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Prosaposin
Sphingolipid Metabolism Diseases ⁎ Thomas Kolter, Konrad Sandhoff
Characterization of a Mutation in a Family with Saposin B Deficiency
A Saposin Deficiency Model in Drosophila: Lysosomal Storage, Progressive Neurodegeneration and Sensory Physiological Decline
Structure of Saposin a Lipoprotein Discs
Impaired Prosaposin Lysosomal Trafficking in Frontotemporal Lobar
Impaired Β-Glucocerebrosidase Activity and Processing in Frontotemporal Dementia Due to Progranulin Mutations Andrew E
The Parkinson's-Disease-Associated Receptor GPR37 Undergoes
Prosaposin Precursor Protein: Functions and Medical Applications
Glucocerebrosidase: Functions in and Beyond the Lysosome
The Evolutionary History of Prosaposin: Two Successive Tandem-Duplication Events Gave Rise to the Four Saposin Domains in Vertebrates
GPR37 and GPR37L1 Are Receptors for the Neuroprotective and Glioprotective Factors Prosaptide and Prosaposin
Is Modulation of Glucocerebrosidase a Viable New Treatment for Parkinson's Disease?
The Roles of Progranulin and Tmem106b in Lysosomal
(Sphingolipid Activator Proteins) in Lysosomal Storage And
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Identification of Prosaposin and Transgelin As Potential Biomarkers for Gallbladder Cancer Using Quantitative Proteomics
Neuronal Ceroid Lipofuscinosis
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Prosaposin and Its Receptors, GRP37 and GPR37L1, Protects Neurons Against in Vivo Neuropathological Disorders
Sphingolipids and Lysosomal Pathologies☆
The Mechanism of Sphingolipid Processing Revealed by a GALC-Sapa Complex Structure
The Role of Saposins in Auditory and Vestibular Systems
Saposins Modulate Human Invariant Natural Killer T Cells Self-Reactivity and Facilitate Lipid Exchange with Cd1d Molecules Durin
Lysosomal Lipid Storage Diseases
Genome-Wide Crispri/A Screens in Human Neurons Link Lysosomal Failure to Ferroptosis
Insights Into the Diagnosis and Treatment of Lysosomal Storage Diseases
A Saposin Deficiency Model in Drosophila: Lysosomal Storage, Progressive Neurodegeneration, Sensory Physiological Decline and Defective Calcium Homeostasis
Translational Studies of Molecular Interactions in Parkinson’S Disease
Prosaposin Facilitates Sortilin-Independent Lysosomal Trafficking of Progranulin
Lysosomal Storage Diseases
Characterization of Lysosomal Proteins Progranulin and Prosaposin And
The Ins and Outs of Cathepsins: Physiological Function and Role in Disease Management
The Niemann-Pick Type C2 Protein Loads Isoglobotrihexosylceramide Onto Cd1d Molecules and Contributes to the Thymic Selection of NKT Cells
ASSOCIATION of a NONSENSE MUTATION at the CODON for GLU 54 in the GM2A GENE with AB VARIANT Cimzgangliosidosis: CHARACTERIZING the Intronf EXON JUNCTIONS of the GENE
Atypical Juvenile Presentation of GM2 Gangliosidosis AB in a Patient MARK Compound-Heterozygote for C.259G > T and C.164C > T Mutations in the ☆ GM2A Gene
Modulation of Thrombospondin-1 in the Lung Microenvironment: Implications for Targeting Metastasis
Prosaposin Is a Regulator of Progranulin Levels and Oligomerization
A Mutation in the Saposin a Domain of the Sphingolipid Activator Protein
PSAP Gene Prosaposin
Exploiting the Potential of Drosophila Models in Lysosomal Storage Disorders: Pathological Mechanisms and Drug Discovery