المؤلفون: Kurpiel B, Thomas MS, Mubeen M, Ring KL, Modesitt SC, Moskaluk CA, Mills AM

المصدر: International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists [Int J Gynecol Pathol] 2022 Jan 01; Vol. 41 (1), pp. 1-11.

نوع المنشور: 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: Germ-Line Mutation*, Colorectal Neoplasms, Hereditary Nonpolyposis/*genetics , Endometrial Neoplasms/*genetics , Mismatch Repair Endonuclease PMS2/*genetics , MutL Protein Homolog 1/*genetics, Adult ; Aged ; Aged, 80 and over ; Colorectal Neoplasms, Hereditary Nonpolyposis/pathology ; DNA Methylation ; DNA Mismatch Repair ; Endometrial Neoplasms/pathology ; Female ; Humans ; Immunohistochemistry ; Middle Aged ; Mismatch Repair Endonuclease PMS2/metabolism ; MutL Protein Homolog 1/metabolism ; Promoter Regions, Genetic/genetics ; Retrospective Studies

المؤلفون: Yamaguchi K; Division of Clinical Genome Research, Advanced Clinical Research Center, The Institute of Medical Science, The University of Tokyo, Tokyo, 108-8639, Japan., Kasajima R; Division of Health Medical Intelligence, Human Genome Center, The Institute of Medical Science, The University of Tokyo, Tokyo, 108-8639, Japan.; Molecular Pathology and Genetics Division, Kanagawa Cancer Center Research Institute, Kanagawa, 241-8518, Japan., Takane K; Division of Clinical Genome Research, Advanced Clinical Research Center, The Institute of Medical Science, The University of Tokyo, Tokyo, 108-8639, Japan., Hatakeyama S; Division of Clinical Genome Research, Advanced Clinical Research Center, The Institute of Medical Science, The University of Tokyo, Tokyo, 108-8639, Japan., Shimizu E; Division of Health Medical Intelligence, Human Genome Center, The Institute of Medical Science, The University of Tokyo, Tokyo, 108-8639, Japan., Yamaguchi R; Division of Health Medical Intelligence, Human Genome Center, The Institute of Medical Science, The University of Tokyo, Tokyo, 108-8639, Japan.; Division of Cancer Systems Biology, Aichi Cancer Center Research Institute, Aichi, 464-8681, Japan.; Division of Cancer Informatics, Nagoya University Graduate School of Medicine, Aichi, 466-8550, Japan., Katayama K; Division of Health Medical Intelligence, Human Genome Center, The Institute of Medical Science, The University of Tokyo, Tokyo, 108-8639, Japan., Arai M; The Committee of HNPCC Registry and Genetic Testing Project, Japanese Society for Cancer of the Colon and Rectum (JSCCR), Tokyo, 102-0075, Japan., Ishioka C; The Committee of HNPCC Registry and Genetic Testing Project, Japanese Society for Cancer of the Colon and Rectum (JSCCR), Tokyo, 102-0075, Japan., Iwama T; The Committee of HNPCC Registry and Genetic Testing Project, Japanese Society for Cancer of the Colon and Rectum (JSCCR), Tokyo, 102-0075, Japan., Kaneko S; The Committee of HNPCC Registry and Genetic Testing Project, Japanese Society for Cancer of the Colon and Rectum (JSCCR), Tokyo, 102-0075, Japan., Matsubara N; The Committee of HNPCC Registry and Genetic Testing Project, Japanese Society for Cancer of the Colon and Rectum (JSCCR), Tokyo, 102-0075, Japan., Moriya Y; The Committee of HNPCC Registry and Genetic Testing Project, Japanese Society for Cancer of the Colon and Rectum (JSCCR), Tokyo, 102-0075, Japan., Nomizu T; The Committee of HNPCC Registry and Genetic Testing Project, Japanese Society for Cancer of the Colon and Rectum (JSCCR), Tokyo, 102-0075, Japan., Sugano K; The Committee of HNPCC Registry and Genetic Testing Project, Japanese Society for Cancer of the Colon and Rectum (JSCCR), Tokyo, 102-0075, Japan., Tamura K; The Committee of HNPCC Registry and Genetic Testing Project, Japanese Society for Cancer of the Colon and Rectum (JSCCR), Tokyo, 102-0075, Japan., Tomita N; The Committee of HNPCC Registry and Genetic Testing Project, Japanese Society for Cancer of the Colon and Rectum (JSCCR), Tokyo, 102-0075, Japan., Yoshida T; The Committee of HNPCC Registry and Genetic Testing Project, Japanese Society for Cancer of the Colon and Rectum (JSCCR), Tokyo, 102-0075, Japan., Sugihara K; The Committee of HNPCC Registry and Genetic Testing Project, Japanese Society for Cancer of the Colon and Rectum (JSCCR), Tokyo, 102-0075, Japan., Nakamura Y; Cancer Precision Medicine Center, Japanese Foundation for Cancer Research, Tokyo, 135-8550, Japan., Miyano S; Division of Health Medical Intelligence, Human Genome Center, The Institute of Medical Science, The University of Tokyo, Tokyo, 108-8639, Japan.; Systems Biology for Intractable Diseases, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, 113-8510, Japan., Imoto S; Division of Health Medical Intelligence, Human Genome Center, The Institute of Medical Science, The University of Tokyo, Tokyo, 108-8639, Japan., Furukawa Y; Division of Clinical Genome Research, Advanced Clinical Research Center, The Institute of Medical Science, The University of Tokyo, Tokyo, 108-8639, Japan. yofurukawa@g.ecc.u-tokyo.ac.jp.; The Committee of HNPCC Registry and Genetic Testing Project, Japanese Society for Cancer of the Colon and Rectum (JSCCR), Tokyo, 102-0075, Japan. yofurukawa@g.ecc.u-tokyo.ac.jp., Ikenoue T; Division of Clinical Genome Research, Advanced Clinical Research Center, The Institute of Medical Science, The University of Tokyo, Tokyo, 108-8639, Japan.

