Pistorius SR - Search Results

1

Identification of six novel MSH2 and MLH1 germline mutations in HNPCC.

Krüger S, Plaschke J, Jeske B, Görgens H, Pistorius SR, Bier A, Kreuz FR, Theissig F, Aust DE, Saeger HD, Schackert HK. Krüger S, et al. Among authors: pistorius sr. Hum Mutat. 2003 Apr;21(4):445-6. doi: 10.1002/humu.9121. Hum Mutat. 2003. PMID: 12655562

2

Ten novel MSH2 and MLH1 germline mutations in families with HNPCC.

Krüger S, Bier A, Plaschke J, Höhl R, Aust DE, Kreuz FR, Pistorius SR, Saeger HD, Rothhammer V, Al-Taie O, Schackert HK. Krüger S, et al. Among authors: pistorius sr. Hum Mutat. 2004 Oct;24(4):351-2. doi: 10.1002/humu.9278. Hum Mutat. 2004. PMID: 15365996

3

Seven novel MLH1 and MSH2 germline mutations in hereditary nonpolyposis colorectal cancer.

Krüger S, Plaschke J, Pistorius S, Jeske B, Haas S, Krämer H, Hinterseher I, Bier A, Kreuz FR, Theissig F, Saeger HD, Schackert HK. Krüger S, et al. Hum Mutat. 2002 Jan;19(1):82. doi: 10.1002/humu.9004. Hum Mutat. 2002. PMID: 11754112

4

Involvement of hMSH6 in the development of hereditary and sporadic colorectal cancer revealed by immunostaining is based on germline mutations, but rarely on somatic inactivation.

Plaschke J, Krüger S, Pistorius S, Theissig F, Saeger HD, Schackert HK. Plaschke J, et al. Int J Cancer. 2002 Feb 10;97(5):643-8. doi: 10.1002/ijc.10097. Int J Cancer. 2002. PMID: 11807791

5

Loss of MSH3 protein expression is frequent in MLH1-deficient colorectal cancer and is associated with disease progression.

Plaschke J, Krüger S, Jeske B, Theissig F, Kreuz FR, Pistorius S, Saeger HD, Iaccarino I, Marra G, Schackert HK. Plaschke J, et al. Cancer Res. 2004 Feb 1;64(3):864-70. doi: 10.1158/0008-5472.can-03-2807. Cancer Res. 2004. PMID: 14871813

6

Genomic rearrangements in MSH2, MLH1 or MSH6 are rare in HNPCC patients carrying point mutations.

Pistorius S, Görgens H, Plaschke J, Hoehl R, Krüger S, Engel C, Saeger HD, Schackert HK. Pistorius S, et al. Cancer Lett. 2007 Apr 8;248(1):89-95. doi: 10.1016/j.canlet.2006.06.002. Epub 2006 Jul 11. Cancer Lett. 2007. PMID: 16837128

7

Clinical consequences of molecular diagnosis in families with mismatch repair gene germline mutations.

Pistorius SR, Kruppa C, Haas S, Plaschke J, Kruger S, Bulitta CJ, Nagel M, Saeger HD, Schackert HK. Pistorius SR, et al. Int J Colorectal Dis. 2000 Nov;15(5-6):255-63. doi: 10.1007/s003840000261. Int J Colorectal Dis. 2000. PMID: 11151427

8

An intronic germline transition in the HNPCC gene hMSH2 is associated with sporadic colorectal cancer.

Goessl C, Plaschke J, Pistorius S, Hahn M, Frank S, Hampl M, Görgens H, Koch R, Saeger HD, Schackert HK. Goessl C, et al. Eur J Cancer. 1997 Oct;33(11):1869-74. doi: 10.1016/s0959-8049(97)00219-0. Eur J Cancer. 1997. PMID: 9470849

9

Sequence analysis of the mismatch repair gene hMSH6 in the germline of patients with familial and sporadic colorectal cancer.

Plaschke J, Kruppa C, Tischler R, Bocker T, Pistorius S, Dralle H, Rüschoff J, Saeger HD, Fishel R, Schackert HK. Plaschke J, et al. Int J Cancer. 2000 Mar 1;85(5):606-13. doi: 10.1002/(sici)1097-0215(20000301)85:5<606::aid-ijc2>3.0.co;2-b. Int J Cancer. 2000. PMID: 10699937

10

[Can molecular genetic knowledge from studies of hereditary carcinoma be applied to sporadic colorectal carcinoma?].

Pistorius S, Schackert HK, Saeger HD. Pistorius S, et al. Kongressbd Dtsch Ges Chir Kongr. 2001;118:820-4. Kongressbd Dtsch Ges Chir Kongr. 2001. PMID: 11824368 German.

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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

37 results

Search Page

Filters