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

Journal Abstract Search


406 related items for PubMed ID: 31350093

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. The HIF pathway and erythrocytosis.
    Lee FS, Percy MJ.
    Annu Rev Pathol; 2011 Apr 03; 6():165-92. PubMed ID: 20939709
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. 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]

  • 6. Congenital erythrocytosis.
    Mallik N, Das R, Malhotra P, Sharma P.
    Eur J Haematol; 2021 Jul 15; 107(1):29-37. PubMed ID: 33840141
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. VHL gene methylation contributes to excessive erythrocytosis in chronic mountain sickness rat model by upregulating the HIF-2α/EPO pathway.
    Yang M, Zhu M, Song K, Wuren T, Yan J, Ge RL, Ji L, Cui S.
    Life Sci; 2021 Feb 01; 266():118873. PubMed ID: 33309718
    [Abstract] [Full Text] [Related]

  • 9. Oxygen sensing: recent insights from idiopathic erythrocytosis.
    Lee FS, Percy MJ, McMullin MF.
    Cell Cycle; 2006 May 01; 5(9):941-5. PubMed ID: 16687917
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Mutations of von Hippel-Lindau tumor-suppressor gene and congenital polycythemia.
    Pastore Y, Jedlickova K, Guan Y, Liu E, Fahner J, Hasle H, Prchal JF, Prchal JT.
    Am J Hum Genet; 2003 Aug 01; 73(2):412-9. PubMed ID: 12844285
    [Abstract] [Full Text] [Related]

  • 16. A knock-in mouse model of human PHD2 gene-associated erythrocytosis establishes a haploinsufficiency mechanism.
    Arsenault PR, Pei F, Lee R, Kerestes H, Percy MJ, Keith B, Simon MC, Lappin TRJ, Khurana TS, Lee FS.
    J Biol Chem; 2013 Nov 22; 288(47):33571-33584. PubMed ID: 24121508
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 19. Erythrocytosis: the HIF pathway in control.
    Franke K, Gassmann M, Wielockx B.
    Blood; 2013 Aug 15; 122(7):1122-8. PubMed ID: 23733342
    [Abstract] [Full Text] [Related]

  • 20. Regulation of adult erythropoiesis by prolyl hydroxylase domain proteins.
    Takeda K, Aguila HL, Parikh NS, Li X, Lamothe K, Duan LJ, Takeda H, Lee FS, Fong GH.
    Blood; 2008 Mar 15; 111(6):3229-35. PubMed ID: 18056838
    [Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 21.