المصدر: Journal of human genetics [J Hum Genet] 2021 Nov; Vol. 66 (11), pp. 1053-1060. Date of Electronic Publication: 2021 May 06.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1435-232X (Electronic) Linking ISSN: 14345161 NLM ISO Abbreviation: J Hum Genet Subsets: MEDLINE

مواضيع طبية MeSH: Colorectal Neoplasms/*genetics , Colorectal Neoplasms, Hereditary Nonpolyposis/*genetics , MutL Protein Homolog 1/*genetics , MutS Homolog 2 Protein/*genetics, Colorectal Neoplasms/complications ; Colorectal Neoplasms/pathology ; Colorectal Neoplasms, Hereditary Nonpolyposis/complications ; Colorectal Neoplasms, Hereditary Nonpolyposis/pathology ; DNA Mismatch Repair/genetics ; Female ; Genetic Predisposition to Disease ; Genetic Testing/standards ; Germ-Line Mutation/genetics ; Humans ; Male ; Mass Screening ; MutL Protein Homolog 1/ultrastructure ; MutS Homolog 2 Protein/ultrastructure ; Nanopore Sequencing ; Polymorphism, Single Nucleotide/genetics ; Protein Conformation

المؤلفون: Georgeson P; Department of Clinical Pathology, The University of Melbourne, Melbourne, Victoria, Australia.; University of Melbourne Centre for Cancer Research, Victorian Comprehensive Cancer Centre, Melbourne, Victoria, Australia., Pope BJ; Department of Clinical Pathology, The University of Melbourne, Melbourne, Victoria, Australia.; University of Melbourne Centre for Cancer Research, Victorian Comprehensive Cancer Centre, Melbourne, Victoria, Australia.; Melbourne Bioinformatics, The University of Melbourne, Melbourne, Victoria, Australia., Rosty C; Department of Clinical Pathology, The University of Melbourne, Melbourne, Victoria, Australia.; University of Melbourne Centre for Cancer Research, Victorian Comprehensive Cancer Centre, Melbourne, Victoria, Australia.; Envoi Pathology, Brisbane, Queensland, Australia.; University of Queensland, School of Medicine, Herston, Queensland, Australia., Clendenning M; Department of Clinical Pathology, The University of Melbourne, Melbourne, Victoria, Australia.; University of Melbourne Centre for Cancer Research, Victorian Comprehensive Cancer Centre, Melbourne, Victoria, Australia., Mahmood K; Department of Clinical Pathology, The University of Melbourne, Melbourne, Victoria, Australia.; University of Melbourne Centre for Cancer Research, Victorian Comprehensive Cancer Centre, Melbourne, Victoria, Australia.; Melbourne Bioinformatics, The University of Melbourne, Melbourne, Victoria, Australia., Joo JE; Department of Clinical Pathology, The University of Melbourne, Melbourne, Victoria, Australia.; University of Melbourne Centre for Cancer Research, Victorian Comprehensive Cancer Centre, Melbourne, Victoria, Australia., Walker R; Department of Clinical Pathology, The University of Melbourne, Melbourne, Victoria, Australia.; University of Melbourne Centre for Cancer Research, Victorian Comprehensive Cancer Centre, Melbourne, Victoria, Australia., Hutchinson RA; Department of Clinical Pathology, The University of Melbourne, Melbourne, Victoria, Australia.; University of Melbourne Centre for Cancer Research, Victorian Comprehensive Cancer Centre, Melbourne, Victoria, Australia., Preston S; Department of Clinical Pathology, The University of Melbourne, Melbourne, Victoria, Australia.; University of Melbourne Centre for Cancer Research, Victorian Comprehensive Cancer Centre, Melbourne, Victoria, Australia., Como J; Department of Clinical Pathology, The University of