戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 cesses such as LTP, LTD, spine motility, and axonal pathfinding.
2 o help direct olfactory sensory neuron (OSN) axonal pathfinding.
3 and that this antagonism is important during axonal pathfinding.
4 lls either to specify cell fate or to direct axonal pathfinding.
5 last proliferation, neuronal positioning and axonal pathfinding.
6  direct evidence that they are essential for axonal pathfinding.
7 otactin, a cell surface receptor involved in axonal pathfinding.
8 from proliferation to synaptic modulation to axonal pathfinding.
9 s that govern specification of cell fate and axonal pathfinding.
10 , and that the space cadet gene functions in axonal pathfinding.
11 e neuronal cell body and is not required for axonal pathfinding.
12 germinal center kinase family play a role in axonal pathfinding.
13 ility and that NMD acts locally to influence axonal pathfinding.
14 s in diverse developmental processes such as axonal pathfinding and cell adhesion.
15  suggest that APP overexpression may perturb axonal pathfinding and circuit formation in developing D
16                    In addition, we find that axonal pathfinding and fasciculation are abnormal in cor
17    Null mutation of the GAP-43 gene disrupts axonal pathfinding and is generally lethal shortly after
18 the repulsive effect of the Eph receptors in axonal pathfinding and may facilitate tumor cell invasio
19 s, including C&E, cochlear cell orientation, axonal pathfinding and neuronal migration.
20 ion along the dorso-ventral axis but also in axonal pathfinding and organisation of the axonal scaffo
21                GAP-43 has been implicated in axonal pathfinding and sprouting, synaptic plasticity, a
22 s) help control neuronal fate determination, axonal pathfinding and synaptic communication and plasti
23  in the expression of proteins essential for axonal pathfinding and/or neuronal differentiation in bo
24 is known to promote neuronal survival, guide axonal pathfinding, and participate in activity-dependen
25 les in vertebrate tissue boundary formation, axonal pathfinding, and stem cell regeneration by steeri
26 , however, so it is unknown which aspects of axonal pathfinding are controlled by their activities.
27 oss of optic nerve astrocytes, and anomalous axonal pathfinding at the optic chiasm.
28 the first to show that ADCY8 is required for axonal pathfinding before axons reach their targets.
29 vely studied for their role in dendritic and axonal pathfinding, but less is known about their potent
30 ral vascular development but is required for axonal pathfinding by several populations of neurons in
31 ranscripts in vivo coincides temporally with axonal pathfinding by spinal neurons, supporting a role
32                                Corresponding axonal pathfinding defects were specific to NOVA2 defici
33 gest that EphA8/Eek receptors play a role in axonal pathfinding during development of the mammalian n
34 that morphogen gradients also serve to guide axonal pathfinding during development of the nervous sys
35 em for studying the mechanisms that underlie axonal pathfinding during development, little is known a
36 oping Xenopus retinotectal system results in axonal pathfinding errors.
37                        Mechanisms underlying axonal pathfinding have been investigated for decades, a
38                             We have examined axonal pathfinding in mice lacking the secreted bone mor
39 rmore, there is a long-lasting alteration in axonal pathfinding in secondary motoneurons that is not
40                     Thus, cell migration and axonal pathfinding in the AVM neurons appear to involve
41  functions, including neuronal migration and axonal pathfinding in the brain.
42  communication during development, including axonal pathfinding in the nervous system and cell-cell i
43                                              Axonal pathfinding in the nervous system is mediated in
44         Ephrin/Eph signalling is crucial for axonal pathfinding in vertebrates and invertebrates.
45 ith particularly well-characterized roles in axonal pathfinding, in the healing of damaged epithelia
46  as well as mutants with specific defects in axonal pathfinding, including exit from the spinal cord
47  and signaling through this isoform mediates axonal pathfinding, independent of the MuSK downstream c
48  establish a previously unknown mechanism of axonal pathfinding involving vascular-derived endothelin
49 to act as repellants in vertebrate embryonic axonal pathfinding may also inhibit regeneration.
50 ts of neuronal development such as embryonic axonal pathfinding, neuroblast proliferation in the larv
51  cell proliferation, cell specification, and axonal pathfinding of discrete neuronal populations.
52  UNC-42 and that UNC-42 is also required for axonal pathfinding of neurons in the circuit.
53 d that embryonic exposure to nicotine alters axonal pathfinding of spinal secondary motoneurons in ze
54  in the optic nerve and retina, and abnormal axonal pathfinding of the ganglion cell axons at the opt
55                 The mechanisms that underlie axonal pathfinding of vomeronasal neurons from the vomer
56 le abnormalities, suggesting that defects in axonal pathfinding or synapse formation may cause the ob
57 ocesses during axonal development, including axonal pathfinding, orientation of axons in chemotactic
58 t the nicotine-induced changes in motoneuron axonal pathfinding persisted into adulthood.
59       This activity may play a major role in axonal pathfinding, refinement of topographic maps, dend
60 ortical layer structures were disrupted, and axonal pathfinding was impaired.
61                     Netrin-1 is critical for axonal pathfinding which shares similarities with format
62 neration after injury depends on accuracy of axonal pathfinding, which is primarily believed to be in

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。