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1 fibers, similar to synaptic contacts seen in nervous tissue.
2 ization of a novel neuropeptide from Aplysia nervous tissue.
3     Both proteoglycans were detected only in nervous tissue.
4 ot been demonstrated previously in mammalian nervous tissue.
5 segregate the most severely injured zones of nervous tissue.
6 series of complex biochemical alterations of nervous tissue.
7  play a critical role in maintaining healthy nervous tissue.
8 t P1-P5 were the only CD200R(+) cells in the nervous tissue.
9 ection and subsequent persistence in sensory nervous tissue.
10 vel to neurons and blood vessels deep within nervous tissue.
11 CYM-5442 partitions significantly in central nervous tissue.
12 s Th and DC accumulation and function in the nervous tissue.
13 neficial host repair of infected and damaged nervous tissue.
14 e pathogenic mutations specifically in human nervous tissue.
15 ently reactivated within the immune-deprived nervous tissue.
16 ant role in the development and stability of nervous tissue.
17 h a high proportion of the genes specific to nervous tissue.
18 ghly scattering preparations, such as living nervous tissue.
19 of CPEB (ApCPEB77 and ApCEPB49) from Aplysia nervous tissue.
20 henotype arises from a lack of expression in nervous tissue.
21 FGF-2 to cell surface signaling receptors in nervous tissue.
22 ecific isoforms are found in the ovaries and nervous tissue.
23 he first member of this family identified in nervous tissue.
24  for XLerk in the developing mesenchymal and nervous tissue.
25 o play important roles in the development of nervous tissues.
26 racellular deposits of protein aggregates in nervous tissues.
27 nctional alpha homomeric receptors in mature nervous tissues.
28 on in lipoproteins and membranes, especially nervous tissues.
29 se stem cells as chaperones for degenerating nervous tissues.
30  lowest in postmortem central and peripheral nervous tissues.
31 nous "capsaicin-like" substance in mammalian nervous tissues.
32    On the other hand it was not found in non-nervous tissues.
33 is expressed in brain as well as several non-nervous tissues.
34  a 83kDa protein which is highly enriched in nervous tissues.
35 on both glycoproteins and glycolipids in the nervous tissues.
36 -type channels, are exclusively expressed in nervous tissues.
37 oimmune defects that can polarize toward the nervous tissue after the selective disruption of CD28/B7
38 being used for tumors adjacent to bowels and nervous tissue, albeit with somewhat less ablative poten
39 at have a role in the central and peripheral nervous tissue also have a role in cutaneous melanocytes
40 ate the autoimmune process when entering the nervous tissue and become reactivated upon local encount
41  scanning confocal microscopy of rat central nervous tissue and C6 glioma cells, we found that a sign
42                  Steroid sulfation occurs in nervous tissue and endogenous sulfated steroids can act
43 vement in the development and maintenance of nervous tissue and in the mechanisms of neuroprotection
44 1 edits adenosines in nuclear transcripts of nervous tissue and is required in the fetal liver of the
45 h plasmalogens are the most abundant form in nervous tissue and myelin; however, the role of plasmalo
46 AAH activity increases AEA concentrations in nervous tissue and reduces sensory hypersensitivity in a
47 eins are functional ligands of glypican-1 in nervous tissue and suggest that their interactions may b
48 ogenous ALS2 is shown here to be enriched in nervous tissue and to be peripherally bound to the cytop
49 ost cell types within central and peripheral nervous tissues and have been functionally linked to man
50 otein, is detected in peripheral and central nervous tissues and participates in neural progenitor ma
51 cated that the expression of alpha1 GlyRs in nervous tissues and spinal cord neurons (SCNs) were simi
52 ed on their presence in normal or neoplastic nervous tissue, and included the extra-cellular matrix m
53 flammatory cytokine release in the serum and nervous tissue, and inhibited chemokine expression and i
54 pressed in fetal brain and fetal sympathetic nervous tissues, and the expression level was strictly c
55 dance and related developmental processes in nervous tissue, are ligands of the glycosylphosphatidyli
56 (8R)-lipoxygenase co-exist in intact Aplysia nervous tissue but are differentially activated by sever
57 strated a consistent cross-sectional area of nervous tissue, but decreasing amounts of collagen poste
58 KLC1, KLC2) genes are expressed in mammalian nervous tissue, but the functional significance of this
59  form non-amyloid inclusions in the affected nervous tissues, but the role of these proteinaceous agg
60 factor (REST) helps preserve the identity of nervous tissue by silencing neuronal genes in non-neural
61 l of patients with cancer and NF1, excluding nervous tissue cancers, was worse than that of comparabl
62 use Ret(MEN2B) derived from the hyperplastic nervous tissue competes with endogenous renal Ret for gf
63 evident and could contribute to irreversible nervous tissue damage in NCC patients.
