Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Rosa Valentina Talarico"'
Autor:
Rosamaria Capuano, Paola Spitalieri, Rosa Valentina Talarico, Ana Carolina Domakoski, Alexandro Catini, Roberto Paolesse, Eugenio Martinelli, Giuseppe Novelli, Federica Sangiuolo, Corrado Di Natale
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-12 (2017)
Abstract Cellular metabolism of stem cell biology is still an unexplored field. However, considering the amount of information carried by metabolomes, this is a promising field for a fast identification of stem cells itself and during the differentia
Externí odkaz:
https://doaj.org/article/812f86c2db0f491c84d6bc6ed303bce3
Autor:
Maria Rosaria D'Apice, Massimo Sanchez, Ion Udroiu, Rosa Valentina Talarico, Chiara Fiorillo, Jessica Marinaccio, Antonella Sgura, Michela Murdocca, Claudia De Masi, Giuseppe Novelli, Monica D’Adamo, Paola Spitalieri, Federica Sangiuolo, Paolo Sbraccia
Mandibular hypoplasia, Deafness and Progeroid features with concomitant Lipodystrophy define a rare systemic disorder, named MDPL Syndrome, due to almost always a de novo variant in POLD1 gene, encoding the DNA polymerase δ. We report a MDPL female
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a070eb7d1067fbb331ec0b9c30444525
http://hdl.handle.net/2108/285060
http://hdl.handle.net/2108/285060
Autor:
Michela, Murdocca, Paola, Spitalieri, Claudia, De Masi, Ion, Udroiu, Jessica, Marinaccio, Massimo, Sanchez, Rosa Valentina, Talarico, Chiara, Fiorillo, Monica, D'Adamo, Paolo, Sbraccia, Maria Rosaria, D'Apice, Giuseppe, Novelli, Antonella, Sgura, Federica, Sangiuolo
Publikováno v:
Aging (Albany NY)
Mandibular hypoplasia, Deafness and Progeroid features with concomitant Lipodystrophy define a rare systemic disorder, named MDPL Syndrome, due to almost always a de novo variant in POLD1 gene, encoding the DNA polymerase δ. We report a MDPL female
Autor:
Sabina Pucci, Simone Dinarelli, Giovanni Longo, Paola Spitalieri, Silvia Caioli, Ruggiero Mango, Giuseppe Novelli, Cristina Zona, Marco Girasole, Rosa Valentina Talarico, Michela Murdocca, Annalisa Botta, Annalucia Serafino, Federica Sangiuolo
Publikováno v:
Journal of Molecular and Cellular Cardiology 118 (2018): 95–109. doi:10.1016/j.yjmcc.2018.03.012
info:cnr-pdr/source/autori:Spitalieri, Paola; Talarico, Rosa V.; Caioli, Silvia; Murdocca, Michela; Serafino, Annalucia; Girasole, Marco; Dinarelli, Simone; Longo, Giovanni; Pucci, Sabina; Botta, Annalisa; Novelli, Giuseppe; Zona, Cristina; Mango, Ruggiero; Sangiuolo, Federica/titolo:Modelling the pathogenesis of Myotonic Dystrophy type 1 cardiac phenotype through human iPSC-derived cardiomyocytes/doi:10.1016%2Fj.yjmcc.2018.03.012/rivista:Journal of Molecular and Cellular Cardiology/anno:2018/pagina_da:95/pagina_a:109/intervallo_pagine:95–109/volume:118
info:cnr-pdr/source/autori:Spitalieri, Paola; Talarico, Rosa V.; Caioli, Silvia; Murdocca, Michela; Serafino, Annalucia; Girasole, Marco; Dinarelli, Simone; Longo, Giovanni; Pucci, Sabina; Botta, Annalisa; Novelli, Giuseppe; Zona, Cristina; Mango, Ruggiero; Sangiuolo, Federica/titolo:Modelling the pathogenesis of Myotonic Dystrophy type 1 cardiac phenotype through human iPSC-derived cardiomyocytes/doi:10.1016%2Fj.yjmcc.2018.03.012/rivista:Journal of Molecular and Cellular Cardiology/anno:2018/pagina_da:95/pagina_a:109/intervallo_pagine:95–109/volume:118
