BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

161 related articles for article (PubMed ID: 27254754)

  • 21. Regionally reduced brain volume, altered serotonin neurochemistry, and abnormal behavior in mice null for the circadian rhythm output gene Magel2.
    Mercer RE; Kwolek EM; Bischof JM; van Eede M; Henkelman RM; Wevrick R
    Am J Med Genet B Neuropsychiatr Genet; 2009 Dec; 150B(8):1085-99. PubMed ID: 19199291
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Loss of MAGEL2 in Prader-Willi syndrome leads to decreased secretory granule and neuropeptide production.
    Chen H; Victor AK; Klein J; Tacer KF; Tai DJ; de Esch C; Nuttle A; Temirov J; Burnett LC; Rosenbaum M; Zhang Y; Ding L; Moresco JJ; Diedrich JK; Yates JR; Tillman HS; Leibel RL; Talkowski ME; Billadeau DD; Reiter LT; Potts PR
    JCI Insight; 2020 Sep; 5(17):. PubMed ID: 32879135
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Loss of magel2, a candidate gene for features of Prader-Willi syndrome, impairs reproductive function in mice.
    Mercer RE; Wevrick R
    PLoS One; 2009; 4(1):e4291. PubMed ID: 19172181
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Two mouse models carrying truncating mutations in Magel2 show distinct phenotypes.
    Ieda D; Negishi Y; Miyamoto T; Johmura Y; Kumamoto N; Kato K; Miyoshi I; Nakanishi M; Ugawa S; Oishi H; Saitoh S
    PLoS One; 2020; 15(8):e0237814. PubMed ID: 32804975
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The Prader-Willi syndrome murine imprinting center is not involved in the spatio-temporal transcriptional regulation of the Necdin gene.
    Watrin F; Le Meur E; Roeckel N; Ripoche MA; Dandolo L; Muscatelli F
    BMC Genet; 2005 Jan; 6():1. PubMed ID: 15634360
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The impact of oxytocin on neurite outgrowth and synaptic proteins in Magel2-deficient mice.
    Reichova A; Schaller F; Bukatova S; Bacova Z; Muscatelli F; Bakos J
    Dev Neurobiol; 2021 May; 81(4):366-388. PubMed ID: 33609001
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Cellular and disease functions of the Prader-Willi Syndrome gene
    Tacer KF; Potts PR
    Biochem J; 2017 Jun; 474(13):2177-2190. PubMed ID: 28626083
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Colocalization of Oxtr with Prader-Willi syndrome transcripts in the trigeminal ganglion of neonatal mice.
    Vaidyanathan R; Schaller F; Muscatelli F; Hammock EAD
    Hum Mol Genet; 2020 Jul; 29(12):2065-2075. PubMed ID: 32420597
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A single postnatal injection of oxytocin rescues the lethal feeding behaviour in mouse newborns deficient for the imprinted Magel2 gene.
    Schaller F; Watrin F; Sturny R; Massacrier A; Szepetowski P; Muscatelli F
    Hum Mol Genet; 2010 Dec; 19(24):4895-905. PubMed ID: 20876615
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Magel2-null mice are hyper-responsive to setmelanotide, a melanocortin 4 receptor agonist.
    Bischof JM; Van Der Ploeg LH; Colmers WF; Wevrick R
    Br J Pharmacol; 2016 Sep; 173(17):2614-21. PubMed ID: 27339818
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Necdin plays a role in the serotonergic modulation of the mouse respiratory network: implication for Prader-Willi syndrome.
    Zanella S; Watrin F; Mebarek S; Marly F; Roussel M; Gire C; Diene G; Tauber M; Muscatelli F; Hilaire G
    J Neurosci; 2008 Feb; 28(7):1745-55. PubMed ID: 18272695
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Magel2 truncation alters select behavioral and physiological outcomes in a rat model of Schaaf-Yang syndrome.
    Reznik DL; Yang MV; Albelda de la Haza P; Jain A; Spanjaard M; Theiss S; Schaaf CP; Malovannaya A; Strong TV; Veeraragavan S; Samaco RC
    Dis Model Mech; 2023 Feb; 16(2):. PubMed ID: 36637363
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Analysis of the hypothalamic oxytocin system and oxytocin receptor-expressing astrocytes in a mouse model of Prader-Willi syndrome.
    Althammer F; Wimmer MC; Krabichler Q; Küppers S; Schimmer J; Fröhlich H; Dötsch L; Gruber T; Wunsch S; Schubert T; Kirchner MK; Stern JE; Charlet A; Grinevich V; Schaaf CP
    J Neuroendocrinol; 2022 Dec; 34(12):e13217. PubMed ID: 36458331
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndrome.
    Bittel DC; Kibiryeva N; Butler MG
    Pediatrics; 2006 Oct; 118(4):e1276-83. PubMed ID: 16982806
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Sleeve gastrectomy leads to weight loss in the Magel2 knockout mouse.
    Arble DM; Pressler JW; Sorrell J; Wevrick R; Sandoval DA
    Surg Obes Relat Dis; 2016 Dec; 12(10):1795-1802. PubMed ID: 27396546
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Three patients with Schaaf-Yang syndrome exhibiting arthrogryposis and endocrinological abnormalities.
    Enya T; Okamoto N; Iba Y; Miyazawa T; Okada M; Ida S; Naruto T; Imoto I; Fujita A; Miyake N; Matsumoto N; Sugimoto K; Takemura T
    Am J Med Genet A; 2018 Mar; 176(3):707-711. PubMed ID: 29359444
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Baby food and bedtime: Evidence for opposite phenotypes from different genetic and epigenetic alterations in Prader-Willi and Angelman syndromes.
    Salminen II; Crespi BJ; Mokkonen M
    SAGE Open Med; 2019; 7():2050312118823585. PubMed ID: 30728968
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth.
    Lee S; Walker CL; Karten B; Kuny SL; Tennese AA; O'Neill MA; Wevrick R
    Hum Mol Genet; 2005 Mar; 14(5):627-37. PubMed ID: 15649943
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Contaminated and unusual food combinations: what do people with Prader-Willi syndrome choose?
    Dykens EM
    Ment Retard; 2000 Apr; 38(2):163-71. PubMed ID: 10804706
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Prader-Willi Syndrome and Schaaf-Yang Syndrome: Neurodevelopmental Diseases Intersecting at the
    Fountain MD; Schaaf CP
    Diseases; 2016 Jan; 4(1):. PubMed ID: 28933382
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.