Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Salvatore Pulcrano"'
Autor:
Rosaria Meccariello, Gian Carlo Bellenchi, Salvatore Pulcrano, Sebastian Luca D’Addario, Domenico Tafuri, Nicola B. Mercuri, Ezia Guatteo
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 17 (2024)
Over the last few decades, emerging evidence suggests that non-coding RNAs (ncRNAs) including long-non-coding RNA (lncRNA), microRNA (miRNA) and circular-RNA (circRNA) contribute to the molecular events underlying progressive neuronal degeneration, a
Externí odkaz:
https://doaj.org/article/f6bd37bd05184584b344f8476221a3a7
Autor:
Maria De Risi, Michele Tufano, Filomena Grazia Alvino, Maria Grazia Ferraro, Giulia Torromino, Ylenia Gigante, Jlenia Monfregola, Elena Marrocco, Salvatore Pulcrano, Lea Tunisi, Claudia Lubrano, Dulce Papy-Garcia, Yaakov Tuchman, Alberto Salleo, Francesca Santoro, Gian Carlo Bellenchi, Luigia Cristino, Andrea Ballabio, Alessandro Fraldi, Elvira De Leonibus
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-17 (2021)
Lysosomal storage disorders, characterized by altered metabolism of heparan sulfate, cause autistic symptoms followed by dementia in children. Here, the authors show that embryonic dopaminergic neurodevelopmental defects due to altered function of he
Externí odkaz:
https://doaj.org/article/5ebeb3f36eeb489b8e165e8571b181e3
Autor:
Francesco Della Valle, Manjula P. Thimma, Massimiliano Caiazzo, Salvatore Pulcrano, Mirko Celii, Sabir A. Adroub, Peng Liu, Gregorio Alanis-Lobato, Vania Broccoli, Valerio Orlando
Publikováno v:
Stem Cell Reports, Vol 14, Iss 1, Pp 60-74 (2020)
Summary: In mammals, LINE-1 (L1) retrotransposons constitute between 15% and 20% of the genome. Although only a few copies have retained the ability to retrotranspose, evidence in brain and differentiating pluripotent cells indicates that L1 retrotra
Externí odkaz:
https://doaj.org/article/5b877dab7e3747c58a1c35b460267621
Autor:
Luisa Speranza, Kardelen Dalım Filiz, Sarah Goebel, Carla Perrone-Capano, Salvatore Pulcrano, Floriana Volpicelli, Anna Francesconi
Publikováno v:
Biomedicines, Vol 10, Iss 11, p 2692 (2022)
Structural, functional, and molecular alterations in excitatory spines are a common hallmark of many neurodevelopmental disorders including intellectual disability and autism. Here, we describe an optimized methodology, based on combined use of DiI a
Externí odkaz:
https://doaj.org/article/86c24fa70d804e97b93ceeec94c66795
Autor:
Floriana Volpicelli, Roberto De Gregorio, Salvatore Pulcrano, Carla Perrone-Capano, Umberto di Porzio, Gian Carlo Bellenchi
Publikováno v:
PLoS ONE, Vol 15, Iss 5, p e0233918 (2020)
[This corrects the article DOI: 10.1371/journal.pone.0030661.].
Externí odkaz:
https://doaj.org/article/24061e8bb8414fbeb8f525d6cba4d9ca
Autor:
Roberto De Gregorio, Salvatore Pulcrano, Claudia De Sanctis, Floriana Volpicelli, Ezia Guatteo, Lars von Oerthel, Emanuele Claudio Latagliata, Roberta Esposito, Rosa Maria Piscitelli, Carla Perrone-Capano, Valerio Costa, Dario Greco, Stefano Puglisi-Allegra, Marten P. Smidt, Umberto di Porzio, Massimiliano Caiazzo, Nicola Biagio Mercuri, Meng Li, Gian Carlo Bellenchi
Publikováno v:
Stem Cell Reports, Vol 10, Iss 4, Pp 1237-1250 (2018)
Summary: The differentiation of dopaminergic neurons requires concerted action of morphogens and transcription factors acting in a precise and well-defined time window. Very little is known about the potential role of microRNA in these events. By per
Externí odkaz:
https://doaj.org/article/3c07e32b8cbb4c9bbf1ce3db9c93dc16
Autor:
Floriana Volpicelli, Roberto De Gregorio, Salvatore Pulcrano, Carla Perrone-Capano, Umberto di Porzio, Gian Carlo Bellenchi
Publikováno v:
PLoS ONE, Vol 7, Iss 2, p e30661 (2012)
Due to their correlation with major human neurological diseases, dopaminergic neurons are some of the most studied neuronal subtypes. Mesencephalic dopaminergic (mDA) differentiation requires the activation of a cascade of transcription factors, amon