Myotonic Dystrophy type 1 (DM1) is a multisystemic disease, autosomal dominant, caused by a CTG repeat expansion in DMPK gene. We assessed the appropriateness of patient-specific induced pluripotent stem cell-derived cardiomyocytes (CMs) as a model t
Autor:
Augusto Orlandi, Paola Spitalieri, Rosella Cicconi, Roberto Paolesse, Ana Carolina Domakoski, Eugenio Martinelli, Rosamaria Capuano, Corrado Di Natale, Rosa Valentina Talarico, Federica Sangiuolo, Maria Giovanna Scioli, Alexandro Catini, Giuseppe Novelli
Publikováno v:
Scientific Reports
Scientific Reports, Vol 8, Iss 1, Pp 1-12 (2018)
Scientific Reports, Vol 8, Iss 1, Pp 1-12 (2018)
Several investigations point out that the volatile fraction of metabolites, often called volatilome, might signal the difference processes occurring in living beings, both in vitro and in vivo. These studies have been recently applied to stem cells b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b70f9704718c9e5e3f5dff129b0ad8a6
http://hdl.handle.net/2108/210816
http://hdl.handle.net/2108/210816
Autor:
Rosamaria, Capuano, Rosa Valentina, Talarico, Paola, Spitalieri, Roberto, Paolesse, Giuseppe, Novelli, Federica, Sangiuolo, Corrado, Di Natale
Publikováno v:
Bio Protoc
Human induced pluripotent stem cells (hiPSCs) are a promising tool in cell-based therapies for degenerative diseases. A safe application of hiPSCs in vivo, requires the detection of the presence of residual undifferentiated pluripotent cells that can
Publikováno v:
Toward the Future: The New Challenges of the Cell Therapy and Potential of Regenerative Medicine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::37d3690cfe02294e5d216d007a4ff380
https://doi.org/10.2174/9781681084374117010009
https://doi.org/10.2174/9781681084374117010009
Autor:
Rosa Valentina Talarico, Paola Spitalieri, Giuseppe Novelli, Corrado Di Natale, Rosamaria Capuano, Federica Sangiuolo, Roberto Paolesse
Publikováno v:
BIO-PROTOCOL. 7
Human induced pluripotent stem cells (hiPSCs) are a promising tool in cell-based therapies for degenerative diseases. A safe application of hiPSCs in vivo, requires the detection of the presence of residual undifferentiated pluripotent cells that can
Autor:
Ana Carolina Domakoski, Rosamaria Capuano, Rosa Valentina Talarico, Giuseppe Novelli, Federica Sangiuolo, Alexandro Catini, Roberto Paolesse, Paola Spitalieri, Eugenio Martinelli, Corrado Di Natale
Although cellular metabolism of pluripotent stem cells is still largely unexplored, metabolomics is a promising approach for a fast identification of stem cells during the differentiation process. In this paper we report the first investigation of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65545b5b89bf55f859b72d5d393b2717
http://hdl.handle.net/2108/244432
http://hdl.handle.net/2108/244432
Autor:
Rosa Valentina Talarico, Michela Murdocca, Massimo Sanchez, Giuseppe Novelli, Paola Spitalieri, Federica Sangiuolo, Silvia Anna Ciafrè
Publikováno v:
International Journal of Molecular Sciences
Spinal Muscular Atrophy (SMA) is a neuromuscular disease caused by mutations in the Survival Motor Neuron 1 gene, resulting in very low levels of functional Survival of Motor Neuron (SMN) protein. SMA human induced Pluripotent Stem Cells (hiPSCs) rep