Christensen E - Search Results

1

Mutations in AXIN2 cause colorectal cancer with defective mismatch repair by activating beta-catenin/TCF signalling.

Liu W, Dong X, Mai M, Seelan RS, Taniguchi K, Krishnadath KK, Halling KC, Cunningham JM, Boardman LA, Qian C, Christensen E, Schmidt SS, Roche PC, Smith DI, Thibodeau SN. Liu W, et al. Among authors: christensen e. Nat Genet. 2000 Oct;26(2):146-7. doi: 10.1038/79859. Nat Genet. 2000. PMID: 11017067 No abstract available.

2

Higher risk of mismatch repair-deficient colorectal cancer in alpha(1)-antitrypsin deficiency carriers and cigarette smokers.

Yang P, Cunningham JM, Halling KC, Lesnick TG, Burgart LJ, Wiegert EM, Christensen ER, Lindor NM, Katzmann JA, Thibodeau SN. Yang P, et al. Among authors: christensen er. Mol Genet Metab. 2000 Dec;71(4):639-45. doi: 10.1006/mgme.2000.3089. Mol Genet Metab. 2000. PMID: 11136557

3

The frequency of hereditary defective mismatch repair in a prospective series of unselected colorectal carcinomas.

Cunningham JM, Kim CY, Christensen ER, Tester DJ, Parc Y, Burgart LJ, Halling KC, McDonnell SK, Schaid DJ, Walsh Vockley C, Kubly V, Nelson H, Michels VV, Thibodeau SN. Cunningham JM, et al. Among authors: christensen er. Am J Hum Genet. 2001 Oct;69(4):780-90. doi: 10.1086/323658. Epub 2001 Aug 24. Am J Hum Genet. 2001. PMID: 11524701 Free PMC article.

4

Analysis of the RNASEL gene in familial and sporadic prostate cancer.

Wang L, McDonnell SK, Elkins DA, Slager SL, Christensen E, Marks AF, Cunningham JM, Peterson BJ, Jacobsen SJ, Cerhan JR, Blute ML, Schaid DJ, Thibodeau SN. Wang L, et al. Among authors: christensen e. Am J Hum Genet. 2002 Jul;71(1):116-23. doi: 10.1086/341281. Epub 2002 May 17. Am J Hum Genet. 2002. PMID: 12022038 Free PMC article.

5

Hypermethylation of the hMLH1 promoter in colon cancer with microsatellite instability.

Cunningham JM, Christensen ER, Tester DJ, Kim CY, Roche PC, Burgart LJ, Thibodeau SN. Cunningham JM, et al. Among authors: christensen er. Cancer Res. 1998 Aug 1;58(15):3455-60. Cancer Res. 1998. PMID: 9699680

6

HMSH6 alterations in patients with microsatellite instability-low colorectal cancer.

Parc YR, Halling KC, Wang L, Christensen ER, Cunningham JM, French AJ, Burgart LJ, Price-Troska TL, Roche PC, Thibodeau SN. Parc YR, et al. Among authors: christensen er. Cancer Res. 2000 Apr 15;60(8):2225-31. Cancer Res. 2000. PMID: 10786688

7

Role of HPC2/ELAC2 in hereditary prostate cancer.

Wang L, McDonnell SK, Elkins DA, Slager SL, Christensen E, Marks AF, Cunningham JM, Peterson BJ, Jacobsen SJ, Cerhan JR, Blute ML, Schaid DJ, Thibodeau SN. Wang L, et al. Among authors: christensen e. Cancer Res. 2001 Sep 1;61(17):6494-9. Cancer Res. 2001. PMID: 11522646

8

The application of fluorescent in situ hybridization to detect Mbcr/abl fusion in variant Ph chromosomes in CML and ALL.

Dewald GW, Schad CR, Christensen ER, Tiede AL, Zinsmeister AR, Spurbeck JL, Thibodeau SN, Jalal SM. Dewald GW, et al. Among authors: christensen er. Cancer Genet Cytogenet. 1993 Nov;71(1):7-14. doi: 10.1016/0165-4608(93)90196-s. Cancer Genet Cytogenet. 1993. PMID: 8275455

9

Luteinizing hormone beta polymorphism and risk of familial and sporadic prostate cancer.

Elkins DA, Yokomizo A, Thibodeau SN, J Schaid D, Cunningham JM, Marks A, Christensen E, McDonnell SK, Slager S, J Peterson B, J Jacobsen S, R Cerhan J, L Blute M, J Tindall D, Liu W. Elkins DA, et al. Among authors: christensen e. Prostate. 2003 Jun 15;56(1):30-6. doi: 10.1002/pros.10220. Prostate. 2003. PMID: 12746844

10

Detection of RB1 deletions by fluorescence in situ hybridization in malignant hematologic disorders.

Juneau AL, Kaehler M, Christensen ER, Schad CR, Zinsmeister AR, Lust J, Hanson C, Dewald GW. Juneau AL, et al. Among authors: christensen er. Cancer Genet Cytogenet. 1998 Jun;103(2):117-23. doi: 10.1016/s0165-4608(97)00408-1. Cancer Genet Cytogenet. 1998. PMID: 9614909

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