ライフサイエンスコーパス: amputate

1 matocrit changes or parts of the network are amputated.

2 pre-existing organizers were simultaneously amputated.

3 ble or Doppler pulse) more likely were to be amputated (31% vs. 13%; p < 0.04).

4 ncrease a disability with further surgery or amputate a patient's limb without clear evidence of LR i

5 l organization of this nucleus in neonatally amputated adult rats.

6 tracked the frequency of each lineage within amputated and fully regenerated limbs.

7 result, the patient's leg did not have to be amputated and he is undergoing rehabilitation.

8 Amputated animals failed to increase stem cell prolifera

9 ls and stem cell (neoblast) proliferation in amputated animals identifying candidate stem cell, regen

10 Amputated apices from vegetative wildtype cells of the u

11 of regeneration is more rapid in proximally amputated appendages compared with distal amputations.

12 We amputated appendages in a variety of cave-adapted and su

13 possess a spectacular ability to regenerate amputated appendages, based on formation and maintenance

14 fishes and urodele amphibians can regenerate amputated appendages, whereas this ability is restricted

15 We show that the suckers of amputated arms never attach to octopus skin because a ch

16 singly, octopuses seem to identify their own amputated arms, as they treat arms of other octopuses li

17 n by central control because, in contrast to amputated arms, behaving octopuses sometime grab amputat

18 tated arms, behaving octopuses sometime grab amputated arms.

19 onal forelimb-stump representation from rats amputated as adults was significantly smaller (P < 0.05)

20 duce a regeneration response in mouse digits amputated at a proximal level of the terminal phalangeal

21 as distal in all cases except for 2 patients amputated at the midforearm level.

22 In wild-type zebrafish caudal fins, amputated blood vessels heal their ends by 24 h postampu

23 l motion restriction, and preservation of an amputated body part.

24 odele amphibians and teleost fish regenerate amputated body parts via a process called epimorphic reg

25 ultimately orchestrates regeneration of the amputated bone and surrounding soft tissue.

26 ilure of the wound epidermis to close across amputated bone.

27 will regenerate the complex structure of an amputated caudal fin to a degree that the original and r

28 Two-day-old zebrafish regenerate their amputated caudal fins within 3 days.

29 a trabecular bone network that replaces the amputated cortical bone.

30 defined as the reattachment of a completely amputated digit that necessitated anastomosis of both ar

31 em cells (mBMSCs) to regenerate a proximally amputated digit tip.

32 on in vitro, and when re-introduced into the amputated digit, these cells display directed migration

33 he cortical region previously devoted to the amputated digits.

34 Larvae amputated during the refractory stage exhibit a much bro

35 The in vivo impact of viruses that have an amputated enhancer was investigated in an extremely sens

36 proliferation continuously acting across the amputated fin from early stages of vertebrate regenerati

37 In the amputated fin, hspd1 is required for the induction of me

38 Zebrafish innately regenerate amputated fins by mechanisms that expand and precisely p

39 Moreover, amputated fins depleted of osteoblasts regenerated new f

40 Many fish and salamander species regenerate amputated fins or limbs, restoring the size and shape of

41 se Mps1, factors crucial for regeneration of amputated fins, also caused rapid, progressive loss of f

42 they are highly regenerative, able to regrow amputated fins, as well as a lesioned brain, retina, spi

43 mportant for late epimorphic regeneration of amputated fins.

44 since sheath cells can behave inductively in amputated follicles after regenerating the papilla, this

45 cedure may help to lower the number of limbs amputated for vascular disease.

46 velopmental stage, tissue composition of the amputated fragment, and axial position of the cut plane.

47 positional information on the two ends of an amputated fragment.

48 hment and regeneration of multiple organs in amputated fragments.

49 Pathological and histological exam of a foot amputated from an affected child revealed complete absen

50 body size confirm it was a predator, but the amputated hind limb on the right side indicate itself ha

51 kade of peripheral activity by QX-314 at the amputated hindpaw 120 min after amputation did not signi

52 ne expression in muscular specimens from the amputated ischemic legs of diabetic patients.

53 t), and from the most proximal region of the amputated leg were studied.

54 y enlarged sciatic nerve in the stump of the amputated leg.

55 Sections of sural nerve were removed from amputated legs of patients with vascular disease or diab

56 flies frequently survive freezing by rapidly amputating legs before ice crystallization can spread to

57 The novel model consists of taking a freshly amputated limb and incorporating it into an ex situ pump

58 The perception of an amputated limb arising from stimulation of reinnervated

59 affect the development of contralateral, un-amputated limb buds.

60 We found that M1 maps of the amputated limb in TMSR patients were similar in terms of

61 echnique allows some sensory nerves from the amputated limb to reinnervate overlying chest skin.

62 hnologies to stimulate regrowth of a lost or amputated limb with a patterned replicate, as salamander

63 r missing somatosensory information from the amputated limb.