Melbourne, Melbourne, Victoria, Australia.; University of Melbourne Centre for Cancer Research, Victorian Comprehensive Cancer Centre, Melbourne, Victoria, Australia., Joseland S; Department of Clinical Pathology, The University of Melbourne, Melbourne, Victoria, Australia.; University of Melbourne Centre for Cancer Research, Victorian Comprehensive Cancer Centre, Melbourne, Victoria, Australia., Win AK; Centre for Epidemiology and Biostatistics, The University of Melbourne, Melbourne, Victoria, Australia.; Genetic Medicine and Family Cancer Clinic, The Royal Melbourne Hospital, Melbourne, Victoria, Australia., Macrae FA; Genetic Medicine and Family Cancer Clinic, The Royal Melbourne Hospital, Melbourne, Victoria, Australia.; Colorectal Medicine and Genetics, The Royal Melbourne Hospital, Melbourne, Victoria, Australia., Hopper JL; Centre for Epidemiology and Biostatistics, The University of Melbourne, Melbourne, Victoria, Australia., Mouradov D; Personalised Oncology Division, Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.; Department of Medical Biology, The University of Melbourne, Melbourne, Victoria, Australia., Gibbs P; Personalised Oncology Division, Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.; Department of Medical Biology, The University of Melbourne, Melbourne, Victoria, Australia.; Department of Medical Oncology, Western Health, Victoria, Australia., Sieber OM; Personalised Oncology Division, Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.; Department of Medical Biology, The University of Melbourne, Melbourne, Victoria, Australia.; Department of Surgery, The University of Melbourne, Parkville, Victoria, Australia.; Department of Biochemistry and Molecular Biology, Monash University, Clayton, Victoria, Australia., O'Sullivan DE; Department of Oncology, University of Calgary, Calgary, Alberta, Canada.; Department of Community Health Sciences, University of Calgary Cumming School of Medicine, Calgary, Alberta, Canada., Brenner DR; Department of Oncology, University of Calgary, Calgary, Alberta, Canada.; Department of Community Health Sciences, University of Calgary Cumming School of Medicine, Calgary, Alberta, Canada.; Department of Cancer Epidemiology and Prevention Research, Alberta Health Services, Calgary, Alberta, Canada., Gallinger S; Lunenfeld Tanenbaum Research Institute, Mount Sinai Hospital, The University of Toronto, Toronto, Ontario, Canada.; Ontario Institute for Cancer Research, Toronto, Ontario, Canada.; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada., Jenkins MA; University of Melbourne Centre for Cancer Research, Victorian Comprehensive Cancer Centre, Melbourne, Victoria, Australia.; Centre for Epidemiology and Biostatistics, The University of Melbourne, Melbourne, Victoria, Australia., Winship IM; Genetic Medicine and Family Cancer Clinic, The Royal Melbourne Hospital, Melbourne, Victoria, Australia.; Department of Medicine, The University of Melbourne, Melbourne, Victoria, Australia., Buchanan DD; Department of Clinical Pathology, The University of Melbourne, Melbourne, Victoria, Australia daniel.buchanan@unimelb.edu.au.; University of Melbourne Centre for Cancer Research, Victorian Comprehensive Cancer Centre, Melbourne, Victoria, Australia.; Genetic Medicine and Family Cancer Clinic, The Royal Melbourne Hospital, Melbourne, Victoria, Australia.

المصدر: Gut [Gut] 2021 Nov; Vol. 70 (11), pp. 2138-2149. Date of Electronic Publication: 2021 Jan 07.

