FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

M Blazková

Research Profile

Geographic Areas

Czech Republic

Disorders

Chemicals & Drugs

Genes & Molecular Sequences

Alleles

Physiology

Procedures

Concepts & Ideas

Molecular Sequence Data

Co-author Network

Publications

TOP 3
Katerina Kanková; J Záhejský; I Márová; Jan Muzík; Viera Kuhrová; M Blazková; Vladimír Znojil; Michal Beránek; Jirí Vácha
Polymorphisms in the RAGE gene influence susceptibility to diabetes-associated microvascular dermatoses in NIDDM.
Karel Klepárnik; Zdena Malá; L Pribyla; M Blazková; A Vasků; Petr Bocek
Ultrafast detection of microsatellite repeat polymorphism in endothelin 1 gene by electrophoresis in short capillaries.
V Pekarík; M Blazková; Libor Kozák
Haplotype analysis of the fragile X syndrome gene FMR1 in the Czech Republic.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of M Blazková (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2001: Katerina Kanková; J Záhejský; I Márová; Jan Muzík; Viera Kuhrová; M Blazková; Vladimír Znojil; Michal Beránek; Jirí Vácha
Polymorphisms in the RAGE gene influence susceptibility to diabetes-associated microvascular dermatoses in NIDDM.
Journal of diabetes and its complications 2001;15(4):185-92.
2000: Karel Klepárnik; Zdena Malá; L Pribyla; M Blazková; A Vasků; Petr Bocek
Ultrafast detection of microsatellite repeat polymorphism in endothelin 1 gene by electrophoresis in short capillaries.
Electrophoresis 2000;21(1):238-46.
1999: V Pekarík; M Blazková; Libor Kozák
Haplotype analysis of the fragile X syndrome gene FMR1 in the Czech Republic.
American journal of medical genetics 1999;84(3):214-6.
1998: Lenka Fajkusová; V Pekarík; J Hájek; Viera Kuhrová; M Blazková; Jirí Fajkus
Characterization of two nonsense mutations in the human dystrophin gene.
Journal of neurogenetics 1998;12(3):183-9.
1998: A Vasků; Miroslav Soucek; Vladimír Znojil; I Rihácek; Svatava Tschöplová; L Strelcová; K Cídl; M Blazková; Dobroslav Hájek; Lydie Izakovicová Hollá; Jirí Vácha
Angiotensin I-converting enzyme and angiotensinogen gene interaction and prediction of essential hypertension.
Kidney international 1998;53(6):1479-82.
1998: Karel Klepárník; Zdena Malá; Z Havác; M Blazková; Lydie Izakovicová Hollá; Petr Bocek
Fast detection of a (CA)18 microsatellite repeat in the IgE receptor gene by capillary electrophoresis with laser-induced fluorescence detection.
Electrophoresis 1998;19(2):249-55.
1997: Libor Kozák; M Blazková; Viera Kuhrová; A Pijácková; S Růzicková; S St'astná
Mutation and haplotype analysis of phenylalanine hydroxylase alleles in classical PKU patients from the Czech Republic: identification of four novel mutations.
Journal of medical genetics 1997;34(11):893-8.
1997: S Růzicková; Libor Kozák; M Blazková; J Kapras; S St'astná
[Mutation of the phenylalanine hydroxylase gene in the population of central Bohemia. Relation to the clinical picture of phenylketonuria].
Casopís lékar̆ů c̆eských 1997;136(9):282-5.
1995: Libor Kozák; Viera Kuhrová; M Blazková; V Romano; Lenka Fajkusová; D Dvoráková; A Pijácková
Phenylketonuria mutations and their relation to RFLP haplotypes at the PAH locus in Czech PKU families.
Human genetics 1995;96(4):472-6.
1995: Libor Kozák; Viera Kuhrová; M Blazková; Lenka Fajkusová; D Dvoráková; A Pijácková
[Advances in the diagnosis of phenylketonuria with the introduction of direct detection of PAH gene mutation].
Casopís lékar̆ů c̆eských 1995;134(12):385-7.