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Elevated erythroferrone distinguishes erythrocytosis with inherited defects in oxygen-sensing pathway from primary familial and congenital polycythaemia.
Sochorcova L, Hlusickova Kapralova K, Fialova Kucerova J, Pospisilova D, Prochazkova D, Jahoda O, Kurekova S, Kralova B, Divoka M, Navratilova J, Manakova J, Kriegova E, Indrak K, Faber E, Divoky V, Horvathova M. Sochorcova L, et al. Among authors: kralova b. Br J Haematol. 2023 Aug;202(3):674-685. doi: 10.1111/bjh.18891. Epub 2023 May 28. Br J Haematol. 2023. PMID: 37246471
Cooperation of germ line JAK2 mutations E846D and R1063H in hereditary erythrocytosis with megakaryocytic atypia.
Kapralova K, Horvathova M, Pecquet C, Fialova Kucerova J, Pospisilova D, Leroy E, Kralova B, Milosevic Feenstra JD, Schischlik F, Kralovics R, Constantinescu SN, Divoky V. Kapralova K, et al. Among authors: kralova b. Blood. 2016 Sep 8;128(10):1418-23. doi: 10.1182/blood-2016-02-698951. Epub 2016 Jul 7. Blood. 2016. PMID: 27389715 Free article.
Cooccurring JAK2 V617F and R1063H mutations increase JAK2 signaling and neutrophilia in myeloproliferative neoplasms.
Mambet C, Babosova O, Defour JP, Leroy E, Necula L, Stanca O, Tatic A, Berbec N, Coriu D, Belickova M, Kralova B, Lanikova L, Vesela J, Pecquet C, Saussoy P, Havelange V, Diaconu CC, Divoky V, Constantinescu SN. Mambet C, et al. Among authors: kralova b. Blood. 2018 Dec 20;132(25):2695-2699. doi: 10.1182/blood-2018-04-843060. Epub 2018 Oct 30. Blood. 2018. PMID: 30377194 Free article. No abstract available.
Alpha-L-fucosidase isoenzyme iso2 from Paenibacillus thiaminolyticus.
Benešová E, Lipovová P, Krejzová J, Kovaľová T, Buchtová P, Spiwok V, Králová B. Benešová E, et al. Among authors: kralova b. BMC Biotechnol. 2015 May 27;15:36. doi: 10.1186/s12896-015-0160-x. BMC Biotechnol. 2015. PMID: 26013545 Free PMC article.
38 results