A multiple sclerosis-associated variant of CBLB links genetic risk with type I IFN function.
about
Translational utility of experimental autoimmune encephalomyelitis: recent developmentsCbl-b-deficient mice express alterations in trafficking-related molecules but retain sensitivity to the multiple sclerosis therapeutic agent, FTY720.Genetic determinants of risk and progression in multiple sclerosis.Genetic variants associated with autoimmunity drive NFκB signaling and responses to inflammatory stimuliCCAAT/Enhancer-binding protein β promotes pathogenesis of EAE.Modulation of Immune Cell Functions by the E3 Ligase Cbl-b.Post-Translational Modification Profiling-Functional Proteomics for the Analysis of Immune Regulation.Gut dysbiosis breaks immunological tolerance toward the central nervous system during young adulthood.Regulation of Lymphatic GM-CSF Expression by the E3 Ubiquitin Ligase Cbl-b
P2860
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P2860
A multiple sclerosis-associated variant of CBLB links genetic risk with type I IFN function.
description
2014 nî lūn-bûn
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2014年の論文
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2014年論文
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2014年論文
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2014年論文
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2014年論文
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2014年論文
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2014年论文
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2014年论文
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2014年论文
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name
A multiple sclerosis-associate ...... risk with type I IFN function.
@en
type
label
A multiple sclerosis-associate ...... risk with type I IFN function.
@en
prefLabel
A multiple sclerosis-associate ...... risk with type I IFN function.
@en
P2093
P50
P356
P1476
A multiple sclerosis-associate ...... risk with type I IFN function
@en
P2093
Christian Schulze
Klarissa Hanja Stürner
Roland Martin
Uwe Borgmeyer
P304
P356
10.4049/JIMMUNOL.1303077
P407
P577
2014-09-26T00:00:00Z