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Select item 111593221.

Association between genetic polymorphisms of the base excision repair gene MUTYH and increased colorectal cancer risk in a Japanese population

Hong Tao, Kazuya Shinmura, Masaya Suzuki, Suminori Kono, Ryuichi Mibu, Masao Tanaka, Yoshihiro Kakeji, Yoshihiko Maehara, Takeshi Okamura, Kouji Ikejiri, Kitaroh Futami, Youichi Yasunami, Takafumi Maekawa, Kenji Takenaka, Hitoshi Ichimiya, Nobutoshi Imaizumi, Haruhiko Sugimura

Cancer Sci. 2008 Feb; 99(2): 355–360. Published online 2008 Feb 6. doi: 10.1111/j.1349-7006.2007.00694.x

PMCID:: PMC11159322

Abstract Article PDF–146K

Select item 111208962.

Exploring the Role of the MUTYH Gene in Breast, Ovarian and Endometrial Cancer

Carla Lintas, Benedetta Canalis, Alessia Azzarà, Giovanna Sabarese, Giuseppe Perrone, Fiorella Gurrieri

Genes (Basel) 2024 May; 15(5): 554. Published online 2024 Apr 26. doi: 10.3390/genes15050554

PMCID:: PMC11120896

Abstract Article PDF–1.5M

Select item 109014353.

Pan-Cancer Interrogation of MUTYH Variants Reveals Biallelic Inactivation and Defective Base Excision Repair Across a Spectrum of Solid Tumors

Channing J. Paller, Hanna Tukachinsky, Alexandra Maertens, Brennan Decker, Julian R. Sampson, Jeremy P. Cheadle, Emmanuel S. Antonarakis

JCO Precis Oncol. 2024; 8: e2300251. Published online 2024 Feb 23. doi: 10.1200/PO.23.00251

PMCID:: PMC10901435

Abstract Article PDF–1.1M

Select item 108363114.

Increased KRAS G12C Prevalence, High Tumor Mutational Burden, and Specific Mutational Signatures Are Associated With MUTYH Mutations: A Pan-Cancer Analysis

Umut Disel, Smruthy Sivakumar, Tim Pham, Zoe Fleischmann, R I Anu, Ethan S Sokol, Razelle Kurzrock

Oncologist. 2024 Feb; 29(2): e213–e223. Published online 2023 Aug 17. doi: 10.1093/oncolo/oyad230

PMCID:: PMC10836311

Abstract Article PDF–12M

Select item 104647245.

ASSOCIATION OF BASE EXCISION REPAIR PATHWAY GENES OGG1, XRCC1 AND MUTYH POLYMORPHISMS AND THE LEVEL OF 8-OXO-GUANINE WITH INCREASED RISK OF COLORECTAL CANCER OCCURRENCE

Jacek Kabziński, Ireneusz Majsterek

Int J Occup Med Environ Health. 2022; 35(5): 625–633. Published online 2022 Sep 1. doi: 10.13075/ijomeh.1896.01901

PMCID:: PMC10464724

Abstract Article PDF–298K

Select item 104366656.

Summary of the experiences, knowledge, medical management, and family communication of monoallelic MUTYH carriers

Danielle B. McKenna, Pauleen Sanchez, Jacquelyn Powers, Jamie Brower, Louise Wang, Rebecca Mueller, Heather Symecko, Jada G. Hamilton, Temima Wildman, Susan M. Domchek, Fergus J. Couch, Judy E. Garber, Kenneth Offit, Mark E. Robson, Bryson W. Katona

J Genet Couns. Author manuscript; available in PMC 2024 Apr 1.

Published in final edited form as: J Genet Couns. 2023 Apr; 32(2): 342–350. Published online 2022 Oct 17. doi: 10.1002/jgc4.1641

PMCID:: PMC10436665

Abstract Article PDF–258K

Select item 100468177.

Evolutionary Origin of MUTYH Germline Pathogenic Variations in Modern Humans

Fengxia Xiao, Jiaheng Li, Philip Naderev Panuringan Lagniton, Si Hoi Kou, Huijun Lei, Benjamin Tam, San Ming Wang

Biomolecules. 2023 Mar; 13(3): 429. Published online 2023 Feb 24. doi: 10.3390/biom13030429

PMCID:: PMC10046817

Abstract Article PDF–6.7M

Select item 99436638.

