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1 om developing seeds of Hedera helix (English ivy).
2 conserved except for T117R and P179I (castor/ivy).
3 e seen in certain species, including English ivy.
4 riod, including his daughter, Lady Theodosia Ivy.
5 and urushiol, the contact allergen of poison ivy.
6 cy, growth, and population biomass of poison ivy.
7                               Five (Alvarez, Ivy, Aaron, Grossman, and Donaldson) are no longer with
8 oparticles results in a low viscosity of the ivy adhesive, and thus a favorable wetting behavior on t
9  expressed sequence tags (ESTs) from English ivy, an Araliaceae species, and sunflower, an Asteraceae
10 acids lining the substrate binding cavity of ivy and castor desaturases are conserved except for T117
11                  Of 12 synthesised peptides, IVY and ILDL were the most potent, having ACE IC50 value
12                                              Ivy and neurogliaform cells are not only numerous but al
13                                   Effects in Ivy and neurogliaform cells are seen at similar concentr
14 ly targeting, neurogliaform family of cells (Ivy and neurogliaform cells) is a previously unrecognize
15 s of CA1, activation of muORs hyperpolarizes Ivy and neurogliaform cells.
16 ired recordings between synaptically coupled Ivy and pyramidal cells show that Ivy cell terminals are
17 logues of the periplasmic lysozyme inhibitor Ivy and the membrane-bound lysozyme inhibitor MliC.
18 ng between the adventitious roots of English ivy and the surface of substrates.
19                              Mutants lacking ivy and/or mliC were generated.
20 , the toxic catechol from poison oak, poison ivy, and poison sumac, has been developed utilizing the
21 ly coupled Ivy and pyramidal cells show that Ivy cell terminals are dramatically inhibited by muOR ac
22       Thus, as neurogliaform cells (NGC) and Ivy cells (IvC) represent the main nNOS(+) interneurons,
23 CP-AMPAR-dependent LTP in NOS-immunopositive ivy cells and SM-expressing O-LM cells to afferent fiber
24                          We also report that Ivy cells display the recently described phenomenon of p
25                                              Ivy cells express nitric oxide synthase, neuropeptide Y,
26 h millisecond precision, the highly abundant Ivy cells express presynaptically acting neuromodulators
27 ntingent manner, whereas persistently firing ivy cells might control network excitability and homeost
28 xide synthase- and neuropeptide Y-expressing ivy cells provided synaptic and extrasynaptic dendritic
29       Paired recordings in vitro showed that Ivy cells receive depressing EPSPs from pyramidal cells,
30                                   Basket and ivy cells showed distinct spike-timing dynamics, firing
31 n contrast, regular-spiking basket cells and ivy cells were less likely to be innervated by mossy fib
32  active GABAergic cells during SWRs, whereas ivy cells were silent.
33  in addition to the dendritically projecting ivy cells, and the septum-projecting spiny stratum lucid
34 ly rising and decaying inhibitory input from Ivy cells.
35                                             "Ivy" cells, named after their dense and fine axons inner
36                              Basket, but not ivy, cells changed their firing rates during movement, s
37                                  Deletion of ivy decreased Y. pestis' ability to counter lysozyme and
38  proposed adhesion mechanisms underlying the ivy-derived adhesive.
39                   Human subjects with poison-ivy dermatitis had a similar cytokine signature followin
40 sional skin, and skin from lesions of poison ivy dermatitis, however, have increased levels of telome
41                                          The ivy desaturase also converted 16:1delta(9)-ACP and 18:1d
42                            Expression of the ivy desaturase in Arabidopsis resulted in the accumulati
43        The multifunctional properties of the ivy desaturase make it well suited for further dissectio
44 or more periplasmic proteins including OsmY, Ivy, DppA, OppA, and HdeB.
45                            Y. pestis lacking Ivy had attenuated virulence, unless animals were neutro
46 vered that the adventitious roots of English ivy (Hedera helix) exude a yellowish mucilage that promo
47  similar size in developing seeds of English ivy (Hedera helix), an Araliaceae species that also accu
48 sensitivity reactions such as that to poison ivy) immune responses.
49                                              Ivy is required to counter lysozyme during infection, bu
50 trate that SERS-active, superhydrophobic and ivy-like nanostructured films of a molecular semiconduct
51  the adhesion mechanisms revealed by English ivy may forward the progress toward understanding the ge
52                   It is not known how poison ivy might respond to increasing concentrations of atmosp
53 d by these molecular events, a reconstructed ivy-mimetic adhesive composite was developed by integrat
54                                          The Ivy mutant induced inflammation to a degree similar to t
55         The spheroidal shape of the AGP-rich ivy nanoparticles results in a low viscosity of the ivy
56 s developed by integrating purified AGP-rich ivy nanoparticles with pectic polysaccharides and calciu
57 ulation of contact sensitivity to the poison ivy/oak catechol was studied at the level of class II MH
58 e site of contact with allergens like poison ivy or nickel.
59 ct dermatitis, such as in response to poison ivy or poison oak, and chronic low-dose ultraviolet B ir
60  The governor named a committee and accepted Ivy's offer to chair the panel.
61                           Late in the trial, Ivy testified--drawing on the authority of this committe
62  Last, Y. pseudotuberculosis did not require Ivy to counter lysozyme and for virulence.
63                          Contact with poison ivy (Toxicodendron radicans) is one of the most widely r

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