64 patterning and cellular architecture of the amputated limb.

65 ber ratio (p < 0.01) in muscle biopsies from amputated limbs and Grad measured pre-operatively at the

66 The regrowth of amputated limbs and the distal tips of digits represent

67 Salamanders are capable of regenerating amputated limbs by generating a mass of lineage-restrict

68 In group 1 (n = 4), we perfused 4 amputated limbs for 12 hours using warm (27 degrees C-32

69 In this study, we show that exposing amputated limbs to beryllium nitrate disrupts blastema f

70 mexicanum) is capable of fully regenerating amputated limbs, but denervation of the limb inhibits th

71 ma chondrogenesis and cartilage formation in amputated limbs.

72 ardiac, neural and retinal tissues, and even amputated limbs.

73 ly expressed between proximally and distally amputated limbs.

74 ly vertebrates capable of fully regenerating amputated limbs.

75 y motor cortical (MI) neurons of chronically amputated monkeys exposed to control a multiple-degree-o

76 In targeted reinnervation, amputated nerves are redirected to proximal muscles and

77 TMR, a surgical technique that redirects amputated nerves into motor targets, has been proposed a

78 egenerated tissue or organ that replaces the amputated one.

79 elopment in cells whose caps either had been amputated or had spontaneously aborted.

80 zebrafish, achieve complete regeneration of amputated or injured myocardium through the proliferatio

81 e preoperative assessment of the patient and amputated part is important to define associated trauma

82 Amputated patients have an impaired physical HR-QOL but

83 the goal to restore function in paralyzed or amputated patients.

84 Males display regenerative defects in amputated pectoral fins, caused by impaired blastemal pr

85 Following equinox inhibition, amputated planarians fail to maintain wound-induced gene

86 In the present study, we amputate portions of the arms of Archaster typicus starf

87 ine or UXO victims who had one or more limbs amputated ranged from 19.5% to 82.6%.

88 At the brainstem level, neonatally amputated rat cuneate neurons possessed the following re

89 y smaller (P < 0.05) than that of neonatally amputated rats (4.3 +/- 1.3 mm(2) vs. 6.6 +/- 1.5 mm(2),

90 eral stimulation vs. neurons from neonatally amputated rats (48% vs. 16%, respectively).

91 reorganization observed in SI of neonatally amputated rats may reflect functional alterations occurr

92 In contrast, cuneate neurons of adult amputated rats were 70% stump responsive, 2% responsive

93 6)-C(8) dorsal root ganglia neurons of adult amputated rats were unresponsive to peripheral stimulati

94 ed the thalamocortical pathway in 2 forelimb-amputated rats.

95 with the stump and hindlimb SI in neonatally amputated rats.

96 t, surgically connected in series within the amputated residuum such that contraction of one muscle s

97 enitor cells responsible for regeneration of amputated salamander limbs and fish fins.

98 rogenitor cells that enables regeneration of amputated salamander limbs or fish fins.

99 body integrity dysphoria express a desire to amputate seemingly healthy parts of their body.

100 ntage of the motor neuron pool (%MNP) on the amputated side than on the intact side.

101 , the threshold for muscle activation on the amputated side was lower than that of the intact side, b

102 normal, some distal limb motoneurons on the amputated side were smaller in size and simpler in form.

103 icantly less intracortical inhibition on the amputated side.

104 estricted in a segment-specific manner, thus amputated skeletal elements regenerate distally patterne

105 ation that results in the replacement of the amputated structures.

106 cal tracers into the muscles proximal to the amputated stump labeled a larger extent of motoneurons t

107 ts that differentiate in continuity with the amputated stump.

108 We hypothesize that electric currents at amputated stumps play significant roles in tail regenera

109 Lizards regenerate amputated tails but fail to recapitulate the dorsoventra

110 Treatment of amputated tails with SB-431542, a specific and reversibl

111 es with the remarkable ability to regenerate amputated tails.

112 t the facultative machinery that regenerates amputated teleost fins also has a surprisingly vigorous

113 A new study finds that ants amputate the limbs of nestmates, which saves them from i

114 These tails were amputated through the labelled region and the distributi

115 tion of regenerative bioelectric dynamics in amputated trunk fragments of planaria stochastically res

116 erated phenotype (tailless) of RNAi of hh in amputated trunk fragments.

117 Almost everyone who has a limb amputated will experience a phantom limb--the vivid impr

118 The willingness to surgically debride and amputate without hesitation at a very early point may be

119 patterning, and functional restoration of an amputated X. laevis hindlimb following a 24-hour exposur

120 he former forepaw representation in forelimb amputated young adult rats (n=5) at 7 to 24 weeks after

121 In amputated zebrafish fins, mature osteoblasts dedifferent

122 blasts can fully support the regeneration of amputated zebrafish fins.