Folia Biologica
Journal of Cellular and Molecular Biology, Charles University 

Individual author index pages

• E. Flachsová
• I. C. Verma
• D. Ulbrichová
• R. Saxena
• J. Zeman
• V. Saudek
• C. S. Raman
• Pavel Martásek

Other articles of these authors

• Stable COX17 Downregulation Leads to Alterations in Mitochondrial Ultrastructure, Decreased Copper Content and Impaired Cytochrome c Oxidase Biogenesis in HEK293 Cells

  M. Vanišová, D. Burská, J. Křížová, T. Daňhelovská, Ž. Dosoudilová, J. Zeman, L. Stibůrek, Hana Hansíková

  2019, Vol. 65, Issue 4, pp. 181-187
• Buccal Respiratory Chain Complexes I and IV Quantities in Huntington’s Disease Patients

  P. Dušek, M. Rodinová, I. Lišková, J. Klempíř, J. Zeman, J. Roth, Hana Hansíková

  2018, Vol. 64, Issue 1, pp. 31-34
• 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

  2017, Vol. 63, Issue 5-6, pp. 165-173
• Novel Mutation (T273R) in Thyroid Hormone Receptor β Gene Provides Further Insight into Cryptic Negative Regulation by Thyroid Hormone

  Filip Kaššák, V. Hána, V. Saudek, M. Kostrouchová

  2017, Vol. 63, Issue 2, pp. 60-66
• 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

  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

  2016, Vol. 62, Issue 2, pp. 82-89
• Hepatoerythropoietic Porphyria Caused by a Novel Homoallelic Mutation in Uroporphyrinogen Decarboxylase Gene in Egyptian Patients

  M. S. Farrag, I. Mikula, E. Richard, V. Saudek, H. De Verneuil, Pavel Martásek

  2015, Vol. 61, Issue 6, pp. 219-226
• A Novel Mutation in the FECH Gene in a Czech Family with Erythropoietic Protoporphyria and a Population Study of IVS3-48C Variant Contributing to the Disease

  M. S. Farrag, J. Kučerová, L. Šlachtová, O. Šeda, J. Šperl, Pavel Martásek

  2015, Vol. 61, Issue 6, pp. 227-232
• Prorenin Receptor Homologue VHA-20 is Critical for Intestinal pH Regulation, Ion and Water Management and Larval Development in

  V. Zima, K. Šebková, K. Šimečková, T. Dvořák, V. Saudek, Marta Kostrouchová

  2015, Vol. 61, Issue 5, pp. 168-177
• Non-Invasive Screening of Cytochrome c Oxidase Deficiency in Children Using a Dipstick Immunocapture Assay

  M. Rodinová, E. Trefilová, T. Honzík, M. Tesařová, J. Zeman, Hana Hansíková

  2014, Vol. 60, Issue 6, pp. 268-274
• Lipoprotein Lipase Deficiency: Clinical, Biochemical and Molecular Characteristics in Three Patients with Novel Mutations in the LPL Gene

  H. Kolářová, M. Tesařová, Š. Švecová, V. Stránecký, A. Přistoupilová, T. Zima, J. Uhrová, S. Y. Volgina, J. Zeman, Tomáš Honzík

  2014, Vol. 60, Issue 5, pp. 235-243
• Stress Perception and (GT)n Repeat Polymorphism in Haem Oxygenase 1 Promoter Are Both Risk Factors in Development of Eating Disorders

  L. Šlachtová, D. Kaminská, M. Chvál, L. Králík, Pavel Martásek, H. Papežová

  2013, Vol. 59, Issue 6, pp. 233-239
• SMED-TLX-1 (NR2E1) Is Critical for Tissue and Body Plan Maintenance in Schmidtea mediterranea in Fasting/Feeding Cycles

  O. Raška, V. Kostrouchová, F. Behenský, P. Yilma, V. Saudek, Z. Kostrouch, Marta Kostrouchová

  2011, Vol. 57, Issue 6, pp. 223-231