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1 nd survival, and increased maturation in the ventral region.
2 the computing of identity information in the ventral region.
3 hs of ventral leg structures in the anterior-ventral region.
4 lamina: a caudal-dorsal region and a rostral-ventral region.
5 from the ventral fin base and innervates the ventral region.
6 RNA, however, is also present outside of the ventral region.
7 neither recrossing nor projecting back into ventral regions.
8 the task with colour stimuli activated more ventral regions.
9 s of content-related ("what") predictions in ventral regions.
10 l cells, but oriented parallel to the lip in ventral regions.
11 regions, whereas type II neurons localize to ventral regions.
12 her their axons terminate in intermediate or ventral regions.
13 egions was not offset by loss of aeration in ventral regions.
14 l lung regions without markedly compromising ventral regions.
15 D2 receptor upregulation in dorsal, but not ventral, region.
17 position by prevention of axonal growth into ventral regions, (2) the prevention of axonal extension
18 ecreased proliferation of progenitors in the ventral region and decreased expression of the ventral m
19 0 and E12 is essential for the patterning of ventral regions and the generation of cell types that ar
20 ughout the CNS, including Wnt7a and Wnt7b in ventral regions and Wnt1, Wnt3, Wnt3a, and Wnt4 in dorsa
21 entricular (dorsal) and the suprachiasmatic (ventral) regions, and limits dorsally with the preoptic
22 lder adults showed less activity in anterior-ventral regions associated with controlled use of semant
26 lion cells were observed within the temporal-ventral region by approximately 48 hpf, more than 8 hour
30 lei of the torus semicircularis, whereas the ventral region did not show significant effects of stimu
31 es that the fossil snake was pale-colored in ventral regions; dorsal and lateral regions were green w
33 inal cord included penetration of axons into ventral regions from which they would normally be repell
35 ession of the neuroectodermal genes into the ventral region in snail mutant is a possible cause of de
36 micircular canal nerves project primarily to ventral regions including the TON, ventral DON, intermed
37 (i.e., color was cued), and alpha power from ventral regions increased when color was irrelevant.
38 d by Grem2, separate an initially homogenous ventral region into distinct ventral and intermediate sk
43 ypes both in Drosophila and vertebrates; the ventral region of Drosophila is homologous to the dorsal
44 Dense terminal projections arose from the ventral region of M1, and moderate projections from LPMC
45 Significant apoptosis was detected in the ventral region of mutant embryos within the definitive e
47 portion of Rt sent a heavy projection to the ventral region of the anterior Ec, whereas the more caud
53 c receives additional input from an anterior-ventral region of the claustrum, which has been reported
55 ) neuronal differentiation in the dorsal and ventral region of the dysraphic neural tube occurs remar
59 activity of the Pipe sulfotransferase in the ventral region of the follicular epithelium that surroun
63 cting SOX17+ biliary progenitor cells to the ventral region of the gut requires the notch effector He
66 creased proliferation of NSCs located in the ventral region of the hippocampus while the mitotic inde
67 task showed more activation in the anterior ventral region of the inferior/middle frontal gyrus (BA
69 d to the interpeduncular nucleus (IP) in the ventral region of the midbrain-hindbrain transition.
70 gion near the Eustachian tube orifice at the ventral region of the middle ear cavity, consisting most
72 t, Six1 expression was first detected in the ventral region of the otic pit and later is restricted t
74 ined with a higher frequency (77-82 Hz) in a ventral region of the premotor cortex to produce a third
75 ty was detected at embryonic day 12.5 in the ventral region of the rhombencephalon and spinal cord an
76 ontextual monitoring demands, whereas a more ventral region of the right prefrontal cortex showed ret
80 effects on oligodendrocyte production in the ventral region of the spinal cord; however, less is know
81 icated that both groups activated dorsal and ventral regions of an anterior-limbic network, but the B
82 f endogenous CamKII activity from dorsal and ventral regions of embryos revealed elevated activity on
83 econd class of cells, most commonly found in ventral regions of LAd, had longer latency responses, bu
84 eased the density of serotonergic axons with ventral regions of spinal segments L1-L5, (3) and that N
85 icant activation of DA release in dorsal and ventral regions of the basal ganglia of healthy voluntee
87 area Te1 labeled axons and terminals in the ventral regions of the dorsal and ventral subnuclei of t
89 ch resource for analyzing how the dorsal and ventral regions of the embryo communicate with each othe
90 lanar contact with tissues of the lateral or ventral regions of the embryo could also contribute to t
92 t of the bulb associated with peripheral and ventral regions of the epithelium, our results challenge
93 mechanisms and general strategies at play in ventral regions of the forming spinal cord, where sonic
95 ously demonstrated that hyperactivity within ventral regions of the hippocampus (vHipp) drives the do
97 e theta is known to propagate from dorsal to ventral regions of the hippocampus, these data suggest t
99 rasting theories propose that the dorsal and ventral regions of the lateral prefrontal cortex are inn
100 nalis (BNST), posterior dorsal and posterior ventral regions of the medial amygdala (MePD and MePV, r
106 t enhancers, which direct gene expression in ventral regions of the neurogenic ectoderm in response t
110 , or both peptides were also detected in the ventral regions of the rostral hypothalamus, dorsolatera
111 Prdxs and Trxs in groups of cells located in ventral regions of the spinal cord that express motor ne
113 V2 functions as a BMP4 feedback inhibitor in ventral regions of the Xenopus embryo; (2) CV2 complexes
115 of each ISV leave the aorta only between the ventral regions of two adjacent somites, and migrate dor
116 support the idea that dorsal, as opposed to ventral, regions of the striatum are a locus of vulnerab
117 hibition accompanied by decrease in CBF from ventral region or sympathoexcitation accompanied by incr
118 mozygous mutant embryos developed with their ventral region outside of the yolk sac, had two independ
120 ysis of the shape of the similarity space in ventral regions provides evidence for a continuum in the
121 ory interactions, whereby genes expressed in ventral regions repress those expressed in more dorsal r
122 onitoring demands were emphasized, while the ventral region showed greater activation when external c
123 during the monitored search task and a more ventral region showing activation under the externally c
125 iprocal striatonigral terminal fields, and a ventral region that receives a specific striatonigral pr
126 ollow from the anatomy and laterality of the ventral regions that interact with the dorsal attention
127 the contralateral lower visual field and the ventral region the contralateral upper visual field.
128 a concomitant impairment of gas exchange in ventral regions, thus leading to a significant increase
129 entral, intermediate regions and part of the ventral region, Vd/Vc/Vi, and Vv) expressed high levels
130 ity between the posterior-dorsal and lateral-ventral regions was corroborated by a multivariate analy
132 on, focusing Wnt1 signaling to the posterior-ventral region where it suppresses nodal expression.
133 reliably activated middle-occipital temporal-ventral regions which are known to participate in the de
134 fect of task was much greater in dorsal than ventral regions, with object category and task relevance
135 hat stimulation of more rostral and somewhat ventral regions within an ICC lamina achieves lower thre
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