For: | Curia MC, Catalano T, Aceto GM. MUTYH: Not just polyposis. World J Clin Oncol 2020; 11(7): 428-449 [PMID: 32821650 DOI: 10.5306/wjco.v11.i7.428] |
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URL: | https://www.wjgnet.com/1948-5204/full/v11/i7/428.htm |
Number | Citing Articles |
1 |
Yunxiao Zhong, Xinya Zhang, Ruibing Feng, Yu Fan, Zhang Zhang, Qing‐Wen Zhang, Jian‐Bo Wan, Yitao Wang, Hua Yu, Guodong Li. OGG1: An emerging multifunctional therapeutic target for the treatment of diseases caused by oxidative DNA damage. Medicinal Research Reviews 2024; doi: 10.1002/med.22068
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2 |
Patricia Esperon, Florencia Neffa, Walter Pavicic, Florencia Spirandelli, Karin Alvarez, María José Mullins, Benedito Mauro Rossi, Rodrigo Felipe Góngora e Silva, Carlos Vaccaro, Francisco Lopéz-Köstner, Jorge Rugeles, Adriana Della Valle, Mev Dominguez-Valentin. A comprehensive characterization of the spectrum of MUTYH germline pathogenic variants in Latin America. Familial Cancer 2024; doi: 10.1007/s10689-024-00382-3
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3 |
Yushu Liu, Mohammadamin Edrisi, Zhi Yan, Huw A Ogilvie, Luay Nakhleh. NestedBD: Bayesian inference of phylogenetic trees from single-cell copy number profiles under a birth-death model. Algorithms for Molecular Biology 2024; 19(1) doi: 10.1186/s13015-024-00264-4
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4 |
Yuri Mizuno, Nona Abolhassani, Guianfranco Mazzei, Kunihiko Sakumi, Takashi Saito, Takaomi C. Saido, Toshiharu Ninomiya, Toru Iwaki, Ryo Yamasaki, Jun-ichi Kira, Yusaku Nakabeppu, Zhao Zhong Chong. MUTYH Actively Contributes to Microglial Activation and Impaired Neurogenesis in the Pathogenesis of Alzheimer’s Disease. Oxidative Medicine and Cellular Longevity 2021; 2021(1) doi: 10.1155/2021/8635088
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5 |
Joseph McGrath, Dillin J Rhatigan, Danielle Donahue, Mackenzie Fannin, Nuria Lawson. Infiltrating Ductal Breast Carcinoma in a Male Patient With Associated BARD1 Mutation. Cureus 2024; doi: 10.7759/cureus.66216
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6 |
Pelin Ercoskun, Cigdem Yuce Kahraman, Guller Ozkan, Abdulgani Tatar. Genetic Characterization of Hereditary Cancer Syndromes Based on Targeted Next-Generation Sequencing. Molecular Syndromology 2022; 13(2): 123 doi: 10.1159/000518927
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7 |
A.B. Semenova, M.M. Byakhova, M.V. Makarova, V.N. Galkin, M.V. Nemtsova, D.K. Chernevskiy, A.M. Danishevich, V.G. Shatalov, A.V. Babkina, N.G. Popova, S.M. Gadzhieva. The structure of pathogenic germline variants in colorectal cancer in Moscow patients. Arkhiv patologii 2023; 85(6): 16 doi: 10.17116/patol20238506116
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8 |
Katarína Fabišíková, Olívia Hamidová, Regína Lohajová Behulová, Katarína Závodná, Petra Priščáková, Vanda Repiská. Case Report: The Role of Molecular Analysis of the MUTYH Gene in Asymptomatic Individuals. Frontiers in Genetics 2020; 11 doi: 10.3389/fgene.2020.590486
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9 |
Luca Savino, Maria Carmela Di Marcantonio, Carmelo Moscatello, Roberto Cotellese, Lucia Centurione, Raffaella Muraro, Gitana Maria Aceto, Gabriella Mincione. Effects of H2O2 Treatment Combined With PI3K Inhibitor and MEK Inhibitor in AGS Cells: Oxidative Stress Outcomes in a Model of Gastric Cancer. Frontiers in Oncology 2022; 12 doi: 10.3389/fonc.2022.860760
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10 |
