Characterization of a 3;6 translocation associated with renal cell carcinoma

The most frequent cause of familial clear cell renal cell carcinoma (RCC) is von Hippel–Lindau disease and the VHL tumor suppressor gene (TSG) is inactivated in most sporadic clear cell RCC. Although there is relatively little information on the mechanisms of tumorigenesis of clear cell RCC without...

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Veröffentlicht in:	Genes chromosomes & cancer 2007-04, Vol.46 (4), p.311-317
Hauptverfasser:	Foster, Rebecca E., Abdulrahman, Mahera, Morris, Mark R., Prigmore, Elena, Gribble, Susan, Ng, Beeling, Gentle, Dean, Ready, Steven, Weston, Phil M. T., Wiesener, Michael S., Kishida, Takeshi, Yao, Masahiro, Davison, Val, Barbero, Jose Luis, Chu, Carol, Carter, Nigel P., Latif, Farida, Maher, Eamonn R.
Format:	Artikel
Sprache:	eng
Schlagworte:	Carcinoma, Renal Cell - genetics Cell Line, Transformed Chromosomes, Human, Pair 3 - genetics Chromosomes, Human, Pair 6 - genetics Humans Male Middle Aged Molecular Sequence Data Translocation, Genetic
Online-Zugang:	Volltext
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