(Q47583371)

English

Evaluation of temperature gradient capillary electrophoresis for detection of the Factor V Leiden mutation: coincident identification of a novel polymorphism in Factor V.

scientific article published in January 2003

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/14529318

Evaluation of temperature gradient capillary electrophoresis for detection of the Factor V Leiden mutation: coincident identification of a novel polymorphism in Factor V. (English)

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/14529318

Factor V Leiden

1 reference

based on heuristic

inferred from title

author name string

Kathleen Murphy

1

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/14529318

Michael Hafez

2

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/14529318

Juliet Philips

3

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/14529318

Kellie Yarnell

4

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/14529318

Kevin Gutshall

5

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/14529318

Karin Berg

6

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/14529318

publication date

1 January 2003

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/14529318

Molecular Diagnosis and Therapy

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/14529318

7

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/14529318

1

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/14529318

35-40

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/14529318

https://scigraph.springernature.com/pub.10.1007/bf03260018

0 references

Ethnic distribution of factor V Leiden in 4047 men and women. Implications for venous thromboembolism screening

1 reference

https://api.crossref.org/works/10.1007%2FBF03260018

21 January 2018

Integrated platform for detection of DNA sequence variants using capillary array electrophoresis

1 reference

https://api.crossref.org/works/10.1007%2FBF03260018

21 January 2018

Mutation in blood coagulation factor V associated with resistance to activated protein C.

1 reference

https://api.crossref.org/works/10.1007%2FBF03260018

21 January 2018

Quantification of PCR bias caused by a single nucleotide polymorphism in SMN gene dosage analysis.

1 reference

https://api.crossref.org/works/10.1007%2FBF03260018

21 January 2018

Rapid detection of the factor V Leiden (1691 G > A) and haemochromatosis (845 G > A) mutation by fluorescence resonance energy transfer (FRET) and real time PCR.

1 reference

https://api.crossref.org/works/10.1007%2FBF03260018

21 January 2018

Evaluation of a tissue factor dependent factor V assay to detect factor V Leiden: demonstration of high sensitivity and specificity for a generally applicable assay for activated protein C resistance

1 reference

https://api.crossref.org/works/10.1007%2FBF03260018

21 January 2018

PCR bias toward the wild-type k-ras and p53 sequences: implications for PCR detection of mutations and cancer diagnosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/14529318

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Colorimetric microwell plate detection of the factor V Leiden mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/14529318

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genotyping method for methylenetetrahydrofolate reductase (C677T thermolabile variant) using heteroduplex technology

1 reference

https://pubmed.ncbi.nlm.nih.gov/14529318

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction, stroke, and venous thrombosis in apparently healthy men

1 reference

https://pubmed.ncbi.nlm.nih.gov/14529318

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factor V Leiden (G1691A), the prothrombin 3'-untranslated region variant (G20210A) and thermolabile methylenetetrahydrofolate reductase (C677T): a single genetic test genotypes all three loci--determination of frequencies in the S. Wales population

1 reference

https://pubmed.ncbi.nlm.nih.gov/14529318

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Accurate and rapid "multiplex heteroduplexing" method for genotyping key enzymes involved in folate/homocysteine metabolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/14529318

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allelic discrimination of factor V Leiden using a 5' nuclease assay

1 reference

https://pubmed.ncbi.nlm.nih.gov/14529318

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chemiluminescent detection of factor V Leiden in a routine laboratory

1 reference

https://pubmed.ncbi.nlm.nih.gov/14529318

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two rare confounding polymorphisms proximal to the factor V Leiden mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/14529318

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The polymerase chain reaction with sequence specific primers for the detection of the factor V mutation associated with activated protein C resistance

1 reference

https://pubmed.ncbi.nlm.nih.gov/14529318

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic diagnosis of factor V Leiden using heteroduplex technology

1 reference

https://pubmed.ncbi.nlm.nih.gov/14529318

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High risk of thrombosis in patients homozygous for factor V Leiden (activated protein C resistance)

1 reference

https://pubmed.ncbi.nlm.nih.gov/14529318

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Non-PCR-dependent detection of the factor V Leiden mutation from genomic DNA using a homogeneous invader microtiter plate assay

1 reference

https://pubmed.ncbi.nlm.nih.gov/14529318

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF03260018

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/14529318

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/14529318

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