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1 447 (0,127s)

Result

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

The role of somatic JAK2 mutations in clonal myeloproliferative neoplasms is well established. Germline JAK2 mutations have previously been described in cases with hereditary polyclonal thrombocytosis. In our work, for the first time in the ...

FD - Onkologie a hematologie

  • 2016
  • Jx
  • Link
Result

Idiopathic erythrocytosis and other non-clonal polycythemias

Idiopathic erythrocytosis, other non-clonal polycythemias...

FD - Onkologie a hematologie

  • 2006
  • Jx
Result

Erythrocytosis in children and adolescents-classification, characterization, and consensus recommendations for the diagnostic approach

changes in polycythemia vera (PV) and of different types of congenital erythrocytosis to patients with erythrocytosis. Although widely accepted for adult patients this approach by erythrocytosis. The "congenital erythr...

FD - Onkologie a hematologie

  • 2013
  • Jx
  • Link
Result

Erythrocytosis in Children and Adolescents-Classification, Characterization, and Consensus Recommendations for the Diagnostic Approach

Erythrocytosis is characterized by the expansion of the erythrocyte compartment range. Absolute erythrocytosis as defined by an increase of the total red cell mass is distinct from relative erythrocytosis which is caused by...

FD - Onkologie a hematologie

  • 2013
  • Jx
Result

Developmental changes in iron metabolism and erythropoiesis in mice with human erythropoietin receptor

erythrocytosis-causing human EPOR gene mutation (mtHEPOR) and shown that mtHEPOR embryos develop erythrocytosis around embryonic day (ED)17.5, followed by transient amelioration of erythrocytosis in perinatal life and its ...

Cell biology

  • 2022
  • Jimp
  • Link
Result

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

The molecular pathophysiology of congenital erythrocytosis, a rare red blood cell disorder characterized by increased red cell mass, is heterogenous and not completely understood. The disease-causing pathogenic variant in many patients remai...

Hematology

  • 2023
  • Jimp
  • Link
Result

The role of erythrocytapheresis in secondary erythrocytosis therapy

The autors describe their 20 years experience with the Large Volume Erythrocytapheresis.They carry out about 1000 hemaphereses/year,out of which LVE accounted for 5-10 %....

FD - Onkologie a hematologie

  • 2002
  • Jx
Result

Erythrocytosis in kidney transplantation

FJ - Chirurgie včetně transplantologie

  • 1994
  • X
Result

A novel germline hyperactivating JAK2 mutation L604F

Somatic JAK2 mutations are the main molecular cause of the vast majority of polycythemia vera (PV) cases. According to a recent structural model, the prevalent acquired V617F mutation improves the stability of the JAK2 dimer, thereby enhancing the co...

Hematology

  • 2003
  • Jimp
  • Link
Result

Losartan, an angiotensin II type 1 receptor antagonist, lowers hematocrit in posttransplant erythrocytosis.

FD - Onkologie a hematologie

  • 1998
  • Jx
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