Corrigendum to ‘Coinheritance of germline mutations in APC and MUTYH genes defines the clinical outcome of adenomatous polyposis syndromes’ [Gene Dis (10) (2023), 1187–1189]

Autor: Giovanna Forte, Filomena Cariola, Antonia Lucia Buonadonna, Anna Filomena Guglielmi, Andrea Manghisi, Katia De Marco, Valentina Grossi, Candida Fasano, Martina Lepore Signorile, Paola Sanese, Rosanna Bagnulo, Nicoletta Resta, Vittoria Disciglio, Cristiano Simone

Publikováno v: Genes and Diseases, Vol 11, Iss 2, Pp 1084- (2024)

Externí odkaz: https://doaj.org/article/85689712f5434c3caf431daeca8fc522

Coinheritance of germline mutations in APC and MUTYH genes defines the clinical outcome of adenomatous polyposis syndromes

Autor: Giovanna Forte, Filomena Cariola, Antonia Lucia Buonadonna, Anna Filomena Guglielmi, Andrea Manghisi, Katia De Marco, Valentina Grossi, Candida Fasano, Martina Lepore Signorile, Paola Sanese, Rosanna Bagnulo, Nicoletta Resta, Vittoria Disciglio, Cristiano Simone

Publikováno v: Genes and Diseases, Vol 10, Iss 4, Pp 1187-1189 (2023)

Externí odkaz: https://doaj.org/article/98534bd75c294ac18e9690010718e4ac

Coinheritance of germline mutations in APC and MUTYH genes defines the clinical outcome of adenomatous polyposis syndromes

Autor: Giovanna Forte, Filomena Cariola, Antonia Lucia Buonadonna, Anna Filomena Guglielmi, Andrea Manghisi, Katia De Marco, Valentina Grossi, Candida Fasano, Martina Lepore Signorile, Paola Sanese, Rosanna Bagnulo, Nicoletta Resta, Vittoria Disciglio, Cristiano Simone

Publikováno v: Genes & Diseases.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::96342a1972069b6c16e55e0a65d0fb22
https://doi.org/10.1016/j.gendis.2022.11.017

Characterization of a rare variant (c.2635-2AG) of the MSH2 gene in a family with Lynch syndrome

Autor: Floranna Guglielmi, Claudio Lotesoriere, Candida Fasano, Ivan Lolli, Anna Maria Valentini, Andrea Manghisi, Cristiano Simone, L. Russo, Vittoria Disciglio, Giovanna Forte, Filomena Cariola, Antonio Di Carlo, Maria Lucia Caruso

Publikováno v: The International journal of biological markers.

Introduction: Lynch syndrome is caused by germline mutations in one of the mismatch repair genes ( MLH1, MSH2, MSH6, and PMS2) or in the EPCAM gene. Lynch syndrome is defined on the basis of clinical, pathological, and genetic findings. Accordingly,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc22efdc0ea340b55978cf4076d1afbb
https://pubmed.ncbi.nlm.nih.gov/29690800

Exploring the Relationship of rs2802292 with Diabetes and NAFLD in a Southern Italian Cohort—Nutrihep Study.

Autor: Forte, Giovanna¹ (AUTHOR) giovanna.forte@irccsdebellis.it, Donghia, Rossella² (AUTHOR) rossella.donghia@irccsdebellis.it, Lepore Signorile, Martina¹ (AUTHOR) martina.lepore@irccsdebellis.it, Tatoli, Rossella² (AUTHOR) rossella.tatoli@irccsdebellis.it, Bonfiglio, Caterina² (AUTHOR) catia.bonfiglio@irccsdebellis.it, Losito, Francesco³ (AUTHOR) francesco.losito@irccsdebellis.it, De Marco, Katia¹ (AUTHOR) katia.demarco@irccsdebellis.it, Manghisi, Andrea¹ (AUTHOR) andrea.manghisi@irccsdebellis.it, Guglielmi, Filomena Anna¹ (AUTHOR) floranna.guglielmi@irccsdebellis.it, Disciglio, Vittoria¹ (AUTHOR) vittoria.disciglio@irccsdebellis.it, Fasano, Candida¹ (AUTHOR) candida.fasano@irccsdebellis.it, Sanese, Paola¹ (AUTHOR) paola.sanese@irccsdebellis.it, Cariola, Filomena¹ (AUTHOR) filo.cariola@irccsdebellis.it, Buonadonna, Antonia Lucia¹ (AUTHOR) lucia.buonadonna@irccsdebellis.it, Grossi, Valentina¹ (AUTHOR) valentina.grossi@irccsdebellis.it, Giannelli, Gianluigi⁴ (AUTHOR) gianluigi.giannelli@irccsdebellis.it, Simone, Cristiano^1,5 (AUTHOR) valentina.grossi@irccsdebellis.it

Publikováno v: International Journal of Molecular Sciences. Sep2024, Vol. 25 Issue 17, p9512. 13p.