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1 ture microdissection was used to isolate the retinal blood vessels.
2 nt epithelium, whereas DGLbeta is limited to retinal blood vessels.
3 iber bundle patterns occurs just above major retinal blood vessels.
4 nner plexiform layer, occasionally alongside retinal blood vessels.
5 anglion cell layers, nerve fiber layers, and retinal blood vessels.
6 ntegrity of the retina, and condition of the retinal blood vessels.
7 netrin-4 was found to be localised to mature retinal blood vessels.
8 e located in the nerve fiber layer and along retinal blood vessels and have been hypothesized to part
9 VIII) immunoreactivity was observed in large retinal blood vessels and in capillaries in some individ
13 , as did endothelial cells of some posterior retinal blood vessels and some retinal pigment epithelia
17 tes highly realistic digital models of human retinal blood vessels, based on established biophysical
18 Occasional cell bodies were associated with retinal blood vessels, but their identity as pericytes,
19 insight into the possible role of tbdn-1 in retinal blood vessels by characterizing its expression p
22 e layer (RNFL) thickness, macular volume and retinal blood vessel diameter were measured and paramete
28 beta2 and gamma3 chains regulate subsequent retinal blood vessel growth and maintain vascular integr
31 n vivo, GSK101 increased the permeability of retinal blood vessels in wild type but not in TRPV4 knoc
32 ession of FcRn receptor was confirmed in the retinal blood vessels, iris blood vessels, optic nerve v
33 sistent with the concept that the absence of retinal blood vessels is essential for foveal pit develo
38 rity and diabetic retinopathy, overgrowth of retinal blood vessels results in the formation of pathol
43 ndothelial precursors stabilizes and rescues retinal blood vessels that would ordinarily completely d