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Vytautas Ivaskevicius

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Molecular Genetics & Genomic Medicine|August 7, 2015
Structural and functional influences of coagulation factor XIII subunit B heterozygous missense mutantsAnne Thomas, Arijit Biswas, Vytautas Ivaskevicius, et al.
Blood Reviews|June 7, 2011
An update of the mutation profile of Factor 13 A and B genesArijit Biswas, Vytautas Ivaskevicius, Rainer Seitz, et al.
Human Mutation|August 6, 2013
In vitro secretion deficits are common among human coagulation factor XIII subunit B missense mutants: correlations with patient phenotypes and molecular modelsArijit Biswas, Anne Thomas, Carville G Bevans, et al.
Journal of Thrombosis and Thrombolysis|March 28, 2019
Exploring the structural similarity yet functional distinction between coagulation factor XIII-B and complement factor H sushi domainsMohammad Suhail Akhter, Sneha Singh, Hamideh Yadegari, et al.
Haematologica|March 30, 2013
Insights into pathological mechanisms of missense mutations in C-terminal domains of von Willebrand factor causing qualitative or quantitative von Willebrand diseaseHamideh Yadegari, Julia Driesen, Anna Pavlova, et al.
Haematologica|February 16, 2005
Identification of 32 novel mutations in the factor VIII gene in Indian patients with hemophilia ARafeeq P H Ahmed, Vytautas Ivaskevicius, Meganathan Kannan, et al.
Annals of the New York Academy of Sciences|November 30, 2006
Protection from type 1 diabetes by vitamin D receptor haplotypesElizabeth Ramos-Lopez, Thomas Jansen, Vytautas Ivaskevicius, et al.
Blood|August 21, 2016
Intron retention resulting from a silent mutation in the VWF gene that structurally influences the 5' splice siteHamideh Yadegari, Arijit Biswas, Mohammad Suhail Akhter, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 8, 2008
The first case of combined coagulation factor V and coagulation factor VIII deficiency in Poland due to a novel p.Tyr135Asn missense mutation in the MCFD2 geneVytautas Ivaskevicius, Jerzy Windyga, Beata Baran, et al.
Human Mutation|July 2, 2016
Coagulation Factor XIIIA Subunit Missense Mutations Affect Structure and Function at the Various Steps of Factor XIII ActionAnne Thomas, Arijit Biswas, Johannes Dodt, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Molecular Genetics & Genomic Medicine|August 7, 2015
Structural and functional influences of coagulation factor XIII subunit B heterozygous missense mutantsAnne Thomas, Arijit Biswas, Vytautas Ivaskevicius, et al.
Blood Reviews|June 7, 2011
An update of the mutation profile of Factor 13 A and B genesArijit Biswas, Vytautas Ivaskevicius, Rainer Seitz, et al.
Human Mutation|August 6, 2013
In vitro secretion deficits are common among human coagulation factor XIII subunit B missense mutants: correlations with patient phenotypes and molecular modelsArijit Biswas, Anne Thomas, Carville G Bevans, et al.
Journal of Thrombosis and Thrombolysis|March 28, 2019
Exploring the structural similarity yet functional distinction between coagulation factor XIII-B and complement factor H sushi domainsMohammad Suhail Akhter, Sneha Singh, Hamideh Yadegari, et al.
Haematologica|March 30, 2013
Insights into pathological mechanisms of missense mutations in C-terminal domains of von Willebrand factor causing qualitative or quantitative von Willebrand diseaseHamideh Yadegari, Julia Driesen, Anna Pavlova, et al.
Haematologica|February 16, 2005
Identification of 32 novel mutations in the factor VIII gene in Indian patients with hemophilia ARafeeq P H Ahmed, Vytautas Ivaskevicius, Meganathan Kannan, et al.
Annals of the New York Academy of Sciences|November 30, 2006
Protection from type 1 diabetes by vitamin D receptor haplotypesElizabeth Ramos-Lopez, Thomas Jansen, Vytautas Ivaskevicius, et al.
Blood|August 21, 2016
Intron retention resulting from a silent mutation in the VWF gene that structurally influences the 5' splice siteHamideh Yadegari, Arijit Biswas, Mohammad Suhail Akhter, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 8, 2008
The first case of combined coagulation factor V and coagulation factor VIII deficiency in Poland due to a novel p.Tyr135Asn missense mutation in the MCFD2 geneVytautas Ivaskevicius, Jerzy Windyga, Beata Baran, et al.
Human Mutation|July 2, 2016
Coagulation Factor XIIIA Subunit Missense Mutations Affect Structure and Function at the Various Steps of Factor XIII ActionAnne Thomas, Arijit Biswas, Johannes Dodt, et al.
Pageof 2