BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

328 related articles for article (PubMed ID: 25189721)

  • 1. 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]  

  • 2. Diagnostic workflow for hereditary erythrocytosis and thrombocytosis.
    McMullin MF
    Hematology Am Soc Hematol Educ Program; 2019 Dec; 2019(1):391-396. PubMed ID: 31808840
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular study of congenital erythrocytosis in 70 unrelated patients revealed a potential causal mutation in less than half of the cases (Where is/are the missing gene(s)?).
    Bento C; Almeida H; Maia TM; Relvas L; Oliveira AC; Rossi C; Girodon F; Fernandez-Lago C; Aguado-Diaz A; Fraga C; Costa RM; Araújo AL; Silva J; Vitória H; Miguel N; Silveira MP; Martin-Nuñez G; Ribeiro ML
    Eur J Haematol; 2013 Oct; 91(4):361-8. PubMed ID: 23859443
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic variants of erythropoietin (EPO) and EPO receptor genes in familial erythrocytosis.
    Vočanec D; Prijatelj T; Debeljak N; Kunej T
    Int J Lab Hematol; 2019 Apr; 41(2):162-167. PubMed ID: 30507031
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Thrombocytosis.
    Skoda RC
    Hematology Am Soc Hematol Educ Program; 2009; ():159-67. PubMed ID: 20008195
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic basis of congenital erythrocytosis: mutation update and online databases.
    Bento C; Percy MJ; Gardie B; Maia TM; van Wijk R; Perrotta S; Della Ragione F; Almeida H; Rossi C; Girodon F; Aström M; Neumann D; Schnittger S; Landin B; Minkov M; Randi ML; Richard S; Casadevall N; Vainchenker W; Rives S; Hermouet S; Ribeiro ML; McMullin MF; Cario H; ; Chauveau A; Gimenez-Roqueplo AP; Bressac-de-Paillerets B; Altindirek D; Lorenzo F; Lambert F; Dan H; Gad-Lapiteau S; Catarina Oliveira A; Rossi C; Fraga C; Taradin G; Martin-Nuñez G; Vitória H; Diaz Aguado H; Palmblad J; Vidán J; Relvas L; Ribeiro ML; Luigi Larocca M; Luigia Randi M; Pedro Silveira M; Percy M; Gross M; Marques da Costa R; Beshara S; Ben-Ami T; Ugo V;
    Hum Mutat; 2014 Jan; 35(1):15-26. PubMed ID: 24115288
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Hereditary thrombocytosis: the genetic landscape.
    Han EY; Catherwood M; McMullin MF
    Br J Haematol; 2021 Sep; 194(6):1098-1105. PubMed ID: 34341988
    [No Abstract]   [Full Text] [Related]  

  • 9. The complete evaluation of erythrocytosis: congenital and acquired.
    Patnaik MM; Tefferi A
    Leukemia; 2009 May; 23(5):834-44. PubMed ID: 19295544
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Algorithmic evaluation of hereditary erythrocytosis: Pathways and caveats.
    Oliveira JL
    Int J Lab Hematol; 2019 May; 41 Suppl 1():89-94. PubMed ID: 31069987
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Narrative review: Thrombocytosis, polycythemia vera, and JAK2 mutations: The phenotypic mimicry of chronic myeloproliferation.
    Spivak JL
    Ann Intern Med; 2010 Mar; 152(5):300-6. PubMed ID: 20194236
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Advances in understanding the pathogenesis of familial thrombocythaemia.
    Teofili L; Larocca LM
    Br J Haematol; 2011 Mar; 152(6):701-12. PubMed ID: 21303356
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Familial chronic myeloproliferative disorders: the state of the art.
    Rumi E
    Hematol Oncol; 2008 Sep; 26(3):131-8. PubMed ID: 18484677
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A family with hereditary thrombocythaemia and normal genes for thrombopoietin and c-Mpl.
    Tecuceanu N; Dardik R; Rabizadeh E; Raanani P; Inbal A
    Br J Haematol; 2006 Nov; 135(3):348-51. PubMed ID: 16995886
    [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. The frequency of JAK2 exon 12 mutations in idiopathic erythrocytosis patients with low serum erythropoietin levels.
    Percy MJ; Scott LM; Erber WN; Harrison CN; Reilly JT; Jones FG; Green AR; McMullin MF
    Haematologica; 2007 Dec; 92(12):1607-14. PubMed ID: 18055983
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Characterization of murine JAK2V617F-positive myeloproliferative disease.
    Bumm TG; Elsea C; Corbin AS; Loriaux M; Sherbenou D; Wood L; Deininger J; Silver RT; Druker BJ; Deininger MW
    Cancer Res; 2006 Dec; 66(23):11156-65. PubMed ID: 17145859
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The MPL mutation.
    Guglielmelli P; Calabresi L
    Int Rev Cell Mol Biol; 2021; 365():163-178. PubMed ID: 34756243
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Congenital erythrocytosis.
    Mallik N; Das R; Malhotra P; Sharma P
    Eur J Haematol; 2021 Jul; 107(1):29-37. PubMed ID: 33840141
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Markers of myeloproliferative diseases in childhood polycythemia vera and essential thrombocythemia.
    Teofili L; Giona F; Martini M; Cenci T; Guidi F; Torti L; Palumbo G; Amendola A; Foà R; Larocca LM
    J Clin Oncol; 2007 Mar; 25(9):1048-53. PubMed ID: 17369568
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.