ライフサイエンスコーパス: dorsoventral patterning

1 ning also play a role in anteroposterior and dorsoventral patterning.

2 s a model system for the study of vertebrate dorsoventral patterning.

3 together with defects in anteroposterior and dorsoventral patterning.

4 of pituitary progenitors but not for initial dorsoventral patterning.

5 e ventral wall closure indicative of altered dorsoventral patterning.

6 ies Axin overexpression resulting in altered dorsoventral patterning.

7 dient of BMP signaling that is essential for dorsoventral patterning.

8 odal gene cyclops (cyc) are not required for dorsoventral patterning.

9 understanding of the maternal regulation of dorsoventral patterning.

10 ised trunk development but did not eliminate dorsoventral patterning.

11 tant background, results in abnormal retinal dorsoventral patterning.

12 ephaly identify the condition as a defect in dorsoventral patterning.

13 d armi mutations disrupt anteroposterior and dorsoventral patterning.

14 iption, the critical first step in embryonic dorsoventral patterning.

15 catalytic activity and function in embryonic dorsoventral patterning.

16 efects in NPS are a result of the diminished dorsoventral patterning activity of LMX1B protein during

17 To further investigate the role En plays in dorsoventral patterning and AER formation, we have used

18 the Toll-like receptor (TLR) family mediate dorsoventral patterning and cellular adhesion in insects

19 elated embryonic punt phenotypes, defects in dorsoventral patterning and dorsal closure, correspond t

20 tor Pt-Ets4 is needed for cumulus integrity, dorsoventral patterning and for the activation of Pt-hun

21 sults suggest a role for translation in leaf dorsoventral patterning and indicate that ribosomes are

22 r of the Myb family has been found to couple dorsoventral patterning and proximodistal outgrowth duri

23 ivity of the protease domain is required for dorsoventral patterning and that the Nudel protease is a

24 t characterized for their roles in mediating dorsoventral patterning and the innate immune response.

25 ormally required sequentially for both early dorsoventral patterning and the specification and patter

26 enes have distinct or redundant functions in dorsoventral patterning and to provide critical tests of

27 vents involving outgrowth, proximodistal and dorsoventral patterning, and epithelial tubulogenesis.

28 Similarly, the maternal regulation of dorsoventral patterning, and in particular the maternal

29 autonomous effects of Spemann's organizer on dorsoventral patterning are executed in part by diffusib

30 Previously, aubergine has been implicated in dorsoventral patterning, as eggs from aubergine mutant m

31 disturbing this inhibitory pathway disrupts dorsoventral patterning at the onset of gastrulation.

32 (Rld1) semi-dominant maize mutations affect dorsoventral patterning by causing adaxialization of aba

33 nidentified dorsalizing factor that mediates dorsoventral patterning by directly or indirectly antago

34 r we also find that auxin levels feedback on dorsoventral patterning by spatially organizing HD-ZIPII

35 nts that lack vox function have little or no dorsoventral patterning defect, and inactivation of eith

36 Mutant females are sterile and show dorsoventral patterning defects during oogenesis.

37 xpression patterns of CF2 result in specific dorsoventral patterning defects in egg chambers and in e

38 tions secondary to early anteroposterior and dorsoventral patterning defects, or to misspecification

39 In addition to dorsoventral patterning defects, split top mutants displ

40 dCtBP products exhibit both segmentation and dorsoventral patterning defects, which can be attributed

41 ich is essential for antifungal immunity and dorsoventral patterning during early development.

42 ges over time, with BMPs required for global dorsoventral patterning during early gastrulation and fo

43 sm that is shared by the Wnt/Fz circuits for dorsoventral patterning during early Xenopus development

44 oligodendrocytes reflects a deregulation of dorsoventral patterning during expansion in vitro, raisi

45 have implicated Chordin in the regulation of dorsoventral patterning during gastrulation.

46 and was accompanied by the repression of the dorsoventral patterning gene Irx3.

47 e found homozygous missense mutations in the dorsoventral-patterning gene WNT7A and confirmed their f

48 Genetic interactions of SoxNeuro and the dorsoventral patterning genes ventral nerve chord defect

49 e evolutionarily conserved expression of the dorsoventral patterning genes, BMP2/4 and chordin, in no

50 ment of the amnioserosa is controlled by the dorsoventral patterning genes.

51 nates is laid down by segmentation genes and dorsoventral patterning genes.

52 Dorsoventral patterning in Drosophila has long been know

53 Indicating that the hem regulates dorsoventral patterning in the cortical hemisphere, the

54 rimary action of Pax6 is to generate correct dorsoventral patterning in the diencephalon.

55 ed in the context of the current evidence in dorsoventral patterning in the Drosophila neuroectoderm.

56 been proposed to be important regulators of dorsoventral patterning in the early embryo.

57 nn Organizer alone may not be sufficient for dorsoventral patterning in the marginal zone and that an

58 ired for the establishment or maintenance of dorsoventral patterning in the retina, as we observe nor

59 genetic proteins (BMPs) are key mediators of dorsoventral patterning in vertebrates and are required

60 hat of others, we propose a model for somite dorsoventral patterning in which competing diffusible si

61 he earliest events known to be necessary for dorsoventral patterning in Xenopus embryos.

62 ein (BMP) signaling pathway is implicated in dorsoventral patterning in Xenopus.

