Terms: = Colorectal cancer AND MUTYH, MYH, 4595, ENSG00000132781, hMYH, MGC4416, MYHbeta AND Treatment
52 results:
1. Updated European guidelines for clinical management of familial adenomatous polyposis (FAP), mutyh-associated polyposis (MAP), gastric adenocarcinoma, proximal polyposis of the stomach (GAPPS) and other rare adenomatous polyposis syndromes: a joint EHTG-ESCP revision.
Zaffaroni G; Mannucci A; Koskenvuo L; de Lacy B; Maffioli A; Bisseling T; Half E; Cavestro GM; Valle L; Ryan N; Aretz S; Brown K; Buttitta F; Carneiro F; Claber O; Blanco-Colino R; Collard M; Crosbie E; Cunha M; Doulias T; Fleming C; Heinrich H; Hüneburg R; Metras J; Nagtegaal I; Negoi I; Nielsen M; Pellino G; Ricciardiello L; Sagir A; Sánchez-Guillén L; Seppälä TT; Siersema P; Striebeck B; Sampson JR; Latchford A; Parc Y; Burn J; Möslein G
Br J Surg; 2024 May; 111(5):. PubMed ID: 38722804
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2. Multiple colorectal adenomas syndrome: The role of mutyh mutation and the polyps' number in clinical management and colorectal cancer risk.
Negro S; Bao QR; Scarpa M; Scognamiglio F; Pucciarelli S; Remo A; Agostini M; D'Angelo E; Mammi I; Schiavi F; Rossi S; Zingone F; Ferrara F; Fantin A; Cristofori C; Guido E; Rizzotto ER; Intini R; Bergamo F; Fassan M; Salviati L; Urso EDL
Dig Liver Dis; 2024 Jun; 56(6):1087-1094. PubMed ID: 38071180
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3. A one-stop approach to diagnosing hereditary colorectal cancer in the Chinese population.
Li C; Song W; Xu Y; Guo T; Zhou X; Liu F; Xu Y
J Gastroenterol Hepatol; 2023 Nov; 38(11):1980-1987. PubMed ID: 37749864
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4. Uncommon variants detected via hereditary cancer panel and suggestions for genetic counseling.
Özdemir Z; Çevik E; Öksüzoğlu ÖBÇ; Doğan M; Ateş Ö; Esin E; Bilgetekin İ; Demirci U; Köseoğlu Ç; Topal A; Karadurmuş N; Erdem HB; Bahsi T
Mutat Res; 2023; 827():111831. PubMed ID: 37453313
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5. [Surgical strategies for hereditary colorectal cancer].
Kelm M; Wiegering A; Germer CT; Flemming S
Chirurgie (Heidelb); 2023 May; 94(5):412-416. PubMed ID: 36856815
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6. Strong Hereditary Predispositions to colorectal cancer.
Hryhorowicz S; Kaczmarek-Ryś M; Lis-Tanaś E; Porowski J; Szuman M; Grot N; Kryszczyńska A; Paszkowski J; Banasiewicz T; Pławski A
Genes (Basel); 2022 Dec; 13(12):. PubMed ID: 36553592
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7. A Previously Unrecognized Molecular Landscape of Lynch Syndrome in the Mexican Population.
Padua-Bracho A; Velázquez-Aragón JA; Fragoso-Ontiveros V; Nuñez-Martínez PM; Mejía Aguayo ML; Sánchez-Contreras Y; Ramirez-Otero MA; De la Fuente-Hernández MA; Vidal-Millán S; Wegman-Ostrosky T; Pedroza-Torres A; Arriaga-Canon C; Herrera-Montalvo LA; Alvarez-Gómez RM
Int J Mol Sci; 2022 Sep; 23(19):. PubMed ID: 36232851
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8. Management of familial adenomatous polyposis and mutyh-associated polyposis; new insights.
