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1 dity at the base of the tail with a flexible lumbar region.
2 elevated in the CSF cells collected from the lumbar region.
3 otor neuron bodies of lamina IX in the lower lumbar region.
4 of morbidity, especially for the "low back" lumbar region.
5 ociceptive IgG-FcgammaR signaling around the lumbar region.
6 ound examination because of the pain in left lumbar region.
7 on of neurons projecting to the cervical and lumbar regions.
8 educed Fos-LI at the cervical but not at the lumbar regions.
9 rmations of vertebrae in the midthoracic and lumbar regions.
10 ate caudally to the lower thoracic and upper lumbar regions.
11 with a higher proportion at cervical versus lumbar regions.
12 e 60% reduction of spinal motoneurons in the lumbar region and a more than 80% reduction in the senso
13 stigate features of the IGF 11778 pelvis and lumbar region based on torso preparations and supplement
14 ten repetitions of PPT measurement over the lumbar region bilaterally at two sessions in twenty heal
15 tions for bipedalism, including an elongated lumbar region, both in the number of vertebrae and their
16 ase is also decreased in spinal cord slices (lumbar region) from animals undergoing CCI, although in
17 root ganglia (DRG), predominantly within the lumbar regions in 6-month-old mice, but spreading to the
18 ociceptive IgG, which accumulates around the lumbar region, including within the dorsal root ganglia
19 red systemically (intraperitoneal) or to the lumbar region (intrathecal), attenuated mechanical allod
20 s-LI was selectively induced in cervical and lumbar regions ipsilateral to forepaw and hindpaw inflam
22 Ov8 has good detection accuracy for both the lumbar region (mAP50 = 99.50%) and the vertebral disc (m
24 its potential involvement in MN loss in the lumbar region of spinal cord of mutant SOD transgenic (G
25 P was injected into the lower thoracic/upper lumbar region of the spinal cord of eight homozygous sg/
26 the MSDB, wide dynamic range neurons in the lumbar region of the spinal cord were recorded in respon
27 (glial cells markers) were quantified in the lumbar region of the spinal cord, prefrontal cortex (PFC
33 y primarily affecting the cervical and dorso-lumbar regions, scoliosis and respiratory insufficiency.