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

بيانات الدورية: Publisher: British Medical Assn Country of Publication: England NLM ID: 2985108R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1468-3288 (Electronic) Linking ISSN: 00175749 NLM ISO Abbreviation: Gut Subsets: MEDLINE

مواضيع طبية MeSH: DNA Glycosylases* , Germ-Line Mutation* , MutL Protein Homolog 1*, Adenomatous Polyposis Coli/*genetics , Colorectal Neoplasms/*genetics, DNA Mismatch Repair ; Female ; Genetic Predisposition to Disease ; Heterozygote ; Humans ; Male ; Middle Aged ; Syndrome ; Exome Sequencing

المؤلفون: Oliveira JW; Faculdade Evangélica Mackenzie do Paraná - Curitiba (PR), Brazil., Moraes RA; Faculdade Evangélica Mackenzie do Paraná - Curitiba (PR), Brazil., Mehanna SH; Faculdade Evangélica Mackenzie do Paraná - Curitiba (PR), Brazil., Linhares JC; Hospital Universitário Evangélico Mackenzie, Pathology Service - Curitiba (PR), Brazil.

المصدر: Arquivos brasileiros de cirurgia digestiva : ABCD = Brazilian archives of digestive surgery [Arq Bras Cir Dig] 2023 Oct 23; Vol. 36, pp. e1771. Date of Electronic Publication: 2023 Oct 23 (Print Publication: 2023).

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Colégio Brasileiro de Cirurgia Digestiva Country of Publication: Brazil NLM ID: 9100283 Publication Model: eCollection Cited Medium: Internet ISSN: 2317-6326 (Electronic) Linking ISSN: 01026720 NLM ISO Abbreviation: Arq Bras Cir Dig Subsets: MEDLINE

مواضيع طبية MeSH: Colorectal Neoplasms*/genetics , Colorectal Neoplasms*/surgery , Colorectal Neoplasms*/diagnosis , Microsatellite Instability*, Female ; Humans ; Male ; Middle Aged ; Biomarkers, Tumor ; Cross-Sectional Studies ; DNA Mismatch Repair ; Hospitals ; MutL Protein Homolog 1/genetics ; Prevalence ; Retrospective Studies ; Aged

المؤلفون: Preti B; Division of Medical Oncology, Department of Oncology, Western University, London, ON N6A 3K7, Canada., Schenkel L; Division of Molecular Diagnostics, Western University, London, ON N6A 3K7, Canada., Cecchini M; Department of Pathology and Laboratory Medicine, Western University, London, ON N6A 3K7, Canada., Romagnoli T; Department of Pathology and Laboratory Medicine, Western University, London, ON N6A 3K7, Canada.; Schulich School of Medicine & Dentistry, Western University, London, ON N6A 3K7, Canada., Sanatani MS; Division of Medical Oncology, Department of Oncology, Western University, London, ON N6A 3K7, Canada., French K; Temerty Faculty of Medicine, University of Toronto, Toronto, ON M5S 1A1, Canada., Colquhoun P; Department of Surgery, Western University, London, ON N6A 3K7, Canada., Vincent MD; Division of Medical Oncology, Department of Oncology, Western University, London, ON N6A 3K7, Canada.

المصدر: Current oncology (Toronto, Ont.) [Curr Oncol] 2023 Oct 06; Vol. 30 (10), pp. 9039-9048. Date of Electronic Publication: 2023 Oct 06.

نوع المنشور: Case Reports

بيانات الدورية: Publisher: MDPI Country of Publication: Switzerland NLM ID: 9502503 Publication Model: Electronic Cited Medium: Internet ISSN: 1718-7729 (Electronic) Linking ISSN: 11980052 NLM ISO Abbreviation: Curr Oncol Subsets: MEDLINE

مواضيع طبية MeSH: Mosaicism* , Neoadjuvant Therapy* , Colonic Neoplasms*/drug therapy , Colonic Neoplasms*/genetics, Humans ; Male ; Middle Aged ; Microsatellite Instability ; Mutation ; MutL Protein Homolog 1/genetics

