Seipin ablation in mice results in severe generalized lipodystrophy. (25/37)

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Serum retinol binding protein 4 is not decreased in congenital generalized lipodystrophy: a case series. (26/37)

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Overexpression of a short human seipin/BSCL2 isoform in mouse adipose tissue results in mild lipodystrophy. (27/37)

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Mitochondrial oxidative phosphorylation is impaired in patients with congenital lipodystrophy. (28/37)

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Seipin: from human disease to molecular mechanism. (29/37)

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Alterations in lipid signaling underlie lipodystrophy secondary to AGPAT2 mutations. (30/37)

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Identification of a novel nonsense mutation and a missense substitution in the AGPAT2 gene causing congenital generalized lipodystrophy type 1. (31/37)

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Leptin's role in lipodystrophic and nonlipodystrophic insulin-resistant and diabetic individuals. (32/37)

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