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Glycolipid
Sphingolipid Metabolism Diseases ⁎ Thomas Kolter, Konrad Sandhoff
Structural Evidence for Adaptive Ligand Binding of Glycolipid Transfer Protein
Sphingolipids and Cell Signaling: Relationship Between Health and Disease in the Central Nervous System
Metabolism of Brain Glycolipid Fatty Acids '': Yasuo Kishimoto and Norman S
Sphingosine Kinases and Their Metabolites Modulate Endolysosomal Trafficking in Photoreceptors
Supplementary Table S1 List of Proteins Identified with LC-MS/MS in the Exudates of Ustilaginoidea Virens Mol
Mutagenesis of Human Alpha-Galactosidase a for the Treatment of Fabry Disease
Differentiation of Murine Leukemia Cells:I-I Antigenic
L-Glucosylceramide: Synthesis, Properties, and Resistance
How Does Alpha Galactosidase Deficiency
SPHINGOSINE KINASE INHIBITION AMELIORATES CHRONIC HYPOPERFUSION-INDUCED WHITE MATTER LESIONS 112 4.1 Introduction
Glucocerebrosidase: Functions in and Beyond the Lysosome
Enzymatic Synthesis of Glycolipid Surfactants
Globoid Cell Leukodystrophy: Deficiency of Lactosyl Ceramide
Sphingosine Kinase Blockade Leads to Increased Natural Killer T Cell Responses to Mantle Cell Lymphoma
Glycolipid Synthesis in Normal and Virus-Transformed Hamster Cell
Secretory Sphingomyelinase in Health and Disease
Isolation and Characterization of Sphingolipids in Arabidopsis Thaliana
Top View
Human Acid Sphingomyelinase Structures Provide Insight to Molecular Basis of Niemann-Pick Disease Yan-Feng Zhou Analytical Discovery Therapeutics
Sphingolipids (GSL) Takes Place at the Intracellular Membranes of Endoplas- Mic Reticulum and the Golgi Apparatus in Eukaryonic Cells
Anti‑Glycolipid Disorder Effect of Epigallocatechin‑3‑Gallate on High‑Fat Diet and STZ‑Induced T2DM in Mice
Gaucher Disease
P-Galactosidase in Tissue Culture Derived from Human Skin and Bone Marrow: Enzyme Defect in Gmlgangliosidosis
Lamellar Bodies of Human Epidermis
Sphingolipids and Kidney Disease: Possible Role of Preeclampsia and Intrauterine Growth Restriction (IUGR)
Sphingolipids and Lysosomal Pathologies☆
Association of the Glycolipid Pattern with Antigenic Alterations in Mouse Fibroblasts Transformed by Murine Sarcoma Virus1
[Frontiers in Bioscience 16, 1797-1810, January 1, 2011] 1797
Lysosomal Storage Diseases ª the Author(S) 2014 DOI: 10.1177/2326409813517663 Iem.Sagepub.Com
Metabolism of Glycosphingolipids and Their Role in the Pathophysiology of Lysosomal Storage Disorders
Contributions of Glycolipid Biosurfactants and Glycolipid- Modified Materials to Antimicrobial Strategy: a Review
Psychosine Variants As Antigens for Natural Killer T Cells† Cite This: Chem
Sachs Disease
Studies in Glycolipids
Editorial: Effects of Membrane Lipids on Protein Function
Novel Mutations in the Glucocerebrosidase Gene of Indian Patients with Gaucher Disease
A New Glucocerebrosidase Chaperone Reduces Α-Synuclein and Glycolipid
Lysosomal Lipid Storage Diseases
Tailored Design of NKT-Stimulatory Glycolipids for Polarization of Immune Responses Jung-Tung Hung1, Jing-Rong Huang1 and Alice L
Altered Sphingolipid Metabolism Induced by Tumor Hypoxia – New Vistas in Glycolipid Tumor Markers
Taliglucerase Alfa (Elelyso) Reference Number: ERX.SPMN.138 Effective Date: 10/16 Coding Implications Last Review Date: 09/16 Revision Log
Lysosomal Storage Disorders: the Cellular Impact of Lysosomal Dysfunction
Alpha Galactosidase
Sphingolipid-Transporting Proteins As Cancer Therapeutic Targets
Sphingolipid Biochemistry Handbook of Lipid Research Editor: Donald J
Lysosomal Storage Diseases
Mechanism of Glucocerebrosidase Activation and Dysfunction in Gaucher Disease Unraveled by Molecular Dynamics and Deep Learning
GRAS Notice 740 for Glycolipids from Dacryopinax Spathularia
The Glycosylation Design Space for Recombinant Lysosomal Replacement Enzymes Produced in CHO Cells
Metab. Phospholipids, Glycolipids