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Ivan Sebesta

Showing results (11-20 of 16) with videos related to

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Clinica Chimica Acta; International Journal of Clinical Chemistry|October 4, 2011
Novel mutations in xanthine dehydrogenase/oxidase cause severe hypouricemia: biochemical and molecular genetic analysis in two Czech families with xanthinuria type IBlanka Stiburkova, Jakub Krijt, Petr Vyletal, et al.
European Journal of Human Genetics : EJHG|February 7, 2013
Novel allelic variants and evidence for a prevalent mutation in URAT1 causing renal hypouricemia: biochemical, genetics and functional analysisBlanka Stiburkova, Ivan Sebesta, Kimiyoshi Ichida, et al.
Nucleosides, Nucleotides & Nucleic Acids|July 5, 2008
Polymorphisms of the TPMT gene in the Czech healthy population and patients with inflammatory bowel diseaseOndrej Slanar, Martin Bortlík, Helena Buzková, et al.
Nucleosides, Nucleotides & Nucleic Acids|April 22, 2020
Modified forearm ischemic test in hypouricemic patientsIvan Sebesta, Daisuke Miyamoto, Blanka Stiburkova, et al.
Biomedicines|July 27, 2022
Analysis of Purine Metabolism to Elucidate the Pathogenesis of Acute Kidney Injury in Renal HypouricemiaDaisuke Miyamoto, Nana Sato, Koji Nagata, et al.
European Journal of Human Genetics : EJHG|March 14, 2003
Familial juvenile hyperuricaemic nephropathy (FJHN): linkage analysis in 15 families, physical and transcriptional characterisation of the FJHN critical region on chromosome 16p11.2 and the analysis of seven candidate genesBlanka Stibůrková, Jacek Majewski, Katerina Hodanová, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 4, 2011
Novel mutations in xanthine dehydrogenase/oxidase cause severe hypouricemia: biochemical and molecular genetic analysis in two Czech families with xanthinuria type IBlanka Stiburkova, Jakub Krijt, Petr Vyletal, et al.
European Journal of Human Genetics : EJHG|February 7, 2013
Novel allelic variants and evidence for a prevalent mutation in URAT1 causing renal hypouricemia: biochemical, genetics and functional analysisBlanka Stiburkova, Ivan Sebesta, Kimiyoshi Ichida, et al.
Nucleosides, Nucleotides & Nucleic Acids|July 5, 2008
Polymorphisms of the TPMT gene in the Czech healthy population and patients with inflammatory bowel diseaseOndrej Slanar, Martin Bortlík, Helena Buzková, et al.
Nucleosides, Nucleotides & Nucleic Acids|April 22, 2020
Modified forearm ischemic test in hypouricemic patientsIvan Sebesta, Daisuke Miyamoto, Blanka Stiburkova, et al.
Biomedicines|July 27, 2022
Analysis of Purine Metabolism to Elucidate the Pathogenesis of Acute Kidney Injury in Renal HypouricemiaDaisuke Miyamoto, Nana Sato, Koji Nagata, et al.
European Journal of Human Genetics : EJHG|March 14, 2003
Familial juvenile hyperuricaemic nephropathy (FJHN): linkage analysis in 15 families, physical and transcriptional characterisation of the FJHN critical region on chromosome 16p11.2 and the analysis of seven candidate genesBlanka Stibůrková, Jacek Majewski, Katerina Hodanová, et al.
Pageof 2