Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3

M Martin, L Maßhöfer, P Temming, S Rahmann… - Nature …, 2013 - nature.com
Gene expression profiles and chromosome 3 copy number divide uveal melanomas into two
distinct classes correlating with prognosis,,. Using exome sequencing, we identified …

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

F Tschentscher, J Hüsing, T Hölter, E Kruse… - Cancer research, 2003 - AACR
Uveal melanoma is the most common intraocular malignancy. About 50% of patients die of
metastases, which almost exclusively originate from primary tumors that have lost one …

Methylation and silencing of the retinoic acid receptor-β2 gene in breast cancer

M Widschwendter, J Berger, M Hermann… - Journal of the …, 2000 - academic.oup.com
Background: A growing body of evidence supports the hypotheses that the retinoic acid
receptor β2 (RAR-β2) gene is a tumor suppressor gene and that the chemopreventive …

A comprehensive molecular study on Coffin–Siris and Nicolaides–Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered …

D Wieczorek, N Bögershausen… - Human molecular …, 2013 - academic.oup.com
Chromatin remodeling complexes are known to modify chemical marks on histones or to
induce conformational changes in the chromatin in order to regulate transcription. De novo …

[HTML][HTML] Acquired IFNγ resistance impairs anti-tumor immunity and gives rise to T-cell-resistant melanoma lesions

A Sucker, F Zhao, N Pieper, C Heeke… - Nature …, 2017 - nature.com
Melanoma treatment has been revolutionized by antibody-based immunotherapies. IFNγ
secretion by CD8+ T cells is critical for therapy efficacy having anti-proliferative and pro …

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

M Zeschnigk, C Lich, K Buiting, W Doerfler… - European Journal of …, 1997 - karger.com
The analysis of allelic methylation differences in 15ql 1-ql 3 has been established as a valid
test for the Angelman and Prader-Willi syndromes. Current tests use methylation-sensitive …

[HTML][HTML] The interdisciplinary diagnosis and treatment of intraocular tumors

N Bornfeld, E Biewald, S Bauer… - Deutsches Ärzteblatt …, 2018 - ncbi.nlm.nih.gov
Background Recent years have seen major changes in the diagnosis and treatment of solid
intraocular tumors, mainly owing to an improved molecular biological understanding of their …

Comparing the prognostic value of BAP1 mutation pattern, chromosome 3 status, and BAP1 immunohistochemistry in uveal melanoma

JAP van de Nes, J Nelles, S Kreis… - The American journal …, 2016 - journals.lww.com
Uveal melanoma (UM), a tumor of the eye, can be divided into 2 major classes correlating
with patients' prognosis. Gene expression profiles and chromosome 3 status are correlated …

A novel real-time PCR assay for quantitative analysis of methylated alleles (QAMA): analysis of the retinoblastoma locus

M Zeschnigk, S Böhringer, EA Price… - Nucleic acids …, 2004 - academic.oup.com
Altered methylation patterns have been found to play a role in developmental disorders,
cancer and aging. Increasingly, changes in DNA methylation are used as molecular markers …

Involvement of M-cadherin in terminal differentiation of skeletal muscle cells

M Zeschnigk, D Kozian, C Kuch… - Journal of cell …, 1995 - journals.biologists.com
Cadherins are a gene family encoding calcium-dependent cell adhesion proteins which are
thought to act in the establishment and maintenance of tissue organization. M-cadherin, one …