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 |
2002 | 1 |
2007 | 1 |
2024 | 0 |
Search Results
4 results
Results by year
Filters applied: . Clear all
Page 1
Differential distribution of the MeCP2 splice variants in the postnatal mouse brain.
J Comp Neurol. 2007 Apr 1;501(4):526-42. doi: 10.1002/cne.21264.
J Comp Neurol. 2007.
PMID: 17278130
The phenotypic consequences of MECP2 mutations extend beyond Rett syndrome.
Hammer S, Dorrani N, Dragich J, Kudo S, Schanen C.
Hammer S, et al.
Ment Retard Dev Disabil Res Rev. 2002;8(2):94-8. doi: 10.1002/mrdd.10023.
Ment Retard Dev Disabil Res Rev. 2002.
PMID: 12112734
Review.
Item in Clipboard
Functional analyses of MeCP2 mutations associated with Rett syndrome using transient expression systems.
Kudo S, Nomura Y, Segawa M, Fujita N, Nakao M, Dragich J, Schanen C, Tamura M.
Kudo S, et al.
Brain Dev. 2001 Dec;23 Suppl 1:S165-73. doi: 10.1016/s0387-7604(01)00345-x.
Brain Dev. 2001.
PMID: 11738866
Item in Clipboard
Neurotrophic factor regulation of human immunodeficiency virus type 1 replication in human blood-derived macrophages through modulation of coreceptor expression.
Harrold SM, Dragic JM, Brown SL, Achim CL.
Harrold SM, et al.
Adv Exp Med Biol. 2001;493:41-7. doi: 10.1007/0-306-47611-8_5.
Adv Exp Med Biol. 2001.
PMID: 11727779
No abstract available.
Item in Clipboard
Cite
Cite