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Galactosylceramidase
Mannosidases Are the Putative Catabolic Enzymes Which
Supplementary Table S4. FGA Co-Expressed Gene List in LUAD
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Molecular Cloning and Knockdown of Galactocerebrosidase in Zebrafish
Glycosphingolipids Are Modulators of Disease Pathogenesis in Amyotrophic Lateral Sclerosis
GALC Gene Galactosylceramidase
(12) United States Patent (10) Patent No.: US 9,689,046 B2 Mayall Et Al
Human Induced Pluripotent Stem Cell–Derived Podocytes Mature Into Vascularized Glomeruli Upon Experimental Transplantation
Chaperone Therapy for Krabbe Disease: Potential for Late-Onset GALC Mutations
Altered Trafficking and Processing of GALC Mutants Correlates with Globoid Cell Leukodystrophy Severity
The Unique Phenotype of Lipid-Laden Macrophages
Pdf NTSAD Chart of Allied Diseases
Enzyme-Replacement Therapy in Lysosomal Storage
Survey of Diagnosis of Lysosomal Storage Disorders
Research Article Complex and Multidimensional Lipid Raft Alterations in a Murine Model of Alzheimer’S Disease
Central Nervous System Pathology Progresses Independently of KC and CXCR2 in Globoid-Cell Leukodystrophy Adarsh S
Ab253391 Lysolivetm Lysosomal Β-Galactosidase Assay Kit
Glucocerebrosidase: Functions in and Beyond the Lysosome
Top View
Thesis May Be Reproduced, Stored Or Transmitted in Any Form Or by Any Means, Without Permission of the Author
S41467-020-19179-W.Pdf
Generated by SRI International Pathway Tools Version 25.0, Authors S
Alpha Galactosidase a Activity in Parkinson's Disease
Supplemental Figures 04 12 2017
Expression and Purification of Human Lysosomal Β-Galactosidase from Pichia Pastoris
The Link Between Gaucher Disease and Parkinson's Disease Sheds
Galactosylceramidase Deficiency Causes Bone Marrow
All Enzymes in BRENDA™ the Comprehensive Enzyme Information System
Rapid Isolation of Glomeruli Coupled with Gene Expression Profiling Identifies Downstream Targets in Pod1 Knockout Mice
Loss of Acid Sphingomyelinase Ameliorates Disease Progression In
Amfep Guidance on REACH Pre-Registration of Enzymes
Glucosylsphingosine Accumulation in Mice and Patients with Type 2 Gaucher Disease Begins Early in Gestation
(12) Patent Application Publication (10) Pub. No.: US 2015/0240226A1 Mathur Et Al
New Therapeutic Approaches for Krabbe Disease: the Potential of Pharmacological Chaperones
Acid Sphingomyelinase Inhibition Results in Profound Rescue
Supplementary Material (ESI) for Natural Product Reports
Proteomic Landscape of the Human Choroid–Retinal Pigment Epithelial Complex
Towards Broad Spectrum Activity-Based Glycosidase Probes: Synthesis and Evaluation Cite This: Chem
Structural Snapshots Illustrate the Catalytic Cycle of Β-Galactocerebrosidase, the Defective Enzyme in Krabbe Disease
Effects of Inhibitors of FGFR3 on Gene Transcription
Krabbe Disease Successfully Treated Via Monotherapy of Intrathecal Gene Therapy
Anti-Galactosylceramidase Antibody (ARG58731)
(19) United States (12) Patent Application Publication (10) Pub
Convergent Functional Genomic Studies of Omega-3 Fatty Acids in Stress Reactivity, Bipolar Disorder and Alcoholism
Insights Into Krabbe Disease from Structures Of
Metabolske Sykdommer V02
Emerging Novel Concept of Chaperone Therapies for Protein Misfolding Diseases
Web Table 5Corrected
Table 10: H. Sapiens Recon 1 Network Confidence Scores and Citations
Probe Set ID Gene Symbol* Gene Name* Change St Error 1393245 AT
Effect of Bone Marrow Transplantation on Enzyme Levels and Clinical Course in the Neurologically Affected Twitcher Mouse
Lysosomal Storage Diseases
A Specific Activity-Based Probe to Monitor Family GH59 Galactosylceramidase, the Enzyme Deficient in Krabbe Disease
Glygen As a Case Study by Jeet Vora BS In
Responsive Nuclear Proteins in Collecting Duct Cells
Lysosomal Storage Disease in the Brain: Mutations of the Β-Mannosidase Gene Identified in Autosomal Dominant Nystagmus
Gene–Phenotype Associations Involving Human-Residential Bifidobacteria (HRB) Reveal Significant Species- and Strain-Specificity in Carbohydrate Catabolism
Generated by SRI International Pathway Tools Version 25.0, Authors S
Galactosylceramidase, Psychosine, and Galactocerebrosides