64 in of patients with MLD and generally marked nervous tissue damage in the LSDs here evaluated.
65                                 Vascular and nervous tissue derived from the ancestral, anterior-most
66 onic lysosphingolipid occurring naturally in nervous tissues, dose-dependently inhibited PLC activati
67 is expressed in a number of chondrocytic and nervous tissues during embryogenesis.
68 n completely abolishes viral spread in human nervous tissue ex vivo and in an in vivo mouse model.
69 at E17 but equalize in most regions of adult nervous tissue, except for the glomerular and granule ce
70 ng study, both drugs persisted in peripheral nervous tissues for weeks, in contrast to their rapid cl
71 issue formation after tissue injury, gaps in nervous tissue formed during phagocytosis of dying cells
72 ues and reveal neuropeptide distributions in nervous tissue from Aplysia californica.
73 sis in the squirrel brain, and thus supports nervous tissue function at low body temperature during h
74  receptor is expressed almost exclusively in nervous tissues, GPRC105 is expressed primarily in bone
75 lin-dependent kinase 5 (cdk5), isolated from nervous tissue, has been shown to phosphorylate the huma
76              However, the effects of HOCl on nervous tissue have not been examined.
77 er rapidly and are exceptionally abundant in nervous tissue, high Ins levels in the range of 2-15 mm
78 l interactions, and neurite outgrowth during nervous tissue histogenesis.
79 ell-cell and cell-matrix interactions during nervous tissue histogenesis.
80 true for recent interpretations of preserved nervous tissues in fossil ecdysozoans.
81 es in the clinical score, disease incidence, nervous tissue inflammation, and Th1, Th2, and Th17 cyto
82 stem, whereas in insects and crustaceans the nervous tissue is produced by stem cells.
83 in in tissues other than the muscle, such as nervous tissue, is a critical component of MCMD.
84 ally similar to that of ordinary synapses in nervous tissue, much less is known about the composition
85 e lacking ERalpha expression specifically in nervous tissue (nestin-ERalpha(-/-)).
86 evels of the CGRP receptor hRAMP1 subunit in nervous tissue (nestin/hRAMP1).
87 one (ELH) from peptidergic neurons in intact nervous tissue of Aplysia.
88 ion patterns and subcellular localization in nervous tissue of glypican, a major glycosylphosphatidyl
89  ubiquitinated protein inclusions present in nervous tissue of most cases of both amyotrophic lateral
90 e-NH(2) (FMRFamide)-gated Na(+) channel from nervous tissue of the pond snail Helisoma trivolvis (HtF
91    Virus replication was not observed in the nervous tissue of the synganglion, Malpighian tubules, a
92 ion of TrkC underlies regenerative events in nervous tissues of patients with Chagas' disease.
93                           Cdk5 purified from nervous tissue phosphorylates neuronal cytoskeletal prot
94 the cellular sites of synthesis of two major nervous tissue proteoglycans, neurocan and phosphacan, i
95 unctional amino acid prevalent in developing nervous tissues, regulates the number of rod photorecept
96 piratory airways and parts of the peripheral nervous tissue running through the lungs.
97 cal studies of embryonic and early postnatal nervous tissue showed an overlapping localization of TAG
98                                          Two nervous tissue-specific chondroitin sulfate proteoglycan
99                                          The nervous tissue-specific chondroitin sulfate proteoglycan
100      We have studied the interactions of the nervous tissue-specific chondroitin sulfate proteoglycan
101                                              Nervous tissue subjected to hyperthermic pre-conditionin
102 s and tissues, including the brain and other nervous tissue such as the retina and spinal cord, liver
103 etinoic acid (RA)-induced differentiation to nervous tissue, suggesting that EGFR plays a role in dif
104 ripts in a variety of central and peripheral nervous tissues suggests a greater degree of receptor su
105 hacan, a chondroitin sulfate proteoglycan of nervous tissue that also represents the extracellular do
106 inum; five of five tumors examined contained nervous tissue that strongly expressed NR2 subunits and
107 eurotrophic role in the extralingual central nervous tissue that underpins synaptic function, memory
108  CNS Ags involves the migration of APCs from nervous tissue to peripheral lymphoid tissues, similarly
109 istopathological examination determined that nervous tissue was better preserved in FGF-13 treated ra
110 the effects of reducing lysosomal storage in nervous tissues, we injected recombinant adeno-associate
111 iated pathological alterations of kidney and nervous tissue were not detected during the observation
112 s can associate closely with or migrate into nervous tissue where differentiation appears to be deter
113                 We found that NADA occurs in nervous tissues, with the highest concentrations being f
114 ely used, noninvasive method for stimulating nervous tissue, yet its mechanisms of effect are poorly

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