المؤلفون: Pivovarcikova K; Šikl's Department of Pathology, The Faculty of Medicine and Faculty Hospital in Pilsen, Charles University, Alej Svobody 80, 304 60, Pilsen, Czech Republic. pivovarcikovak@fnplzen.cz.; Biopticka Laborator S.R.O., Pilsen, Czech Republic. pivovarcikovak@fnplzen.cz., Pitra T; Department of Urology, Faculty of Medicine in Plzeň, Charles University in Prague, Pilsen, Czech Republic., Alaghehbandan R; Cleveland Clinic, Department of Anatomic Pathology, Robert J. Tomsich Pathology and Laboratory Medicine Institute, Cleveland, OH, USA., Buchova K; Šikl's Department of Pathology, The Faculty of Medicine and Faculty Hospital in Pilsen, Charles University, Alej Svobody 80, 304 60, Pilsen, Czech Republic., Steiner P; Šikl's Department of Pathology, The Faculty of Medicine and Faculty Hospital in Pilsen, Charles University, Alej Svobody 80, 304 60, Pilsen, Czech Republic.; Biopticka Laborator S.R.O., Pilsen, Czech Republic., Hajkova V; Šikl's Department of Pathology, The Faculty of Medicine and Faculty Hospital in Pilsen, Charles University, Alej Svobody 80, 304 60, Pilsen, Czech Republic.; Biopticka Laborator S.R.O., Pilsen, Czech Republic., Ptakova N; Šikl's Department of Pathology, The Faculty of Medicine and Faculty Hospital in Pilsen, Charles University, Alej Svobody 80, 304 60, Pilsen, Czech Republic.; Biopticka Laborator S.R.O., Pilsen, Czech Republic., Subrt I; Department of Medical Genetics, Faculty of Medicine in Plzeň, Charles University in Prague, Pilsen, Czech Republic., Skopal J; Šikl's Department of Pathology, The Faculty of Medicine and Faculty Hospital in Pilsen, Charles University, Alej Svobody 80, 304 60, Pilsen, Czech Republic., Svajdler P; Šikl's Department of Pathology, The Faculty of Medicine and Faculty Hospital in Pilsen, Charles University, Alej Svobody 80, 304 60, Pilsen, Czech Republic.; Cytopathos S. R. O., Bratislava, Slovakia., Farcas M; Šikl's Department of Pathology, The Faculty of Medicine and Faculty Hospital in Pilsen, Charles University, Alej Svobody 80, 304 60, Pilsen, Czech Republic.; Onco Team Diagnostic, Bucharest, Romania., Slisarenko M; Šikl's Department of Pathology, The Faculty of Medicine and Faculty Hospital in Pilsen, Charles University, Alej Svobody 80, 304 60, Pilsen, Czech Republic., Michalova K; Šikl's Department of Pathology, The Faculty of Medicine and Faculty Hospital in Pilsen, Charles University, Alej Svobody 80, 304 60, Pilsen, Czech Republic.; Biopticka Laborator S.R.O., Pilsen, Czech Republic., Strakova Peterikova A; Šikl's Department of Pathology, The Faculty of Medicine and Faculty Hospital in Pilsen, Charles University, Alej Svobody 80, 304 60, Pilsen, Czech Republic.; Biopticka Laborator S.R.O., Pilsen, Czech Republic., Hora M; Department of Urology, Faculty of Medicine in Plzeň, Charles University in Prague, Pilsen, Czech Republic., Michal M; Šikl's Department of Pathology, The Faculty of Medicine and Faculty Hospital in Pilsen, Charles University, Alej Svobody 80, 304 60, Pilsen, Czech Republic.; Biopticka Laborator S.R.O., Pilsen, Czech Republic., Daum O; Šikl's Department of Pathology, The Faculty of Medicine and Faculty Hospital in Pilsen, Charles University, Alej Svobody 80, 304 60, Pilsen, Czech Republic.; Biopticka Laborator S.R.O., Pilsen, Czech Republic., Svajdler M; Šikl's Department of Pathology, The Faculty of Medicine and Faculty Hospital in Pilsen, Charles University, Alej Svobody 80, 304 60, Pilsen, Czech Republic.; Biopticka Laborator S.R.O., Pilsen, Czech Republic.; Cytopathos S. R. O., Bratislava, Slovakia., Hes O; Šikl's Department of Pathology, The Faculty of Medicine and Faculty Hospital in Pilsen, Charles University, Alej Svobody 80, 304 60, Pilsen, Czech Republic.; Biopticka Laborator S.R.O., Pilsen, Czech Republic.

