176 related articles for article (PubMed ID: 22638770)
1. Analysis of a Finnish family confirms RHBDF2 mutations as the underlying factor in tylosis with esophageal cancer.
Saarinen S; Vahteristo P; Lehtonen R; Aittomäki K; Launonen V; Kiviluoto T; Aaltonen LA
Fam Cancer; 2012 Sep; 11(3):525-8. PubMed ID: 22638770
[TBL] [Abstract][Full Text] [Related]
2. RHBDF2 mutations are associated with tylosis, a familial esophageal cancer syndrome.
Blaydon DC; Etheridge SL; Risk JM; Hennies HC; Gay LJ; Carroll R; Plagnol V; McRonald FE; Stevens HP; Spurr NK; Bishop DT; Ellis A; Jankowski J; Field JK; Leigh IM; South AP; Kelsell DP
Am J Hum Genet; 2012 Feb; 90(2):340-6. PubMed ID: 22265016
[TBL] [Abstract][Full Text] [Related]
3. [RHBDF2 mutations in familial palmoplantar keratoderma associated with tylosis oesophageal cancer].
Dereure O
Ann Dermatol Venereol; 2012; 139(8-9):605-6. PubMed ID: 22963978
[No Abstract] [Full Text] [Related]
4. Envoplakin, a possible candidate gene for focal NEPPK/esophageal cancer (TOC): the integration of genetic and physical maps of the TOC region on 17q25.
Risk JM; Ruhrberg C; Hennies H; Mills HS; Di Colandrea T; Evans KE; Ellis A; Watt FM; Bishop DT; Spurr NK; Stevens HP; Leigh IM; Reis A; Kelsell DP; Field JK
Genomics; 1999 Jul; 59(2):234-42. PubMed ID: 10409435
[TBL] [Abstract][Full Text] [Related]
5. Tylosis with oesophageal cancer: Diagnosis, management and molecular mechanisms.
Ellis A; Risk JM; Maruthappu T; Kelsell DP
Orphanet J Rare Dis; 2015 Sep; 10():126. PubMed ID: 26419362
[TBL] [Abstract][Full Text] [Related]
6. Tylosis associated with squamous cell carcinoma of the oesophagus (TOC): Report of an African family with a novel RHBDF2 variant.
Mokoena T; Smit JGM; Karusseit VO; Dorfling CM; van Rensburg EJ
Clin Genet; 2018 May; 93(5):1114-1116. PubMed ID: 29372562
[No Abstract] [Full Text] [Related]
7. Novel microsatellite markers and single nucleotide polymorphisms refine the tylosis with oesophageal cancer (TOC) minimal region on 17q25 to 42.5 kb: sequencing does not identify the causative gene.
Langan JE; Cole CG; Huckle EJ; Byrne S; McRonald FE; Rowbottom L; Ellis A; Shaw JM; Leigh IM; Kelsell DP; Dunham I; Field JK; Risk JM
Hum Genet; 2004 May; 114(6):534-40. PubMed ID: 15007728
[TBL] [Abstract][Full Text] [Related]
8. Whole Exome Sequencing Identified a Novel Mutation of the RHBDF2 Gene in a Chinese Family of Tylosis with Esophageal Cancer.
Qu L; Sha S; Zou QL; Gao XH; Xiao T; Chen HD; He CC
Acta Derm Venereol; 2019 Jun; 99(7):699-700. PubMed ID: 30938830
[No Abstract] [Full Text] [Related]
9. Tissue-specific role of RHBDF2 in cutaneous wound healing and hyperproliferative skin disease.
Hosur V; Lyons BL; Burzenski LM; Shultz LD
BMC Res Notes; 2017 Nov; 10(1):573. PubMed ID: 29116018
[TBL] [Abstract][Full Text] [Related]
10. RHBDF2-Regulated Growth Factor Signaling in a Rare Human Disease, Tylosis With Esophageal Cancer: What Can We Learn From Murine Models?
