Cribriform neuroepithelial tumor (CRINET): a nonrhabdoid ventricular tumor with INI1 loss and relatively favorable prognosis. - Wikidata - wikimedia - TriplyDB

Cribriform neuroepithelial tumor (CRINET): a nonrhabdoid ventricular tumor with INI1 loss and relatively favorable prognosis.

Cribriform neuroepithelial tumor (CRINET): a nonrhabdoid ventricular tumor with INI1 loss and relatively favorable prognosis.

http://www.wikidata.org/entity/Q48406841

about

SWI/SNF chromatin remodeling complexes and cancer Atypical teratoid/rhabdoid tumors: challenges and search for solutions Prognostic value of MIB-1, p53, epidermal growth factor receptor, and INI1 in childhood chordomas.Primary atypical teratoid/rhabdoid tumor of central nervous system in children: a clinicopathological analysis and review of literature in China.Cribriform neuroepithelial tumor in the third ventricle: a case report and literature review.Atypical teratoid/rhabdoid tumors-current concepts, advances in biology, and potential future therapies.Molecular diagnostics of CNS embryonal tumors.Intracranial tumors in infants: long-term functional outcome, survival, and its predictors.Loss of INI1 protein expression defines a subgroup of aggressive central nervous system primitive neuroectodermal tumors.Rhabdoid tumors: clinical approaches and molecular targets for innovative therapy.Biology and Treatment of Rhabdoid Tumor.Uncommon pediatric tumors of the posterior fossa: pathologic and molecular features.Co-occurrence of histone H3 K27M and BRAF V600E mutations in paediatric midline grade I ganglioglioma.Cribriform neuroepithelial tumor: molecular characterization of a SMARCB1-deficient non-rhabdoid tumor with favorable long-term outcome.High-Resolution Genomic Analysis of Cribriform Neuroepithelial Tumors of the Central Nervous System.Atypical teratoid rhabdoid tumors of the posterior fossa in children.Cribriform neuroepithelial tumor arising in the lateral ventricle.Atypical teratoid rhabdoid tumors (ATRTs): the British Columbia's Children's Hospital's experience, 1986-2006.Atypical teratoid/rhabdoid tumor with retained INI1 (SMARCB1) expression and loss of BRG1 (SMARCA4).Meningeal SWI/SNF related, matrix-associated, actin-dependent regulator of chromatin, subfamily B member 1 (SMARCB1)-deficient tumours: an emerging group of meningeal tumours.SMARCB1-deficient Tumors of Childhood: A Practical Guide.SNF5 as a prognostic factor in skull base chordoma.Cribriform neuroepithelial tumour: novel clinicopathological, ultrastructural and cytogenetic findings.Development of an Atypical Teratoid Rhabdoid Tumor in a Meningioma.Atypical teratoid rhabdoid tumor mimicking beta-catenin-positive nodular medulloblastoma.Atypical teratoid/rhabdoid tumour in an adult with disseminated mediastinal germ cell tumour Choroid plexus carcinomas are characterized by complex chromosomal alterations related to patient age and prognosis

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P2860

Cribriform neuroepithelial tumor (CRINET): a nonrhabdoid ventricular tumor with INI1 loss and relatively favorable prognosis.

http://www.wikidata.org/entity/Q48406841

description

2009 nî lūn-bûn

@nan

2009年の論文

@ja

2009年学术文章

@wuu

2009年学术文章

@zh

2009年学术文章

@zh-cn

2009年学术文章

@zh-hans

2009年学术文章

@zh-my

2009年学术文章

@zh-sg

2009年學術文章

@yue

2009年學術文章

@zh-hant

name

Cribriform neuroepithelial tum ...... elatively favorable prognosis.

@en

Cribriform neuroepithelial tumor

@nl

type

label

Cribriform neuroepithelial tum ...... elatively favorable prognosis.

@en

Cribriform neuroepithelial tumor

@nl

prefLabel

Cribriform neuroepithelial tum ...... elatively favorable prognosis.

@en

Cribriform neuroepithelial tumor

@nl

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Journal of Neuropathology & Experimental Neurology

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Cribriform neuroepithelial tum ...... elatively favorable prognosis.

@en

P2093

Brigitte Wrede

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Hansjörg Schmid

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Markus Bergmann

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Michael C Frühwald

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Stefan Gesk

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Uwe Kordes

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Werner Paulus

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P2860

Familial anaplastic ependymoma: evidence of loss of chromosome 22 in tumour cells

Genomic analysis using high-density single nucleotide polymorphism-based oligonucleotide arrays and multiplex ligation-dependent probe amplification provides a comprehensive analysis of INI1/SMARCB1 in malignant rhabdoid tumors

The 2007 WHO classification of tumours of the central nervous system

Intensive Multimodality Treatment for Children With Newly Diagnosed CNS Atypical Teratoid Rhabdoid Tumor

An immunohistochemical study of the primitive and maturing elements of human cerebral medulloepitheliomas.

Loss of INI1 expression is characteristic of both conventional and proximal-type epithelioid sarcoma.

The IL-4 and IL-13 pseudomonas exotoxins: new hope for brain tumor therapy.

Long-term survival and transmission of INI1-mutation via nonpenetrant males in a family with rhabdoid tumour predisposition syndrome.

Central nervous system medulloepithelioma: a series of eight cases including two arising in the pons.

Immunohistochemical analysis of INI1 protein in malignant pediatric CNS tumors: Lack of INI1 in atypical teratoid/rhabdoid tumors and in a fraction of primitive neuroectodermal tumors without rhabdoid phenotype.

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12

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68

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Martin Hasselblatt

Reinhard Schneppenheim

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2009-12-01T00:00:00Z

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19915490

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