المصدر: Virchows Archiv : an international journal of pathology [Virchows Arch] 2023 Oct; Vol. 483 (4), pp. 517-526. Date of Electronic Publication: 2023 Aug 23.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Springer International Country of Publication: Germany NLM ID: 9423843 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-2307 (Electronic) Linking ISSN: 09456317 NLM ISO Abbreviation: Virchows Arch Subsets: MEDLINE

مواضيع طبية MeSH: Colorectal Neoplasms, Hereditary Nonpolyposis*/diagnosis , Colorectal Neoplasms, Hereditary Nonpolyposis*/genetics , Colorectal Neoplasms, Hereditary Nonpolyposis*/pathology , Carcinoma, Transitional Cell*/genetics , Urinary Bladder Neoplasms* , Urology*, Male ; Female ; Humans ; Middle Aged ; Aged ; MutL Protein Homolog 1/genetics ; Mismatch Repair Endonuclease PMS2/genetics ; Germ-Line Mutation ; DNA Mismatch Repair

المؤلفون: Sandoval RL; Hospital Sírio-Libanês, Brasília, Brazil.; Dana-Farber Cancer Institute, 450 Brookline Avenue Dana 1126, 02215, Boston, MA, USA., Horiguchi M; Dana-Farber Cancer Institute, 450 Brookline Avenue Dana 1126, 02215, Boston, MA, USA.; Harvard Medical School, Boston, MA, USA., Ukaegbu C; Dana-Farber Cancer Institute, 450 Brookline Avenue Dana 1126, 02215, Boston, MA, USA., Furniss CS; Dana-Farber Cancer Institute, 450 Brookline Avenue Dana 1126, 02215, Boston, MA, USA., Uno H; Dana-Farber Cancer Institute, 450 Brookline Avenue Dana 1126, 02215, Boston, MA, USA.; Harvard Medical School, Boston, MA, USA., Syngal S; Dana-Farber Cancer Institute, 450 Brookline Avenue Dana 1126, 02215, Boston, MA, USA.; Harvard Medical School, Boston, MA, USA.; Brigham and Women's Hospital, Boston, MA, USA., Yurgelun MB; Dana-Farber Cancer Institute, 450 Brookline Avenue Dana 1126, 02215, Boston, MA, USA. matthew_yurgelun@dfci.harvard.edu.

المصدر: Familial cancer [Fam Cancer] 2023 Oct; Vol. 22 (4), pp. 459-465. Date of Electronic Publication: 2023 Aug 12.

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

بيانات الدورية: Publisher: Springer Country of Publication: Netherlands NLM ID: 100898211 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1573-7292 (Electronic) Linking ISSN: 13899600 NLM ISO Abbreviation: Fam Cancer Subsets: MEDLINE

مواضيع طبية MeSH: Colorectal Neoplasms*/diagnosis , Colorectal Neoplasms*/genetics , Colorectal Neoplasms, Hereditary Nonpolyposis*/diagnosis , Colorectal Neoplasms, Hereditary Nonpolyposis*/genetics , Colorectal Neoplasms, Hereditary Nonpolyposis*/pathology , Neoplastic Syndromes, Hereditary*, Humans ; DNA Mismatch Repair/genetics ; Germ-Line Mutation ; Microsatellite Instability ; MutL Protein Homolog 1/genetics

