ライフサイエンスコーパス: protoplasmic

1 cal and immunocytochemical phenotype between protoplasmic and fibrous astrocytes.

2 e knowledge of how the complex morphology of protoplasmic astrocytes affects their 3D relationships w

3 Protoplasmic astrocytes are critically important to ener

4 Protoplasmic astrocytes are increasingly thought to inte

5 In all mammals, protoplasmic astrocytes are organized into spatially non

6 postnatal months prior to its expression in protoplasmic astrocytes at 41 postconceptional weeks onw

7 Released glutamate acts on receptors on the protoplasmic astrocytes closely apposed to the synapse t

8 Mammalian protoplasmic astrocytes develop a dense ramified meshwor

9 Our findings show that protoplasmic astrocytes establish primarily exclusive te

10 ing was used to directly isolate neurons and protoplasmic astrocytes from the cortex of adult mice.

11 are precursors of oligodendrocytes and some protoplasmic astrocytes in gray matter.

12 We report here that protoplasmic astrocytes in human neocortex are 2.6-fold

13 iated astrocytes account for the majority of protoplasmic astrocytes in neocortex.

14 To this end, protoplasmic astrocytes in the adult rat dentate gyrus w

15 e interactions in detail, groups of adjacent protoplasmic astrocytes in the CA1 stratum radiatum were

16 e rise to a subset of immature, postmitotic, protoplasmic astrocytes in the gray matter of the spinal

17 es throughout the CNS and a subpopulation of protoplasmic astrocytes in the gray matter of the ventra

18 n both gray and white matter and a subset of protoplasmic astrocytes in the gray matter of the ventra

19 as NG2 cells in the embryonic brain generate protoplasmic astrocytes in the gray matter of the ventra

20 g oligodendrocytes and in a subpopulation of protoplasmic astrocytes in the gray matter of ventrolate

21 Human protoplasmic astrocytes manifest a threefold larger diam

22 inct contrast to those reported for reactive protoplasmic astrocytes of the gray matter, in which the

23 on of any of the three VGLUTs by gray matter protoplasmic astrocytes of the primary somatosensory cor

24 pared from acutely resected surgical tissue, protoplasmic astrocytes propagate Ca(2+) waves with a sp

25 nule layer, D-serine is found transiently in protoplasmic astrocytes surrounding glomeruli, where it

26 This racemase has been localized to protoplasmic astrocytes that ensheath synapses and modul

27 astrocytes initiates a conversion of normal, protoplasmic astrocytes to astrocytes that display sever

28 fap(+/R236H), resulting in the conversion of protoplasmic astrocytes to cells that have lost their bu

29 The protoplasmic astrocytes were either isolated or formed s

30 nctions in balancing the number of dorsal GM protoplasmic astrocytes with dorsal WM fibrous astrocyte

31 intranuclear inclusions were also present in protoplasmic astrocytes, including Bergmann glia in the

32 ration resulted in expression in neurons and protoplasmic astrocytes, respectively.

33 etinal ganglion cell (RGC) somata and axons, protoplasmic astrocytes, vascular endothelial cells, and

34 e telencephalon, D-serine is concentrated in protoplasmic astrocytes, which are abundant in neuropil

35 alized to perivascular end feet in the CD44- protoplasmic astrocytes.

36 was possible to document the development of protoplasmic astrocytes.

37 res that contain both projection neurons and protoplasmic astrocytes.

38 distinct gene expression pattern relative to protoplasmic astrocytes.

39 nal populations, yet abundant in fibrous and protoplasmic astrocytes.

40 cus strongly upregulate Gfap in grey matter (protoplasmic) astrocytes, implying that signalling throu

41 , and solely by phenotypic transformation of protoplasmic astroglia in gray matter.

42 sheath (OS), and within this sheath are the protoplasmic cell cylinder (PC) and periplasmic flagella

43 mbrane sheath, and within this sheath is the protoplasmic cell cylinder and subterminally attached pe

44 a tight-fitting ribbon that wraps around the protoplasmic cell cylinder in a right-handed sense.

45 s) subterminally attached to each end of the protoplasmic cell cylinder, and surrounding the cell is

46 alkaline plasmolysis and separated from the protoplasmic cylinder by sucrose density gradient ultrac

47 rimitia motility that posits rotation of the protoplasmic cylinder within the outer sheath.

48 eta-NADH oxidase activity and the absence of protoplasmic cylinder-associated proteins observed by Co

49 and, in T. pallidum, is tightly bound to the protoplasmic cylinder.

50 The OMV fractions were free of protoplasmic-cylinder material, as judged by immunoblott

51 tions of OMVs were distinct from that of the protoplasmic-cylinder material, which was found in the s

52 d increase in the density of plasma membrane protoplasmic face intramembrane particles.

53 The particle density in the protoplasmic face of the oocyte plasma membrane increase

54 The density of particles on the protoplasmic face of the plasma membrane of oocytes expr

55 nits), clusters of particles appeared in the protoplasmic face of the plasma membrane.

56 eze-fracture particle, which appeared in the protoplasmic face only after EAAT3 expression.

57 novel transmembrane particles in the P-face (protoplasmic face) of oocytes injected with TrkA cRNA, b

58 vity of brevican occurs predominantly in the protoplasmic islet in the internal granular layer after

59 irst described by Santiago Ramon y Cajal as "protoplasmic kisses that appear to constitute the final

60 It maps given data configuration into a protoplasmic network.

61 The protoplasmic networks also show a degree of similarity t

62 ter perhaps representing a shift from CD44- "protoplasmic" to CD44+ "fibrous"-like astrocytes.

63 degrees C, the electrical resistance of the protoplasmic tube increases from approximately 3 MOmega

64 mould spans the sources with networks of its protoplasmic tube.

65 lime mould span two electrodes with a single protoplasmic tube: if the tube is heated to approximatel

66 Networks of protoplasmic tubes of organism Physarum polycehpalum are

67 ; proposing that the network connectivity of protoplasmic tubes shows pathway-dependent plasticity.

68 uld computers we explore conductivity of the protoplasmic tubes; proposing that the network connectiv