Mangold E - Search Results

1

"Second hit" in sebaceous tumors from Muir-Torre patients with germline mutations in MSH2: allele loss is not the preferred mode of inactivation.

Kruse R, Rütten A, Hosseiny-Malayeri HR, Bisceglia M, Friedl W, Propping P, Ruzicka T, Mangold E. Kruse R, et al. Among authors: mangold e. J Invest Dermatol. 2001 Mar;116(3):463-5. doi: 10.1046/j.1523-1747.2001.01265.x. J Invest Dermatol. 2001. PMID: 11231323 Free article.

2

Loss of DNA mismatch repair proteins in skin tumors from patients with Muir-Torre syndrome and MSH2 or MLH1 germline mutations: establishment of immunohistochemical analysis as a screening test.

Mathiak M, Rütten A, Mangold E, Fischer HP, Ruzicka T, Friedl W, Propping P, Kruse R. Mathiak M, et al. Among authors: mangold e. Am J Surg Pathol. 2002 Mar;26(3):338-43. doi: 10.1097/00000478-200203000-00007. Am J Surg Pathol. 2002. PMID: 11859205

3

Frequency of microsatellite instability in unselected sebaceous gland neoplasias and hyperplasias.

Kruse R, Rütten A, Schweiger N, Jakob E, Mathiak M, Propping P, Mangold E, Bisceglia M, Ruzicka T. Kruse R, et al. Among authors: mangold e. J Invest Dermatol. 2003 May;120(5):858-64. doi: 10.1046/j.1523-1747.2003.12125.x. J Invest Dermatol. 2003. PMID: 12713593 Free article.

4

MSH6 mutation in Muir-Torre syndrome: could this be a rare finding?

Mangold E, Rahner N, Friedrichs N, Buettner R, Pagenstecher C, Aretz S, Friedl W, Ruzicka T, Propping P, Rütten A, Kruse R. Mangold E, et al. Br J Dermatol. 2007 Jan;156(1):158-62. doi: 10.1111/j.1365-2133.2006.07607.x. Br J Dermatol. 2007. PMID: 17199584 No abstract available.

5

A modified multiplex PCR assay for detection of large deletions in MSH2 and MLH1.

Wang Y, Friedl W, Sengteller M, Jungck M, Filges I, Propping P, Mangold E. Wang Y, et al. Among authors: mangold e. Hum Mutat. 2002 Mar;19(3):279-86. doi: 10.1002/humu.10042. Hum Mutat. 2002. PMID: 11857745

6

Hereditary nonpolyposis colorectal cancer: frequent occurrence of large genomic deletions in MSH2 and MLH1 genes.

Wang Y, Friedl W, Lamberti C, Jungck M, Mathiak M, Pagenstecher C, Propping P, Mangold E. Wang Y, et al. Among authors: mangold e. Int J Cancer. 2003 Feb 20;103(5):636-41. doi: 10.1002/ijc.10869. Int J Cancer. 2003. PMID: 12494471

7

Hereditary nonpolyposis colorectal cancer: pitfalls in deletion screening in MSH2 and MLH1 genes.

Wehner M, Mangold E, Sengteller M, Friedrichs N, Aretz S, Friedl W, Propping P, Pagenstecher C. Wehner M, et al. Among authors: mangold e. Eur J Hum Genet. 2005 Aug;13(8):983-6. doi: 10.1038/sj.ejhg.5201421. Eur J Hum Genet. 2005. PMID: 15870828

8

Tumours from MSH2 mutation carriers show loss of MSH2 expression but many tumours from MLH1 mutation carriers exhibit weak positive MLH1 staining.

Mangold E, Pagenstecher C, Friedl W, Fischer HP, Merkelbach-Bruse S, Ohlendorf M, Friedrichs N, Aretz S, Buettner R, Propping P, Mathiak M. Mangold E, et al. J Pathol. 2005 Dec;207(4):385-95. doi: 10.1002/path.1858. J Pathol. 2005. PMID: 16216036

9

Nine novel pathogenic germline mutations in MLH1, MSH2, MSH6 and PMS2 in families with Lynch syndrome.

Rahner N, Friedrichs N, Wehner M, Steinke V, Aretz S, Friedl W, Buettner R, Mangold E, Propping P, Walldorf C. Rahner N, et al. Among authors: mangold e. Acta Oncol. 2007;46(6):763-9. doi: 10.1080/02841860701230217. Acta Oncol. 2007. PMID: 17653898

10

A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndrome.

Mangold E, Pagenstecher C, Leister M, Mathiak M, Rütten A, Friedl W, Propping P, Ruzicka T, Kruse R. Mangold E, et al. J Med Genet. 2004 Jul;41(7):567-72. doi: 10.1136/jmg.2003.012997. J Med Genet. 2004. PMID: 15235030 Free PMC article. No abstract available.

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