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Screening for mutations by enzyme mismatch cleavage with T4 endonuclease VII.

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4 August 2017

Screening for mutations by enzyme mismatch cleavage with T4 endonuclease VII. (English)

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4 August 2017

Youil R

1

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4 August 2017

Kemper BW

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2

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4 August 2017

Cotton RG

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3

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4 August 2017

language of work or name

English

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publication date

1 January 1995

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4 August 2017

Proceedings of the National Academy of Sciences of the United States of America

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4 August 2017

92

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4 August 2017

87-91

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4 August 2017

1

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4 August 2017

Identification and in vitro expression of mutations causing dihydropteridine reductase deficiency

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42822

retrieved

8 July 2018

Mutations in the murine homologue of the Menkes gene in dappled and blotchy mice

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stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42822

retrieved

8 July 2018

Current methods of mutation detection

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42822

retrieved

8 July 2018

Initiation of heteroduplex-loop repair by T4-encoded endonuclease VII in vitro

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42822

retrieved

8 July 2018

Pyruvate dehydrogenase deficiency caused by deletion of a 7-bp repeat sequence in the E1 alpha gene

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42822

retrieved

8 July 2018

Large-scale preparation of T4 endonuclease VII from over-expressing bacteria.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42822

retrieved

8 July 2018

Simultaneous screening for beta-thalassemia mutations by chemical cleavage of mismatch.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42822

retrieved

8 July 2018

Enzymes and molecular mechanisms of genetic recombination

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42822

retrieved

8 July 2018

T4 endonuclease VII cleaves holliday structures

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7816853

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening for phenylketonuria mutations by DNA amplification with the polymerase chain reaction

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7816853

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Model for the interaction of DNA junctions and resolving enzymes

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7816853

retrieved

12 December 2020

based on heuristic

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T4 endonuclease VII resolves cruciform DNA with nick and counter-nick and its activity is directed by local nucleotide sequence

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7816853

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Use of the chemical cleavage of mismatch method for prenatal diagnosis of alpha-1-antitrypsin deficiency

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7816853

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chemical cleavage of mismatch to detect mutations

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7816853

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Endonuclease VII of phage T4 triggers mismatch correction in vitro

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7816853

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new codon 15 rhodopsin gene mutation in autosomal dominant retinitis pigmentosa is associated with sectorial disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7816853

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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4 August 2017

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4 August 2017

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4 August 2017

ResearchGate publication ID

15382062

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(Q34804051)

Screening for mutations by enzyme mismatch cleavage with T4 endonuclease VII.

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