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Monogenic forms of childhood obesity due to mutations in the leptin gene.
Not available
S-EPMC4644131
|
biostudies-literature
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Severe Early-Onset Obesity Due to Bioinactive Leptin Caused by a p.N103K Mutation in the Leptin Gene.
Not available
S-EPMC4570156
|
biostudies-literature
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Functional and Phenotypic Characteristics of Human Leptin Receptor Mutations.
Not available
S-EPMC6293235
|
biostudies-literature
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Activating Connexin43 gap junctions primes adipose tissue for therapeutic intervention.
Not available
S-EPMC9293664
|
biostudies-literature
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The mitochondrial dicarboxylate carrier prevents hepatic lipotoxicity by inhibiting white adipocyte lipolysis.
Not available
S-EPMC8292187
|
biostudies-literature
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Measurement of immunofunctional leptin to detect and monitor patients with functional leptin deficiency.
Not available
S-EPMC5292973
|
biostudies-literature
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miR-146a regulates insulin sensitivity via NPR3.
Not available
S-EPMC8004521
|
biostudies-literature
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