ライフサイエンスコーパス: embryological

1 Embryological ablation of preplate cells led to an early

2 We report the cloning, distribution, and embryological activity of the Xenopus Smad7 (XSmad7).

3 eatic development, and highlights an unknown embryological activity of Vg1RBP.

4 Because of this embryological activity, we have renamed this clone Coco,

5 nto a blastocoel, revealing an unanticipated embryological affinity between nematodes and all other t

6 Discussion emphasizes embryological, anatomical and clinical aspects of the ma

7 Although embryological and anatomic observations suggest that the

8 Through embryological and biochemical experiments we find that:

9 The embryological and evolutionary origins of tympanal organ

10 origins of various tissues and will present embryological and experimental evidence to illustrate ho

11 Embryological and genetic analyses have revealed that Sp

12 progress is being made in elucidating their embryological and genetic basis.

13 Embryological and genetic evidence indicates that the ve

14 genomic tools and the many mouse and chicken embryological and genetic resources should increasingly

15 formation from fate mapping and experimental embryological and genetic studies is illuminating the me

16 Using pharmacological, embryological and molecular approaches, we determined th

17 Embryological and molecular data suggest that the AVE is

18 Embryological and molecular evidence suggests that placo

19 tion, work on chicken has provided important embryological and molecular insights, whereas studies in

20 tion are well understood in Drosophila, both embryological and molecular studies suggest significant

21 We present evidence, using both embryological and molecular techniques, indicating that

22 organizer of Xenopus using a combination of embryological and molecular techniques.

23 s (including vestimentiferans) share several embryological and morphological features with annelids,

24 han 300 extinct and extant taxa, integrating embryological and paleontological data.

25 Increasingly, developmental, embryological, and functional genomic approaches have al

26 the past 10 years a combination of genetic, embryological, and molecular analyses has provided detai

27 Morphological, embryological, and molecular biological characteristics

28 nd mathematical modelling with molecular and embryological approaches, we identify a contractile forc

29 ation of molecular genetic, biochemical, and embryological assays has begun to reveal the identity an

30 of almost normal development in a variety of embryological assays.

31 issue formation in zebrafish, and provide an embryological basis for zebrafish and mouse bifurcated n

32 To investigate the embryological basis of these defects, we characterized t

33 We have investigated the embryological cause of Zic2-associated HPE and the relat

34 We describe the first embryological characterization of this gene in chordates

35 ority of the right ventricle and provides an embryological context for understanding cardiac outflow

36 These results are discussed in embryological context with an eye toward understanding t

37 These embryological criteria can refocus arguments on paired f

38 onstituent embryos relative to commonly used embryological criteria.

39 he evolution of developmental duration using embryological data and information on incubation and fle

40 Embryological data suggest that endothelial cells (ECs)

41 At embryological days 16-18, increased proliferation rate,

42 ompatible with native counterpart throughout embryological development and into adulthood.

43 the beta-catenin/Tcf complex is involved in embryological development and is upregulated in various

44 Knowledge of embryological development and the normal characteristics

45 l transduction pathways that are crucial for embryological development and tissue differentiation and

46 This finding confirms an early disruption in embryological development in males with schizophrenia an

47 ted, and their expression or function during embryological development is unknown.

48 'recapitulation'-the theory that the present embryological development of a species reflects its evol

49 Comparative anatomy and similarities in the embryological development of ears in divergent taxa sugg

50 This differentiation program resembled the embryological development of these distinct types of hya

51 tumorigenesis, circadian rhythm regulation, embryological development, and osteoclastogenesis.

52 enes and chemical signals for the control of embryological development, morphogenesis and tissue patt

53 echanisms that control cell migration during embryological development, such as epithelial to mesench

54 We review here the origin of HSCs during embryological development, the relationship between hema

55 ing thoracic aortic disease, integrating its embryological development, wall composition, pathophysio

56 of normal physiological functions including embryological development, wound healing, and tissue reg

57 alies occur as a result of failure in normal embryological development.