SCR Disease Name: Turcot syndrome

المؤلفون: Walker R; Colorectal Oncogenomics Group, Department of Clinical Pathology, The University of Melbourne, 305 Grattan Street, Parkville, VIC, 3010, Australia. romy.walker@unimelb.edu.au.; University of Melbourne Centre for Cancer Research, Victorian Comprehensive Cancer Centre, 305 Grattan Street, Parkville, VIC, 3010, Australia. romy.walker@unimelb.edu.au., Clendenning M; Colorectal Oncogenomics Group, Department of Clinical Pathology, The University of Melbourne, 305 Grattan Street, Parkville, VIC, 3010, Australia.; University of Melbourne Centre for Cancer Research, Victorian Comprehensive Cancer Centre, 305 Grattan Street, Parkville, VIC, 3010, Australia., Joo JE; Colorectal Oncogenomics Group, Department of Clinical Pathology, The University of Melbourne, 305 Grattan Street, Parkville, VIC, 3010, Australia.; University of Melbourne Centre for Cancer Research, Victorian Comprehensive Cancer Centre, 305 Grattan Street, Parkville, VIC, 3010, Australia., Xue J; Colorectal Oncogenomics Group, Department of Clinical Pathology, The University of Melbourne, 305 Grattan Street, Parkville, VIC, 3010, Australia.; University of Melbourne Centre for Cancer Research, Victorian Comprehensive Cancer Centre, 305 Grattan Street, Parkville, VIC, 3010, Australia., Mahmood K; Colorectal Oncogenomics Group, Department of Clinical Pathology, The University of Melbourne, 305 Grattan Street, Parkville, VIC, 3010, Australia.; University of Melbourne Centre for Cancer Research, Victorian Comprehensive Cancer Centre, 305 Grattan Street, Parkville, VIC, 3010, Australia.; Melbourne Bioinformatics, The University of Melbourne, Melbourne, Parkville, VIC, 3010, Australia., Georgeson P; Colorectal Oncogenomics Group, Department of Clinical Pathology, The University of Melbourne, 305 Grattan Street, Parkville, VIC, 3010, Australia.; University of Melbourne Centre for Cancer Research, Victorian Comprehensive Cancer Centre, 305 Grattan Street, Parkville, VIC, 3010, Australia., Como J; Colorectal Oncogenomics Group, Department of Clinical Pathology, The University of Melbourne, 305 Grattan Street, Parkville, VIC, 3010, Australia.; University of Melbourne Centre for Cancer Research, Victorian Comprehensive Cancer Centre, 305 Grattan Street, Parkville, VIC, 3010, Australia., Joseland S; Colorectal Oncogenomics Group, Department of Clinical Pathology, The University of Melbourne, 305 Grattan Street, Parkville, VIC, 3010, Australia.; University of Melbourne Centre for Cancer Research, Victorian Comprehensive Cancer Centre, 305 Grattan Street, Parkville, VIC, 3010, Australia., Preston SG; Colorectal Oncogenomics Group, Department of Clinical Pathology, The University of Melbourne, 305 Grattan Street, Parkville, VIC, 3010, Australia.; University of Melbourne Centre for Cancer Research, Victorian Comprehensive Cancer Centre, 305 Grattan Street, Parkville, VIC, 3010, Australia., Chan JM; Colorectal Oncogenomics Group, Department of Clinical Pathology, The University of Melbourne, 305 Grattan Street, Parkville, VIC, 3010, Australia.; University of Melbourne Centre for Cancer Research, Victorian Comprehensive Cancer Centre, 305 Grattan Street, Parkville, VIC, 3010, Australia., Jenkins MA; University of Melbourne Centre for Cancer Research, Victorian Comprehensive Cancer Centre, 305 Grattan Street, Parkville, VIC, 3010, Australia.; Centre for Epidemiology and Biostatistics, The University of Melbourne, Parkville, VIC, 3010, Australia., Rosty C; Colorectal Oncogenomics Group, Department of Clinical Pathology, The University of Melbourne, 305 Grattan Street, Parkville, VIC, 3010, Australia.; University of Melbourne Centre for Cancer Research, Victorian Comprehensive Cancer Centre, 305 Grattan Street, Parkville, VIC, 3010, Australia.; Envoi Specialist Pathologists, Brisbane, QLD, 4059, Australia.; University of Queensland, Brisbane, QLD, 4072, Australia., Macrae FA; Genomic Medicine and Familial Cancer Centre, The Royal Melbourne Hospital, Parkville, VIC, 3000, Australia.; Colorectal Medicine and Genetics, The Royal Melbourne Hospital, Parkville, VIC, 3000, Australia.; Department of Medicine, The University of Melbourne, Melbourne, VIC, 3000, Australia., Di Palma S; Clinical Genetics Unit, Austin Health, Melbourne, VIC, 3084, Australia., Campbell A; Clinical Genetics Unit, Austin Health, Melbourne, VIC, 3084, Australia., Winship IM; Genomic Medicine and Familial Cancer Centre, The Royal Melbourne Hospital, Parkville, VIC, 3000, Australia.; Department of Medicine, The University of Melbourne, Melbourne, VIC, 3000, Australia., Buchanan DD; Colorectal Oncogenomics Group, Department of Clinical Pathology, The University of Melbourne, 305 Grattan Street, Parkville, VIC, 3010, Australia.; University of Melbourne Centre for Cancer Research, Victorian Comprehensive Cancer Centre, 305 Grattan Street, Parkville, VIC, 3010, Australia.; Genomic Medicine and Familial Cancer Centre, The Royal Melbourne Hospital, Parkville, VIC, 3000, Australia.

المصدر: Familial cancer [Fam Cancer] 2023 Oct; Vol. 22 (4), pp. 423-428. Date of Electronic Publication: 2023 Jun 15.

