Terms: = Colorectal cancer AND STK11, LKB1, 6794, ENSG00000118046, Q15831, PJS AND Diagnosis
34 results:
1. Tumor loss-of-function mutations in stk11/lkb1 induce cachexia.
Iyengar P; Gandhi AY; Granados J; Guo T; Gupta A; Yu J; Llano EM; Zhang F; Gao A; Kandathil A; Williams D; Gao B; Girard L; Malladi VS; Shelton JM; Evers BM; Hannan R; Ahn C; Minna JD; Infante RE
JCI Insight; 2023 Apr; 8(8):. PubMed ID: 37092555
[TBL] [Abstract] [Full Text] [Related]
2. 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
[TBL] [Abstract] [Full Text] [Related]
3. Whole Genome Sequencing Applied in Familial Hamartomatous Polyposis Identifies Novel Structural Variations.
Kariv R; Dahary D; Yaron Y; Petel-Galil Y; Malcov M; Rosner G
Genes (Basel); 2022 Aug; 13(8):. PubMed ID: 36011318
[TBL] [Abstract] [Full Text] [Related]
4. diagnosis and Management of cancer Risk in the Gastrointestinal Hamartomatous Polyposis Syndromes: Recommendations From the US Multi-Society Task Force on colorectal cancer.
Boland CR; Idos GE; Durno C; Giardiello FM; Anderson JC; Burke CA; Dominitz JA; Gross S; Gupta S; Jacobson BC; Patel SG; Shaukat A; Syngal S; Robertson DJ
Gastroenterology; 2022 Jun; 162(7):2063-2085. PubMed ID: 35487791
[TBL] [Abstract] [Full Text] [Related]
5. diagnosis and management of cancer risk in the gastrointestinal hamartomatous polyposis syndromes: recommendations from the U.S. Multi-Society Task Force on colorectal cancer.
Boland CR; Idos GE; Durno C; Giardiello FM; Anderson JC; Burke CA; Dominitz JA; Gross S; Gupta S; Jacobson BC; Patel SG; Shaukat A; Syngal S; Robertson DJ
Gastrointest Endosc; 2022 Jun; 95(6):1025-1047. PubMed ID: 35487765
[TBL] [Abstract] [Full Text] [Related]
6. diagnosis and Management of cancer Risk in the Gastrointestinal Hamartomatous Polyposis Syndromes: Recommendations From the US Multi-Society Task Force on colorectal cancer.
Boland CR; Idos GE; Durno C; Giardiello FM; Anderson JC; Burke CA; Dominitz JA; Gross S; Gupta S; Jacobson BC; Patel SG; Shaukat A; Syngal S; Robertson DJ
Am J Gastroenterol; 2022 Jun; 117(6):846-864. PubMed ID: 35471415
[TBL] [Abstract] [Full Text] [Related]
7. Germline variant testing in serrated polyposis syndrome.
Murphy A; Solomons J; Risby P; Gabriel J; Bedenham T; Johnson M; Atkinson N; Bailey AA; Bird-Lieberman E; Leedham SJ; East JE; Biswas S
J Gastroenterol Hepatol; 2022 May; 37(5):861-869. PubMed ID: 35128723
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8. Paediatric polyposis syndromes: burden of disease and current concepts.
Phen C; Rojas I
Curr Opin Pediatr; 2021 Oct; 33(5):509-514. PubMed ID: 34261898
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9. Delayed diagnosis of Peutz-Jeghers syndrome due to pathological information loss or mistake in family/personal history.
Jiang YL; Xu XD; Li BR; Yu ED; Zhao ZY; Liu H
Orphanet J Rare Dis; 2021 Jun; 16(1):261. PubMed ID: 34103092
[TBL] [Abstract] [Full Text] [Related]
10. Wnt/β-catenin signaling as an emerging potential key pharmacological target in cholangiocarcinoma.
Zhang GF; Qiu L; Yang SL; Wu JC; Liu TJ
Biosci Rep; 2020 Mar; 40(3):. PubMed ID: 32140709
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11. [diagnosis and treatment for 46 cases of Peutz-Jeghers syndrome].
