المؤلفون: Carnevali IW; UO Anatomia Patologica Ospedale di Circolo ASST-Settelaghi, 21100 Varese, Italy.; Centro di Ricerca per lo Studio dei Tumori Eredo-Famigliari, Università dell'Insubria, 21100 Varese, Italy., Cini G; Unit of Functional Oncogenomics and Genetics, Centro di Riferimento Oncologico di Aviano (CRO) IRCCS, 33081 Aviano, Italy., Libera L; Centro di Ricerca per lo Studio dei Tumori Eredo-Famigliari, Università dell'Insubria, 21100 Varese, Italy.; Department of Medicine and Thecnological Innovation, Università dell'Insubria, 21100 Varese, Italy., Sahnane N; UO Anatomia Patologica Ospedale di Circolo ASST-Settelaghi, 21100 Varese, Italy.; Centro di Ricerca per lo Studio dei Tumori Eredo-Famigliari, Università dell'Insubria, 21100 Varese, Italy., Facchi S; Centro di Ricerca per lo Studio dei Tumori Eredo-Famigliari, Università dell'Insubria, 21100 Varese, Italy.; Department of Medicine and Thecnological Innovation, Università dell'Insubria, 21100 Varese, Italy., Viel A; Unit of Functional Oncogenomics and Genetics, Centro di Riferimento Oncologico di Aviano (CRO) IRCCS, 33081 Aviano, Italy., Sessa F; UO Anatomia Patologica Ospedale di Circolo ASST-Settelaghi, 21100 Varese, Italy.; Centro di Ricerca per lo Studio dei Tumori Eredo-Famigliari, Università dell'Insubria, 21100 Varese, Italy.; Department of Medicine and Thecnological Innovation, Università dell'Insubria, 21100 Varese, Italy., Tibiletti MG; Centro di Ricerca per lo Studio dei Tumori Eredo-Famigliari, Università dell'Insubria, 21100 Varese, Italy.

المصدر: Genes [Genes (Basel)] 2023 Nov 09; Vol. 14 (11). Date of Electronic Publication: 2023 Nov 09.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: MDPI Country of Publication: Switzerland NLM ID: 101551097 Publication Model: Electronic Cited Medium: Internet ISSN: 2073-4425 (Electronic) Linking ISSN: 20734425 NLM ISO Abbreviation: Genes (Basel) Subsets: MEDLINE

مواضيع طبية MeSH: Colorectal Neoplasms, Hereditary Nonpolyposis*/genetics , Colorectal Neoplasms, Hereditary Nonpolyposis*/pathology , Endometrial Neoplasms*/diagnosis, Female ; Humans ; MutL Protein Homolog 1/genetics ; Microsatellite Instability ; Genetic Predisposition to Disease ; DNA Methylation/genetics ; Carcinogenesis/genetics

المؤلفون: Carnevali I; UO Anatomia Patologica, ASST Settelaghi, Ospedale di Circolo.; Centro di ricerca dei tumori eredo-familiari., Sahnane N; UO Anatomia Patologica, ASST Settelaghi, Ospedale di Circolo.; Centro di ricerca dei tumori eredo-familiari., Chiaravalli AM; UO Anatomia Patologica, ASST Settelaghi, Ospedale di Circolo.; Centro di ricerca dei tumori eredo-familiari., Di Lauro E; UO Anatomia Patologica, ASST Settelaghi, Ospedale di Circolo., Facco C; UO Anatomia Patologica, ASST Settelaghi, Ospedale di Circolo., Facchi S; UO Anatomia Patologica, ASST Settelaghi, Ospedale di Circolo., Casarin J; Dipartimento di Ostetricia e Ginecologia, ASST Settelaghi, University of Insubria, Varese, Italy., Ghezzi F; Centro di ricerca dei tumori eredo-familiari.; Dipartimento di Ostetricia e Ginecologia, ASST Settelaghi, University of Insubria, Varese, Italy., Sessa F; UO Anatomia Patologica, ASST Settelaghi, Ospedale di Circolo.; Centro di ricerca dei tumori eredo-familiari., Tibiletti MG; UO Anatomia Patologica, ASST Settelaghi, Ospedale di Circolo.; Centro di ricerca dei tumori eredo-familiari.

