Alterations of common chromosome fragile sites in hematopoietic malignancies (Q35787503)

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scientific article published on April 2004

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English	Alterations of common chromosome fragile sites in hematopoietic malignancies	scientific article published on April 2004

Statements

instance of

scholarly article

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stated in

Europe PubMed Central

PubMed publication ID

15168591

retrieved

10 August 2017

review article

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stated in

Europe PubMed Central

title

Alterations of common chromosome fragile sites in hematopoietic malignancies (English)

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stated in

Europe PubMed Central

PubMed publication ID

15168591

retrieved

10 August 2017

author name string

Hideshi Ishii

series ordinal

1

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stated in

Europe PubMed Central

PubMed publication ID

15168591

retrieved

10 August 2017

Yusuke Furukawa

series ordinal

2

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stated in

Europe PubMed Central

PubMed publication ID

15168591

retrieved

10 August 2017

publication date

1 April 2004

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stated in

Europe PubMed Central

PubMed publication ID

15168591

retrieved

10 August 2017

published in

International Journal of Hematology

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stated in

Europe PubMed Central

PubMed publication ID

15168591

retrieved

10 August 2017

volume

79

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stated in

Europe PubMed Central

PubMed publication ID

15168591

retrieved

10 August 2017

issue

3

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stated in

Europe PubMed Central

PubMed publication ID

15168591

retrieved

10 August 2017

page(s)

238-242

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Europe PubMed Central

PubMed publication ID

15168591

retrieved

10 August 2017

cites work

Tumor suppressor genes in normal and malignant hematopoiesis

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/15168591

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12 December 2020

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inferred from PubMed ID database lookup

WW domain containing oxidoreductase gene expression is altered in non-small cell lung cancer

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA polymerase alpha inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Designed FHIT alleles establish that Fhit-induced apoptosis in cancer cells is limited by substrate binding

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

WWOX: a candidate tumor suppressor gene involved in multiple tumor types

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

WWOX, a novel WW domain-containing protein mapping to human chromosome 16q23.3-24.1, a region frequently affected in breast cancer

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

FHIT in human cancer

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Constitutive fragile sites and cancer.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/15168591

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple molecular alterations of FHIT in betel-associated oral carcinoma

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/15168591

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic alterations of the tumor suppressor gene WWOX in esophageal squamous cell carcinoma

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

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12 December 2020

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Common fragile sites.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Altered methylation patterns in cancer cell genomes: cause or consequence?

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/15168591

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aberrant expression and deletion of FHIT gene in leukemias

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allele loss and promoter hypermethylation of VHL, RAR-beta, RASSF1A, and FHIT tumor suppressor genes on chromosome 3p in esophageal squamous cell carcinoma

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical significance of fragile histidine triad gene expression in adult acute lymphoblastic leukemia

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aberrant promoter methylation profile of bladder cancer and its relationship to clinicopathological features

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene therapy of hepatocellular carcinoma

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ATR Regulates Fragile Site Stability

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/15168591

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Compilation of published comparative genomic hybridization studies

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/15168591

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequent aberration of FHIT gene expression in acute leukemias.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

JNK1 physically interacts with WW domain-containing oxidoreductase (WOX1) and inhibits WOX1-mediated apoptosis

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile and unstable chromosomes in cancer: causes and consequences

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methylation of the 5' CpG island of the FHIT gene is closely associated with transcriptional inactivation in esophageal squamous cell carcinomas

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Induction of apoptosis and inhibition of tumorigenicity and tumor growth by adenovirus vector-mediated fragile histidine triad (FHIT) gene overexpression

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/15168591

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of FRA16D/WWOX and FRA3B/FHIT genes in hematopoietic malignancies

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tumour suppressor genes in sporadic epithelial ovarian cancer

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/15168591

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary Renal-Cell Carcinoma Associated with a Chromosomal Translocation

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

FHIT expression and hypermethylation in esophageal squamous cell carcinoma

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

5'-CpG island methylation of the FHIT gene is associated with reduced protein expression and higher clinical stage in cervical carcinomas

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Potential cancer therapy with the fragile histidine triad gene: review of the preclinical studies

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aberrant transcripts of the FHIT gene are expressed in normal and leukaemic haemopoietic cells

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

WWOX, the common chromosomal fragile site, FRA16D, cancer gene

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The p53 tumour suppressor gene: a model for molecular epidemiology of human cancer

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Significance of FHIT expression in chronic myelogenous leukemia

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic and epigenetic alterations of tumor suppressor and tumor-related genes in gastric cancer

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The role of PML in tumor suppression

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aberrant FHIT transcripts in acute myeloid leukaemia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

WWOX, the FRA16D gene, behaves as a suppressor of tumor growth

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequence of the FRA3B common fragile region: Implications for the mechanism of FHIT deletion

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role of TCL1 and ALL1 in human leukemias and development

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomes in lymphomas and solid tumors

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

5' CpG island methylation of the FHIT gene is correlated with loss of gene expression in lung and breast cancer

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aberrant FHIT mRNA transcripts are present in malignant and normal haematopoiesis, but absence of FHIT protein is restricted to leukaemia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The tumor-suppressor gene FHIT is involved in the regulation of apoptosis and in cell cycle control

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

FRA3B and other common fragile sites: the weakest links

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of unstable sequences within the common fragile site at 3p14.2: implications for the mechanism of deletions within fragile histidine triad gene/common fragile site at 3p14.2 in tumors

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cancer-specific chromosome alterations in the constitutive fragile region FRA3B.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two-hit inactivation of FHIT by loss of heterozygosity and hypermethylation in breast cancer

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular characterization of FRAXB and comparative common fragile site instability in cancer cells

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aberrant promoter methylation profile of prostate cancers and its relationship to clinicopathological features

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated t(3;8) breakpoint, is abnormal in digestive tract cancers

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Replacement of Fhit in cancer cells suppresses tumorigenicity

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/15168591

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chronic myelogenous leukemia

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of FHIT expression in acute lymphoblastic leukemia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Self-fusion of the ALL1 gene. A new genetic mechanism for acute leukemia

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

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12 December 2020

based on heuristic

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Chronic myelogenous leukemia as a paradigm of early cancer and possible curative strategies

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15168591

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12 December 2020

based on heuristic

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Identifiers

DOI

10.1532/IJH97.03145

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15168591

retrieved

10 August 2017

Dimensions Publication ID

1022193984

0 references

PubMed publication ID

15168591

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15168591

retrieved

10 August 2017

 

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