ライフサイエンスコーパス: sense organ

1 ition proximal to the accessory cells of the sense organ.

2 applications in both cochlear and vestibular sense organs.

3 te or invaginate to form cranial ganglia and sense organs.

4 s in the function of auditory and vestibular sense organs.

5 reflected by the number and functionality of sense organs.

6 gress to form sensory ganglia and the paired sense organs.

7 the differentiation and function of ciliated sense organs.

8 e generally based on bilaterally symmetrical sense organs.

9 or precise calibration of muscle spindles as sense organs.

10 s and a basicranium underlying the brain and sense organs.

11 atory behaviour involving active movement of sense organs.

12 r is commonly observed in animals with light-sensing organs.

13 aused by the aberrant development of gravity-sensing organs.

14 ent rhodopsins (RH) are present in the light-sensing organs.

15 In non-mammalian, hair cell-bearing sense organs amplification is associated with mechano-el

16 rebellar Purkinje cells, atrophic vestibular sense organs and enlarged ventricles.

17 activity at single-cell resolution in larval sense organs and in the proboscis or leg of the adult fl

18 cell types, including elements of the paired sense organs and neurons in cranial sensory ganglia.

19 they develop in register to form functional sense organs and sensory circuits.

20 tebrates, cranial placodes contribute to all sense organs and sensory ganglia and arise from a common

21 In the vertebrate head, crucial parts of the sense organs and sensory ganglia develop from special re

22 ally for disorders of the nervous system and sense organs and skin and subcutaneous tissue.

23 lacode generates the auditory and vestibular sense organs and their afferent neurons; however, how au

24 contribute to the development of the cranial sense organs and their associated ganglia.

25 of the otic placode correspond to particular sense organs and their innervating neurons.

26 r system give rise to behavior and how force-sensing organs and sensory neurons work.

27 leading to the morphogenesis of the face and sense organs, and to that of the neck, including the ant

28 prostate as well as in other non-temperature-sensing organs, and is regulated by downstream receptor-

29 -3.44%), diseases of the nervous system and sense organs (APC = -6.01%), and diseases of the respira

30 Sense organs are often actively controlled by motor proc

31 tles, SOPs of chordotonal (stretch receptor) sense organs are tightly clustered.

32 tion but, under natural behaving conditions, sense organs are under active, motor control.

33 lator receptor sites in mammalian vestibular sense organs at locations corresponding to efferent inne

34 efects in the development of a male-specific sense organ because of a failure in the proliferation of

35 brate skull evolved to protect the brain and sense organs, but with the appearance of jaws and associ

36 In all three sense organs, cilia defects are followed by degeneration

37 Ancestrally, it comprises neuromasts - small sense organs containing mechanosensory hair cells - dist

38 m thickened ectodermal placodes into complex sense organs containing numerous, diverse neuronal subty

39 gene expression patterns in the major light-sensing organ (cotyledons) and in rapidly elongating hyp

40 cription in the intestine and specifies male sense organ differentiation in the nervous system.

41 egulates yolk protein transcription and male sense-organ differentiation.

42 silla in the labellum, the pharyngeal labral sense organ, dorsal and ventral cibarial organs, as well

43 suggesting that efferent innervation to this sense organ employs other receptor types.

44 ral line, a distributed linear array of flow sensing organs, for underwater hydrodynamic imaging and

45 Although the anatomy of this sense organ has been well documented, the molecular mech

46 their shapes, we examined the formation of a sense organ in C. elegans.

47 knowledge of regeneration in the specialized sense organs in both nonmammalian vertebrates and mammal

48 c responses to stimulation of the vestibular sense organs in the inner ear.

49 igration as collectives of cells, depositing sense organs in their wake.

50 shown previously that the number of external sense organs increases with each moult.

51 e semicircular canal system, one of the main sense organs involved in neural control of locomotion.

52 The fly pharyngeal sense organs lie at the transition between external and

53 termines daughter cell fates in the external sense organ lineage by inhibiting Notch signaling.

54 ughter cell fates in the Drosophila external sense organ lineage requires asymmetric localization of

55 In the external sense organ lineage, the phosphotyrosine binding domain

56 The subgenual organ is a scolopidial sense organ located in the tibia of many insects.

57 ls living in dark environments without light-sensing organs may not be presumed to be light insensiti

58 formation, and finally OFF to permit proper sense organ morphology.

59 acodes contribute to the cranial ganglia and sense organs of the head and, together with neural crest

60 It is specifically expressed in type I sense organs of the peripheral nervous system by the sup

61 of Basic Medical Sciences, Neuroscience, and Sense Organs of the University of Bari, Bari, Italy, 17

62 tem: they give rise to the paired peripheral sense organs (olfactory organs, inner ears and anamniote

63 ically in their contribution to macrochaete (sense organ) patterning on the notum of Drosophila melan

64 gether, our data demonstrate that pharyngeal sense organs play an important role in directing sustain

65 novel patterning mechanism which determines sense organ positioning in Drosophila.

66 hila neurogenesis, a key mechanism promoting sense organ precursor (SOP) fate is the synergy between

67 The adult external sense organ precursor (SOP) lineage is a model system fo

68 Expression of brm(K804R) in the adult sense organ precursor lineage causes phenotypes similar

69 We show that during sense organ precursor specification in Drosophila, the c

70 The selection of Drosophila melanogaster sense organ precursors (SOPs) for sensory bristles is a

71 and in the newly recruited leg disc femoral sense organ precursors was found to be controlled by the

72 controlled neural recruitment of chordotonal sense organ precursors.

73 establish the size and shape of a zebrafish sense organ primordium.

74 The development of Drosophila embryonic sense organs provides a neuronal migration paradigm wher

75 prospero function leads to 'double bristle' sense organs (reflecting a IIb-to-IIa transformation) or

76 nd hair cells of all vestibular and cochlear sense organs, Reissner's membrane, saccular membrane, an

77 including formation of V rays, male-specific sense organs required for mating.

78 The stick insect sense organs show a case of an elaborate scolopidial sen

79 Precursors for vestibular and auditory sense organs show the same distribution.

80 = 1.55), diseases of the nervous system and sense organs (SMR = 1.31), nonmalignant respiratory dise

81 bristle fate as well as promote alternative sense organ subtypes.

82 arization vision, and peculiar locations for sense organs such as the infrared sensors on the abdomen

83 ed in the rostral head region and in certain sense organs such as the inner ear.

84 gans show a case of an elaborate scolopidial sense organ that evolved in addition to the subgenual or

85 s, the nervous system changes the effects of sense organs that signal forces on a leg when the direct

86 With maturation of the sense organs, the developing brain relies less on sponta

87 cuticular surface, the shafts of the bristle sense organs, the lateral extensions of the arista, and

88 nd signals, which is needed for the auditory sense organ to detect sounds over a wide intensity range

89 s that convey olfactory information from the sense organ to the cortical and subcortical olfactory ce

90 s for rapid transmission of information from sense organs to responding muscles.

91 the development and function of the auditory sense organs, we performed a forward genetics screen in

92 of acoustic signals is initiated at auditory sense organs, where mechanosensory hair cells convert so

93 escribe the development of putative internal sense organs, which do not differentiate until larval st

94 b-to-IIa transformation) or 'single bristle' sense organs with abnormal neuronal differentiation (ref

95 The inner ear is a complex vertebrate sense organ, yet it arises from a simple epithelium, the

96 ired in spatial coordinate systems linked to sense organs, yet movement must be executed in coordinat