Structural snapshots of base excision by the cancer-associated variant MutY N146S reveal a retaining mechanism

Merve Demir, L Peyton Russelburg, Wen-Jen Lin, Carlos H Trasviña-Arenas, Beili Huang, Philip K Yuen, Martin P Horvath, Sheila S David

Nucleic Acids Res. 2023 Feb 22; 51(3): 1034–1049. Published online 2023 Jan 12. doi: 10.1093/nar/gkac1246

PMCID:: PMC9943663

Abstract Article PDF–5.5M

Select item 95413779.

Germline MUTYH mutations and high‐grade gliomas: Novel evidence for a potential association

Gábor Bedics, Lili Kotmayer, Erik Zajta, Lajos László Hegyi, Edit Ágota Brückner, Hajnalka Rajnai, Lilla Reiniger, Csaba Bödör, Miklós Garami, Bálint Scheich

Genes Chromosomes Cancer. 2022 Oct; 61(10): 622–628. Published online 2022 May 21. doi: 10.1002/gcc.23054

PMCID:: PMC9541377

Abstract Article PDF–5.7M

Select item 927042710.

Inherited MUTYH mutations cause elevated somatic mutation rates and distinctive mutational signatures in normal human cells

Philip S. Robinson, Laura E. Thomas, Federico Abascal, Hyunchul Jung, Luke M. R. Harvey, Hannah D. West, Sigurgeir Olafsson, Bernard C. H. Lee, Tim H. H. Coorens, Henry Lee-Six, Laura Butlin, Nicola Lander, Rebekah Truscott, Mathijs A. Sanders, Stefanie V. Lensing, Simon J. A. Buczacki, Rogier ten Hoopen, Nicholas Coleman, Roxanne Brunton-Sim, Simon Rushbrook, Kourosh Saeb-Parsy, Fiona Lalloo, Peter J. Campbell, Iñigo Martincorena, Julian R. Sampson, Michael R. Stratton

Nat Commun. 2022; 13: 3949. Published online 2022 Jul 8. doi: 10.1038/s41467-022-31341-0

PMCID:: PMC9270427

Abstract Article PDF–1.6M

Select item 914520011.

Oxidative Damage in Sporadic Colorectal Cancer: Molecular Mapping of Base Excision Repair Glycosylases MUTYH and hOGG1 in Colorectal Cancer Patients

Miriam J. Kavec, Marketa Urbanova, Pavol Makovicky, Alena Opattová, Kristyna Tomasova, Michal Kroupa, Klara Kostovcikova, Anna Siskova, Nazila Navvabi, Michaela Schneiderova, Veronika Vymetalkova, Ludmila Vodickova, Pavel Vodicka

Int J Mol Sci. 2022 May; 23(10): 5704. Published online 2022 May 20. doi: 10.3390/ijms23105704

PMCID:: PMC9145200

Abstract Article PDF–2.3M

Select item 910523512.

Cullin 3 Exon 9 Deletion in Familial Hyperkalemic Hypertension Impairs Cullin3-Ring-E3 Ligase (CRL3) Dynamic Regulation and Cycling

Ilektra Kouranti, Waed Abdel Khalek, Stephani Mazurkiewicz, Irmine Loisel-Ferreira, Alexis M. Gautreau, Lionel Pintard, Xavier Jeunemaitre, Eric Clauser

Int J Mol Sci. 2022 May; 23(9): 5151. Published online 2022 May 5. doi: 10.3390/ijms23095151

PMCID:: PMC9105235

Abstract Article PDF–5.8M

Select item 908038613.

Intronic Variant of MUTYH Gene Exhibits A Strong Association with Early Onset of Breast Cancer Susceptibility in Indonesian Women Population

Sonar Soni Panigoro, Erlin Listiyaningsih, Ika Nurlaila, Bharuno Mahesworo, Alam Ahmad Hidayat, Arif Budiarto, Digdo Sudigyo, Dian Amirullah, Simon Simon, James Baurley, Bens Pardamean

Asian Pac J Cancer Prev. 2021 Dec; 22(12): 3985–3991. doi: 10.31557/APJCP.2021.22.12.3985

PMCID:: PMC9080386

Abstract Article PDF–424K

Select item 868363314.

Filling the gap: A thorough investigation for the genetic diagnosis of unsolved polyposis patients with monoallelic MUTYH pathogenic variants

Anastasia Dell’Elice, Giulia Cini, Mara Fornasarig, Franco Armelao, Daniela Barana, Francesca Bianchi, Guido Claudio Casalis Cavalchini, Antonella Maffè, Isabella Mammi, Monica Pedroni, Antonio Percesepe, Italo Sorrentini, Mariagrazia Tibiletti, Roberta Maestro, Michele Quaia, Alessandra Viel

Mol Genet Genomic Med. 2021 Dec; 9(12): e1831. Published online 2021 Oct 26. doi: 10.1002/mgg3.1831

PMCID:: PMC8683633

Abstract Article PDF–1.1M

Select item 866412915.

