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Immune system irregularities in lysosomal storage disorders
Julian A. Castaneda
, Ming J. Lim
,
Jonathan D. Cooper
, David A. Pearce
Roy and Diana Vagelos Division of Biology & Biomedical Sciences (DBBS)
Bursky Center for Human Immunology & Immunotherapy Programs (CHiiPs)
Division of Genetics and Genomic Medicine
DBBS - Neurosciences
DBBS - Developmental, Regenerative and Stem Cell Biology
DBBS - Molecular Genetics and Genomics
Research output
:
Contribution to journal
›
Review article
›
peer-review
96
Scopus citations
Overview
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Dive into the research topics of 'Immune system irregularities in lysosomal storage disorders'. Together they form a unique fingerprint.
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Biochemistry, Genetics and Molecular Biology
Antigen Presentation
100%
Lysosome
100%
Genetic Disorder
50%
Mediator
50%
Cell Function
50%
Sly Syndrome
50%
Cellular Secretion
50%
Antigen Presenting Cell
50%
Niemann-Pick Disease
50%
Gaucher's Disease
50%
Mast Cell
50%
Batten Disease
50%
Neuronal Ceroid Lipofuscinosis
50%
Cytotoxic T Cell
50%
Perforin
50%
GM2 Gangliosidoses
50%
Metabolic Intermediate
50%
Mannosidosis
50%
Hyperactivity
50%
Neuroscience
Lysosome
100%
Leukodystrophy
50%
Cell Function
50%
Hyperactivity
50%
Pick's Disease
50%
Antigen Presenting Cell
50%
T Cell
50%
Mast Cell
50%
Neuronal Ceroid Lipofuscinosis
50%
Cellular Secretion
50%
Proteolipid
50%
Mannosidosis
50%
Perforin
50%
Keyphrases
Lysosomal Storage Disease
100%
Immune System
100%
Lysosomal Compartment
33%
Lysosome
22%
Mast Cells
11%
Antigen Presentation
11%
Cytotoxic T Lymphocytes
11%
Inherited Disease
11%
Inflammatory Mediators
11%
Immune Suppression
11%
Cell Behavior
11%
Clinical Data
11%
Antigen-presenting Cells
11%
Hyperactivity
11%
Mucopolysaccharidosis VII
11%
NP-C
11%
Biochemical Studies
11%
Cell Secretion
11%
Disease-specific
11%
Neurological Impairment
11%
Globoid Cell Leukodystrophy
11%
Perforin
11%
Gaucher Disease
11%
Neuronal Ceroid Lipofuscinosis
11%
Immune System Function
11%
Antigen Processing
11%
Neuroimmune Response
11%
Biological Materials
11%
Pore-forming
11%
GM2 Gangliosidosis
11%
Proteolipids
11%
Metabolic Intermediates
11%
Alpha-mannosidosis
11%