Copy number variation (CNV) analysis and mutation analysis of the 6q14.1–6q16.3 genes SIM1 and MRAP2 in Prader Willi like patients-Reference-Cited by-同舟云学术

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Copy number variation (CNV) analysis and mutation analysis of the 6q14.1–6q16.3 genes SIM1 and MRAP2 in Prader Willi like patients

Published:2016-03 Issue:3 Volume:117 Page:383-388
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Geets Ellen,Zegers Doreen,Beckers Sigri,Verrijken An,Massa Guy,Van Hoorenbeeck Kim,Verhulst Stijn,Van Gaal Luc,Van Hul Wim

Funder

Interuniversity Attraction Pole Project

University of Antwerp

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference39 articles.

1. Association between class III obesity (BMI of 40–59kg/m2) and mortality: a pooled analysis of 20 prospective studies;Kitahara;PLoS Med.,2014

2. Obesity as a medical problem;Kopelman;Nature,2000

3. Monogenic and complex forms of obesity: insights from genetics reveal the leptin-melanocortin signaling pathway as a common player;Zegers;Crit. Rev. Eukaryot. Gene Expr.,2012

4. Melanocortin-4 receptor in energy homeostasis and obesity pathogenesis;Hinney;Prog. Mol. Biol. Transl. Sci.,2013

5. Prader-Willi Syndrome;Driscoll,1993

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3. Modulation of Canine Melanocortin-3 and -4 Receptors by Melanocortin-2 Receptor Accessory Protein 1 and 2;Biomolecules;2022-11-01

4. Arginine 125 Is an Essential Residue for the Function of MRAP2;International Journal of Molecular Sciences;2022-08-30

5. Recommendations for the diagnosis and management of childhood Prader-Willi syndrome in China;Orphanet Journal of Rare Diseases;2022-06-13

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