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Jan P Kraus

Showing results (61-70 of 70) with videos related to

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FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 11, 2009
Genetic or nutritional disorders in homocysteine or folate metabolism increase protein N-homocysteinylation in miceHieronim Jakubowski, Joanna Perla-Kaján, Richard H Finnell, et al.
Biochemical and Biophysical Research Communications|November 24, 2004
Plasma albumin cysteinylation is regulated by cystathionine beta-synthaseDavid Bar-Or, C Gerald Curtis, Andrea Sullivan, et al.
Biochemistry|November 17, 2004
The redox behavior of the heme in cystathionine beta-synthase is sensitive to pHSamuel Pazicni, Gudrun S Lukat-Rodgers, Jana Oliveriusová, et al.
Molecular Genetics and Metabolism|July 20, 2010
Cystathionine beta-synthase null homocystinuric mice fail to exhibit altered hemostasis or lowering of plasma homocysteine in response to betaine treatmentKenneth N Maclean, Jakub Sikora, Viktor Kožich, et al.
Human Mutation|May 15, 2002
High homocysteine and thrombosis without connective tissue disorders are associated with a novel class of cystathionine beta-synthase (CBS) mutationsKenneth N Maclean, Mette Gaustadnes, Jana Oliveriusová, et al.
Plos One|January 19, 2012
Brain phenotype of transgenic mice overexpressing cystathionine β-synthaseVinciane Régnier, Jean-Marie Billard, Sapna Gupta, et al.
Molecular Genetics and Metabolism|May 12, 2009
Cystathionine gamma-lyase: Clinical, metabolic, genetic, and structural studiesJan P Kraus, Jindrich Hasek, Viktor Kozich, et al.
Molecular Genetics and Metabolism|July 20, 2010
A novel transgenic mouse model of CBS-deficient homocystinuria does not incur hepatic steatosis or fibrosis and exhibits a hypercoagulative phenotype that is ameliorated by betaine treatmentKenneth N Maclean, Jakub Sikora, Viktor Kožich, et al.
Human Mutation|October 31, 2006
Diversity of cystathionine beta-synthase haplotypes bearing the most common homocystinuria mutation c.833T>C: a possible role for gene conversionPetr Vyletal, Jitka Sokolová, David N Cooper, et al.
Orphanet Journal of Rare Diseases|January 12, 2013
Propionic acidemia: clinical course and outcome in 55 pediatric and adolescent patientsSarah C Grünert, Stephanie Müllerleile, Linda De Silva, et al.
Pageof 7

Showing results (61-70 of 70) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 70 results.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 11, 2009
Genetic or nutritional disorders in homocysteine or folate metabolism increase protein N-homocysteinylation in miceHieronim Jakubowski, Joanna Perla-Kaján, Richard H Finnell, et al.
Biochemical and Biophysical Research Communications|November 24, 2004
Plasma albumin cysteinylation is regulated by cystathionine beta-synthaseDavid Bar-Or, C Gerald Curtis, Andrea Sullivan, et al.
Biochemistry|November 17, 2004
The redox behavior of the heme in cystathionine beta-synthase is sensitive to pHSamuel Pazicni, Gudrun S Lukat-Rodgers, Jana Oliveriusová, et al.
Molecular Genetics and Metabolism|July 20, 2010
Cystathionine beta-synthase null homocystinuric mice fail to exhibit altered hemostasis or lowering of plasma homocysteine in response to betaine treatmentKenneth N Maclean, Jakub Sikora, Viktor Kožich, et al.
Human Mutation|May 15, 2002
High homocysteine and thrombosis without connective tissue disorders are associated with a novel class of cystathionine beta-synthase (CBS) mutationsKenneth N Maclean, Mette Gaustadnes, Jana Oliveriusová, et al.
Plos One|January 19, 2012
Brain phenotype of transgenic mice overexpressing cystathionine β-synthaseVinciane Régnier, Jean-Marie Billard, Sapna Gupta, et al.
Molecular Genetics and Metabolism|May 12, 2009
Cystathionine gamma-lyase: Clinical, metabolic, genetic, and structural studiesJan P Kraus, Jindrich Hasek, Viktor Kozich, et al.
Molecular Genetics and Metabolism|July 20, 2010
A novel transgenic mouse model of CBS-deficient homocystinuria does not incur hepatic steatosis or fibrosis and exhibits a hypercoagulative phenotype that is ameliorated by betaine treatmentKenneth N Maclean, Jakub Sikora, Viktor Kožich, et al.
Human Mutation|October 31, 2006
Diversity of cystathionine beta-synthase haplotypes bearing the most common homocystinuria mutation c.833T>C: a possible role for gene conversionPetr Vyletal, Jitka Sokolová, David N Cooper, et al.
Orphanet Journal of Rare Diseases|January 12, 2013
Propionic acidemia: clinical course and outcome in 55 pediatric and adolescent patientsSarah C Grünert, Stephanie Müllerleile, Linda De Silva, et al.
Pageof 7