M. Horvathova

发表

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.

Developmental changes in iron metabolism and erythropoiesis in mice with human gain‐of‐function erythropoietin receptor

K. Kapralova, V. Divoky, Jihyun Song, 2022, American journal of hematology.

Hepcidin levels in Diamond-Blackfan anemia reflect erythropoietic activity and transfusion dependency

V. Divoky, L. Radová, P. Džubák, 2014, Haematologica.

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.

Erythropoietin-driven signaling ameliorates the survival defect of DMT1-mutant erythroid progenitors and erythroblasts

K. Kapralova, V. Divoky, D. Pospíšilová, 2012, Haematologica.

Hepcidin in newly diagnosed inflammatory bowel disease in children

V. Mihál, D. Pospíšilová, E. Karaskova, 2018, Journal of paediatrics and child health.

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 .

HIF-mediated increased ROS from reduced mitophagy and decreased catalase causes neocytolysis

J. Prchal, R. Christensen, P. Thiagarajan, 2015, Journal of Molecular Medicine.

Heme oxygenase 1 is expressed in murine erythroid cells where it controls the level of regulatory heme.

D. Garcia-Santos, Monika Horváthová, P. Ponka, 2014, Blood.

RUNX1 and NF-E2 upregulation is not specific for MPNs, but is seen in polycythemic disorders with augmented HIF signaling.

K. Kapralova, V. Divoky, J. Prchal, 2014, Blood.

Molecular basis of hereditary iron homeostasis defects

V. Divoky, Monika Horváthová, P. Ponka, 2010, Hematology.

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.

Inhibition of heme oxygenase ameliorates anemia and reduces iron overload in a β-thalassemia mouse model.

D. Garcia-Santos, Amel Hamdi, Zuzana Saxova, 2018, Blood.

Inhibition of heme oxygenase ameliorates anemia and reduces iron overload in β-thalassemia mouse model Short Title : Thalassemia treatment by heme oxygenase inhibition

D. Garcia-Santos, Amel Hamdi, Zuzana Saxova, 2017 .

Delayed hemoglobin switching and perinatal neocytolysis in mice with gain-of-function erythropoietin receptor

H. Votavova, V. Divoky, J. Prchal, 2015, Journal of Molecular Medicine.

Cooperation of germ line JAK2 mutations E846D and R1063H in hereditary erythrocytosis with megakaryocytic atypia.

C. Pecquet, R. Kralovics, K. Kapralova, 2016, Blood.

Most pediatric patients with essential thrombocythemia show hypersensitivity to erythropoietin in vitro, with rare JAK2 V617F-positive erythroid colonies.

V. Divoky, J. Starý, V. Mihál, 2008, Leukemia research.

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

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

HIF-mediated increased ROS from reduced mitophagy and decreased catalase causes neocytolysis

J. Prchal, R. Christensen, P. Thiagarajan, 2015, Journal of Molecular Medicine.

Characterization of iron metabolism and erythropoiesis in erythrocyte membrane defects and thalassemia traits.

M. Hajdúch, V. Mihál, D. Pospíšilová, 2016, Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia.

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.

Elevated erythroferrone distinguishes erythrocytosis with inherited defects in oxygen‐sensing pathway from primary familial and congenital polycythaemia

D. Pospíšilová, K. Indrák, J. Navrátilová, 2023, British journal of haematology.

JAK2 E846D Germline Mutation Associated with Erythrocytosis Causes Increased and Prolonged Epo-Induced Activation of STAT5

K. Kapralova, D. Pospíšilová, S. Constantinescu, 2014 .

Increased blood reactive oxygen species and hepcidin in obstructive sleep apnea precludes expected erythrocytosis

C. Lundby, T. Ganz, K. Indrák, 2023, American journal of hematology.

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.

Heme oxygenase 1 is expressed in murine erythroid cells where it controls the level of regulatory heme.

P. Ponka, A. Sheftel, M. Schranzhofer, 2014, Blood.