Kiechle M - Search Results

1

Interaction of Werner and Bloom syndrome genes with p53 in familial breast cancer.

Wirtenberger M, Frank B, Hemminki K, Klaes R, Schmutzler RK, Wappenschmidt B, Meindl A, Kiechle M, Arnold N, Weber BH, Niederacher D, Bartram CR, Burwinkel B. Wirtenberger M, et al. Among authors: kiechle m. Carcinogenesis. 2006 Aug;27(8):1655-60. doi: 10.1093/carcin/bgi374. Epub 2006 Feb 25. Carcinogenesis. 2006. PMID: 16501249 Clinical Trial.

2

[Clinical counseling and care of women with genetic predisposition to breast and ovarian carcinoma].

Schmutzler RK, Kempe A, Kiechle M, Beckmann MW. Schmutzler RK, et al. Among authors: kiechle m. Dtsch Med Wochenschr. 1999 May 7;124(18):563-6. doi: 10.1055/s-2007-1024360. Dtsch Med Wochenschr. 1999. PMID: 10356583 Review. German. No abstract available.

3

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

4

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

5

FISH-microdissection (FISH-MD) analysis of complex chromosome rearrangements.

Weimer J, Kiechle M, Arnold N. Weimer J, et al. Among authors: kiechle m. Cytogenet Cell Genet. 2000;88(1-2):114-8. doi: 10.1159/000015502. Cytogenet Cell Genet. 2000. PMID: 10773683

6

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

7

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

8

Comparison of comparative genomic hybridization and interphase fluorescence in situ hybridization in ovarian carcinomas: possibilities and limitations of both techniques.

Jacobsen A, Arnold N, Weimer J, Kiechle M. Jacobsen A, et al. Among authors: kiechle m. Cancer Genet Cytogenet. 2000 Oct 1;122(1):7-12. doi: 10.1016/s0165-4608(00)00263-6. Cancer Genet Cytogenet. 2000. PMID: 11104025

9

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

10

Coincident PTCH and BRCA1 germline mutations in a patient with nevoid basal cell carcinoma syndrome and familial breast cancer.

Reifenberger J, Arnold N, Kiechle M, Reifenberger G, Hauschild A. Reifenberger J, et al. Among authors: kiechle m. J Invest Dermatol. 2001 Mar;116(3):472-4. doi: 10.1046/j.1523-1747.2001.01279-2.x. J Invest Dermatol. 2001. PMID: 11231326 Free article. No abstract available.

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