Search Results - Blažková, Michaela

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  1. 1
    Aging and high-fat diet feeding lead to peripheral insulin resistance and sex-dependent changes in brain of mouse model of tau pathology THY-Tau22

    Aging and high-fat diet feeding lead to peripheral insulin resistance and sex-dependent changes in brain of mouse model of tau pathology THY-Tau22 by Kacířová, Miroslava, Železná, Blanka, Blažková, Michaela, Holubová, Martina, Popelová, Andrea, Kuneš, Jaroslav, Šedivá, Blanka, Maletínská, Lenka

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  2. 2
    Polymorphisms in the RAGE gene influence susceptibility to diabetes-associated microvascular dermatoses in NIDDM

    Polymorphisms in the RAGE gene influence susceptibility to diabetes-associated microvascular dermatoses in NIDDM by Kaňková, Kateřina, Záhejský, Jiřı́, Márová, Ivana, Mužı́k, Jan, Kuhrová, Viera, Blažková, Michaela, Znojil, Vladimı́r, Beránek, Michal, Vácha, Jiřı́

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  3. 3
    Characterization of Two Nonsense Mutations in the Human Dystrophin Gene

    Characterization of Two Nonsense Mutations in the Human Dystrophin Gene by Fajkusová, Lenka, Pekarˆík, VladimÍR, Hájek, JiRˆÍ, Kuhrová, Viera, Blazˆková, Michaela, Fajkus, JiRˆÍ

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  4. 4
    Ultrafast detection of microsatellite repeat polymorphism in endothelin 1 gene by electrophoresis in short capillaries

    Ultrafast detection of microsatellite repeat polymorphism in endothelin 1 gene by electrophoresis in short capillaries by Klepárnik, K, Malá, Z, Pribyla, L, Blazková, M, Vasků, A, Bocek, P

    Published in Electrophoresis
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  5. 5
    Mutation and haplotype analysis of phenylalanine hydroxylase alleles in classical PKU patients from the Czech Republic: identification of four novel mutations

    Mutation and haplotype analysis of phenylalanine hydroxylase alleles in classical PKU patients from the Czech Republic: identification of four novel mutations by Kozak, L, Blazkova, M, Kuhrova, V, Pijackova, A, Ruzickova, S, St'astna, S

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  6. 6
    R395W, K497E and P664L: Three missense mutations in the LDL receptor gene in Czech patients with familial hypercholesterolemia

    R395W, K497E and P664L: Three missense mutations in the LDL receptor gene in Czech patients with familial hypercholesterolemia by Kuhrová, Viera, Kozák, Libor, Soška, Vladimír, Fajkusová, Lenka, Stejskal, Jaroslav, Blažková, Michaela, Freiberger, Tomáš, Jurtíková, Alžběta

    Published in Human mutation
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  7. 7
    Phenylketonuria mutations and their relation to RFLP haplotypes at the PAH locus in Czech PKU families

    Phenylketonuria mutations and their relation to RFLP haplotypes at the PAH locus in Czech PKU families by KOZAK, L, KUHROVA, V, BLAZKOVA, M, ROMANO, V, FAJKUSOVA, L, DVORAKOVA, D, PIJACKOVA, A

    Published in Human genetics
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  8. 8
    Mutation spectrum and phenylalanine hydroxylase RFLP/VNTR background in 44 Romanian phenylketonuric alleles

    Mutation spectrum and phenylalanine hydroxylase RFLP/VNTR background in 44 Romanian phenylketonuric alleles by Popescu, Teodora, Blazkova, Michaela, Kozak, Libor, Jebeleanu, Gheorghe, Popescu, Antonia

    Published in Human mutation
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  9. 9
    Genetic polymorphism of rage and diabetic late skin complications

    Genetic polymorphism of rage and diabetic late skin complications by Kaòková, Kateøina, Blazková, Michaela, Márová, Ivana

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  10. 10
    Haplotype analysis of the fragile X syndrome gene FMR1 in the Czech Republic

    Haplotype analysis of the fragile X syndrome gene FMR1 in the Czech Republic by Pekarík, Vladimír, Blazková, Michaela, Kozák, Libor

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