Sézary syndrome without erythroderma.
Paris, France. In J Am Acad Dermatol, Jun 2015
Peripheral blood lymphocytes from 3 of 4 patients tested strongly expressed PLS3, Twist-1, and KIR3DL2.
Comparative proteomic analysis of hypertrophic chondrocytes in osteoarthritis.
Irákleion, Greece. In Clin Proteomics, 2014
We also observed that the proteins GSTP1, PLS3, MYOF, HSD17B12, PRDX2, APCS, PLA2G2A SERPINH1/HSP47 and MVP, show distinct synthesis levels, characteristic for OA or control chondrocytes.
New Genetic Forms of Childhood-Onset Primary Osteoporosis.
Stockholm, Sweden. In Horm Res Paediatr, 2014
This Mini Review discusses monogenetic forms of childhood-onset primary osteoporosis, with the main focus on osteoporosis caused by mutations in WNT1 and PLS3, two of the most recently discovered genes underlying early-onset osteoporosis.
PLS3 mutations in X-linked osteoporosis with fractures.
Amsterdam, Netherlands. In N Engl J Med, 2013
Plastin 3 (PLS3), a protein involved in the formation of filamentous actin (F-actin) bundles, appears to be important in human bone health, on the basis of pathogenic variants in PLS3 in five families with X-linked osteoporosis and osteoporotic fractures that we report here.