ライフサイエンスコーパス: glabrous

1 s Balsas teosinte leaf sheaths are green and glabrous.

2 papillae development, did not complement the glabrous 1 mutant of Arabidopsis.

3 GLABROUS 1, a myb gene required for trichome development

4 S-dependent proteolysis of two of these TFs, GLABROUS 3 (GL3) and ENHANCER OF GL3 (EGL3), is mediated

5 neighboring uninjured fibers into denervated glabrous and hairy plantar skin of male mice.

6 Neurons terminating along the glabrous and hairy skin border exhibit hybrid morphologi

7 s, mediate first pain to heat stimulation of glabrous and hairy skin in humans.

8 e-Dawley rats and macaque monkeys, including glabrous and hairy skin, corneas, eyelids, and the lip.

9 In the glabrous and hairy skin, rare Merkel endings and transve

10 Additionally, molecular profiles of neonatal glabrous and hairy skin-innervating neurons largely over

11 rent primary afferent classes that innervate glabrous and hairy skin.

12 We modeled boundary layer dynamics over glabrous and pubescent leaves (assuming non-exchanging t

13 tant trichome initiation genes compared with glabrous B. napus leaves and consistent with the Arabido

14 xed nerve to a skeletal muscle combined with glabrous dermal skin transplantation, thus forming a bi-

15 e zone is somatotopically organized with the glabrous digits represented centrally, bordered on the m

16 re associated with the representation of the glabrous digits, with D5 represented most dorsal followe

17 re associated with the representation of the glabrous forepaw digits and pads and adjacent non-cluste

18 Application of gibberellic acid to glabrous ga1-3 plants consistently induces earlier forma

19 Mammals use glabrous (hairless) skin of their hands and feet to navi

20 rains and stimulus site (glabrous lip versus glabrous hand).

21 encode C2H2 transcription factors related to GLABROUS INFLORESCENCE STEMS (GIS).

22 hand inputs, amplification and refinement of glabrous inputs, and relocations of representations.

23 This is despite glabrous itch arising from many medical conditions such

24 The null mutant ga1-3 produces completely glabrous leaves when grown in SD conditions.

25 nments, whereas L. luteus and L. albus, with glabrous leaves, are adaptable to humid conditions.

26 pneumatic stimulus trains and stimulus site (glabrous lip versus glabrous hand).

27 All C-polymodal nociceptors in glabrous (n = 4) but none in hairy skin (n = 4) were pos

28 apidly adapting mechanoreceptors innervating glabrous (non-hairy) skin form Meissner corpuscles, whil

29 However, the glabrous noses of moles are an exception.

30 , yielded many colonies which were initially glabrous, off white becoming velvety, greyish brown on a

31 ntergenic noncomplementation and a synthetic glabrous phenotype.

32 When mutated, egl3 gives totally glabrous plants only in the gl3 mutant background.

33 lasting thermal hyperalgesia was apparent in glabrous skin (1 h to >72 h).

34 Itch arising from glabrous skin (palms and soles) has attracted limited at

35 MCs) are cutaneous mechanoreceptors found in glabrous skin and are exquisitely sensitive to light tou

36 ing the gentlest detectable forces acting on glabrous skin and fine sensorimotor control.

37 All glabrous skin and muscle spindle units and in hairy skin

38 us axons at the dermal-epidermal junction in glabrous skin and of myelinated and unmyelinated axons i

39 The afferent inputs from hairy and glabrous skin are distinct with respect to both the prof

40 Laser stimulation of hairy and glabrous skin at the same energy elicited remarkably sim

41 Therefore, we developed a mouse glabrous skin behavioral assay to investigate the contri

42 We have utilized glabrous skin biopsies, a minimally invasive procedure,

43 imager was used to continuously monitor rat glabrous skin blood perfusion in both hind paws, while a

44 l for texture discrimination tasks involving glabrous skin but not whiskers.

45 gradual and rapid non-painful heating of non-glabrous skin by sensitizing the sensory nerves that med

46 Active vasodilatation (AVD) in human, non-glabrous skin depends on functional cholinergic fibres b

47 These results suggest that sweating in non-glabrous skin during post-IHG exercise ischaemia is acti

48 find that disproportionate representation of glabrous skin emerges over postnatal development at the

49 natomical analysis revealed slightly reduced glabrous skin epidermal innervation and substantial alte

50 Mechanoreceptive afferents innervating the glabrous skin exhibit temporal patterning in their respo

51 Primary sensory neurons innervating hindpaw glabrous skin from Slurp2X knock-out mice exhibit increa

52 number of free nerve endings was detected in glabrous skin from SNS-gp130(-/-) compared with control

53 nd density of the nonvascular innervation in glabrous skin from the hands of aged nondiabetic rhesus

54 cant attention, unlike in primates where the glabrous skin has been the focus.

55 shold mechanoreceptors (LTMRs) in the rodent glabrous skin has received scant attention, unlike in pr

56 mechanoreceptor subtypes homotypically tile glabrous skin in a manner that is offset with respect to

57 nt of SkBF responses to local heating of non-glabrous skin in humans.

58 her nominal temperature had to be applied to glabrous skin in order to achieve psychophysical ratings

59 fying somatosensory receptor distribution in glabrous skin is usually difficult because of the divers

60 of itch and opens up new avenues for future glabrous skin itch research.

61 ry skin itch, do not play important roles in glabrous skin itch, demonstrating a mechanistic differen

62 Activation of MrgprC11(+) neurons induced glabrous skin itch, while ablation of MrgprC11(+) neuron

63 reviously identified pruriceptive neurons in glabrous skin itch.

