Kiechle M - Search Results

1

Polymorphisms in the Janus kinase 2 (JAK)/signal transducer and activator of transcription (STAT) genes: putative association of the STAT gene region with familial breast cancer.

Vaclavicek A, Bermejo JL, Schmutzler RK, Sutter C, Wappenschmidt B, Meindl A, Kiechle M, Arnold N, Weber BH, Niederacher D, Burwinkel B, Bartram CR, Hemminki K, Försti A. Vaclavicek A, et al. Among authors: kiechle m. Endocr Relat Cancer. 2007 Jun;14(2):267-77. doi: 10.1677/ERC-06-0077. Endocr Relat Cancer. 2007. PMID: 17639043

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

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

5

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

6

Breastfeeding and breast cancer risk by age 50 among women in Germany.

Chang-Claude J, Eby N, Kiechle M, Bastert G, Becher H. Chang-Claude J, et al. Among authors: kiechle m. Cancer Causes Control. 2000 Sep;11(8):687-95. doi: 10.1023/a:1008907901087. Cancer Causes Control. 2000. PMID: 11065005

7

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

8

Comparative genomic hybridization detects genetic imbalances in primary ovarian carcinomas as correlated with grade of differentiation.

Kiechle M, Jacobsen A, Schwarz-Boeger U, Hedderich J, Pfisterer J, Arnold N. Kiechle M, et al. Cancer. 2001 Feb 1;91(3):534-40. Cancer. 2001. PMID: 11169935

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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