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1.

Recent progress in Lynch syndrome and other familial colorectal cancer syndromes.

Boland, Patrick M; Yurgelun, Matthew B; Boland, C Richard.

CA Cancer J Clin ; 68(3): 217-231, 2018 05.

Artículo en Inglés | MEDLINE | ID: mdl-29485237

2.

A conserved motif in the disordered linker of human MLH1 is vital for DNA mismatch repair and its function is diminished by a cancer family mutation.

Wolf, Karla; Kosinski, Jan; Gibson, Toby J; Wesch, Nicole; Dötsch, Volker; Genuardi, Maurizio; Cordisco, Emanuela Lucci; Zeuzem, Stefan; Brieger, Angela; Plotz, Guido.

Nucleic Acids Res ; 51(12): 6307-6320, 2023 07 07.

Artículo en Inglés | MEDLINE | ID: mdl-37224528

3.

Comparative molecular genomic analyses of a spontaneous rhesus macaque model of mismatch repair-deficient colorectal cancer.

Ozirmak Lermi, Nejla; Gray, Stanton B; Bowen, Charles M; Reyes-Uribe, Laura; Dray, Beth K; Deng, Nan; Harris, R Alan; Raveendran, Muthuswamy; Benavides, Fernando; Hodo, Carolyn L; Taggart, Melissa W; Colbert Maresso, Karen; Sinha, Krishna M; Rogers, Jeffrey; Vilar, Eduardo.

PLoS Genet ; 18(4): e1010163, 2022 04.

Artículo en Inglés | MEDLINE | ID: mdl-35446842

4.

Clonal origin and genomic diversity in Lynch syndrome-associated endometrial cancer with multiple synchronous tumors: Identification of the pathogenicity of MLH1 p.L582H.

Takahashi, Kotaro; Yachida, Nozomi; Tamura, Ryo; Adachi, Sosuke; Kondo, Shuhei; Abé, Tatsuya; Umezu, Hajime; Nyuzuki, Hiromi; Okuda, Shujiro; Nakaoka, Hirofumi; Yoshihara, Kosuke.

Genes Chromosomes Cancer ; 63(3): e23231, 2024 Mar.

Artículo en Inglés | MEDLINE | ID: mdl-38459936

5.

PMS2 or PMS2CL? Characterization of variants detected in the 3' of the PMS2 gene.

Bouras, Ahmed; Lefol, Cedrick; Ruano, Eric; Grand-Masson, Chloé; Wang, Qing.

Genes Chromosomes Cancer ; 63(1): e23193, 2024 Jan.

Artículo en Inglés | MEDLINE | ID: mdl-37534630

6.

Identification of Comprehensive Biomarkers in Patients With Mismatch Repair-Deficient Colon Adenocarcinoma Based on Parallel Multiomics.

Li, Zhengjun; Teng, Linxin; Pan, Zhiwei; Yang, Yang; Zhu, Junlin; Wu, Xiaobin; Qian, Yunzhi; Qian, Haihua; Bian, Yaoyao; Chen, Ying; Chen, Weiping; Bi, Lei.

Lab Invest ; 104(2): 100306, 2024 02.

Artículo en Inglés | MEDLINE | ID: mdl-38104864

7.

Molecular analysis of cancer genomes in children with Lynch syndrome: Exploring causal associations.

Weijers, Dilys D; Hirsch, Steffen; Bakhuizen, Jette J; van Engelen, Nienke; Kester, Lennart A; Kranendonk, Mariëtte E G; Hiemcke-Jiwa, Laura S; de Vos-Kerkhof, Evelien; Loeffen, Jan L C; Autry, Robert J; Pajtler, Kristian W; Jäger, Natalie; Jongmans, Marjolijn C J; Kuiper, Roland P.

Int J Cancer ; 154(8): 1455-1463, 2024 Apr 15.

Artículo en Inglés | MEDLINE | ID: mdl-38175816

8.

Characterization of mismatch-repair/microsatellite instability-discordant endometrial cancers.

