INI1 expression is retained in composite rhabdoid tumors, including rhabdoid meningiomas (Q28239308)

ORCID Public Data File 2021

Louis P. Dehner

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object named as

Louis P Dehner

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author name string

Christine E Fuller

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Alexander R Judkins

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Jaclyn A Biegel

Histopathology and prognosis of Wilms tumorResults from the first national wilms' tumor study

5

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language of work or name

English

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publication date

July 2005

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published in

Modern Pathology

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volume

18

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issue

7

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page(s)

951-8

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cites work

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Constitutional mutations of the hSNF5/INI1 gene predispose to a variety of cancers

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No evidence for hypermethylation of the hSNF5/INI1 promoter in pediatric rhabdoid tumors

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Rhabdoid transformation of tumor cells in meningiomas: a histologic indication of increased proliferative activity: report of four cases.

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"Rhabdoid" meningioma: an aggressive variant

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Lung carcinoma with rhabdoid cells: a clinicopathological study and survival analysis of 14 cases

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The tumor suppressor hSNF5/INI1 modulates cell growth and actin cytoskeleton organization

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