Zobrazeno 1 - 10
of 30
pro vyhledávání: '"patrizia bianchi"'
Autor:
Emma Puighermanal, Marta Luna-Sánchez, Alejandro Gella, Gunter van der Walt, Andrea Urpi, María Royo, Paula Tena-Morraja, Isabella Appiah, Maria Helena de Donato, Fabien Menardy, Patrizia Bianchi, Anna Esteve-Codina, Laura Rodríguez-Pascau, Cristina Vergara, Mercè Gómez-Pallarès, Giovanni Marsicano, Luigi Bellocchio, Marc Martinell, Elisenda Sanz, Sandra Jurado, Francesc Xavier Soriano, Pilar Pizcueta, Albert Quintana
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-21 (2024)
Abstract Mutations in mitochondrial energy-producing genes lead to a heterogeneous group of untreatable disorders known as primary mitochondrial diseases (MD). Leigh syndrome (LS) is the most common pediatric MD and is characterized by progressive ne
Externí odkaz:
https://doaj.org/article/622861ac6cc14a5babd24370dd72d435
Autor:
Patricia Prada-Dacasa, Andrea Badell, Laura Sánchez-Benito, patrizia bianchi, Albert Quintana
Publikováno v:
Bio-Protocol, Vol 10, Iss 17 (2020)
Respiratory dysfunction is among the main cause of severe and fatal pathologies worldwide. The use of effective experimental models and methodologies for the study of the pulmonary pathophysiology is necessary to prevent, control and cure these disea
Externí odkaz:
https://doaj.org/article/b5ad8454ac41463e91ca66bc4365157d
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 16, p 8523 (2021)
Symbiosis between the mitochondrion and the ancestor of the eukaryotic cell allowed cellular complexity and supported life. Mitochondria have specialized in many key functions ensuring cell homeostasis and survival. Thus, proper communication between
Externí odkaz:
https://doaj.org/article/05bae7e012ef45fc87f02d020d38daa4
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 22, Iss 8523, p 8523 (2021)
International Journal of Molecular Sciences, Vol 22, Iss 8523, p 8523 (2021)
Funding: This work was supported by a Juan de la Cierva grant (IJC2018-036938-I). A.Q. received funds from the European Research Council (Starting grant NEUROMITO, ERC-2014-StG-638106), MINECO Proyectos I + D de Excelencia (SAF2014-57981P; SAF2017-88
Publikováno v:
Bio Protoc
Respiratory dysfunction is among the main cause of severe and fatal pathologies worldwide. The use of effective experimental models and methodologies for the study of the pulmonary pathophysiology is necessary to prevent, control and cure these disea
Autor:
Stefano Camerucci, Marco Pavone, Antonella Villanova, Caterina Di Mauro, Biagio Valente, Paola Giovannetti, Sergio Crescenzi, Andrea Filabozzi, Livia Archibugi, Maria Cristina Scamuffa, Claudio Medori, Sergio Centofanti, Paolo Balducci, Giuseppe Lanna, Giovanni Spinelli, Gianfranco Delle Fave, Enzo Nunnari, Emilio Merletti, Riccarda Cremaschi, Rosanna Cantarini, Gabriele Capurso, Giuseppe Giancaspro, Piera Pasquali, Francesca Paris, Alfonso Fiorillo, A. Chiriatti, Patrizia Colantonio, Davide Di Renzi, Patrizia Bianchi, Almerindo Rossi, Marco Taborchi, Alessandro Aceti, Francesco Buono, Angela Piacenti
Publikováno v:
Digestive and Liver Disease. 49:535-539
Background Data on chronic pancreatitis prevalence are scanty and usually limited to hospital-based studies. Aim Investigating chronic pancreatitis prevalence in primary care. Methods Participating primary care physicians reported the prevalence of c
Autor:
Elisabetta Ciani, Fiorenza Stagni, Stefania Trazzi, Andrea Giacomini, Sandra Guidi, Renata Bartesaghi, Patrizia Bianchi, Marco Emili
Publikováno v:
CNS & Neurological Disorders - Drug Targets. 16
BACKGROUND & OBJECTIVE Down syndrome, a genetic condition caused by triplication of chromosome 21, is characterized by widespread neurogenesis reduction and cognitive impairment. Unlike other brain functions, smell is not impaired at early life stage
Autor:
Odile Boespflug-Tanguy, Marie-Noëlle Bonnet-Dupeyron, Mélina Bégou, Johan Auwerx, Jone López-Erauskin, Aurora Pujol, Nathalie Launay, Céline Guéret-Gonthier, Catherine Vaurs-Barrière, Pablo Ranea-Robles, Patrizia Bianchi, Stéphane Fourcade, Bérengère Petit, Laia Morató, Montserrat Ruiz, Cristina Guilera
Publikováno v:
Brain Pathology
Brain Pathology, 2017, ⟨10.1111/bpa.12571⟩
Brain Pathology, Wiley, 2017, ⟨10.1111/bpa.12571⟩
Dipòsit Digital de la UB
Universidad de Barcelona
Brain Pathology, Wiley, 2017, 〈10.1111/bpa.12571〉
Brain Pathology, 2017, ⟨10.1111/bpa.12571⟩
Brain Pathology, Wiley, 2017, ⟨10.1111/bpa.12571⟩
Dipòsit Digital de la UB
Universidad de Barcelona
Brain Pathology, Wiley, 2017, 〈10.1111/bpa.12571〉
Pelizaeus‐Merzbacher disease (PMD) is a fatal hypomyelinating disorder characterized by early impairment of motor development, nystagmus, choreoathetotic movements, ataxia and progressive spasticity. PMD is caused by variations in the proteolipid p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21be927e5d376dd6689ba3c95b010238
https://hal.uca.fr/hal-01662573
https://hal.uca.fr/hal-01662573
Publikováno v:
Neural Regeneration Research
The purpose of this work was to investigate whether, by intranasal administration, the nerve growth factor bypasses the blood-brain barrier and turns over the spinal cord neurons and if such therapeutic approach could be of value in the treatment of
Autor:
Nyoman D. Kurniawan, Sandra Guidi, Alessandro Giuliani, Renata Bartesaghi, Laura Calzà, Karine Mardon, Fiorenza Stagni, Elisabetta Ciani, Marianna De Franceschi, Andrea Giacomini, Patrizia Bianchi, Randal X. Moldrich
Publikováno v:
Brain. 137:380-401
Intellectual impairment is a strongly disabling feature of Down's syndrome, a genetic disorder of high prevalence (1 in 700-1000 live births) caused by trisomy of chromosome 21. Accumulating evidence shows that widespread neurogenesis impairment is a