ライフサイエンスコーパス: spinal column

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1 T and KO mouse visceral yolk sac, brain, and spinal column.

2 m that ensures the bilateral symmetry of the spinal column.

3 artilage in the intervertebral joints of the spinal column.

4 ease resulting in chronic deformation of the spinal column.

5 me-space distribution of HSV-1 in the intact spinal column.

6 tervertebral discs during development of the spinal column.

7 ion disorders, birth defects that affect the spinal column.

8 egulated to ensure bilateral symmetry of the spinal column.

9 ow a remarkable capacity to regenerate their spinal column after injury, an ability that stands in st

10 s within the neural tube, and absence of the spinal column and most of the ribs.

11 al cords remain but are enclosed in a single spinal column as in the human diastematomyelia.

12 familiar with all surgical approaches to the spinal column but also be proficient in using various re

13 rogenitor cells alters cartilage biology and spinal column development.

14 e include cardiac, lung, craniofacial, limb, spinal column, eye, inner ear and urogenital defects.

15 Analysis of dissected spinal column from Taf9b KO mice confirmed that TAF9B al

16 Instability of the spinal column has been recognized as a significant cause

17 yrinth of the placenta, embryonic brain, and spinal column in wild-type (WT) mice.

18 sensory cortex is highly dependent on dorsal spinal column inputs, and other spinal pathways do not s

19 spinal cord is dysplastic, and the overlying spinal column is absent.

20 tor neuron syndrome after irradiation to the spinal column is caused by a proximal motor polyradiculo

21 SMN protein in the brain and throughout the spinal column of neonatal SMA mice.

22 ion of glycolysis with [(18)F]FDG in various spinal column segments; (ii) [(18)F]FDG PET/CT can detec

23 y was biased to be ~170 times greater at the spinal column than at the sciatic nerve.

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