ライフサイエンスコーパス: chordotonal organ

1 ry neurons in Johnston's organ, the antennal chordotonal organ.

2 ngly uniform mechanosensory transducers, the chordotonal organs.

3 is required for the clustering of embryonic chordotonal organs.

4 elated to ancestral states as proprioceptive chordotonal organs.

5 nd graviception are combined in the antennal chordotonal organs.

6 ally in every stage of its expression during chordotonal organ and photoreceptor development.

7 r cells are developmentally related and that chordotonal organs and insect bristle organs are mechani

8 which form an integral component of the fly chordotonal organs and mediate mechanosensation.

9 It is expressed in the chordotonal organs and photoreceptor cells, and flies th

10 eural gene for the development of Drosophila chordotonal organs and photoreceptor cells.

11 We suggest that the reason chordotonal organs and photoreceptors share a requiremen

12 nal (ato) is the proneural gene required for chordotonal organs and R8 photoreceptors, whereas the ac

13 New evidence showing that chordotonal organs and vertebrate auditory hair cells ar

14 s required a functional clock and functional chordotonal organs and was accompanied by phase-shifts o

15 of nocte in this process and identifying the chordotonal organs as relevant sensory structures.

16 as well as the Drosophila flagellar ears use chordotonal organs as the auditory mechanoreceptors.

17 n the crab Cancer borealis and the coxobasal chordotonal organ (CBCTO) in the crab Carcinus maenas.

18 Reducing the function of the gene nocte in chordotonal organs changes their structure and function

19 the body wall and can detect vibration with chordotonal organs (Cho).

20 la atonal (ato) is the proneural gene of the chordotonal organs (CHOs) in the peripheral nervous syst

21 Expressing Math1 induced ectopic chordotonal organs (CHOs) in wild-type flies and partial

22 echanosensory neurons in the larval PNS, the chordotonal organs (chos), in providing sensory feedback

23 oneural gene that governs the development of chordotonal organs (CHOs), which serve as stretch recept

24 During chordotonal organ development, the 3' enhancer directs e

25 ed to describe the remodeling of the femoral chordotonal organ (FCO) in the prothoracic legs.

26 The femoro-tibial chordotonal organ (FCO) of the hindleg monitors extensio

27 interaction of FTi movement(13-15) (femoral chordotonal organ [fCO]) and load(13)(,)(15)(,)(16) (tib

28 ory organ in the Drosophila leg, the femoral chordotonal organ (FeCO).

29 Whereas ectopic ato expression induces chordotonal organ formation, ectopic scute expression pr

30 c-HLH protein required for photoreceptor and chordotonal organ formation.

31 sively studied in the sensory neurons of the chordotonal organ from the coxobasal joint (CBCO) of the

32 ession of dei was lost, resulting in loss of chordotonal organ functionality and defective larval loc

33 ted effects on the structure and function of chordotonal organ in fly model.

34 tial for the formation of photoreceptors and chordotonal organs in Drosophila.

35 ctions bond cells of the nascent (embryonic) chordotonal organs in early neurogenesis.

36 trate the effects of scaling on the antennal chordotonal organs in insects.

37 ion produces external sensory organs but not chordotonal organs in the wing.

38 elicits cytoplasmic expression in embryonic chordotonal organs, in Johnston's organ, and in sperm fl

39 in promotes oenocyte formation and supresses chordotonal organ induction by acting both downstream an

40 l and functional roles for IFT-A proteins in chordotonal organs, insect mechanosensory organs with ci

41 microtubule organization in the cap cells of chordotonal organs is altered in mutant larvae.

42 anosensory afferents of the massive array of chordotonal organs (Johnston's organ) of the adult anten

43 esults in collapse of scolopale cells within chordotonal organs, leading to deficits in larval vibrat

44 tiation of cap versus scolopale cells in the chordotonal organ lineage by, respectively, activating a

45 ophila by daily temperature changes requires chordotonal organs, mechanosensory structures that funct

46 tor nanchung (Nan)-expressing neurons in the chordotonal organs mediate this sleep induction: flies i

47 hannel nanchung, located in the antennae and chordotonal organs, mediate orbital motion-induced sleep

48 val leg, together with 13 femoral and tibial chordotonal organ neurons, persist into the developing a

49 of the structure and scaling of the antennal chordotonal organs of the extremely miniaturized parasit

50 Chordotonal organs perform proprioceptive and other mech

51 nal ears derived from proprioceptive pleural chordotonal organs (plCOs).

52 the developing eye imaginal disc, embryonic chordotonal organ precursors and the midline glia.

53 ' region drive tissue-specific expression in chordotonal organ precursors in the embryo and larval le

54 e precursors of the adult femoral and tibial chordotonal organs respectively.

55 eurons degenerate but some hair sensilla and chordotonal organ sensory neurons survive metamorphosis.

56 ed for the development of precursors of both chordotonal organs (stretch receptors) and photoreceptor

57 ted sensory neurons in Johnston's organ, the chordotonal organ that is the sensory element of the fly

58 in sperm flagella and ciliated dendrites of chordotonal organs that mediate hearing and larval touch

59 asured mechanical properties of a particular chordotonal organ-the lateral pentascolopidial (lch5) or

60 Nan-Iav) and are localized in mechanosensory chordotonal organs which confer gravitaxis, hearing and