64 prC11(+) neurons are the major mediators for glabrous skin itch.

65 11(+) neurons reduced both acute and chronic glabrous skin itch.

66 o glabrous skin, such that those innervating glabrous skin make synaptic connections that expand thei

67 In retrogradely labelled neurons from the glabrous skin of adult male Sprague-Dawley rats, NCX act

68 and Pacinian (PC) afferents, innervating the glabrous skin of anesthetized macaque monkeys.

69 that hyperkeratotic calluses arising in the glabrous skin of individuals with PC and Krt16 null mice

70 I (SA-II) afferents, which are absent in the glabrous skin of monkeys.

71 after injection of capsaicin (CAP) into the glabrous skin of one hindpaw of anesthetized rats.

72 ponses of all tactile fibers innervating the glabrous skin of the hand to any spatiotemporal stimulus

73 On the glabrous skin of the hand, the gradient of spatial acuit

74 creased sensitivity to mechanical stimuli in glabrous skin of the hindpaw.

75 s between the hairy skin of the arm, and the glabrous skin of the palm, which is not innervated by CT

76 similarly drove widespread K8 expression in glabrous skin of the paws, but in the whisker pads and b

77 ing mechanosensory afferents innervating the glabrous skin of the rat foot.

78 stry showed betaArr1 immunoreactivity in the glabrous skin of the rat hindpaw.

79 labels 32% of the unmyelinated axons in the glabrous skin of the rat hindpaw.

80 Afferents from the glabrous skin of toes 1-5 terminated in a ventromedial t

81 hreshold level mechanical stimulation of the glabrous skin on the contralateral forepaw.

82 nately large numbers of neurons dedicated to glabrous skin sensation, in part reflecting a higher den

83 g gentle touch, mechanoreceptors innervating glabrous skin still make more powerful synapses in the b

84 croneurographical II-AMH responses following glabrous skin stimulation could have been the result of

85 hairy skin stimulation, and CHEPs following glabrous skin stimulation had significantly longer laten

86 study was to assess the effect of hairy and glabrous skin stimulation on neural transmission of noci

87 The larger-caliber axons in the ventral glabrous skin terminate as Pacinian corpuscles deep in t

88 a higher proportion of unmyelinated axons in glabrous skin than in hairy skin.

89 inely identified myelinated dermal nerves in glabrous skin that appeared similar to myelinated fibres

90 r Protein Gene Product 9.5 were performed in glabrous skin to determine the percentage of total fiber

91 In the present study, an analysis of glabrous skin was conducted in human donors to assess th

92 nsory stimuli were applied to the upper lip (glabrous skin) and the chin (hairy skin).

93 er corpuscle size, and Merkel cell number in glabrous skin, although no change in the total number of

94 ic nails, painful hyperkeratotic calluses in glabrous skin, and lesions involving other epithelial ap

95 Finally, BMP5 and BMP7 are enriched in glabrous skin, and signaling through type I bone morphog

96 idence that first pain to heat does exist in glabrous skin, and suggests that similar nociceptive aff

97 not alter the number of Merkel cells in the glabrous skin, but it did enhance the number of myelinat

98 The complex mechanical structure of the glabrous skin, composed of multiple layers and intricate

99 In mouse mutants with ectopic glabrous skin, mechanosensory neurons form end-organs ap

100 g receptive fields of positive DRG neurones: glabrous skin, near hair follicles and in skeletal muscl

101 nsitization in hind foot hairy skin, but not glabrous skin, rapidly activates a descending inhibitory

102 , Meissner, and Pacinian mechanoreceptors in glabrous skin, respectively.

103 In the glabrous skin, strong betaArr1 immunoreactivity was dete

104 t depends on proximity of their terminals to glabrous skin, such that those innervating glabrous skin

105 In glabrous skin, yohimbine had no effect on an equivalent

106 rophysiological recordings using an in vitro glabrous skin-nerve preparation show increased nocicepto

107 ory end organs that densely occupy mammalian glabrous skin.

108 fference in itch sensation between hairy and glabrous skin.

109 s well as in texture perception in primate's glabrous skin.

110 chanoreceptors that innervate both hairy and glabrous skin.

111 ion that II-AMHs are lacking in this primate glabrous skin.

112 o the dynamics of epidermal renewal in human glabrous skin.

113 at transduce steady indentation in hairy and glabrous skin.

114 to terminate as Ruffini corpuscles in human glabrous skin.

115 eceptors are present on sensory axons in rat glabrous skin.

116 utaneous nociceptors and some of the CPMs in glabrous skin.

117 age reversed along the representation of the glabrous snout.

118 nally hairy Brassica species compared with a glabrous species opens doors for the scientific communit

119 Individual TAC-Cells were positioned on the glabrous surface of the right hand, and midline of the u

120 5 ms duration, 1800 mum displacement) to the glabrous surface of the upper lip in order to index the

121 small leaves, where the Reynolds number over glabrous surfaces would be low.

122 gar and other routine mycological media were glabrous to soft, moist, heaped, deeply folded or convol

123 f the foot tended to surround those from the glabrous toes.

124 th the GLABROUS1 (GL1) and TRANSPARENT TESTA GLABROUS (TTG) genes.

125 units, n = 6; slowly adapting (SA) hairy and glabrous units, n = 2; and muscle spindle (MS) units n =

126 ch) hair units, n = 6; rapidly adapting (RA) glabrous units, n = 6; slowly adapting (SA) hairy and gl

127 Culture of the kidney tissue yielded white, glabrous, yeast-like colonies.