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

بيانات الدورية: Publisher: Springer Country of Publication: Netherlands NLM ID: 100898211 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1573-7292 (Electronic) Linking ISSN: 13899600 NLM ISO Abbreviation: Fam Cancer Subsets: MEDLINE

مواضيع طبية MeSH: Colorectal Neoplasms, Hereditary Nonpolyposis*/diagnosis , Colorectal Neoplasms, Hereditary Nonpolyposis*/genetics , Colorectal Neoplasms, Hereditary Nonpolyposis*/pathology , Endometrial Neoplasms*/genetics, Female ; Humans ; Germ-Line Mutation ; DNA-Binding Proteins/genetics ; DNA-Binding Proteins/metabolism ; DNA ; DNA Mismatch Repair ; MutL Protein Homolog 1/genetics ; Microsatellite Instability

المؤلفون: Bolivar AM; Department of Clinical Cancer Prevention, The University of Texas MD Anderson Cancer Center, Houston, TX, USA., Duzagac F; Department of Clinical Cancer Prevention, The University of Texas MD Anderson Cancer Center, Houston, TX, USA., Sinha KM; Department of Clinical Cancer Prevention, The University of Texas MD Anderson Cancer Center, Houston, TX, USA., Vilar E; Department of Clinical Cancer Prevention, The University of Texas MD Anderson Cancer Center, Houston, TX, USA; Clinical Cancer Genetics Program, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. Electronic address: EVilar@mdanderson.org.

المصدر: Molecular aspects of medicine [Mol Aspects Med] 2023 Oct; Vol. 93, pp. 101204. Date of Electronic Publication: 2023 Jul 19.

نوع المنشور: Journal Article; Review; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Elsevier Science Country of Publication: England NLM ID: 7603128 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1872-9452 (Electronic) Linking ISSN: 00982997 NLM ISO Abbreviation: Mol Aspects Med Subsets: MEDLINE

مواضيع طبية MeSH: Colorectal Neoplasms, Hereditary Nonpolyposis*/genetics , Colorectal Neoplasms, Hereditary Nonpolyposis*/prevention & control, Humans ; DNA-Binding Proteins/genetics ; MutL Protein Homolog 1/genetics ; Mismatch Repair Endonuclease PMS2/genetics ; Vaccine Development

المؤلفون: Kaneko M; First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan., Nakashima M; Department of Biochemistry, Hamamatsu University of School of Medicine, Hamamatsu, Japan., Sugiura K; First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan., Ishida N; Department of Endoscopic and Photodynamic Medicine, Hamamatsu University of School of Medicine, Hamamatsu, Japan., Tamura S; First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan., Tani S; First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan., Yamade M; First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan., Hamaya Y; First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan., Osawa S; Department of Endoscopic and Photodynamic Medicine, Hamamatsu University of School of Medicine, Hamamatsu, Japan., Tatsuta K; Department of Surgery, Hamamatsu University of School of Medicine, Hamamatsu, Japan., Kurachi K; Department of Surgery, Hamamatsu University of School of Medicine, Hamamatsu, Japan., Baba S; Department of Diagnostic Pathology, Hamamatsu University School of Medicine, Hamamatsu, Japan., Iwashita Y; Department of Tumor Pathology, Hamamatsu University School of Medicine, Hamamatsu, Japan., Arai T; Department of Pathology, Tokyo Metropolitan Geriatric Hospital and Institute of Gerontology, Tokyo, Japan., Sugimura H; Department of Tumor Pathology, Hamamatsu University School of Medicine, Hamamatsu, Japan., Maekawa M; Department of Laboratory Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan., Sugimoto K; First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan., Iwaizumi M; Department of Laboratory Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan.

المصدر: Medicine [Medicine (Baltimore)] 2023 Sep 22; Vol. 102 (38), pp. e35022.

نوع المنشور: Observational Study; Journal Article

بيانات الدورية: Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 2985248R Publication Model: Print Cited Medium: Internet ISSN: 1536-5964 (Electronic) Linking ISSN: 00257974 NLM ISO Abbreviation: Medicine (Baltimore) Subsets: MEDLINE

مواضيع طبية MeSH: Carcinoma, Medullary* , Adenocarcinoma* , Colorectal Neoplasms*/genetics , Colorectal Neoplasms*/surgery, Humans ; Mutation ; Genetic Testing ; MutL Protein Homolog 1/genetics