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1 -dependent process when triggered ex vivo by colony stimulating factor-1.
2 elial growth factor, tissue factor (TF), and colony-stimulating factor 1.
3 yte-macrophage colony-stimulating factor and colony-stimulating factor-1.
4 ptors for platelet-derived growth factor and colony-stimulating factor-1.
5 IL-34, which was a known cytokine receptor, colony-stimulating factor 1 (also called macrophage colo
6 entiated into osteoclasts in the presence of colony stimulating factor-1 and receptor activator of NF
7 alpha(-/-) hematopoietic cells treated with colony-stimulating factor 1 and RANK ligand (RANKL), as
8 on of the putative tooth eruption molecules, colony-stimulating factor-1 and c-fos, both of which are
10 m the platelet-derived growth factor (PDGF), colony stimulating factor-1, and epidermal growth factor
11 ctivator of Nuclear factor-kappaB ligand and colony-stimulating factor-1, and decrease the expression
12 pression and proliferative responsiveness to colony-stimulating factor-1; and (c) elevated expression
13 Inhibition of TAM recruitment using an anti-colony-stimulating factor-1 antibody compromised the sur
14 stabilization, including macrophage-specific colony-stimulating factor 1, carbonic anhydrase 2, Bcl2,
16 etween interleukin 1 receptor antagonist and colony-stimulating factor 1, colony-stimulating factor 2
17 a stable complex with the chimeric receptor colony stimulating factor 1 (CSF)-Met and wild type DEP-
21 how that microglia develop in mice that lack colony stimulating factor-1 (CSF-1) but are absent in CS
24 autophosphorylated Tyr559 in the JMD of the colony stimulating factor-1 (CSF-1) receptor (CSF-1R) bi
26 acellular ligand binding domain of the human colony stimulating factor-1 (CSF-1) receptor to sequence
29 dary events occur, such as the expression of colony stimulating factor-1 (CSF-1) which play a critica
30 ormyl-methionyl-leucyl-phenylalanine (FMLP), colony stimulating factor-1 (CSF-1), IgG-coated particle
31 n the gene for the macrophage growth factor, colony stimulating factor-1 (CSF-1), that are severely d
32 at the op locus which are totally devoid of colony stimulating factor-1 (CSF-1), the major growth fa
34 w tested the roles of Cdc42, Rac, and Rho in colony stimulating factor-1 (CSF-1)-induced macrophage m
36 ar precursor cells under the control of both colony stimulating factor-1 (CSF-1, or M-CSF) and recept
37 ng signaling by the major macrophage mitogen colony-stimulating factor 1 (CSF-1) (also known as macro
38 s a signaling effector engaged by macrophage colony-stimulating factor 1 (CSF-1) and receptor activat
40 ted with gamma interferon (IFN-gamma) DNA or colony-stimulating factor 1 (CSF-1) DNA prior to ocular
41 rapid osteoclast differentiation induced by colony-stimulating factor 1 (CSF-1) in Csf1-null toothle
42 of LCs in mice deficient in the receptor for colony-stimulating factor 1 (CSF-1) in steady-state cond
43 r tyrosine at codon 809 (Y809F) of the human colony-stimulating factor 1 (CSF-1) receptor (CSF-1R) im
47 arr virus (EBV) BARF1 gene encodes a soluble colony-stimulating factor 1 (CSF-1) receptor that neutra
49 s of either epidermal growth factor (EGF) or colony-stimulating factor 1 (CSF-1) stimulate collection
51 other tyrosine kinases including, KIT, FLT3, colony-stimulating factor 1 (CSF-1), and RET, which are
55 for the mononuclear phagocytic growth factor colony-stimulating factor 1 (CSF-1), we have demonstrate
56 phosphorylated at residue threonine 72 in a colony-stimulating factor 1 (CSF-1)- and mitogen-activat
57 clear that alloantibody can, in concert with colony-stimulating factor 1 (CSF-1)-dependent donor macr
58 ly suppresses OC differentiation by limiting colony-stimulating factor 1 (CSF-1)-dependent proliferat
65 te to regulate specific genes in response to colony-stimulating factor-1 (CSF-1) and receptor activat
68 radients of epidermal growth factor (EGF) or colony-stimulating factor-1 (CSF-1) can induce invasion
70 otic because of a frameshift mutation in the colony-stimulating factor-1 (CSF-1) gene (Csf1(tl)).
71 recessive null osteopetrotic mutation in the colony-stimulating factor-1 (CSF-1) gene, we show that C
78 e investigated how costimulation by cAMP and colony-stimulating factor-1 (CSF-1) or interleukin-3 (IL
80 H3T3 fibroblasts co-expressing a form of the colony-stimulating factor-1 (CSF-1) receptor that is par
81 extracellular, ligand-binding domain of the colony-stimulating factor-1 (CSF-1) receptor to the tran
82 o-oncogene, which encodes for the macrophage colony-stimulating factor-1 (CSF-1) receptor, has been o
86 es, activation of WASPbs upon treatment with colony-stimulating factor-1 (CSF-1) was detected globall
90 2) mouse model of pancreatic islet cancer to colony-stimulating factor-1 (CSF-1)-deficient Csf1(op/op
92 gnal-regulated kinase (ERK) is necessary for colony-stimulating factor-1 (CSF-1)-mediated c-Myc expre
102 osine kinase inhibitor, blocks expression of colony stimulating factor 1 (CSF1) by a small subpopulat
107 n neutralizing antibodies against macrophage colony-stimulating factor 1 (CSF1 or MCSF) or F4/80.
