Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 92

1.

Cooperative function of Tbx1 and Brn4 in the periotic mesenchyme is necessary for cochlea formation.

Braunstein EM, Crenshaw EB 3rd, Morrow BE, Adams JC.

J Assoc Res Otolaryngol. 2008 Mar;9(1):33-43. doi: 10.1007/s10162-008-0110-6. Epub 2008 Jan 30.

2.

Tbx1 and Brn4 regulate retinoic acid metabolic genes during cochlear morphogenesis.

Braunstein EM, Monks DC, Aggarwal VS, Arnold JS, Morrow BE.

BMC Dev Biol. 2009 May 29;9:31. doi: 10.1186/1471-213X-9-31.

3.

Targeted mutagenesis of the POU-domain gene Brn4/Pou3f4 causes developmental defects in the inner ear.

Phippard D, Lu L, Lee D, Saunders JC, Crenshaw EB 3rd.

J Neurosci. 1999 Jul 15;19(14):5980-9.

4.

Deficiency of transcription factor Brn4 disrupts cochlear gap junction plaques in a model of DFN3 non-syndromic deafness.

Kidokoro Y, Karasawa K, Minowa O, Sugitani Y, Noda T, Ikeda K, Kamiya K.

PLoS One. 2014 Sep 26;9(9):e108216. doi: 10.1371/journal.pone.0108216. eCollection 2014.

5.

Pou3f4 deficiency causes defects in otic fibrocytes and stria vascularis by different mechanisms.

Song MH, Choi SY, Wu L, Oh SK, Lee HK, Lee DJ, Shim DB, Choi JY, Kim UK, Bok J.

Biochem Biophys Res Commun. 2011 Jan 7;404(1):528-33. doi: 10.1016/j.bbrc.2010.12.019. Epub 2010 Dec 7.

PMID:
21144821
6.

TBX1 is required for inner ear morphogenesis.

Vitelli F, Viola A, Morishima M, Pramparo T, Baldini A, Lindsay E.

Hum Mol Genet. 2003 Aug 15;12(16):2041-8.

PMID:
12913075
7.

Tissue-specific roles of Tbx1 in the development of the outer, middle and inner ear, defective in 22q11DS patients.

Arnold JS, Braunstein EM, Ohyama T, Groves AK, Adams JC, Brown MC, Morrow BE.

Hum Mol Genet. 2006 May 15;15(10):1629-39. Epub 2006 Apr 6.

8.

Otic mesenchyme expression of Cre recombinase directed by the inner ear enhancer of the Brn4/Pou3f4 gene.

Ahn KJ, Passero F Jr, Crenshaw EB 3rd.

Genesis. 2009 Mar;47(3):137-41. doi: 10.1002/dvg.20454.

PMID:
19217071
9.

Changes in the subcellular localization of the Brn4 gene product precede mesenchymal remodeling of the otic capsule.

Phippard D, Heydemann A, Lechner M, Lu L, Lee D, Kyin T, Crenshaw EB 3rd.

Hear Res. 1998 Jun;120(1-2):77-85.

PMID:
9667433
10.

Identification of putative retinoic acid target genes downstream of mesenchymal Tbx1 during inner ear development.

Monks DC, Morrow BE.

Dev Dyn. 2012 Mar;241(3):563-73. doi: 10.1002/dvdy.23731. Epub 2012 Feb 1.

11.

Mice overexpressing genes from the 22q11 region deleted in velo-cardio-facial syndrome/DiGeorge syndrome have middle and inner ear defects.

Funke B, Epstein JA, Kochilas LK, Lu MM, Pandita RK, Liao J, Bauerndistel R, Schüler T, Schorle H, Brown MC, Adams J, Morrow BE.

Hum Mol Genet. 2001 Oct 15;10(22):2549-56.

PMID:
11709542
12.

The sex-linked fidget mutation abolishes Brn4/Pou3f4 gene expression in the embryonic inner ear.

Phippard D, Boyd Y, Reed V, Fisher G, Masson WK, Evans EP, Saunders JC, Crenshaw EB 3rd.

Hum Mol Genet. 2000 Jan 1;9(1):79-85.

PMID:
10587581
13.

Deafness in mice lacking the T-box transcription factor Tbx18 in otic fibrocytes.

Trowe MO, Maier H, Schweizer M, Kispert A.

Development. 2008 May;135(9):1725-34. doi: 10.1242/dev.014043. Epub 2008 Mar 19.

14.

Mutation of the POU-domain gene Brn4/Pou3f4 affects middle-ear sound conduction in the mouse.

Samadi DS, Saunders JC, Crenshaw EB 3rd.

Hear Res. 2005 Jan;199(1-2):11-21.

PMID:
15574296
15.

Conditional and constitutive expression of a Tbx1-GFP fusion protein in mice.

Freyer L, Nowotschin S, Pirity MK, Baldini A, Morrow BE.

BMC Dev Biol. 2013 Aug 23;13:33. doi: 10.1186/1471-213X-13-33.

16.
17.

Pou3f4-mediated regulation of ephrin-b2 controls temporal bone development in the mouse.

Raft S, Coate TM, Kelley MW, Crenshaw EB 3rd, Wu DK.

PLoS One. 2014 Oct 9;9(10):e109043. doi: 10.1371/journal.pone.0109043. eCollection 2014.

18.

Tbx1 is required for proper neural crest migration and to stabilize spatial patterns during middle and inner ear development.

Moraes F, Nóvoa A, Jerome-Majewska LA, Papaioannou VE, Mallo M.

Mech Dev. 2005 Feb;122(2):199-212.

19.

Loss of Sox9 in the periotic mesenchyme affects mesenchymal expansion and differentiation, and epithelial morphogenesis during cochlea development in the mouse.

Trowe MO, Shah S, Petry M, Airik R, Schuster-Gossler K, Kist R, Kispert A.

Dev Biol. 2010 Jun 1;342(1):51-62. doi: 10.1016/j.ydbio.2010.03.014. Epub 2010 Mar 24.

20.

The 22q11 deletion syndrome candidate gene Tbx1 determines thyroid size and positioning.

Fagman H, Liao J, Westerlund J, Andersson L, Morrow BE, Nilsson M.

Hum Mol Genet. 2007 Feb 1;16(3):276-85. Epub 2006 Dec 12.

PMID:
17164259

Supplemental Content

Support Center