Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Carlo Della Ragione"'
Autor:
Raffaella Liccardo, Antonio Nolano, Matilde Lambiase, Carlo Della Ragione, Marina De Rosa, Paola Izzo, Francesca Duraturo
Publikováno v:
Biomedicines, Vol 8, Iss 6, p 167 (2020)
Background: The loss or low expression of DNA mismatch repair (MMR) genes can result in genomic instability and tumorigenesis. One such gene, MSH2, is mutated or rearranged in Lynch syndrome (LS), which is characterized by a high risk of tumor develo
Externí odkaz:
https://doaj.org/article/8e3539812d24414682a2470e060731cf
Autor:
Carlo Della Ragione, Marina De Rosa, Nunzio Mitilini, Paola Izzo, Francesca Duraturo, Raffaella Liccardo
Publikováno v:
Cancer Management and Research. 11:6719-6725
Background: Lynch syndrome is associated with genetic variants in mismatch repair (MMR) genes. Pathogenic variants in the MLH1 and MSH2 genes occur in most families in which the phenotype is highly penetrant. These testing criteria are likely to miss
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5710ae63a8237216a65c6526765041f
https://doi.org/10.2147/cmar.s167348
https://doi.org/10.2147/cmar.s167348
Autor:
Matilde Lambiase, Antonio Nolano, Raffaella Liccardo, Francesca Duraturo, Carlo Della Ragione, Paola Izzo, Marina De Rosa
Publikováno v:
Biomedicines
Volume 8
Issue 6
Biomedicines, Vol 8, Iss 167, p 167 (2020)
Volume 8
Issue 6
Biomedicines, Vol 8, Iss 167, p 167 (2020)
Background: The loss or low expression of DNA mismatch repair (MMR) genes can result in genomic instability and tumorigenesis. One such gene, MSH2, is mutated or rearranged in Lynch syndrome (LS), which is characterized by a high risk of tumor develo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e59a7a09ab8d756e7f4d7900380e8b98
https://pubmed.ncbi.nlm.nih.gov/32575404
https://pubmed.ncbi.nlm.nih.gov/32575404
Autor:
Raffaella, Liccardo, Carlo, Della Ragione, Nunzio, Mitilini, Marina, De Rosa, Paola, Izzo, Francesca, Duraturo
Publikováno v:
Cancer Management and Research
Background: Lynch syndrome is associated with genetic variants in mismatch repair (MMR) genes. Pathogenic variants in the MLH1 and MSH2 genes occur in most families in which the phenotype is highly penetrant. These testing criteria are likely to miss
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c2990f8f658ab97cccb49e40b843b32f
https://pubmed.ncbi.nlm.nih.gov/31410062
https://pubmed.ncbi.nlm.nih.gov/31410062