Unique Patterns of Allelic Imbalance Distinguish Type 1 from Type 2 Sporadic Papillary Renal Cell Carcinoma
- 1 September 2002
- journal article
- Published by Elsevier in The American Journal of Pathology
- Vol. 161 (3) , 997-1005
- https://doi.org/10.1016/s0002-9440(10)64260-5
Abstract
No abstract availableKeywords
This publication has 50 references indexed in Scilit:
- Translocation (X;1) Associated with a Nonpapillary Carcinoma in a Young Woman: A New Definition for an Xp11.2 RCC SubtypeCancer Genetics and Cytogenetics, 1999
- Gene structure of the human MET proto-oncogeneOncogene, 1997
- The t(X;1)(p11.2;q21.2) translocation in papillary renal cell carcinoma fuses a novel gene PRCC to the TFE3 transcription factor geneHuman Molecular Genetics, 1996
- Papillary Renal Cell CarcinomaDiagnostic Molecular Pathology, 1996
- Chromosome imbalances in papillary renal cell carcinoma and first cytogenetic data of familial cases analyzed by comparative genomic hybridizationCytogenetic and Genome Research, 1996
- Distinct Xp11.2 breakpoints in two renal cell carcinomas exhibiting X;autosome translocationsGenes, Chromosomes and Cancer, 1995
- Contribution of Chromosome 9p21-22 Deletion to the Progression of Human Renal Cell CarcinomaJapanese Journal of Cancer Research, 1995
- Mapping the X chromosome breakpoint in two papillary renal cell carcinoma cell lines with a t(X;1)(p11.2;q21.2)and the first report of a female caseCytogenetic and Genome Research, 1995
- Mutations of the VHL tumour suppressor gene in renal carcinomaNature Genetics, 1994
- PCR-Based RFLP Screening of the Commonly Deleted 3p Loci in Renal Cortical NeoplasmsDiagnostic Molecular Pathology, 1993