(Q40726338)

English

A single nucleotide polymorphism at the splice donor site of the human MYH base excision repair genes results in reduced translation efficiency of its transcripts

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scholarly article

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Europe PubMed Central

PubMed publication ID

23 September 2017

A single nucleotide polymorphism at the splice donor site of the human MYH base excision repair genes results in reduced translation efficiency of its transcripts (English)

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

single-nucleotide polymorphism

1 reference

based on heuristic

inferred from title

Kazuya Shinmura

2

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

author name string

Satoru Yamaguchi

1

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Takayuki Saitoh

3

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Seiichi Takenoshita

4

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Hiroyuki Kuwano

5

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Jun Yokota

6

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Europe PubMed Central

PubMed publication ID

23 September 2017

language of work or name

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based on heuristic

inferred from title

publication date

1 May 2002

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

7

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

461-474

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Cloning of a human homolog of the yeast OGG1 gene that is involved in the repair of oxidative DNA damage

1 reference

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Escherichia coli mutY gene encodes an adenine glycosylase active on G-A mispairs

1 reference

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hMYH cell cycle-dependent expression, subcellular localization and association with replication foci: evidence suggesting replication-coupled repair of adenine:8-oxoguanine mispairs

1 reference

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21 January 2018

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1 reference

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RNA surveillance. Unforeseen consequences for gene expression, inherited genetic disorders and cancer

1 reference

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21 January 2018

Differential DNA recognition and glycosylase activity of the native human MutY homolog (hMYH) and recombinant hMYH expressed in bacteria

1 reference

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21 January 2018

Role of the nonsense-mediated decay factor hUpf3 in the splicing-dependent exon-exon junction complex

1 reference

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21 January 2018

Genetic polymorphisms and alternative splicing of the hOGG1 gene, that is involved in the repair of 8-hydroxyguanine in damaged DNA.

1 reference

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21 January 2018

Compilation and analysis of sequences upstream from the translational start site in eukaryotic mRNAs

1 reference

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21 January 2018

Influences of mRNA secondary structure on initiation by eukaryotic ribosomes

1 reference

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21 January 2018

Effects of intercistronic length on the efficiency of reinitiation by eucaryotic ribosomes

1 reference

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21 January 2018

The scanning model for translation: an update

1 reference

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21 January 2018

Initiation of translation in prokaryotes and eukaryotes

1 reference

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21 January 2018

The exon-exon junction complex provides a binding platform for factors involved in mRNA export and nonsense-mediated mRNA decay

1 reference

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21 January 2018

Mutation of the CDKN2A 5' UTR creates an aberrant initiation codon and predisposes to melanoma

1 reference

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21 January 2018

A mammalian DNA repair enzyme that excises oxidatively damaged guanines maps to a locus frequently lost in lung cancer

1 reference

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21 January 2018

Communication of the position of exon-exon junctions to the mRNA surveillance machinery by the protein RNPS1

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2002.00532.X

21 January 2018

MutT protein specifically hydrolyses a potent mutagenic substrate for DNA synthesis

1 reference

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21 January 2018

The GO system protects organisms from the mutagenic effect of the spontaneous lesion 8-hydroxyguanine (7,8-dihydro-8-oxoguanine)

1 reference

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21 January 2018

Identification of human MutY homolog (hMYH) as a repair enzyme for 2-hydroxyadenine in DNA and detection of multiple forms of hMYH located in nuclei and mitochondria

1 reference

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21 January 2018

Cloning and characterization of hOGG1, a human homolog of the OGG1 gene of Saccharomyces cerevisiae

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2002.00532.X

21 January 2018

Cloning and characterization of a mammalian 8-oxoguanine DNA glycosylase

1 reference

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21 January 2018

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

1 reference

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RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression

1 reference

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21 January 2018

Insertion of specific bases during DNA synthesis past the oxidation-damaged base 8-oxodG

1 reference

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21 January 2018

Adenine excisional repair function of MYH protein on the adenine:8-hydroxyguanine base pair in double-stranded DNA.

1 reference

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21 January 2018

Cloning and sequencing a human homolog (hMYH) of the Escherichia coli mutY gene whose function is required for the repair of oxidative DNA damage

1 reference

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21 January 2018

Differential subcellular localization of human MutY homolog (hMYH) and the functional activity of adenine:8-oxoguanine DNA glycosylase

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2002.00532.X

21 January 2018

Loss of heterozygosity in neuroblastomas--an overview

1 reference

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21 January 2018

Nuclear localization of the human mutY homologue hMYH.

1 reference

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Mutation in a splice-donor site of the APC gene in a family with polyposis and late age of colonic cancer death

1 reference

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An activating splice donor mutation in the thrombopoietin gene causes hereditary thrombocythaemia.

1 reference

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Comprehensive allelotyping of human hepatocellular carcinoma

1 reference

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Two different 5′ splice site mutations in the growth hormone gene causing autosomal dominant growth hormone deficiency

1 reference

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21 January 2018

Identifiers

10.1046/J.1365-2443.2002.00532.X

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

ResearchGate publication ID

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