Hosur V; Farley ML; Low BE; Burzenski LM; Shultz LD; Wiles MV
Front Genet; 2018; 9():233. PubMed ID: 30022999
[TBL] [Abstract][Full Text] [Related]
11. Analysis of the function of ADAM17 in iRhom2 curly-bare and tylosis with esophageal cancer mutant mice.
Rabinowitsch AI; Maretzky T; Weskamp G; Haxaire C; Tueshaus J; Lichtenthaler SF; Monette S; Blobel CP
J Cell Sci; 2023 Jul; 136(13):. PubMed ID: 37282854
[TBL] [Abstract][Full Text] [Related]
12. The tylosis esophageal cancer (TOC) locus: more than just a familial cancer gene.
Risk JM; Mills HS; Garde J; Dunn JR; Evans KE; Hollstein M; Field JK
Dis Esophagus; 1999; 12(3):173-6. PubMed ID: 10631907
[TBL] [Abstract][Full Text] [Related]
13. Loss of heterozygosity in sporadic oesophageal tumors in the tylosis oesophageal cancer (TOC) gene region of chromosome 17q.
von Brevern M; Hollstein MC; Risk JM; Garde J; Bennett WP; Harris CC; Muehlbauer KR; Field JK
Oncogene; 1998 Oct; 17(16):2101-5. PubMed ID: 9798681
[TBL] [Abstract][Full Text] [Related]
14. Palmoplantar Hyperkeratosis and Strong Family History of Esophageal Cancer: Tylosis or Not?
Abidali H; Muna-Aguon P; Vela S; Nanda R
Am J Gastroenterol; 2018 Nov; 113(11):1733-1734. PubMed ID: 30214015
[No Abstract] [Full Text] [Related]
15. Candidate susceptibility variants for esophageal squamous cell carcinoma.
Donner I; Katainen R; Tanskanen T; Kaasinen E; Aavikko M; Ovaska K; Artama M; Pukkala E; Aaltonen LA
Genes Chromosomes Cancer; 2017 Jun; 56(6):453-459. PubMed ID: 28165652
[TBL] [Abstract][Full Text] [Related]
16. Tylosis esophageal cancer locus on chromosome 17q25.1 is commonly deleted in sporadic human esophageal cancer.
Iwaya T; Maesawa C; Ogasawara S; Tamura G
Gastroenterology; 1998 Jun; 114(6):1206-10. PubMed ID: 9609757
[TBL] [Abstract][Full Text] [Related]
17. An investigation of the tylosis with oesophageal cancer (TOC) locus in Iranian patients with oesophageal squamous cell carcinoma.
Shahabi M; Noori Daloii MR; Langan JE; Rowbottom L; Jahanzad E; Khoshbin E; Taghikhani M; Field JK; Risk JM
Int J Oncol; 2004 Aug; 25(2):389-95. PubMed ID: 15254736
[TBL] [Abstract][Full Text] [Related]
18. Infrequent mutation of the human envoplakin gene is closely linked to the tylosis oesophageal cancer locus in sporadic oesophageal squamous cell carcinomas.
Iwaya T; Maesawa C; Kimura T; Ogasawara S; Ikeda K; Kimura Y; Noda Y; Ishida K; Sato N; Saito K; Masuda T
Oncol Rep; 2005 Apr; 13(4):703-7. PubMed ID: 15756445
[TBL] [Abstract][Full Text] [Related]
19. Down-regulation of the cytoglobin gene, located on 17q25, in tylosis with oesophageal cancer (TOC): evidence for trans-allele repression.
McRonald FE; Liloglou T; Xinarianos G; Hill L; Rowbottom L; Langan JE; Ellis A; Shaw JM; Field JK; Risk JM
Hum Mol Genet; 2006 Apr; 15(8):1271-7. PubMed ID: 16510494
[TBL] [Abstract][Full Text] [Related]
20. Tylosis A with squamous cell carcinoma of the oesophagus in a Spanish family.
Varela AB; Blanco RodrÃguez MM; Boullosa PE; Silva JG
Eur J Gastroenterol Hepatol; 2011 Mar; 23(3):286-8. PubMed ID: 21285883
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