58 een given to its acquisition, evolution, and embryological development.

59 lity of nuclear chromosomal determinants for embryological development.

60 n is integral to both cancer progression and embryological development.

61 This Seminar describes embryological developmental processes, epidemiology, kno

62 These embryological differences imply that anterior and poster

63 of precision results in numerous examples of embryological disorders or even cancer.

64 y, which could represent specific markers of embryological dysmorphogenesis underlying schizophrenia.

65 ding a unique opportunity to explore complex embryological events in a detailed and highly quantitati

66 m into groupings based on known genetics and embryological events.

67 Embryological evidence clearly identifies the three wing

68 We argue that, although comparative embryological evidence correctly identifies the homology

69 Here we provide functional, biochemical, and embryological evidence identifying the SCP (small C-term

70 pparent conflict between paleontological and embryological evidence regarding the homology of the dig

71 In this paper, we present anatomical and embryological evidence showing that pectoral motoneurons

72 and yangochiropterans), providing the first embryological evidence that the echolocation system evol

73 Embryological experiments demonstrate that mesoderm indu

74 Classic embryological experiments directly assessed the potency

75 Embryological experiments had suggested that the skin pr

76 Classical embryological experiments have demonstrated that dorsal-

77 Classic embryological experiments have established that the earl

78 Genetic and embryological experiments have established the Caenorhab

79 Embryological experiments have indicated the existence o

80 Early embryological experiments identified the notochord and t

81 Classical embryological experiments suggest that a posterior signa

82 Manteia allows the comparison of embryological, expression, molecular and etiological dat

83 Mammals and birds have common embryological facial structures, and appear to employ th

84 ix, influenced by genetic predisposition and embryological factors as well as arterial hypertension.

85 lopmental features, especially regarding the embryological fate of the blastopore.

86 report that Hydatella expresses several rare embryological features that, in combination, are found o

87 Overall, our study establishes an embryological framework for pectoral/shoulder girdle for

88 portant role in germ cell specification, the embryological function of BMP15 remains unknown.

89 e use a multidisciplinary approach employing embryological, genetic, and genomic techniques to interr

90 urely mutant embryos will greatly facilitate embryological, genetic, genomic, and biochemical studies

91 animal model we demonstrate that there is an embryological HCM phenotype.

92 We used embryological imaging techniques to examine the morphoge

93 Our comparative embryological investigations found that there is no deve

94 tion in vivo demonstrates a new strategy for embryological manipulation and allows us to address a lo

95 We developed a novel approach for embryological manipulation of the developing larval tiss

96 Experimental embryological manipulations and molecular studies show t

97 Data from embryological manipulations suggest that either sensory

98 trulation in C elegans and permits classical embryological manipulations.

99 or interpreting gene expression patterns and embryological manipulations.

100 limb development, we employed several other embryological manipulations.

101 agnosed as PTA in the absence of evidence of embryological mechanism.

102 nce findings and classified when possible by embryological mechanisms RESULTS: The most common locati

103 plication of powerful genetic, cellular, and embryological methodologies make zebrafish a useful mode

104 We combine state-of-the-art embryological methods with low-input RNA-seq to develop

105 In the past, classical embryological models have explained how patterned struct

106 e these findings with current anatomical and embryological models.

107 ccessibility of the system, and with various embryological, molecular and genetic approaches, signifi

108 ripheral nervous systems exhibit significant embryological, morphological, and functional differences

109 Some analyses of embryological, morphological, and paleontological data s

110 s that adversely affect both respiratory and embryological nodal cilia are a significant cause of het

111 e entire early embryo, and the molecular and embryological of basis these processes are beginning to

112 ly resemble each other despite the different embryological origin and physiological properties of the

113 In this review, we will consider their embryological origin and the genes controlling their mor

114 ermaphroditism, while the non-duality of the embryological origin of teleost gonads might explain why

115 red with common cancers, consistent with the embryological origin of TGCT.

