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1 racardiac injections of HRP and were rapidly decapitated.
2 hich were capable of regenerating heads when decapitated.
3  1.75 mCi/kg [3H]AA (i.v.), anesthetized and decapitated 20 min after infusion onset, and brains were
4 3 weeks of activity-wheel running, rats were decapitated and brains were extracted.
5 uman patients, who have a high percentage of decapitated and decaudated spermatozoa (DDS), whose seme
6   Aerial tissues of treated plants were then decapitated and soil was rehydrated to determine the gro
7 sensory function of these noncephalic cells, decapitated animals display a clear photoavoidance respo
8 e absence of expression at the apical end of decapitated animals of reg-16, a head formation-deficien
9                        The viral Gag protein decapitates cellular mRNAs apparently to decoy this enzy
10                             A preparation of decapitated Drosophila melanogaster has been used for di
11                                    Rats were decapitated every 30 min from 0830 h-1100 h and hourly f
12 changes in agonist responsiveness persist in decapitated flies that are aged for 12 h.
13 tor agonist, induces reflexive locomotion in decapitated flies.
14     However, whereas sporadic translocations decapitate Myc from 5' proximal regulatory elements, mos
15                         The mice were either decapitated or perfused in-situ and brain samples collec
16                                     However, decapitated plants and explants both showed similar up-r
17 scription factor and MAP kinase) in roots of decapitated plants to investigate the tissue-specific lo
18 uxin efflux from axillary buds of intact and decapitated plants without affecting auxin flow in the m
19   Both genes were induced just as rapidly in decapitated plants, suggesting that the rapid response t
20  reduction and hormone synthesis and also in decapitated plants.
21  much diminished auxin supply in in vitro or decapitated plants.
22 plants respond better to auxin than those on decapitated plants.
23            IE leaves senesced sooner even in decapitated poplars where source-sink relationships and
24 ine receptors by using a behaviorally active decapitated preparation that allows for direct applicati
25  and the application of insulin eye drops to decapitated rats still resulted in the accumulation of i
26 ng the effects of eye drop administration in decapitated rats.
27 tiation is strictly dependent on the tip; in decapitated slugs no new waves are initiated and slug mo
28  indicative of additional zeatin-type CKs in decapitated stems being supplied by roots and thus promo
29  sensitivity hypothesis, we immersed marked, decapitated sunflower (Helianthus annuus L.) hypocotyl s
30 iation of new apical meristems was forced by decapitating the plants above the injection site.
31 stochemical evaluation, additional rats were decapitated without prior SE or 2, 5, or 14 d after SE.