Friedl W - Search Results

1

Is the mismatch repair deficient type of Muir-Torre syndrome confined to mutations in the hMSH2 gene?

Kruse R, Lamberti C, Wang Y, Ruelfs C, Bruns A, Esche C, Lehmann P, Ruzicka T, Rütten A, Friedl W, Propping P. Kruse R, et al. Among authors: friedl w. Hum Genet. 1996 Dec;98(6):747-50. doi: 10.1007/s004390050298. Hum Genet. 1996. PMID: 8931714

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: friedl w. Am J Surg Pathol. 2002 Mar;26(3):338-43. doi: 10.1097/00000478-200203000-00007. Am J Surg Pathol. 2002. PMID: 11859205

3

Attenuated familial adenomatous polyposis due to a mutation in the 3' part of the APC gene. A clue for understanding the function of the APC protein.

Friedl W, Meuschel S, Caspari R, Lamberti C, Krieger S, Sengteller M, Propping P. Friedl W, et al. Hum Genet. 1996 May;97(5):579-84. doi: 10.1007/BF02281864. Hum Genet. 1996. PMID: 8655134

4

Muir-Torre syndrome: clinical features and molecular genetic analysis.

Esche C, Kruse R, Lamberti C, Friedl W, Propping P, Lehmann P, Ruzicka T. Esche C, et al. Among authors: friedl w. Br J Dermatol. 1997 Jun;136(6):913-7. Br J Dermatol. 1997. PMID: 9217825

5

Hereditary nonpolyposis colorectal cancer: causative role of a germline missense mutation in the hMLH1 gene confirmed by the independent occurrence of the same somatic mutation in tumour tissue.

Wang Y, Friedl W, Lamberti C, Ruelfs C, Kruse R, Propping P. Wang Y, et al. Among authors: friedl w. Hum Genet. 1997 Sep;100(3-4):362-4. doi: 10.1007/s004390050517. Hum Genet. 1997. PMID: 9272156

6

Hereditary nonpolyposis colorectal cancer (HNPCC): eight novel germline mutations in hMSH2 or hMLH1 genes.

Wehner M, Buschhausen L, Lamberti C, Kruse R, Caspari R, Propping P, Friedl W. Wehner M, et al. Among authors: friedl w. Hum Mutat. 1997;10(3):241-4. doi: 10.1002/(SICI)1098-1004(1997)10:3<241::AID-HUMU12>3.0.CO;2-#. Hum Mutat. 1997. PMID: 9298827 No abstract available.

7

A novel missense mutation in the DNA mismatch repair gene hMLH1 present among East Asians but not among Europeans.

Wang Y, Friedl W, Lamberti C, Nöthen MM, Kruse R, Propping P. Wang Y, et al. Among authors: friedl w. Hum Hered. 1998 Mar-Apr;48(2):87-91. doi: 10.1159/000022786. Hum Hered. 1998. PMID: 9526167

8

Muir-Torre phenotype has a frequency of DNA mismatch-repair-gene mutations similar to that in hereditary nonpolyposis colorectal cancer families defined by the Amsterdam criteria.

Kruse R, Rütten A, Lamberti C, Hosseiny-Malayeri HR, Wang Y, Ruelfs C, Jungck M, Mathiak M, Ruzicka T, Hartschuh W, Bisceglia M, Friedl W, Propping P. Kruse R, et al. Among authors: friedl w. Am J Hum Genet. 1998 Jul;63(1):63-70. doi: 10.1086/301926. Am J Hum Genet. 1998. PMID: 9634524 Free PMC article.

9

Microsatellite instability-a useful diagnostic tool to select patients at high risk for hereditary non-polyposis colorectal cancer: a study in different groups of patients with colorectal cancer.

Lamberti C, Kruse R, Ruelfs C, Caspari R, Wang Y, Jungck M, Mathiak M, Malayeri HR, Friedl W, Sauerbruch T, Propping P. Lamberti C, et al. Among authors: friedl w. Gut. 1999 Jun;44(6):839-43. doi: 10.1136/gut.44.6.839. Gut. 1999. PMID: 10323887 Free PMC article.

10

Cystic sebaceous tumors as marker lesions for the Muir-Torre syndrome: a histopathologic and molecular genetic study.

Rütten A, Burgdorf W, Hügel H, Kutzner H, Hosseiny-Malayeri HR, Friedl W, Propping P, Kruse R. Rütten A, et al. Among authors: friedl w. Am J Dermatopathol. 1999 Oct;21(5):405-13. doi: 10.1097/00000372-199910000-00001. Am J Dermatopathol. 1999. PMID: 10535567

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

249 results

Search Page