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ASAH1
Implications in Parkinson's Disease
Understanding the Molecular Pathobiology of Acid Ceramidase Deficiency
ASAH1 Variant Causing a Mild SMA Phenotype with No Myoclonic Epilepsy: a Clinical, Biochemical and Molecular Study
Perkinelmer Genomics to Request the Saliva Swab Collection Kit for Patients That Cannot Provide a Blood Sample As Whole Blood Is the Preferred Sample
Requisition for DNA Testing
Generation of Sphingosine-1-Phosphate Is Enhanced in Biliary Tract Cancer Patients and Is Associated with Lymphatic Metastasis
Population Genetic Analysis of the N-Acylsphingosine Amidohydrolase Gene Associated with Mental Activity in Humans
Additional Tables.Xlsx
Targeting Acid Ceramidase to Improve the Radiosensitivity of Rectal Cancer
Disorders of Sphingolipid Synthesis, Sphingolipidoses, Niemann-Pick Disease Type C and Neuronal Ceroid Lipofuscinoses
Altered Mrna Expression Levels of the Major Components of Sphingolipid Metabolism, Ceramide Synthases and Their Clinical Implication in Colorectal Cancer
Glucocerebrosidase: Functions in and Beyond the Lysosome
Vitamin K2 As a New Modulator of the Ceramide De Novo Synthesis Pathway
Glucosylsphingosine Promotes Α-Synuclein Pathology in Mutant GBA- Associated Parkinson's Disease
Acid Ceramidase Depletion Impairs Neuronal Survival and Induces Morphological Defects in Neurites Associated with Altered Gene Transcription and Sphingolipid Content
Necroptosis in Primate Luteolysis
TFEB Links MYC Signaling to Epigenetic Control of Myeloid Differentiation and Acute Myeloid Leukemia
Molecular Basis of Acid Ceramidase Deficiency in a Neonatal Form of Farber Disease” in Molecular Genetics and Metabolism
Top View
ADX609 3301 Athena Newborndx Gene Panel Update 3-30-20.Indd
Acid Ceramidase Deficiency: Farber Disease and SMA-PME Fabian P
ASAH1 Gene N-Acylsphingosine Amidohydrolase 1
Molecular Mechanism of Activation of the Immunoregulatory Amidase NAAA
The Link Between Gaucher Disease and Parkinson's Disease Sheds
Identification of Palmitoyl Protein Thioesterase 1 Substrates Defines Roles for Synaptic Depalmitoylation
Loss of α2-6 Sialylation Promotes the Transformation Of
The Origins of Glucosylsphingosine in Gaucher Disease John J
Comprehensive Lysosomal Storage Disorders Panel with GBA and IDS
Cross-Talks Among GBA Mutations, Glucocerebrosidase, and Α
Acid Sphingomyelinase Inhibition Results in Profound Rescue
Systems Biology Analysis of the Lung Cancer‑Related Secretome
Pathogenic Variants in GNPTAB and GNPTG Encoding Distinct Subunits
Disruption of Sphingolipid Metabolism Augments Ceramide-Induced Autophagy in Preeclampsia
Metabolism of Glycosphingolipids and Their Role in the Pathophysiology of Lysosomal Storage Disorders
Analysis of Pathogenic Alterations in the Cln3 Mouse Model (Mus
Synuclein Proteinopathy in a Cellular Model of Parkinson's Disease
C26-Ceramide As Highly Sensitive Biomarker for the Diagnosis Of
Identification of Synaptic PPT1 Substrates Highlight Roles of Depalmitoylation in Disulfide Bond Formation and Synaptic Function
Supplemental Data Tuberous Sclerosis Complex-Associated CNS
Exogenous Flupirtine As Potential Treatment for CLN3 Disease
Supplemental Table S1 Percentage of the Distance from Chip-Seq Peak to the Nearest Transcription Sample 0-5
Table S11. up Or Down Regulated Genes in Tcof1 Over-Expressed
Identification of Novel Clinical Applications for Acid Sphingomyelinase Inhibitors
Epilepsy Test Requisition
Genomic Unity® Testing Comprehensive Neurology Testing Services Obtaining a Molecular Diagnosis for Neurology Patients Can Be Challenging
Lysosomal Acid Ceramidase ASAH1 Controls the Transition Between
Individual Genome Sequence Gene List (By Disease)
Inhibition of Sphingolipid Synthesis Improves Outcomes and Survival in GARP Mutant Wobbler Mice, a Model of Motor Neuron Degeneration
(ASA) in Parkinson's Disease: from Pathogenesis to Biomarker Potential
Myocardial Gene Expression Associated with Genetic Cardiac Hypertrophy in the Absence of Hypertension
Lysosomal Storage Disease in the Brain: Mutations of the Β-Mannosidase Gene Identified in Autosomal Dominant Nystagmus
Comprehensive Analysis of HEXB Protein Reveal Forty Two Novel Nssnps That May Lead to Sandhoff Disease (SD) Using Bioinformatics
Farber Disease: Understanding a Fatal Childhood Disorder and Dissecting Ceramide Biology Mark S