ライフサイエンスコーパス: zonule

1 nterior and posterior lens surfaces, and the zonule.

2 ues, is a prominent constituent of the mouse zonule.

3 ng vitreous interconnected with the vitreous zonule.

4 fibrillin-1 microfibrils, which compose the zonule.

5 MTSL4 in the formation or maintenance of the zonule.

6 seudoexfoliation (PEX)-induced laxity of the zonule.

7 s mediated by the ciliary muscle through the zonule.

8 r along the insertions of disrupted anterior zonules.

9 formation of microfibril bundles in ciliary zonules.

10 s also develop abnormally long anterior lens zonules.

11 lving the lens-associated MAGP1-rich ciliary zonules.

12 ts because it causes less damage to weakened zonules.

13 ior capsule, anterior cortical vitreous, and zonules.

14 stretched zonules; and (2) extensive loss of zonules.

15 plied manually either by grasping a group of zonules 180 degrees apart with tying forceps (three lens

16 Fibrillin microfibrils form the ocular zonule and are present in the drainage apparatus of the

17 Our findings quantify the movements of the zonule and ciliary muscle during accommodation, and iden

18 The human vitreous zonule and lens equator move forward (anteriorly) during

19 r impact on shape change than the equatorial zonule and that choice of capsular thickness values can

20 A strong relation between the posterior zonule and the anterior hyaloid membrane was observed.

21 elopment immune cells migrate on the ciliary zonules and localize among the equatorial epithelial cel

22 We review the anatomy of the ciliary zonules and their spatial relationship with the ciliary

23 ulling forward the choroid, retina, vitreous zonule, and the neighboring vitreous interconnected with

24 ; (1) uneven, disrupted zonules or stretched zonules; and (2) extensive loss of zonules.

25 opment and arrangement of the murine ciliary zonule are similar to those of humans, and consequently

26 The zonules are attached at the lens capsule equator.

27 lts demonstrate that lens-associated ciliary zonules are directly involved in the lens immune respons

28 lens surfaces to steepen, or the equatorial zonules are under increased tension while the anterior a

29 ls of the lens adjacent to where the ciliary zonules associate with the lens capsule.

30 ed to mount human cadaveric lenses, with the zonule, ciliary body, and sclera attached, inside an env

31 4.2-10) tissues including the lens, capsule, zonules, ciliary body, and sclera were mounted in an opt

32 ned postmortem, including the lens, capsule, zonules, ciliary body, and sclera were mounted in an opt

33 ars) were dissected leaving intact the lens, zonules, ciliary body, hyaloid membrane, anterior vitreo

34 High strain in the ciliary body and zonule corresponded with angle recession and lens displa

35 Damage to ciliary zonules during ECP may not manifest until subsequent gla

36 possible alteration or damage to the ciliary zonules during uncomplicated endoscopic cyclophotocoagul

37 g immune cells are activated to travel along zonule fibers that extend anteriorly along the equatoria

38 ADAMTSL4 is required for stable anchorage of zonule fibers to the lens capsule.

39 lens luxation caused by compromised ciliary zonule formation without a typical phenotype related to

40 to further elucidate the molecular basis of zonule formation, the pathophysiology of EL and ADAMTSL4

41 using retinal degeneration and abnormal lens zonules in human.

42 so restored unfragmented and bundled ciliary zonules in Ltbp2(-/-) mouse eyes under organ culture.

43 t vitrectomy may not affect the integrity of zonules in phakic patients, at least for patients with v

44 ve ability after transection of the anterior zonules in simulated accommodation experiments.

45 ive change in distances between the vitreous zonule insertion zone and the posterior lens equator or

46 be associated with early-onset long anterior zonules (LAZ) and late-onset retinal degeneration (L-ORD

47 Patients with known risk factors for weak zonules may consider choosing alternative intraocular pr

48 models show that the anterior and posterior zonules may have a greater impact on shape change than t

49 yes, the anterior and posterior parts of the zonule need independent force directions.

50 , and structural organization of the ciliary zonule of the mouse.

51 r segment structures, such as the cornea and zonule, often occurs.

52 ell-defined zonule(s); (1) uneven, disrupted zonules or stretched zonules; and (2) extensive loss of

53 ssue is whether during accommodation all the zonules relax causing the central and peripheral lens su

54 sed tension while the anterior and posterior zonules relax causing the lens surface to peripherally f

55 sistent with the general belief that all the zonules relax during accommodation.

56 ith relaxation of the anterior and posterior zonules replicates the topographical changes observed du

57 ed as the following: (0) clear, well-defined zonule(s); (1) uneven, disrupted zonules or stretched zo

58 conditions that can affect the integrity of zonules, such as uveitis or ectopia lentis; (6) eyes wit

59 Fibulin-2 was not present in ocular ciliary zonules, tendon, and the connective tissue around kidney

60 astic capsule with attached ligaments called zonules that mediate ciliary muscle forces to alter lens

61 il-associated protein-1 (MAGP1)-rich ciliary zonules that originate from the vasculature-rich ciliary

62 ls the shape of the lens through the ciliary zonules to focus the image onto the retina.

63 f trypan blue under the iris and through the zonules to the posterior capsule.

64 The insertion site of the posterior zonule was examined.

65 The organization of the zonule was visualized using antibodies to Fbn1, Fbn2, an

66 ography, imaging of the anterior capsule and zonules was performed.