180 related articles for article (PubMed ID: 24533580)
1. Polycythaemia-inducing mutations in the erythropoietin receptor (EPOR): mechanism and function as elucidated by epidermal growth factor receptor-EPOR chimeras.
Gross M; Ben-Califa N; McMullin MF; Percy MJ; Bento C; Cario H; Minkov M; Neumann D
Br J Haematol; 2014 May; 165(4):519-28. PubMed ID: 24533580
[TBL] [Abstract][Full Text] [Related]
2. Erythropoietin hypersensitivity in primary familial and congenital polycythemia: role of tyrosines Y285 and Y344 in erythropoietin receptor cytoplasmic domain.
Arcasoy MO; Karayal AF
Biochim Biophys Acta; 2005 Apr; 1740(1):17-28. PubMed ID: 15878737
[TBL] [Abstract][Full Text] [Related]
3. Increased cell surface expression of C-terminal truncated erythropoietin receptors in polycythemia.
Motohashi T; Nakamura Y; Osawa M; Hiroyama T; Iwama A; Shibuya A; Nakauchi H
Eur J Haematol; 2001 Aug; 67(2):88-93. PubMed ID: 11722595
[TBL] [Abstract][Full Text] [Related]
4. Genetic heterogeneity of primary familial and congenital polycythemia.
Kralovics R; Prchal JT
Am J Hematol; 2001 Oct; 68(2):115-21. PubMed ID: 11559951
[TBL] [Abstract][Full Text] [Related]
5. Two new EPO receptor mutations: truncated EPO receptors are most frequently associated with primary familial and congenital polycythemias.
Kralovics R; Indrak K; Stopka T; Berman BW; Prchal JF; Prchal JT
Blood; 1997 Sep; 90(5):2057-61. PubMed ID: 9292543
[TBL] [Abstract][Full Text] [Related]
6. Familial polycythemia due to truncations of the erythropoietin receptor.
Forget BG; Degan BA; Arcasoy MO
Trans Am Clin Climatol Assoc; 2000; 111():38-44; discussion 44-5. PubMed ID: 10881330
[TBL] [Abstract][Full Text] [Related]
7. A human erythropoietin receptor gene mutant causing familial erythrocytosis is associated with deregulation of the rates of Jak2 and Stat5 inactivation.
Arcasoy MO; Harris KW; Forget BG
Exp Hematol; 1999 Jan; 27(1):63-74. PubMed ID: 9923445
[TBL] [Abstract][Full Text] [Related]
8. "Benign erythrocytosis" and other familial and congenital polycythemias.
Prchal JT; Sokol L
Eur J Haematol; 1996 Oct; 57(4):263-8. PubMed ID: 8982288
[TBL] [Abstract][Full Text] [Related]
9. Delayed hemoglobin switching and perinatal neocytolysis in mice with gain-of-function erythropoietin receptor.
Divoky V; Song J; Horvathova M; Kralova B; Votavova H; Prchal JT; Yoon D
J Mol Med (Berl); 2016 May; 94(5):597-608. PubMed ID: 26706855
[TBL] [Abstract][Full Text] [Related]
10. Advances in understanding the pathogenesis of primary familial and congenital polycythaemia.
Huang LJ; Shen YM; Bulut GB
Br J Haematol; 2010 Mar; 148(6):844-52. PubMed ID: 20096014
[TBL] [Abstract][Full Text] [Related]
11. Primary familial polycythaemia associated with a novel point mutation in the erythropoietin receptor.
Furukawa T; Narita M; Sakaue M; Otsuka T; Kuroha T; Masuko M; Azegami T; Kishi K; Takahashi M; Utsumi J; Koike T; Aizawa Y
Br J Haematol; 1997 Oct; 99(1):222-7. PubMed ID: 9359528
[TBL] [Abstract][Full Text] [Related]
12. The erythropoietin receptor gene is not linked with the polycythemia phenotype in a family with autosomal dominant primary polycythemia.
Kralovics R; Sokol L; Broxson EH; Prchal JT
Proc Assoc Am Physicians; 1997 Nov; 109(6):580-5. PubMed ID: 9394420
[TBL] [Abstract][Full Text] [Related]
13. Absence of polycythemia in a child with a unique erythropoietin receptor mutation in a family with autosomal dominant primary polycythemia.
Kralovics R; Sokol L; Prchal JT
J Clin Invest; 1998 Jul; 102(1):124-9. PubMed ID: 9649565
[TBL] [Abstract][Full Text] [Related]
14. Mimicry of erythropoietin and interleukin-6 signalling by an antibody/cytokine receptor chimera in murine myeloid 32D cells.
Kawahara M; Ueda H; Tsumoto K; Kumagai I; Nagamune T
J Biochem; 2007 Apr; 141(4):563-71. PubMed ID: 17442704
[TBL] [Abstract][Full Text] [Related]
15. A possible involvement of Stat5 in erythropoietin-induced hemoglobin synthesis.
Wakao H; Chida D; Damen JE; Krystal G; Miyajima A
Biochem Biophys Res Commun; 1997 May; 234(1):198-205. PubMed ID: 9168989
[TBL] [Abstract][Full Text] [Related]
16. Cbl ubiquitination of p85 is essential for Epo-induced EpoR endocytosis.
Bulut GB; Sulahian R; Yao H; Huang LJ
Blood; 2013 Dec; 122(24):3964-72. PubMed ID: 24113870
[TBL] [Abstract][Full Text] [Related]
17. A new point mutation in EPOR inducing a short deletion in congenital erythrocytosis.
Chauveau A; Luque Paz D; Lecucq L; Le Gac G; Le Maréchal C; Gueguen P; Berthou C; Ugo V
Br J Haematol; 2016 Feb; 172(3):475-7. PubMed ID: 26010769
[No Abstract] [Full Text] [Related]
18. Primary familial polycythemia: a frameshift mutation in the erythropoietin receptor gene and increased sensitivity of erythroid progenitors to erythropoietin.
Sokol L; Luhovy M; Guan Y; Prchal JF; Semenza GL; Prchal JT
Blood; 1995 Jul; 86(1):15-22. PubMed ID: 7795221
[TBL] [Abstract][Full Text] [Related]
19. Hereditary erythrocytosis, thrombocytosis and neutrophilia.
Hong WJ; Gotlib J
Best Pract Res Clin Haematol; 2014 Jun; 27(2):95-106. PubMed ID: 25189721
[TBL] [Abstract][Full Text] [Related]
20. Ligand-induced EpoR internalization is mediated by JAK2 and p85 and is impaired by mutations responsible for primary familial and congenital polycythemia.
Sulahian R; Cleaver O; Huang LJ
Blood; 2009 May; 113(21):5287-97. PubMed ID: 19336760
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
