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1 c Wnt/beta-catenin signaling during visceral left-right patterning.
2 required for ciliogenesis, HH signaling, and left-right patterning.
3 e but is frequently associated with abnormal left-right patterning.
4 tward fluid flow and, thus, abnormalities in left-right patterning.
5 a5 in the formation of Kupffer's vesicle and left-right patterning.
6 uncovered Megf8 as an essential regulator of left-right patterning.
7 vesicle, they can have very weak effects on left-right patterning.
8 minant in the specification of cilia used in left-right patterning.
9 , a ciliated organ thought to play a role in left-right patterning.
10 t remains unclear how retinoic acid mediates left-right patterning.
11 mechanism for transcriptional control during left-right patterning.
12 shment of the mesendoderm and later visceral left-right patterning.
13 eft side, but not the right side, for normal left-right patterning.
14 gand essential for mesendoderm formation and left-right patterning.
15 ve been implicated in mesoderm induction and left-right patterning.
16 node, in which cilia-generated flow promotes left-right patterning.
17 etermined by the effect of its expression on left-right patterning.
18 a single motile cilium by cells involved in left-right patterning.
19 ns as part of a fundamental, early aspect of left-right patterning.
20 t is necessary for normal cilia motility and left-right patterning.
21 a process that affects both gastrulation and left-right patterning.
22 crucial for airway clearance, fertility and left-right patterning.
23 s that the notochord plays an active role in left/right patterning.
24 e finding that a number of genes involved in left/right patterning also play a role in anteroposterio
25 requirements for Zic3 in node morphogenesis, left-right patterning and cardiac development and sugges
27 y vertebrate development, for example during left-right patterning and in cardiovascular and neural d
28 ia in the gastrocoel roof plate that control left-right patterning and in shorter multicilia in exter
29 y required in epiblast derivatives to affect left-right patterning and its expression in epiblast is
30 found that low frequency vibrations altered left-right patterning and tail morphogenesis, but did no
31 ng of another TGF-beta ligand, nodal, during left-right patterning and the development of anterior he
32 sed by mutations in genes that control early left-right patterning and the earliest steps in cardioge
33 ected relationship between somitogenesis and left-right patterning, and suggest that bilateral somite
36 attributed to the CHD, airway clearance and left-right patterning both require motile cilia function
37 essed ubiquitously during critical stages of left-right patterning but its later expression in the de
38 e activation within the IC, promoting proper left-right patterning, cardiopulmonary development and r
39 ignaling as an obligate aspect of very early left-right patterning conserved to two vertebrate specie
42 cts on the incidence of neural tube defects, left-right patterning defects and abnormal tail morphoge
43 restriction of mutant phenotypes and lack of left-right patterning defects in schlei animals suggest
48 Morphant embryos displayed both cardiac and left/right patterning defects as well as disruption of t
49 covered a spontaneous mouse mutation causing left/right patterning defects together with defects in a
50 fects in development of the limb, heart, and left-right patterning, defects that resemble those obser
51 equences of abnormal midline development for left-right patterning depend on the time of onset, durat
55 ry in plants also affect very early steps of left-right patterning in nematode and frog embryos, as w
56 oved understanding of the genetic control of left-right patterning in the early embryo is leading to
57 iven cilia create fluid flow that determines left-right patterning in the early mammalian embryo.
58 neate the spatial requirement of Zic3 during left-right patterning in the mammalian embryo, and provi
59 normalities such as cyclopia, and defects in left-right patterning, indicating that Smad2 may mediate
60 cle, loss of flow is associated with loss of left-right patterning, indicating that the 'nodal flow'
62 ests that, whatever the molecular mechanism, left-right patterning is unlikely to be due to a blastod
64 m of CHDs and suggest that the disruption of left-right patterning may play an important role in CHD.
65 adaptation to a sessile lifestyle depends on left-right patterning mechanisms present in the free-swi
69 ng the normal function of excitable tissues, left-right patterning, organogenesis and wound healing.
70 The first defined asymmetric signal in the left-right patterning pathway is Shh, which is initially
71 e Xenopus embryo and, moreover, suggest that left-right patterning preceding cardiac morphogenesis in
73 subtype frequently associated with defective left-right patterning, probably through perturbation of
74 specific protein depletion demonstrated that left-right patterning requires Coco exclusively on the r
76 mporal and spatial requirements, for Zic3 in left-right patterning, we generated conditional Zic3 mic
77 with CHD and heterotaxy (Htx), a disorder of left-right patterning, we previously identified a duplic
78 heart disease and heterotaxy, a disorder of left-right patterning, we previously identified the guan