István Sohár
Publications by Year
Research Areas
Lysosomal Storage Disorders Research, Cellular transport and secretion, Glycosylation and Glycoproteins Research, Peptidase Inhibition and Analysis, Muscle metabolism and nutrition
Most-Cited Works
- → Association of Mutations in a Lysosomal Protein with Classical Late-Infantile Neuronal Ceroid Lipofuscinosis(1997)581 cited
- → Activation of Microglia Acidifies Lysosomes and Leads to Degradation of Alzheimer Amyloid Fibrils(2007)285 cited
- → Quantitation of oxidative damage to tissue proteins(1999)192 cited
- → Mutational Analysis of the Defective Protease in Classic Late-Infantile Neuronal Ceroid Lipofuscinosis, a Neurodegenerative Lysosomal Storage Disorder(1999)178 cited
- → The Human CLN2 Protein/Tripeptidyl-Peptidase I Is a Serine Protease That Autoactivates at Acidic pH(2001)138 cited
- → A mutation in the cathepsin D gene (CTSD) in American Bulldogs with neuronal ceroid lipofuscinosis(2006)130 cited
- → A frame shift mutation in canine TPP1 (the ortholog of human CLN2) in a juvenile Dachshund with neuronal ceroid lipofuscinosis(2006)123 cited
- → Stretch-induced prostaglandins and protein turnover in cultured skeletal muscle(1990)112 cited
- → Rat Brain Contains High Levels of Mannose-6-phosphorylated Glycoproteins Including Lysosomal Enzymes and Palmitoyl-Protein Thioesterase, an Enzyme Implicated in Infantile Neuronal Lipofuscinosis(1996)112 cited
- → The human brain mannose 6‐phosphate glycoproteome: A complex mixture composed of multiple isoforms of many soluble lysosomal proteins(2005)103 cited