ライフサイエンスコーパス: photoreceptive

1 euro-2a) is sufficient to render these cells photoreceptive.

2 ng because it requires accurate alignment of photoreceptive and optical components on a curved surfac

3 onservation of the process that patterns the photoreceptive and support structures of the eye.

4 Therefore, other important clock-related photoreceptive and synchronization mechanisms must exist

5 nd diversifying their preeminently elaborate photoreceptive arsenal.

6 ess imply either that CRYb retains circadian-photoreceptive capacities or that additional CRY-indepen

7 nd murine IRBP promoters are unmethylated in photoreceptive cells but methylated in other tissues.

8 ars or more that rods and cones are the only photoreceptive cells in the retina.

9 has an endogenous circadian clock as well as photoreceptive cells that regulate this clock.

10 The melanopsin-IR cells have photoreceptive characteristics optimal for circadian rhy

11 nvestigate turnover of protein components in photoreceptive cone outer segments (COSs), the labeled c

12 To assess the nature of the photoreceptive defect in Rpe65 null mice, we eliminated

13 show, using a transgenic approach, that the photoreceptive, Drosophila-like type 1 Cry and the trans

14 lectron microscopy, and behavioral assays of photoreceptive function in zebrafish.

15 urviving retinal neurons to take on the lost photoreceptive function.

16 ement strategy taking account of the complex photoreceptive inputs to these non-visual responses is p

17 s of a complete circadian system, comprising photoreceptive inputs, molecular clockworks and an easil

18 onfirmed the presence of a non-visual ocular photoreceptive mechanism similar to that described in bl

19 retinography, which showed one cone-mediated photoreceptive mechanism with a maximum sensitivity of 5

20 Photoreceptive, melanopsin-expressing retinal ganglion c

21 can be grouped into two classes, with their photoreceptive membrane derived either from cilia or mic

22 s (HAMP1 and HAMP2) in HtrII that bridge the photoreceptive membrane domain of the complex and the cy

23 terior to the brain, Drosophila CRY may be a photoreceptive molecule and also part of the pacemaker m

24 Melanopsin has been proposed as an important photoreceptive molecule for the mammalian circadian syst

25 er, for the majority of these processes, the photoreceptive molecules involved are unknown.

26 ty rhythms in Drosophila relies on different photoreceptive molecules.

27 Our results indicate that this bilayered photoreceptive net is anatomically distinct from the rod

28 We have discovered an expansive photoreceptive 'net' in the mouse inner retina, visualiz

29 A recently identified class of photoreceptive neuron in the retina underlies this funct

30 nd in parts of the brain associated with the photoreceptive ocellus.

31 ng flagellum [4, 5], demonstrating this is a photoreceptive organelle composed of lipid droplets.

32 ar green alga Chlamydomonas reinhardtii is a photoreceptive organelle required for phototaxis.

33 ensory ability found across the Metazoa, and photoreceptive organs are intricate and diverse in their

34 To better understand the evolution of photoreceptive organs, we established the cephalopod Dor

35 pineal gland, or other canonical deep-brain photoreceptive organs.

36 With this powerful mouse model, the photoreceptive origins of any response can be readily id

37 Recently a parallel, non-rod, non-cone photoreceptive pathway, arising from a population of ret

38 Unique photoreceptive properties of intrinsically photosensitiv

39 The photoreceptive properties of the explanted tissues indic

40 t extends to a small number of intrinsically photoreceptive retinal ganglion cells (ipRGCs), expressi

41 However, a population of atypical photoreceptive retinal ganglion cells (RGCs) expresses t

42 ions of projections from mouse intrinsically photoreceptive retinal ganglion cells, and with data fro

43 localization to the inner retina, supports a photoreceptive role for CRY2 in human retina.

44 in a vertebrate eye and suggest a conserved photoreceptive role for cryptochromes in vertebrates.

45 mer location, mouse CRY may play a circadian-photoreceptive role, along with that mediated by rhodops

46 pacemaking neurons are themselves circadian photoreceptive structures.

47 nal rod-cone system, a melanopsin-associated photoreceptive system exists that conveys photic informa

48 first direct evidence of a non-rod, non-cone photoreceptive system in humans.

49 onal characterization of a non-rod, non-cone photoreceptive system in the mammalian CNS.

50 Here, we investigated whether additional photoreceptive systems participate in these responses.

51 , and suggest that it may mediate non-visual photoreceptive tasks such as the regulation of circadian

52 sues suggests a role in vision and nonvisual photoreceptive tasks, such as photic control of skin pig

53 e formation but rather may mediate nonvisual photoreceptive tasks, such as the regulation of circadia

54 pineals of all nonmammalian vertebrates are photoreceptive, whereas those of mammals do not normally