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

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

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

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

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

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

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

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

36 These embryological criteria can refocus arguments on paired f

37 Embryological data suggest that endothelial cells (ECs)

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

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

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

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

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

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

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

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

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

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

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

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

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

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

52 lity of nuclear chromosomal determinants for embryological development.

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

54 This Seminar describes embryological developmental processes, epidemiology, kno

55 These embryological differences imply that anterior and poster

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

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

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

59 Embryological evidence clearly identifies the three wing

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

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

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

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

64 Embryological experiments demonstrate that mesoderm indu

65 Embryological experiments had suggested that the skin pr

66 Classical embryological experiments have demonstrated that dorsal-

67 Genetic and embryological experiments have established the Caenorhab

68 Embryological experiments have indicated the existence o

69 Early embryological experiments identified the notochord and t

70 Classical embryological experiments suggest that a posterior signa

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

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

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

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

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

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

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

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

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

80 Experimental embryological manipulations and molecular studies show t

81 Data from embryological manipulations suggest that either sensory

82 or interpreting gene expression patterns and embryological manipulations.

83 limb development, we employed several other embryological manipulations.

84 trulation in C elegans and permits classical embryological manipulations.

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

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

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

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

89 e these findings with current anatomical and embryological models.

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

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

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

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

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

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

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

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

98 The embryological origin of the PE is presently unclear.

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

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

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

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

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

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

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

106 ription factors in these tissues of distinct embryological origin.

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

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

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

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

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

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

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

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

115 d differentiation of tissues having multiple embryological origins.

116 Although some embryological pathways have been elucidated, the molecul

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

118 Due to embryological, physiological, and microbial differences,

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

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

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

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

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

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

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

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

127 Recent embryological studies are beginning to establish that th

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

129 Genetic and embryological studies have begun to elucidate the proces

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

131 Classical embryological studies have shown that the surrounding ex

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

133 Experimental embryological studies indicate that caudal elongation of

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

135 Genetic and embryological studies over the past decade have informed

136 Although classical embryological studies performed several decades ago in c

137 In embryological studies phenocopies of these abnormalities

138 5, it is now possible to reconcile classical embryological studies with molecular mechanisms of cardi

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

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

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

142 We have combined embryological techniques with array technology to identi

143 bryos using cell biological, biophysical and embryological techniques.

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

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