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1 a) from the bloodsucking mite (Ornithonyssus bursa).
2 lly abundant in the bone marrow, spleen, and bursa.
3 e-specific and includes embryonic thymus and bursa.
4 bout the hip, especially in the trochanteric bursa.
5 ,000 lincRNA loci were identified in chicken bursa.
6 ge lesion that was filling the suprapatellar bursa.
7 all eyes, and corresponded to the premacular bursa.
8 itoneally or orthotopically into the ovarian bursa.
9 egates into either kidney capsule or ovarian bursa.
10 myc-induced neoplastic transformation in the bursa.
11 sion of protease inhibitors into the ovarian bursa.
12  failed to induce hemorrhagic lesions in the bursa.
13 mpanied by an infiltration of T cells in the bursa.
14  with proviral c-myc integrations within the bursa.
15 atomic area of the trochanteric or iliopsoas bursa (55 [60%] of 91 sites).
16                               The premacular bursa, also called the posterior precortical vitreous po
17 Bulgaria was a FMDV collected during 2010 in Bursa (Anatolia, Turkey).
18     Communication between the bicipitoradial bursa and elbow joint was not observed.
19 th no human or murine equivalent such as the bursa and Harderian gland.
20  Proviral c-myc integrations are detected in bursa and other tissues from 6 day-old lymphoma-suscepti
21  integrations arise at the same frequency in bursa and other tissues of both strains, and they do not
22 gene expression distinct from that of normal bursa and partially shared with the short-latency lympho
23 u-expressing B cells declined rapidly in the bursa and periphery in the absence of Ag after hatch; ho
24                                          The bursa and space of Martegiani coexisted in 97.8% of eyes
25 leum, cecum, and feces) and visceral organs (bursa and spleen) after challenge with homologous (Typhi
26  shows a high level of CD1 expression in the bursa and spleen.
27  differences in the morphology of the corpus bursa and the heavy muscular area of the ductus ejaculat
28 ith a complex of adjacent fibrocartilages, a bursa, and a fat-pad, and is functionally much more than
29 13 was expressed at high levels in embryonic bursa, and decreased significantly after hatching, corre
30  instances, the virus was recovered from the bursa, and the presence or absence of mutation in these
31 t into mature B cells and migration from the bursa are blocked in the mutants.
32 bursal atrophy or hemorrhagic lesions in the bursa, as seen with the variant or classical virulent st
33 ed annellides was isolated from a left elbow bursa aspirate and was identified as an Exophiala specie
34                                              Bursa aurealis insertion in SAV2335, encoding a polytopi
35  intermediate lysostaphin resistance carried bursa aurealis insertions in genes specifying GTP pyroph
36                                      Herein, bursa aurealis, a mariner-based transposon, was used for
37 ed distinct lincRNA expression signatures in bursa between MD resistant and susceptible lines of chic
38 and microscopic sections revealed no primary bursa between the lateral femoral epicondyle and the ITT
39   Although apoptosis is low in the embryonic bursa, cell death increases markedly after hatching.
40     Three bursae comprising the trochanteric bursa complex were injected, and conventional radiograph
41                             The trochanteric bursa covered the posterior facet and the lateral insert
42                       Width and depth of the bursa did not correlate with age (R(2) width = 0.0316; R
43                           The bicipitoradial bursa enveloped the biceps tendon, with internal septati
44  with D78 or mutant virus and analyzed their bursa for histopathological lesions.
45                                          The bursa fused broadly with the extension of the preoptic a
46      In the first intermetatarsal space, the bursa had a specific appearance as it coursed along the
47                                              Bursa had no detectable CD4(+)CD25(+) cells.
48 ated fluid collections in the bicipitoradial bursa in all cases, with compression of branches of the
49                               Bicipitoradial bursa in eight cadaveric elbows were injected with a sol
50 bursa, that was separate from the premacular bursa in horizontal scans centered on the fovea and was
51                                        As O. bursa infestations reduce population viability in hihi,
52 elatively high levels in the spleen, thymus, bursa, intestine, and lungs.
53                             The trochanteric bursa is delineated with fat on both sides and can be se
54            The anatomy of the bicipitoradial bursa is demonstrated with radiography and MR imaging of
55                   Oligoclonal, NF-containing bursas lacked detectable c-myc overexpression and demons
56                       The subgluteus minimus bursa lies in the area of the anterior facet, underneath
57  (44.4%), co-existing subacromial-subdeltoid bursa/long head of bicep tendon sheath effusion (44.4%),
58 inal epithelial protein not expressed in the bursa, mediates this effect.
59                                           No bursa membrane is formed, and the oviduct remains uncoil
60  = 1), schwannoma (n = 1), or bicipitoradial bursa (n = 1).
