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    Results: 1 to 20 of 175

    1.

    Mutational screening of the CART gene in obese children: identifying a mutation (Leu34Phe) associated with reduced resting energy expenditure and cosegregating with obesity phenotype in a large family.

    del Giudice EM, Santoro N, Cirillo G, D'Urso L, Di Toro R, Perrone L.

    Diabetes. 2001 Sep;50(9):2157-60.PMID: 11522684 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    Molecular screening of the proopiomelanocortin (POMC ) gene in Italian obese children: report of three new mutations.

    Miraglia del Giudice E, Cirillo G, Santoro N, D'Urso L, Carbone MT, Di Toro R, Perrone L.

    Int J Obes Relat Metab Disord. 2001 Jan;25(1):61-7.PMID: 11244459 [PubMed - indexed for MEDLINE]Related articles

    3.

    Sequence variants in the human cocaine and amphetamine-regulated transcript (CART) gene in subjects with early onset obesity.

    Echwald SM, Sørensen TI, Andersen T, Hansen C, Tommerup N, Pedersen O.

    Obes Res. 1999 Nov;7(6):532-6.PMID: 10574510 [PubMed - indexed for MEDLINE]Related articles

    4.

    Low frequency of melanocortin-4 receptor (MC4R) mutations in a Mediterranean population with early-onset obesity.

    Miraglia Del Giudice E, Cirillo G, Nigro V, Santoro N, D'Urso L, Raimondo P, Cozzolino D, Scafato D, Perrone L.

    Int J Obes Relat Metab Disord. 2002 May;26(5):647-51.PMID: 12032748 [PubMed - indexed for MEDLINE]Related articlesFree article

    5.

    Sequencing of the putative promoter region of the cocaine- and amphetamine-regulated-transcript gene and identification of polymorphic sites associated with obesity.

    Yamada K, Yuan X, Otabe S, Koyanagi A, Koyama W, Makita Z.

    Int J Obes Relat Metab Disord. 2002 Jan;26(1):132-6.PMID: 11791158 [PubMed - indexed for MEDLINE]Related articlesFree article

    6.

    Several mutations in the melanocortin-4 receptor gene including a nonsense and a frameshift mutation associated with dominantly inherited obesity in humans.

    Hinney A, Schmidt A, Nottebom K, Heibült O, Becker I, Ziegler A, Gerber G, Sina M, Görg T, Mayer H, Siegfried W, Fichter M, Remschmidt H, Hebebrand J.

    J Clin Endocrinol Metab. 1999 Apr;84(4):1483-6.PMID: 10199800 [PubMed - indexed for MEDLINE]Related articlesFree article

    7.

    The CART gene and human obesity: mutational analysis and population genetics.

    Challis BG, Yeo GS, Farooqi IS, Luan J, Aminian S, Halsall DJ, Keogh JM, Wareham NJ, O'Rahilly S.

    Diabetes. 2000 May;49(5):872-5.PMID: 10905499 [PubMed - indexed for MEDLINE]Related articlesFree article

    8.

    The Leu34Phe ProCART mutation leads to cocaine- and amphetamine-regulated transcript (CART) deficiency: a possible cause for obesity in humans.

    Yanik T, Dominguez G, Kuhar MJ, Del Giudice EM, Loh YP.

    Endocrinology. 2006 Jan;147(1):39-43. Epub 2005 Oct 6.PMID: 16210370 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    A novel non-synonymous mutation in the melanocortin-4 receptor gene (MC4R) in a 2-year-old Austrian girl with extreme obesity.

    Rettenbacher E, Tarnow P, Brumm H, Prayer D, Wermter AK, Hebebrand J, Biebermann H, Hinney A, Widhalm K.

    Exp Clin Endocrinol Diabetes. 2007 Jan;115(1):7-12.PMID: 17286227 [PubMed - indexed for MEDLINE]Related articles

    10.

    Ghrelin gene: identification of missense variants and a frameshift mutation in extremely obese children and adolescents and healthy normal weight students.

    Hinney A, Hoch A, Geller F, Schäfer H, Siegfried W, Goldschmidt H, Remschmidt H, Hebebrand J.

    J Clin Endocrinol Metab. 2002 Jun;87(6):2716.PMID: 12050239 [PubMed - indexed for MEDLINE]Related articlesFree article

    11.

