Ask
Search
My library
ORKG

ORKG Ask

Our mission is to organize scholarly knowledge and make it accessible to humans and machines.

About

About ORKG Ask
Report issue
Statistics
Contact

Legal

Terms of use
Data protection (sheet)
Imprint
Accessibility
License

Technical

We
open source
System status
Changelog
Frontend: v1.41.0
Backend: v1.13.4

We use cookies to provide a better user experience.

Data Protection

Semi-automated detection of the factor V mutation by allele specific amplification and capillary electrophoresis

Locht, A.T.F. van de
Kuypers, A.W.H.M.
Verbruggen, H.W.
Linssen, P.C.M.
Nováková, I.R.O.
Mensink, E.J.B.M.

Publication date

January 1995

Abstract

Contains fulltext : 21120___.PDF (publisher's version ) (Open Access

Extracted data

Related items

Genetic diagnosis of factor V Leiden using heteroduplex technology

Bowen, Derrick John
Standen, G. R.
Granville, S.
Bowley, S.
Wood, N. A.
Bidwell, J.

January 1997

A new genetic test has been developed for detection of the mutation known as factor V Leiden. The te...

100 channel electrophoresis prototypes for application to an ultra-high throughput mutational spectrometer

Beltran, Michael J. (Michael Joseph)

January 2007

Thesis (S.B.)--Massachusetts Institute of Technology, Dept. of Mechanical Engineering, 2007.Includes...

Use of first nucleotide change technology to determine the frequency of factor V Leiden in a population of Australian blood donors

Pecheniuk, N.M.
Marsh, N.A.
Walsh, T.P.
Dale, J.L.

November 1997

Activated protein C resistance (APCR), the most common risk factor for venous thrombosis, is the res...

C677T mutation of methylenetetrahydrofolate reductase gene determined in blood or plasma by multiple-injection capillary electrophoresis and laser-induced fluorescence detection

Ulvik, A.
Refsum, H.
Kluijtmans, L.A.J.
Ueland, P.M.

January 1997

Contains fulltext : 25391___.PDF (publisher's version ) (Open Access

Design and validation of a conformation-sensitive capillary electrophoresis system for mutation identification of the COL7A1 gene with automated peak comparison.

Akker, P.C. van den
Hettema, W.
Meijer, R.
Jonkman, M.F.
Hofstra, R.M.
Scheffer, H.

January 2009

Item does not contain fulltextDystrophic epidermolysis bullosa is a heritable skin disease in which ...

Automated Detection of the Factor V Leiden Mutation Using the LCx Microparticle

Enzyme Immunoassay

January 2015

V, produces an Arg506Gln substitution and is the most common genetic risk factor for venous thrombos...

Fluorescencebased SSCP analysis with automatic allele detection demonstrated for the factor V Leiden mutation. Clin Chem

Tanja Walz
Marion Bodis
Wolfgang Herrmann (klinisch-chemisches Zen

January 1998

rz.uni-sb.de) Resistance of coagulation factor V to activated protein C is caused by a point mutatio...

Design and Validation of a Conformation-Sensitive Capillary Electrophoresis System for Mutation Identification of the COL7A1 Gene with Automated Peak Comparison

van den Akker, Peter C.
Hettema, Wendy
Meijer, Rowdy
Jonkman, Marcel F.
Hofstra, Robert M. W.
Scheffer, Hans

October 2009

Dystrophic epidermolysis bullosa is a heritable skin disease in which blisters occur because of a de...

A matrix-assisted laser desorption/ionization time-of-flight based method for screening the 1691G --> A mutation in the factor V gene

HUNG K
SUN X
DING H
KALAFATIS M
GUO B.
SIMIONI, PAOLO

January 2002

A point mutation, 1691 G --> A in the coagulation factor V gene results in an Arg506 --> Gln amino a...

High throughput DNA sequence variant detection by conformation sensitive capillary electrophoresis and automated peak comparison

Davies, Helen
Dicks, Ed
Stephens, Philip
Cox, Charles
Teague, Jon
Greenman, Chris
Bignell, Graham
O'Meara, Sarah
Edkins, Sarah
Parker, Adrian
Stevens, Claire
Menzies, Andrew
Blow, Matt
Bottomley, Bill
Dronsfield, Mark
Futreal, P. Andrew
Stratton, Michael R.
Wooster, Richard

March 2006

AbstractWe report the development of a heteroduplex-based mutation detection method using multicapil...

Screening for genetic mutations [1]

Carlsson, C
Tsui, LC
Zielenski, J
Nielsen, PE
Noolandi, J
Zare, RN
Dulay, MT
Norden, B
Jonsson, M

January 1996

Scientific Correspondence: Rapid detection of single-base substitution by PNA-DNA hybridization in c...

Microelectronic Array Technology

Jess G. Evans
Cindy Lee-tataseo

March 2015

Background: Methods for analysis of the single-nucle-otide polymorphism (SNP) known as factor V Leid...

Simultaneous determination of methylenetetrahydrofolate reductase C677T and

January 2015

factor V G1691A genotypes by mutagenically separated PCR and multiple-injection capillary electropho...

Direct detection of a missense mutation causing severe hemophilia A by PCR amplification and fluorescence scanning.

Marchetti G
Gemmati D
Patracchini P
Volinia S
Castagnoli A
Tosi B
Capelli M
Bernardi F.

January 1990

The amplification of Factor VIII gene-specific sequences, obtained by polymerase chain reaction, was...

Capillary electrophoresis in molecular diagnostics

Kuypers, A.W.H.M.

