'Cold SSCP': a simple, rapid and non-radioactive method for optimized single-strand conformation polymorphism analyses (Q34994306)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8367279%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

title

'Cold SSCP': a simple, rapid and non-radioactive method for optimized single-strand conformation polymorphism analyses (English)

1 reference

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30 October 2019

author

Christopher M Weghorst

4

1 reference

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30 October 2019

author name string

T Hongyo

1

1 reference

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30 October 2019

G S Buzard

2

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30 October 2019

R J Calvert

3

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30 October 2019

language of work or name

English

0 references

publication date

1 August 1993

1 reference

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30 October 2019

published in

Nucleic Acids Research

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30 October 2019

volume

21

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30 October 2019

issue

16

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30 October 2019

page(s)

3637-3642

1 reference

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A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

30 October 2019

cites work

1 reference

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Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

8 July 2018

1 reference

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Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309858

Non-radioactive single strand conformation polymorphism (SSCP) using the Pharmacia 'PhastSystem'.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309858

Non-isotopic detection of single strand conformation polymorphism (PCR-SSCP): a rapid and sensitive technique in diagnosis of phenylketonuria

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309858

Diagnostic single strand conformational polymorphism, (SSCP): a simplified non-radioisotopic method as applied to a Tay-Sachs B1 variant

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309858

Nonisotopic SSCP and competitive PCR for DNA quantification: p53 in breast cancer cells

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309858

F-SSCP: fluorescence-based polymerase chain reaction-single-strand conformation polymorphism (PCR-SSCP) analysis.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309858

Neurotrophic factor-like activity in Drosophila

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309858

Screening for mutations by RNA single-strand conformation polymorphism (rSSCP): comparison with DNA-SSCP

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309858

Cloning of the essential myotonic dystrophy region and mapping of the putative defect

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309858

The unstable and methylatable mutations causing the fragile X syndrome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309858

A novel CFTR mutation, 4035delA, detected by non-radioactive SSCP analysis

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309858

Mutation analysis of genetic diseases by asymmetric-PCR SSCP and ethidium bromide staining: application to neurofibromatosis and cystic fibrosis

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309858

Identification and characterization of sporadic and inherited mutations in exon 31 of the neurofibromatosis (NF1) gene.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309858

New mutant gene (transthyretin Arg 58) in cases with hereditary polyneuropathy detected by non-isotope method of single-strand conformation polymorphism analysis.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309858

Nonisotopic SSCP detection in PCR products by ethidium bromide staining

26 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8367279

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Methods in laboratory investigation. Rapid and simple detection of c-Ki-ras2 gene codon 12 mutations by nonradioisotopic single-strand conformation polymorphism analysis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8367279

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Detection and characterization of new genetic mutations in individuals heterozygous for lactate dehydrogenase-B(H) deficiency using DNA conformation polymorphism analysis and silver staining

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8367279

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/NAR/21.16.3637

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8367279%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8367279%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

1 reference