POU3F4

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
section_title =
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/nature03440

External links

*

PBB_Controls
update_page = yes
require_manual_inspection = no
update_protein_box = yes
update_summary = yes
update_citations = yes


Wikimedia Foundation. 2010.

Игры ⚽ Нужна курсовая?

Look at other dictionaries:

  • Nonsyndromic deafness — is hearing loss that is not associated with other signs and symptoms. In contrast, syndromic deafness involves hearing loss that occurs with abnormalities in other parts of the body. Genetic changes are related to the following types of… …   Wikipedia

  • POU-Gen — Die POU Familie ist eine Gruppe von Transkriptionsfaktoren mit einer hochkonservierten Homöodomäne. Im menschlichen Genom wurden 15 POU Gene gefunden. Das Genom der Modellorganismen Drosophila und Caenorhabditis elegans weist dagegen nur fünf… …   Deutsch Wikipedia

  • Octamer transcription factor — An octamer transcription factor is a transcription factor which binds to the ATTTGCAT sequence.[1] Examples include: Oct 1 POU2F1 Oct 2 POU2F2 Oct 3/4 – POU5F1 Oct 6 – …   Wikipedia

  • POU-Familie — Die POU Familie ist eine Gruppe von Transkriptionsfaktoren mit einer hochkonservierten Homöodomäne. Im menschlichen Genom wurden 15 POU Gene gefunden. Das Genom der Modellorganismen Drosophila und Caenorhabditis elegans weist dagegen nur fünf… …   Deutsch Wikipedia

  • Genetic disorder — For a non technical introduction to the topic, see Introduction to genetics. Genetic disorder Classification and external resources MeSH D030342 A genetic disorder is an illness caused by abnormalities in genes or …   Wikipedia

  • Androgen insensitivity syndrome — Classification and external resources AIS results when the function of the androgen receptor (AR) is impaired. The AR protein (pictured) mediates the effects of androgens in the human body. ICD 10 E …   Wikipedia

  • Cleft lip and palate — For other uses, see Cleft. Cleft lip and palate Classification and external resources …   Wikipedia

  • Septo-optic dysplasia — Classification and external resources ICD 10 Q04.4 ICD 9 742.2 …   Wikipedia

  • Tietz syndrome — Not to be confused with Tietze syndrome. Tietz syndrome Classification and external resources ICD 10 E70.3 (ILDS E70.358) OMIM 103500 …   Wikipedia

  • Congenital hypothyroidism — Classification and external resources ICD 10 E00, E03.0, E03.1 …   Wikipedia

Share the article and excerpts

Direct link
Do a right-click on the link above
and select “Copy Link”