about
Human 70-kDa SHP-1L differs from 68-kDa SHP-1 in its C-terminal structure and catalytic activityCD22 associates with protein tyrosine phosphatase 1C, Syk, and phospholipase C-gamma(1) upon B cell activationTargeted disruption of SHIP leads to hemopoietic perturbations, lung pathology, and a shortened life spanGenetic modifiers of systemic lupus erythematosus in FcgammaRIIB(-/-) miceLeishmania major intracellular survival is not altered in SHP-1 deficient mev or CD45-/- mice.Lymphoid tyrosine phosphatase and autoimmunity: human genetics rediscovers tyrosine phosphatases.Why is PTPN22 a good candidate susceptibility gene for autoimmune disease?Modulation of the ERG K+ current by the tyrosine phosphatase, SHP-1.Dendritic cells under investigation in autoimmune disease.Genetic evidence that Shp-2 tyrosine phosphatase is a signal enhancer of the epidermal growth factor receptor in mammals.A deletion mutation in the SH2-N domain of Shp-2 severely suppresses hematopoietic cell development.Survival of monocytes and macrophages and their role in health and disease.SHP-1 negatively regulates neuronal survival by functioning as a TrkA phosphatase
P2860
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P2860
description
1994 nî lūn-bûn
@nan
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
1994年论文
@zh
1994年论文
@zh-cn
name
Molecular basis of the motheaten phenotype.
@en
type
label
Molecular basis of the motheaten phenotype.
@en
prefLabel
Molecular basis of the motheaten phenotype.
@en
P2860
P1476
Molecular basis of the motheaten phenotype.
@en
P2860
P304
P356
10.1111/J.1600-065X.1994.TB00852.X
P577
1994-04-01T00:00:00Z