(Q24681580)

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Transcriptional map of 170-kb region at chromosome 11p15.5: identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samples

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Transcriptional map of 170-kb region at chromosome 11p15.5: identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samples (English)

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mutational analysis

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based on heuristic

inferred from title

Carlo Maria Croce

11

object named as

C M Croce

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author name string

C Schwienbacher

1

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S Sabbioni

2

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M Campi

3

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A Veronese

4

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G Bernardi

5

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A Menegatti

6

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I Hatada

7

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T Mukai

8

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H Ohashi

9

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G Barbanti-Brodano

10

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M Negrini

12

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language of work or name

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publication date

31 March 1998

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Proceedings of the National Academy of Sciences of the United States of America

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95

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7

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3873-8

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The IPL gene on chromosome 11p15.5 is imprinted in humans and mice and is similar to TDAG51, implicated in Fas expression and apoptosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19930

7 April 2017

Direct selection: a method for the isolation of cDNAs encoded by large genomic regions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19930

7 April 2017

Cloning and stable maintenance of 300-kilobase-pair fragments of human DNA in Escherichia coli using an F-factor-based vector

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19930

7 April 2017

An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19930

7 April 2017

A novel gene product that couples TCR signaling to Fas(CD95) expression in activation-induced cell death

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19930

7 April 2017

Tumor cell growth arrest caused by subchromosomal transferable DNA fragments from chromosome 11

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19930

7 April 2017

Disruption of imprinting caused by deletion of the H19 gene region in mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19930

7 April 2017

GOK: a gene at 11p15 involved in rhabdomyosarcoma and rhabdoid tumor development.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19930

28 September 2017

Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19930

28 September 2017

Three tumor-suppressor regions on chromosome 11p identified by high-resolution deletion mapping in human non-small-cell lung cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19930

28 September 2017

Differential DNA sequence deletions from chromosomes 3, 11, 13, and 17 in squamous-cell carcinoma, large-cell carcinoma, and adenocarcinoma of the human lung

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19930

28 September 2017

Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19930

28 September 2017

Genetic linkage of Beckwith-Wiedemann syndrome to 11p15.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19930

28 September 2017

Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19930

28 September 2017

Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19930

28 September 2017

cDNA selection: efficient PCR approach for the selection of cDNAs encoded in large chromosomal DNA fragments

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19930

28 September 2017

Chromosomal localisation of two putative 11p oncosuppressor genes involved in human ovarian tumours

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19930

28 September 2017

Localization of a tumor suppressor gene in 11p15.5 using the G401 Wilms' tumor assay

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19930

28 September 2017

Microsatellite analysis of loss of heterozygosity on chromosomes 9q, 11p and 17p in medulloblastomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19930

28 September 2017

Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19930

30 May 2018

Suppression of tumorigenicity in Wilms tumor by the p15.5-p14 region of chromosome 11.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19930

30 May 2018

Chromosome 11p15 deletions in human malignant astrocytomas and primitive neuroectodermal tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19930

30 May 2018

Reduction to homozygosity of genes on chromosome 11 in human breast neoplasia

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.7.3873

21 January 2018

Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.7.3873

21 January 2018

Relaxation of imprinted genes in human cancer.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.7.3873

21 January 2018

Refinement of regional loss of heterozygosity for chromosome 11p15.5 in human breast tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19930

28 November 2018

Chromosomal localization of the human rhabdomyosarcoma locus by mitotic recombination mapping

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.7.3873

21 January 2018

Tumour-suppressor activity of H19 RNA

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.7.3873

21 January 2018

Deletions in human chromosome arms 11p and 13q in primary hepatocellular carcinomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/9520460

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allele loss at the c-Ha-ras1 locus in human ovarian cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/9520460

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of heterozygosity in human germinal tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/9520460

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequent loss of 11p13 and 11p15 loci in male germ cell tumours

1 reference

https://pubmed.ncbi.nlm.nih.gov/9520460

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour

1 reference

https://pubmed.ncbi.nlm.nih.gov/9520460

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Epigenetic lesions at the H19 locus in Wilms' tumour patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/9520460

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Seven megabase yeast artificial chromosome contig at region 11p15: identification of a yeast artificial chromosome spanning the breakpoint of a chromosomal translocation found in a case of Beckwith-Wiedemann syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9520460

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Definition and refinement of chromosome 11 regions of loss of heterozygosity in breast cancer: identification of a new region at 11q23.3

1 reference

https://pubmed.ncbi.nlm.nih.gov/9520460

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of heterozygosity for chromosome 11 in adenocarcinoma of the stomach

1 reference

https://pubmed.ncbi.nlm.nih.gov/9520460

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.95.7.3873

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1998PNAS...95.3873S

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PMC publication ID

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PubMed publication ID

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