المصدر: European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP) [Eur J Cancer Prev] 2022 Jul 01; Vol. 31 (4), pp. 369-376. Date of Electronic Publication: 2021 Sep 13.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Lippincott Williams & Wilkins Country of Publication: England NLM ID: 9300837 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1473-5709 (Electronic) Linking ISSN: 09598278 NLM ISO Abbreviation: Eur J Cancer Prev Subsets: MEDLINE

مواضيع طبية MeSH: Colorectal Neoplasms, Hereditary Nonpolyposis*/diagnosis , Colorectal Neoplasms, Hereditary Nonpolyposis*/epidemiology , Colorectal Neoplasms, Hereditary Nonpolyposis*/genetics , Endometrial Neoplasms*/diagnosis , Endometrial Neoplasms*/epidemiology , Endometrial Neoplasms*/genetics , Ovarian Neoplasms*/diagnosis , Ovarian Neoplasms*/epidemiology , Ovarian Neoplasms*/genetics, DNA Mismatch Repair/genetics ; DNA Repair Enzymes/genetics ; DNA-Binding Proteins/metabolism ; Female ; Humans ; Immunohistochemistry ; Microsatellite Instability ; Mismatch Repair Endonuclease PMS2/genetics ; Mismatch Repair Endonuclease PMS2/metabolism ; MutL Protein Homolog 1/genetics ; MutL Protein Homolog 1/metabolism

المؤلفون: Cini G; Unit of Functional Oncogenomics and Genetics, Centro di Riferimento Oncologico di Aviano (CRO) IRCCS, Via F. Gallini 2, 33081 Aviano, Italy., Carnevali I; Department of Pathology, Circolo Hospital ASST Settelaghi, via O. Rossi 9, 21100, Varese, Italy; Research Center for the Study of Hereditary and Familial Tumors, Department of Medicine and Surgery, University of Insubria, via O. Rossi 9, 21100, Varese, Italy., Sahnane N; Department of Pathology, Circolo Hospital ASST Settelaghi, via O. Rossi 9, 21100, Varese, Italy; Research Center for the Study of Hereditary and Familial Tumors, Department of Medicine and Surgery, University of Insubria, via O. Rossi 9, 21100, Varese, Italy., Chiaravalli AM; Department of Pathology, Circolo Hospital ASST Settelaghi, via O. Rossi 9, 21100, Varese, Italy; Research Center for the Study of Hereditary and Familial Tumors, Department of Medicine and Surgery, University of Insubria, via O. Rossi 9, 21100, Varese, Italy., Dell'Elice A; Unit of Functional Oncogenomics and Genetics, Centro di Riferimento Oncologico di Aviano (CRO) IRCCS, Via F. Gallini 2, 33081 Aviano, Italy., Maestro R; Unit of Functional Oncogenomics and Genetics, Centro di Riferimento Oncologico di Aviano (CRO) IRCCS, Via F. Gallini 2, 33081 Aviano, Italy., Pin E; Division of Affinity Proteomics, Department of Protein Science, SciLifeLab, The Royal Institute of Technology KTH, Tomtebodavägen 23B, 171 65 Solna, Stockholm, Sweden., Bestetti I; Research Laboratory of Medical Cytogenetics and Molecular Genetics, IRCCS Istituto Auxologico Italiano, Via Zucchi, 18 - 20095 Cusano Milanino (MI); Department of Medical Biotechnology and Translational Medicine, University of Milan, Via Vanvitelli 32, 20133 Milan, Italy., Radovic S; IGA Technology Services Srl, Via J. Linussio, 51, 33100 Udine, Italy., Armelao F; U.O. Gastroenterologia ed Endoscopia Digestiva, Ospedale S. Chiara, APSS, Via A. de Gasperi 79 - 38123, Trento, Italy., Viel A; Unit of Functional Oncogenomics and Genetics, Centro di Riferimento Oncologico di Aviano (CRO) IRCCS, Via F. Gallini 2, 33081 Aviano, Italy. Electronic address: aviel@cro.it., Tibiletti MG; Department of Pathology, Circolo Hospital ASST Settelaghi, via O. Rossi 9, 21100, Varese, Italy; Research Center for the Study of Hereditary and Familial Tumors, Department of Medicine and Surgery, University of Insubria, via O. Rossi 9, 21100, Varese, Italy.

