- POU3F4
POU domain, class 3, transcription factor 4, also known as POU3F4, is a human
gene .cite web | title = Entrez Gene: POU3F4 POU domain, class 3, transcription factor 4| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=5456| accessdate = ]PBB_Summary
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summary_text =References
Further reading
PBB_Further_reading
citations =
*cite journal | author=Bitner-Glindzicz M, Turnpenny P, Höglund P, "et al." |title=Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3. |journal=Hum. Mol. Genet. |volume=4 |issue= 8 |pages= 1467–9 |year= 1995 |pmid= 7581392 |doi=
*cite journal | author=de Kok YJ, van der Maarel SM, Bitner-Glindzicz M, "et al." |title=Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4. |journal=Science |volume=267 |issue= 5198 |pages= 685–8 |year= 1995 |pmid= 7839145 |doi=
*cite journal | author=Douville PJ, Atanasoski S, Tobler A, "et al." |title=The brain-specific POU-box gene Brn4 is a sex-linked transcription factor located on the human and mouse X chromosomes. |journal=Mamm. Genome |volume=5 |issue= 3 |pages= 180–2 |year= 1994 |pmid= 7911044 |doi=
*cite journal | author=Malik KF, Jaffe H, Brady J, Young WS |title=The class III POU factor Brn-4 interacts with other class III POU factors and the heterogeneous nuclear ribonucleoprotein U. |journal=Brain Res. Mol. Brain Res. |volume=45 |issue= 1 |pages= 99–107 |year= 1997 |pmid= 9105675 |doi=
*cite journal | author=de Kok YJ, Cremers CW, Ropers HH, Cremers FP |title=The molecular basis of X-linked deafness type 3 (DFN3) in two sporadic cases: identification of a somatic mosaicism for a POU3F4 missense mutation. |journal=Hum. Mutat. |volume=10 |issue= 3 |pages= 207–11 |year= 1997 |pmid= 9298820 |doi= 10.1002/(SICI)1098-1004(1997)10:3<207::AID-HUMU5>3.0.CO;2-F |doilabel=10.1002/(SICI)1098-1004(1997)10:3207::AID-HUMU53.0.CO;2-F
*cite journal | author=Phippard D, Heydemann A, Lechner M, "et al." |title=Changes in the subcellular localization of the Brn4 gene product precede mesenchymal remodeling of the otic capsule. |journal=Hear. Res. |volume=120 |issue= 1-2 |pages= 77–85 |year= 1998 |pmid= 9667433 |doi=
*cite journal | author=Hagiwara H, Tamagawa Y, Kitamura K, Kodera K |title=A new mutation in the POU3F4 gene in a Japanese family with X-linked mixed deafness (DFN3). |journal=Laryngoscope |volume=108 |issue= 10 |pages= 1544–7 |year= 1998 |pmid= 9778298 |doi=
*cite journal | author=Shimazaki T, Arsenijevic Y, Ryan AK, "et al." |title=A role for the POU-III transcription factor Brn-4 in the regulation of striatal neuron precursor differentiation. |journal=EMBO J. |volume=18 |issue= 2 |pages= 444–56 |year= 1999 |pmid= 9889200 |doi= 10.1093/emboj/18.2.444
*cite journal | author=Xia AP, Kikuchi T, Minowa O, "et al." |title=Late-onset hearing loss in a mouse model of DFN3 non-syndromic deafness: morphologic and immunohistochemical analyses. |journal=Hear. Res. |volume=166 |issue= 1-2 |pages= 150–8 |year= 2002 |pmid= 12062767 |doi=
*cite journal | author=Ross MT, Grafham DV, Coffey AJ, "et al." |title=The DNA sequence of the human X chromosome. |journal=Nature |volume=434 |issue= 7031 |pages= 325–37 |year= 2005 |pmid= 15772651 |doi= 10.1038/nature03440External links
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