Fol. Biol. 2016, 62, 82-89
X-Chromosome Inactivation Analysis in Different Cell Types and Induced Pluripotent Stem Cells Elucidates the Disease Mechanism in a Rare Case of Mucopolysaccharidosis Type II in a Female
Individual author index pages
- M. Řeboun
- J. Rybová
- R. Dobrovolný
- J. Včelák
- T. Veselková
- G. Štorkánová
- D. Mušálková
- M. Hřebíček
- J. Ledvinová
- M. Magner
- J. Zeman
- K. Pešková
- Lenka Dvořáková
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2019, Vol. 65, Issue 4, pp. 181-187 -
Buccal Respiratory Chain Complexes I and IV Quantities in Huntington’s Disease Patients
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Molecular Diagnostics of Copper-Transporting Protein Mutations Allows Early Onset Individual Therapy of Menkes Disease
L. Králík, E. Flachsová, H. Hansíková, V. Saudek, J. Zeman, Pavel Martásek
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Non-Invasive Screening of Cytochrome c Oxidase Deficiency in Children Using a Dipstick Immunocapture Assay
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Lipoprotein Lipase Deficiency: Clinical, Biochemical and Molecular Characteristics in Three Patients with Novel Mutations in the LPL Gene
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2014, Vol. 60, Issue 5, pp. 235-243 -
Association of Obesity Susceptibility Gene Variants with Metabolic Syndrome and Related Traits in 1,443 Czech Adolescents
Lenka Dušátková, H. Zamrazilová, B. Sedláčková, J. Včelák, P. Hlavatý, I. Aldhoon Hainerová, V. Korenková, O. Bradnová, B. Bendlová, M. Kunešová, V. Hainer
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Rapid Isolation of Lysosomal Membranes from Cultured Cells
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Role of Common Canalicular Transporter Gene Variations in Aetiology of Idiopathic Gallstones in Childhood
J. Bronský, Milan Jirsa, J. Nevoral, M. Hřebíček
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