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1 ups of rats: Sham, CCI-alone and CCI-BMMNCs (AUTO).
2 ower, too, in the allo group (p = 0.0186 vs. auto).
3 ICallo) to autologous transplantation alone (auto).
4 nsplants are more effective than autologous (auto).
5 unosuppression, VBP autotransplantation (VBP-auto).
6  regulatory loop (R-loop) by > 10(4)-fold (k(auto) = 2.6 +/- 0.3 s(-1)).
7 re recipients of cellular therapy (Allo, 35; Auto, 37; CAR T, 5; median time from cellular therapy, 7
8              The DKM (1) underwent a facile (auto) acid-mediated methanolysis to yield seco-shornephi
9 g kidney tubulopathy and cardiomyopathy are "auto- activating", even in the absence of Folliculin, th
10              Moreover, RECQ1 regulates PARP1 auto-(ADP-ribosyl)ation and the choice between long-patc
11 SA-FXM method from 94 patients (enriched for auto+/allo+ pairs; n = 64) against 110 donors (338 tests
12  promises novel insights into mechanisms of (auto-/allo-)immune diseases and more rationally designed
13                                           An auto-/alloantigen is tentatively implicated in disease i
14 mpled with a conventional automatic sampler (Auto) and by grab (Grab) sampling.
15 f patients.CONCLUSIONIn this series of Allo, Auto, and CAR T recipients, we report overall favorable
16 otein complex is a favored target for allo-, auto-, and drug-dependent antibodies associated with imm
17 otodeboronation process, augmented by self-, auto-, and oxidative (phenolic) catalysis when the pH is
18                   Although high-affinity IgG auto- and alloantibodies are important drivers of kidney
19             They prevent immune responses to auto- and alloantigens and are thus under close scrutiny
20 ymic and peripheral T-cell responses against auto- and alloantigens.
21  including marrow stimulation, osteochondral auto- and allografting, and autologous chondrocyte impla
22 Current bone-regenerative strategies such as auto- and allografts are invasive by nature, with advers
23  FCGR genes has been associated with various auto- and alloimmune diseases.
24 nctions to inhibit aggressive T(H)1-mediated auto- and alloimmune responses.
25 ia time, diabetogenic immunosuppression, and auto- and alloimmunity.
26           We investigated this phenomenon in auto- and allopolyploids of the Festuca-Lolium complex p
27 een parental genomes, although comparison of auto- and allopolyploids suggests that intergenomic inco
28 en chloroplasts and mitochondria and between auto- and allopolyploids.
29 er WGD and across generations in Arabidopsis auto- and allopolyploids.
30 only cotransplanted along with islets during auto- and allotransplantations.
31 -component peptide system that is capable of auto- and cross-catalysis and allows for the selective a
32 he search for chemical systems in which both auto- and cross-catalysis can occur has therefore attrac
33 les and used this information to predict the auto- and cross-catalysis pathways and the resulting pla
34 approach makes use of the sequence-dependent auto- and cross-catalytic functional characteristics of
35  of privileged replicator structures through auto- and cross-catalyzed reaction cycles is created fro
36        Here we measure an extensive range of auto- and cross-correlated spin relaxation rates at mult
37 ) depends on the accurate measurement of the auto- and cross-correlation function (ACF and CCF) ampli
38 hm that simultaneously analyzes all distinct auto- and cross-correlation functions from 15 independen
39  effect of reaction kinetics on the shape of auto- and cross-correlation functions.
40                                              Auto- and cross-correlation of spectral data facilitates
41 ompare the TE with standard measures such as auto- and cross-correlation, showing that the TE has a d
42 cleotide interactions by means of a modified auto- and cross-covariance function, (iv) nucleotide the
43 ggestive of immediate-early genes capable of auto- and cross-induction through cis-acting regulatory
44 R) activation was also necessary for trefoil auto- and cross-induction, and both spasmolytic polypept
45 at the 3'UTRs of their own transcripts in an auto- and cross-regulated mechanism that limits their ex
46 vation, Tal1, Gata2, and Gata3 are linked by auto- and cross-regulation as well as regulatory interac
47 ts revealed MYB31 and MYB42 participation in auto- and cross-regulation in all three species.
48 rovide evidence for a concerted role for DLX auto- and cross-regulation in the establishment of a nes
49 stral (autosomal) DDX3X gene transmuted into auto- and cross-regulation of DDX3X and DDX3Y as these s
50              These loops can be generated by auto- and cross-regulation of expression of CREB protein
51 nd those of six other Dmrt genes, indicating auto- and cross-regulation of these genes.
52 mbryos and present evidence for existence of auto- and cross-regulatory control of expression among t
53                   We also discover extensive auto- and cross-regulatory interactions among the Hoxa1
54 ength to the emerging importance of positive auto- and cross-regulatory interactions between Hox gene
55 b2 and Hoxa1, is integrated into a series of auto- and cross-regulatory loops between Hox genes.
56 the critical ternary complexes formed by the auto- and crosscatalytic templates.
57 tein families and form extensive networks of auto- and crossregulation.
58 oduction, serum IgG1 and IgG2 levels of both auto- and heteroantibodies, and soluble CD44.
59 oduction, serum IgG1 and IgG2 levels of both auto- and heteroantibodies, and soluble CD44.
60 luding pro- and anti-inflammatory cytokines, auto- and heteroantibody productions) or antigen-specifi
61 excitability, and its control by presynaptic auto- and heteroreceptors on presynaptic terminals.