Yong Yang, Jieqing Yu, Yuanping Xiong, Jiansheng Xiao, Daofeng Dai, Feng Zhang. Prognostic Analysis of Differentially Expressed DNA Damage Repair Genes in Bladder Cancer. Pathology and Oncology Research 2022; 28 doi: 10.3389/pore.2022.1610267
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11 |
Melissa Duarte, Clara Milikowski. Gastrointestinal polyposis with associated cutaneous manifestations. Pathology 2022; 54(2): 157 doi: 10.1016/j.pathol.2021.08.009
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12 |
Sofia Tzoumpa, Nicolas Sevenet, Claudia‐Luisa Bejar‐Ardiles, Béatrice Villette, Coralie Zumelzu, Robert Benamouzig, Frédéric Caux, Eve Maubec. Multiple basal cell carcinomas revealing a biallelic MUTYH gene mutation in a 39‐year‐old male patient. Journal of the European Academy of Dermatology and Venereology 2023; 37(3) doi: 10.1111/jdv.18592
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13 |
Silvia Negro, Quoc Riccardo Bao, Marco Scarpa, Federico Scognamiglio, Salvatore Pucciarelli, Andrea Remo, Marco Agostini, Edoardo D'Angelo, Isabella Mammi, Francesca Schiavi, Silvia Rossi, Fabiana Zingone, Francesco Ferrara, Alberto Fantin, Chiara Cristofori, Ennio Guido, Erik Rosa Rizzotto, Rossana Intini, Francesca Bergamo, Matteo Fassan, Leonardo Salviati, Emanuele D.L. Urso. Multiple colorectal adenomas syndrome: The role of MUTYH mutation and the polyps’ number in clinical management and colorectal cancer risk. Digestive and Liver Disease 2024; 56(6): 1087 doi: 10.1016/j.dld.2023.11.034
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14 |
Arthur S. Aelvoet, Francesco Buttitta, Luigi Ricciardiello, Evelien Dekker. Management of familial adenomatous polyposis and MUTYH-associated polyposis; new insights. Best Practice & Research Clinical Gastroenterology 2022; : 101793 doi: 10.1016/j.bpg.2022.101793
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15 |
Luigi Magrin, Daniele Fanale, Chiara Brando, Lidia Rita Corsini, Ugo Randazzo, Marianna Di Piazza, Vittorio Gurrera, Erika Pedone, Tancredi Didier Bazan Russo, Salvatore Vieni, Gianni Pantuso, Antonio Russo, Viviana Bazan. MUTYH-associated tumor syndrome: The other face of MAP. Oncogene 2022; 41(18): 2531 doi: 10.1038/s41388-022-02304-y
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16 |
Exome sequencing identifies novel genes and variants in patients with Hirschsprung disease. Journal of Pediatric Surgery 2023; 58(4): 723 doi: 10.1016/j.jpedsurg.2022.11.011
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17 |
Samhita De, Sourav Paul, Anirban Manna, Chirantan Majumder, Koustav Pal, Nicolette Casarcia, Arijit Mondal, Sabyasachi Banerjee, Vinod Kumar Nelson, Suvranil Ghosh, Joyita Hazra, Ashish Bhattacharjee, Subhash Chandra Mandal, Mahadeb Pal, Anupam Bishayee. Phenolic Phytochemicals for Prevention and Treatment of Colorectal Cancer: A Critical Evaluation of In Vivo Studies. Cancers 2023; 15(3): 993 doi: 10.3390/cancers15030993
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18 |
Ghada Al-Kafaji, Ghufran Jassim, Amani AlHajeri, Amna Mohamed Tayeb Alawadhi, Mariam Fida, Ibrahim Sahin, Faisal Alali, Elias Fadel, Amy McCart Reed. Investigation of germline variants in Bahraini women with breast cancer using next-generation sequencing based-multigene panel. PLOS ONE 2023; 18(9): e0291015 doi: 10.1371/journal.pone.0291015
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19 |
Polyanna Oliveira, Paula Correa, Angelina Acosta, Juliana Freitas, Taísa Machado-Lopes, Thais Bomfim-Palma, Ândrea Ribeiro-dos-Santos, Sidney Santos, Roberto Nascimento, Ivana Nascimento, Kiyoko Abe-Sandes. Screening for Mutations in Hereditary Cancer Susceptibility Genes in a Region with High Endogamy in Brazil. Global Medical Genetics 2023; 10(04): 376 doi: 10.1055/s-0043-1777449
