Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Cristina Lapucci"'
Autor:
Graziano Santoro, Fabiana Cro, Federica Poma, Cristina Kullmann, Cristina Lapucci, Maurizio Ferrari
Publikováno v:
Clinical Case Reports, Vol 10, Iss 9, Pp n/a-n/a (2022)
Abstract Here, we describe a case report of a Sardinian woman diagnosed as pure beta‐thalassemia carrier for her anemia who underwent to alpha‐thalassemia genetic testing that revealed she was heterozygous for both thalssemias. This allowed to re
Externí odkaz:
https://doaj.org/article/4ce3c3b6204c4a8b88f3215e00173021
Autor:
Anna Maria Grimaldi, Cristina Lapucci, Marco Salvatore, Mariarosaria Incoronato, Maurizio Ferrari
Publikováno v:
Biomedicines, Vol 10, Iss 11, p 2766 (2022)
Bladder cancer is the 10th most common cancer type worldwide. Cystoscopy represents the gold standard for bladder cancer diagnosis, but this procedure is invasive and painful, hence the need to identify new biomarkers through noninvasive procedures.
Externí odkaz:
https://doaj.org/article/509ac63620424314a457551aa5cf3b5c
Autor:
Graziano Santoro, Cristina Lapucci, Marco Giannoccaro, Simona Caporilli, Martina Rusin, Anna Seidenari, Maurizio Ferrari, Antonio Farina
Publikováno v:
Diagnostics, Vol 11, Iss 11, p 2108 (2021)
The present pilot study investigates whether an abnormal miRNA profile in NIPT plasma samples can explain the finding of a low cell-free DNA (cfDNA) fetal fraction (cfDNAff) in euploid fetuses and non-obese women. Twelve women who underwent neoBona®
Externí odkaz:
https://doaj.org/article/2a8e843759b243ffb7628b3a5e8c65e1
Autor:
Enrico Tagliafico, Isabella Bernardis, Marina Grasso, Maria Rosaria D'Apice, Cristina Lapucci, Annalisa Botta, Daniela Francesca Giachino, Maria Marinelli, Paola Primignani, Silvia Russo, Ilaria Sani, Manuela Seia, Sergio Fini, Paola Rimessi, Elena Tenedini, Anna Ravani, Maurizio Genuardi, Alessandra Ferlini, Molecular Genetics Working Group of the Italian Society of Human Genetics, SIGU
Publikováno v:
PLoS ONE, Vol 13, Iss 11, p e0206855 (2018)
Genetic testing availability in the health care system is rapidly increasing, along with the diffusion of next-generation sequencing (NGS) into diagnostics. These issues make imperative the knowledge-drive optimization of testing in the clinical sett
Externí odkaz:
https://doaj.org/article/e0be3ab1c9574e378228b83edd270268
Publikováno v:
Case Reports in Obstetrics and Gynecology, Vol 2015 (2015)
Panorama Plus (Natera), a single-nucleotide polymorphism- (SNP-) based approach that relies on the identification of maternal and fetal allele distributions, allows the detection of common aneuploidies and also incorporates a panel of 5 microdeletion
Externí odkaz:
https://doaj.org/article/9f2e5c9a6c424a5a84ac755c1d308f48
Autor:
Simona Caporilli, Antonio Farina, Maurizio Ferrari, Cristina Lapucci, Marco Giannoccaro, Anna Seidenari, Martina Rusin, Graziano Santoro
Publikováno v:
Diagnostics, Vol 11, Iss 2108, p 2108 (2021)
Diagnostics
Diagnostics
The present pilot study investigates whether an abnormal miRNA profile in NIPT plasma samples can explain the finding of a low cell-free DNA (cfDNA) fetal fraction (cfDNAff) in euploid fetuses and non-obese women. Twelve women who underwent neoBona®
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::588dd6a93a3602c156948eed9ccbde91
https://www.mdpi.com/2075-4418/11/11/2108
https://www.mdpi.com/2075-4418/11/11/2108
Autor:
