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1 ervous systems are asymmetric about the left-right axis.
2 f thoraco-abdominal viscera across a left-to-right axis.
3 ry in nodal family signaling across the left-right axis.
4 somite formation is regulated along the left-right axis.
5 ys a key role in establishing the avian left-right axis.
6 rrelates with normal development of the left-right axis.
7 ulation for proper establishment of the left-right axis.
8 ature GDF1 is sufficient to reverse the left-right axis.
9 ng events that establish the vertebrate left-right axis.
10 at allow embryos to reliably orient the left-right axis.
11 initially broken to define a consistent left-right axis.
12 and birth positions with regard to the left-right axis.
14 s required for the establishment of the left-right axis and for normal expression of Nodal, and the v
15 c-acid signalling is uniform across the left-right axis and occurs in node ectoderm but not node meso
16 ly, neurons must be specified along the left-right axis, assigned left-side versus right-side identit
18 it is symmetrically expressed along the left-right axis at early stages of embryonic and cardiac deve
19 o be asymmetrically expressed along the left-right axis before the development of organ asymmetry.
21 eobox gene, plays a crucial role in the left-right axis determination and dextral looping of the vert
23 that Pitx2c plays a crucial role in the left-right axis determination and rightward heart looping dur
24 terning of the spinal cord, a defect in left-right axis determination and severe polydactyly (extra d
27 f biological responses, from control of left-right axis determination in embryonic development to adu
29 d Sonic Hedgehog genes are required for left-right axis determination in the mouse embryo, but that t
30 ly govern gut formation and patterning, left-right axis determination, and development of the central
31 c development and upstream processes of left-right axis determination, and to consider how perturbati
33 n several mammalian processes including left-right axis determination, sperm motility, and photorecep
38 nes have emerged from recent studies of left-right axis development in chick, frog and mouse, which h
39 A history of pulmonary embolism (p = 0.04), right-axis deviation (p = 0.02), right ventricular (RV)
42 have been implicated in initiating the left-right axis during embryonic development, but how cilia r
43 f EGF-CFC genes and Nodal signalling in left-right axis formation is conserved from fish to humans.
45 ibited a spectrum of defects related to left-right axis formation, including visceral situs inversus,
51 e, structural cardiac defects, abnormal left-right axis, hepatorenal and pancreatic cysts, and embryo
52 e symposium on 'Making and breaking the left-right axis: implications of laterality in development an
53 ans are consistently oriented along the left-right axis in all vertebrates, and perturbations of left
55 Furthermore, the orientation of the left-right axis in conjoined twins is dependent upon which ce
56 symmetries, or can "rescue" a perturbed left-right axis in conjoined twins to normal orientation (sit
58 fication program that occurs across the left/right axis in the nervous system of the nematode C. eleg
62 Functional diversification across the left/right axis is a common feature of many nervous systems.
64 nternal organs asymmetrically along the left-right axis is critical for their proper adult function.
66 e-dimensional vertebrate body plan, the left-right axis is linked to the dorsoventral and anteriopost
67 n mutations in ZIC3 are associated with left-right axis malformations (MIM 306955, 208530, 207100).
68 tx2 isoform, pitx2c, in determining the left-right axis of amphibian embryos, we examined the heart a
71 actions regulate the development of the left-right axis of asymmetry; however, the identities of ECM
72 n about molecular cues that specify the left-right axis of the body, fashioning the asymmetric morpho
74 s of cilia in diverse processes such as left-right axis pattern formation, cerebrospinal fluid flow,
76 d focus on the role of FGF signaling on left-right axis patterning, showing that FGF functions at lea
77 he embryonic mechanism that orients the left-right axis relative to the dorsoventral and anteroposter
78 ion of Vg1 protein can fully invert the left-right axis (situs inversus), can randomize left-right as
79 ouse node is instrumental in initiating left-right axis specification and identify Nodal as the key m
80 he cilia protein Arl13b is required for left right axis specification as its absence results in heter
81 nical Wnt signaling with the control of left-right axis specification, and provide an entry point for
82 tral roles in mesendoderm induction and left-right axis specification, but the mechanisms regulating
83 pectrum of phenotypes, including random left-right axis specification, polycystic kidney disease, liv
87 develop distinct asymmetries along the left-right axis, which are consistently aligned with the ante
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