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20 |
Zangbéwendé Guy Ouedraogo, Florian Ceruti, Mathis Lepage, Mathilde Gay-Bellile, Nancy Uhrhammer, Flora Ponelle-Chachuat, Yannick Bidet, Maud Privat, Mathias Cavaillé. Detection Rate and Spectrum of Pathogenic Variations in a Cohort of 83 Patients with Suspected Hereditary Risk of Kidney Cancer. Genes 2023; 14(11): 1991 doi: 10.3390/genes14111991
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21 |
Fouad Bouso, Akhaled Zaher. Genetic Complexity in Recurrent Basal Cell Carcinoma: A MUTYH Variant Case Report. Cureus 2024; doi: 10.7759/cureus.55677
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22 |
Marcella Nunziato, Federica Di Maggio, Matilde Pensabene, Maria Valeria Esposito, Flavio Starnone, Carmine De Angelis, Alessandra Calabrese, Massimiliano D’Aiuto, Gerardo Botti, Sabino De Placido, Valeria D’Argenio, Francesco Salvatore. Multi-gene panel testing increases germline predisposing mutations’ detection in a cohort of breast/ovarian cancer patients from Southern Italy. Frontiers in Medicine 2022; 9 doi: 10.3389/fmed.2022.894358
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23 |
A. V. Endutkin, D. O. Zharkov. GO System, a DNA Repair Pathway to Cope with Oxidative Damage. Molecular Biology 2021; 55(2): 193 doi: 10.1134/S0026893321020072
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24 |
Carmelo Moscatello, Maria Carmela Di Marcantonio, Luca Savino, Emira D’Amico, Giordano Spacco, Pasquale Simeone, Paola Lanuti, Raffaella Muraro, Gabriella Mincione, Roberto Cotellese, Gitana Maria Aceto. Emerging Role of Oxidative Stress on EGFR and OGG1-BER Cross-Regulation: Implications in Thyroid Physiopathology. Cells 2022; 11(5): 822 doi: 10.3390/cells11050822
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25 |
Yuyue Qiu, Xinru Hu, Xiaoping Zeng, Hongmei Wang. Triple kill: DDR inhibitors, radiotherapy and immunotherapy leave cancer cells with no escape. Acta Biochimica et Biophysica Sinica 2022; 54(11): 1569 doi: 10.3724/abbs.2022153
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26 |
Giovanna D’Elia, Gemma Caliendo, Luana Passariello, Luisa Albanese, Jasmine Makker, Anna Maria Molinari, Maria Teresa Vietri. Hereditary Cancer Syndrome in a Family with Double Mutation in BRIP1 and MUTYH Genes. Genes 2023; 14(2): 428 doi: 10.3390/genes14020428
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27 |
Eugénie Chevalier, Robert Benamouzig. Chemoprevention in hereditary digestive neoplasia: A comprehensive review. Therapeutic Advances in Gastroenterology 2023; 16 doi: 10.1177/17562848231215585
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28 |
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29 |
Edward J. Saunders, Tokhir Dadaev, Mark N. Brook, Sarah Wakerell, Koveela Govindasami, Reshma Rageevakumar, Nafisa Hussain, Andrea Osborne, Diana Keating, Artitaya Lophatananon, Kenneth R. Muir, Burcu F. Darst, David V. Conti, Christopher A. Haiman, Antonis C. Antoniou, Rosalind A. Eeles, Zsofia Kote-Jarai. Identification of Genes with Rare Loss of Function Variants Associated with Aggressive Prostate Cancer and Survival. European Urology Oncology 2024; 7(2): 248 doi: 10.1016/j.euo.2024.02.003
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30 |
Ibrahim Sahin, Hanife Saat. New Perspectives on the Recurrent Monoallelic Germline Mutations of DNA Repair and Checkpoint Genes and Clinical Variability. Genetic Testing and Molecular Biomarkers 2022; 26(1): 17 doi: 10.1089/gtmb.2021.0108
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