Riedinger, Courtney J; Esnakula, Ashwini; Haight, Paulina J; Suarez, Adrian A; Chen, Wei; Gillespie, Jessica; Villacres, Alyssa; Chassen, Alexis; Cohn, David E; Goodfellow, Paul J; Cosgrove, Casey M.

Cancer ; 130(3): 385-399, 2024 Feb 01.

Artículo en Inglés | MEDLINE | ID: mdl-37751191

9.

Massively parallel functional testing of MSH2 missense variants conferring Lynch syndrome risk.

Jia, Xiaoyan; Burugula, Bala Bharathi; Chen, Victor; Lemons, Rosemary M; Jayakody, Sajini; Maksutova, Mariam; Kitzman, Jacob O.

Am J Hum Genet ; 108(1): 163-175, 2021 01 07.

Artículo en Inglés | MEDLINE | ID: mdl-33357406

10.

Lynch Syndrome Genetics and Clinical Implications.

Peltomäki, Päivi; Nyström, Minna; Mecklin, Jukka-Pekka; Seppälä, Toni T.

Gastroenterology ; 164(5): 783-799, 2023 04.

Artículo en Inglés | MEDLINE | ID: mdl-36706841

11.

Province-Wide Ascertainment of Lynch Syndrome in Manitoba.

Rothenmund, Heidi; Lambert, Pascal; Khan, Deirdre; Kim, Christina; Sharma, Bhavya; Serfas, Kim; Chodirker, Bernard; Singh, Harminder.

Clin Gastroenterol Hepatol ; 22(3): 642-652.e2, 2024 Mar.

Artículo en Inglés | MEDLINE | ID: mdl-37879520

12.

Constitutional Microsatellite Instability, Genotype, and Phenotype Correlations in Constitutional Mismatch Repair Deficiency.

Gallon, Richard; Phelps, Rachel; Hayes, Christine; Brugieres, Laurence; Guerrini-Rousseau, Léa; Colas, Chrystelle; Muleris, Martine; Ryan, Neil A J; Evans, D Gareth; Grice, Hannah; Jessop, Emily; Kunzemann-Martinez, Annabel; Marshall, Lilla; Schamschula, Esther; Oberhuber, Klaus; Azizi, Amedeo A; Baris Feldman, Hagit; Beilken, Andreas; Brauer, Nina; Brozou, Triantafyllia; Dahan, Karin; Demirsoy, Ugur; Florkin, Benoît; Foulkes, William; Januszkiewicz-Lewandowska, Danuta; Jones, Kristi J; Kratz, Christian P; Lobitz, Stephan; Meade, Julia; Nathrath, Michaela; Pander, Hans-Jürgen; Perne, Claudia; Ragab, Iman; Ripperger, Tim; Rosenbaum, Thorsten; Rueda, Daniel; Sarosiek, Tomasz; Sehested, Astrid; Spier, Isabel; Suerink, Manon; Zimmermann, Stefanie-Yvonne; Zschocke, Johannes; Borthwick, Gillian M; Wimmer, Katharina; Burn, John; Jackson, Michael S; Santibanez-Koref, Mauro.

Gastroenterology ; 164(4): 579-592.e8, 2023 04.

Artículo en Inglés | MEDLINE | ID: mdl-36586540

13.

Epigenetic MLH1 silencing concurs with mismatch repair deficiency in sporadic, naturally occurring colorectal cancer in rhesus macaques.

Deycmar, Simon; Johnson, Brendan J; Ray, Karina; Schaaf, George W; Ryan, Declan Patrick; Cullin, Cassandra; Dozier, Brandy L; Ferguson, Betsy; Bimber, Benjamin N; Olson, John D; Caudell, David L; Whitlow, Christopher T; Solingapuram Sai, Kiran Kumar; Romero, Emily C; Villinger, Francois J; Burgos, Armando G; Ainsworth, Hannah C; Miller, Lance D; Hawkins, Gregory A; Chou, Jeff W; Gomes, Bruno; Hettich, Michael; Ceppi, Maurizio; Charo, Jehad; Cline, J Mark.

