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

256 related items for PubMed ID: 18431404

  • 1. A cAMP-specific phosphodiesterase (PDE8B) that is mutated in adrenal hyperplasia is expressed widely in human and mouse tissues: a novel PDE8B isoform in human adrenal cortex.
    Horvath A, Giatzakis C, Tsang K, Greene E, Osorio P, Boikos S, Libè R, Patronas Y, Robinson-White A, Remmers E, Bertherat J, Nesterova M, Stratakis CA.
    Eur J Hum Genet; 2008 Oct; 16(10):1245-53. PubMed ID: 18431404
    [Abstract] [Full Text] [Related]

  • 2. Abnormalities of cAMP signaling are present in adrenocortical lesions associated with ACTH-independent Cushing syndrome despite the absence of mutations in known genes.
    Bimpaki EI, Nesterova M, Stratakis CA.
    Eur J Endocrinol; 2009 Jul; 161(1):153-61. PubMed ID: 19429701
    [Abstract] [Full Text] [Related]

  • 3. Phosphodiesterase 11A expression in the adrenal cortex, primary pigmented nodular adrenocortical disease, and other corticotropin-independent lesions.
    Boikos SA, Horvath A, Heyerdahl S, Stein E, Robinson-White A, Bossis I, Bertherat J, Carney JA, Stratakis CA.
    Horm Metab Res; 2008 May; 40(5):347-53. PubMed ID: 18491255
    [Abstract] [Full Text] [Related]

  • 4. Mutation in PDE8B, a cyclic AMP-specific phosphodiesterase in adrenal hyperplasia.
    Horvath A, Mericq V, Stratakis CA.
    N Engl J Med; 2008 Feb 14; 358(7):750-2. PubMed ID: 18272904
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. The roles of cyclic nucleotide phosphodiesterases (PDEs) in steroidogenesis.
    Tsai LC, Beavo JA.
    Curr Opin Pharmacol; 2011 Dec 14; 11(6):670-5. PubMed ID: 21962440
    [Abstract] [Full Text] [Related]

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

  • 11. Molecular cloning and characterization of human PDE8B, a novel thyroid-specific isozyme of 3',5'-cyclic nucleotide phosphodiesterase.
    Hayashi M, Matsushima K, Ohashi H, Tsunoda H, Murase S, Kawarada Y, Tanaka T.
    Biochem Biophys Res Commun; 1998 Sep 29; 250(3):751-6. PubMed ID: 9784418
    [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. PRKAR1A mutations in primary pigmented nodular adrenocortical disease.
    Cazabat L, Ragazzon B, Groussin L, Bertherat J.
    Pituitary; 2006 Sep 29; 9(3):211-9. PubMed ID: 17036196
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 18. Pde8b haploinsufficiency in mice is associated with modest adrenal defects, impaired steroidogenesis, and male infertility, unaltered by concurrent PKA or Wnt activation.
    Leal LF, Szarek E, Berthon A, Nesterova M, Faucz FR, London E, Mercier C, Abu-Asab M, Starost MF, Dye L, Bilinska B, Kotula-Balak M, Antonini SR, Stratakis CA.
    Mol Cell Endocrinol; 2021 Feb 15; 522():111117. PubMed ID: 33338547
    [Abstract] [Full Text] [Related]

  • 19. Detection of somatic beta-catenin mutations in primary pigmented nodular adrenocortical disease (PPNAD).
    Tadjine M, Lampron A, Ouadi L, Horvath A, Stratakis CA, Bourdeau I.
    Clin Endocrinol (Oxf); 2008 Sep 15; 69(3):367-73. PubMed ID: 18419788
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 13.