Difference between revisions of "Talk:HDBR and HuDSeN Collection"

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PMID 20979583  
 
PMID 20979583  
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Authors choosing OnlineOpen will retain copyright in their articles and will be offered a choice of creative commons licenses. All Research Councils UK (RCUK), COAF/Wellcome Trust and FWF funded authors will be directed to the Creative Commons Attribution license (CC-BY). https://creativecommons.org/licenses/by/4.0/
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==2005==
 
==2005==

Latest revision as of 10:42, 26 February 2016

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Cite this page: Hill, M.A. (2021, December 2) Embryology HDBR and HuDSeN Collection. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/Talk:HDBR_and_HuDSeN_Collection


2010

The HUDSEN Atlas: a three-dimensional (3D) spatial framework for studying gene expression in the developing human brain

J Anat. 2010 Oct;217(4):289-99. doi: 10.1111/j.1469-7580.2010.01290.x.

Kerwin J1, Yang Y, Merchan P, Sarma S, Thompson J, Wang X, Sandoval J, Puelles L, Baldock R, Lindsay S.

Abstract

We are developing a three-dimensional (3D) atlas of the human embryonic brain using anatomical landmarks and gene expression data to define major subdivisions through 12 stages of development [Carnegie Stages (CS) 12-23; approximately 26-56 days post conception (dpc)]. Virtual 3D anatomical models are generated from intact specimens using optical projection tomography (OPT). Using MAPAINT software, selected gene expression data, gathered using standard methods of in situ hybridization and immunohistochemistry, are mapped to a representative 3D model for each chosen Carnegie stage. In these models, anatomical domains, defined on the basis of morphological landmarks and comparative knowledge of expression patterns in vertebrates, are linked to a developmental neuroanatomic ontology. Human gene expression patterns for genes with characteristic expression in different vertebrates (e.g. PAX6, GAD65 and OLIG2) are being used to confirm and/or refine the human anatomical domain boundaries. We have also developed interpolation software that digitally generates a full domain from partial data. Currently, the 3D models and a preliminary set of anatomical domains and ontology are available on the atlas pages along with gene expression data from approximately 100 genes in the HUDSEN Human Spatial Gene Expression Database (http://www.hudsen.org). The aim is that full 3D data will be generated from expression data used to define a more detailed set of anatomical domains linked to a more advanced anatomy ontology and all of these will be available online, contributing to the long-term goal of the atlas, which is to help maximize the effective use and dissemination of data wherever it is generated. © 2010 The Authors. Journal of Anatomy © 2010 Anatomical Society of Great Britain and Ireland.

  • Embryos were staged and fixed overnight in 4% paraformaldehyde at 4 C before being stored in 70% ethanol
  • prior to OPT imaging or wax embedding and sectioning at 8 micron.
  • Placental tissue was sampled for karyotype analysis prior to fixation.


PMID 20979583

Authors choosing OnlineOpen will retain copyright in their articles and will be offered a choice of creative commons licenses. All Research Councils UK (RCUK), COAF/Wellcome Trust and FWF funded authors will be directed to the Creative Commons Attribution license (CC-BY). https://creativecommons.org/licenses/by/4.0/


2005

MRC-Wellcome Trust Human Developmental Biology Resource: enabling studies of human developmental gene expression

Trends Genet. 2005 Nov;21(11):586-90. Epub 2005 Sep 9.

Lindsay S1, Copp AJ.

Abstract

A striking finding of the human and mouse genome sequencing projects is that, although there are many differences between the two species, they have similar numbers of genes. The differences arise during development and are driven, in part, by changes in gene expression. The MRC-Wellcome Trust Human Developmental Biology Resource (HDBR) is a unique resource that provides human embryonic and foetal tissues to the scientific community, enabling gene-expression studies at these crucial periods of development.

PMID 16154230