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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

40 Chordotonal organs perform proprioceptive and other mech

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

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

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

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

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

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

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

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

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