(Q35745691)

10 August 2017

Characterization of genomic alterations in hepatoblastomas. A role for gains on chromosomes 8q and 20 as predictors of poor outcome (English)

1 reference

10 August 2017

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R G Weber

1

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10 August 2017

T Pietsch

series ordinal

2

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10 August 2017

D von Schweinitz

series ordinal

3

1 reference

10 August 2017

P Lichter

series ordinal

4

1 reference

10 August 2017

language of work or name

English

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publication date

1 August 2000

1 reference

The American Journal of Pathology

10 August 2017

1 reference

10 August 2017

157

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10 August 2017

571-578

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10 August 2017

2

1 reference

describes a project that uses

10 August 2017

HepT1

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HepT3

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cites work

Comparative genomic hybridization analysis of hepatoblastomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850131

Karyotypic analyses of hepatoblastoma. Report of two cases and review of the literature suggesting chromosomal loci responsible for the pathogenesis of this disease

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850131

Assessment of genetic changes in hepatocellular carcinoma by comparative genomic hybridization analysis: relationship to disease stage, tumor size, and cirrhosis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850131

Genetic analysis of ovarian germ cell tumors by comparative genomic hybridization.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850131

Risk of cancer during the first four years of life in children from The Beckwith-Wiedemann Syndrome Registry

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850131

Analysis of genomic alterations in benign, atypical, and anaplastic meningiomas: toward a genetic model of meningioma progression

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850131

Cytogenetic abnormalities and clonal evolution in an adult hepatoblastoma

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850131

Hepatoblastoma and APC gene mutation in familial adenomatous polyposis.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850131

Gains, losses, and amplification of genomic material in rhabdomyosarcoma analyzed by comparative genomic hybridization

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850131

Characterization of the continuous cell line HepT1 derived from a human hepatoblastoma.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850131

Detection of chromosomal aberrations by means of molecular cytogenetics: painting of chromosomes and chromosomal subregions and comparative genomic hybridization

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850131

Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850131

Detection of amplified DNA sequences by reverse chromosome painting using genomic tumor DNA as probe

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850131

Quantitative analysis of comparative genomic hybridization

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850131

Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumors

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850131

Primary hepatic tumors of childhood

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850131

Cancer incidence, survival, and mortality for children younger than age 15 years

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850131

Hepatoblastoma in families with polyposis coli

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850131

Hepatitis B virus. The major etiology of hepatocellular carcinoma

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850131

Chromosome 2 abnormalities (+Der 2) in two cases of childhood rhabdomyosarcoma

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850131

Trisomy 2 as the sole chromosomal abnormality in a hepatoblastoma

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850131

Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850131

Risk of hepatoblastoma in familial adenomatous polyposis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850131

Establishment of a cell line and its clonal sublines from a patient with hepatoblastoma

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850131

Childhood hepatoblastomas frequently carry a mutated degradation targeting box of the beta-catenin gene.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850131

Computer image analysis of comparative genomic hybridization.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850131

Genetic changes in inherited and sporadic ovarian carcinomas by comparative genomic hybridization: extensive similarity except for a difference at chromosome 2q24-q32

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850131

Hepatoblastoma and hepatocarcinoma in infancy and childhood. Report of 47 cases

25 September 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964567-1

Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964567-1

Hepatoblastoma characterized by trisomy 20 and double minutes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964567-1

Consistent cytogenetic aberrations in hepatoblastoma: a common pathway of genetic alterations in embryonal liver and skeletal muscle malignancies?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964567-1

Trisomy 2 and 20 in two hepatoblastomas

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964567-1

Chromosome aberrations in an alpha-fetoprotein-producing hepatoblastoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964567-1

Trisomy 2, trisomy 20, and del(17p) as sole chromosomal abnormalities in three cases of hepatoblastoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964567-1

Significance of extra copies of chromosome 20 and the long arm of chromosome 2 in hepatoblastoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964567-1

The first recurring chromosome translocation in hepatoblastoma: der(4)t(1;4)(q12;q34)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964567-1

Fluorescence in situ hybridization reveals trisomy 2q by insertion into 9p in hepatoblastoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964567-1

Cytogenetic analysis of hepatoblastoma: hypothesis of cytogenetic evolution in such tumors and results of a multicentric study

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964567-1

Loss of heterozygosity on chromosome 1 in human hepatoblastoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964567-1

Efficiency and toxicity of ifosfamide, cisplatin and doxorubicin in the treatment of childhood hepatoblastoma. Study Committee of the Cooperative Paediatric Liver Tumour Study HB89 of the German Society for Paediatric Oncology and Haematology

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964567-1

Comparative genomic hybridization analysis of hepatoblastomas: additional evidence for a genetic link with Wilms tumor and rhabdomyosarcoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964567-1

Comparative genomic hybridization analysis of Wilms tumors

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964567-1

Comparative genomic hybridization and its application to Wilms' tumorigenesis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964567-1

Recurrent chromosomal abnormalities in hepatocellular carcinoma detected by comparative genomic hybridization

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964567-1

Molecular genetics of Wiedemann-Beckwith syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964567-1

Identification of a 1-cM region of common deletion on 4q35 associated with progression of hepatocellular carcinoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964567-1

Prognostic factors and staging systems in childhood hepatoblastoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964567-1

Chromosomal analysis of sixteen human rhabdomyosarcomas

7 January 2021

1 reference

12 December 2020

Retrospective study on amplification of N-myc and c-myc genes in pediatric solid tumors and its association with prognosis and tumor differentiation

1 reference

12 December 2020

Loss of maternal alleles on chromosome arm 11p in hepatoblastoma

1 reference

12 December 2020

Somatic mutations of the APC gene in sporadic hepatoblastomas

1 reference

12 December 2020

Recurrent chromosomal abnormalities in hepatocellular carcinoma detected by comparative genomic hybridization

1 reference

12 December 2020

Minimal sizes of deletions detected by comparative genomic hybridization

1 reference

12 December 2020

Oncogene amplification and expression in pediatric solid tumors

1 reference

12 December 2020

10.1016/S0002-9440(10)64567-1

Identifiers

DOI

1 reference

10 August 2017

1 reference

10 August 2017

1 reference