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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.
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
25 leum, cecum, and feces) and visceral organs (bursa and spleen) after challenge with homologous (Typhi
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
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
35 intermediate lysostaphin resistance carried bursa aurealis insertions in genes specifying GTP pyroph
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
40 Three bursae comprising the trochanteric bursa complex were injected, and conventional radiograph
48 ated fluid collections in the bicipitoradial bursa in all cases, with compression of branches of the
50 bursa, that was separate from the premacular bursa in horizontal scans centered on the fovea and was
57 (44.4%), co-existing subacromial-subdeltoid bursa/long head of bicep tendon sheath effusion (44.4%),
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
69 g genes during B cell development within the bursa of Fabricius, a lymphoid organ unique to birds.
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
80 ted with the development of lymphomas in the bursa of Farbricius of chickens; these arise with a shor
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
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
96 ther endothelin 2 or angiotensin 2) into the bursa restored the vasoconstriction of apical vessels an
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
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
104 The superior level contained the synovial bursa, the plantar and dorsal interosseous muscles and t
113 iversification by gene conversion in chicken bursa was not supported by studies of RAG2 protein in th
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
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