Kiechle M - Search Results

1

TP53 germline mutations in the context of families with hereditary breast and ovarian cancer: a clinical challenge.

Grill S, Ramser J, Hellebrand H, Pfarr N, Boxberg M, Brambs C, Ditsch N, Meindl A, Groß E, Meitinger T, Kiechle M, Quante AS. Grill S, et al. Among authors: kiechle m. Arch Gynecol Obstet. 2021 Jun;303(6):1557-1567. doi: 10.1007/s00404-020-05883-x. Epub 2020 Nov 27. Arch Gynecol Obstet. 2021. PMID: 33245408 Free PMC article.

2

A comparison of BRCA1 mutation analysis by direct sequencing, SSCP and DHPLC.

Gross E, Arnold N, Goette J, Schwarz-Boeger U, Kiechle M. Gross E, et al. Among authors: kiechle m. Hum Genet. 1999 Jul-Aug;105(1-2):72-8. doi: 10.1007/s004399900092. Hum Genet. 1999. PMID: 10480358

3

A highly sensitive, fast, and economical technique for mutation analysis in hereditary breast and ovarian cancers.

Arnold N, Gross E, Schwarz-Boeger U, Pfisterer J, Jonat W, Kiechle M. Arnold N, et al. Among authors: kiechle m. Hum Mutat. 1999;14(4):333-9. doi: 10.1002/(SICI)1098-1004(199910)14:4<333::AID-HUMU9>3.0.CO;2-C. Hum Mutat. 1999. PMID: 10502781

4

Identification of specific BRCA1 and BRCA2 variants by DHPLC.

Gross E, Arnold N, Pfeifer K, Bandick K, Kiechle M. Gross E, et al. Among authors: kiechle m. Hum Mutat. 2000 Oct;16(4):345-53. doi: 10.1002/1098-1004(200010)16:4<345::AID-HUMU7>3.0.CO;2-#. Hum Mutat. 2000. PMID: 11013445

5

Ten novel BRCA1 and BRCA2 mutations in breast and/or ovarian cancer families from northern Germany.

Kiechle M, Gross E, Schwarz-Boeger U, Pfisterer J, Jonat W, Gerber WD, Albacht B, Fischer B, Schlegelberger B, Arnold N. Kiechle M, et al. Hum Mutat. 2000 Dec;16(6):529-30. doi: 10.1002/1098-1004(200012)16:6<529::AID-HUMU14>3.0.CO;2-K. Hum Mutat. 2000. PMID: 11102986

6

Mutation analysis of p53 in ovarian tumors by DHPLC.

Gross E, Kiechle M, Arnold N. Gross E, et al. Among authors: kiechle m. J Biochem Biophys Methods. 2001 Jan 30;47(1-2):73-81. doi: 10.1016/s0165-022x(00)00153-6. J Biochem Biophys Methods. 2001. PMID: 11179763

7

High-throughput genotyping by DHPLC of the dihydropyrimidine dehydrogenase gene implicated in (fluoro)pyrimidine catabolism.

Gross E, Seck K, Neubauer S, Mayr J, Hellebrand H, Ratanaphan A, Lutz V, Stockinger H, Kiechle M. Gross E, et al. Among authors: kiechle m. Int J Oncol. 2003 Feb;22(2):325-32. Int J Oncol. 2003. PMID: 12527930

8

[Mutations in the dihydropyrimidine dehydrogenase gene and their role in 5-fluororuracil intolerance].

Gross E, Seck K, Kiechle M. Gross E, et al. Among authors: kiechle m. Zentralbl Gynakol. 2002 Dec;124(12):574-9. doi: 10.1055/s-2002-40170. Zentralbl Gynakol. 2002. PMID: 12822071 German.

9

Detailed analysis of five mutations in dihydropyrimidine dehydrogenase detected in cancer patients with 5-fluorouracil-related side effects.

Gross E, Ullrich T, Seck K, Mueller V, de Wit M, von Schilling C, Meindl A, Schmitt M, Kiechle M. Gross E, et al. Among authors: kiechle m. Hum Mutat. 2003 Dec;22(6):498. doi: 10.1002/humu.9201. Hum Mutat. 2003. PMID: 14635116

10

[Counselling, genetic testing and prevention in women with hereditary breast- and ovarian cancer. Interdisciplinary recommendations of the consortium "Hereditary Breast- and Ovarian Cancer" of the German Cancer AiD].

Schmutzler R, Schlegelberger B, Meindl A, Gerber WD, Kiechle M; Hereditary Breast- and Ovarian Cancer Consortium, German Cancer AiD. Schmutzler R, et al. Among authors: kiechle m. Zentralbl Gynakol. 2003 Dec;125(12):494-506. doi: 10.1055/s-2003-44815. Zentralbl Gynakol. 2003. PMID: 14755360 German.

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