Jia Y; Fu H; Li N; Kang Q; Sheng J
Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2018 Dec; 43(12):1323-1327. PubMed ID: 30643048
[TBL] [Abstract] [Full Text] [Related]
12. Optimization of the diagnosis of inherited colorectal cancer using NGS and capture of exonic and intronic sequences of panel genes.
Baert-Desurmont S; Coutant S; Charbonnier F; Macquere P; Lecoquierre F; Schwartz M; Blanluet M; Vezain M; Lanos R; Quenez O; Bou J; Bouvignies E; Fourneaux S; Manase S; Vasseur S; Mauillon J; Gerard M; Marlin R; Bougeard G; Tinat J; Frebourg T; Tournier I
Eur J Hum Genet; 2018 Nov; 26(11):1597-1602. PubMed ID: 29967336
[TBL] [Abstract] [Full Text] [Related]
13. Clinical manifestations and stk11 germline mutations in Taiwanese patients with Peutz-Jeghers syndrome.
Chiang JM; Chen TC
Asian J Surg; 2018 Sep; 41(5):480-485. PubMed ID: 28869103
[TBL] [Abstract] [Full Text] [Related]
14. cancer Screening Recommendations and Clinical Management of Inherited Gastrointestinal cancer Syndromes in Childhood.
Achatz MI; Porter CC; Brugières L; Druker H; Frebourg T; Foulkes WD; Kratz CP; Kuiper RP; Hansford JR; Hernandez HS; Nathanson KL; Kohlmann WK; Doros L; Onel K; Schneider KW; Scollon SR; Tabori U; Tomlinson GE; Evans DGR; Plon SE
Clin Cancer Res; 2017 Jul; 23(13):e107-e114. PubMed ID: 28674119
[TBL] [Abstract] [Full Text] [Related]
15. Laparoscopic restorative proctocolectomy with ileal pouch-anal anastomosis for Peutz-Jeghers syndrome with synchronous rectal cancer.
Zhong ME; Niu BZ; Ji WY; Wu B
World J Gastroenterol; 2016 Jun; 22(22):5293-6. PubMed ID: 27298573
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16. [Rare hereditary syndromes associated with polyposis and the development of malignant tumors].
Kazubskaya TP; Kozlova VM; Filippova MG; Тrofimov EI; Belev NF; Sokolova IN; Tamrazov RI; Pavlovskaya AI; Kondratyeva TT
Arkh Patol; 2016; 78(2):10-18. PubMed ID: 27070770
[TBL] [Abstract] [Full Text] [Related]
17. Hereditary non-BRCA gynecological tumors.
Vellone VG; Paudice M; Varesco L
Minerva Ginecol; 2016 Oct; 68(5):579-86. PubMed ID: 26930387
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18. Oral mucosal stigmata in hereditary-cancer syndromes: From germline mutations to distinctive clinical phenotypes and tailored therapies.
Ponti G; Tomasi A; Manfredini M; Pellacani G
Gene; 2016 May; 582(1):23-32. PubMed ID: 26850131
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19. Prevalence of germline mutations in cancer predisposition genes in patients with pancreatic cancer.
Grant RC; Selander I; Connor AA; Selvarajah S; Borgida A; Briollais L; Petersen GM; Lerner-Ellis J; Holter S; Gallinger S
Gastroenterology; 2015 Mar; 148(3):556-64. PubMed ID: 25479140
[TBL] [Abstract] [Full Text] [Related]
20. [Hereditary predisposition to cancers of the digestive tract, breast, gynecological and gonadal: focus on the Peutz-Jeghers].
Turpin A; Cattan S; Leclerc J; Wacrenier A; Manouvrier-Hanu S; Buisine MP; Lejeune-Dumoulin S
Bull Cancer; 2014 Sep; 101(9):813-22. PubMed ID: 25036236
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