Results 131 to 140 of about 79,437 (329)

Abnormal mannose-6-phosphate receptor trafficking impairs recombinant alpha-glucosidase uptake in Pompe disease fibroblasts

open access: yesPathoGenetics, 2008
BackgroundPompe disease (PD) is a metabolic myopathy caused by α-glucosidase (GAA) deficiency and characterized by generalized glycogen storage. Heterogeneous GAA gene mutations result in wide phenotypic variability, ranging from the severe classic ...
M. Cardone   +9 more
semanticscholar   +1 more source

Herpes simplex virus glycoprotein D acquires mannose 6-phosphate residues and binds to mannose 6-phosphate receptors.

open access: yesJournal of Biological Chemistry, 1994
Herpes simplex viruses (HSV) use multiple and sequential receptors to enter host cells. HSV glycoprotein D (gD) has been implicated in binding to cellular receptors that facilitate virus penetration into cells. We used soluble forms of gD that were expressed in Chinese hamster ovary cells to characterize and identify a putative cellular receptor for ...
Kevin S. Dingwell   +6 more
openaire   +3 more sources

Targeting MAN1B1 potently enhances bladder cancer antitumor immunity via deglycosylation of CD47

open access: yesCancer Communications, EarlyView.
Abstract Background Only a few bladder cancer patients benefit from anti‐programmed cell death protein 1/programmed cell death ligand 1 immunotherapy. The cluster of differentiation 47 (CD47) plays an important role in tumor immune evasion. CD47 is a highly glycosylated protein, however, the mechanisms governing CD47 glycosylation and its potential ...
Jie Zhang   +20 more
wiley   +1 more source

Rhabdomyosarcoma targeting with tuned porous silicon nanoparticles

open access: yesNano Select
We describe porous silicon nanoparticles (pSiNP) chemically functionalized with an analog of mannose 6‐phosphate (AMFA) and a porphyrin derivative to target aggressive pediatric Rhabdomyosarcoma (RMS) tumor cells.
Sofia Dominguez‐Gil   +10 more
doaj   +1 more source

Mannose 6-phosphate receptor-mediated transport of sulfamidase across the blood-brain barrier in the newborn mouse.

open access: yesMolecular Therapy, 2008
Mucopolysaccharidosis type IIIA (MPS IIIA), which is a lysosomal storage disorder (LSD) caused by inherited deficiency of sulfamidase, is characterized by severe, progressive central nervous system (CNS) dysfunction.
A. Urayama, J. Grubb, W. Sly, W. Banks
semanticscholar   +1 more source

Glycosidases Interact Selectively With Mannose‐6‐Phosphate Receptors of Bull Spermatozoa

open access: yesJournal of Cellular Biochemistry, 2016
ABSTRACTGlycosidases may play a role in sperm maturation during epididymal transit. In this work, we describe the interaction of these enzymes with bull spermatozoa. We found that β‐galactosidase associated to spermatozoa can be released under low ionic strength conditions, whereas the interaction of N‐acetyl‐β‐D‐glucosaminidase and β‐glucuronidase ...
Aguilera, Andrea Carolina   +4 more
openaire   +4 more sources

Reactivity of Carbohydrate Phosphodiesters, Potential Targets of Antibacterial Agents

open access: yesChemistry &Biodiversity, EarlyView.
A simple carbohydrate phosphodiester model was synthesized to compare the reactivity of phosphodiester bonds within carbohydrates and RNA. ABSTRACT While monosaccharide units in bacterial carbohydrates may be linked with phosphodiester bonds, human carbohydrates exclusively contain glycosidic linkages.
Eero Sillanpää   +2 more
wiley   +1 more source

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