Zeschnigk M - Search Results

1

Comprehensive methylation analysis in typical and atypical PWS and AS patients with normal biparental chromosomes 15.

Runte M, Färber C, Lich C, Zeschnigk M, Buchholz T, Smith A, Van Maldergem L, Bürger J, Muscatelli F, Gillessen-Kaesbach G, Horsthemke B, Buiting K. Runte M, et al. Among authors: zeschnigk m. Eur J Hum Genet. 2001 Jul;9(7):519-26. doi: 10.1038/sj.ejhg.5200661. Eur J Hum Genet. 2001. PMID: 11464243

2

Imprinted segments in the human genome: different DNA methylation patterns in the Prader-Willi/Angelman syndrome region as determined by the genomic sequencing method.

Zeschnigk M, Schmitz B, Dittrich B, Buiting K, Horsthemke B, Doerfler W. Zeschnigk M, et al. Hum Mol Genet. 1997 Mar;6(3):387-95. doi: 10.1093/hmg/6.3.387. Hum Mol Genet. 1997. PMID: 9147641

3

A single-tube PCR test for the diagnosis of Angelman and Prader-Willi syndrome based on allelic methylation differences at the SNRPN locus.

Zeschnigk M, Lich C, Buiting K, Doerfler W, Horsthemke B. Zeschnigk M, et al. Eur J Hum Genet. 1997 Mar-Apr;5(2):94-8. Eur J Hum Genet. 1997. PMID: 9195159

4

Methylation analysis of the PWS/AS region does not support an enhancer-competition model.

Schumacher A, Buiting K, Zeschnigk M, Doerfler W, Horsthemke B. Schumacher A, et al. Among authors: zeschnigk m. Nat Genet. 1998 Aug;19(4):324-5. doi: 10.1038/1211. Nat Genet. 1998. PMID: 9697691 No abstract available.

5

Detection of homozygous deletions in tumors by hybridization of representational difference analysis (RDA) products to chromosome-specific YAC clone arrays.

Zeschnigk M, Horsthemke B, Lohmann D. Zeschnigk M, et al. Nucleic Acids Res. 1999 Nov 1;27(21):e30. doi: 10.1093/nar/27.21.e30. Nucleic Acids Res. 1999. PMID: 10518625 Free PMC article.

6

A PCR test for the detection of hypermethylated alleles at the retinoblastoma locus.

Zeschnigk M, Lohmann D, Horsthemke B. Zeschnigk M, et al. J Med Genet. 1999 Oct;36(10):793-4. doi: 10.1136/jmg.36.10.793. J Med Genet. 1999. PMID: 10528863 Free PMC article. No abstract available.

7

Identification of chromosomes 3, 6, and 8 aberrations in uveal melanoma by microsatellite analysis in comparison to comparative genomic hybridization.

Tschentscher F, Prescher G, Zeschnigk M, Horsthemke B, Lohmann DR. Tschentscher F, et al. Among authors: zeschnigk m. Cancer Genet Cytogenet. 2000 Oct 1;122(1):13-7. doi: 10.1016/s0165-4608(00)00266-1. Cancer Genet Cytogenet. 2000. PMID: 11104026

8

Partial deletions of the long and short arm of chromosome 3 point to two tumor suppressor genes in uveal melanoma.

Tschentscher F, Prescher G, Horsman DE, White VA, Rieder H, Anastassiou G, Schilling H, Bornfeld N, Bartz-Schmidt KU, Horsthemke B, Lohmann DR, Zeschnigk M. Tschentscher F, et al. Among authors: zeschnigk m. Cancer Res. 2001 Apr 15;61(8):3439-42. Cancer Res. 2001. PMID: 11309305

9

Tumor classification based on gene expression profiling shows that uveal melanomas with and without monosomy 3 represent two distinct entities.

Tschentscher F, Hüsing J, Hölter T, Kruse E, Dresen IG, Jöckel KH, Anastassiou G, Schilling H, Bornfeld N, Horsthemke B, Lohmann DR, Zeschnigk M. Tschentscher F, et al. Among authors: zeschnigk m. Cancer Res. 2003 May 15;63(10):2578-84. Cancer Res. 2003. PMID: 12750282

10

Somatic mosaicism in patients with Angelman syndrome and an imprinting defect.

Nazlican H, Zeschnigk M, Claussen U, Michel S, Boehringer S, Gillessen-Kaesbach G, Buiting K, Horsthemke B. Nazlican H, et al. Among authors: zeschnigk m. Hum Mol Genet. 2004 Nov 1;13(21):2547-55. doi: 10.1093/hmg/ddh296. Epub 2004 Sep 22. Hum Mol Genet. 2004. PMID: 15385437

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