Isochromosome breakpoints on 17p in medulloblastoma are flanked by different classes of DNA sequence repeats (Q29037387)

27 March 2017

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10

Bernhard Radlwimmer

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Andreas Hochhaus

object named as

Andreas Hochhaus

7

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Claudia Schoch

8

object named as

Claudia Schoch

1 reference

27 March 2017

9

Peter Lichter

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27 March 2017

2

Andrey Korshunov

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27 March 2017

author name string

Frank Mendrzyk

1

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27 March 2017

Grischa Toedt

3

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27 March 2017

Frank Schwarz

4

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27 March 2017

Bernhard Korn

5

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27 March 2017

Stefan Joos

6

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27 March 2017

publication date

2006

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Genes, Chromosomes and Cancer

27 March 2017

published in

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27 March 2017

volume

45

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27 March 2017

issue

4

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27 March 2017

page(s)

401-410

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Use of targeted array-based CGH for the clinical diagnosis of chromosomal imbalance: is less more?

27 March 2017

cites work

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Histopathological and molecular prognostic markers in medulloblastoma: c-myc, N-myc, TrkC, and anaplasia.

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NUP98 gene rearrangements and the clonal evolution of chronic myelogenous leukemia

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Recent segmental duplications in the human genome

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The breakpoint region of the most common isochromosome, i(17q), in human neoplasia is characterized by a complex genomic architecture with large, palindromic, low-copy repeats

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Development and validation of a CGH microarray for clinical cytogenetic diagnosis

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REN(KCTD11) is a suppressor of Hedgehog signaling and is deleted in human medulloblastoma

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Biologic risk stratification of medulloblastoma: the real time is now.

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Human genes encoding U3 snRNA associate with coiled bodies in interphase cells and are clustered on chromosome 17p11.2 in a complex inverted repeat structure

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Brain and other central nervous system tumors: rates, trends, and epidemiology.

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Using full probability models to compute probabilities of actual interest to decision makers

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Cytogenetic and molecular genetic evolution of chronic myeloid leukemia.

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Postoperative neoadjuvant chemotherapy before radiotherapy as compared to immediate radiotherapy followed by maintenance chemotherapy in the treatment of medulloblastoma in childhood: results of the German prospective randomized trial HIT '91.

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Combined histopathological and molecular cytogenetic stratification of medulloblastoma patients.

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Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries

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Identification of tumour-specific epigenetic events in medulloblastoma development by hypermethylation profiling

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7 January 2021

Isolated isochromosome 17q: a distinct type of mixed myeloproliferative disorder/myelodysplastic syndrome with an aggressive clinical course

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Genomic and protein expression profiling identifies CDK6 as novel independent prognostic marker in medulloblastoma

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Cytogenetic analysis of 109 pediatric central nervous system tumors.

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Isochromosome 17q is a negative prognostic factor in poor-risk childhood medulloblastoma patients

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Structure and evolution of the Smith-Magenis syndrome repeat gene clusters, SMS-REPs.

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High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays

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Analysis of the centromeric regions of the human genome assembly

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

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7 January 2021

Mapping of the breakpoints on the short arm of chromosome 17 in neoplasms with an i(17q)

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7 January 2021

High-resolution deletion mapping of chromosome arm 17p in childhood primitive neuroectodermal tumors reveals a common chromosomal disruption within the Smith-Magenis region, an unstable region in chromosome band 17p11.2.

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7 January 2021

Automated array-based genomic profiling in chronic lymphocytic leukemia: development of a clinical tool and discovery of recurrent genomic alterations

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7 January 2021

Transcription mapping in a medulloblastoma breakpoint interval and Smith-Magenis syndrome candidate region: identification of 53 transcriptional units and new candidate genes

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7 January 2021

Segmental duplications and copy-number variation in the human genome

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7 January 2021

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

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7 January 2021

The structure and evolution of centromeric transition regions within the human genome

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7 January 2021

Normalization of cDNA microarray data

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7 January 2021

Molecular characterization of a genetically unstable region containing the SMS critical area and a breakpoint cluster for human PNETs

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7 January 2021

Metastasis stage, adjuvant treatment, and residual tumor are prognostic factors for medulloblastoma in children: conclusions from the Children's Cancer Group 921 randomized phase III study.

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Identifiers

DOI

10.1002/GCC.20304

1 reference