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ACER3
Implications in Parkinson's Disease
Methods
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
Detection of Selection Signatures in Farmed Coho Salmon (Oncorhynchus Kisutch) Using Dense Genome‑Wide Information M
Generation of Sphingosine-1-Phosphate Is Enhanced in Biliary Tract Cancer Patients and Is Associated with Lymphatic Metastasis
Acid Ceramidase Controls Apoptosis and Increases Autophagy in Human Melanoma Cells Treated with Doxorubicin
Disorders of Sphingolipid Synthesis, Sphingolipidoses, Niemann-Pick Disease Type C and Neuronal Ceroid Lipofuscinoses
Adipocyte-Specific Deficiency of De Novo Sphingolipid Biosynthesis Leads to Lipodystrophy and Insulin Resistance
Loss of the Sphingolipid Desaturase DEGS1 Causes Hypomyelinating Leukodystrophy
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
Autocrine IFN Signaling Inducing Profibrotic Fibroblast Responses By
Macaque Gene Symbols Were Mapped to Human Gene Symbols on June 2011
SUPPLEMENTARY MATERIALS and METHODS PBMC Transcriptomics
The Link Between Gaucher Disease and Parkinson's Disease Sheds
ACER3-Related Leukoencephalopathy: Expanding
PDF Output of CLIC (Clustering by Inferred Co-Expression)
The Origins of Glucosylsphingosine in Gaucher Disease John J
Top View
Mutations in Sphingolipid Metabolism Genes Are Associated with ADHD
Perilipin 2 Improves Insulin Sensitivity in Skeletal Muscle Despite Elevated Intramuscular Lipid Levels
Improving Diagnosis, Understanding, and Treatment of Farber Disease
ACER3-Realted Leukoencephalopathy: Expanding the Clinical and Imaging Findings Spectrum Due to Novel Variants
Supplementary File 1
Aneuploid Cell Survival Relies Upon Sphingolipid Homeostasis
Acid Ceramidase Deficiency in Mice Results in a Broad Range Of
Inborn Metabolic Diseases, DOI 10.1007/978-3-662-49771-5 , © Springer-Verlag Berlin Heidelberg 2016 644 Subject Index
A Gene Expression Estimator of Intramuscular Fat Percentage for Use in Both Cattle and Sheep
Identification of Acer2 As a First Susceptibility Gene for Lithium-Induced Nephrogenic Diabetes Insipidus in Mice
Structural Basis for the Activation of Acid Ceramidase
Supplementary Table 1
Metabolske Sykdommer V02
Role of Sphingolipids and Metabolizing Enzymes in Hematological Malignancies
Supplemental Data Tuberous Sclerosis Complex-Associated CNS
Expression Profiling of Constitutive Mast Cells Reveals a Unique Identity
Transcriptomics Identified a Critical Role for Th2 Cell-Intrinsic Mir-155 In
Generated by SRI International Pathway Tools Version 25.0 on Mon
In Spino-Cerebellar Tissue, Ataxin-2 Expansion Affects Ceramide-Sphingomyelin Metabolism
Alkaline Ceramidase Catalyzes the Hydrolysis of Ceramides Via a Catalytic Mechanism Shared by Zn2+-Dependent Amidases
Hnrnp K Co-Immunoprecipitated Transcripts Regulated by BDNF
Loss of the Sphingolipid Desaturase DEGS1 Causes Hypomyelinating Leukodystrophy
Rapid Mendelian Sequencing Gene List December 2018
Leukodystrophy Panel Versie V2 (265 Genen) Centrum Voor Medische Genetica Gent
Supplementary Table 1. a Full List of Cancer Genes
Genomic Unity® Neurology Analysis
Structure of a Human Intramembrane Ceramidase Explains Enzymatic
ASLAN003, a Potent Dihydroorotate Dehydrogenase Inhibitor for Differentiation of Acute Myeloid Leukemia
Structure of a Human Intramembrane Ceramidase Explains Enzymatic Dysfunction Found in Leukodystrophy
Probe List HTG Transcriptome Panel
Ceramide Metabolism Enzymes—Therapeutic Targets Against Cancer