Identification of a 428-kb homozygously deleted region disrupting the SEZ6L gene at 22q12.1 in a lung cancer cell line (Q33933200)

30 July 2017

Identification of a 428-kb homozygously deleted region disrupting the SEZ6L gene at 22q12.1 in a lung cancer cell line (English)

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30 July 2017

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Nishioka M

1

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30 July 2017

Kohno T

2

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30 July 2017

Takahashi M

3

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30 July 2017

Niki T

4

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30 July 2017

Yamada T

5

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30 July 2017

Sone S

6

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30 July 2017

Yokota J

7

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30 July 2017

language of work or name

English

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publication date

1 December 2000

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30 July 2017

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30 July 2017

19

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54

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30 July 2017

6251-6260

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https://scigraph.springernature.com/pub.10.1038/sj.onc.1204031

30 July 2017

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Short, direct repeats at the breakpoints of deletions of the retinoblastoma gene

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Chromosomal rearrangements occur in S. cerevisiae rfa1 mutator mutants due to mutagenic lesions processed by double-strand-break repair

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The DNA sequence of human chromosome 22

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Association of CDKN2A(p16)/CDKN2B(p15) alterations and homozygous chromosome arm 9p deletions in human lung carcinoma.

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SEZ-6: promoter selectivity, genomic structure and localized expression in the brain.

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Silencing of the VHL tumor-suppressor gene by DNA methylation in renal carcinoma

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

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Allelotype and replication error phenotype of small cell lung carcinoma.

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How many tumor suppressor genes are involved in human lung carcinogenesis?

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Breakpoint junction of interstitial homozygous deletion at chromosome 2q33 in a small cell lung carcinoma

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Inactivation of the PTEN/MMAC1/TEP1 gene in human lung cancers.

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p53 splice acceptor site mutation and increased HsRAD51 protein expression in Bloom's syndrome GM1492 fibroblasts

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Absence of hSNF5/INI1 mutation in human lung cancer.

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5′ CpG island methylation is associated with transcriptional silencing of the tumour suppressor p16/CDKN2/MTS1 in human cancers

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Polypyrimidine tract sequences direct selection of alternative branch sites and influence protein binding.

21 January 2018

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Breakpoint Junctions of Chromosome 9p Deletions in Two Human Glioma Cell Lines

21 January 2018

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Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2

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Cloning of a breast cancer homozygous deletion junction narrows the region of search for a 3p21.3 tumor suppressor gene

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Cloning and expression of SEZ-6, a brain-specific and seizure-related cDNA.

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Comparative allelotype of early and advanced stage non-small cell lung carcinomas.

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Cytogenetic analysis of 63 non-small cell lung carcinomas: recurrent chromosome alterations amid frequent and widespread genomic upheaval.

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A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor.

21 January 2018

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Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer

21 January 2018

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Mutations truncating the EP300 acetylase in human cancers

21 January 2018

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Frequent Chromosome 8q Gains in Human Small Cell Lung Carcinoma Detected by Arbitrarily Primed-PCR Genomic Fingerprinting

21 January 2018

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Amplotyping of microdissected, methanol-fixed lung carcinoma by arbitrarily primed polymerase chain reaction

21 January 2018

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7 January 2021

SSCP analysis of long DNA fragments in low pH gel

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7 January 2021

Recurrent allelic deletions of chromosome arms 15q and 16q in human small cell lung carcinomas

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7 January 2021

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

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7 January 2021

Mutation at position -12 of intron 45 (c-->t) plays a prevalent role in the partial skipping of exon 46 from the transcript of allele alphaLELY in erythroid cells

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7 January 2021

Identifiers

DOI

10.1038/SJ.ONC.1204031

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Dimensions Publication ID

30 July 2017

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