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CLN3
Palmitoyl-Protein Thioesterase 1 Deficiency in Drosophila Melanogaster Causes Accumulation
Yeast Genome Gazetteer P35-65
Dysregulation of Autophagy As a Common Mechanism in Lysosomal
©Ferrata Storti Foundation
ROS and Hypoxia Signaling Regulate Periodic Metabolic Arousal During Insect Dormancy to Coordinate Glucose, Amino Acid, and Lipid Metabolism
Disorders of Sphingolipid Synthesis, Sphingolipidoses, Niemann-Pick Disease Type C and Neuronal Ceroid Lipofuscinoses
Mechanism of Secondary Ganglioside and Lipid Accumulation in Lysosomal Disease
C6cc08797c1.Pdf
Molecular Interactions of Neuronal Ceroid Lipofuscinosis Protein CLN3
Lysosomal Enzyme Activities As Possible CSF Biomarkers Of
Supplementary File 1 (PDF, 225 Kib)
Acid Ceramidase Depletion Impairs Neuronal Survival and Induces Morphological Defects in Neurites Associated with Altered Gene Transcription and Sphingolipid Content
Lineage-Specific Effector Signatures of Invariant NKT Cells Are Shared Amongst Δγ T, Innate Lymphoid, and Th Cells
The Crystal Structure of Palmitoyl Protein Thioesterase 1 and the Molecular Basis of Infantile Neuronal Ceroid Lipofuscinosis
Btn1, the Schizosaccharomyces Pombe Homologue of the Human Batten Disease Gene CLN3, Regulates Vacuole Homeostasis Yannick Gachet, Sandra Codlin, Jeremy S
Altered Expression of Ganglioside Metabolizing Enzymes Results in GM3 Ganglioside Accumulation in Cerebellar Cells of a Mouse Mo
The CLN3 Gene and Protein: What We Know
Programmed Lectures
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Dissection of the Genetic Background of Childhood Onset Progressive Myoclonic Epilepsies
Induced Pluripotent Stem Cell Models of Lysosomal Storage Disorders Daniel K
Neuronal Ceroid-Lipofuscinosis, CLN3-Related
Mutation Leading to a Sulfatase Deficiency Is Associated
Glucocerebrosidase Mutations and Parkinson's Disease
The CLN3 Gene Is a Novel Molecular Target for Cancer Drug Discovery1
Targeted Genes and Methodology Details for Inborn Errors of Metabolism Custom Gene Panel
Neuronal Ceroid Lipofuscinosis: a Common Pathway?
Progressive Pathogenesis of Juvenile Neuronal Ceroid Lipofuscinosis
A Knock-In Reporter Model of Batten Disease
Analysis of Pathogenic Alterations in the Cln3 Mouse Model (Mus
Altered Expression of Ganglioside Metabolizing Enzymes
Tripeptidyl Peptidase I, the Late Infantile Neuronal Ceroid Lipofuscinosis Gene Product, Initiates the Lysosomal Degradation of Subunit C of ATP Synthase1
NCBI ID Symbol 2 A2M 53947 A4GALT 51146 A4GNT 8086 AAAS
Exogenous Flupirtine As Potential Treatment for CLN3 Disease
Synaptic Dysfunction in Lysosomal Storage Disorders: Pathogenic
Supplemental Table 1. List of Candidate Gene Filters Used in the Analysis of Exome Sequencing. MYOPATHY NEUROPATHY MND ABHD5
Neuronal Network Dysfunction Precedes Storage and Neurodegeneration in a Lysosomal Storage Disorder