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Items: 1 to 20 of 187

1.

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
2.

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.

3.

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
4.

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
5.

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
6.

Comprehensive characterization of annexin I alterations in esophageal squamous cell carcinoma.

Hu N, Flaig MJ, Su H, Shou JZ, Roth MJ, Li WJ, Wang C, Goldstein AM, Li G, Emmert-Buck MR, Taylor PR.

Clin Cancer Res. 2004 Sep 15;10(18 Pt 1):6013-22.

7.

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.

8.

Allelic loss on chromosome 13q14 and mutation in deleted in cancer 1 gene in esophageal squamous cell carcinoma.

Li WJ, Hu N, Su H, Wang C, Goldstein AM, Wang Y, Emmert-Buck MR, Roth MJ, Guo WJ, Taylor PR.

Oncogene. 2003 Jan 16;22(2):314-8.

PMID:
12527901
9.

Polymorphism and allelic loss at the AS3 locus on 13q12-13 in esophageal squamous cell carcinoma.

Harada H, Uchida N, Shimada Y, Kumimoto H, Shinoda M, Imamura M, Ishizaki K.

Int J Oncol. 2001 May;18(5):1003-7.

PMID:
11295048
10.

Lymph node metastasis is associated with allelic loss on chromosome 13q12-13 in esophageal squamous cell carcinoma.

Harada H, Tanaka H, Shimada Y, Shinoda M, Imamura M, Ishizaki K.

Cancer Res. 1999 Aug 1;59(15):3724-9.

11.

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
12.
13.

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
14.

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
15.

Infrequent mutation in the BRCA2 gene in esophageal squamous cell carcinoma.

Hu N, Li G, Li WJ, Wang C, Goldstein AM, Tang ZZ, Roth MJ, Dawsey SM, Huang J, Wang QH, Ding T, Giffen C, Taylor PR, Emmert-Buck MR.

Clin Cancer Res. 2002 Apr;8(4):1121-6.

16.

E-cadherin gene mutations are rare in adenocarcinomas of the oesophagus.

Wijnhoven BP, de Both NJ, van Dekken H, Tilanus HW, Dinjens WN.

Br J Cancer. 1999 Jul;80(10):1652-7.

17.

Status of the DPC4 tumor suppressor gene in sporadic colon adenocarcinoma of Croatian patients: identification of a novel somatic mutation.

Popović Hadzija M, Radosevic S, Kovacević D, Lukac J, Hadzija M, Spaventi R, Pavelić K, Kapitanović S.

Mutat Res. 2004 Apr 14;548(1-2):61-73.

PMID:
15063137
18.

High frequency of CDKN2A alterations in esophageal squamous cell carcinoma from a high-risk Chinese population.

Hu N, Wang C, Su H, Li WJ, Emmert-Buck MR, Li G, Roth MJ, Tang ZZ, Lu N, Giffen C, Albert PS, Taylor PR, Goldstein AM.

Genes Chromosomes Cancer. 2004 Mar;39(3):205-16.

PMID:
14732922
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