(Q41749103)

8 October 2017

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title

An FHIT tumor suppressor gene? (English)

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8 October 2017

Le Beau MM

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8 October 2017

Drabkin H

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8 October 2017

Glover TW

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8 October 2017

Gemmill R

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8 October 2017

Rassool FV

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8 October 2017

McKeithan TW

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8 October 2017

Smith DI

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8 October 2017

publication date

1 April 1998

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Genes, Chromosomes and Cancer

8 October 2017

published in

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8 October 2017

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8 October 2017

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8 October 2017

page(s)

281-289

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Fhit, a putative tumor suppressor in humans, is a dinucleoside 5',5"'-P1,P3-triphosphate hydrolase

8 October 2017

cites work

1 reference

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Chromosome 3p14 homozygous deletions and sequence analysis of FRA3B.

21 January 2018

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Expression of fragile sites triggers intrachromosomal mammalian gene amplification and sets boundaries to early amplicons

21 January 2018

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Identification of intragenic mutations in the von Hippel-Lindau disease tumour suppressor gene and correlation with disease phenotype

21 January 2018

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MADR2 maps to 18q21 and encodes a TGFbeta-regulated MAD-related protein that is functionally mutated in colorectal carcinoma

21 January 2018

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Phenotype of mice lacking functional Deleted in colorectal cancer (Dcc) gene

21 January 2018

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Identification of a chromosome 18q gene that is altered in colorectal cancers

21 January 2018

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

21 January 2018

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DPC4, a candidate tumor suppressor gene at human chromosome 18q21.1

21 January 2018

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Identification of a Gene Located at Chromosome 5q21 that Is Mutated in Colorectal Cancers

21 January 2018

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Consistent chromosome 3p deletion and loss of heterozygosity in renal cell carcinoma

21 January 2018

1 reference

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Chromosome breakage at a major fragile site associated with P-glycoprotein gene amplification in multidrug-resistant CHO cells

21 January 2018

1 reference

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Vertebrate homologues of C. elegans UNC-5 are candidate netrin receptors

21 January 2018

1 reference

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Comparative genomic analysis of tumors: detection of DNA losses and amplification

21 January 2018

1 reference

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MCC, a cytoplasmic protein that blocks cell cycle progression from the G0/G1 to S phase

21 January 2018

1 reference

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Loss of heterozygosity of chromosome 3p markers in small-cell lung cancer

21 January 2018

1 reference

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

21 January 2018

1 reference

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Precise localization of theFHIT gene to the common fragile site at 3p14.2 (FRA3B) and characterization of homozygous deletions within FRA3B that affectFHIT transcription in tumor cell lines

21 January 2018

1 reference

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Variable FHIT transcripts in non-neoplastic tissues

21 January 2018

1 reference

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A 350-kb cosmid contig in 3p14.2 that crosses the t(3;8) hereditary renal cell carcinoma translocation breakpoint and 17 aphidicolin-induced FRA3B breakpoints

21 January 2018

1 reference

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LOH at 3p correlates with a poor survival in oral squamous cell carcinoma

21 January 2018

1 reference

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The molecular basis of focal cyst formation in human autosomal dominant polycystic kidney disease type I.

21 January 2018

1 reference

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Preferential integration of marker DNA into the chromosomal fragile site at 3p14: an approach to cloning fragile sites

21 January 2018

1 reference

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Direct cloning of DNA sequences from the common fragile site region at chromosome band 3p14.2.

21 January 2018

1 reference

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The FHIT gene 3p14.2 is abnormal in lung cancer.

21 January 2018

1 reference

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The 9p21 region in bladder cancer cell lines: large homozygous deletion inactivate the CDKN2, CDKN2B and MTAP genes

21 January 2018

1 reference

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NormalFHIT transcripts in renal cell cancer- and lung cancer-derived cell lines, including a cell line with a homozygous deletion in the FRA3B region

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199804%2921%3A4%3C281%3A%3AAID-GCC1%3E3.0.CO%3B2-V

FHIT gene alterations in head and neck squamous cell carcinomas

21 January 2018

1 reference

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The expanding world of trinucleotide repeats

21 January 2018

1 reference

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FRA3B extends over a broad region and contains a spontaneous HPV16 integration site: direct evidence for the coincidence of viral integration sites and fragile sites

21 January 2018

1 reference

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Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeat

21 January 2018

1 reference

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Constitutive fragile sites and cancer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199804%2921%3A4%3C281%3A%3AAID-GCC1%3E3.0.CO%3B2-V

Deletion of a DNA sequence at the chromosomal region 3p21 in all major types of lung cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199804%2921%3A4%3C281%3A%3AAID-GCC1%3E3.0.CO%3B2-V

Cancer biology: Heritable fragile sites in cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199804%2921%3A4%3C281%3A%3AAID-GCC1%3E3.0.CO%3B2-V

Loss of alleles of loci on the short arm of chromosome 3 in renal cell carcinoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199804%2921%3A4%3C281%3A%3AAID-GCC1%3E3.0.CO%3B2-V

10.1002/(SICI)1098-2264(199804)21:4<281::AID-GCC1>3.0.CO;2-V

21 January 2018

Identifiers

DOI

1 reference

8 October 2017

1 reference