المصدر: Cancer genetics [Cancer Genet] 2021 Jun; Vol. 254-255, pp. 1-10. Date of Electronic Publication: 2021 Jan 19.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Elsevier Country of Publication: United States NLM ID: 101539150 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2210-7762 (Print) NLM ISO Abbreviation: Cancer Genet Subsets: MEDLINE

مواضيع طبية MeSH: 3' Untranslated Regions/*genetics , Colorectal Neoplasms, Hereditary Nonpolyposis/*genetics , Colorectal Neoplasms, Hereditary Nonpolyposis/*pathology , DNA-Binding Proteins/*genetics , Muir-Torre Syndrome/*genetics , Muir-Torre Syndrome/*pathology, Base Sequence ; Case-Control Studies ; Female ; Gene Expression Regulation ; Germ-Line Mutation/genetics ; Heterozygote ; Humans ; Male ; MutS Homolog 2 Protein/genetics ; Pedigree ; Phenotype ; Probability ; RNA, Messenger/genetics ; RNA, Messenger/metabolism

المؤلفون: Libera L; Unit of Pathology, Department of Medicine and Surgery, University of Insubria, 21100, Varese, Italy., Craparotta I; IRCCS Institute for Pharmacological Researches Mario Negri, Department of Oncology, 20156, Milano, Italy., Sahnane N; Unit of Pathology, Department of Medicine and Surgery, University of Insubria, 21100, Varese, Italy; Research Center for the study of Hereditary and Familial Tumors, Department of Medicine and Surgery, University of Insubria, 21100, Varese, Italy. Electronic address: n.sahnane@gmail.com., Chiaravalli AM; Research Center for the study of Hereditary and Familial Tumors, Department of Medicine and Surgery, University of Insubria, 21100, Varese, Italy; Unit of Pathology, ASST-Sette Laghi, 21100, Varese, Italy., Mannarino L; IRCCS Institute for Pharmacological Researches Mario Negri, Department of Oncology, 20156, Milano, Italy., Cerutti R; Unit of Pathology, Department of Medicine and Surgery, University of Insubria, 21100, Varese, Italy; Research Center for the study of Hereditary and Familial Tumors, Department of Medicine and Surgery, University of Insubria, 21100, Varese, Italy., Riva C; Unit of Pathology, Department of Medicine and Surgery, University of Insubria, 21100, Varese, Italy; Research Center for the study of Hereditary and Familial Tumors, Department of Medicine and Surgery, University of Insubria, 21100, Varese, Italy., Marchini S; IRCCS Institute for Pharmacological Researches Mario Negri, Department of Oncology, 20156, Milano, Italy., Furlan D; Unit of Pathology, Department of Medicine and Surgery, University of Insubria, 21100, Varese, Italy; Research Center for the study of Hereditary and Familial Tumors, Department of Medicine and Surgery, University of Insubria, 21100, Varese, Italy.

المصدر: Human pathology [Hum Pathol] 2018 Nov; Vol. 81, pp. 235-244. Date of Electronic Publication: 2018 Jul 03.

نوع المنشور: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: W B Saunders Country of Publication: United States NLM ID: 9421547 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1532-8392 (Electronic) Linking ISSN: 00468177 NLM ISO Abbreviation: Hum Pathol Subsets: MEDLINE

مواضيع طبية MeSH: High-Throughput Nucleotide Sequencing* , Microsatellite Instability* , Mutation*, Base Pair Mismatch/*genetics , Biomarkers, Tumor/*genetics , Colorectal Neoplasms, Hereditary Nonpolyposis/*genetics , DNA Mutational Analysis/*methods , Endometrial Neoplasms/*genetics , Gene Expression Profiling/*methods, Adult ; Aged ; Colorectal Neoplasms, Hereditary Nonpolyposis/pathology ; DNA-Binding Proteins ; Endometrial Neoplasms/pathology ; Female ; Gene Silencing ; Genetic Predisposition to Disease ; Humans ; Immunohistochemistry ; Middle Aged ; MutL Protein Homolog 1/genetics ; Nuclear Proteins/genetics ; Phenotype ; Predictive Value of Tests ; Proto-Oncogene Proteins p21(ras)/genetics ; Transcription Factors/genetics

