(Q60689261)

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Polymerase chain reaction—single strand conformation polymorphism or how to detect reliably and efficiently each sequence variation in many samples and many genes

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9 December 2019

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Polymerase chain reaction-single strand conformation polymorphism or how to detect reliably and efficiently each sequence variation in many samples and many genes (English)

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Europe PubMed Central

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9 December 2019

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Jaeckel S

1

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9 December 2019

Epplen JT

2

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9 December 2019

Kauth M

3

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9 December 2019

Miterski B

4

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9 December 2019

Tschentscher F

5

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9 December 2019

Epplen C

6

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9 December 2019

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1 December 1998

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9 December 2019

Electrophoresis

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9 December 2019

19

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9 December 2019

18

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9 December 2019

3055-3061

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9 December 2019

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

1 reference

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

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How sensitive is PCR-SSCP?

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Separation of DNA strands facilitates detection of point mutations by PCR-SSCP

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Simple and rapid determination of the acetaldehyde dehydrogenase (ALDH2) genotypes by nonradioactive single-strand conformation polymorphism analysis

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

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Development of standard reference materials for diagnosis of p53 mutations: analysis by slab gel single strand conformation polymorphism

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7 January 2021

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Separation of random fragments of DNA according to properties of their sequences

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7 January 2021

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Mutation detection by denaturing gradient gel electrophoresis (DGGE).

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7 January 2021

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Factor VIII gene mutations found by a comparative study of SSCP, DGGE and CMC and their analysis on a molecular model of factor VIII protein

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7 January 2021

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A method to detect and characterize point mutations in transcribed genes: amplification and overexpression of the mutant c-Ki-ras allele in human tumor cells

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7 January 2021

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Genotypic selection of mutated DNA sequences using mismatch cleavage analysis, a possible basis for novel mutation assays

1 reference

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7 January 2021

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Reactivity of cytosine and thymine in single-base-pair mismatches with hydroxylamine and osmium tetroxide and its application to the study of mutations

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7 January 2021

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Chemical cleavage of mismatch: a new look at an established method

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Rapid genetic screening for haemochromatosis using heteroduplex technology

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Detecting single base substitutions as heteroduplex polymorphisms

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7 January 2021

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Dideoxy fingerprinting (ddF): A rapid and efficient screen for the presence of mutations

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Bi-directional dideoxy fingerprinting (Bi-ddF): a rapid method for quantitative detection of mutations in genomic regions of 300-600 bp

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7 January 2021

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Directed termination PCR: a one-step approach to mutation detection

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Pathology and pathogenesis of demyelinating diseases.

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Review: cytokines and the pathogenesis of multiple sclerosis

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Genetic predisposition to multiple sclerosis as revealed by immunoprinting

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A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22

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7 January 2021

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A full genome search in multiple sclerosis

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7 January 2021

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A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group

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7 January 2021

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Dense Alu clustering and a potential new member of the NF kappa B family within a 90 kilobase HLA class III segment

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7 January 2021

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Lymphotoxin beta, a novel member of the TNF family that forms a heteromeric complex with lymphotoxin on the cell surface

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Cloning and genomic characterization of LST1: a new gene in the human TNF region

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7 January 2021

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Structure of the human TNF receptor 1 (p60) gene (TNFR1) and localization to chromosome 12p13 [corrected]

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7 January 2021

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Human tumor necrosis factor receptor p75/80 (CD120b) gene structure and promoter characterization

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7 January 2021

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Human IL-3 (multi-CSF): identification by expression cloning of a novel hematopoietic growth factor related to murine IL-3.

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7 January 2021

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Molecular regulation of the human IL-3 gene: inducible T cell-restricted expression requires intact AP-1 and Elf-1 nuclear protein binding sites

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Structural relationship of human interferon alpha genes and pseudogenes

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Optimization of the single-strand conformation polymorphism (SSCP) technique for detection of point mutations.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150191802

7 January 2021

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Protocols for an improved detection of point mutations by SSCP

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High percentage acrylamide gels improve resolution in SSCP analysis

1 reference

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Excess PCR primers may dramatically affect SSCP efficiency

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Determination of human alcohol dehydrogenase and acetaldehyde dehydrogenase genotypes by single strand conformation polymorphism in discontinuous buffer electrophoresis

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Improved single-strand conformation polymorphism analysis by asymmetric polymerase chain reaction with end-labeled primers

1 reference

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1 reference

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Identifiers

10.1002/ELPS.1150191802

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9932793%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9932793%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

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