Arnold N - Search Results

1

Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression.

Darabi H, McCue K, Beesley J, Michailidou K, Nord S, Kar S, Humphreys K, Thompson D, Ghoussaini M, Bolla MK, Dennis J, Wang Q, Canisius S, Scott CG, Apicella C, Hopper JL, Southey MC, Stone J, Broeks A, Schmidt MK, Scott RJ, Lophatananon A, Muir K, Beckmann MW, Ekici AB, Fasching PA, Heusinger K, Dos-Santos-Silva I, Peto J, Tomlinson I, Sawyer EJ, Burwinkel B, Marme F, Guénel P, Truong T, Bojesen SE, Flyger H, Benitez J, González-Neira A, Anton-Culver H, Neuhausen SL, Arndt V, Brenner H, Engel C, Meindl A, Schmutzler RK; German Consortium of Hereditary Breast and Ovarian Cancer; Arnold N, Brauch H, Hamann U, Chang-Claude J, Khan S, Nevanlinna H, Ito H, Matsuo K, Bogdanova NV, Dörk T, Lindblom A, Margolin S; kConFab/AOCS Investigators; Kosma VM, Mannermaa A, Tseng CC, Wu AH, Floris G, Lambrechts D, Rudolph A, Peterlongo P, Radice P, Couch FJ, Vachon C, Giles GG, McLean C, Milne RL, Dugué PA, Haiman CA, Maskarinec G, Woolcott C, Henderson BE, Goldberg MS, Simard J, Teo SH, Mariapun S, Helland Å, Haakensen V, Zheng W, Beeghly-Fadiel A, Tamimi R, Jukkola-Vuorinen A, Winqvist R, Andrulis IL, Knight JA, Devilee P, Tollenaar RA, Figueroa J, García-Closas M, Czene K, Hooning MJ, Ti… See abstract for full author list ➔ Darabi H, et al. Among authors: arnold n. Am J Hum Genet. 2015 Jul 2;97(1):22-34. doi: 10.1016/j.ajhg.2015.05.002. Epub 2015 Jun 11. Am J Hum Genet. 2015. PMID: 26073781 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: arnold n. Hum Genet. 1999 Jul-Aug;105(1-2):72-8. doi: 10.1007/s004399900092. Hum Genet. 1999. PMID: 10480358

3

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 Free article.

4

A network of clinically and functionally relevant genes is involved in the reversion of the tumorigenic phenotype of MDA-MB-231 breast cancer cells after transfer of human chromosome 8.

Seitz S, Frege R, Jacobsen A, Weimer J, Arnold W, von Haefen C, Niederacher D, Schmutzler R, Arnold N, Scherneck S. Seitz S, et al. Among authors: arnold n, arnold w. Oncogene. 2005 Jan 27;24(5):869-79. doi: 10.1038/sj.onc.1208260. Oncogene. 2005. PMID: 15580292

5

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: arnold n. Carcinogenesis. 2006 Aug;27(8):1655-60. doi: 10.1093/carcin/bgi374. Epub 2006 Feb 25. Carcinogenesis. 2006. PMID: 16501249 Clinical Trial.

6

Genetic background of different cancer cell lines influences the gene set involved in chromosome 8 mediated breast tumor suppression.

Seitz S, Korsching E, Weimer J, Jacobsen A, Arnold N, Meindl A, Arnold W, Gustavus D, Klebig C, Petersen I, Scherneck S. Seitz S, et al. Among authors: arnold n, arnold w. Genes Chromosomes Cancer. 2006 Jun;45(6):612-27. doi: 10.1002/gcc.20325. Genes Chromosomes Cancer. 2006. PMID: 16552773

7

Associations of genetic variants in the estrogen receptor coactivators PPARGC1A, PPARGC1B and EP300 with familial breast cancer.

Wirtenberger M, Tchatchou S, Hemminki K, Schmutzhard J, Sutter C, Schmutzler RK, Meindl A, Wappenschmidt B, Kiechle M, Arnold N, Weber BH, Niederacher D, Bartram CR, Burwinkel B. Wirtenberger M, et al. Among authors: arnold n. Carcinogenesis. 2006 Nov;27(11):2201-8. doi: 10.1093/carcin/bgl067. Epub 2006 May 15. Carcinogenesis. 2006. PMID: 16704985

8

The functional genetic variant Ile646Val located in the kinase binding domain of the A-kinase anchoring protein 10 is associated with familial breast cancer.

Wirtenberger M, Schmutzhard J, Hemminki K, Meindl A, Sutter C, Schmutzler RK, Wappenschmidt B, Kiechle M, Arnold N, Weber BH, Niederacher D, Bartram CR, Burwinkel B. Wirtenberger M, et al. Among authors: arnold n. Carcinogenesis. 2007 Feb;28(2):423-6. doi: 10.1093/carcin/bgl164. Epub 2006 Sep 6. Carcinogenesis. 2007. PMID: 16956908

9

Allelic loss analysis by denaturing high-performance liquid chromatography and electrospray ionization mass spectrometry.

Gross E, Hölzl G, Arnold N, Hauenstein E, Jacobsen A, Schulze K, Ramser J, Meindl A, Kiechle M, Oefner PJ. Gross E, et al. Among authors: arnold n. Hum Mutat. 2007 Mar;28(3):303-11. doi: 10.1002/humu.20439. Hum Mutat. 2007. PMID: 17109391

10

Comparison of gene expression data from human and mouse breast cancers: identification of a conserved breast tumor gene set.

Klein A, Wessel R, Graessmann M, Jürgens M, Petersen I, Schmutzler R, Niederacher D, Arnold N, Meindl A, Scherneck S, Seitz S, Graessmann A. Klein A, et al. Among authors: arnold n. Int J Cancer. 2007 Aug 1;121(3):683-8. doi: 10.1002/ijc.22630. Int J Cancer. 2007. PMID: 17410534 Free article.

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