These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

157 related articles for article (PubMed ID: 29269524)

  • 1. New pathogenic mechanisms induced by germline erythropoietin receptor mutations in primary erythrocytosis.
    Pasquier F; Marty C; Balligand T; Verdier F; Grosjean S; Gryshkova V; Raslova H; Constantinescu SN; Casadevall N; Vainchenker W; Bellanné-Chantelot C; Plo I
    Haematologica; 2018 Apr; 103(4):575-586. PubMed ID: 29269524
    [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. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. A novel mutation in the erythropoietin receptor gene is associated with familial erythrocytosis.
    Arcasoy MO; Karayal AF; Segal HM; Sinning JG; Forget BG
    Blood; 2002 Apr; 99(8):3066-9. PubMed ID: 11929803
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Erythropoietin receptor mutations associated with familial erythrocytosis cause hypersensitivity to erythropoietin in the heterozygous state.
    Watowich SS; Xie X; Klingmuller U; Kere J; Lindlof M; Berglund S; de la Chapelle A
    Blood; 1999 Oct; 94(7):2530-2. PubMed ID: 10498627
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Familial erythrocytosis associated with a short deletion in the erythropoietin receptor gene.
    Arcasoy MO; Degar BA; Harris KW; Forget BG
    Blood; 1997 Jun; 89(12):4628-35. PubMed ID: 9192789
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Mouse model of congenital polycythemia: Homologous replacement of murine gene by mutant human erythropoietin receptor gene.
    Divoky V; Liu Z; Ryan TM; Prchal JF; Townes TM; Prchal JT
    Proc Natl Acad Sci U S A; 2001 Jan; 98(3):986-91. PubMed ID: 11158582
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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
    Blood; 2016 Sep; 128(10):1418-23. PubMed ID: 27389715
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutation in the negative regulatory element of the erythropoietin receptor gene in a case of sporadic primary polycythemia.
    Sokol L; Prchal JF; D'Andrea A; Rado TA; Prchal JT
    Exp Hematol; 1994 May; 22(5):447-53. PubMed ID: 8174675
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular genetic analyses in familial and sporadic congenital primary erythrocytosis.
    Rives S; Pahl HL; Florensa L; Bellosillo B; Neusuess A; Estella J; Debatin KM; Kohne E; Schwarz K; Cario H
    Haematologica; 2007 May; 92(5):674-7. PubMed ID: 17488692
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. "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]  

  • 18. 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]  

  • 19. 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]  

  • 20. A novel mutation of the erythropoietin receptor gene associated with primary familial and congenital polycythaemia.
    O'Rourke K; Fairbairn DJ; Jackson KA; Morris KL; Tey SK; Kennedy GA
    Int J Hematol; 2011 Apr; 93(4):542-544. PubMed ID: 21437635
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.