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1 ecific isoforms are found in the ovaries and nervous tissue.
2 he first member of this family identified in nervous tissue.
3  for XLerk in the developing mesenchymal and nervous tissue.
4 fibers, similar to synaptic contacts seen in nervous tissue.
5 ization of a novel neuropeptide from Aplysia nervous tissue.
6     Both proteoglycans were detected only in nervous tissue.
7 ot been demonstrated previously in mammalian nervous tissue.
8  gasdermin D and cognate genes is induced in nervous tissue.
9 tructural integrity and axon orientations in nervous tissue.
10  kidneys and isoform 3 (MT3) is expressed in nervous tissue.
11 sessing favorable material similarities with nervous tissue.
12 well as mesenchymal, adipose, and peripheral nervous tissue.
13 er cellular and non-cellular elements of the nervous tissue.
14 ently reactivated within the immune-deprived nervous tissue.
15 segregate the most severely injured zones of nervous tissue.
16 series of complex biochemical alterations of nervous tissue.
17  play a critical role in maintaining healthy nervous tissue.
18  wiring in Drosophila melanogaster and mouse nervous tissue.
19 t P1-P5 were the only CD200R(+) cells in the nervous tissue.
20 ection and subsequent persistence in sensory nervous tissue.
21  cardiomyocytes but spared blood vessels and nervous tissue.
22 vel to neurons and blood vessels deep within nervous tissue.
23 CYM-5442 partitions significantly in central nervous tissue.
24 s Th and DC accumulation and function in the nervous tissue.
25 neficial host repair of infected and damaged nervous tissue.
26 e pathogenic mutations specifically in human nervous tissue.
27 ant role in the development and stability of nervous tissue.
28 oinvasion (3 days) in peripheral and central nervous tissue.
29 h a high proportion of the genes specific to nervous tissue.
30 ghly scattering preparations, such as living nervous tissue.
31 of CPEB (ApCPEB77 and ApCEPB49) from Aplysia nervous tissue.
32 henotype arises from a lack of expression in nervous tissue.
33 FGF-2 to cell surface signaling receptors in nervous tissue.
34 -type channels, are exclusively expressed in nervous tissues.
35 d (GABA)-a prominent neurotransmitter-in non-nervous tissues.
36 o play important roles in the development of nervous tissues.
37 racellular deposits of protein aggregates in nervous tissues.
38 nctional alpha homomeric receptors in mature nervous tissues.
39 on in lipoproteins and membranes, especially nervous tissues.
40 se stem cells as chaperones for degenerating nervous tissues.
41  lowest in postmortem central and peripheral nervous tissues.
42 nous "capsaicin-like" substance in mammalian nervous tissues.
43    On the other hand it was not found in non-nervous tissues.
44 is expressed in brain as well as several non-nervous tissues.
45  a 83kDa protein which is highly enriched in nervous tissues.
46 on both glycoproteins and glycolipids in the nervous tissues.
47 dolinium retention in central and peripheral nervous tissues (1.8-333.2 nmol Gd/g tissue).
48 oimmune defects that can polarize toward the nervous tissue after the selective disruption of CD28/B7
49 being used for tumors adjacent to bowels and nervous tissue, albeit with somewhat less ablative poten
50 at have a role in the central and peripheral nervous tissue also have a role in cutaneous melanocytes
51 d a steady increase in reports of fossilized nervous tissues among Cambrian total-group euarthropods,
52 ate the autoimmune process when entering the nervous tissue and become reactivated upon local encount
53  scanning confocal microscopy of rat central nervous tissue and C6 glioma cells, we found that a sign
54                  Steroid sulfation occurs in nervous tissue and endogenous sulfated steroids can act
55 vement in the development and maintenance of nervous tissue and in the mechanisms of neuroprotection
56   They have the potential to replace damaged nervous tissue and integrate into the brain or spinal co
57 1 edits adenosines in nuclear transcripts of nervous tissue and is required in the fetal liver of the
58 ly troublesome for energy-demanding cells of nervous tissue and muscle.