110 Previously we showed that activation of the colony-stimulating factor 1 (CSF1) gene by the chromatin
112 l nerve injury induced de novo expression of colony-stimulating factor 1 (CSF1) in injured sensory ne
114 et of inflammatory response genes, including colony-stimulating factor 1 (CSF1), a central regulator
115 ed, is characterised by an overexpression of colony-stimulating factor 1 (CSF1), and is usually cause
118 th muscle that can express varying levels of colony-stimulating factor-1 (CSF1), the expression of wh
120 io lacked such projections, concomitant with Colony stimulating factor 1-dependent changes in xanthop
121 fibrosis, illustrating the critical role of colony-stimulating factor 1-dependent monocyte/macrophag
122 motif ligand 2 that stimulated migration of colony-stimulating factor 1-differentiated macrophages.
123 agy initiated by ULK1 is required for proper colony stimulating factor-1-driven differentiation of hu
125 ne marrow-derived macrophages that depend on colony-stimulating factor-1 for proliferation and surviv
126 t of DNA in the promoter region of the human colony-stimulating factor 1 gene into the left-handed Z-
129 tyrosine kinase activator protein 1 (TKA-1); colony stimulating factor-1; insulin-like growth factor
130 nduced the tumor cells to express macrophage colony-stimulating factor 1 (M-CSF1 or CSF1) and other c
136 systemic deletion of macrophages expressing colony stimulating factor 1 receptor (CSF1R) was initiat
138 affecting the tyrosine kinase domain of the colony stimulating factor 1 receptor (encoded by CSF1R)
139 show that treatment with the pharmacological colony stimulating factor 1 receptor inhibitor PLX5622 s
140 with wild-type, but not macrophage-deficient colony stimulating factor 1 receptor mutant (Csf1r(-/-))
145 dministered a dietary inhibitor (PLX5622) of colony stimulating factor-1 receptor (CSF1R) to deplete
146 laced with the extracellular domain of human colony stimulating factor-1 receptor and expressed in en
149 e uptake in 3T3-L1 adipocytes expressing the colony stimulating factor-1 receptor/insulin receptor ch
150 tumour-to-tumour heterogeneity, response to colony-stimulating factor 1 receptor (CSF-1R) blockade a
151 scriptional events and signals downstream of colony-stimulating factor 1 receptor (CSF-1R) that contr
152 BIT, but not PIR-B, is in a complex with the colony-stimulating factor 1 receptor (CSF-1R), suggestin
153 on of macrophages induces phosphorylation of colony-stimulating factor 1 receptor (CSF-1R), which con
156 method revealed the presence of an activated colony-stimulating factor 1 receptor (CSF1R) kinase in t
157 y discovered that microglia are dependent on colony-stimulating factor 1 receptor (CSF1R) signaling f
158 croglia in the healthy adult mouse depend on colony-stimulating factor 1 receptor (CSF1R) signalling
159 utations in the protein kinase domain of the colony-stimulating factor 1 receptor (CSF1R) which is a
160 hanism is regulated by the activation of the colony-stimulating factor 1 receptor (CSF1R), thus provi
162 acellular domain of VEGFR-2 with that of the colony-stimulating factor 1 receptor did not alleviate t
164 ncluding cellular interleukin-10, bcl-2, and colony-stimulating factor 1 receptor homologues and an e
166 mary acini induced by chronic stimulation of colony-stimulating factor 1 receptor is coupled to endog
167 cked macrophage function in ID8 mice using a colony-stimulating factor 1 receptor kinase inhibitor (G
169 results of studies inhibiting the macrophage colony-stimulating factor 1 receptor,whereas the CD11b(+
172 ession and can be targeted via inhibition of colony-stimulating factor-1 receptor (CSF-1R) to regress
173 tiation is mediated by signaling through the colony-stimulating factor-1 receptor (CSF-1R) which is n
174 laced with the extracellular domain of human colony-stimulating factor-1 receptor (CSF-1R), and these
175 IL-34 signaling via its cognate receptor, colony-stimulating factor-1 receptor (CSF-1R), is requir
176 osine phosphorylated after activation of the colony-stimulating factor-1 receptor (CSF-1R), which als
177 inhibiting either the myeloid cell receptors colony-stimulating factor-1 receptor (CSF1R) or chemokin
178 g in the E13.5 mouse fetal liver express the colony-stimulating factor-1 receptor (CSF1R), previously
182 nsisting of the ligand-binding domain of the colony-stimulating factor-1 receptor spliced to the cyto
183 beta, IL-6, and TNFalpha; (b) loss of CD115 (colony-stimulating factor-1 receptor) expression and pro
184 The cFMS proto-oncogene encodes for the colony-stimulating factor-1 receptor, a receptor-tyrosin
186 cells, we have created a chimeric receptor (colony-stimulating factor-1 receptor/insulin receptor ch
187 ne resorption were studied as the macrophage colony-stimulating factor-1-receptor activator of NF-kap
188 via the A(2A) receptor, inhibits macrophage colony-stimulating factor-1-receptor activator of NF-kap
189 er fracture with the pro-macrophage cytokine colony stimulating factor-1 significantly enhanced soft
190 ma membrane-spanning glycoprotein, pp130, in colony stimulating factor-1 stimulated or unstimulated m
191 ic macrophages, which also exhibit increased colony-stimulating factor-1-stimulated proliferation and
192 Differentiation, in response to RANKL and colony-stimulating factor 1, was evaluated while varying
193 ulating macrophages through the secretion of colony-stimulating factor-1 while the tumor-associated m
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