Pages that link to "Q36965786"

The following pages link to Immune system irregularities in lysosomal storage disorders. (Q36965786):

Displaying 39 items.

• Functional crosstalk between membrane lipids and TLR biology (Q26823479) (← links)
• Impaired neural differentiation of induced pluripotent stem cells generated from a mouse model of Sandhoff disease (Q27316065) (← links)
• Enzyme Replacement in a Human Model of Mucopolysaccharidosis IVA In Vitro and Its Biodistribution in the Cartilage of Wild Type Mice (Q28749673) (← links)
• Progranulin Deficiency Promotes Circuit-Specific Synaptic Pruning by Microglia via Complement Activation (Q30754508) (← links)
• GTPase of the Immune-Associated Nucleotide Protein 5 Regulates the Lysosomal Calcium Compartment in T Lymphocytes (Q30837702) (← links)
• Thymic Alterations in GM2 Gangliosidoses Model Mice (Q33697973) (← links)
• Mitochondrial autophagy promotes cellular injury in nephropathic cystinosis (Q33711275) (← links)
• Immunomodulatory activity of orphan drug Elmiron® in female B6C3F1/N mice (Q33840472) (← links)
• The galactocerebrosidase enzyme contributes to the maintenance of a functional hematopoietic stem cell niche (Q35215402) (← links)
• Manipulating autophagic processes in autoimmune diseases: a special focus on modulating chaperone-mediated autophagy, an emerging therapeutic target (Q35622999) (← links)
• Neuronal and epithelial cell rescue resolves chronic systemic inflammation in the lipid storage disorder Niemann-Pick C. (Q36026905) (← links)
• Gaucher disease geneGBAfunctions in immune regulation (Q36056642) (← links)
• Differential expression of matrix metalloproteinases in the serum of patients with mucopolysaccharidoses (Q36433328) (← links)
• Progressive thalamocortical neuron loss in Cln5 deficient mice: Distinct effects in Finnish variant late infantile NCL. (Q37248270) (← links)
• Normalizing glycosphingolipids restores function in CD4 T cells from lupus patients. (Q37524224) (← links)
• Juvenile neuronal ceroid lipofuscinosis (JNCL) and the eye. (Q37524944) (← links)
• Myelin lesions associated with lysosomal and peroxisomal disorders (Q37785556) (← links)
• Treating inflammation in childhood neurodegenerative disorders (Q37839130) (← links)
• Mucopolysaccharidosis type I: current knowledge on its pathophysiological mechanisms (Q38004963) (← links)
• Treatment options for lysosomal storage disorders: developing insights (Q38046227) (← links)
• Mucopolysaccharide diseases: a complex interplay between neuroinflammation, microglial activation and adaptive immunity. (Q38105045) (← links)
• The Roles of Lysosomes in Inflammation and Autoimmune Diseases (Q38235294) (← links)
• Insights into novel cellular injury mechanisms by gene expression profiling in nephropathic cystinosis (Q38504897) (← links)
• Gaucher disease: Progress and ongoing challenges (Q39028972) (← links)
• Activated and Memory T Lymphocytes in Children with Gaucher Disease (Q39379834) (← links)
• Fabry disease peripheral blood immune cells release inflammatory cytokines: role of globotriaosylceramide (Q42434979) (← links)
• Alterations in the properties of the cell membrane due to glycosphingolipid accumulation in a model of Gaucher disease. (Q47215609) (← links)
• Niemann-Pick disease type C in the newborn period: a single-center experience. (Q47761092) (← links)
• Genomewide association study identifies GALC as susceptibility gene for mucous membrane pemphigoid (Q47840482) (← links)
• Microglia in juvenile neuronal ceroid lipofuscinosis are primed toward a pro-inflammatory phenotype (Q47848197) (← links)
• Enzymes as Immunotherapeutics. (Q48333043) (← links)
• Contribution of inflammatory pathways to Fabry disease pathogenesis (Q50279704) (← links)
• Long time enzyme replacement therapy stabilizes obstructive lung disease and alters peripheral immune cell subsets in Fabry patients. (Q53214046) (← links)
• Characterisation of the T cell and dendritic cell repertoire in a murine model of mucopolysaccharidosis I (MPS I) (Q58418211) (← links)
• Altered immune phenotypes in subjects with Fabry disease and responses to switching from agalsidase alfa to agalsidase beta (Q64085287) (← links)
• Intracerebroventricular enzyme infusion corrects central nervous system pathology and dysfunction in a mouse model of metachromatic leukodystrophy (Q83941327) (← links)
• Neuroinflammation in frontotemporal dementia (Q92035807) (← links)
• Prevalence of antibodies to ganglioside and Hep 2 in Gaucher, Niemann - Pick type C and Sanfilippo diseases (Q92715189) (← links)
• Recent trends in mucopolysaccharidosis research (Q93209008) (← links)