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1 concomitant phosphorylation of proline-rich tyrosine kinase 2.
2 activated the downstream kinase proline-rich tyrosine kinase 2.
3 ne phosphatase 1c with the receptor and with tyrosine kinase 2.
4 tein kinase C, Src kinases, and proline-rich tyrosine kinase 2.
5 of the receptor, STAT1, Janus kinase 1, and tyrosine kinase 2.
6 proteins were identified and include protein-tyrosine kinase 2 (also known as CAKbeta, RAFTK, and CAD
7 e kinase (RAFTK), also known as proline-rich tyrosine kinase 2 and cellular adhesion kinase beta, has
11 tyrosine phosphorylation of Janus kinase 2, tyrosine kinase 2, and STAT3 and STAT4 transcription fac
13 he phosphorylation and activation of protein-tyrosine kinase 2-beta (PTK2B, also referred to as Pyk2)
14 tein 9 (CARD9) disturb the subsequent spleen tyrosine kinase 2-CARD9/BCL10/MALT1-driven signaling cas
16 ntrolene-sensitive, nonreceptor proline-rich tyrosine kinase-2; components of the extracellular signa
19 dicted that the 86 amino acids following the tyrosine kinase 2 domain of beta PDGFR (amino acid resid
20 tyrosine phosphorylation of the proline-rich tyrosine kinase 2, epidermal growth factor receptor (EGF
21 AIMS: Drugs that inhibit the erb-b2 receptor tyrosine kinase 2 (ERBB2 or HER2) are the standard treat
23 the cell membrane, and that Erb-b2 receptor tyrosine kinase 2 (Erbb2) function is required for this
24 In a mouse model of basal ErbB2 receptor tyrosine kinase 2 (ErbB2)-positive breast cancer (ErbB2(
25 mRNA expression of discoidin domain receptor tyrosine kinase 2, fibronectin, and alpha-smooth muscle
26 e with a 2538 G-->A missense mutation in the tyrosine kinase-2 gene (Tyk2) are susceptible to Toxopla
27 r protein-tyrosine kinase Pyk2 (proline-rich tyrosine kinase 2) has been shown previously to regulate
32 ata further suggest that within this complex tyrosine kinase 2 is the tyrosine kinase responsible for
35 with the BCR-ABL fusion kinase and the Janus tyrosine kinase 2 (JAK2) V617F mutation, respectively.
37 ion of JAKs, all JAKs (JAK1, JAK2, JAK3, and tyrosine kinase 2), JAK2, or JAK3, caused a significant
38 ty, including focal adhesion kinase, protein tyrosine kinase-2, Janus kinase, other focal adhesion-as
41 ion study identified the gene encoding lemur tyrosine kinase-2 (LMTK2) as a susceptibility gene for p
42 in kinase C delta and , but not proline-rich tyrosine kinase 2, mediate tumor necrosis factor alpha-i
44 r necrosis factor-alpha-induced proline-rich tyrosine kinase 2 phosphorylation, but at different tyro
47 CH patients with higher pretreatment protein tyrosine kinase 2 (PTK2) messenger RNA levels derived gr
48 sion of one such gene, that encoding protein tyrosine kinase 2 (ptk2, also known as focal adhesion ki
49 ion kinase [FAK] family members proline-rich tyrosine kinase 2 [Pyk-2] and FAK) was also examined usi
52 focal adhesion kinase (FAK) and proline-rich tyrosine kinase 2 (Pyk2) and also reduces the associatio
53 focal adhesion kinase (FAK) and proline-rich tyrosine kinase 2 (Pyk2) and their increased association
54 cells, phosphorylation of a FAK/proline-rich tyrosine kinase 2 (PYK2) consensus site in the alpha-hel
55 eceptor tyrosine kinase proline-rich protein tyrosine kinase 2 (Pyk2) functions as an integrator of m
