A list of normal human embryos which have been cut into serial sections

1910 ◽  
Vol 4 (10) ◽  
pp. 355-367 ◽  
Author(s):  
Franklin P. Mall
1993 ◽  
Vol 86 (5) ◽  
Author(s):  
Mirna Saraga-Babi� ◽  
Vedran Stefanovi� ◽  
Jorma Wartiovaara ◽  
Eero Lehtonen

2016 ◽  
Vol 299 (7) ◽  
pp. 819-827 ◽  
Author(s):  
Zhe Wu Jin ◽  
Kwang Ho Cho ◽  
Hyung Suk Jang ◽  
Gen Murakami ◽  
Jose Francisco Rodríguez-Vázquez

2000 ◽  
Vol 3 (5) ◽  
pp. 439-449 ◽  
Author(s):  
Daphne E. deMello ◽  
Lynne M. Reid

Recently, we have identified in the mouse three processes involved in the early development of pulmonary vasculature: angiogenesis for branching of central vessels, vasculogenesis (lakes in the mesenchyme) for peripheral vessels, and a lytic process to establish luminal connection between the two. We have established that these three processes also operate in the human by studying serial sections of human embryos and early fetuses. Vascular lakes of hematopoietic cells appear at stage 13, i.e., 4+ weeks gestational age (GA), the first intrapulmonary vascular structure to appear. At stage 20 (50.5 days GA), a venous network with luminal connections to central pulmonary veins (PV) is present. Airways have not yet reached these regions of lung.At its first intrapulmonary appearance, the pulmonary artery (PA) is small and thick walled: it runs with the airway but its branching is slower, so many peripheral airways are not accompanied by a PA branch. By contrast, the PV has a peripheral patent network well before the PA.In the pseudoglandular phase, airway branching continues, and the PA catches up so that small PA branches are found with all airways. Later in this phase small nonmuscular vessels lie in the mesenchyme close to airway epithelium.By the early canalicular phase and the age of viability, continuity between pulmonary artery and the peripheral capillary network must be established. In a 10-week fetus several structures suggesting a breakthrough site were seen. Air-blood barrier structure is first seen at 19 weeks. Thus in the lung, the PA and PV are dissociated in their timing and pattern of branching. Early veins are present diffusely through the mesenchyme and establish central luminal connection to the main pulmonary vein before airway or artery are present at this level.


1925 ◽  
Vol 53 (3) ◽  
pp. 533-567 ◽  
Author(s):  
Thomas H. Bryce

This memoir is based upon the study of three normal human embryos belonging to the period of development preceding the cleavage of the paraxial mesoderm into the primitive segments, as well as of certain abnormal specimens of the same early period which have yielded valuable corroborative data, but will not be described in detail. Well-preserved specimens belonging to these early stages are very rare, and our knowledge has been, and can only be, built up from the detailed descriptions of isolated cases by the individual observers into whose hands they happen to fall.


2020 ◽  
Vol 20 (1) ◽  
Author(s):  
L. Powell ◽  
M. Barroso-Gil ◽  
G. J. Clowry ◽  
L. A. Devlin ◽  
E. Molinari ◽  
...  

Abstract Background Joubert syndrome and related disorders (JSRD) and Jeune syndrome are multisystem ciliopathy disorders with overlapping phenotypes. There are a growing number of genetic causes for these rare syndromes, including the recently described genes ARL3 and CEP120. Methods We sought to explore the developmental expression patterns of ARL3 and CEP120 in humans to gain additional understanding of these genetic conditions. We used an RNA in situ detection technique called RNAscope to characterise ARL3 and CEP120 expression patterns in human embryos and foetuses in collaboration with the MRC-Wellcome Trust Human Developmental Biology Resource. Results Both ARL3 and CEP120 are expressed in early human brain development, including the cerebellum and in the developing retina and kidney, consistent with the clinical phenotypes seen with pathogenic variants in these genes. Conclusions This study provides insights into the potential pathogenesis of JSRD by uncovering the spatial expression of two JSRD-causative genes during normal human development.


Author(s):  
Gonzague S. Kistler ◽  
Peter Groscurth

Tubuloreticular structures (TRS) consisting of branching tubules of variable length and with a diameter of 18-30 nm have been described within dilated endoplasmic reticulum cisternae of endothelial and other cells in a variety of conditions. Thus, TRS have been observed in apparently normal human and animal cells, in cells of patients with auto-immune disease (e. g. systemic lupus erythematodes), with neoplasia (leukemias, carcinomas, sarcomas) as well as with a number of viral infections caused by both DNA or RNA viruses. Whereas earlier investigators regarded TRS as viral or virus-like in nature, it is now widely accepted that these structures represent focal proliferations of ER-membranes and that they reflect a cellular response to a broad range of stimuli. The biological significance of TRS has, however, not been resolved.In rubella-infected human embryos and fetuses, vascular lesions are the most frequently observed light microscopical findings.


Author(s):  
Saundra C. Parra ◽  
Ricky Burnette ◽  
Timothy Takaro

Portions of two adjacent normal human alveoli were reconstructed from serial sections in order to examine normal alveolar organization, including anatomical relationships among the different cell types, the connective tissue matrix and gaps in the alveolar septum. Computer reconstructions were prepared from montaged electron micrographs of serial sections. Rotation of these reconstructions in the x, y or z axes allowed examination of the alveoli from many different aspects other than the actual plane of sectioning. Anatomical relationships “between Type I and Type II epithelial cells, alveolar macrophages, and pores of Kohn that could not he deduced from a single plane of the section (random sections) were revealed.


2020 ◽  
Author(s):  
L Powell ◽  
M Barroso-Gil ◽  
Gavin J Clowry ◽  
Laura A Devlin ◽  
Elisa Molinari ◽  
...  

Abstract Background: Joubert syndrome and related disorders (JSRD) and Jeune syndrome are multisystem ciliopathy disorders with overlapping phenotypes. There are a growing number of genetic causes for these rare syndromes, including the recently described genes ARL3 and CEP120.Methods: We sought to explore the developmental expression patterns of ARL3 and CEP120 in humans to gain additional understanding of these genetic conditions. We used an RNA in situ detection technique called RNAscope to characterise ARL3 and CEP120 expression patterns in human embryos and foetuses in collaboration with the MRC-Wellcome Trust Human Developmental Biology Resource.Results: Both ARL3 and CEP120 are expressed in early human brain development, including the cerebellum and in the developing retina and kidney, consistent with the clinical phenotypes seen with pathogenic variants in these genes.Conclusions: This study provides insights into the potential pathogenesis of JSRD by uncovering the spatial expression of two JSRD-causative genes during normal human development.


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