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Items: 1 to 20 of 104

1.

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 15;59(2):234-42.

PMID:
10409435
2.

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.

PMID:
10631907
3.

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.

PMID:
15756445
4.

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.

PMID:
9609757
5.

Characterization of a 500 kb region on 17q25 and the exclusion of candidate genes as the familial Tylosis Oesophageal Cancer (TOC) locus.

Risk JM, Evans KE, Jones J, Langan JE, Rowbottom L, McRonald FE, Mills HS, Ellis A, Shaw JM, Leigh IM, Kelsell DP, Field JK.

Oncogene. 2002 Sep 12;21(41):6395-402.

6.
7.

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.

PMID:
15254736
8.

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;15(8):1271-7. Epub 2006 Mar 1.

PMID:
16510494
9.

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 22;17(16):2101-5.

10.

Close mapping of the focal non-epidermolytic palmoplantar keratoderma (PPK) locus associated with oesophageal cancer (TOC).

Kelsell DP, Risk JM, Leigh IM, Stevens HP, Ellis A, Hennies HC, Reis A, Weissenbach J, Bishop DT, Spurr NK, Field JK.

Hum Mol Genet. 1996 Jun;5(6):857-60.

PMID:
8776604
11.

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. Epub 2004 Mar 9.

PMID:
15007728
12.

Structure and regulation of the envoplakin gene.

Määttä A, Ruhrberg C, Watt FM.

J Biol Chem. 2000 Jun 30;275(26):19857-65.

13.

Fine genetic mapping of diffuse non-epidermolytic palmoplantar keratoderma to chromosome 12q11-q13: exclusion of the mapped type II keratins.

Kelsell DP, Stevens HP, Purkis PE, Talas U, Rustin MH, Leigh IM.

Exp Dermatol. 1999 Oct;8(5):388-91.

PMID:
10536965
14.

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 10;90(2):340-6. doi: 10.1016/j.ajhg.2011.12.008. Epub 2012 Jan 19.

15.

[Palmoplantar keratosis].

Nagai H, Emi M.

Nihon Rinsho. 2000 Jul;58(7):1501-4. Review. Japanese.

PMID:
10921331
16.

Tylosis A with squamous cell carcinoma of the oesophagus in a Spanish family.

Varela AB, Blanco Rodríguez MM, Boullosa PE, Silva JG.

Eur J Gastroenterol Hepatol. 2011 Mar;23(3):286-8. doi: 10.1097/MEG.0b013e328344042d.

PMID:
21285883
17.

Identification of DMC1, a novel gene in the TOC region on 17q25.1 that shows loss of expression in multiple human cancers.

Harada H, Nagai H, Tsuneizumi M, Mikami I, Sugano S, Emi M.

J Hum Genet. 2001;46(2):90-5.

PMID:
11281419
18.

Molecular cloning, tissue expression, and chromosomal assignment of a novel gene encoding a subunit of the human signal-recognition particle.

Harada H, Nagai H, Mine N, Terada Y, Fujiwara H, Mikami I, Tsuneizumi M, Yabe A, Miyazaki K, Yokota T, Imoto I, Inazawa J, Emi M.

J Hum Genet. 2001;46(2):70-5.

PMID:
11281415
19.

Refining the DFNB7-DFNB11 deafness locus using intragenic polymorphisms in a novel gene, TMEM2.

Scott DA, Drury S, Sundstrom RA, Bishop J, Swiderski RE, Carmi R, Ramesh A, Elbedour K, Srikumari Srisailapathy CR, Keats BJ, Sheffield VC, Smith RJ.

Gene. 2000 Apr 4;246(1-2):265-74.

PMID:
10767548
20.

Genetics of gastroesophageal cancer: paradigms, paradoxes, and prognostic utility.

Robertson EV, Jankowski JA.

Am J Gastroenterol. 2008 Feb;103(2):443-9. Epub 2007 Oct 9. Review.

PMID:
17925001

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