R. Mojzíková

发表

DMT1-Mutant Erythrocytes have Shortened Life Span, Accelerated Glycolysis and Increased Oxidative Stress

K. Kapralova, V. Divoky, D. Doležal, 2013, Cellular Physiology and Biochemistry.

The specific PKC-α inhibitor chelerythrine blunts costunolide-induced eryptosis

M. Schaller, F. Lang, V. Divoky, 2020, Apoptosis.

Molecular Characterization of β-Thalassemia in the Czech and Slovak Populations: Mediterranean, Asian and Unique Mutations

V. Divoky, D. Pospíšilová, K. Indrák, 2016, Hemoglobin.

Czech and Slovak Diamond-Blackfan Anemia (DBA) Registry update: Clinical data and novel causative genetic lesions.

J. Blatny, D. Pospíšilová, J. Čermák, 2019, Blood cells, molecules & diseases.

Iron status in patients with pyruvate kinase deficiency: neonatal hyperferritinaemia associated with a novel frameshift deletion in the PKLR gene (p.Arg518fs), and low hepcidin to ferritin ratios

V. Divoky, D. Pospíšilová, K. Indrák, 2014, British journal of haematology.

Missense mutation in RPS7 causes Diamond-Blackfan anemia via alteration of erythrocyte metabolism, protein translation and induction of ribosomal stress.

D. Pospíšilová, J. Čermák, P. Vojta, 2022, Blood cells, molecules & diseases.

Two novel mutations (p.(Ser160Pro) and p.(Arg472Cys)) causing glucose-6-phosphate isomerase deficiency are associated with erythroid dysplasia and inappropriately suppressed hepcidin.

V. Divoky, P. Džubák, D. Pospíšilová, 2017, Blood cells, molecules & diseases.

Partial glutathione reductase deficiency as a cause of diverse clinical manifestations in a family with unstable hemoglobin (Hemoglobin Haná, β63(E7) His-Asn).

P. Doležel, P. Mlejnek, V. Divoky, 2010, Blood cells, molecules & diseases.

Two Novel Mutations in Ribosomal Proteins in the Czech National Diamond-Blackfan Anemia Registry

M. Jarošová, D. Pospíšilová, Zuzana Saxova, 2016 .

Flow cytometric monitoring of the in vitro inhibition of the phosphorylation of CRKL and of SRC family kinases in patients with chronic myelogenous leukemia treated with tyrosine kinase inhibitors

V. Divoky, M. Jarošová, K. Indrák, 2015, International journal of laboratory hematology.

Pharmacological targeting of glucose-6-phosphate dehydrogenase in human erythrocytes by Bay 11–7082, parthenolide and dimethyl fumarate

F. Lang, I. Bernhardt, U. Mrowietz, 2016, Scientific Reports.

Identification of e6a2 BCR-ABL fusion in a Philadelphia-positive CML with marked basophilia: implications for treatment strategy.

V. Divoky, Lenka Calabkova, M. Jarošová, 2011, Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia.

Recurrent episodes of myoglobinuria, mental retardation and seizures but no hemolysis in two brothers with phosphoglycerate kinase deficiency

S. Coppens, A. Aeby, N. Deconinck, 2016, Neuromuscular Disorders.

Major molecular response achieved with dasatinib in a CML patient with F317L BCR-ABL kinase domain mutation.

M. Jarošová, K. Indrák, E. Faber, 2010, Leukemia research.

Role of DNA Damage Response in Suppressing Malignant Progression of Chronic Myeloid Leukemia and Polycythemia Vera: Impact of Different Oncogenes

J. Bartek, J. Gursky, J. Stetka, 2020, Cancers.

Molecular characterization of six new cases of red blood cell hexokinase deficiency yields four novel mutations in HK1.

J. Vives Corrons, R. van Wijk, B. V. van Oirschot, 2016, Blood cells, molecules & diseases.

Prediction of wastewater quality using amperometric bioelectronic tongues.

Charlotte Carlsson, Ulla Wollenberger, Jenny Emnéus, 2016, Biosensors & bioelectronics.

New Mutation in Erythroid-Specific Delta-Aminolevulinate Synthase as the Cause of X-Linked Sideroblastic Anemia Responsive to Pyridoxine

J. Čermák, P. Belohlavkova, J. Kučerová, 2011, Acta Haematologica.

Hydrops fetalis and failure of hematopoietic stem cell transplantation - A long route to the diagnosis of SPTA1-associated hereditary spherocytosis.

T. Kalina, E. Froňková, J. Starý, 2022, Blood Cells, Molecules & Diseases.

Iron status in patients with pyruvate kinase deficiency: neonatal hyperferritinaemia associated with a novel frameshift deletion in the PKLR gene (p.Arg518fs), and low hepcidin to ferritin ratios

D. Pospíšilová, K. Indrák, J. Čermák, 2014, British journal of haematology.

Partial glutathione reductase deficiency as a cause of diverse clinical manifestations in a family with unstable hemoglobin (Hemoglobin Haná, β63(E7) His-Asn).

P. Doležel, P. Mlejnek, D. Pospíšilová, 2010, Blood cells, molecules & diseases.