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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

191 related items for PubMed ID: 33840141

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

  • 2. Update on mutations in the HIF: EPO pathway and their role in erythrocytosis.
    Lappin TR, Lee FS.
    Blood Rev; 2019 Sep; 37():100590. PubMed ID: 31350093
    [Abstract] [Full Text] [Related]

  • 3. The HIF pathway and erythrocytosis.
    Lee FS, Percy MJ.
    Annu Rev Pathol; 2011 Sep; 6():165-92. PubMed ID: 20939709
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. Erythrocytosis-associated HIF-2alpha mutations demonstrate a critical role for residues C-terminal to the hydroxylacceptor proline.
    Furlow PW, Percy MJ, Sutherland S, Bierl C, McMullin MF, Master SR, Lappin TR, Lee FS.
    J Biol Chem; 2009 Apr 03; 284(14):9050-8. PubMed ID: 19208626
    [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, ECE-Consortium, 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, ECE-Consortium.
    Hum Mutat; 2014 Jan 03; 35(1):15-26. PubMed ID: 24115288
    [Abstract] [Full Text] [Related]

  • 7. Involvement of oxygen-sensing pathways in physiologic and pathologic erythropoiesis.
    Semenza GL.
    Blood; 2009 Sep 03; 114(10):2015-9. PubMed ID: 19494350
    [Abstract] [Full Text] [Related]

  • 8. Notch Downregulation and Extramedullary Erythrocytosis in Hypoxia-Inducible Factor Prolyl 4-Hydroxylase 2-Deficient Mice.
    Myllymäki MNM, Määttä J, Dimova EY, Izzi V, Väisänen T, Myllyharju J, Koivunen P, Serpi R.
    Mol Cell Biol; 2017 Jan 15; 37(2):. PubMed ID: 27821476
    [Abstract] [Full Text] [Related]

  • 9. Oxygen sensing: recent insights from idiopathic erythrocytosis.
    Lee FS, Percy MJ, McMullin MF.
    Cell Cycle; 2006 May 15; 5(9):941-5. PubMed ID: 16687917
    [Abstract] [Full Text] [Related]

  • 10. A novel erythrocytosis-associated PHD2 mutation suggests the location of a HIF binding groove.
    Percy MJ, Furlow PW, Beer PA, Lappin TR, McMullin MF, Lee FS.
    Blood; 2007 Sep 15; 110(6):2193-6. PubMed ID: 17579185
    [Abstract] [Full Text] [Related]

  • 11. Erythrocytosis associated with a novel missense mutation in the HIF2A gene.
    van Wijk R, Sutherland S, Van Wesel AC, Huizinga EG, Percy MJ, Bierings M, Lee FS.
    Haematologica; 2010 May 15; 95(5):829-32. PubMed ID: 20007141
    [Abstract] [Full Text] [Related]

  • 12. HIF pathway mutations and erythrocytosis.
    McMullin MF.
    Expert Rev Hematol; 2010 Feb 15; 3(1):93-101. PubMed ID: 21082936
    [Abstract] [Full Text] [Related]

  • 13. Hereditary erythrocytosis, thrombocytosis and neutrophilia.
    Hong WJ, Gotlib J.
    Best Pract Res Clin Haematol; 2014 Jun 15; 27(2):95-106. PubMed ID: 25189721
    [Abstract] [Full Text] [Related]

  • 14. Novel mutations in the EPO-R, VHL and EPAS1 genes in the Congenital Erythrocytosis patients.
    Chandrasekhar C, Pasupuleti SK, Sarma PVGK.
    Blood Cells Mol Dis; 2020 Nov 15; 85():102479. PubMed ID: 32739800
    [Abstract] [Full Text] [Related]

  • 15. Polycythemia and oxygen sensing.
    Maran J, Prchal J.
    Pathol Biol (Paris); 2004 Jun 15; 52(5):280-4. PubMed ID: 15217714
    [Abstract] [Full Text] [Related]

  • 16. A novel biological function of soluble biglycan: Induction of erythropoietin production and polycythemia.
    Frey H, Moreth K, Hsieh LT, Zeng-Brouwers J, Rathkolb B, Fuchs H, Gailus-Durner V, Iozzo RV, de Angelis MH, Schaefer L.
    Glycoconj J; 2017 Jun 15; 34(3):393-404. PubMed ID: 27600268
    [Abstract] [Full Text] [Related]

  • 17. Erythrocytosis associated with EPAS1(HIF2A), EGLN1(PHD2), VHL, EPOR or BPGM mutations: The Mayo Clinic experience.
    Gangat N, Oliveira JL, Porter TR, Hoyer JD, Al-Kali A, Patnaik MM, Pardanani A, Tefferi A.
    Haematologica; 2022 May 01; 107(5):1201-1204. PubMed ID: 35142155
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Erythrocytosis and pulmonary hypertension in a mouse model of human HIF2A gain of function mutation.
    Tan Q, Kerestes H, Percy MJ, Pietrofesa R, Chen L, Khurana TS, Christofidou-Solomidou M, Lappin TR, Lee FS.
    J Biol Chem; 2013 Jun 14; 288(24):17134-44. PubMed ID: 23640890
    [Abstract] [Full Text] [Related]

  • 20. Regulation of Erythropoiesis by the Hypoxia-Inducible Factor Pathway: Effects of Genetic and Pharmacological Perturbations.
    Semenza GL.
    Annu Rev Med; 2023 Jan 27; 74():307-319. PubMed ID: 35773226
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.