59 h plasmalogens are the most abundant form in nervous tissue and myelin; however, the role of plasmalo
60 AAH activity increases AEA concentrations in nervous tissue and reduces sensory hypersensitivity in a
61 eins are functional ligands of glypican-1 in nervous tissue and suggest that their interactions may b
62 ogenous ALS2 is shown here to be enriched in nervous tissue and to be peripherally bound to the cytop
63 ost cell types within central and peripheral nervous tissues and have been functionally linked to man
64 otein, is detected in peripheral and central nervous tissues and participates in neural progenitor ma
65 cated that the expression of alpha1 GlyRs in nervous tissues and spinal cord neurons (SCNs) were simi
66 ed on their presence in normal or neoplastic nervous tissue, and included the extra-cellular matrix m
67 flammatory cytokine release in the serum and nervous tissue, and inhibited chemokine expression and i
68  provided three-dimensional display of bone, nervous tissue, and vasculature at microscale resolution
69 (ELAVL4), which is specifically expressed in nervous tissues, and involved in differentiation and syn
70 pressed in fetal brain and fetal sympathetic nervous tissues, and the expression level was strictly c
71 dance and related developmental processes in nervous tissue, are ligands of the glycosylphosphatidyli
72 (8R)-lipoxygenase co-exist in intact Aplysia nervous tissue but are differentially activated by sever
73 strated a consistent cross-sectional area of nervous tissue, but decreasing amounts of collagen poste
74 KLC1, KLC2) genes are expressed in mammalian nervous tissue, but the functional significance of this
75  form non-amyloid inclusions in the affected nervous tissues, but the role of these proteinaceous agg
76 for quantitative high-resolution analysis of nervous tissues, but varied axonal dispersion angles res
77 factor (REST) helps preserve the identity of nervous tissue by silencing neuronal genes in non-neural
78 l of patients with cancer and NF1, excluding nervous tissue cancers, was worse than that of comparabl
79 use Ret(MEN2B) derived from the hyperplastic nervous tissue competes with endogenous renal Ret for gf
80 theoretically also occur in these peripheral nervous tissues, contributing to the presence of infecti
81 evident and could contribute to irreversible nervous tissue damage in NCC patients.
82 in of patients with MLD and generally marked nervous tissue damage in the LSDs here evaluated.
83                                 Vascular and nervous tissue derived from the ancestral, anterior-most
84  within the vertebral canal, despite evident nervous tissue deterioration after Thiel embalming.
85 onic lysosphingolipid occurring naturally in nervous tissues, dose-dependently inhibited PLC activati
86 several lipids were significantly altered in nervous tissue during oxaliplatin-induced acute pain.
87 is expressed in a number of chondrocytic and nervous tissues during embryogenesis.
88 n completely abolishes viral spread in human nervous tissue ex vivo and in an in vivo mouse model.
89 at E17 but equalize in most regions of adult nervous tissue, except for the glomerular and granule ce
90 ng study, both drugs persisted in peripheral nervous tissues for weeks, in contrast to their rapid cl
91 issue formation after tissue injury, gaps in nervous tissue formed during phagocytosis of dying cells
92 ues and reveal neuropeptide distributions in nervous tissue from Aplysia californica.
93 sis in the squirrel brain, and thus supports nervous tissue function at low body temperature during h
94  receptor is expressed almost exclusively in nervous tissues, GPRC105 is expressed primarily in bone
95 lin-dependent kinase 5 (cdk5), isolated from nervous tissue, has been shown to phosphorylate the huma
96              However, the effects of HOCl on nervous tissue have not been examined.
97 er rapidly and are exceptionally abundant in nervous tissue, high Ins levels in the range of 2-15 mm
98 l interactions, and neurite outgrowth during nervous tissue histogenesis.
99 ell-cell and cell-matrix interactions during nervous tissue histogenesis.
100 true for recent interpretations of preserved nervous tissues in fossil ecdysozoans.
101 es in the clinical score, disease incidence, nervous tissue inflammation, and Th1, Th2, and Th17 cyto
102                    Electrical stimulation of nervous tissue is grounded in well-established biophysic
103 s by which metabolic wastes are cleared from nervous tissue is important for understanding natural fu
104 stem, whereas in insects and crustaceans the nervous tissue is produced by stem cells.
