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1 resentation of the distal hindlimb in dorsal gracile.
2 f the present study was to establish whether gracile afferents to the inferior olive are topographica
4 dorsal column nuclei (DCN, referring to the gracile and cuneate nuclei collectively), external cunea
5 o demonstrate that projecting neurons in the gracile and cuneate nuclei express predominantly the Glu
14 The skeleton was that of an adult man with a gracile build and severe scoliosis of the thoracic spine
15 hare features related to a shallow skull and gracile build with juvenile eutyrannosaurians, reinforci
16 keleton of modern Homo sapiens is relatively gracile compared with other hominoids and earlier homini
17 sauropodomorphs and theropods tending toward gracile crania and low bite forces and ornithischian tax
23 central processes of sensory neurons in the gracile fasciculus of genetically diabetic BB rats, we h
25 intense involvement of the posterior column (gracile fasciculus) in the thoracolumbar spinal cord, a
27 al intermediate septum or the midline of the gracile fasciculus, respectively; 2) terminating primari
29 e most cursorial of these fossils are small, gracile forms often grouped together as the Sphenosuchia
31 ately 35,000 years ago that people with more gracile, fully modern morphology make their appearance.
34 ric analyses of TPL 6 suggest descent from a gracile immigrant population rather than evolution from
35 was related to the dorsoventral locus of the gracile injection site: gracile injections centred dorsa
37 ventral locus of the gracile injection site: gracile injections centred dorsally produced the largest
38 iting the maximum tooth size of species with gracile jaws adapted for high mobility and jaw protrusio
40 vely demonstrates that Alioramus is a small, gracile, long-snouted carnivore that deviates from other
41 ry with populations that evolved from modern gracile morphology in Africa 130,000-160,000 years ago.
43 expected marked increase in the frequency of gracile NAD; however, substantial numbers of dystrophic
44 overrepresentation of short, morphologically gracile, non-local females, alongside two immature indiv
46 projections of sensory neurons to medullary gracile nuclei in aged animals and man, and in a number
47 ated to the cell-cluster architecture of the gracile nuclei in sections processed for cytochrome oxid
52 osomal vacuolization, axonal swelling in the gracile nucleus and impaired neuromotor coordination.
53 horase reactivity was neither altered in the gracile nucleus and mNTS of non-acupoint stimulated rats
54 that EA ST 36 induces nNOS expression in the gracile nucleus and mNTS, and enhanced nNOS-NO in the nu
55 rimary afferent terminals in the ipsilateral gracile nucleus and spinal dorsal horn in three nerve in
56 primarily in the dorsal, lateral rim of the gracile nucleus and the medial rim of the cuneate nucleu
58 dorsal root ganglia, lumbar spinal cord and gracile nucleus at 2, 6 and 14 weeks after sciatic nerve
59 ion and the caudal region of the ipsilateral gracile nucleus compared to the side with intact sciatic
60 us, but was not altered in the contralateral gracile nucleus compared with sham-treated rats (P < 0.0
61 immunopositive terminals in spinal cord and gracile nucleus displayed morphological characteristics
62 oked c-fos expression in the dorsal horn and gracile nucleus following either sciatic nerve section o
64 d single-unit recording was performed in the gracile nucleus in urethane-anesthetized rats to examine
66 viors of the female rat, suggesting that the gracile nucleus is a component of neural systems that co
67 owever, Abeta-evoked c-fos expression in the gracile nucleus may be under some other control since it
68 l-arginine-derived nitric oxide (NO) in the gracile nucleus modifies the hypotensive responses to el
71 medial portion of the dorsal horn and in the gracile nucleus of the brainstem on the side ipsilateral
72 o reveal the somatotopic organization of the gracile nucleus of the dorsal column-trigeminal complex,
73 crease in nNOS expression in the ipsilateral gracile nucleus of young rats, which is still seen in ol
76 NADPHd containing neurons in the ipsilateral gracile nucleus were moderately increased by axotomy ove
79 lls in the rostral region of the ipsilateral gracile nucleus, but was not altered in the contralatera
80 ted in terminals of injured afferents in the gracile nucleus, CGRP was expressed in between 32 and 68
81 uneate nucleus or the dorsomedial rim of the gracile nucleus, respectively; and 3) ascending bilatera
82 gray, area postrema, pontine raphe nucleus, gracile nucleus, spinal trigeminal nucleus, and spinal c
89 in subunit B revealed aberrant expansions of gracile projections into the cuneate and, in one case, e
90 or biotinylated dextran amine were made into gracile, resulting in anterograde labelling often distri
91 deep-snouted Tyrannosaurini and the smaller, gracile, shallow-snouted Alioramini as highly derived eu
92 nt surfaces in combination with a relatively gracile skeleton (i.e., lower bone mass for our body siz
93 ciency, whereas in the Finnish patients with GRACILE syndrome complex III activity was within the nor
94 was an infant who presented with a classical GRACILE syndrome leading to death at 4 months of age.
95 n overload, lactic acidosis and early death (GRACILE syndrome), and Bjornstad syndrome, characterized
97 e in the BCS1L gene in Finnish patients with GRACILE syndrome, as well as five different mutations in
98 tations cause complex III deficiency and the GRACILE syndrome, which in neonates are lethal condition
99 ization was obtained, suggesting that medial gracile targets only the most lateral part of rDAO, wher
100 lay a more severe axonal degeneration of the gracile tract of the medulla and spinal cord than had be