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1 stral bauplan, the quasi-independence of the interfascicular and fascicular cambia, and the inclusion
2                             In contrast, the interfascicular and transverse nuclei differentially inn
3 e, with the highest binding occurring in the interfascicular and ventral nuclei.
4 erminalis has three major nuclei: principal, interfascicular, and transverse, which receive topograph
5 acapsular, oval, magnocellular, ventral, and interfascicular BST nuclei.
6  the rbe-2 mutant increased the width of the interfascicular cambium-derived (ICD) region.
7 f secondarily thickened vascular bundles and interfascicular cells, and inner pith parenchyma cells w
8 condary cell wall material in both xylem and interfascicular cells, and suggests that a common regula
9 pattern of secondary cell wall thickening in interfascicular cells, with some cells apparently underg
10  project principally to the MnR/PMnR and DTg/interfascicular dorsal raphe, both areas rich in seroton
11 st that the lateral DRN and the ventromedial/interfascicular DRN may be anatomically, morphologically
12 ere also observed in the dorsal, lateral and interfascicular DRN subnuclei; fewer neurons were observ
13 s occurred in the lateral, ventromedial, and interfascicular DRN; and 44, 12, and 31% of 5-HT-ir cell
14 ly deposited in the walls of xylem cells and interfascicular fiber cells during normal plant growth a
15                 The spatial specification of interfascicular fiber differentiation is regulated by th
16 s consistent with its role in the control of interfascicular fiber differentiation.
17 repress REV expression, while blh6 and knat7 interfascicular fiber secondary cell wall phenotypes are
18  and KNAT7 overexpression results in thinner interfascicular fiber secondary cell walls, phenotypes t
19 ctionality of CSC movements of the xylem and interfascicular fiber walls of Arabidopsis stems, inferr
20                                          The INTERFASCICULAR FIBERLESS/REVOLUTA (IFL1/REV) gene is es
21 ar fiber differentiation is regulated by the INTERFASCICULAR FIBERLESS1 (IFL1) gene because mutation
22 leucine zipper transcription factor REVOLUTA/INTERFASCICULAR FIBERLESS1 (REV/IFL1).
23 nd BGLU46 proteins are mainly located in the interfascicular fibers and in the protoxylem, respective
24  essential for the normal differentiation of interfascicular fibers and secondary xylem in the inflor
25  show that SND1 is expressed specifically in interfascicular fibers and xylary fibers in stems and th
26 ed about 25 degrees off the stem axis, while interfascicular fibers are bidirectional and highly alig
27  that gene abolishes the formation of normal interfascicular fibers in Arabidopsis stems.
28 ibitor altered the normal differentiation of interfascicular fibers in the inflorescence stems of wil
29 tant defective in the mechanical strength of interfascicular fibers in the inflorescence stems.
30  The nst1-3 mutant shows no lignification in interfascicular fibers, as previously seen in tnt1 trans
31    Secondary walls were affected also in the interfascicular fibers, where neither XTH4 nor XTH9 was
32 tment to secondary cell wall biosynthesis in interfascicular fibers.
33 ce under UV microscopy and red coloration in interfascicular fibers.
34 es exhibited bundle branch reentry and other interfascicular FVTs.
35 for atypical bundle branch reentry and other interfascicular FVTs; (3) examination of P1/P2 activatio
36                                              Interfascicular glia in the normal optic nerve were fain
37 ly strong immunoreactivity in the developing interfascicular glial rows.
38 ally distinct fascicular (collagen-rich) and interfascicular (glycoprotein-rich) ECM phases of tendon
39 , axonal projection pattern, and targets: an interfascicular group, a vagal area group, and an area p
40 ve perikarya of the SNc, paranigral (PN) and interfascicular (IF) nucleus was performed and compared.
41 llagen-rich fascicles surrounded by a softer interfascicular matrix (IFM).
42  composed of fascicles bound together by the interfascicular matrix (IFM).
43 rotein turnover within the glycoprotein-rich interfascicular matrix compared to the collagen-rich fas
44 unding predominantly non-collagenous matrix (interfascicular matrix) can be interrogated independentl
45 exclusively localised to the non-collagenous interfascicular matrix.
46                                              Interfascicular neurons formed a loose longitudinal colu
47  > lateral hypothalamus > accumbens > linear/interfascicular nuclei >/= globus pallidus > prefrontal
48 tary, ventrolateral periaqueductal gray, and interfascicular nuclei.
49 in the ventral tegmental area and the linear/interfascicular nuclei.
50  dysfunction and selective cell death in the interfascicular nucleus of the dorsal raphe (DRif), resu
51 ian paranigral VTA, ventral tier of the SNc, interfascicular nucleus of the VTA, and supramamillary/r
52  tegmental area, central linear nucleus, and interfascicular nucleus).
53  paranigral nucleus, ventral tegmental area, interfascicular nucleus, and dorsal raphe nucleus.
54 acent midline nuclei (caudal linear nucleus, interfascicular nucleus, and rostral linear nucleus of t
55 eld, rostral and caudal linear raphe nuclei, interfascicular nucleus, and supramammillary region.
56 ained within linear arrays characteristic of interfascicular oligodendrocytes.
57 cells lining the lateral ventricles and many interfascicular oligodendroglia of forebrain fiber tract
58 ons in the dorsal, ventrolateral, caudal and interfascicular parts of the DR relative to appropriate
59 ssue development in the stem in place of the interfascicular region that normally separates the vascu
60 dentified with a total lack of lignin in the interfascicular region.
61 60%) and symmetric (49%) in the ventromedial/interfascicular region.
62 olateral region and the rostral ventromedial/interfascicular region.
63 nd a complete absence of secondary growth in interfascicular regions in the stem.
64 rated that the IFL1 gene is expressed in the interfascicular regions in which fibers differentiate, w
65 ucleus and mDA of the ventral tegmental area/interfascicular regions, but remarkably, little to the s
66 elop extraxylary fibers at specific sites in interfascicular regions.
67 specialisation of the IFM to enable repeated interfascicular sliding and recoil.
68                                   Within the interfascicular subnucleus, [3H]8-OH-DPAT binding decrea
69 us was lower than that in the ventral or the interfascicular subnucleus.
70 nerve in the mouse, which we have called the interfascicular trigeminal nucleus (IF5).
71 inals were more frequent in the ventromedial/interfascicular vs. the dorsolateral region (72% of 233