
Motoneuron; Neuregulin 1; Spinal cord Motoneurona; Neuregulina 1; Médula espinal Motoneurona; Neuregulina 1; Medul·la espinal Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease affecting the neuromuscular system for which curr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5e3a5a6011ede7f3bc47683f7f0d90c
https://ddd.uab.cat/record/267003
https://ddd.uab.cat/record/267003
Autor:
Isaac Francos-Quijorna, Assumpció Bosch, Xavier Navarro, Belén García-Lareu, Ana C. Calvo, Rubèn López-Vales, Rosario Osta, Sergi Verdés, Guillem Mòdol-Caballero, Neus Solanes, Mireia Herrando-Grabulosa
Publikováno v:
Neurobiology of Disease, Vol 137, Iss, Pp 104793-(2020)
Altres ajuts: Fundació La Marato-TV3: TV3201428-10 ; AFM-Telethon: 20289 Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder affecting motoneurons (MNs), with no effective treatment currently available. The molecular mechanisms that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7aa2708ebdad5e0f8bc51398d84bc423
https://ddd.uab.cat/record/266956
https://ddd.uab.cat/record/266956