V. Saudek
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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
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 -
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 -
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 -
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
