Sengteller M - Search Results

1

Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families.

Friedl W, Caspari R, Sengteller M, Uhlhaas S, Lamberti C, Jungck M, Kadmon M, Wolf M, Fahnenstich J, Gebert J, Möslein G, Mangold E, Propping P. Friedl W, et al. Among authors: sengteller m. Gut. 2001 Apr;48(4):515-21. doi: 10.1136/gut.48.4.515. Gut. 2001. PMID: 11247896 Free PMC article.

2

Eleven novel germline mutations in the adenomatous polyposis coli (APC) gene.

Paffenholz R, Mandl M, Caspari R, Sengteller M, Propping P, Friedl W. Paffenholz R, et al. Among authors: sengteller m. Hum Mol Genet. 1994 Sep;3(9):1703-4. doi: 10.1093/hmg/3.9.1703. Hum Mol Genet. 1994. PMID: 7833936 No abstract available.

3

A somatic mutation in the adenomatous polyposis coli (APC) gene in peripheral blood cells--implications for predictive diagnosis.

Mandl M, Kadmon M, Sengteller M, Caspari R, Propping P, Friedl W. Mandl M, et al. Among authors: sengteller m. Hum Mol Genet. 1994 Jun;3(6):1009-11. doi: 10.1093/hmg/3.6.1009. Hum Mol Genet. 1994. PMID: 7951213 No abstract available.

4

Frequency of common and novel inactivating APC mutations in 202 families with familial adenomatous polyposis.

Mandl M, Paffenholz R, Friedl W, Caspari R, Sengteller M, Propping P. Mandl M, et al. Among authors: sengteller m. Hum Mol Genet. 1994 Jan;3(1):181-4. doi: 10.1093/hmg/3.1.181. Hum Mol Genet. 1994. PMID: 8162022

5

Familial adenomatous polyposis: a submicroscopic deletion at the APC locus in a family with mentally normal patients.

Mandl M, Caspari R, Jauch A, Böker T, Raschke H, Sengteller M, Propping P, Friedl W. Mandl M, et al. Among authors: sengteller m. Hum Genet. 1996 Feb;97(2):204-8. doi: 10.1007/BF02265266. Hum Genet. 1996. PMID: 8566954

6

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. Among authors: sengteller m. Hum Genet. 1996 May;97(5):579-84. doi: 10.1007/BF02281864. Hum Genet. 1996. PMID: 8655134

7

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: sengteller m. Hum Mutat. 2002 Mar;19(3):279-86. doi: 10.1002/humu.10042. Hum Mutat. 2002. PMID: 11857745

8

Single-step screening method for the most common mutations in familial adenomatous polyposis.

Friedl W, Mandl M, Sengteller M. Friedl W, et al. Among authors: sengteller m. Hum Mol Genet. 1993 Sep;2(9):1481-2. doi: 10.1093/hmg/2.9.1481. Hum Mol Genet. 1993. PMID: 8242076 No abstract available.

9

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: sengteller m. Eur J Hum Genet. 2005 Aug;13(8):983-6. doi: 10.1038/sj.ejhg.5201421. Eur J Hum Genet. 2005. PMID: 15870828

10

Aberrant splicing in MLH1 and MSH2 due to exonic and intronic variants.

Pagenstecher C, Wehner M, Friedl W, Rahner N, Aretz S, Friedrichs N, Sengteller M, Henn W, Buettner R, Propping P, Mangold E. Pagenstecher C, et al. Among authors: sengteller m. Hum Genet. 2006 Mar;119(1-2):9-22. doi: 10.1007/s00439-005-0107-8. Epub 2005 Dec 8. Hum Genet. 2006. PMID: 16341550

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