المؤلفون: Carnevali I; Department of Pathology, Ospedale di Circolo, ASST Settelaghi, Varese; †Department of Medicine and Surgery, University of Insubria, Varese; ‡Unit of Functional Onco-Genomics and Genetics, CRO Aviano, National Cancer Institute, Aviano (PN); and §Department of Obstetrics and Gynecology, Ospedale di Circolo ASST Settelaghi, Varese, Italy., Libera L, Chiaravalli A, Sahnane N, Furlan D, Viel A, Cini G, Cimetti L, Rossi T, Formenti G, Ghezzi F, Riva C, Sessa F, Tibiletti MG

المصدر: International journal of gynecological cancer : official journal of the International Gynecological Cancer Society [Int J Gynecol Cancer] 2017 Sep; Vol. 27 (7), pp. 1543-1549.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: BMJ Country of Publication: England NLM ID: 9111626 Publication Model: Print Cited Medium: Internet ISSN: 1525-1438 (Electronic) Linking ISSN: 1048891X NLM ISO Abbreviation: Int J Gynecol Cancer Subsets: MEDLINE

مواضيع طبية MeSH: Colorectal Neoplasms, Hereditary Nonpolyposis/*diagnosis , Genital Neoplasms, Female/*diagnosis, Adult ; Aged ; Colorectal Neoplasms, Hereditary Nonpolyposis/genetics ; Colorectal Neoplasms, Hereditary Nonpolyposis/metabolism ; DNA Methylation ; DNA Repair Enzymes/biosynthesis ; DNA Repair Enzymes/genetics ; Female ; Genital Neoplasms, Female/genetics ; Genital Neoplasms, Female/metabolism ; Humans ; Immunohistochemistry ; Microsatellite Instability ; Middle Aged ; MutL Protein Homolog 1/biosynthesis ; MutL Protein Homolog 1/genetics ; Promoter Regions, Genetic

المؤلفون: Carnevali IW; Unit of Pathology (I.W.C., C.L., S.N., L.L., C.R., M.G.T.), Ospedale di Circolo Varese-University of InsubriaUnit of Pathology (A.C.), Ospedale Sant'Anna ComoGynaecologic and Obstetric Clinic, University of Insubria (G.F.), Ospedale di Circolo, Varese, Italy., Cimetti L, Sahnane N, Libera L, Cavallero A, Formenti G, Riva C, Tibiletti MG

المصدر: International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists [Int J Gynecol Pathol] 2017 Jan; Vol. 36 (1), pp. 64-70.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 8214845 Publication Model: Print Cited Medium: Internet ISSN: 1538-7151 (Electronic) Linking ISSN: 02771691 NLM ISO Abbreviation: Int J Gynecol Pathol Subsets: MEDLINE

مواضيع طبية MeSH: BRCA1 Protein/*genetics , Carcinosarcoma/*genetics , Colorectal Neoplasms, Hereditary Nonpolyposis/*genetics , DNA-Binding Proteins/*genetics , Neoplastic Syndromes, Hereditary/*genetics , Ovarian Neoplasms/*genetics, Adult ; Carcinosarcoma/diagnosis ; Carcinosarcoma/pathology ; Colorectal Neoplasms, Hereditary Nonpolyposis/complications ; Female ; Genetic Counseling ; Germ-Line Mutation ; Humans ; Middle Aged ; Neoplastic Syndromes, Hereditary/diagnosis ; Neoplastic Syndromes, Hereditary/pathology ; Ovarian Neoplasms/diagnosis ; Ovarian Neoplasms/pathology ; Ovary/pathology ; Tumor Suppressor Protein p53/genetics ; Tumor Suppressor Protein p53/metabolism