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 (Q24643365)

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English	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	scientific article

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scholarly article

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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 (English)

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single-nucleotide polymorphism

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based on heuristic

inferred from title

Hakon Hakonarson

4

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author name string

Eric M Jackson

1

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Angela J Sievert

2

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Xiaowu Gai

3

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Alexander R Judkins

5

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Laura Tooke

6

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Juan Carlos Perin

7

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Hongbo Xie

8

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Tamim H Shaikh

9

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Jaclyn A Biegel

10

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language of work or name

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publication date

15 March 2009

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Clinical Cancer Research

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15

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6

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1923-30

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Detailed analysis of 22q11.2 with a high density MLPA probe set

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668138

7 April 2017

Germline mutation of INI1/SMARCB1 in familial schwannomatosis

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668138

7 April 2017

Cluster analysis and display of genome-wide expression patterns

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7 April 2017

The murine SNF5/INI1 chromatin remodeling factor is essential for embryonic development and tumor suppression

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668138

7 April 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668138

7 April 2017

Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668138

7 April 2017

Circular binary segmentation for the analysis of array-based DNA copy number data

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668138

7 April 2017

High-density single nucleotide polymorphism array analysis in patients with germline deletions of 22q11.2 and malignant rhabdoid tumor

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668138

27 September 2017

hSNF5/INI1-deficient tumours and rhabdoid tumours are convergent but not fully overlapping entities

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27 September 2017

Oligonucleotide microarray analysis of genomic imbalance in children with mental retardation

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27 September 2017

High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668138

27 September 2017

Molecular genetics of atypical teratoid/rhabdoid tumor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668138

27 September 2017

Combined genome-wide allelotyping and copy number analysis identify frequent genetic losses without copy number reduction in medulloblastoma

1 reference

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27 September 2017

SMARCB1/INI1 tumor suppressor gene is frequently inactivated in epithelioid sarcomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668138

27 September 2017

An integrated view of copy number and allelic alterations in the cancer genome using single nucleotide polymorphism arrays

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668138

27 September 2017

High-resolution single-nucleotide polymorphism array and clustering analysis of loss of heterozygosity in human lung cancer cell lines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668138

27 September 2017

Implications of human genome architecture for rearrangement-based disorders: the genomic basis of disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668138

27 September 2017

High-resolution analysis of DNA copy number using oligonucleotide microarrays

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668138

27 September 2017

Segmental duplications: an 'expanding' role in genomic instability and disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668138

27 September 2017

The mammalian SWI/SNF complex and the control of cell growth

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668138

27 September 2017

Region-specific detection of neuroblastoma loss of heterozygosity at multiple loci simultaneously using a SNP-based tag-array platform

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668138

30 May 2018

Continuous and widespread roles for the Swi-Snf complex in transcription

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668138

30 May 2018

Monosomy 22 in rhabdoid or atypical tumors of the brain.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668138

30 May 2018

Non-linkage of familial rhabdoid tumors to SMARCB1 implies a second locus for the rhabdoid tumor predisposition syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668138

28 November 2018

Immunohistochemical analysis of hSNF5/INI1 in pediatric CNS neoplasms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668138

28 November 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668138

28 November 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668138

28 November 2018

Renal medullary carcinoma: rhabdoid features and the absence of INI1 expression as markers of aggressive behavior

1 reference

https://pubmed.ncbi.nlm.nih.gov/19276269

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid detection of submicroscopic chromosomal rearrangements in children with multiple congenital anomalies using high density oligonucleotide arrays

1 reference

https://pubmed.ncbi.nlm.nih.gov/19276269

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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