(Q35189235)

English

Molecular analysis of the rhabdoid predisposition syndrome in a child: a novel germline hSNF5/INI1 mutation and absence of c-myc amplification

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Molecular analysis of the rhabdoid predisposition syndrome in a child: a novel germline hSNF5/INI1 mutation and absence of c-myc amplification (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

author name string

Hironori Fujisawa

1

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Yasushi Takabatake

2

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Toshio Fukusato

3

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Osamu Tachibana

4

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Yoshitake Tsuchiya

5

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Junkoh Yamashita

6

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

publication date

1 July 2003

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Journal of Neuro-Oncology

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

63

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

257-262

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Germline INI1 mutation in a patient with a central nervous system atypical teratoid tumor and renal rhabdoid tumor

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Choroid plexus carcinomas and rhabdoid tumors: phenotypic and genotypic overlap

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spectrum of hSNF5/INI1 somatic mutations in human cancer and genotype-phenotype correlations

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The association of embryonal tumors originating in the kidney and in the brain. A report of seven cases.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rhabdoid tumor of the kidney with primitive neuroectodermal tumor of the central nervous system: associated tumors with different histologic, cytogenetic, and molecular findings

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aberrations of the hSNF5/INI1 gene are restricted to malignant rhabdoid tumors or atypical teratoid/rhabdoid tumors in pediatric solid tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alterations of the hSNF5/INI1 gene in central nervous system atypical teratoid/rhabdoid tumors and renal and extrarenal rhabdoid tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rhabdoid tumor of kidney. A report of 111 cases from the National Wilms' Tumor Study Pathology Center

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations of the INI1 rhabdoid tumor suppressor gene in medulloblastomas and primitive neuroectodermal tumors of the central nervous system.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human SWI/SNF interconverts a nucleosome between its base state and a stable remodeled state

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Amplification of the c-myc gene in human medulloblastoma cell lines and xenografts

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Central nervous system atypical teratoid/rhabdoid tumors of infancy and childhood: definition of an entity

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

C-MYC expression in medulloblastoma and its prognostic value.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular analysis of childhood primitive neuroectodermal tumors defines markers associated with poor outcome

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Extraneural metastasis in a child with atypical teratoid rhabdoid tumor of the central nervous system

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

"Large cell/anaplastic" medulloblastomas: a Pediatric Oncology Group Study.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Indications for a tumor suppressor gene at 22q11 involved in the pathogenesis of ependymal tumors and distinct from hSNF5/INI1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A role for fluorescence in situ hybridization detection of chromosome 22q dosage in distinguishing atypical teratoid/rhabdoid tumors from medulloblastoma/central primitive neuroectodermal tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations of the hSNF5/INI1 Gene in Renal Rhabdoid Tumors With Second Primary Brain Tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

c-MYC interacts with INI1/hSNF5 and requires the SWI/SNF complex for transactivation function

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial posterior fossa brain tumors of infancy secondary to germline mutation of the hSNF5 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Large cell/anaplastic medulloblastomas and medullomyoblastomas: clinicopathological and genetic features.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Newly Established Uterine Cervical Carcinoma Cell Line with Co-amplification of Human Papillomavirus DNA and c-myc Gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germ-line and acquired mutations of INI1 in atypical teratoid and rhabdoid tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human medulloblastomas lack point mutations and homozygous deletions of the hSNF5/INI1 tumour suppressor gene.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic differences between neurocytoma and dysembryoplastic neuroepithelial tumor and oligodendroglial tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Acquisition of the glioblastoma phenotype during astrocytoma progression is associated with loss of heterozygosity on 10q25-qter

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutational analysis of INI1 in sporadic human brain tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Amplification of c-myc in hepatocellular carcinoma: correlation with clinicopathologic features, proliferative activity and p53 overexpression

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1023/A:1024345221792

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

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