116 The embryological origin of the PE is presently unclear.

117 associated with del22q11; we have traced the embryological origin of these abnormalities to defective

118 However, the embryological origin of these neurons and glia is unclea

119 We review the effect of embryological origin on VSMC behavior in atherosclerosis

120 ation and show that both structures share an embryological origin within the lateral plate mesoderm.

121 view, we discuss the anatomical development, embryological origin, lineage relationships, and key reg

122 rs, irrespective of the anatomical location, embryological origin, or physiological properties of ass

123 s and collecting lymphatics sharing a common embryological origin, their P(RSA)(s) would not differ s

124 opposite responses in cells having a common embryological origin, we analyzed individual transcripto

125 oci even in cell lines derived from a common embryological origin.

126 ription factors in these tissues of distinct embryological origin.

127 metrical primordia that may be of equivalent embryological origin: the anterior lateral plate mesoder

128 anscriptional "imprint" consistent with both embryological origins and classic evolutionary relations

129 ons have been studied physiologically, their embryological origins and molecular profiles remain obsc

130 nted alongside existing understanding of the embryological origins for the meninges prior to proposin

131 Heterogeneity of embryological origins is a hallmark of vascular smooth m

132 We want to draw interest to the embryological origins of cells that will develop into wh

133 e, we used genetic fate mapping to chart the embryological origins of the tissues in the mouse larynx

134 The aim of this study was to elucidate the embryological origins of the unique neuronal progenitor

135 d differentiation of tissues having multiple embryological origins.

136 Although some embryological pathways have been elucidated, the molecul

137 bryo size, which we verified by biophysical, embryological, pharmacological and genetic perturbations

138 lopmental genetic machinery that lies behind embryological phenotypes, which were all that could be s

139 Due to embryological, physiological, and microbial differences,

140 bians (salamanders) are important models for embryological, physiological, and natural history resear

141 ide range of experimental genetic, cellular, embryological, physiological, developmental, ecological

142 en though the first wing digit develops from embryological position 2.

143 Using experimental embryological procedures (in chick) and genetic models (

144 ue-specific gene expression, we revealed new embryological processes that are influenced by Hh signal

145 g by this superfamily regulates a variety of embryological processes, and it has a conserved role in

146 Thus the paleo-embryological record may have strong biases on developme

147 ow tract alignment defects may constitute an embryological spectrum rather than distinct anomalies.

148 Previous embryological studies [3] have shown that contact with n

149 n used in mammals as both a valuable tool in embryological studies and as a method for the multiplica

150 Recent embryological studies are beginning to establish that th

151 Here we present Xenopus embryological studies demonstrating an unforeseen role f

152 Genetic and embryological studies have begun to elucidate the proces

153 teractions that descriptive and experimental embryological studies have elucidated in the control of

154 Classical embryological studies have shown that the surrounding ex

155 However, non-rodent embryological studies highlight that many aspects of ear

156 According to a model based on embryological studies in amphibia, dorsoventral patterni

157 Although this was known from embryological studies in extant turtles, important steps

158 Experimental embryological studies indicate that caudal elongation of

159 is concept is also consistent with classical embryological studies of many organ systems involving a

160 Genetic and embryological studies over the past decade have informed

161 Although classical embryological studies performed several decades ago in c

162 In embryological studies phenocopies of these abnormalities

163 5, it is now possible to reconcile classical embryological studies with molecular mechanisms of cardi

164 a squirt', has become an important model for embryological studies, offering a simple blueprint for c

165 this review, we highlight a number of recent embryological studies, using chicken, frog, zebrafish an

166 Here, we combine embryological techniques with array technology to descri

167 We have combined embryological techniques with array technology to identi

168 bryos using cell biological, biophysical and embryological techniques.

169 f vignettes highlighting the rich history of embryological thinking in Asia and Latin America.

170 are aware of the depth and breadth of early embryological thinking outside of Europe.

171 eliable cell fate decisions within the short embryological timescales.

172 hat is expressed by endothelial cells during embryological vascular development.

173 tatic development has come from experimental embryological work as well as from the study of mice and