J Transl Med ; 22(1): 292, 2024 Mar 19.

Artículo en Inglés | MEDLINE | ID: mdl-38504345

14.

Deficient mismatch repair screening of advanced adenomas in the population screening program for colorectal cancer is not effective.

Vink-Börger, Elisa; Dabir, Parag D; Krekels, Joyce; van Kouwen, Mariëtte C A; Ligtenberg, Marjolijn J L; van der Post, Rachel S; Nagtegaal, Iris D.

Histopathology ; 84(6): 1056-1060, 2024 May.

Artículo en Inglés | MEDLINE | ID: mdl-38275207

15.

BRAF^V600E immunohistochemistry can reliably substitute BRAF molecular testing in the Lynch syndrome screening algorithm in colorectal cancer.

Grillo, Federica; Paudice, Michele; Pigozzi, Simona; Dono, Maria; Lastraioli, Sonia; Lugaresi, Marialuisa; Bozzano, Silvia; Tognoni, Camilla; Ali, Murad; Sciallero, Stefania; Puccini, Alberto; Fassan, Matteo; Mastracci, Luca.

Histopathology ; 84(5): 877-887, 2024 Apr.

Artículo en Inglés | MEDLINE | ID: mdl-38173291

16.

The effects of oxaliplatin-based adjuvant chemotherapy in high-risk stage II colon cancer with mismatch repair-deficient: a retrospective study.

Liao, Leen; Tang, Jinghua; Hong, Zhigang; Jiang, Wu; Li, Yuan; Kong, Lingheng; Han, Kai; Hou, Zhenlin; Zhang, Chenzhi; Zhou, Chi; Zhang, Linjie; Sui, Qiaoqi; Xiao, Binyi; Mei, Weijian; Yu, Jiehai; Yang, Wanjun; Pan, Zhizhong; Ding, Pei-Rong.

BMC Cancer ; 24(1): 164, 2024 Feb 02.

Artículo en Inglés | MEDLINE | ID: mdl-38302968

17.

Correlation Between the Severity of Adhesions and Desmoid Disease in Patients With Familial Adenomatous Polyposis: A Prospective Cohort Study.

Faul, Eleanor; Xhaja, Xhileta; Church, James.

Dis Colon Rectum ; 67(2): 273-279, 2024 Feb 01.

Artículo en Inglés | MEDLINE | ID: mdl-36940315

18.

Sarcoma in patients with Lynch syndrome and response to immunotherapy.

Shehata, Michael S; Lofftus, Serena Y; Park, Joon Y; Singh, Arun S; Federman, Noah C; Eilber, Fritz C; Crompton, Joseph G; McCaw, Tyler R.

J Surg Oncol ; 129(4): 820-826, 2024 Mar.

Artículo en Inglés | MEDLINE | ID: mdl-38151827

19.

Tumor board presentation of a woman with metastatic, hormone receptor-positive, mismatch repair-deficient endometrial cancer.

Bennett, Jennifer A; Fleming, Gini F; Kurnit, Katherine C; Mills, Kathryn A; vanWeelden, Willem Jan.

CA Cancer J Clin ; 72(2): 102-111, 2022 03.

Artículo en Inglés | MEDLINE | ID: mdl-35077576

20.

Association between colorectal cancer, the frequency of Bacteroides fragilis, and the level of mismatch repair genes expression in the biopsy samples of Iranian patients.

Nazarinejad, Nooshin; Hajikhani, Bahareh; Vaezi, Amir Abbas; Firoozeh, Farzaneh; Sameni, Fatemeh; Yaslianifard, Somayeh; Goudarzi, Mehdi; Dadashi, Masoud.

BMC Gastroenterol ; 24(1): 82, 2024 Feb 23.

Artículo en Inglés | MEDLINE | ID: mdl-38395750

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