(Q39402100)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22302706%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

title

Contribution of germline mutations to PARK2 gene inactivation in lung adenocarcinoma (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22302706%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

1 reference

Reika Iwakawa

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22302706%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

Aiko Sato-Otsubo

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22302706%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

Seishi Ogawa

series ordinal

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22302706%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

Jun Yokota

series ordinal

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22302706%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

publication date

3 February 2012

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22302706%20AND%20SRC:MED&resulttype=core&format=json

Genes, Chromosomes and Cancer

22 January 2020

number of pages

11

1 reference

based on heuristic

inferred from page(s)

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22302706%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

volume

51

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22302706%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22302706%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

page(s)

462-472

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22302706%20AND%20SRC:MED&resulttype=core&format=json

Hotspots of large rare deletions in the human genome

22 January 2020

cites work

1 reference

Frequency of heterozygous Parkin mutations in healthy subjects: need for careful prospective follow-up examination of mutation carriers.

21 January 2018

1 reference

Parkin, a gene implicated in autosomal recessive juvenile parkinsonism, is a candidate tumor suppressor gene on chromosome 6q25-q27

21 January 2018

1 reference

Prevalence of human papillomavirus 16/18/33 infection and p53 mutation in lung adenocarcinoma

21 January 2018

1 reference

MYC amplification as a prognostic marker of early-stage lung adenocarcinoma identified by whole genome copy number analysis.

21 January 2018

1 reference

A comprehensive analysis of deletions, multiplications, and copy number variations in PARK2

21 January 2018

1 reference

21 January 2018

1 reference

Geographic and ethnic differences in frequencies of two polymorphisms (D/N394 and L/I272) of the parkin gene in sporadic Parkinson's disease.

21 January 2018

1 reference

Parkin variants in North American Parkinson's disease: cases and controls.

21 January 2018

1 reference

Establishment and characterization of 20 human non-small cell lung cancer cell lines in a serum-free defined medium (ACL-4).

21 January 2018

1 reference

Integrated detection and population-genetic analysis of SNPs and copy number variation

21 January 2018

1 reference

Mechanisms of genomic instabilities underlying two common fragile-site-associated loci, PARK2 and DMD, in germ cell and cancer cell lines

21 January 2018

1 reference

Progress in the pathogenesis and genetics of Parkinson's disease

21 January 2018

1 reference

Genetic determinants at the interface of cancer and neurodegenerative disease

21 January 2018

1 reference

A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays

21 January 2018

1 reference

Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update

21 January 2018

1 reference

Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing

21 January 2018

1 reference

Alterations of the tumor suppressor gene Parkin in non-small cell lung cancer

21 January 2018

1 reference

PARK2 deletions occur frequently in sporadic colorectal cancer and accelerate adenoma development in Apc mutant mice.

21 January 2018

1 reference

Discovering tumor suppressor genes through genome-wide copy number analysis

21 January 2018

1 reference

A genome-wide screen for microdeletions reveals disruption of polarity complex genes in diverse human cancers

21 January 2018

1 reference

Transforming gene from human stomach cancers and a noncancerous portion of stomach mucosa

21 January 2018

1 reference

Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase

21 January 2018

1 reference

Somatic mutations of the Parkinson's disease-associated gene PARK2 in glioblastoma and other human malignancies

21 January 2018

1 reference

Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarrays

21 January 2018

1 reference

Genetics of Parkinson's disease and essential tremor

21 January 2018

1 reference

One Hundred and Twenty-Seven Cultured Human Tumor Cell Lines Producing Tumors in Nude Mice23

21 January 2018

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Allelotyping demonstrates common and distinct patterns of chromosomal loss in human lung cancer types

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1002/GCC.21933

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22302706%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

1 reference