63 gative regulatory point during LRP6-mediated dorsoventral patterning in zebrafish and in allograft mo

64 LE cells are specified in response to early dorsoventral patterning information or whether they aris

65 Dorsoventral patterning is mediated by two organizer reg

66 This indicates that dorsoventral patterning is not dependent upon Dorsal-med

67 Dorsoventral patterning is regulated by a system of inte

68 based on embryological studies in amphibia, dorsoventral patterning is regulated by the antagonizing

69 enetic protein 4 (BMP4) is known to regulate dorsoventral patterning, limb bud formation and axis spe

70 col mutants display early defects in dorsoventral patterning manifested by a decrease in the

71 al cord, supporting the hypothesis that some dorsoventral patterning mechanisms are used at all axial

72 gradient in the early Drosophila embryo, the dorsoventral patterning of a frog embryo by bone morphog

73 in (BMP) signaling is an essential factor in dorsoventral patterning of animal embryos but how BMP si

74 rtilized eggs and resulted in defects in the dorsoventral patterning of embryos.

75 s in Bmp signaling pathways to mediate early dorsoventral patterning of neurectodermal and mesendoder

76 Previous work has suggested that the dorsoventral patterning of O and P fates differs in the

77 Dorsoventral patterning of somites into sclerotome and d

78 In vertebrates, the dorsoventral patterning of somitic mesoderm is controlle

79 We have discovered a new role for SMA-9 in dorsoventral patterning of the C. elegans post-embryonic

80 Msx genes have been shown to function in the dorsoventral patterning of the central nervous system in

81 Dorsoventral patterning of the Drosophila embryo is init

82 Dorsoventral patterning of the Drosophila embryo is regu

83 Rel-related transcription factors regulates dorsoventral patterning of the Drosophila embryo, as wel

84 th the gene regulatory network that controls dorsoventral patterning of the Drosophila embryo.

85 al C and trailer hitch are both required for dorsoventral patterning of the Drosophila oocyte.

86 regulating primary germ layer formation and dorsoventral patterning of the early Xenopus embryo.

87 iation by tuning the DPP receptor Saxophone, dorsoventral patterning of the egg shell by regulating t

88 olecules required for anterior-posterior and dorsoventral patterning of the embryo.

89 for structural integrity of the egg and for dorsoventral patterning of the embryo.

90 Dorsoventral patterning of the embryonic neural tube giv

91 identify TGIF2 as the molecular link between dorsoventral patterning of the endoderm and pancreatic s

92 s the most upstream element yet described in dorsoventral patterning of the eye disc.

93 a BMP family member previously implicated in dorsoventral patterning of the eye.

94 cells of the Drosophila ovary - required for dorsoventral patterning of the fly embryo - leads to cel

95 Collectively our results support a model for dorsoventral patterning of the gnathostome pharyngeal ar

96 is important to regulate Wg signaling during dorsoventral patterning of the larval wing.

97 ntaining gene Engrailed (En) plays a role in dorsoventral patterning of the limb.

98 pathway function independently in regulating dorsoventral patterning of the M lineage, with LIN-12/No

99 /from the adaxial epidermis and controls the dorsoventral patterning of the maize leaf.

100 le for the graded action of Nodal signals in dorsoventral patterning of the mesendoderm.

101 These experiments demonstrate that dorsoventral patterning of the mouse posterior mesoderm

102 ate the molecular mechanisms associated with dorsoventral patterning of the neural tube and acquisiti

103 nterruption of Sonic hedgehog (Shh)-mediated dorsoventral patterning of the neural tube and somites.

104 During neural development caudalization and dorsoventral patterning of the neural tube is directed b

105 prechordal plate functions as a morphogen in dorsoventral patterning of the neural tube.

106 ed excess Hh signaling and resultant altered dorsoventral patterning of the neural tube.

107 ons include primary neural induction and the dorsoventral patterning of the neural tube.

108 lts suggest that Wnt members are involved in dorsoventral patterning of the neural tube.

109 derm adjacent to the ventral midline, in the dorsoventral patterning of the neuroectoderm and the neu

110 erived Sonic Hedgehog (Shh) is essential for dorsoventral patterning of the overlying neural tube.

111 gnals through Ednra proteins to direct early dorsoventral patterning of the skeletogenic neural crest

112 the molecular mechanisms associated with the dorsoventral patterning of the spinal cord.

113 d temporal requirements for Tolloid (Mfn) in dorsoventral patterning of the tail.

114 ell proliferation in the cerebral cortex and dorsoventral patterning of the telencephalon and neural

115 We report that dorsoventral patterning of the telencephalon is dramatic

116 particular, loss of Shh has little effect on dorsoventral patterning of the telencephalon when Gli3 i

117 During embryonic development, appropriate dorsoventral patterning of the trachea leads to the form

118 orylated beta-catenin for degradation and in dorsoventral patterning of the Xenopus embryo.

119 A widely accepted model of dorsoventral patterning postulates that a morphogenetic

120 integrated in both anteroposterior (AP) and dorsoventral patterning processes.

121 the integration of distinct rostrocaudal and dorsoventral patterning signals that derive, respectivel

122 analyze multiple morphogen gradients in the dorsoventral patterning system.

123 evidence in support of a mechanism of early dorsoventral patterning that is conserved among vertebra

124 morphogen to establish at least two distinct dorsoventral patterning thresholds.

125 proteoglycan is involved in pipe function in dorsoventral patterning, we generated females carrying f

126 e neurogenesis, raising the possibility that dorsoventral patterning within the central nervous syste