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Berger, C.* ; Klöting, N.

Leptin receptor compound heterozygosity in humans and animal models.

Int. J. Mol. Sci. 22:4475 (2021)
Verlagsversion DOI PMC
Open Access Gold
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Leptin and its receptor are essential for regulating food intake, energy expenditure, glucose homeostasis and fertility. Mutations within leptin or the leptin receptor cause early-onset obesity and hyperphagia, as described in human and animal models. The effect of both heterozygous and homozygous variants is much more investigated than compound heterozygous ones. Recently, we discovered a spontaneous compound heterozygous mutation within the leptin receptor, resulting in a considerably more obese phenotype than described for the homozygous leptin receptor deficient mice. Accordingly, we focus on compound heterozygous mutations of the leptin receptor and their effects on health, as well as possible therapy options in human and animal models in this review.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Review
Schlagwörter Compound Heterozygous Mutation ; Leptin Receptor ; Mouse Model; Janus Kinase/signal Transducer; Early-onset Obesity; Signal Transducer; Mutations; Gene; Lepr; Identification; Activation; Homeostasis; Deficiency
Sprache englisch
Veröffentlichungsjahr 2021
HGF-Berichtsjahr 2021
ISSN (print) / ISBN 1661-6596
e-ISSN 1422-0067
Zeitschrift International Journal of Molecular Sciences
Quellenangaben Band: 22, Heft: 9, Seiten: , Artikelnummer: 4475 Supplement: ,
Verlag MDPI
Verlagsort Basel
Begutachtungsstatus Peer reviewed
Institut(e) Helmholtz Institute for Metabolism, Obesity and Vascular Research (HI-MAG)
POF Topic(s) 30201 - Metabolic Health
Forschungsfeld(er) Helmholtz Diabetes Center
PSP-Element(e) G-506500-001
Förderungen Deutsche Forschungsgemeinschaft (DFG, German Research Foun-dation)
DOI 10.3390/ijms22094475
WOS ID WOS:000650420500001
Scopus ID 85104604844
PubMed ID 33922961
Erfassungsdatum 2021-05-03
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