56 tes the role of the nonreceptor proline-rich tyrosine kinase 2 (PYK2) in Ang II-induced VSMC protein
63 in vitro studies indicated that proline-rich tyrosine kinase 2 (PYK2) is a positive mediator of osteo
65 , expression of the FAK-related proline-rich tyrosine kinase 2 (Pyk2) is elevated and phosphorylated
67 study in this issue shows that proline-rich tyrosine kinase 2 (Pyk2) is responsible for acid-induced
70 l that tyrosine kinases Src and proline-rich tyrosine kinase 2 (Pyk2) regulate SHP-1-dependent LPS-in
78 n focal tyrosine kinase (RAFTK)/proline-rich tyrosine kinase 2 (PYK2), an upstream effector of JNK an
79 yrosine-protein kinase) and the proline-rich tyrosine kinase 2 (Pyk2), and they can also cause robust
81 ns of FAK are shared by its homolog, protein tyrosine kinase 2 (Pyk2), raising the question as to whe
83 rimary response gene-88 (MYD88)/proline-rich tyrosine kinase 2 (PYK2)/LYN complexes, which allows rec
85 egulated focal adhesion protein proline-rich tyrosine kinase-2 (Pyk2) and the effector proteins paxil
87 hosphorylation (Tyr-402) of the proline-rich tyrosine kinase-2 (PYK2) without significant change in a
88 al adhesion kinase (FAK) and/or proline-rich tyrosine kinase-2 (Pyk2), based on two lines of evidence
89 kinase Cs (aPKCs) by activating proline-rich tyrosine kinase-2 (PYK2), ERK pathway components, and ph
90 inhibitable; (b) dependent upon proline-rich tyrosine kinase-2 (PYK2), GRB2, SOS, RAS, RAF, and MEK1;
92 cules downstream of the IFN receptor, namely tyrosine kinase 2, STAT1, and IFN regulatory factor 7, a
93 transcription (STAT) family, including JAK1, tyrosine kinase 2, STAT2, and STAT4 in the human progeni
94 that in cells expressing RAFTK/proline-rich tyrosine kinase 2, such as endothelial and B cells, RAFT
95 Y657 of eNOS and expression of proline-rich tyrosine kinase 2 that phosphorylates this residue were
96 G protein and to PLC-gamma via a downstream tyrosine kinase; 2) the initial AT1 receptor-PLC-beta1 c
97 NG-2 binds the endothelial-specific receptor tyrosine kinase 2 (TIE2) and acts as a negative regulato
98 ion of the angiopoietin receptor endothelial tyrosine kinase 2 (Tie2) or both angiopoietin-1 and angi
99 -specific tunica intima endothelial receptor tyrosine kinase 2 (Tie2) receptor kinase, angiopoietin-1
101 necrosis factor-alpha activates proline-rich tyrosine kinase 2 to cause cytoskeletal disorganization
103 ive (CYT387), which inhibits JAK1, JAK2, and tyrosine kinase 2 (TYK2) at low nanomolar concentrations
105 cule inhibitor with specificity for JAK1 and tyrosine kinase 2 (TYK2) over other JAK family members.
106 mily of cytoplasmic tyrosine kinases) family tyrosine kinase 2 (TYK2) participates in signaling throu
107 cure, but we demonstrate that IL-22 acts via tyrosine kinase 2 (Tyk2), a member of the Jak family.
108 xis, connecting genetic aberrations in FLT3, tyrosine kinase 2 (TYK2), platelet-derived growth factor
109 the pseudokinase domain of the Janus kinase tyrosine kinase 2 (Tyk2), resulting in blockade of recep
113 Concomitantly, IFN-alpha stimulation of tyrosine kinase 2 tyrosine phosphorylation and kinase ac
115 t al. now show that mutation of another Jak, tyrosine kinase 2, underlies another human immunodeficie
116 small interfering RNA targeting proline-rich tyrosine kinase-2, which was also phosphorylated in resp
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