ライフサイエンスコーパス: amputate

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

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

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

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

5 Amputated animals failed to increase stem cell prolifera

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

7 Amputated apices from vegetative wildtype cells of the u

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

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

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

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

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

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

14 tated arms, behaving octopuses sometime grab amputated arms.

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

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

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

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

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

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

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

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

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

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

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

26 he cortical region previously devoted to the amputated digits.

27 Larvae amputated during the refractory stage exhibit a much bro

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

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

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

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

32 Moreover, amputated fins depleted of osteoblasts regenerated new f

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

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

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

36 mportant for late epimorphic regeneration of amputated fins.

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

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

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

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

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

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

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

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

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

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

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

48 patterning and cellular architecture of the amputated limb.

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

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

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

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

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

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

55 ly vertebrates capable of fully regenerating amputated limbs.

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

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

58 egenerated tissue or organ that replaces the amputated one.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

79 icantly less intracortical inhibition on the amputated side.

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

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

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

83 ts that differentiate in continuity with the amputated stump.

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

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

86 es with the remarkable ability to regenerate amputated tails.

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

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

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

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

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

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

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

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