61 tissues, levels are particularly high in the bursa of Fabricius and comparatively low in ovarian foll
62    The young rabbit appendix and the chicken bursa of Fabricius are primary lymphoid organs where the
63  their development; >95% of the cells in the bursa of Fabricius die without entering the secondary im
64   Migration of B-lineage precursors into the bursa of Fabricius is unaffected, whereas development in
65  but S. pullorum preferentially targeted the bursa of Fabricius prior to eliciting intestinal inflamm
66                                    The avian bursa of Fabricius provides an essential microenvironmen
67               B cells removed from the avian bursa of Fabricius rapidly undergo cell death in culture
68 its expression in the tongue, esophagus, and bursa of Fabricius was unaffected.
69 g genes during B cell development within the bursa of Fabricius, a lymphoid organ unique to birds.
70 histological changes in the large intestine, bursa of Fabricius, and cecal tonsil.
71 in-3 was especially prominent in the tongue, bursa of Fabricius, and trachea.
72 expressed on epithelial cells of the chicken bursa of Fabricius, BEN is expressed in a variety of tis
73 ned, whereas IFITM1 is only expressed in the bursa of Fabricius, gastrointestinal tract, cecal tonsil
74                  In follicles of the chicken bursa of Fabricius, myc induction of B-cell neoplasia re
75 chyme and non-intestinal epithelium from the bursa of Fabricius.
76 iesis takes place in GALT, such as the avian bursa of Fabricius.
77 constitute the cellular homolog of the avian bursa of Fabricius.
78 , the virus rapidly destroyed B cells in the bursa of Fabricius.
79  is developmentally regulated in the chicken bursa of Fabricius.
80 ted with the development of lymphomas in the bursa of Farbricius of chickens; these arise with a shor
81      After orthotopic transplantation in the bursa of the mouse ovary, they disseminate into the orga
82 e-encoding adenovirus (AdCre) in the ovarian bursa of triple (MUC1KrasPten) Tg mice triggers ovarian
83  of endothelin receptor antagonists into the bursa of wild-type mice prevented vasoconstriction and f
84 c-myc integration events were amplified from bursas of infected 35-day-old birds, in good agreement w
85 nfect with MDV B cells isolated from spleen, bursa or blood cultured in the presence of soluble CD40L
86  patterns of involvement: either a distended bursa or multiple small abscesses.
87  results suggest that polyploidization in C. bursa-pastoris enhanced its plasticity of response to li
88 We constructed a high-quality assembly of C. bursa-pastoris genome and a transcriptome atlas covering
89 hows a structure similar to that of Capsella bursa-pastoris, a distant mustard relative of Arabidopsi
90 onduct whole-genome resequencing in Capsella bursa-pastoris, a recently formed tetraploid with one of
91                                     Capsella bursa-pastoris, a widespread ruderal plant, is a recent
92  recent data from the allopolyploid Capsella bursa-pastoris.
93                            Prevalence of the bursa premacularis and space of Martegiani and the stage
94 ate the almost invariable coexistence of the bursa premacularis and space of Martegiani.
95                           About half of such bursas rapidly developed lymphomas.
96 ther endothelin 2 or angiotensin 2) into the bursa restored the vasoconstriction of apical vessels an
97                           The bicipitoradial bursa revealed a smooth outline and a wide base along th
98 tome-sequencing (RNA-seq) analysis of normal bursa revealed a transcribed region upstream of TERT in
99 ize day-of-hatch chicks, colonization of the bursa, spleen, and liver was observed, with peak titers
100                                    Bilateral bursa tended to be symmetrical in width but less so in d
101  integrations were much more abundant in the bursa than in other tissues, indicating that cells with
102 a was another lacuna, named the supramacular bursa, that was separate from the premacular bursa in ho
103                               In the chicken bursa, the later stages of B cell development occur in t
104    The superior level contained the synovial bursa, the plantar and dorsal interosseous muscles and t
105                         The mean size of the bursa was 1.8 x 2.5 cm.
106                       Prevalence of detected bursa was 75.4% in patient group aged 0-60 years and 38%
107                       Prevalence of detected bursa was 84.5% in eyes with either no PVD or perifoveal
108                   Anterior to the premacular bursa was another lacuna, named the supramacular bursa,
109                                            A bursa was detected in 57.1% (136/238) of eyes.
110 uperficial branch of the radial nerve by the bursa was found in two specimens.
111                               The premacular bursa was identified in all 102 eyes and was found to ex
112                        The subgluteus medius bursa was located in the superior part of the lateral fa
113 iversification by gene conversion in chicken bursa was not supported by studies of RAG2 protein in th
114 nd anteroposterior (depth) dimensions of the bursa were recorded along with the patient's age.
115      The morphology and relationships of the bursa were studied.
116 aused microscopic lesions and atrophy of the bursa, while the mutant virus failed to induce any patho
117  were subsequently challenged in the ovarian bursa with 10(5) C. trachomatis MoPn IFU at 60, 120, or
118 the mice were challenged in the left ovarian bursa with 10(5) C. trachomatis MoPn IFU.
119 ization, mice were challenged in the ovarian bursa with 10(5) IFU of C. trachomatis MoPn.
120                 Instead, a connection of the bursa with the preoptic area of Martegiani or its extens

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