戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 rative embolisation of RCC metastases to the vertebral column.
2 ed exclusively in mild defects in the caudal vertebral column.
3 , controls segmentation of precursors of the vertebral column.
4  discs (IVD) are essential components of the vertebral column.
5 notochord to constrain these cells along the vertebral column.
6  contributes to neuromuscular control of the vertebral column.
7 cute effects on neuromuscular control of the vertebral column.
8 by the repetition of vertebrae that form the vertebral column.
9 rcoma cases, 198 (4%) were PVOS arising from vertebral column.
10 resegmentation in development from somite to vertebral column.
11 e first two somites do not contribute to the vertebral column.
12 rtebrates is evident in the character of the vertebral column.
13 carring and tissue resorption, have a closed vertebral column.
14 ature at the cervicothoracic boundary of the vertebral column.
15 t of the dome referenced horizontally to the vertebral column.
16 s both in the craniofacial region and in the vertebral column.
17 nding to mammal-like sagittal bending of the vertebral column.
18 esomitic mesoderm (PSM) and give rise to the vertebral column.
19 eletal dysplasia predominantly affecting the vertebral column.
20 morphic) life cycle had an increased rate of vertebral column and body form diversification compared
21 ormation or absence of specific bones of the vertebral column and cranial bones of mesodermal origin,
22 nsformations along the cervical and thoracic vertebral column and defects in sternum morphogenesis.
23       Mutant mice exhibit alterations in the vertebral column and in the bones of the hindlimb.
24 of the segmented embryonic precursors of the vertebral column and musculature.
25 rdate body plan and for the formation of the vertebral column and numerous organs.
26 cral ribs, which provide linkage between the vertebral column and pelvis, contributing to body suppor
27 spicuous in the periodic organization of the vertebral column and peripheral nerves.
28 tameric pattern of axial tissues such as the vertebral column and peripheral nerves.
29 malformations are localized along the entire vertebral column and rib cage and are linked to defectiv
30 6R) mutants manifest skeletal defects in the vertebral column and ribcage, revealing a hitherto undef
31 a morphogen mode, whereas development of the vertebral column and the hind limbs has threshold signal
32 rmal development of the caudal aspect of the vertebral column and the spinal cord., It results in neu
33     Extrinsic vertical muscles attach to the vertebral column and the swimbladder.
34 er in development, expression is seen in the vertebral column and tooth bud.
35  differentiation in the developing skull and vertebral column and understanding how perturbations in
36 e vertebrates are defined by their segmented vertebral column, and vertebral periodicity is thought t
37 mented precursors of the skeletal muscle and vertebral column are generated during vertebrate embryog
38             Although several complete lumbar vertebral columns are known for early hominins, to date,
39 m (PSM) and differentiate into the segmented vertebral column as well as other unsegmented tissues.
40 udal segment, indicating repatterning of the vertebral column associated with the transition from lim
41                   Histologic sections of the vertebral column at embryonic days 15.5 and 17.5 reveale
42 known complete hominin cervical and thoracic vertebral column before 60,000 years ago.
43 dentity are patterned requires understanding vertebral column cellular and developmental biology.
44 into distinct anteroposterior regions of the vertebral column (cervical, trunk, sacral, and caudal),
45                              This reinforced vertebral column, combined with the extensive developmen
46                                The segmented vertebral column comprises a repeat series of vertebrae,
47                                     Anterior vertebral columns comprising T1 through L5 were removed
48 had kidney defects, whereas chimeras without vertebral column defects had highly chimeric kidneys tha
49 ive to birth, with multiple craniofacial and vertebral column defects.
50                          Characterization of vertebral column development allowed examination of the
51 ey are central transcriptional regulators of vertebral column development.
52 le at specific stages of both cerebellar and vertebral column development.
53 tor controlling rhythmic segmentation of the vertebral column during embryonic development.
54 entally revises our current understanding of vertebral column evolution in the earliest tetrapods and
55                                          The vertebral column exhibits segmentation and regionalizati
56 sturgeons, with asymmetric caudal fins and a vertebral column extending into an elongated upper lobe.
