P. Koralkova

发表

Oxidative DNA Damage, Inflammatory Signature, and Altered Erythrocytes Properties in Diamond-Blackfan Anemia

K. Kapralova, V. Divoky, L. Lanikova, 2020, International journal of molecular sciences.

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.

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.

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

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

Rare hereditary red blood cell enzymopathies associated with hemolytic anemia – pathophysiology, clinical aspects, and laboratory diagnosis

R. Wijk, W. W. Solinge, W. Solinge, 2014, 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.

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.

Addiction to DUSP1 protects JAK2V617F-driven polycythemia vera progenitors against inflammatory stress and DNA damage, allowing chronic proliferation

J. Bartek, L. Lanikova, Z. Hodny, 2019, Oncogene.

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.

First description of phosphofructokinase deficiency in spain: identification of a novel homozygous missense mutation in the PFKM gene

J. Grau, R. van Wijk, J. Vives-Corrons, 2013, Front. Physiol..

Low Plasma Citrate Levels and Specific Transcriptional Signatures Associated with Quiescence of CD34+ Progenitors Predict Azacitidine Therapy Failure in MDS/AML Patients

J. Čermák, Z. Krejcík, M. Belickova, 2021, Cancers.

Deep Molecular Response Achieved with Chemotherapy, Dasatinib and Interferon α in Patients with Lymphoid Blast Crisis of Chronic Myeloid Leukaemia

E. Faber, E. Kriegová, T. Papajík, 2023, International journal of molecular sciences.

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.