    The relation between two polymorphisms in the glucocorticoid receptor gene and body mass index, blood pressure and cholesterol in obese patients.

    Di Blasio AM, van Rossum EF, Maestrini S, Berselli ME, Tagliaferri M, Podestà F, Koper JW, Liuzzi A, Lamberts SW.

    Clin Endocrinol (Oxf). 2003 Jul;59(1):68-74.PMID: 12807506 [PubMed - indexed for MEDLINE]Related articles

    12.

    Genetic screening for melanocortin-4 receptor mutations in a cohort of Italian obese patients: description and functional characterization of a novel mutation.

    Santini F, Maffei M, Ceccarini G, Pelosini C, Scartabelli G, Rosellini V, Chiellini C, Marsili A, Lisi S, Tonacchera M, Agretti P, Chiovato L, Mammoli C, Vitti P, Pinchera A.

    J Clin Endocrinol Metab. 2004 Feb;89(2):904-8.PMID: 14764812 [PubMed - indexed for MEDLINE]Related articlesFree article

    13.

    Adolescents carrying a missense mutation in the CART gene exhibit increased anxiety and depression.

    Miraglia del Giudice E, Santoro N, Fiumani P, Dominguez G, Kuhar MJ, Perrone L.

    Depress Anxiety. 2006;23(2):90-2.PMID: 16400624 [PubMed - indexed for MEDLINE]Related articles

    14.

    Mutational analysis of the proopiomelanocortin gene in Caucasians with early onset obesity.

    Echwald SM, Sørensen TI, Andersen T, Tybjaerg-Hansen A, Clausen JO, Pedersen O.

    Int J Obes Relat Metab Disord. 1999 Mar;23(3):293-8.PMID: 10193875 [PubMed - indexed for MEDLINE]Related articles

    15.

    Molecular screening of the ghrelin gene in Italian obese children: the Leu72Met variant is associated with an earlier onset of obesity.

    Miraglia del Giudice E, Santoro N, Cirillo G, Raimondo P, Grandone A, D'Aniello A, Di Nardo M, Perrone L.

    Int J Obes Relat Metab Disord. 2004 Mar;28(3):447-50.PMID: 14724664 [PubMed - indexed for MEDLINE]Related articles

    16.

    A novel nonsense mutation in the melanocortin-4 receptor associated with obesity in a Spanish population.

    Marti A, Corbalán MS, Forga L, Martinez JA, Hinney A, Hebebrand J.

    Int J Obes Relat Metab Disord. 2003 Mar;27(3):385-8.PMID: 12629567 [PubMed - indexed for MEDLINE]Related articles

    17.

    Prevalence of pathogenetic MC4R mutations in Italian children with early onset obesity, tall stature and familial history of obesity.

    Santoro N, Cirillo G, Xiang Z, Tanas R, Greggio N, Morino G, Iughetti L, Vottero A, Salvatoni A, Di Pietro M, Balsamo A, Crinò A, Grandone A, Haskell-Luevano C, Perrone L, del Giudice EM.

    BMC Med Genet. 2009 Mar 12;10:25.PMID: 19284607 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    Screening for variability in the ciliary neurotrophic factor (CNTF) gene: no evidence for association with human obesity.

    Münzberg H, Tafel J, Büsing B, Hinney A, Ziegler A, Mayer H, Siegfried W, Matthaei S, Greten H, Hebebrand J, Hamann A.

    Exp Clin Endocrinol Diabetes. 1998;106(2):108-12.PMID: 9628240 [PubMed - indexed for MEDLINE]Related articles

    19.

    Structural organization and mutational analysis of the human uncoupling protein-2 (hUCP2) gene.

    Tu N, Chen H, Winnikes U, Reinert I, Marmann G, Pirke KM, Lentes KU.

    Life Sci. 1999;64(3):PL41-50.PMID: 10027754 [PubMed - indexed for MEDLINE]Related articles

    20.

    Obesity among children and adolescents with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

    Völkl TM, Simm D, Beier C, Dörr HG.

    Pediatrics. 2006 Jan;117(1):e98-105.PMID: 16396852 [PubMed - indexed for MEDLINE]Related articlesFree article

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