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1 T receptor activation through recruitment of protein tyrosine phosphatase 1B.
2 cting ligands of an allosteric pocket of the protein tyrosine phosphatase 1B.
3 photoreceptors against dephosphorylation by protein tyrosine phosphatase 1B.
4 1 over VH-1-related phosphatase, Cdc25B2, or protein-tyrosine phosphatase 1B.
5 in part by a reduction in the expression of protein-tyrosine phosphatase 1B.
6 yrosine phosphatase-alpha over the cytosolic protein-tyrosine phosphatase-1B.
7 reased skeletal muscle protein expression of protein-tyrosine phosphatase 1B (a negative regulator of
8 a chemical library of 704 compounds against protein tyrosine phosphatase 1B, a diabetes, obesity, an
12 phosphorylation of autophosphorylated Src by protein tyrosine phosphatase 1B allowed Src to be inacti
14 enes for signal transduction proteins (e.g., protein tyrosine phosphatase 1B and regulatory subunits
15 ially S-oxidized and S-nitrosylated forms of protein tyrosine phosphatase 1B, as well as intact and l
16 NAFLD, including the histopathologic marker protein tyrosine phosphatase 1b, AST/ALT ratio, gamma-gl
21 , inhibiting the phosphotyrosine phosphatase protein tyrosine phosphatase 1B further stimulated insul
22 rylation of insulin receptor substrate-1 and protein tyrosine phosphatase-1B gene expression and the
24 nalysis, leukocyte antigen related (LAR) and protein-tyrosine phosphatase 1B had the greatest increas
25 NA levels, protein mass, and activity of the protein-tyrosine phosphatase-1B implicated in the attenu
27 hat both the native and the cleaved forms of protein tyrosine phosphatase 1B interact with p130(Cas)
29 o enzyme inhibition (glycogen phosphorylase, protein tyrosine phosphatase 1B) or by inhibiting renal
32 eraldehyde-3-phosphate dehydrogenase, HSP27, protein-tyrosine phosphatase 1B, protein kinase Calpha,
33 ogen synthase kinase-3beta, forkhead box O1, protein-tyrosine phosphatase-1B, PTEN (phosphatase and t
35 c but enhanced the Ser-50 phosphorylation of protein tyrosine phosphatase 1B (PTP-1B) with a concomit
39 uppressor of cytokine signaling (SOCS)-3 and protein-tyrosine phosphatase 1B (PTP-1B) are two endogen
42 late radial migration in mouse brain via the protein tyrosine phosphatase 1B (PTP1B) and alpha- and b
43 g with assays of zinc content was related to protein tyrosine phosphatase 1B (PTP1B) and extracellula
44 aling and reduced levels of the phosphatases protein tyrosine phosphatase 1B (PTP1B) and phosphatase
46 e of Developmental Cell, two groups identify protein tyrosine phosphatase 1B (PTP1B) as a cause of le
51 ued by expression of a truncated fragment of protein tyrosine phosphatase 1B (PTP1B) corresponding to
67 at increased NO production via inhibition of protein tyrosine phosphatase 1B (PTP1B) is associated wi
74 invasion through enhanced recruitment of the protein tyrosine phosphatase 1B (PTP1B) to a MET/VEGFR2
75 idic benzimidazole sulfonamide inhibitors of protein tyrosine phosphatase 1B (PTP1B) were derived fro
76 A highly potent and selective inhibitor of protein tyrosine phosphatase 1B (PTP1B) with a nanomolar
77 e we show how these pillars are connected in Protein Tyrosine Phosphatase 1B (PTP1B), a drug target f
79 ran and benzothiophene biphenyl analogues of protein tyrosine phosphatase 1B (PTP1B), a target for in
80 tion machinery modulates an interaction with protein tyrosine phosphatase 1B (PTP1B), an ER-associate
81 rreversible sulphinic and sulphonic acids of protein tyrosine phosphatase 1B (PTP1B), an important en
82 imarily to transcriptional downregulation of protein tyrosine phosphatase 1B (PTP1B), an inhibitory p
83 omerase, nucleophosmin-1, chaperonin, actin, protein tyrosine phosphatase 1B (PTP1B), and glucosidase
84 gative inhibitor of insulin signaling, i.e., protein tyrosine phosphatase 1B (PTP1B), and increased p
86 lpain-1 null (Capn1-/-) platelets accumulate protein tyrosine phosphatase 1B (PTP1B), which correlate
87 nalysis of the redox-dependent regulation of protein tyrosine phosphatase 1B (PTP1B), which is revers
91 s implications for the in vivo regulation of protein tyrosine phosphatase 1B (PTP1B, EC 3.1.3.48): th
93 signal termination is less well understood, protein tyrosine phosphatase-1B (PTP1B) is implicated in
96 to discover novel inhibitors for the enzyme protein tyrosine phosphatase-1B (PTP1B), a tyrosine phos
97 cell infiltration, expression of MMP-9, and protein tyrosine phosphatase-1B (PTP1B), which negativel
100 s zinc transport into hepatocytes to inhibit protein-tyrosine phosphatase 1B (PTP1B) activity, which
101 epatocytes with or without expression of the protein-tyrosine phosphatase 1B (PTP1B) and in wild-type
102 enylalanine (F(2)Pmp)-containing peptides to protein-tyrosine phosphatase 1B (PTP1B) and its substrat
111 tically inactive mutant (C215S) of the human protein-tyrosine phosphatase 1B (PTP1B) has been solved
113 h as silencer of cell signaling 1 (SOCS1) or protein-tyrosine phosphatase 1B (PTP1B) in this process.
120 aim of our work was to study the role of the protein-tyrosine phosphatase 1B (PTP1B) on the cellular
122 ermal growth factor (EGF) on the activity of protein-tyrosine phosphatase 1B (PTP1B) was investigated
124 colocalization of S-nitrosothiol (S-NO) and protein-tyrosine phosphatase 1B (PTP1B), and Akt phospho
126 our candidate protein-tyrosine phosphatases (protein-tyrosine phosphatase 1B (PTP1B), SH2 domain-cont
133 To understand the physiological role of protein-tyrosine phosphatase 1B (PTPase 1B) in insulin a
138 had a significantly higher IRbeta-associated protein tyrosine phosphatase-1B than the mean of WL5 and
140 we experimentally validate a cryptic site in protein tyrosine phosphatase 1B using a covalent ligand
144 are distinctly different from those seen in protein tyrosine phosphatase 1B where a five-membered su
146 ave identified a small-molecule inhibitor of protein tyrosine phosphatase 1B with low micromolar inhi
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