Schrock E - Search Results

1

Spectral karyotyping of human, mouse, rat and ape chromosomes--applications for genetic diagnostics and research.

Schrock E, Zschieschang P, O'Brien P, Helmrich A, Hardt T, Matthaei A, Stout-Weider K. Schrock E, et al. Cytogenet Genome Res. 2006;114(3-4):199-221. doi: 10.1159/000094203. Cytogenet Genome Res. 2006. PMID: 16954656 Review.

2

Spectral karyotyping, a 24-colour FISH technique for the identification of chromosomal rearrangements.

Macville M, Veldman T, Padilla-Nash H, Wangsa D, O'Brien P, Schröck E, Ried T. Macville M, et al. Among authors: schrock e. Histochem Cell Biol. 1997 Oct-Nov;108(4-5):299-305. doi: 10.1007/s004180050169. Histochem Cell Biol. 1997. PMID: 9387921

3

Spectral karyotyping refines cytogenetic diagnostics of constitutional chromosomal abnormalities.

Schröck E, Veldman T, Padilla-Nash H, Ning Y, Spurbeck J, Jalal S, Shaffer LG, Papenhausen P, Kozma C, Phelan MC, Kjeldsen E, Schonberg SA, O'Brien P, Biesecker L, du Manoir S, Ried T. Schröck E, et al. Hum Genet. 1997 Dec;101(3):255-62. doi: 10.1007/s004390050626. Hum Genet. 1997. PMID: 9439652

4

High-resolution analysis of chromosomal imbalances using the Affymetrix 10K SNP genotyping chip.

Herr A, Grützmann R, Matthaei A, Artelt J, Schröck E, Rump A, Pilarsky C. Herr A, et al. Among authors: schrock e. Genomics. 2005 Mar;85(3):392-400. doi: 10.1016/j.ygeno.2004.07.015. Genomics. 2005. PMID: 15718106

5

Recurrent chromosomal aberrations in INK4a/ARF defective primary lymphomas predict drug responses in vivo.

Helmrich A, Lee S, O'Brien P, Dörken B, Lowe SW, Schröck E, Schmitt CA. Helmrich A, et al. Among authors: schrock e. Oncogene. 2005 Jun 16;24(26):4174-82. doi: 10.1038/sj.onc.1208600. Oncogene. 2005. PMID: 15824738

6

An inversion involving the mouse Shh locus results in brachydactyly through dysregulation of Shh expression.

Niedermaier M, Schwabe GC, Fees S, Helmrich A, Brieske N, Seemann P, Hecht J, Seitz V, Stricker S, Leschik G, Schrock E, Selby PB, Mundlos S. Niedermaier M, et al. Among authors: schrock e. J Clin Invest. 2005 Apr;115(4):900-9. doi: 10.1172/JCI23675. J Clin Invest. 2005. PMID: 15841179 Free PMC article.

7

Small reciprocal insertion detected by spectral karyotyping (SKY) and delimited by array-CGH analysis.

Matthaei A, Werner W, Gerlach EM, Koerner U, Tinschert S, Nitz I, Herr A, Rump A, Bartsch O, Hinkel KG, Schrock E, Oexle K. Matthaei A, et al. Among authors: schrock e. Eur J Med Genet. 2005 Jul-Sep;48(3):328-38. doi: 10.1016/j.ejmg.2005.04.024. Eur J Med Genet. 2005. PMID: 16179228

8

Common fragile sites are conserved features of human and mouse chromosomes and relate to large active genes.

Helmrich A, Stout-Weider K, Hermann K, Schrock E, Heiden T. Helmrich A, et al. Among authors: schrock e. Genome Res. 2006 Oct;16(10):1222-30. doi: 10.1101/gr.5335506. Epub 2006 Sep 5. Genome Res. 2006. PMID: 16954539 Free PMC article.

9

Identification of the human/mouse syntenic common fragile site FRA7K/Fra12C1--relation of FRA7K and other human common fragile sites on chromosome 7 to evolutionary breakpoints.

Helmrich A, Stout-Weider K, Matthaei A, Hermann K, Heiden T, Schrock E. Helmrich A, et al. Among authors: schrock e. Int J Cancer. 2007 Jan 1;120(1):48-54. doi: 10.1002/ijc.22049. Int J Cancer. 2007. PMID: 17039484

10

Telomere dysfunction and DNA-PKcs deficiency: characterization and consequence.

Williams ES, Klingler R, Ponnaiya B, Hardt T, Schrock E, Lees-Miller SP, Meek K, Ullrich RL, Bailey SM. Williams ES, et al. Among authors: schrock e. Cancer Res. 2009 Mar 1;69(5):2100-7. doi: 10.1158/0008-5472.CAN-08-2854. Epub 2009 Feb 24. Cancer Res. 2009. PMID: 19244120 Free PMC article.

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