ライフサイエンスコーパス: embryology

1 e 'Law of Development' or 'von Baer's law of embryology'.

2 The concept of an "organizer" is basic to embryology.

3 vertebrate zebrafish is a favorite model for embryology.

4 ments that form the foundations of amphibian embryology.

5 data, cis-regulatory analysis, and molecular embryology.

6 protocols for their application to molecular embryology.

7 these approaches in the context of molecular embryology.

8 d to Rosa Beddington, a pioneer in mammalian embryology].

9 for studies on the fundamental mechanisms of embryology and adult physiology and for investigating th

10 ntal questions remaining at the frontiers of embryology and early human development.

11 elopment (called at that time the Journal of Embryology and Experimental Morphology).

12 nsightful papers published in the Journal of Embryology and Experimental Morphology, in which he prov

13 A combination of embryology and gene identification has led us to the cur

14 m is proposed, based wherever possible, upon embryology and genetics.

15 werfully informed by comparative morphology, embryology and genomics of chordates, hemichordates and

16 The work illuminates embryology and has important implications for making mor

17 e GCMB gene impairs normal parathyroid gland embryology and is responsible for isolated hypoparathyro

18 written of the early history of comparative embryology and its influence on the emergence of an evol

19 Here we combine experimental embryology and mathematical modelling to analyse the rol

20 lation of stem cells has evidence in classic embryology and more recently in adult stem cells through

21 arise this information, link it to classical embryology and propose a molecular framework for the est

22 n development, thereby helping advance human embryology and reproductive medicine.

23 segmental organization, and (2) comparative embryology and the neural tube's transverse and longitud

24 ing of the polarity of cholangiocytes, their embryology and ultrastructural anatomy, and in vivo huma

25 tionships between adipose tissue (histology, embryology, and adipogenesis) and cardiovascular medicin

26 nterest since the early days of experimental embryology, and constitutes the best understood system i

27 rvous system is based on studies of anatomy, embryology, and evolution.

28 where cis-regulatory evidence, experimental embryology, and network analysis combine to provide a co

29 major role in the formation of experimental embryology, and they are returning as the need for knowl

30 sue masses is a recurrent theme in mammalian embryology, and this process plays an integral role in t

31 Since 1991, the Human Fertilisation and Embryology Authority (HFEA) has been collecting informat

32 spective study of UK Human Fertilisation and Embryology Authority data, we investigated whether perin

33 s a model with all the benefits of amphibian embryology but crucially only a single Mix and Nodal gen

34 st experienced in molecular cell biology and embryology can reproduce this protocol in 12-16 weeks.

35 been the subject of studies in experimental embryology, cell lineage, and the organization of the la

36 of fossilization and providing insight into embryology during the emergence of metazoan phyla.

37 and provides a platform for advancing human embryology.Early in human embryonic development, it is u

38 As marking tools for experimental embryology emerged, the cellular events of cortical hist

39 European Society of Human Reproduction and Embryology, European Society for Gynaecological Endoscop

40 Classical embryology experiments have indicated the existence of d

41 dominated thinking in amphibian experimental embryology for many decades.

42 treatment modalities, anatomy and pathology, embryology, genetics, epidemiology, and imaging.

43 ications of microarray technologies to mouse embryology/genetics have been limited, due to the nonava

44 gnathostomes), they provide insight into the embryology, genomics, and body plan of the ancestral ver

45 Embryology has offered important insights into key pathw

46 Classical embryology has provided a clear view of the timing and h

47 ut recent progress in molecular genetics and embryology has revealed deep similarities in body-axis f

48 A combination of genetics and embryology has uncovered the organisation and function o

49 Classical experiments in embryology have shown that normal growth, morphogenetic

50 ent would enhance our understanding of basic embryology, improve applications of the technology, supp

51 The results of this comparative embryology in conjunction with genetic experiments on Dr

52 oning and Shh expression, using experimental embryology in ovo in the chick.

53 I here review some of the milestones of embryology in which the sea urchin was the key player, s

54 presenting urodele amphibians, since urodele embryology is basal to amphibians and was conserved duri

55 Pertinent embryology is discussed and the classification is justif

56 ussion of the important events of pancreatic embryology is followed by presentation of congenital ano

57 models are still very complex, and the human embryology is still poorly understood.

58 Developmental biology (including embryology) is proposed as "the stem cell of biological

59 ng amniotes has implications for dinosaurian embryology, life history strategies, and survivorship ac

60 Unearthing embryology-like processes in tumors may allow us to cont

61 Modern Synthesis of genetics and evolution: embryology, macroevolution, and homology.

62 hology, but within the field of experimental embryology mathematical descriptions of anatomical form

63 because they preserve the earliest stages of embryology of animals that represent the initial diversi

64 The embryology of basal angiosperm lineages (Amborella, Nymp

65 sease in the young promises new insight into embryology of cardiac development and improved understan

66 chromatin remodellers, illuminates the patho-embryology of CHARGE syndrome, and suggests a broader fu

67 Although the gross embryology of inner ear development has been documented

68 Finally, in accord with the distinct embryology of retinal pigmented cells, transgenic mice w

69 Some of the classical embryology of the endoderm is discussed and the progress

70 ade great strides in understanding the early embryology of the kidney and the molecular signals invol

71 n lymphangiogenesis, an understanding of the embryology of the mammalian lymphatic system, the recent

72 Whereas the embryology of the normal venous pole and PV is becoming

73 Although the embryology of the palate has long been studied, the past

74 view focuses on recent advances in molecular embryology of the upper and lower urinary tract with an

75 In this review, we present the descriptive embryology of this process as well as the recent data th

76 Combining fields as diverse as comparative embryology, palaeontology, molecular phylogenetics and g

77 ntologies for anatomy, cell types, function, embryology, pathology and other domains.

78 At the level of descriptive embryology, skeletogenesis in Sp and Et has long been kn

79 eing used to answer fundamental questions in embryology, such as how cells self-organize and assemble

80 t as with many conclusions from experimental embryology, the idea that the dorsal lip of the blastopo

81 ersy remains regarding etiology, anatomy and embryology, the role of prenatal diagnosis and mode of d

82 Experiments employing chick embryology, tissue culture, and gene targeting in mice s

83 Using experimental embryology to discriminate among these models, we show h

84 nly used in amphibian and avian experimental embryology, we either grafted or deleted the region of t

85 lecular, genetic and classical techniques of embryology, we have investigated the role of T in allant

86 ng the OCT features, available evidence, and embryology, we propose that the true nature of CHRRPE sh