57  three skeletal characteristics (e.g., thick vertebral column for its length), while an additional fe
58 t xenarthran mammals, which strengthened the vertebral column for locomotion.
59 ellular and tissue-level events required for vertebral column formation, supporting the view that cha
60             The notochord has major roles in vertebral column formation: indirectly by inducing scler
61  already known functions in the mechanics of vertebral column function.
62                      The construction of the vertebral column has been used as a key anatomical chara
63 1 signaling regulates the development of the vertebral column have yet to be determined.
64 e focus on the serial differentiation of the vertebral column in 1,136 extant mammal species, using t
65                                          The vertebral column in the sacral area has large anterior a
66      Different subclades evolve more complex vertebral columns in different configurations and probab
67 oration of long-bone pathological fractures, vertebral column instability, and spinal cord compressio
68 bone fractures, spinal cord compression, and vertebral column instability.
69                                   The mammal vertebral column is a classic example of a metameric str
70                                          The vertebral column is a conserved anatomical structure tha
71                             Formation of the vertebral column is a critical developmental stage in ma
72 vidual vertebrae and distinct regions of the vertebral column is accomplished by Polycomb and Hox pro
73     The periodic or segmental pattern of the vertebral column is established early in development whe
74            The segmental organization of the vertebral column is established early in embryogenesis,
75                                The mammalian vertebral column is highly variable, reflecting adaptati
76  aside the developmentally abnormal Kebara 2 vertebral column, La Chapelle-aux-Saints 1 is joined by
77 he close proximity of the spinal cord to the vertebral column limits many conventional therapeutic op
78 and differentiate after birth along with the vertebral column, little is known about the mechanism of
79                     Here we show an extended vertebral column LV network using three-dimensional imag
80 e embryonic notochord and consequently adult vertebral column malformations.
81 posterior-to-anterior transformations of the vertebral column midsection, similar to mice deficient f
82 combining geometric morphometric analysis of vertebral column morphology with cell lineage tracing of
83  soft tissues and structures surrounding the vertebral column, neurological deficits, and spinal inst
84 cal studies, the morphology of the skull and vertebral column of abelisaurids, have led researchers t
85                              Relative to the vertebral column of other mammals that is subdivided int
86                            Consequently, the vertebral column of Sox5(-/-)/Sox6(-/-) fetuses consiste
87 o previous studies, we show that most of the vertebral column of the Berlin Archaeopteryx possesses i
88 which gives rise to the skeletal muscles and vertebral column of the body.
89                                  Two partial vertebral columns of Australopithecus sediba grant insig
90 ntiated from the teratoma by the presence of vertebral column often with an appropriate arrangement o
91                                          The vertebral column or spine assembles around the notochord
92            In bony fishes, patterning of the vertebral column, or spine, is guided by a metameric blu
93                              The elements of vertebral column pattern under debate include both segme
94            This is most prominent around the vertebral column, pelvis and long bones in CPDX2.
95  col11a2 -/- zebrafish exhibited compromised vertebral column properties, bent their body less while
96                                The mammalian vertebral column provides an opportunity to test these h
97 ovo cell and tissue interactions pattern the vertebral column remains a fundamental, unresolved issue
98                                 The complete vertebral column reveals paired proatlases and a tail lo
99                                          The vertebral column, ribs, and appendicular skeleton were a
100 yonic body axis, such as the spinal cord and vertebral column, takes place in an anterior-to-posterio
101 the 1960s, show features of the shoulder and vertebral column that are significantly similar to those
102 ation, including re-patterning of the caudal vertebral column that is otherwise only seen in salamand
103 d signals are essential for formation of the vertebral column the phenotypes suggested that the lacZ
104 f the mid-RPT from the lateral margin of the vertebral column was measured and calculated as a fracti
105 istologically proved primary osteosarcoma of vertebral column was performed.
106      Pbx1/Pbx2 mutants exhibit a homogeneous vertebral column, with loss of vertebral identity, rudim
107  shifts in vertebral types along most of the vertebral column, with transformations being most obviou

 
Page Top