Cargando…
Molecular topography of the MED12-deleted region in smooth muscle tumors: a possible link between non-B DNA structures and hypermutability
BACKGROUND: Deletions of the gene encoding mediator subcomplex 12 (MED12) in human smooth muscle tumors rank among the most frequent genomic alterations in human tumors at all. In a minority of these cases, small deletions are found. In an attempt to delineate key features of the deletions aimed at...
Autores principales: | Markowski, Dominique Nadine, Nimzyk, Rolf, Belge, Gazanfer, Löning, Thomas, Helmke, Burkhard Maria, Bullerdiek, Jörn |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3712005/ https://www.ncbi.nlm.nih.gov/pubmed/23738817 http://dx.doi.org/10.1186/1755-8166-6-23 |
Ejemplares similares
-
Cytogenetically normal uterine leiomyomas without MED12-mutations – a source to identify unknown mechanisms of the development of uterine smooth muscle tumors
por: Holzmann, Carsten, et al.
Publicado: (2014) -
HMGA2 expression distinguishes between different types of postpubertal testicular germ cell tumour
por: Kloth, Lars, et al.
Publicado: (2015) -
Correlated Expression of HMGA2 and PLAG1 in Thyroid Tumors, Uterine Leiomyomas and Experimental Models
por: Klemke, Markus, et al.
Publicado: (2014) -
Fibroid explants reveal a higher sensitivity against MDM2-inhibitor nutlin-3 than matching myometrium
por: Markowski, Dominique N, et al.
Publicado: (2012) -
Genome-wide acquired uniparental disomy as well as chromosomal gains and losses in an uterine epithelioid leiomyoma
por: Holzmann, Carsten, et al.
Publicado: (2014)