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Sarka Krejcova

Observed names: S Krejcova, S Krejcová, SARKA KREJCOVA, Š. Krejčová
OpenAlex ID: A5036594792
X-linked Alport Syndrome
2000 · JEAN PHILIPPE JAIS, BERTRAND KNEBELMANN, et al. · Journal of the American Society of Nephrology · 604
Plexin B3 promotes neurite outgrowth, interacts homophilically, and interacts with Rin
2005 · Christine Hartwig, Andres Veske, et al. · BMC Neuroscience · 53
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Interaction of Bestrophin-1 and Ca2+ Channel β-Subunits: Identification of New Binding Domains on the Bestrophin-1 C-Terminus
2011 · Vladimir M. Milenkovic, Sarka Krejcova, et al. · PLoS ONE · 50
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Plexin B3 is genetically associated with verbal performance and white matter volume in human brain
2006 · D Rujescu, E M Meisenzahl, et al. · Molecular Psychiatry · 46
A human specific haplotype in Plexin B3 is associated with verbal performance and brain white matter volume
2007 · D Rujescu, E M Meisenzahl, et al. · Molecular Psychiatry · 3
243 Genotype/phenotype correlations in Duchenne/Becker muscular dystrophy
1999 · J. Kraus, Š. Krejčová, et al. · European Journal of Paediatric Neurology · 1
Implication for an Intracellular Functional Role of Bestrophin-1
2007 · S Krejcová, Rudgar Neussert, et al. · Investigative Ophthalmology & Visual Science
[New diagnostic possibilities in Alport's syndrome].
1999 · J Stejskal, S Krejcová, et al. · PubMed
[DNA diagnosis of the fragile X chromosome syndrome--FRAXA using PCR].
1998 · A Bóday, V Mat'oska, et al. · PubMed
[Use of CA repeat polymorphism in direct and indirect diagnosis of Duchenne and Becker muscular dystrophy].
1997 · Z Musová, V Mat'oska, et al. · PubMed
Works count: 11
Citation count: 757
H-index: 4
I10-index: 4
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