January 1998

Contains fulltext : 18640.pdf (publisher's version ) (Open Access)117 p

Genetic diagnosis of factor V Leiden using heteroduplex technology

Bowen, Derrick John
Standen, G. R.
Granville, S.
Bowley, S.
Wood, N. A.
Bidwell, J.

January 1997

A new genetic test has been developed for detection of the mutation known as factor V Leiden. The te...

100 channel electrophoresis prototypes for application to an ultra-high throughput mutational spectrometer

Beltran, Michael J. (Michael Joseph)

January 2007

Thesis (S.B.)--Massachusetts Institute of Technology, Dept. of Mechanical Engineering, 2007.Includes...

Use of first nucleotide change technology to determine the frequency of factor V Leiden in a population of Australian blood donors

Pecheniuk, N.M.
Marsh, N.A.
Walsh, T.P.
Dale, J.L.

November 1997

Activated protein C resistance (APCR), the most common risk factor for venous thrombosis, is the res...

C677T mutation of methylenetetrahydrofolate reductase gene determined in blood or plasma by multiple-injection capillary electrophoresis and laser-induced fluorescence detection

Ulvik, A.
Refsum, H.
Kluijtmans, L.A.J.
Ueland, P.M.

January 1997

Contains fulltext : 25391___.PDF (publisher's version ) (Open Access

Design and validation of a conformation-sensitive capillary electrophoresis system for mutation identification of the COL7A1 gene with automated peak comparison.

Akker, P.C. van den
Hettema, W.
Meijer, R.
Jonkman, M.F.
Hofstra, R.M.
Scheffer, H.

January 2009

Item does not contain fulltextDystrophic epidermolysis bullosa is a heritable skin disease in which ...

Automated Detection of the Factor V Leiden Mutation Using the LCx Microparticle

Enzyme Immunoassay

January 2015

V, produces an Arg506Gln substitution and is the most common genetic risk factor for venous thrombos...

Fluorescencebased SSCP analysis with automatic allele detection demonstrated for the factor V Leiden mutation. Clin Chem

Tanja Walz
Marion Bodis
Wolfgang Herrmann (klinisch-chemisches Zen

January 1998

rz.uni-sb.de) Resistance of coagulation factor V to activated protein C is caused by a point mutatio...

Design and Validation of a Conformation-Sensitive Capillary Electrophoresis System for Mutation Identification of the COL7A1 Gene with Automated Peak Comparison

van den Akker, Peter C.
Hettema, Wendy
Meijer, Rowdy
Jonkman, Marcel F.
Hofstra, Robert M. W.
Scheffer, Hans

October 2009

Dystrophic epidermolysis bullosa is a heritable skin disease in which blisters occur because of a de...

A matrix-assisted laser desorption/ionization time-of-flight based method for screening the 1691G --> A mutation in the factor V gene

HUNG K
SUN X
DING H
KALAFATIS M
GUO B.
SIMIONI, PAOLO

January 2002

A point mutation, 1691 G --> A in the coagulation factor V gene results in an Arg506 --> Gln amino a...

High throughput DNA sequence variant detection by conformation sensitive capillary electrophoresis and automated peak comparison

Davies, Helen
Dicks, Ed
Stephens, Philip
Cox, Charles
Teague, Jon
Greenman, Chris
Bignell, Graham
O'Meara, Sarah
Edkins, Sarah
Parker, Adrian
Stevens, Claire
Menzies, Andrew
Blow, Matt
Bottomley, Bill
Dronsfield, Mark
Futreal, P. Andrew
Stratton, Michael R.
Wooster, Richard

March 2006

AbstractWe report the development of a heteroduplex-based mutation detection method using multicapil...

Screening for genetic mutations [1]

Carlsson, C
Tsui, LC
Zielenski, J
Nielsen, PE
Noolandi, J
Zare, RN
Dulay, MT
Norden, B
Jonsson, M

January 1996

Scientific Correspondence: Rapid detection of single-base substitution by PNA-DNA hybridization in c...

Microelectronic Array Technology

Jess G. Evans
Cindy Lee-tataseo

March 2015

Background: Methods for analysis of the single-nucle-otide polymorphism (SNP) known as factor V Leid...

Simultaneous determination of methylenetetrahydrofolate reductase C677T and

January 2015

factor V G1691A genotypes by mutagenically separated PCR and multiple-injection capillary electropho...

Direct detection of a missense mutation causing severe hemophilia A by PCR amplification and fluorescence scanning.

Marchetti G
Gemmati D
Patracchini P
Volinia S
Castagnoli A
Tosi B
Capelli M
Bernardi F.

January 1990

The amplification of Factor VIII gene-specific sequences, obtained by polymerase chain reaction, was...

Capillary electrophoresis in molecular diagnostics

Kuypers, A.W.H.M.

January 1998

Contains fulltext : 18640.pdf (publisher's version ) (Open Access)117 p

Genetic diagnosis of factor V Leiden using heteroduplex technology

Bowen, Derrick John
Standen, G. R.
Granville, S.
Bowley, S.
Wood, N. A.
Bidwell, J.

January 1997

A new genetic test has been developed for detection of the mutation known as factor V Leiden. The te...

100 channel electrophoresis prototypes for application to an ultra-high throughput mutational spectrometer

Beltran, Michael J. (Michael Joseph)

January 2007

Thesis (S.B.)--Massachusetts Institute of Technology, Dept. of Mechanical Engineering, 2007.Includes...

Use of first nucleotide change technology to determine the frequency of factor V Leiden in a population of Australian blood donors

Pecheniuk, N.M.
Marsh, N.A.
Walsh, T.P.
Dale, J.L.

November 1997

Activated protein C resistance (APCR), the most common risk factor for venous thrombosis, is the res...