Quantitative high-confidence human mitochondrial proteome and its dynamics in cellular context

Marcel Morgenstern, Christian D. Peikert, Philipp Lübbert, Ida Suppanz, Cinzia Klemm, Oliver Alka, Conny Steiert, Nataliia Naumenko, Alexander Schendzielorz, Laura Melchionda, Wignand W.D. Mühlhäuser, Bettina Knapp, Jakob D. Busch, Sebastian B. Stiller, Stefan Dannenmaier, Caroline Lindau, Mariya Licheva, Christopher Eickhorst, Riccardo Galbusera, Ralf M. Zerbes, Michael T. Ryan, Claudine Kraft, Vera Kozjak-Pavlovic, Friedel Drepper, Sven Dennerlein, Silke Oeljeklaus, Nikolaus Pfanner, Nils Wiedemann, Bettina Warscheid

Cell Metab. 2021 Dec 7; 33(12): 2464–2483.e18. doi: 10.1016/j.cmet.2021.11.001

PMCID:: PMC8664129

Abstract Article

Select item 826063216.

Evaluating the utility of tumour mutational signatures for identifying hereditary colorectal cancer and polyposis syndrome carriers

Peter Georgeson, Bernard J. Pope, Christophe Rosty, Mark Clendenning, Khalid Mahmood, Jihoon E. Joo, Romy Walker, Ryan Hutchinson, Susan Preston, Julia Como, Sharelle Joseland, Aung K. Win, Finlay A. Macrae, John L. Hopper, Dmitry Mouradov, Peter Gibbs, Oliver M. Sieber, Dylan E. O’Sullivan, Darren R. Brenner, Steve Gallinger, Mark A. Jenkins, Ingrid M. Winship, Daniel D. Buchanan

Gut. Author manuscript; available in PMC 2021 Nov 1.

Published in final edited form as: Gut. 2021 Nov; 70(11): 2138–2149. Published online 2021 Jan 7. doi: 10.1136/gutjnl-2019-320462

PMCID:: PMC8260632

Abstract Article PDF–3.1M

Select item 823326017.

Male and female breast cancer: the two faces of the same genetic susceptibility coin

Susana Nunes Silva, Bruno Costa Gomes, Saudade André, Ana Félix, António Sebastião Rodrigues, José Rueff

Breast Cancer Res Treat. 2021; 188(1): 295–305. Published online 2021 May 3. doi: 10.1007/s10549-021-06159-x

PMCID:: PMC8233260

Abstract Article PDF–870K

Select item 787891818.

MUTYH is associated with hepatocarcinogenesis in a non-alcoholic steatohepatitis mouse model

Hiroki Sakamoto, Koji Miyanishi, Shingo Tanaka, Ryo Ito, Kota Hamaguchi, Akira Sakurada, Masanori Sato, Tomohiro Kubo, Takahiro Osuga, Kazuyuki Murase, Kohichi Takada, Yusaku Nakabeppu, Masayoshi Kobune, Junji Kato

Sci Rep. 2021; 11: 3599. Published online 2021 Feb 11. doi: 10.1038/s41598-021-83138-8

PMCID:: PMC7878918

Abstract Article PDF–5.4M

Select item 785490419.

CHARACTERIZING GERMLINE APC AND MUTYH VARIANTS IN ASHKENAZI JEWS COMPARED TO OTHER INDIVIDUALS

Chinedu Ukaegbu, Zohar Levi, Tara D. Fehlmann, Hajime Uno, Anu Chittenden, Jennifer A. Inra, Shilpa Grover, Fay Kastrinos, Sapna Syngal, Matthew B. Yurgelun

Fam Cancer. Author manuscript; available in PMC 2022 Apr 1.

Published in final edited form as: Fam Cancer. 2021 Apr; 20(2): 111–116. Published online 2020 Aug 3. doi: 10.1007/s10689-020-00198-x

PMCID:: PMC7854904

Abstract Article PDF–320K

Select item 760362720.

MUTYH Deficiency Is Associated with Attenuated Pulmonary Fibrosis in a Bleomycin-Induced Model

Qingmin Sun, Jingwen Chen, Lizhi Xu, Jiaqi Kang, Xin Wu, Yan Ren, Yusaku Nakabeppu, Yaping Wang

Oxid Med Cell Longev. 2020; 2020: 4828256. Published online 2020 Oct 16. doi: 10.1155/2020/4828256

PMCID:: PMC7603627

Abstract Article PDF–2.5M

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