62 e chemistry of complex samples by decrypting auto- and heterospectral correlations that may exist bet
63 le autoregulatory models for E2EPF involving auto- and multiubiquitination.
64                       A greater frequency of auto- and neutralizing antibodies against IFN-alpha2 or
65 lpha L29F, beta N108Q) is stabilized against auto- and NO-induced oxidation as compared to rHb (beta
66 se of the complex relationship between Syk's auto- and other internal phosphorylation sites, scaffold
67  used to select subpopulations for which the auto- and pair-correlation analysis can be performed sep
68 ular environment, quantification of averaged auto- and pair-correlation profiles may obscure importan
69  of Hoxb1 expression in rhombomere 4 through auto- and para-regulatory interactions.
70 ivation of T lymphocytes and functions as an auto- and paracrine growth factor.
71  and a dramatically increased sensitivity to auto- and paracrine Wnts.
72 ferences between the contraction patterns of auto- and photo-cure were minimal.
73  measure lipid hydroperoxides by the both in auto- and photo-oxidation systems.
74 oad neutralization and its relationship with auto- and polyreactivity and may aid design of vaccine i
75  of the Golgi and activate it there for both auto- and Rab substrate phosphorylation.
76 er (D) compared with - 0.71 +/- 0.91D in the auto- and subjective refraction, respectively (p = 0.001
77 tutions in the SCD and the FHA domain impair auto- and trans-kinase activities of Chk2.
78                                      Slik is auto- and trans-phosphorylated in vivo.
79            Moreover, they support a role for auto- and trans-regulation of Gfi1 by GFI1 and GFI1B in
80 ne/threonine kinase activity, impairing both auto- and transkinase activities of Bcr.
81 for immunomodulation to achieve tolerance to auto- and transplantation Ags.
82 n of immunoglobulin M, which then serves as (auto-) antigen for a prosurvival BCR signal.
83                                         Such auto- antigen specificity and/or cross-reactivity may di
84 for example tonic B-cell signaling, chronic (auto)-antigen exposure, and self-binding properties of t
85                                         Both auto- as well as photo-curing composites were analyzed.
86 edian QS of augmented models were lower than auto, but not significantly different from each other (W
87                                              Auto-, cross- and para-regulatory interactions help esta
88 by inputs from Meis and Pbx proteins and Hox auto-/cross-regulatory interactions.
89 ipients of allogeneic (Allo) and autologous (Auto) hematopoietic cell transplant and CD19-directed ch
90             Allogeneic (ALLO) or autologous (AUTO) HSCT was employed, respectively, in 141 and 102 HR
91 to our understanding of normal and abnormal (auto) immune responses.
92     The physiological relevance for humoral (auto-)immunity was corroborated by exacerbated lupuslike
93 o and in vivo assays, as well as 2 relevant (auto-) inflammatory murine models.
94 ationship of AE with Th1- and Th17-mediated (auto-)inflammatory conditions such as diabetes mellitus
95  infection or tissue injury, likely to curb (auto)-inflammatory responses.
96                  The primary hindcast model (auto) is an Autoregressive Integrated Moving average mod
97 comes for patients who underwent autologous (auto, n = 128) or HLA-identical sibling (allo, n = 76) S
98            The oligotrophic ocean is neither auto- nor heterotrophic, but functionally diverse.
99  selectivity of action to facilitate intra-, auto-, or paracrine mechanisms that define and influence
100  DCs cultured in the laboratory can suppress auto- or alloimmunity.
101 lucagon secretion was observed in either the auto- or allotransplant recipients, whereas healthy cont
102 el was evaluated in19 monkeys that underwent auto- or allotransplantation, with or without subtherape
103 ons did not indicate any underlying positive auto- or cross-regulation of Mash1.
104 i-stage epithelial carcinogenesis, including auto- or paracrine growth stimulation, upregulation of a
105 ene amplification, activating mutations, and auto- or paracrine mechanisms.
106   Thus, shed soluble chemokines can generate auto- or paracrine signals by binding and activating the
107              The domain does not support the auto- or trans-kinase activity of p210 BCR/ABL or its ab
108 is hypothesized to occur as a consequence of auto- or transphosphorylation on tyrosine residues assoc
109 eptor dependent and independent, act through auto-, para- or intracrine mechanisms and can be modifie
110                  We also provide evidence of auto-, para-, and feedback regulation among these factor
111  levels in Hyp mice, its putative role as an auto-/paracrine osteomalacia-causing factor has not been
112                          Here we describe an auto-/paracrine physiologic circuit that controls quiesc
113  the signaling components, the logic of this auto-/paracrine signaling module in growth control remai
114 es the accumulation of pyrophosphate through auto-/paracrine suppression of TNAP.
115 riming of CAR T-cell susceptibility involved auto-/paracrine type-I IFN signaling loops and could spr
116                           Here we report an "auto"-regulatory feedback mechanism between plasmacytoid
117 se bifurcation theory and numerical methods (AUTO) to characterize the codimension-one and -two bifur
118                                        Thus, auto-/transphosphorylation of S379 is required for Chk2
119 on by ATM, followed by Chk2 oligomerization, auto-/transphosphorylation, and activation.
120 e direct enumeration and characterization of auto-, tumor-, or neo-Ag-reactive T cells within the nai
121 arison of safety and efficacy of autologous (auto) versus allogeneic (allo) bone marrow-derived hMSCs
122                 In Experiment 2, we used an "auto- vs. self-play" manipulation to eliminate outcome d

 
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