Characterization of FRA6E and its potential role in autosomal recessive juvenile parkinsonism and ovarian cancer. (Q54763867)

3 June 2018

title

Characterization of FRA6E and its potential role in autosomal recessive juvenile parkinsonism and ovarian cancer. (English)

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3 June 2018

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parkinsonian syndrome

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Stacy R Denison

1

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3 June 2018

Gwen Callahan

2

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3 June 2018

Nicole A Becker

3

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3 June 2018

Leslie A Phillips

4

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3 June 2018

David I Smith

5

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3 June 2018

publication date

1 September 2003

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3 June 2018

Genes, Chromosomes and Cancer

published in

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3 June 2018

volume

38

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3 June 2018

issue

1

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3 June 2018

page(s)

40-52

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3 June 2018

A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease

cites work

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7 January 2021

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

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7 January 2021

Evidence that instability within the FRA3B region extends four megabases

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7 January 2021

Characterization of the common fragile site FRA9E and its potential role in ovarian cancer

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7 January 2021

Biological Characterization of Human Epithelial Ovarian Carcinoma Cells in Primary Culture: The Insulin-like Growth Factor System

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7 January 2021

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

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7 January 2021

Transcriptional profiling reveals that several common fragile-site genes are downregulated in ovarian cancer

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7 January 2021

The genetics of Parkinson's disease

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7 January 2021

M6P/IGF2R gene is mutated in human hepatocellular carcinomas with loss of heterozygosity

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7 January 2021

The importance of gene dosage studies: mutational analysis of the parkin gene in early-onset parkinsonism

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7 January 2021

A role for common fragile site induction in amplification of human oncogenes

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7 January 2021

Fish mapping of YAC clones at human chromosomal band 7q31.2: Identification of YACS spanning FRA7G within the common region of LOH in breast and prostate cancer

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7 January 2021

FRA7G extends over a broad region: coincidence of human endogenous retroviral sequences (HERV-H) and small polydispersed circular DNAs (spcDNA) and fragile sites

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7 January 2021

Parkin suppresses unfolded protein stress-induced cell death through its E3 ubiquitin-protein ligase activity

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7 January 2021

Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2

1 reference

7 January 2021

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

1 reference

7 January 2021

Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation

1 reference

7 January 2021

M6P/IGF2R is mutated in squamous cell carcinoma of the lung

1 reference

7 January 2021

The Characterization of the Common Fragile Site FRA16D and Its Involvement in Multiple Myeloma Translocations

1 reference

7 January 2021

Replication of a common fragile site, FRA3B, occurs late in S phase and is delayed further upon induction: implications for the mechanism of fragile site induction

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7 January 2021

Tumor cell growth inhibition by caveolin re-expression in human breast cancer cells

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7 January 2021

Characterization of the human common fragile site FRA2G

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7 January 2021

Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism. The European Consortium on Genetic Susceptibility in Parkinson's Disease and the French Parkinson's Disease Genetics Study Gro

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7 January 2021

Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration site.

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7 January 2021

The mannose 6-phosphate/insulin-like growth factor 2 receptor (M6P/IGF2R), a putative breast tumor suppressor gene

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7 January 2021

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

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7 January 2021

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

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7 January 2021

Viral integration, fragile sites, and proto-oncogenes in human neoplasia

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7 January 2021

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

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7 January 2021

A novel region of deletion on chromosome 6q23.3 spanning less than 500 Kb in high grade invasive epithelial ovarian cancer

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7 January 2021

Characterization of the human TESTIN gene localized in the FRA7G region at 7q31.2

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7 January 2021

New mutation (R42P) of the parkin gene in the ubiquitinlike domain associated with parkinsonism

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7 January 2021

The Sequence of the Human Genome

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7 January 2021

Themes and variations on ubiquitylation

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7 January 2021

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

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7 January 2021

Parkin functions as an E2-dependent ubiquitin- protein ligase and promotes the degradation of the synaptic vesicle-associated protein, CDCrel-1

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7 January 2021

Identifiers

DOI

10.1002/GCC.10236

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3 June 2018

release_xbadrak4dneivofty2acf55aue

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/xbadrak4dneivofty2acf55aue

24 November 2022

mapped directly with Wikidata item

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3 June 2018