Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2001 | 2 |
2008 | 1 |
2024 | 0 |
Search Results
3 results
Results by year
Filters applied: . Clear all
Page 1
A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome.
Nat Genet. 2001 Mar;27(3):322-6. doi: 10.1038/85899.
Nat Genet. 2001.
PMID: 11242117
Closely related proteins MBD2 and MBD3 play distinctive but interacting roles in mouse development.
Hendrich B, Guy J, Ramsahoye B, Wilson VA, Bird A.
Hendrich B, et al.
Genes Dev. 2001 Mar 15;15(6):710-23. doi: 10.1101/gad.194101.
Genes Dev. 2001.
PMID: 11274056
Free PMC article.
Item in Clipboard
Deficiency of Mbd2 attenuates Wnt signaling.
Phesse TJ, Parry L, Reed KR, Ewan KB, Dale TC, Sansom OJ, Clarke AR.
Phesse TJ, et al.
Mol Cell Biol. 2008 Oct;28(19):6094-103. doi: 10.1128/MCB.00539-08. Epub 2008 Jul 21.
Mol Cell Biol. 2008.
PMID: 18644872
Free PMC article.
Item in Clipboard
Cite
Cite