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1  from an increase in the axial length of the eyeball.
2 era giving an extra degree of support to the eyeball.
3 d solely by the mechanical properties of the eyeball.
4  tissue, and the global layer inserts on the eyeball.
5 mal onto the denuded stroma of an enucleated eyeball.
6 s placed on the bare stroma of an enucleated eyeball.
7 uded cornea before incubating the enucleated eyeball.
8 ceCT) on a 5-week-old chick brain, and right eyeball.
9 ntified in rabbit cornea and sclera of whole eyeballs.
10 nput and are accompanied by rotations of the eyeball [1].
11                       Without perturbing the eyeball, 3 microL of tear fluid was sampled from the mar
12 s (17 cases) did not directly compromise the eyeball, 58.82% (10 of these cases) of which corresponde
13 followed by cornea (16%), conjunctiva (14%), eyeball (9.1%), temporal artery (3.9%) and other locatio
14 is found in the mechanical properties of the eyeball, although neural computations remain necessary a
15 e sclera forms the fibrous outer coat of the eyeball and acts as a supportive framework.
16 lmic artery and its branches vascularise the eyeball and its contents.
17         One involved in the formation of the eyeball and the second involved in the formation of the
18  crucial for the coordinated movement of the eyeballs and for visual acuity.
19 aller body size, different allometry, larger eyeballs and more dorsoventrally compressed heads.
20  expression along with reduced m6A levels in eyeballs and T cells of experimental autoimmune uveitis
21 olymerization were used to make anisotropic 'eyeball' and striped particles, polymer capsules and sem
22 esultant inversion of the lashes abrades the eyeball, and the abrasion leads to corneal opacification
23             Further, we demonstrate that the eyeballs are a source of diffusible all-trans retinoic a
24 e orbit to exclude any foreign bodies in the eyeball, as well as pantomographies to evaluate the dent
25 retina and the lens, collectively called the eyeball, as well as the formation of auxiliary eye struc
26 activated ganglion cell population exits the eyeball; as reported, this triphasic event is invariably
27 ypermetropia with apparent shortening of the eyeball associated with one or more scleral abnormalitie
28 (ADG) is a unique neutral lipid found in the eyeball-associated Harderian gland (HG) of the mouse and
29  sheets were isolated from CD-1 albino mouse eyeballs by incubating for 18 hours at 4 degrees C in 15
30 s of them in systems ranging from electronic eyeball cameras to deformable light-emitting displays.
31 ificant progress in the realization of such "eyeball" cameras, including examples of fully functional
32 ut whether the outer coats of these abnormal eyeballs, cornea anteriorly and sclera posteriorly, are
33 lved in the normal enlargement of the rabbit eyeball during postnatal growth.
34 , retinal detachment, disorganization of the eyeball, endophthalmitis, uveal prolapse, OTS classifica
35                    Rabbits were then killed, eyeballs enucleated, and their ocular volumes determined
36 ucinations (odds ratio: 8.68, P < 0.001) and eyeball/eyelid movements or sensations (odds ratio: 4.35
37 f the right orbit that caused dislocation of eyeball, for which she underwent medial orbitotomy.
38                               In addition, 8 eyeballs from healthy donors were used for biochemical a
39 single or double injections of bFGF into the eyeball had no effect on RGC survival.
40                                              Eyeballs having these refractive errors are known to exh
41  Bilateral ONSD was measured 3 mm behind the eyeball in axial and sagittal planes and mean value was
42 ral orbitotomy, all PCAs were cut behind the eyeball in both groups of animals.
43 rinciple, we use an air-puff stimulus to the eyeball in order to elicit cerebellar activity that is w
44 rug delivery to the posterior segment of the eyeball in pigs.
45  also find that (2) the temporal side of the eyeball is more heavily pigmented than the nasal side.
46 hat (1) the posterior option of the anterior eyeball is more pigmented closer to the equator, suggest
47 e, however, is based on what is known as the eyeball method of data assessment.
48 ildren under 15 years old with trauma to the eyeball or its adnexa were included.
49                                 Normal mouse eyeballs or whole-mount corneas encompassing the entire
50                           This suggests that eyeball pigmentation in macaques is distributed to reduc
51                               Excised feline eyeballs preserved in corneal storage medium and with ei
52 al criterion standard for measuring abnormal eyeball protrusion is still the historic Hertel exophtha
53 nd 8 [35%] male) showed a mean difference in eyeball protrusion of 3.3 mm and 16 healthy volunteers (
54 e (3 mm) cut from the scleral surface of the eyeball, sclera, RPE-choroid, retina, lens, and ciliary
55                                   Individual eyeball structures, such as chromophores, were found to
56                  Abnormal positioning of the eyeball suggested the extraocular muscles involvement.
57 , in the absence of proper protection of the eyeballs, the structures that are crucial for vision can
58 bserve the morphology and vascularity of the eyeball was applied.
59            Postoperative enlargement of both eyeballs was monitored by measuring the axial length and
60                         On postnatal day 17, eyeballs were enucleated.
61 at-mounted conjunctivae or cross sections of eyeballs were harvested from BALB/c mice (6-8 weeks of a
62                           Corneas of excised eyeballs were inoculated with green fluorescent protein
63                         Normal C57BL/6 mouse eyeballs were sampled from embryonic day (E) 10.5 to pos
64                                    Adult rat eyeballs with rectus EOMs attached and TAs were dissecte
65 lids is to provide maximal protection to the eyeball without interfering with vision.