Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Sabrina Santoleri"'
Autor:
Francesco Galli, Laricia Bragg, Maira Rossi, Daisy Proietti, Laura Perani, Marco Bacigaluppi, Rossana Tonlorenzi, Tendai Sibanda, Miriam Caffarini, Avraneel Talapatra, Sabrina Santoleri, Mirella Meregalli, Beatriz Bano-Otalora, Anne Bigot, Irene Bozzoni, Chiara Bonini, Vincent Mouly, Yvan Torrente, Giulio Cossu
Publikováno v:
EMBO Molecular Medicine, Vol 16, Iss 4, Pp 927-944 (2024)
Abstract Cell therapy for muscular dystrophy has met with limited success, mainly due to the poor engraftment of donor cells, especially in fibrotic muscle at an advanced stage of the disease. We developed a cell-mediated exon skipping that exploits
Externí odkaz:
https://doaj.org/article/2901b421c44741348f703c80bba345e6
Autor:
Francesco Galli, Laricia Bragg, Maira Rossi, Daisy Proietti, Laura Perani, Marco Bacigaluppi, Rossana Tonlorenzi, Tendai Sibanda, Miriam Caffarini, Avraneel Talapatra, Sabrina Santoleri, Mirella Meregalli, Beatriz Bano-Otalora, Anne Bigot, Irene Bozzoni, Chiara Bonini, Vincent Mouly, Yvan Torrente, Giulio Cossu
Publikováno v:
EMBO Molecular Medicine, Vol 16, Iss 10, Pp 2654-2654 (2024)
Externí odkaz:
https://doaj.org/article/5f7f0ae2ba184d8d97e0eb107a271912
Autor:
Claudia Fuoco, Roberto Rizzi, Antonella Biondo, Emanuela Longa, Anna Mascaro, Keren Shapira‐Schweitzer, Olga Kossovar, Sara Benedetti, Maria L Salvatori, Sabrina Santoleri, Stefano Testa, Sergio Bernardini, Roberto Bottinelli, Claudia Bearzi, Stefano M Cannata, Dror Seliktar, Giulio Cossu, Cesare Gargioli
Publikováno v:
EMBO Molecular Medicine, Vol 7, Iss 4, Pp 411-422 (2015)
Abstract Extensive loss of skeletal muscle tissue results in mutilations and severe loss of function. In vitro‐generated artificial muscles undergo necrosis when transplanted in vivo before host angiogenesis may provide oxygen for fibre survival. H
Externí odkaz:
https://doaj.org/article/48b3e289f04c41fe9cb0ec66cf68ed38
Autor:
Paula Martin, Azat Abdullin, Rashid Giniatullin, Sabrina Santoleri, Jari Koistinaho, Taina Pihlajaniemi, Anastasia Shakirzyanova, Ilkka Miinalainen, Michael A. Fox, Hongmin Tu, Heli Härönen, Anne Heikkinen, Zarin Zainul, Raija Sormunen, Israel Silman, Nikolay Naumenko, Tuomo Oikarainen
Publikováno v:
Human Molecular Genetics. 26:2076-2090
Both transmembrane and extracellular cues, one of which is collagen XIII, regulate the formation and function of the neuromuscular synapse, and their absence results in myasthenia. We show that the phenotypical changes in collagen XIII knock-out mice
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a006c7ab8550096f6f9a4a88c32f9d5
https://doi.org/10.1093/hmg/ddx101
https://doi.org/10.1093/hmg/ddx101
Autor:
Zarin Zainul, Antti Kemppainen, Anne Heikkinen, Raija Sormunen, Heli Härönen, Rashid Giniatullin, Nikolay Naumenko, Anastasia Shakirzyanova, Taina Pihlajaniemi, Ilkka Miinalainen, Sabrina Santoleri
Publikováno v:
The European journal of neuroscience. 49(11)
Transmembrane collagen XIII has been linked to maturation of the musculoskeletal system. Its absence in mice (Col13a1-/- ) results in impaired neuromuscular junction (NMJ) differentiation and function, while transgenic overexpression (Col13a1oe ) lea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12632f10e3f2af4c48142f1acd4c30b1
https://pubmed.ncbi.nlm.nih.gov/30667565
https://pubmed.ncbi.nlm.nih.gov/30667565
Autor:
Giulio Cossu, Claudia Fuoco, Cesare Gargioli, Stefano Cannata, Sabrina Santoleri, Francesco Tedesco, Stefania Antonini, Maria Lavinia Salvatori, Sergio Bernardini, Keren Shapira-Schweitzer, Dror Seliktar, Antonella Biondo
Publikováno v:
Skeletal Muscle
Skeletal Muscle, Vol 2, Iss 1, p 24 (2012)
Skeletal Muscle; Vol 2
Skeletal Muscle, Vol 2, Iss 1, p 24 (2012)
Skeletal Muscle; Vol 2
Background Cell-transplantation therapies have attracted attention as treatments for skeletal-muscle disorders; however, such research has been severely limited by poor cell survival. Tissue engineering offers a potential solution to this problem by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aaee914f4b78bf1c89f4289c18d190be
https://pubmed.ncbi.nlm.nih.gov/23181356
https://pubmed.ncbi.nlm.nih.gov/23181356
Autor:
Giovanni, Chillemi, Paola, Fiorani, Alessandro, Bruselles, Silvia, Castelli, Alessia, Campagna, Ofelia, Sarra, Cinzia, Tesauro, Monica, Fiorentini, Oscar, Vassallo, Ilda, D'Annessa, Sabrina, Santoleri, Alessandro, Desideri
Publikováno v:
The Italian journal of biochemistry. 56(2)
Eukaryotic topoisomerase I is an essential enzyme that regulates the changes in DNA topology, relaxing the superhelical tension associated with DNA replication, transcription and recombination. Human topoisomerase I is of significant medical interest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4e883bfb86127096155a7d52170212fe
https://pubmed.ncbi.nlm.nih.gov/17722651
https://pubmed.ncbi.nlm.nih.gov/17722651