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

612 related items for PubMed ID: 9620771

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

  • 2. Obesity in the mouse model of pro-opiomelanocortin deficiency responds to peripheral melanocortin.
    Yaswen L, Diehl N, Brennan MB, Hochgeschwender U.
    Nat Med; 1999 Sep; 5(9):1066-70. PubMed ID: 10470087
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Obesity due to proopiomelanocortin deficiency: three new cases and treatment trials with thyroid hormone and ACTH4-10.
    Krude H, Biebermann H, Schnabel D, Tansek MZ, Theunissen P, Mullis PE, Grüters A.
    J Clin Endocrinol Metab; 2003 Oct; 88(10):4633-40. PubMed ID: 14557433
    [Abstract] [Full Text] [Related]

  • 6. A case of early-onset obesity, hypocortisolism, and skin pigmentation problem due to a novel homozygous mutation in the proopiomelanocortin (POMC) gene in an Indian boy.
    Hung CN, Poon WT, Lee CY, Law CY, Chan AY.
    J Pediatr Endocrinol Metab; 2012 Oct; 25(1-2):175-9. PubMed ID: 22570972
    [Abstract] [Full Text] [Related]

  • 7. Proopiomelanocortin (POMC): the cutaneous roles of its melanocortin products and receptors.
    Millington GW.
    Clin Exp Dermatol; 2006 May; 31(3):407-12. PubMed ID: 16681590
    [Abstract] [Full Text] [Related]

  • 8. Early-onset severe obesity with ACTH deficiency and red hair in a boy: the POMC deficiency.
    Ozen S, Aldemir O.
    Genet Couns; 2012 May; 23(4):493-5. PubMed ID: 23431750
    [Abstract] [Full Text] [Related]

  • 9. A missense mutation disrupting a dibasic prohormone processing site in pro-opiomelanocortin (POMC) increases susceptibility to early-onset obesity through a novel molecular mechanism.
    Challis BG, Pritchard LE, Creemers JW, Delplanque J, Keogh JM, Luan J, Wareham NJ, Yeo GS, Bhattacharyya S, Froguel P, White A, Farooqi IS, O'Rahilly S.
    Hum Mol Genet; 2002 Aug 15; 11(17):1997-2004. PubMed ID: 12165561
    [Abstract] [Full Text] [Related]

  • 10. Systematic mutation screening of the pro-opiomelanocortin gene: identification of several genetic variants including three different insertions, one nonsense and two missense point mutations in probands of different weight extremes.
    Hinney A, Becker I, Heibült O, Nottebom K, Schmidt A, Ziegler A, Mayer H, Siegfried W, Blum WF, Remschmidt H, Hebebrand J.
    J Clin Endocrinol Metab; 1998 Oct 15; 83(10):3737-41. PubMed ID: 9768693
    [Abstract] [Full Text] [Related]

  • 11. Two Cases With an Early Presented Proopiomelanocortin Deficiency-A Long-Term Follow-Up and Systematic Literature Review.
    Gregoric N, Groselj U, Bratina N, Debeljak M, Zerjav Tansek M, Suput Omladic J, Kovac J, Battelino T, Kotnik P, Avbelj Stefanija M.
    Front Endocrinol (Lausanne); 2021 Oct 15; 12():689387. PubMed ID: 34177811
    [Abstract] [Full Text] [Related]

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

  • 13. Unexpected endocrine features and normal pigmentation in a young adult patient carrying a novel homozygous mutation in the POMC gene.
    Clément K, Dubern B, Mencarelli M, Czernichow P, Ito S, Wakamatsu K, Barsh GS, Vaisse C, Leger J.
    J Clin Endocrinol Metab; 2008 Dec 15; 93(12):4955-62. PubMed ID: 18765507
    [Abstract] [Full Text] [Related]

  • 14. The neuroendocrine circuitry controlled by POMC, MSH, and AGRP.
    Biebermann H, Kühnen P, Kleinau G, Krude H.
    Handb Exp Pharmacol; 2012 Dec 15; (209):47-75. PubMed ID: 22249810
    [Abstract] [Full Text] [Related]

  • 15. Obesity and Hyperphagia With Increased Defective ACTH: A Novel POMC Variant.
    van der Valk ES, Kleinendorst L, Delhanty PJD, van der Voorn B, Visser JA, van Haelst MM, de Graaff LCG, Huisman M, White A, Ito S, Wakamatsu K, de Rijke YB, van den Akker ELT, Iyer AM, van Rossum EFC.
    J Clin Endocrinol Metab; 2022 Aug 18; 107(9):e3699-e3704. PubMed ID: 35737586
    [Abstract] [Full Text] [Related]

  • 16. Delayed diagnosis of proopiomelanocortin (POMC) deficiency with type 1 diabetes in a 9-year-old girl and her infant sibling.
    Ozsu E, Bahm A.
    J Pediatr Endocrinol Metab; 2017 Oct 26; 30(10):1137-1140. PubMed ID: 28915118
    [Abstract] [Full Text] [Related]

  • 17. [Monogenic forms of obesity: from mice to human].
    Clément K.
    Ann Endocrinol (Paris); 2000 Dec 26; 61 Suppl 6():39-49. PubMed ID: 11148335
    [Abstract] [Full Text] [Related]

  • 18. Duplication of the POMC gene in the paddlefish (Polyodon spathula): analysis of gamma-MSH, ACTH, and beta-endorphin regions of ray-finned fish POMC.
    Danielson PB, Alrubaian J, Muller M, Redding JM, Dores RM.
    Gen Comp Endocrinol; 1999 Nov 26; 116(2):164-77. PubMed ID: 10562447
    [Abstract] [Full Text] [Related]

  • 19. Lack of red hair phenotype in a North-African obese child homozygous for a novel POMC null mutation: nonsense-mediated decay RNA evaluation and hair pigment chemical analysis.
    Cirillo G, Marini R, Ito S, Wakamatsu K, Scianguetta S, Bizzarri C, Romano A, Grandone A, Perrone L, Cappa M, Miraglia Del Giudice E.
    Br J Dermatol; 2012 Dec 26; 167(6):1393-5. PubMed ID: 22612534
    [No Abstract] [Full Text] [Related]

  • 20. A fully functional proopiomelanocortin/melanocortin-1 receptor system regulates the differentiation of human scalp hair follicle melanocytes.
    Kauser S, Thody AJ, Schallreuter KU, Gummer CL, Tobin DJ.
    Endocrinology; 2005 Feb 26; 146(2):532-43. PubMed ID: 15498881
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 31.