CONFIGURATIONS, POWER TOPOLOGIES AND APPLICATIONS OF HYBRID DISTRIBUTION TRANSFORMERS


Curvilinear, symmetrical, and profound pigment deposition on the posterior lens capsule in a patient with bilateral pigmentary dispersion syndrome

Julia Canestraro,1 Jerome Sherman2 1SUNY College of Optometry, New York, NY, USA; 2Department of Clinical Education, SUNY College of Optometry, New m02n3ll/a York, NY, USA Introduction: The classic presentation of pigmentary dispersion syndrome (PDS) often consists of midperipheral iris transillumination defects, Krukenberg’s spindle, and den

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Crystal structure of the N-acetylmannosamine kinase domain of GNE.

UDP-GlcNAc 2-epimerase/ManNAc 6-kinase, GNE, is a bi-functional enzyme that plays a key role in sialic acid biosynthesis.Mutations of the GNE protein cause sialurea or autosomal recessive inclusion body myopathy/Nonaka myopathy.GNE is the only human protein that contains a kinase domain belonging to the ROK (repressor, ORF, kinase) family.We solved

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