Megan Schwarz, Denis Torre, Daniel Lozano-Ojalvo, Anthony T. Tan, Tommaso Tabaglio, Slim Mzoughi, Rodrigo Sanchez-Tarjuelo, Nina Le Bert, Joey Ming Er Lim, Sandra Hatem, Kevin Tuballes, Carmen Camara, Eduardo Lopez-Granados, Estela Paz-Artal, Rafael Correa-Rocha, Alberto Ortiz, Marcos Lopez-Hoyos, Jose Portoles, Isabel Cervera, Maria Gonzalez-Perez, Irene Bodega-Mayor, Patricia Conde, Jesús Oteo-Iglesias, Alberto M. Borobia, Antonio J. Carcas, Jesús Frías, Cristóbal Belda-Iniesta, Jessica S. Y. Ho, Kemuel Nunez, Saboor Hekmaty, Kevin Mohammed, William M. Marsiglia, Juan Manuel Carreño, Arvin C. Dar, Cecilia Berin, Giuseppe Nicoletti, Isabella Della Noce, Lorenzo Colombo, Cristina Lapucci, Graziano Santoro, Maurizio Ferrari, Kai Nie, Manishkumar Patel, Vanessa Barcessat, Sacha Gnjatic, Jocelyn Harris, Robert Sebra, Miriam Merad, Florian Krammer, Seunghee Kim-schulze, Ivan Marazzi, Antonio Bertoletti, Jordi Ochando, Ernesto Guccione
Publikováno v:
Nature biotechnology. 40(11)
et al.
Fast, high-throughput methods for measuring the level and duration of protective immune responses to SARS-CoV-2 are needed to anticipate the risk of breakthrough infections. Here we report the development of two quantitative PCR assays fo
Fast, high-throughput methods for measuring the level and duration of protective immune responses to SARS-CoV-2 are needed to anticipate the risk of breakthrough infections. Here we report the development of two quantitative PCR assays fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c01734224edd0b310de2dfe157af710
https://pubmed.ncbi.nlm.nih.gov/35697804
https://pubmed.ncbi.nlm.nih.gov/35697804
Autor:
Danila Morano, Silvia Berto, Antonio Farina, Daniela Prandstraller, Lara Walczer Baldinazzo, Cristina Lapucci
Publikováno v:
Molecular Diagnosis & Therapy. 22:235-240
Objective: Maternal plasma is a source of circulating placental nucleic acids. In this study, we validated previous observations on abnormal levels of circulating messenger RNA (mRNA) for the tenascin-X gene in pregnancies with ventricular septal def
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99c8317b1876551e393f6a55ca2ad5bb
https://doi.org/10.1007/s40291-018-0321-4
https://doi.org/10.1007/s40291-018-0321-4
Autor:
Cristina Lapucci, Daniela Prandstraller, Silvia Berto, Antonella Perolo, Antonio Farina, Nicola Rizzo, Elena Contro, Diego Arcelli, Lara Stefani
Publikováno v:
Molecular Diagnosis & Therapy. 21:653-661
Objective: Maternal plasma is a source of circulating placental nucleic acids. This study was designed to detect aberrantly expressed placental mRNA genes circulating in the maternal plasma of pregnancies affected with fetal conotruncal anomalies (CN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e75f78ab6816992d6e8af46e077590f
https://doi.org/10.1007/s40291-017-0295-7
https://doi.org/10.1007/s40291-017-0295-7
Autor:
Daniela Prandstraller, Cristina Lapucci, Nicola Rizzo, Silvia Berto, Antonella Perolo, Antonio Farina, Alessandra Curti
Publikováno v:
Prenatal Diagnosis. 36:738-743
Objective To verify the hypothesis that aberrant placental mRNA genes related to cardiogenesis can be detected in maternal plasma at the second trimester of pregnancy. Methods NanoString technology was used to identify aberrant genes, comparing 39 wo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99eb7be25816c0865b5280e29b50c95a
https://doi.org/10.1002/pd.4853
https://doi.org/10.1002/pd.4853