Schoell B - Search Results

1

Comparison of genomic abnormalities between BRCAX and sporadic breast cancers studied by comparative genomic hybridization.

Gronwald J, Jauch A, Cybulski C, Schoell B, Böhm-Steuer B, Lener M, Grabowska E, Górski B, Jakubowska A, Domagała W, Chosia M, Scott RJ, Lubiński J. Gronwald J, et al. Among authors: schoell b. Int J Cancer. 2005 Mar 20;114(2):230-6. doi: 10.1002/ijc.20723. Int J Cancer. 2005. PMID: 15540206

2

Comparative genomic hybridization in childhood acute lymphoblastic leukemia: correlation with interphase cytogenetics and loss of heterozygosity analysis.

Scholz I, Popp S, Granzow M, Schoell B, Holtgreve-Grez H, Takeuchi S, Schrappe M, Harbott J, Teigler-Schlegel A, Zimmermann M, Fischer C, Koeffler HP, Bartram CR, Jauch A. Scholz I, et al. Among authors: schoell b. Cancer Genet Cytogenet. 2001 Jan 15;124(2):89-97. doi: 10.1016/s0165-4608(00)00330-7. Cancer Genet Cytogenet. 2001. PMID: 11172898

3

Isochromosome 1q as an early genetic event in a child with intracranial ependymoma characterized by molecular cytogenetics.

Granzow M, Popp S, Weber S, Schoell B, Holtgreve-Grez H, Senf L, Hager D, Boschert J, Scheurlen W, Jauch A. Granzow M, et al. Among authors: schoell b. Cancer Genet Cytogenet. 2001 Oct 1;130(1):79-83. doi: 10.1016/s0165-4608(01)00465-4. Cancer Genet Cytogenet. 2001. PMID: 11672779

4

Study of 30 patients with unexplained developmental delay and dysmorphic features or congenital abnormalities using conventional cytogenetics and multiplex FISH telomere (M-TEL) integrity assay.

Popp S, Schulze B, Granzow M, Keller M, Holtgreve-Grez H, Schoell B, Brough M, Hager HD, Tariverdian G, Brown J, Kearney L, Jauch A. Popp S, et al. Among authors: schoell b. Hum Genet. 2002 Jul;111(1):31-9. doi: 10.1007/s00439-002-0739-x. Epub 2002 Jun 13. Hum Genet. 2002. PMID: 12136233

5

Multicolor karyotype analyses of mouse embryonic stem cells.

Guo J, Jauch A, Heidi HG, Schoell B, Erz D, Schrank M, Janssen JW. Guo J, et al. Among authors: schoell b. In Vitro Cell Dev Biol Anim. 2005 Sep-Oct;41(8-9):278-83. doi: 10.1290/990771.1. In Vitro Cell Dev Biol Anim. 2005. PMID: 16409114

6

Specific loss of chromosomes 1, 2, 6, 10, 13, 17, and 21 in chromophobe renal cell carcinomas revealed by comparative genomic hybridization.

Speicher MR, Schoell B, du Manoir S, Schröck E, Ried T, Cremer T, Störkel S, Kovacs A, Kovacs G. Speicher MR, et al. Among authors: schoell b. Am J Pathol. 1994 Aug;145(2):356-64. Am J Pathol. 1994. PMID: 7519827 Free PMC article.

7

Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31.

Williamson C, Cavaco BM, Jauch A, Dixon PH, Forbes S, Harding B, Holtgreve-Grez H, Schoell B, Pereira MC, Font AP, Loureiro MM, Sobrinho LG, Santos MA, Thakker RV. Williamson C, et al. Among authors: schoell b. J Bone Miner Res. 1999 Feb;14(2):230-9. doi: 10.1359/jbmr.1999.14.2.230. J Bone Miner Res. 1999. PMID: 9933477 Free article.

8

Multiplex FISH telomere integrity assay identifies an unbalanced cryptic translocation der(5)t(3;5)(q27;p15.3) in a family with three mentally retarded individuals.

Granzow M, Popp S, Keller M, Holtgreve-Grez H, Brough M, Schoell B, Rauterberg-Ruland I, Hager HD, Tariverdian G, Jauch A. Granzow M, et al. Among authors: schoell b. Hum Genet. 2000 Jul;107(1):51-7. doi: 10.1007/s004390000321. Hum Genet. 2000. PMID: 10982035

9

High resistance to X-rays and therapeutic carbon ions in glioblastoma cells bearing dysfunctional ATM associates with intrinsic chromosomal instability.

Dokic I, Mairani A, Brons S, Schoell B, Jauch A, Krunic D, Debus J, Régnier-Vigouroux A, Weber KJ. Dokic I, et al. Among authors: schoell b. Int J Radiat Biol. 2015 Feb;91(2):157-65. doi: 10.3109/09553002.2014.937511. Epub 2014 Sep 8. Int J Radiat Biol. 2015. PMID: 24991884

10

Molecular cytogenetic analysis of formalin-fixed, paraffin-embedded solid tumors by comparative genomic hybridization after universal DNA-amplification.

Speicher MR, du Manoir S, Schröck E, Holtgreve-Grez H, Schoell B, Lengauer C, Cremer T, Ried T. Speicher MR, et al. Among authors: schoell b. Hum Mol Genet. 1993 Nov;2(11):1907-14. doi: 10.1093/hmg/2.11.1907. Hum Mol Genet. 1993. PMID: 8281155

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