105 in in tissues other than the muscle, such as nervous tissue, is a critical component of MCMD.
106 ally similar to that of ordinary synapses in nervous tissue, much less is known about the composition
107 e lacking ERalpha expression specifically in nervous tissue (nestin-ERalpha(-/-)).
108 evels of the CGRP receptor hRAMP1 subunit in nervous tissue (nestin/hRAMP1).
109 ctive milieu' that unifies all components of nervous tissue (neuronal and glial compartments, extrace
110 one (ELH) from peptidergic neurons in intact nervous tissue of Aplysia.
111 ion patterns and subcellular localization in nervous tissue of glypican, a major glycosylphosphatidyl
112  ubiquitinated protein inclusions present in nervous tissue of most cases of both amyotrophic lateral
113 e-NH(2) (FMRFamide)-gated Na(+) channel from nervous tissue of the pond snail Helisoma trivolvis (HtF
114    Virus replication was not observed in the nervous tissue of the synganglion, Malpighian tubules, a
115  show that striking activation occurs in the nervous tissue of these parasite life-stages; CaMKII was
116 ion of TrkC underlies regenerative events in nervous tissues of patients with Chagas' disease.
117 ng findings from receptor systems in central nervous tissue or exogenously expressing immortalized ce
118                           Cdk5 purified from nervous tissue phosphorylates neuronal cytoskeletal prot
119 eds of serial ganglia form a central core of nervous tissue processing sensory input, issuing motor c
120 the cellular sites of synthesis of two major nervous tissue proteoglycans, neurocan and phosphacan, i
121    Upregulation of CG2120 in D. melanogaster nervous tissues reduces copulation latency, consistent w
122 ce, resilience, compensation) aspects of the nervous tissue reflecting exposome-driven life-long plas
123 ction during successful retinal (and central nervous tissue) regeneration.
124 unctional amino acid prevalent in developing nervous tissues, regulates the number of rod photorecept
125  pharmacological target for the treatment of nervous tissue-related tumors.
126 piratory airways and parts of the peripheral nervous tissue running through the lungs.
127 ngle-cell RNA sequencing analysis of central nervous tissue samples to gain insights into the underly
128 cal studies of embryonic and early postnatal nervous tissue showed an overlapping localization of TAG
129      We have studied the interactions of the nervous tissue-specific chondroitin sulfate proteoglycan
130                                          Two nervous tissue-specific chondroitin sulfate proteoglycan
131                                          The nervous tissue-specific chondroitin sulfate proteoglycan
132                                              Nervous tissue subjected to hyperthermic pre-conditionin
133 s and tissues, including the brain and other nervous tissue such as the retina and spinal cord, liver
134 etinoic acid (RA)-induced differentiation to nervous tissue, suggesting that EGFR plays a role in dif
135 ripts in a variety of central and peripheral nervous tissues suggests a greater degree of receptor su
136 hacan, a chondroitin sulfate proteoglycan of nervous tissue that also represents the extracellular do
137 inum; five of five tumors examined contained nervous tissue that strongly expressed NR2 subunits and
138 eurotrophic role in the extralingual central nervous tissue that underpins synaptic function, memory
139  CNS Ags involves the migration of APCs from nervous tissue to peripheral lymphoid tissues, similarly
140 isease severity and the degree of the virus' nervous tissue tropism and should be examined in future
141 istopathological examination determined that nervous tissue was better preserved in FGF-13 treated ra
142     Because of elevated RNA editing in their nervous tissues, we hypothesized that RNA regulation may
143 the effects of reducing lysosomal storage in nervous tissues, we injected recombinant adeno-associate
144 iated pathological alterations of kidney and nervous tissue were not detected during the observation
145 s can associate closely with or migrate into nervous tissue where differentiation appears to be deter
146 eno-associated virus (AAV) variants - target nervous tissues with differing efficiencies.
147                 We found that NADA occurs in nervous tissues, with the highest concentrations being f
148 ely used, noninvasive method for stimulating nervous tissue, yet its mechanisms of effect are poorly

 
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