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Nature Reviews Molecular Cell Biology, ISSN 1471-0072, 09/2009, Volume 10, Issue 9, pp. 597 - 608
Journal Article
Journal of Cellular Physiology, ISSN 0021-9541, 03/2017, Volume 232, Issue 3, pp. 463 - 476
Journal Article
Journal of Immunology, ISSN 0022-1767, 01/2018, Volume 200, Issue 2, pp. 483 - 499
T cells use the endocytic pathway for key cell biological functions, including receptor turnover and maintenance of the immunological synapse. Some of the... 
EARLY ENDOSOMAL TRANSPORT | PROTEIN EHD1 | IMMUNE SYNAPSE | SURFACE EXPRESSION | DOWN-REGULATION | CENTRAL-NERVOUS-SYSTEM | IMMUNOLOGY | IMMUNOLOGICAL SYNAPSE | PLASMA-MEMBRANE | INTRAFLAGELLAR TRANSPORT | AUTOIMMUNE ENCEPHALOMYELITIS | Multigene Family | Encephalomyelitis, Autoimmune, Experimental - metabolism | Vesicular Transport Proteins - metabolism | Encephalomyelitis, Autoimmune, Experimental - immunology | Lymphoid Tissue - immunology | CD4-Positive T-Lymphocytes - immunology | Multiprotein Complexes - metabolism | Endocytosis | Lysosomes - metabolism | T-Lymphocytes - metabolism | Proteolysis | Female | Encephalomyelitis, Autoimmune, Experimental - genetics | Nuclear Proteins - genetics | Gene Expression | Receptors, Antigen, T-Cell - metabolism | Lymphocyte Activation | Vesicular Transport Proteins - genetics | CD4-Positive T-Lymphocytes - metabolism | Lymphoid Tissue - metabolism | DNA-Binding Proteins - genetics | Gene Knockout Techniques | CD3 Complex - metabolism | Mice, Knockout | Protein Transport | Carrier Proteins - genetics | Animals | Protein Binding | T-Lymphocytes - immunology | Mice | Cell proliferation | Regulators | Oligodendrocyte-myelin glycoprotein | Encephalomyelitis | Myelin | Secretion | Glycoprotein | SNAP receptors | Homology | Immunological synapses | Lymphocytes T | CD3 antigen | Experimental allergic encephalomyelitis | CD4 antigen | Proteins | T-cell receptor | Immunology | Interleukin 2 | Lymphocytes | Rodents | Recycling | Regulatory proteins
Journal Article
Molecular Neurodegeneration, ISSN 1750-1326, 09/2016, Volume 11, Issue 1
Christianson Syndrome, a recently identified X-linked neurodevelopmental disorder, is caused by mutations in the human gene SLC9A6 encoding the recycling... 
Ubiquitination | Protein misfolding | NHE6/SLC9A6 | Christianson syndrome | Membrane trafficking | X-linked intellectual disability | Apoptosis | Endosomal pH homeostasis | Gene mutations | Physiological aspects | Causes of | Nervous system | Degeneration | Genetic aspects | Research
Journal Article