Externí odkaz:
https://doaj.org/article/9402b735a5dd41ce89c6284366b6aa2e
Autor:
Salvatore Pulcrano, Umberto di Porzio
Publikováno v:
Academia Letters.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6ad6b93782b49243d72733ca60922d7
https://doi.org/10.20935/al4185
https://doi.org/10.20935/al4185
Autor:
Salvatore Pulcrano, Mariangela Cerreta, Gian Carlo Bellenchi, Davide Nardone, Ferdinando Febbraio, Linda Leone, Giuseppe Manco, Angelo Ciaramella
Publikováno v:
Biotechnology and applied biochemistry (2021). doi:10.1002/bab.2249
info:cnr-pdr/source/autori:Nardone D.; Ciaramella A.; Cerreta M.; Pulcrano S.; Bellenchi G.C.; Leone L.; Manco G.; Febbraio F./titolo:Selymatra: A web application for protein-profiling analysis of mass spectra/doi:10.1002%2Fbab.2249/rivista:Biotechnology and applied biochemistry/anno:2021/pagina_da:/pagina_a:/intervallo_pagine:/volume
info:cnr-pdr/source/autori:Nardone D.; Ciaramella A.; Cerreta M.; Pulcrano S.; Bellenchi G.C.; Leone L.; Manco G.; Febbraio F./titolo:Selymatra: A web application for protein-profiling analysis of mass spectra/doi:10.1002%2Fbab.2249/rivista:Biotechnology and applied biochemistry/anno:2021/pagina_da:/pagina_a:/intervallo_pagine:/volume
Surface enhanced laser desorption/ionization-time of flight (SELDI-TOF) mass spectrometry is a variant of the matrix-assisted laser desorption/ionization-time of flight (MALDI-TOF) mass spectrometry. It is used in many cases especially for the analys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20635e22d1b1e09696ec31829132ed6a
https://pubmed.ncbi.nlm.nih.gov/34487563
https://pubmed.ncbi.nlm.nih.gov/34487563
Autor:
Yaakov Tuchman, Michele Tufano, Filomena Grazia Alvino, Alberto Salleo, Giulia Torromino, Ylenia Gigante, Jlenia Monfregola, Maria Grazia Ferraro, Maria De Risi, Elvira De Leonibus, Alessandro Fraldi, Andrea Ballabio, Dulce Papy-Garcia, Lea Tunisi, Claudia Lubrano, Francesca Santoro, Salvatore Pulcrano, Gian Carlo Bellenchi, Elena Marrocco, Luigia Cristino
Publikováno v:
Nature communications 12 (2021). doi:10.1038/s41467-021-23903-5
info:cnr-pdr/source/autori:De Risi M.; Tufano M.; Alvino F.G.; Ferraro M.G.; Torromino G.; Gigante Y.; Monfregola J.; Marrocco E.; Pulcrano S.; Tunisi L.; Lubrano C.; Papy-Garcia D.; Tuchman Y.; Salleo A.; Santoro F.; Bellenchi G.C.; Cristino L.; Ballabio A.; Fraldi A.; De Leonibus E./titolo:Altered heparan sulfate metabolism during development triggers dopamine-dependent autistic-behaviours in models of lysosomal storage disorders/doi:10.1038%2Fs41467-021-23903-5/rivista:Nature communications/anno:2021/pagina_da:/pagina_a:/intervallo_pagine:/volume:12
Nature Communications
Nature Communications, Vol 12, Iss 1, Pp 1-17 (2021)
info:cnr-pdr/source/autori:De Risi M.; Tufano M.; Alvino F.G.; Ferraro M.G.; Torromino G.; Gigante Y.; Monfregola J.; Marrocco E.; Pulcrano S.; Tunisi L.; Lubrano C.; Papy-Garcia D.; Tuchman Y.; Salleo A.; Santoro F.; Bellenchi G.C.; Cristino L.; Ballabio A.; Fraldi A.; De Leonibus E./titolo:Altered heparan sulfate metabolism during development triggers dopamine-dependent autistic-behaviours in models of lysosomal storage disorders/doi:10.1038%2Fs41467-021-23903-5/rivista:Nature communications/anno:2021/pagina_da:/pagina_a:/intervallo_pagine:/volume:12
Nature Communications
Nature Communications, Vol 12, Iss 1, Pp 1-17 (2021)
Lysosomal storage disorders characterized by altered metabolism of heparan sulfate, including Mucopolysaccharidosis (MPS) III and MPS-II, exhibit lysosomal dysfunctions leading to neurodegeneration and dementia in children. In lysosomal storage disor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97c87bc7247dabaa4f4bdf6a666e2442
https://doi.org/10.1038/s41467-021-23903-5
https://doi.org/10.1038/s41467-021-23903-5