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CLN6
An Interactive Web Application to Explore Regeneration-Associated Gene Expression and Chromatin Accessibility
Palmitoyl-Protein Thioesterase 1 Deficiency in Drosophila Melanogaster Causes Accumulation
CLN8 Mutations Presenting with a Phenotypic Continuum of Neuronal Ceroid Lipofuscinosis—Literature Review and Case Report
Requisition for DNA Testing
Enhanced Expression of Manganese-Dependent Superoxide Dismutase in Human and Sheep CLN6 Tissues
Supplemental Table 1A. Differential Gene Expression Profile of Adehcd40l and Adehnull Treated Cells Vs Untreated Cells
CLN6 Gene CLN6, Transmembrane ER Protein
Disorders of Sphingolipid Synthesis, Sphingolipidoses, Niemann-Pick Disease Type C and Neuronal Ceroid Lipofuscinoses
1 SUPPLEMENTAL DATA Figure S1. Poly I:C Induces IFN-Β Expression
FREE Sequencing MLD Invitae Detect Lysosomalstorage Diseases (Lsds) Genetic Testing Program
Lysosomal Storage Disorders
Supplementary File 1 (PDF, 225 Kib)
Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss
Supplementary Figure 1. Dystrophic Mice Show Unbalanced Stem Cell Niche
Summary of New Classification
Supplementary Table 3. Genes Specifically Regulated by Zol (Non-Significant for Fluva)
Macaque Gene Symbols Were Mapped to Human Gene Symbols on June 2011
The CLN3 Gene and Protein: What We Know
Top View
Programmed Lectures
Dissection of the Genetic Background of Childhood Onset Progressive Myoclonic Epilepsies
CLN6 Disease
Downloaded from Pharmgkb (Accessed 11/2018 by Webgestalt 334 Tool)) Databases
Identification of Two Novel Null Variants in CLN8 By
Comprehensive Lysosomal Storage Disorders Panel with GBA and IDS
The Genetic Nomenclature of Recessive Cerebellar Ataxias
Mutation Leading to a Sulfatase Deficiency Is Associated
Exome Sequencing Enhanced Package Department of Pathology and Laboratory Medicine Feb 2012 UCLA Molecular Diagnostics Laboratories Page:1
Targeted Genes and Methodology Details for Inborn Errors of Metabolism Custom Gene Panel
Proteomic Landscape of the Human Choroid–Retinal Pigment Epithelial Complex
Neuronal Ceroid Lipofuscinosis: a Common Pathway?
Moving Towards Effective Therapeutic Strategies for Neuronal Ceroid Lipofuscinosis Ryan D
Recent Studies of Ovine Neuronal Ceroid Lipofuscinoses from BARN, the Batten Animal Research Network☆
SUPPLEMENTARY APPENDIX Targetable Driver Mutations in Multicentric Reticulohistiocytosis
Lysosomal Storage Disease Overview
You Can Check If Genes Are Captured by the Agilent Sureselect V5 Exome
Gene Expression Profiling in Vlincl CLN6-Deficient Fibroblasts: Insights Into Pathobiology