116764 ⎘
Hydrolases acting on peptide bonds, i.e. peptidases (3.4); Dipeptidyl-peptidases and tripeptidyl-peptidases (3.4.14) Tripeptidyl-peptidase I (3.4.14.9)
GENE THERAPY FOR CEROID LIPOFUSCINOSES
#2METHODS FOR TREATING LYSOSOMAL STORAGE DISEASES
#3METHODS FOR TREATING LYSOSOMAL STORAGE DISEASES
#4GENE THERAPY FOR NEURONAL CEROID LIPOFUSCINOSES
#5GENE THERAPY FOR CEROID LIPOFUSCINOSES
#6GENE THERAPY FOR OCULAR MANIFESTATIONS OF CLN2 DISEASE
#7Methods for Treating CLN2 Disease in Pediatric Subjects
#8AAV VECTOR TREATMENT METHODS FOR LATE INFANTILE NEURONAL CEROID LIPOFUSCINOSIS TYPE 2
#9PROLINE TOLERANT TRIPEPTIDYL PEPTIDASES AND USES THEREOF
#10Selective recovery
#11Anti-Human Transferrin Receptor Antibody Permeating Blood-Brain Barrier
#12METHOD FOR PRODUCING A PROTEIN HYDROLYSATE EMPLOYING AN ASPERGILLUS FUMIGATUS TRIPEPTIDYL PEPTIDASE
#13TPP-1 formulations and methods for treating CLN2 disease
#14USE OF PROLINE TOLERANT TRIPEPTIDYL PEPTIDASES IN FEED ADDITIVE COMPOSITIONS
#15Gene therapy for ceroid lipofuscinoses
#16Selective recovery
#17Selective recovery
#18SCALABLE HIGH RECOVERY METHODS FOR PRODUCING HIGH YIELD RECOMBINANT ADENO-ASSOCIATED VIRAL (rAAV) VECTOR AND RECOMBINANT ADENO-ASSOCIATED VIRAL (rAAV) VECTORS PRODUCED THEREBY
#19GENE TRANSFER COMPOSITIONS, METHODS AND USES FOR TREATING NEURODEGENERATIVE DISEASES
#20TPP-1 formulations and methods for treating CLN2 disease
#21Selective recovery
#22METHODS FOR TREATING NEURODEGENERATIVE DISEASES USING GENE THERAPY TO DELAY DISEASE ONSET AND PROGRESSION WHILE PROVIDING COGNITIVE PROTECTION
#23Selective recovery
#24Anti-human transferrin receptor antibody permeating blood-brain barrier
#25PROLINE TOLERANT TRIPEPTIDYL PEPTIDASES AND USES THEREOF
#26Selective recovery
#27Targeting peptides for directing adeno-associated viruses (AAVs)
#28METHODS AND COMPOSITIONS FOR TREATMENT OF NEURODEGENERATIVE DISEASES
#29TPP-1 formulations and methods for treating CLN2 disease
#30Recombinant AAV capsid protein
#31Human lysosomal protein and methods of its use
#32Substances and Methods for the Treatment of Lysosmal Storage Diseases
#33Methods of treating a deficiency of functional tripeptidyl peptidase I (CLN2) protein
#34CLN2 TREATMENT OF ALZHEIMER'S DISEASE
#35Methods of treating a deficiency of functional tripeptidyl peptidase I (CLN2) protein
#36Human lysosomal protein and methods of its use
#37Methods of reducing storage products using tripeptidyl peptidase I (CLN2) protein
#38Method of expressing human lysosomal protein in brain cells