ライフサイエンスコーパス: vertebral column

1 ed exclusively in mild defects in the caudal vertebral column.

2 , controls segmentation of precursors of the vertebral column.

3 discs (IVD) are essential components of the vertebral column.

4 notochord to constrain these cells along the vertebral column.

5 contributes to neuromuscular control of the vertebral column.

6 cute effects on neuromuscular control of the vertebral column.

7 by the repetition of vertebrae that form the vertebral column.

8 rcoma cases, 198 (4%) were PVOS arising from vertebral column.

9 resegmentation in development from somite to vertebral column.

10 e first two somites do not contribute to the vertebral column.

11 rtebrates is evident in the character of the vertebral column.

12 carring and tissue resorption, have a closed vertebral column.

13 ature at the cervicothoracic boundary of the vertebral column.

14 t of the dome referenced horizontally to the vertebral column.

15 s both in the craniofacial region and in the vertebral column.

16 morphic) life cycle had an increased rate of vertebral column and body form diversification compared

17 ormation or absence of specific bones of the vertebral column and cranial bones of mesodermal origin,

18 nsformations along the cervical and thoracic vertebral column and defects in sternum morphogenesis.

19 Mutant mice exhibit alterations in the vertebral column and in the bones of the hindlimb.

20 of the segmented embryonic precursors of the vertebral column and musculature.

21 rdate body plan and for the formation of the vertebral column and numerous organs.

22 tameric pattern of axial tissues such as the vertebral column and peripheral nerves.

23 malformations are localized along the entire vertebral column and rib cage and are linked to defectiv

24 6R) mutants manifest skeletal defects in the vertebral column and ribcage, revealing a hitherto undef

25 a morphogen mode, whereas development of the vertebral column and the hind limbs has threshold signal

26 rmal development of the caudal aspect of the vertebral column and the spinal cord., It results in neu

27 er in development, expression is seen in the vertebral column and tooth bud.

28 differentiation in the developing skull and vertebral column and understanding how perturbations in

29 e vertebrates are defined by their segmented vertebral column, and vertebral periodicity is thought t

30 mented precursors of the skeletal muscle and vertebral column are generated during vertebrate embryog

31 Although several complete lumbar vertebral columns are known for early hominins, to date,

32 m (PSM) and differentiate into the segmented vertebral column as well as other unsegmented tissues.

33 known complete hominin cervical and thoracic vertebral column before 60,000 years ago.

34 dentity are patterned requires understanding vertebral column cellular and developmental biology.

35 The segmented vertebral column comprises a repeat series of vertebrae,

36 Anterior vertebral columns comprising T1 through L5 were removed

37 had kidney defects, whereas chimeras without vertebral column defects had highly chimeric kidneys tha

38 ive to birth, with multiple craniofacial and vertebral column defects.

39 Characterization of vertebral column development allowed examination of the

40 ey are central transcriptional regulators of vertebral column development.

41 le at specific stages of both cerebellar and vertebral column development.

42 tor controlling rhythmic segmentation of the vertebral column during embryonic development.

43 entally revises our current understanding of vertebral column evolution in the earliest tetrapods and

44 The vertebral column exhibits segmentation and regionalizati

45 t xenarthran mammals, which strengthened the vertebral column for locomotion.

46 The notochord has major roles in vertebral column formation: indirectly by inducing scler

47 already known functions in the mechanics of vertebral column function.

48 The construction of the vertebral column has been used as a key anatomical chara

49 1 signaling regulates the development of the vertebral column have yet to be determined.

50 The vertebral column in the sacral area has large anterior a

51 bone fractures, spinal cord compression, and vertebral column instability.

52 The vertebral column is a conserved anatomical structure tha

53 Formation of the vertebral column is a critical developmental stage in ma

54 vidual vertebrae and distinct regions of the vertebral column is accomplished by Polycomb and Hox pro

55 The periodic or segmental pattern of the vertebral column is established early in development whe

56 The mammalian vertebral column is highly variable, reflecting adaptati

57 he close proximity of the spinal cord to the vertebral column limits many conventional therapeutic op

58 and differentiate after birth along with the vertebral column, little is known about the mechanism of

59 e embryonic notochord and consequently adult vertebral column malformations.

60 posterior-to-anterior transformations of the vertebral column midsection, similar to mice deficient f

61 soft tissues and structures surrounding the vertebral column, neurological deficits, and spinal inst

62 Consequently, the vertebral column of Sox5(-/-)/Sox6(-/-) fetuses consiste

63 which gives rise to the skeletal muscles and vertebral column of the body.

64 Two partial vertebral columns of Australopithecus sediba grant insig

65 ntiated from the teratoma by the presence of vertebral column often with an appropriate arrangement o

66 The elements of vertebral column pattern under debate include both segme

67 This is most prominent around the vertebral column, pelvis and long bones in CPDX2.

68 ovo cell and tissue interactions pattern the vertebral column remains a fundamental, unresolved issue

69 The vertebral column, ribs, and appendicular skeleton were a

70 the 1960s, show features of the shoulder and vertebral column that are significantly similar to those

71 ation, including re-patterning of the caudal vertebral column that is otherwise only seen in salamand

72 d signals are essential for formation of the vertebral column the phenotypes suggested that the lacZ

73 f the mid-RPT from the lateral margin of the vertebral column was measured and calculated as a fracti

74 istologically proved primary osteosarcoma of vertebral column was performed.

75 Pbx1/Pbx2 mutants exhibit a homogeneous vertebral column, with loss of vertebral identity, rudim

76 shifts in vertebral types along most of the vertebral column, with transformations being most obviou