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Refinado por: assunto: Mutation remover
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1
A tale of two pathways: Review of immune checkpoint inhibitors in DNA mismatch repair‐deficient and microsatellite instability‐high endometrial cancers
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A tale of two pathways: Review of immune checkpoint inhibitors in DNA mismatch repair‐deficient and microsatellite instability‐high endometrial cancers

Liu, Ying L. ; Weigelt, Britta

Cancer, 2024-05, Vol.130 (10), p.1733-1746 [Periódico revisado por pares]

United States: Wiley Subscription Services, Inc

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2
Mitotic abnormalities precede microsatellite instability in lynch syndrome-associated colorectal tumourigenesis
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Artigo
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Mitotic abnormalities precede microsatellite instability in lynch syndrome-associated colorectal tumourigenesis

Pussila, Marjaana ; Laiho, Aleksi ; Törönen, Petri ; Björkbacka, Pauliina ; Nykänen, Sonja ; Pylvänäinen, Kirsi ; Holm, Liisa ; Mecklin, Jukka-Pekka ; Renkonen-Sinisalo, Laura ; Lehtonen, Taru ; Lepistö, Anna ; Linden, Jere ; Mäki-Nevala, Satu ; Peltomäki, Päivi ; Nyström, Minna

EBioMedicine, 2024-05, Vol.103, p.105111-105111, Article 105111 [Periódico revisado por pares]

Netherlands: Elsevier B.V

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3
Clinical features and impact of p53 status on sporadic mismatch repair deficiency and Lynch syndrome in uterine cancer
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Artigo
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Clinical features and impact of p53 status on sporadic mismatch repair deficiency and Lynch syndrome in uterine cancer

Kato, Mayumi Kobayashi ; Fujii, Erisa ; Asami, Yuka ; Momozawa, Yukihide ; Hiranuma, Kengo ; Komatsu, Masaaki ; Hamamoto, Ryuji ; Ebata, Takahiro ; Matsumoto, Koji ; Ishikawa, Mitsuya ; Kohno, Takashi ; Kato, Tomoyasu ; Yoshida, Hiroshi ; Shiraishi, Kouya

Cancer science, 2024-05, Vol.115 (5), p.1646-1655 [Periódico revisado por pares]

England: John Wiley & Sons, Inc

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4
Genomic Landscape of Lynch Syndrome Colorectal Neoplasia Identifies Shared Mutated Neoantigens for Immunoprevention
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Artigo
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Genomic Landscape of Lynch Syndrome Colorectal Neoplasia Identifies Shared Mutated Neoantigens for Immunoprevention

Bolivar, Ana M. ; Duzagac, Fahriye ; Deng, Nan ; Reyes-Uribe, Laura ; Chang, Kyle ; Wu, Wenhui ; Bowen, Charles M. ; Taggart, Melissa W. ; Thirumurthi, Selvi ; Lynch, Patrick M. ; You, Y. Nancy ; Rodriguez-Pascual, Jesus ; Lipkin, Steven M. ; Kopetz, Scott ; Scheet, Paul ; Lizee, Gregory A. ; Reuben, Alexandre ; Sinha, Krishna M. ; Vilar, Eduardo

Gastroenterology (New York, N.Y. 1943), 2024-05, Vol.166 (5), p.787-801.e11 [Periódico revisado por pares]

United States: Elsevier Inc

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5
BRAF V600E immunohistochemistry can reliably substitute BRAF molecular testing in the Lynch syndrome screening algorithm in colorectal cancer
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Artigo
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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, 2024-04, Vol.84 (5), p.877-887 [Periódico revisado por pares]

England

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6
Inherited BRCA1 and RNF43 pathogenic variants in a familial colorectal cancer type X family
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Artigo
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Inherited BRCA1 and RNF43 pathogenic variants in a familial colorectal cancer type X family

Chan, James M. ; Clendenning, Mark ; Joseland, Sharelle ; Georgeson, Peter ; Mahmood, Khalid ; Joo, Jihoon E. ; Walker, Romy ; Como, Julia ; Preston, Susan ; Chai, Shuyi Marci ; Chu, Yen Lin ; Meyers, Aaron L. ; Pope, Bernard J. ; Duggan, David ; Fink, J. Lynn ; Macrae, Finlay A. ; Rosty, Christophe ; Winship, Ingrid M. ; Jenkins, Mark A. ; Buchanan, Daniel D.

Familial cancer, 2024-03, Vol.23 (1), p.9-21 [Periódico revisado por pares]

Dordrecht: Springer Netherlands

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7
Clonal origin and genomic diversity in Lynch syndrome‐associated endometrial cancer with multiple synchronous tumors: Identification of the pathogenicity of MLH1 p.L582H
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Artigo
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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, 2024-03, Vol.63 (3), p.e23231-n/a [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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8
Association between colorectal cancer, the frequency of Bacteroides fragilis, and the level of mismatch repair genes expression in the biopsy samples of Iranian patients
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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 gastroenterology, 2024-02, Vol.24 (1), p.82-82, Article 82 [Periódico revisado por pares]

England: BioMed Central

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9
Characterization of mismatch‐repair/microsatellite instability‐discordant endometrial cancers
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Artigo
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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, 2024-02, Vol.130 (3), p.385-399 [Periódico revisado por pares]

United States: Wiley Subscription Services, Inc

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10
De novo germline pathogenic variant in Lynch Syndrome: A rare event or the tip of the iceberg?
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De novo germline pathogenic variant in Lynch Syndrome: A rare event or the tip of the iceberg?

Brignola, Clorinda ; Volorio, Sara ; De Vecchi, Giovanna ; Zaffaroni, Daniela ; Dall’Olio, Valentina ; Mariette, Frederique ; Sardella, Domenico ; Capra, Fabio ; Signoroni, Stefano ; Rausa, Emanuele ; Vitellaro, Marco ; Pensotti, Valeria ; Ricci, Maria Teresa

Tumori, 2024-02, Vol.110 (1), p.69-73 [Periódico revisado por pares]

London, England: SAGE Publications

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