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1.
Attenuated cell cycle and DNA damage response transcriptome signatures and overrepresented cell adhesion processes imply accelerated progression in patients with lower-risk myelodysplastic neoplasms.
Int J Cancer
; 154(9): 1652-1668, 2024 May 01.
Article
in English
| MEDLINE | ID: mdl-38180088
2.
Elevated erythroferrone distinguishes erythrocytosis with inherited defects in oxygen-sensing pathway from primary familial and congenital polycythaemia.
Br J Haematol
; 202(3): 674-685, 2023 08.
Article
in English
| MEDLINE | ID: mdl-37246471
3.
Increased blood reactive oxygen species and hepcidin in obstructive sleep apnea precludes expected erythrocytosis.
Am J Hematol
; 98(8): 1265-1276, 2023 08.
Article
in English
| MEDLINE | ID: mdl-37350302
4.
Deep Molecular Response Achieved with Chemotherapy, Dasatinib and Interferon α in Patients with Lymphoid Blast Crisis of Chronic Myeloid Leukaemia.
Int J Mol Sci
; 24(3)2023 Jan 20.
Article
in English
| MEDLINE | ID: mdl-36768374
5.
Developmental changes in iron metabolism and erythropoiesis in mice with human gain-of-function erythropoietin receptor.
Am J Hematol
; 97(10): 1286-1299, 2022 10.
Article
in English
| MEDLINE | ID: mdl-35815815
6.
The specific PKC-α inhibitor chelerythrine blunts costunolide-induced eryptosis.
Apoptosis
; 25(9-10): 674-685, 2020 10.
Article
in English
| MEDLINE | ID: mdl-32638182
7.
Oxidative DNA Damage, Inflammatory Signature, and Altered Erythrocytes Properties in Diamond-Blackfan Anemia.
Int J Mol Sci
; 21(24)2020 Dec 17.
Article
in English
| MEDLINE | ID: mdl-33348919
8.
Iron chelation and 2-oxoglutarate-dependent dioxygenase inhibition suppress mantle cell lymphoma's cyclin D1.
J Cell Mol Med
; 23(11): 7785-7795, 2019 11.
Article
in English
| MEDLINE | ID: mdl-31517438
9.
Two novel mutations (p.(Ser160Pro) and p.(Arg472Cys)) causing glucose-6-phosphate isomerase deficiency are associated with erythroid dysplasia and inappropriately suppressed hepcidin.
Blood Cells Mol Dis
; 69: 23-29, 2018 03.
Article
in English
| MEDLINE | ID: mdl-28803808
10.
Cooperation of germ line JAK2 mutations E846D and R1063H in hereditary erythrocytosis with megakaryocytic atypia.
Blood
; 128(10): 1418-23, 2016 09 08.
Article
in English
| MEDLINE | ID: mdl-27389715
11.
Hemoglobinopathies.
Vnitr Lek
; 64(5): 476-487, 2018.
Article
in English
| MEDLINE | ID: mdl-30193516
12.
Loss of Major DNase I Hypersensitive Sites in Duplicated ß-globin Gene Cluster Incompletely Silences HBB Gene Expression.
Hum Mutat
; 37(11): 1153-1156, 2016 11.
Article
in English
| MEDLINE | ID: mdl-27492747
13.
Molecular characterization of six new cases of red blood cell hexokinase deficiency yields four novel mutations in HK1.
Blood Cells Mol Dis
; 59: 71-6, 2016 07.
Article
in English
| MEDLINE | ID: mdl-27282571
14.
RUNX1 and NF-E2 upregulation is not specific for MPNs, but is seen in polycythemic disorders with augmented HIF signaling.
Blood
; 123(3): 391-4, 2014 Jan 16.
Article
in English
| MEDLINE | ID: mdl-24297870
15.
Molecular Characterization of ß-Thalassemia in the Czech and Slovak Populations: Mediterranean, Asian and Unique Mutations.
Hemoglobin
; 40(3): 156-62, 2016 Jun.
Article
in English
| MEDLINE | ID: mdl-26956563
16.
Novel homozygous VHL mutation in exon 2 is associated with congenital polycythemia but not with cancer.
Blood
; 121(19): 3918-24, 2013 May 09.
Article
in English
| MEDLINE | ID: mdl-23538339
17.
Cooccurring JAK2 V617F and R1063H mutations increase JAK2 signaling and neutrophilia in myeloproliferative neoplasms.
Blood
; 132(25): 2695-2699, 2018 12 20.
Article
in English
| MEDLINE | ID: mdl-30377194
18.
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.
Br J Haematol
; 165(4): 556-63, 2014 May.
Article
in English
| MEDLINE | ID: mdl-24533562
19.
DMT1-mutant erythrocytes have shortened life span, accelerated glycolysis and increased oxidative stress.
Cell Physiol Biochem
; 34(6): 2221-31, 2014.
Article
in English
| MEDLINE | ID: mdl-25562168
20.
ß-Thalassemia due to intronic LINE-1 insertion in the ß-globin gene (HBB): molecular mechanisms underlying reduced transcript levels of the ß-globin(L1) allele.
Hum Mutat
; 34(10): 1361-5, 2013 Oct.
Article
in English
| MEDLINE | ID: mdl-23878091