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 |
---|---|
1999 | 2 |
2012 | 1 |
2024 | 0 |
Search Results
3 results
Results by year
Filters applied: . Clear all
Page 1
Targeted mutagenesis of the POU-domain gene Brn4/Pou3f4 causes developmental defects in the inner ear.
J Neurosci. 1999 Jul 15;19(14):5980-9. doi: 10.1523/JNEUROSCI.19-14-05980.1999.
J Neurosci. 1999.
PMID: 10407036
Free PMC article.
Altered cochlear fibrocytes in a mouse model of DFN3 nonsyndromic deafness.
Minowa O, Ikeda K, Sugitani Y, Oshima T, Nakai S, Katori Y, Suzuki M, Furukawa M, Kawase T, Zheng Y, Ogura M, Asada Y, Watanabe K, Yamanaka H, Gotoh S, Nishi-Takeshima M, Sugimoto T, Kikuchi T, Takasaka T, Noda T.
Minowa O, et al.
Science. 1999 Aug 27;285(5432):1408-11. doi: 10.1126/science.285.5432.1408.
Science. 1999.
PMID: 10464101
Item in Clipboard
Otic mesenchyme cells regulate spiral ganglion axon fasciculation through a Pou3f4/EphA4 signaling pathway.
Coate TM, Raft S, Zhao X, Ryan AK, Crenshaw EB 3rd, Kelley MW.
Coate TM, et al.
Neuron. 2012 Jan 12;73(1):49-63. doi: 10.1016/j.neuron.2011.10.029.
Neuron. 2012.
PMID: 22243746
Free PMC article.
Item in Clipboard
Cite
Cite