Titlebook: Lysosomes; Paul Saftig Book 2005 Springer-Verlag US 2005 Chaperone.Organelle.Resorption.enzymes.proteins

Filament

书目名称Lysosomes影响因子(影响力)




书目名称Lysosomes影响因子(影响力)学科排名




书目名称Lysosomes网络公开度




书目名称Lysosomes网络公开度学科排名




书目名称Lysosomes被引频次




书目名称Lysosomes被引频次学科排名




书目名称Lysosomes年度引用




书目名称Lysosomes年度引用学科排名




书目名称Lysosomes读者反馈




书目名称Lysosomes读者反馈学科排名

世俗

Transport of Lysosomal Enzymes,n identified. The hydrolases are enclosed by a membrane containing a set of highly glycosylated lysosomal membrane proteins. Lysosomal enzymes are also components of cell type-specific compartments referred to as lysosome-related organelles which include melanosomes, lytic gran-ules, MHC class II co

安慰

Adaptor Proteins in Lysosomal Biogenesis,sicles which bud from the donor compartment and are transported to and fuse with the proper acceptor compartment. The proteins forming the vesicle-coat bind to the cytoplasmic domains of the cargo proteins and recruit additional proteins like clathrin to the site of vesicle formation. These proteins

白杨鱼

Lysosomal Membrane Proteins,of fusion events beween lysosomes and other organelles, and transport of degradation products to the cytoplasm. Lysosomal membrane proteins are usually highly glycosylated proteins decorating the luminal surface of lysosomal membranes. LAMP-1, LAMP-2 and LIMP-2 are the most abundant components of th

Mechanics

Lysosomal Proteases,issue- or cell type-specific manner. Although we still call them lysosomal proteases, the enzymes are usually detected within all vesicles of the endocytic pathway. In specific cell types, they might even become secreted and might fulfill important tasks in the direct pericellular surrounding. Funct

Culmination

愉快吗

EXCEL

Cholesterol Transport in Lysosomes,has many possible fates within the cell, including incorporation into membranes, metabolic conversion to a number of different products, covalent modification of specific proteins, regulation of gene expression, and efflux from the cell. Distinct trafficking pathways are thought to exist for de novo

NUL

Therapy of Lysosomal Storage Diseases,r macromolecules to low molecular components that are transported to the cytoplasm for reutilization in the biosynthetic pathways of the cell. Up to now more than 50 different lysosomal hydrolases catalyzing the degradation of proteins, lipids, nucleic acids and carbohydrates have been identified. T

外观

Lysosomal Proteome and Transcriptome,nd others in the 1950s. Nevertheless, a lot of questions are still open, and some of them can be addressed using screening techniques. Among them are questions about the structure of the lysosomal mem-brane, the function of its proteins, and the effect of lysosomal dysfunction on cell functions. Alt