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SUMF1
SUMF1 Enhances Sulfatase Activities in Vivo in Five Sulfatase Deficiencies
Supplementary Table S4. FGA Co-Expressed Gene List in LUAD
Human Induced Pluripotent Stem Cell–Derived Podocytes Mature Into Vascularized Glomeruli Upon Experimental Transplantation
Invitae Detect Lysosomal Storage Diseases (Lsds) Genetic Testing Program
Excessive Burden of Lysosomal Storage Disorder Gene Variants in Parkinson’S Disease
Disorders of Sphingolipid Synthesis, Sphingolipidoses, Niemann-Pick Disease Type C and Neuronal Ceroid Lipofuscinoses
Endosomal-Lysosomal Processing of Neurodegeneration-Associated Proteins in Astrocytes
Lysosomal Storage Disorders
Hunter Syndrome)
TFEB Links MYC Signaling to Epigenetic Control of Myeloid Differentiation and Acute Myeloid Leukemia
Natural Disease History and Characterisation of SUMF1
STAT3 Targets Suggest Mechanisms of Aggressive Tumorigenesis in Diffuse Large B Cell Lymphoma
Cardiac Fibroblast Proliferation Rates and Collagen Expression Mature Early and Are Unaltered with Advancing Age
Genetic Carrier Screening Technical Bulletin
Us 2018 / 0305689 A1
Lysosomal Storage Disease Panel by Next-Generation Sequencing
Case of Multiple Sulfatase Deficiency and Ocular Albinism: a Diagnostic Odyssey
Oncogene Regulated Release of Extracellular Vesicles
Top View
Comprehensive Lysosomal Storage Disorders Panel with GBA and IDS
Astrocyte Dysfunction Triggers Neurodegeneration in a Lysosomal Storage Disorder
Abnormal Sphingolipid World in Inflammation Specific for Lysosomal
Lysosomal Storage Diseases: Diagnostic Confirmation and Management of Presymptomatic Individuals Raymond Y
Genetic Testing of Leukodystrophies Unraveling Extensive Heterogeneity
Proteomic Landscape of the Human Choroid–Retinal Pigment Epithelial Complex
Effects of Inhibitors of FGFR3 on Gene Transcription
Lysosomal Storage Diseases ª the Author(S) 2014 DOI: 10.1177/2326409813517663 Iem.Sagepub.Com
Lysosomes As a Therapeutic Target
SUMF1 Mutations Affecting Stability and Activity of Formylglycine
Invitae Detect Lysosomal Storage Diseases (Lsds) Genetic Testing Program
Intravenously Administered Gene Therapy for Neuronopathic Gaucher Disease
Quantitative Analysis of the Mitochondrial Proteome in Human Ovarian Carcinomas
Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force
Inherited Metabolic Disorders Presenting with Ataxia
JNCL, Batten Disease)
Is Associated with Chronic Obstructive Pulmonary Disease Julie Weidner1, Linnea Jarenbäck1, Kim De Jong2, Judith M
Activities of Genes Controlling Sphingolipid Metabolism in Human Fibroblasts Treated with Flavonoids