Aelvoet AS; Buttitta F; Ricciardiello L; Dekker E
Best Pract Res Clin Gastroenterol; 2022; 58-59():101793. PubMed ID: 35988966
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9. Sirt3 Regulates Response to Oxidative Stress by Interacting with BER Proteins in colorectal cancer.
Kabzinski J; Walczak A; Majsterek I
Genet Res (Camb); 2022; 2022():7299555. PubMed ID: 35440893
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10. Mismatch repair deficiency and mutyh variants in small intestine-neuroendocrine tumors.
Helderman NC; Elsayed FA; van Wezel T; Terlouw D; Langers AMJ; van Egmond D; Kilinç G; Hristova H; Farina Sarasqueta A; Morreau H; Nielsen M; Suerink M;
Hum Pathol; 2022 Jul; 125():11-17. PubMed ID: 35417733
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11. Molecular characteristics of young-onset colorectal cancer in Vietnamese patients.
Do MD; Nguyen TH; Le KT; Le LHG; Nguyen BH; Le KT; Doan TPT; Ho CQ; Nguyen HN; Tran TD; Vu HA
Asia Pac J Clin Oncol; 2022 Dec; 18(6):678-685. PubMed ID: 35098669
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12. 30 year experience of index case identification and outcomes of cascade testing in high-risk breast and colorectal cancer predisposition genes.
Woodward ER; Green K; Burghel GJ; Bulman M; Clancy T; Lalloo F; Schlecht H; Wallace AJ; Evans DG
Eur J Hum Genet; 2022 Apr; 30(4):413-419. PubMed ID: 34866136
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13. Forty-eight-year-old female mutyh carrier presenting with five concurrent primary cancers.
Arroyave A; Nodit L; Clegg D; Russ A
Cancer Rep (Hoboken); 2022 Feb; 5(2):e1455. PubMed ID: 34173730
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14. Surveillance recommendations for patients with Lynch syndrome and FAP : a monocentric study.
Baert L; Claes K; De Man M; Tate DJ; Geboes K
Acta Gastroenterol Belg; 2020; 83(3):399-405. PubMed ID: 33094586
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15. A case report of a patient with first phenotype of papillary thyroid carcinoma and heterochronous multiprimary tumor harboring germline mutyh Arg19*/Gly286Glu mutations.
Wang M; Zhu F; Luo N; Han T; Wang M
Oral Oncol; 2021 Jan; 112():104987. PubMed ID: 32888815
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16. Presentation and Follow-up of Familial Adenomatous Polyposis: Differences Between APC and mutyh Mutations.
Bademci R; Bollo J; Ramón Y Cajal T; Martínez MC; Hernández MP; Targarona EM
Cir Esp (Engl Ed); 2020 Oct; 98(8):465-471. PubMed ID: 32505560
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17. Oxidative Damage in Sporadic colorectal cancer: Molecular Mapping of Base Excision Repair Glycosylases in colorectal cancer Patients.
Vodicka P; Urbanova M; Makovicky P; Tomasova K; Kroupa M; Stetina R; Opattova A; Kostovcikova K; Siskova A; Schneiderova M; Vymetalkova V; Vodickova L
Int J Mol Sci; 2020 Apr; 21(7):. PubMed ID: 32252452
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18. Efficacy of immune checkpoint blockade in mutyh-associated hereditary colorectal cancer.
Volkov NM; Yanus GA; Ivantsov AO; Moiseenko FV; Matorina OG; Bizin IV; Moiseyenko VM; Imyanitov EN
Invest New Drugs; 2020 Jun; 38(3):894-898. PubMed ID: 31377904
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19. mutyh-associated polyposis.
Toboeva MK; Shelygin YA; Frolov SA; Kuzminov MA; Tsukanov AS
Ter Arkh; 2019 Mar; 91(2):97-100. PubMed ID: 31094179
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20. [Advance in research on the correlation between genotypes of susceptible mutations and clinical phenotype of familial adenomatous polyposis].
He S; Du J; Liu F
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Dec; 34(6):919-923. PubMed ID: 29188631
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