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V Kozich

Showing results (21-30 of 50) with videos related to

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Vnitrni Lekarstvi|May 1, 1990
[A low-energy protein diet--its effect on lipid and protein metabolism]M Kunesová, V Hainer, V Stich, et al.
Human Mutation|April 11, 2001
Haplotyping of wild type and I278T alleles of the human cystathionine beta-synthase gene based on a cluster of novel SNPs in IVS12M Linnebank, A Homberger, J P Kraus, et al.
Journal of Inherited Metabolic Disease|January 31, 2003
CblE type of homocystinuria due to methionine synthase reductase deficiency: clinical and molecular studies and prenatal diagnosis in two familiesP Zavadakova, B Fowler, J Zeman, et al.
Human Mutation|December 19, 2001
Cystathionine beta-synthase deficiency in Central Europe: discrepancy between biochemical and molecular genetic screening for homocystinuric allelesJ Sokolová, B Janosíková, J D Terwilliger, et al.
Casopis Lekaru Ceskych|June 7, 2012
[Prenatal diagnosis of lysosomal enzymopathies in the Czech Republic]H Poupetová, J Ledvinová, D Chudoba, et al.
Human Molecular Genetics|November 1, 1993
Molecular basis of cystathionine beta-synthase deficiency in pyridoxine responsive and nonresponsive homocystinuriaF L Hu, Z Gu, V Kozich, et al.
American Journal of Human Genetics|May 19, 2001
Impaired heme binding and aggregation of mutant cystathionine beta-synthase subunits in homocystinuriaM Janosík, J Oliveriusová, B Janosíková, et al.
Journal of Inherited Metabolic Disease|July 1, 1997
Analysis of CBS alleles in Czech and Slovak patients with homocystinuria: report on three novel mutations E176K, W409X and 1223 + 37 del99V Kozich, M Janosík, J Sokolová, et al.
Ceskoslovenska Pediatrie|November 1, 1990
[Non-ketotic hyperglycinemia]J Zeman, V Kozich, S Stastná, et al.
Human Molecular Genetics|April 1, 1995
Hyperhomocysteinemia in premature arterial disease: examination of cystathionine beta-synthase alleles at the molecular levelV Kozich, E Kraus, R de Franchis, et al.
Pageof 5

Showing results (21-30 of 50) with videos related to

Sort By:
Pageof 5
Vnitrni Lekarstvi|May 1, 1990
[A low-energy protein diet--its effect on lipid and protein metabolism]M Kunesová, V Hainer, V Stich, et al.
Human Mutation|April 11, 2001
Haplotyping of wild type and I278T alleles of the human cystathionine beta-synthase gene based on a cluster of novel SNPs in IVS12M Linnebank, A Homberger, J P Kraus, et al.
Journal of Inherited Metabolic Disease|January 31, 2003
CblE type of homocystinuria due to methionine synthase reductase deficiency: clinical and molecular studies and prenatal diagnosis in two familiesP Zavadakova, B Fowler, J Zeman, et al.
Human Mutation|December 19, 2001
Cystathionine beta-synthase deficiency in Central Europe: discrepancy between biochemical and molecular genetic screening for homocystinuric allelesJ Sokolová, B Janosíková, J D Terwilliger, et al.
Casopis Lekaru Ceskych|June 7, 2012
[Prenatal diagnosis of lysosomal enzymopathies in the Czech Republic]H Poupetová, J Ledvinová, D Chudoba, et al.
Human Molecular Genetics|November 1, 1993
Molecular basis of cystathionine beta-synthase deficiency in pyridoxine responsive and nonresponsive homocystinuriaF L Hu, Z Gu, V Kozich, et al.
American Journal of Human Genetics|May 19, 2001
Impaired heme binding and aggregation of mutant cystathionine beta-synthase subunits in homocystinuriaM Janosík, J Oliveriusová, B Janosíková, et al.
Journal of Inherited Metabolic Disease|July 1, 1997
Analysis of CBS alleles in Czech and Slovak patients with homocystinuria: report on three novel mutations E176K, W409X and 1223 + 37 del99V Kozich, M Janosík, J Sokolová, et al.
Ceskoslovenska Pediatrie|November 1, 1990
[Non-ketotic hyperglycinemia]J Zeman, V Kozich, S Stastná, et al.
Human Molecular Genetics|April 1, 1995
Hyperhomocysteinemia in premature arterial disease: examination of cystathionine beta-synthase alleles at the molecular levelV Kozich, E Kraus, R de Franchis, et al.
Pageof 5