ライフサイエンスコーパス: coextensive

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1 -8 expression and of polarizing activity are coextensive.

2 S-cone contributions to this ganglion cell's coextensive blue-ON/yellow-OFF receptive field are large

3 gely cancel, explaining the small, spatially coextensive but spectrally antagonistic receptive field

4 We found coextensive cutaneous and auditory responses in caudomed

5 ded amygdala are innervated by substantially coextensive distributions of neurons in the prefrontal a

6 mplex cells had ON and OFF regions that were coextensive in space.

7 small bistratified cell displays a spatially coextensive receptive field in which the S-ON-input is i

8 id not affect chromatic balance or the basic coextensive receptive field structure, suggesting that t

9 weights to different BY ganglion cells, the coextensive receptive fields must be already present in

10 Finally, because BY ganglion cells have coextensive +S and -(L+M) receptive fields, and each S c

11 sual hemifield was observed in V1, which was coextensive with a region of dense myelination.

12 ligned in narrow parasagittal bands that are coextensive with activated glial cells.

13 erminal fields of the Vv were observed to be coextensive with afferent cell groups in the preoptic ar

14 Primary motor cortex was coextensive with an agranular area of cortex marked by a

15 Furthermore, these areas were coextensive with distinct myeloarchitectonic appearances

16 First, a beta-glucan-enriched domain, coextensive with GAXs of low degrees of arabinosyl subst

17 g from laminae V and VII neurons that may be coextensive with its cerebellothalamic input.

18 ganized to form a polarized network that was coextensive with microtubules in cell protrusions.

19 vity and appeared to originate from a region coextensive with that of the linear receptive field cent

20 bulin is a giant filamentous protein that is coextensive with the actin filaments of the skeletal mus

21 separation) with the hair cell membrane and coextensive with the micrometers-long synaptic terminals

22 narrow region of the RVLM that appears to be coextensive with the pre-BotC of adult rats.

23 al distribution of group Ia contacts was not coextensive with the radially organized dendrites of mot

24 dy, we show that the rx expression domain is coextensive with the region identified as the retinal fi

25 ir influence to an LGN region visuotopically coextensive with the size of the minimum response field

26 yperintense (light) areas in MTC images were coextensive with the SN as delineated histologically.

27 (dark) areas in T2-weighted images were not coextensive with the SN but extended partially into the

28 The second focus was coextensive with the somatosensory representation of the

29 ounded by an annular grating that was either coextensive with the target (unsegmented) or appeared se

30 [3H]8-OH-DPAT binding was coextensive with the TrpOH-immunoreactive cell bodies an

31 suotopic information to V1 that is spatially coextensive with the V1 neuron's optimal stimulus size m

32 microm-long segment of ventrolateral medulla coextensive with the ventral respiratory group.

33 These endodermal deficits are precisely coextensive with the zone of mesodermal deficiency, sugg

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