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1 of nervous systems are asymmetric about the left-right axis.
2 ymmetry in nodal family signaling across the left-right axis.
3 eral somite formation is regulated along the left-right axis.
4 e plays a key role in establishing the avian left-right axis.
5 rn correlates with normal development of the left-right axis.
6 gastrulation for proper establishment of the left-right axis.
7 hat mature GDF1 is sufficient to reverse the left-right axis.
8 terning events that establish the vertebrate left-right axis.
9 ms that allow embryos to reliably orient the left-right axis.
10 eages and birth positions with regard to the left-right axis.
11 o is initially broken to define a consistent left-right axis.
13 LIC is required for the establishment of the left-right axis and for normal expression of Nodal, and
14 tinoic-acid signalling is uniform across the left-right axis and occurs in node ectoderm but not node
15 rically, neurons must be specified along the left-right axis, assigned left-side versus right-side id
17 xes, it is symmetrically expressed along the left-right axis at early stages of embryonic and cardiac
18 own to be asymmetrically expressed along the left-right axis before the development of organ asymmetr
20 d homeobox gene, plays a crucial role in the left-right axis determination and dextral looping of the
21 ctivation of KIF3A produces abnormalities of left-right axis determination and embryonic lethality.
22 rate that Pitx2c plays a crucial role in the left-right axis determination and rightward heart loopin
23 l patterning of the spinal cord, a defect in left-right axis determination and severe polydactyly (ex
26 nge of biological responses, from control of left-right axis determination in embryonic development t
27 ese genes was not associated with defects in left-right axis determination in humans or zebrafish.
28 f8 and Sonic Hedgehog genes are required for left-right axis determination in the mouse embryo, but t
29 imately govern gut formation and patterning, left-right axis determination, and development of the ce
30 ardiac development and upstream processes of left-right axis determination, and to consider how pertu
32 ole in several mammalian processes including left-right axis determination, sperm motility, and photo
37 te genes have emerged from recent studies of left-right axis development in chick, frog and mouse, wh
40 node have been implicated in initiating the left-right axis during embryonic development, but how ci
41 ole of EGF-CFC genes and Nodal signalling in left-right axis formation is conserved from fish to huma
43 e exhibited a spectrum of defects related to left-right axis formation, including visceral situs inve
49 rrhage, structural cardiac defects, abnormal left-right axis, hepatorenal and pancreatic cysts, and e
50 ellite symposium on 'Making and breaking the left-right axis: implications of laterality in developme
51 l organs are consistently oriented along the left-right axis in all vertebrates, and perturbations of
54 ght asymmetries, or can "rescue" a perturbed left-right axis in conjoined twins to normal orientation
58 specification program that occurs across the left/right axis in the nervous system of the nematode C.
61 of internal organs asymmetrically along the left-right axis is critical for their proper adult funct
63 three-dimensional vertebrate body plan, the left-right axis is linked to the dorsoventral and anteri
65 Human mutations in ZIC3 are associated with left-right axis malformations (MIM 306955, 208530, 20710
66 ne pitx2 isoform, pitx2c, in determining the left-right axis of amphibian embryos, we examined the he
69 interactions regulate the development of the left-right axis of asymmetry; however, the identities of
70 known about molecular cues that specify the left-right axis of the body, fashioning the asymmetric m
72 ctions of cilia in diverse processes such as left-right axis pattern formation, cerebrospinal fluid f
74 Dawid focus on the role of FGF signaling on left-right axis patterning, showing that FGF functions a
75 ed, the embryonic mechanism that orients the left-right axis relative to the dorsoventral and anterop
76 pression of Vg1 protein can fully invert the left-right axis (situs inversus), can randomize left-rig
77 how the cilia protein Arl13b is required for left right axis specification as its absence results in
78 the mouse node is instrumental in initiating left-right axis specification and identify Nodal as the
79 ncanonical Wnt signaling with the control of left-right axis specification, and provide an entry poin
80 y central roles in mesendoderm induction and left-right axis specification, but the mechanisms regula
81 ide spectrum of phenotypes, including random left-right axis specification, polycystic kidney disease
85 rates develop distinct asymmetries along the left-right axis, which are consistently aligned with the
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