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PUBMED FOR HANDHELDS

Journal Abstract Search


136 related items for PubMed ID: 33666293

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  • 24. Quality of life outcomes in two phase 3 trials of setmelanotide in patients with obesity due to LEPR or POMC deficiency.
    Kühnen P, Wabitsch M, von Schnurbein J, Chirila C, Mallya UG, Callahan P, Gnanasakthy A, Poitou C, Krabusch PM, Stewart M, Clément K.
    Orphanet J Rare Dis; 2022 Feb 05; 17(1):38. PubMed ID: 35123544
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  • 32. [Monogenic forms of obesity: from mice to human].
    Clément K.
    Ann Endocrinol (Paris); 2000 Dec 05; 61 Suppl 6():39-49. PubMed ID: 11148335
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  • 33. Two Distinctive POMC Promoters Modify Gene Expression in Cushing Disease.
    Araki T, Tone Y, Yamamoto M, Kameda H, Ben-Shlomo A, Yamada S, Takeshita A, Yamamoto M, Kawakami Y, Tone M, Melmed S.
    J Clin Endocrinol Metab; 2021 Aug 18; 106(9):e3346-e3363. PubMed ID: 34061962
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  • 35. Hypothalamic-specific proopiomelanocortin deficiency reduces alcohol drinking in male and female mice.
    Zhou Y, Rubinstein M, Low MJ, Kreek MJ.
    Genes Brain Behav; 2017 Apr 18; 16(4):449-461. PubMed ID: 27870313
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  • 38. Mice lacking pro-opiomelanocortin are sensitive to high-fat feeding but respond normally to the acute anorectic effects of peptide-YY(3-36).
    Challis BG, Coll AP, Yeo GS, Pinnock SB, Dickson SL, Thresher RR, Dixon J, Zahn D, Rochford JJ, White A, Oliver RL, Millington G, Aparicio SA, Colledge WH, Russ AP, Carlton MB, O'Rahilly S.
    Proc Natl Acad Sci U S A; 2004 Mar 30; 101(13):4695-700. PubMed ID: 15070780
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  • 39. A rare cause of neonatal hypoglycemia in two siblings: TBX19 gene mutation.
    Unal E, Yıldırım R, Taş FF, Tekin S, Sen A, Haspolat YK.
    Hormones (Athens); 2018 Jun 30; 17(2):269-273. PubMed ID: 29858850
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