Show simple item record

dc.contributor.authorKramer, Edgar
dc.date.accessioned2018-07-24T11:52:33Z
dc.date.available2018-07-24T11:52:33Z
dc.date.issued2018
dc.identifier.urihttp://hdl.handle.net/10026.1/11873
dc.description.abstract

Human neurodegenerative disease are currently difficult to model in rodents and only a handful of transgenic mice show a phenotype related to the human disease. This is most likely due to several reasons such as restricted life expectation of rodents, restricted environmental influences in the holding cages and slightly different gene and protein sequences. To overcome this limitation and to generate some more disease relevant mouse models bespoke alterations have to be made in mice. A promising approach to generate human disease relevant mouse models is to humanize the mice. This includes expression of human proteins in mice by viruses or transgenic constructs in a constitutive or regulated fashion, replacing mouse genes with human genes, introducing hole human chromosomes or adding human cells into the mouse organisms. In this talk I will present examples of this mouse humanization techniques from the neurodegeneration field and highlight the advantages and disadvantages of these different humanized mouse models.

dc.language.isoen
dc.titleHumanized mice to investigate neurodegenerative diseases
dc.typeconference
dc.typeinproceedings
plymouth.date-start2018-06-27
plymouth.date-finish2018-06-29
plymouth.conference-nameExperimental models in physiology
plymouth.organisational-group/Plymouth
plymouth.organisational-group/Plymouth/Faculty of Health
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA01 Clinical Medicine
plymouth.organisational-group/Plymouth/Users by role
plymouth.organisational-group/Plymouth/Users by role/Academics
dc.publisher.placeUniversity of Exeter, Exeter, United Kingdom
dcterms.dateAccepted2018-01-01
dc.rights.embargodate2023-7-19
dc.rights.embargoperiodNo embargo
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.typeConference Paper/Proceeding/Abstract


Files in this item

Thumbnail
Thumbnail

This item appears in the following Collection(s)

Show simple item record


All items in PEARL are protected by copyright law.
Author manuscripts deposited to comply with open access mandates are made available in accordance with publisher policies. Please cite only the published version using the details provided on the item record or document. In the absence of an open licence (e.g. Creative Commons), permissions for further reuse of content should be sought from the publisher or author.
Theme by 
Atmire NV