(Q54355228)

28 May 2018

title

Clonal trisomies 7,10 and 12, normal 3p and absence of VHL gene mutation in a clear cell tubulopapillary carcinoma of the kidney. (English)

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28 May 2018

author name string

Alexander Wolfe

1

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28 May 2018

Sheila M Dobin

2

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28 May 2018

Petr Grossmann

3

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28 May 2018

Michal Michal

4

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28 May 2018

Ludvik R Donner

5

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28 May 2018

publication date

7 August 2011

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28 May 2018

published in

Virchows Archiv

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28 May 2018

volume

459

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28 May 2018

issue

4

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28 May 2018

page(s)

457-463

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28 May 2018

https://scigraph.springernature.com/pub.10.1007/s00428-011-1137-3

exact match

0 references

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Inactivation of the von Hippel-Lindau (VHL) tumour suppressor gene and allelic losses at chromosome arm 3p in primary renal cell carcinoma: evidence for a VHL-independent pathway in clear cell renal tumourigenesis

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Spectrum of epithelial neoplasms in end-stage renal disease: an experience from 66 tumor-bearing kidneys with emphasis on histologic patterns distinct from those in sporadic adult renal neoplasia

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Strength of molecular cytogenetic analyses for adjusting the diagnosis of renal cell carcinomas with both clear cells and papillary features: a study of three cases

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Clear-cell papillary renal cell carcinoma: molecular and immunohistochemical analysis with emphasis on the von Hippel-Lindau gene and hypoxia-inducible factor pathway-related proteins.

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Benign renal angiomyoadenomatous tumor: a previously unreported renal tumor

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Renal angiomyoadenomatous tumor: morphologic, immunohistochemical, and molecular genetic study of a distinct entity

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Clear cell papillary renal cell carcinoma and clear cell renal cell carcinoma arising in acquired cystic disease of the kidney: an immunohistochemical and genetic study.

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Clear cell papillary renal cell carcinoma: a distinct histopathologic and molecular genetic entity

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12 December 2020

10.1007/S00428-011-1137-3

Identifiers

DOI

1 reference

28 May 2018

1 reference

28 May 2018