Published in J Invest Dermatol on January 17, 2014
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Mutations in lipoprotein lipase that block binding to the endothelial cell transporter GPIHBP1. Proc Natl Acad Sci U S A (2011) 1.09
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Unexpected expression pattern for glycosylphosphatidylinositol-anchored HDL-binding protein 1 (GPIHBP1) in mouse tissues revealed by positron emission tomography scanning. J Biol Chem (2010) 1.03
Mal de Meleda (MDM) caused by mutations in the gene for SLURP-1 in patients from Germany, Turkey, Palestine, and the United Arab Emirates. Hum Genet (2002) 1.00
Brain regions and genes affecting limb-clasping responses. Brain Res Rev (2011) 0.99
Reciprocal metabolic perturbations in the adipose tissue and liver of GPIHBP1-deficient mice. Arterioscler Thromb Vasc Biol (2011) 0.99
Upregulation of nuclear factor-kappaB expression by SLURP-1 is mediated by alpha7-nicotinic acetylcholine receptor and involves both ionic events and activation of protein kinases. Am J Physiol Cell Physiol (2010) 0.98
Protein 4.1B contributes to the organization of peripheral myelinated axons. PLoS One (2011) 0.98
Desmosomal genodermatoses. Br J Dermatol (2012) 0.98
A novel missense mutation in the gene encoding SLURP-1 in patients with Mal de Meleda from northern Tunisia. Br J Dermatol (2003) 0.96
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Reversal of neuropathy phenotypes in conditional mouse model of Charcot-Marie-Tooth disease type 2E. Hum Mol Genet (2010) 0.95
Crooked, coiled and crimpled are three Ly6-like proteins required for proper localization of septate junction components. Development (2010) 0.94
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Clinical and genetic studies of 3 large, consanguineous, Algerian families with Mal de Meleda. Arch Dermatol (2000) 0.92
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Motor and sensory neuropathy due to myelin infolding and paranodal damage in a transgenic mouse model of Charcot-Marie-Tooth disease type 1C. Hum Mol Genet (2013) 0.86
The Ly6 neurotoxin-like molecule target of wit regulates spontaneous neurotransmitter release at the developing neuromuscular junction in Drosophila. Dev Neurobiol (2012) 0.84
Epidermal triglyceride levels are correlated with severity of ichthyosis in Dorfman-Chanarin syndrome. J Dermatol Sci (2009) 0.82
Mutations in a keratin 6 isomer (K6c) cause a type of focal palmoplantar keratoderma. J Invest Dermatol (2010) 0.82
The Ly6 protein coiled is required for septate junction and blood brain barrier organisation in Drosophila. PLoS One (2011) 0.81
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Sudan-IV-positive material in fingernails of patient affected with mal de Meleda. Dermatologica (1986) 0.76
Lipid composition of outer stratum corneum in hereditary palmoplantar keratodermas. Dermatology (2003) 0.76
Palmoplantar Keratoderma in Slurp2-Deficient Mice. J Invest Dermatol (2015) 0.76