Arnold N - Search Results

1

SNPs in ultraconserved elements and familial breast cancer risk.

Yang R, Frank B, Hemminki K, Bartram CR, Wappenschmidt B, Sutter C, Kiechle M, Bugert P, Schmutzler RK, Arnold N, Weber BH, Niederacher D, Meindl A, Burwinkel B. Yang R, et al. Among authors: arnold n. Carcinogenesis. 2008 Feb;29(2):351-5. doi: 10.1093/carcin/bgm290. Epub 2008 Jan 3. Carcinogenesis. 2008. PMID: 18174240

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: arnold n. 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. 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

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

Weimer J, Kiechle M, Arnold N. Weimer J, et al. Among authors: arnold n. 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: arnold n. 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

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: arnold n. Cancer Genet Cytogenet. 2000 Oct 1;122(1):7-12. doi: 10.1016/s0165-4608(00)00263-6. Cancer Genet Cytogenet. 2000. PMID: 11104025

7

Mutation analysis of p53 in ovarian tumors by DHPLC.

Gross E, Kiechle M, Arnold N. Gross E, et al. Among authors: arnold n. 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

8

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: arnold n. 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.

9

Limited relevance of the CHEK2 gene in hereditary breast cancer.

Dufault MR, Betz B, Wappenschmidt B, Hofmann W, Bandick K, Golla A, Pietschmann A, Nestle-Krämling C, Rhiem K, Hüttner C, von Lindern C, Dall P, Kiechle M, Untch M, Jonat W, Meindl A, Scherneck S, Niederacher D, Schmutzler RK, Arnold N. Dufault MR, et al. Among authors: arnold n. Int J Cancer. 2004 Jun 20;110(3):320-5. doi: 10.1002/ijc.20073. Int J Cancer. 2004. PMID: 15095295

10

Large BRCA1 gene deletions are found in 3% of German high-risk breast cancer families.

Hartmann C, John AL, Klaes R, Hofmann W, Bielen R, Koehler R, Janssen B, Bartram CR, Arnold N, Zschocke J. Hartmann C, et al. Among authors: arnold n. Hum Mutat. 2004 Dec;24(6):534. doi: 10.1002/humu.9291. Hum Mutat. 2004. PMID: 15532023

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