Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Alessandra Morgante"'
Autor:
Alessandra Ulivieri, Luca Lavra, Fiorenza Magi, Alessandra Morgante, Leonardo Calò, Patrizio Polisca, Leila B. Salehi, Salvatore Sciacchitano
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-13 (2022)
Abstract Prolongation of cardiac repolarization (QT interval) represents a dangerous and potentially life-threatening electrical event affecting the heart. Thyroid hormones (THs) are critical for cardiac development and heart function. However, littl
Externí odkaz:
https://doaj.org/article/45d4986c2186402cab95fe2b57f81153
Autor:
Salvatore Sciacchitano, Carlo Capalbo, Christian Napoli, Andrea Negro, Luciano De Biase, Adriano Marcolongo, Paolo Anibaldi, Valentina Salvati, Lea Petrella, Luca Merlo, Daniela Alampi, Elisa Alessandri, Chiara Loffredo, Alessandra Ulivieri, Luca Lavra, Fiorenza Magi, Alessandra Morgante, Leila B. Salehi, Claudia De Vitis, Rita Mancini, Flaminia Coluzzi, Monica Rocco
Publikováno v:
Journal of Translational Medicine, Vol 19, Iss 1, Pp 1-18 (2021)
Abstract Background Nonthyroidal Illness Syndrome (NTIS) can be detected in many critical illnesses. Recently, we demonstrated that this condition is frequently observed in COVID-19 patients too and it is correlated with the severity the disease. How
Externí odkaz:
https://doaj.org/article/6a0564040064407393f87c777bb37eb4
Autor:
Luca Lavra, Fiorenza Magi, Alessandra Ulivieri, Alessandra Morgante, Marianna Paulis, Luca Sala, Matteo Pedrazzini, Patrizio Polisca, Marcella Rocchetti, Leonardo Calò, Salvatore Sciacchitano, Leila B. Salehi
Publikováno v:
Stem Cell Research, Vol 54, Iss , Pp 102418- (2021)
In this study we describe the generation and characterization of an human induced pluripotent stem cell (hiPSC) line from a long QT syndrome type 1 (LQT1) patient carrying the KCNQ1 c.940 G > A (p.Gly314Ser) mutation. This patient-specific iPSC line
Externí odkaz:
https://doaj.org/article/3dee8cd02ef6407b96a8a6deaf2c1067
Autor:
Salvatore Sciacchitano, Luca Lavra, Alessandra Morgante, Alessandra Ulivieri, Fiorenza Magi, Gian Paolo De Francesco, Carlo Bellotti, Leila B. Salehi, Alberto Ricci
Publikováno v:
International Journal of Molecular Sciences, Vol 19, Iss 2, p 379 (2018)
Galectin-3 (Gal-3) regulates basic cellular functions such as cell–cell and cell–matrix interactions, growth, proliferation, differentiation, and inflammation. It is not surprising, therefore, that this protein is involved in the pathogenesis of
Externí odkaz:
https://doaj.org/article/f63c70ad9c0d4994ba41853569a5d15f
Autor:
Matteo Pedrazzini, Alessandra Morgante, Marianna Paulis, Salvatore Sciacchitano, Fiorenza Magi, Leonardo Calò, Alessandra Ulivieri, Marcella Rocchetti, Luca Lavra, Leila B. Salehi, Luca Sala, Patrizio Polisca
Publikováno v:
Stem Cell Research, Vol 54, Iss, Pp 102418-(2021)
In this study we describe the generation and characterization of an human induced pluripotent stem cell (hiPSC) line from a long QT syndrome type 1 (LQT1) patient carrying the KCNQ1 c.940 G > A (p.Gly314Ser) mutation. This patient-specific iPSC line
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd04edd4aa821b1df06bf4d020d8ac89
http://hdl.handle.net/10281/339398
http://hdl.handle.net/10281/339398
Autor:
Luca Lavra, Fiorenza Magi, Leila B. Salehi, Alessandra Ulivieri, Lea Petrella, Monica Rocco, Salvatore Sciacchitano, Luca Merlo, Andrea Negro, Alessandra Morgante, Chiara Loffredo, Rita Mancini, Elisa Alessandri, Luciano De Biase, Carlo Capalbo, Paolo Anibaldi, Flaminia Coluzzi, Valentina Salvati, Claudia De Vitis, D. Alampi, Adriano Marcolongo, Christian Napoli
Publikováno v:
Journal of Translational Medicine, Vol 19, Iss 1, Pp 1-18 (2021)
Journal of Translational Medicine
Journal of Translational Medicine
Background Nonthyroidal Illness Syndrome (NTIS) can be detected in many critical illnesses. Recently, we demonstrated that this condition is frequently observed in COVID-19 patients too and it is correlated with the severity the disease. However, the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb9afd7b9bbefed706d0d4f10793d081
http://hdl.handle.net/11573/1591395
http://hdl.handle.net/11573/1591395
Autor:
Leila B. Salehi, Carlo Bellotti, Alberto Ricci, Alessandra Morgante, Salvatore Sciacchitano, Luca Lavra, Fiorenza Magi, Alessandra Ulivieri, Gian Paolo De Francesco
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 19, Iss 2, p 379 (2018)
International Journal of Molecular Sciences, Vol 19, Iss 2, p 379 (2018)
Galectin-3 (Gal-3) regulates basic cellular functions such as cell–cell and cell–matrix interactions, growth, proliferation, differentiation, and inflammation. It is not surprising, therefore, that this protein is involved in the pathogenesis of
Co-segregation of DM2 with a recessive CLCN1 mutation in juvenile onset of myotonic dystrophy type 2
Autor:
Olayinka Raheem, Laura Valentina Renna, Fabrizio Rinaldi, Annalisa Botta, Enrico Bugiardini, Bjarne Udd, Giovanni Meola, Valeria A. Sansone, Giuseppe Novelli, Rosanna Cardani, Sini Penttilä, Alessandra Morgante, M. Giagnacovo, Tiina Suominen
Publikováno v:
Journal of Neurology. 259:2090-2099
Myotonic dystrophy type 2 (DM2) is a common adult onset muscular dystrophy caused by a dominantly transmitted (CCTG)( n ) expansion in intron 1 of the CNBP gene. In DM2 there is no obvious evidence for an intergenerational increase of expansion size,
Autor:
Claudio Catalli, Fabrizio Rinaldi, Annalisa Botta, Giuseppe Novelli, Raniero Iraci, Alessandra Morgante
Myotonic dystrophy type 2 (DM2, OMIM #602688) is a multisystemic hereditary degenerative disease caused by a tetranucleotide CCTG expansion in the ZNF9 gene. Routine testing strategies for DM2 require the use of Southern blot or long-range PCR, but t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c6782eb7b96c77cd112551b2e64a247
http://hdl.handle.net/2108/10344
http://hdl.handle.net/2108/10344
Publikováno v:
Analytical biochemistry. 235(1)