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Arylsulfatase A
Sphingolipid Metabolism Diseases ⁎ Thomas Kolter, Konrad Sandhoff
Characterization of a Mutation in a Family with Saposin B Deficiency
Supplementary Table S4. FGA Co-Expressed Gene List in LUAD
2016 Mock Exam General Pathology Answer Sheet
Structural Study of the Acid Sphingomyelinase Protein Family
A Possible Role for Arylsulfatase G in Dermatan Sulfate Metabolism
Human Induced Pluripotent Stem Cell–Derived Podocytes Mature Into Vascularized Glomeruli Upon Experimental Transplantation
Lab Dept: Chemistry Test Name: ARYLSULFATASE A, LEUKOCYTES
Metachromatic Leukodystrophy Improved Diagnosis and Prognosis
Arylsulfatase G Inactivation Causes Loss of Heparan Sulfate 3-O-Sulfatase Activity and Mucopolysaccharidosis in Mice
Molecular Interactions Underlying Neuronal Ceroid Lipofuscinoses CLN1 and CLN5
Arylsulfatase a and the Campbell Family: a Molecular Story from the CBM
Proteome Mapping of Human Skim Milk Proteins in Term and Preterm Milk † † ‡ § § Claire E
Oviduct: Fertilization and 232:1 R1–R26 Review Embryo Development PROOF ONLY Oviduct: Roles in Fertilization and Early Embryo Development
Autocrine IFN Signaling Inducing Profibrotic Fibroblast Responses By
Tissue Expression Profiles Unveil the Gene Interaction of Hepatopancreas
Supplemental Figures 04 12 2017
Natural Disease History and Characterisation of SUMF1
Top View
Lentiviral Vectors
Biosynthesis and Processing of Prostatic and Lysosomal Acid Phosphatases in a Prostate Carcinoma Cell Line PC-3SF121
Comprehensive Genetic Test Menu Diagnostic Services Genetics Genetic Test Menu
Comparative and Evolutionary Studies of Vertebrate Arylsulfatase B
Pdf 362.09 K
United States Patent (19) 11 Patent Number: 5,972,615 an Et Al
Fluorimetric Assays for N-Acetylgalactosamine-6-Sulfatase
Exome Sequencing Enhanced Package Department of Pathology and Laboratory Medicine Feb 2012 UCLA Molecular Diagnostics Laboratories Page:1
Lysosomal Storage Diseases: Diagnostic Confirmation and Management of Presymptomatic Individuals Raymond Y
Proteomic Landscape of the Human Choroid–Retinal Pigment Epithelial Complex
Potential Role As a Biomarker in Prostate Cancer
Sphingolipids and Lysosomal Pathologies☆
Supplementary Materials
Lysosomal Storage Diseases ª the Author(S) 2014 DOI: 10.1177/2326409813517663 Iem.Sagepub.Com
Pathology and Laboratory Cpt Code Changes for 2018
Gene Expression Profiling in Vlincl CLN6-Deficient Fibroblasts: Insights Into Pathobiology
Various Sulfatase Activities in Leukocytes and Cultured Skin Fibroblasts from Heterozygotes for the Multiple Sulfatase Deficiency (Mukosulfatidosis)
Diagnosis of Pseudo-Arylsulfatase a Deficiency with Electrophoretic Techniques
Metabolske Sykdommer V02
Complementation of Arylsulfatase a in Somatichybrids of Metachromatic
Lysosomal Lipid Storage Diseases
Structural Studies of Acid Phosphatases from Pathogenic
Infantile Batten Disease: Effective Therapy and Novel Model Charles Shyng Washington University in St
Mucopolysaccharidosis IVA) Identifies 39 Novel GALNS Mutations
Official Symbol Accession Alias / Previous Symbol Official Full Name
WO 2008/148063 Al
Individual Genome Sequence Gene List (By Disease)
Mucopolysaccharidosis IVA Mutations in Chinese Patients: 16 Novel Mutations
(12) Patent Application Publication (10) Pub. No.: US 2009/0203605 A1 Segatoriet Al
The Emerging and Diverse Roles of Bis(Monoacylglycero) Phosphate Lipids in Cellular Physiology and Disease
Responsive Nuclear Proteins in Collecting Duct Cells
Lysosmal Enzyme Specimen Collection Guide
Transcriptomic and Micrornaomic Profiling Reveals Multi-Faceted Mechanisms to Cope with Phosphate Stress in a Dinoflagellate
Catalytic Promiscuity and the Evolution of New Enzymatic Activities Patrick J O’Brien and Daniel Herschlag
Arylsulfatase B Mediates the Sulfonation-Transport Interplay in Human Embryonic Kidney 293 Cells Overexpressing Sulfotransferase 1A3 S
S1- Alphabetical List of Aging-Related Genes
Exploiting the Potential of Drosophila Models in Lysosomal Storage Disorders: Pathological Mechanisms and Drug Discovery