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Title:CTNNB1 syndrome mouse models
Authors:ID Lainšček, Duško (Author)
ID Forstnerič, Vida (Author)
ID Miroševič, Špela (Author)
Files:URL URL - Source URL, visit https://link.springer.com/article/10.1007/s00335-025-10105-3
 
.pdf PDF - Presentation file, download (1,51 MB)
MD5: D441F80549A84EBBC40E878C78F03B5F
 
Language:English
Typology:1.02 - Review Article
Organization:Logo KI - National Institute of Chemistry
Publication status:Published
Publication version:Version of Record
Publication date:01.01.2025
Publisher:Springer
Year of publishing:2025
Number of pages:str. [390]-402
Numbering:Vol. 36, [ǂiss. ]2
PID:20.500.12556/DiRROS-22599 New window
UDC:577
ISSN on article:1432-1777
DOI:10.1007/s00335-025-10105-3 New window
COBISS.SI-ID:224354307 New window
Copyright:© The Author(s) 2025
Note:Nasl. z nasl. zaslona; Opis vira z dne 29. 1. 2025;
Publication date in DiRROS:09.06.2025
Views:477
Downloads:218
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Record is a part of a journal

Title:Mammalian genome
Shortened title:Mamm. genome
Publisher:Springer
ISSN:1432-1777
COBISS.SI-ID:2525972 New window

Document is financed by a project

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:P4-0176
Name:Sintezna biologija in imunologija
Funder:ARIS - Slovenian Research and Innovation Agency
Project number:J4-4563
Name:Uporaba izboljšanega sistema CRISPR/Cas za nevirusno produkcijo celic CAR-T
Funder:ARIS - Slovenian Research and Innovation Agency
Project number:J7-4537
Name:POVEZAVA MED GENOTIPOM IN FENOTIPOM PRI SINDROMU CTNNB1 IN NOVI PRISTOPI K ZDRAVLJENJU TEGA SINDROMA

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Licensing start date:20.01.2025
Applies to:Text and Data Mining valid from 2025-01-20 Version of Record valid from 2025-01-20

Secondary language

Language:Slovenian
Keywords:biokemija, nevrorazvojna motnja, bolezni, zdravljenje, genska terapija, CTNNB1


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