Cox TC - Search Results

1

Hmx1 is required for the normal development of somatosensory neurons in the geniculate ganglion.

Quina LA, Tempest L, Hsu YW, Cox TC, Turner EE. Quina LA, et al. Among authors: cox tc. Dev Biol. 2012 May 1;365(1):152-63. doi: 10.1016/j.ydbio.2012.02.022. Dev Biol. 2012. PMID: 22586713 Free PMC article.

2

Deletion of a conserved regulatory element required for Hmx1 expression in craniofacial mesenchyme in the dumbo rat: a newly identified cause of congenital ear malformation.

Quina LA, Kuramoto T, Luquetti DV, Cox TC, Serikawa T, Turner EE. Quina LA, et al. Among authors: cox tc. Dis Model Mech. 2012 Nov;5(6):812-22. doi: 10.1242/dmm.009910. Epub 2012 Jun 26. Dis Model Mech. 2012. PMID: 22736458 Free PMC article.

3

Genetic evidence for conserved non-coding element function across species-the ears have it.

Turner EE, Cox TC. Turner EE, et al. Among authors: cox tc. Front Physiol. 2014 Jan 21;5:7. doi: 10.3389/fphys.2014.00007. eCollection 2014. Front Physiol. 2014. PMID: 24478720 Free PMC article.

4

The genetics of auricular development and malformation: new findings in model systems driving future directions for microtia research.

Cox TC, Camci ED, Vora S, Luquetti DV, Turner EE. Cox TC, et al. Eur J Med Genet. 2014 Aug;57(8):394-401. doi: 10.1016/j.ejmg.2014.05.003. Epub 2014 May 29. Eur J Med Genet. 2014. PMID: 24880027 Free PMC article. Review.

5

Discovery and characterization of spontaneous mouse models of craniofacial dysmorphology.

Palmer K, Fairfield H, Borgeia S, Curtain M, Hassan MG, Dionne L, Yong Karst S, Coombs H, Bronson RT, Reinholdt LG, Bergstrom DE, Donahue LR, Cox TC, Murray SA. Palmer K, et al. Among authors: cox tc. Dev Biol. 2016 Jul 15;415(2):216-227. doi: 10.1016/j.ydbio.2015.07.023. Epub 2015 Jul 31. Dev Biol. 2016. PMID: 26234751 Free PMC article.

6

A distal 594 bp ECR specifies Hmx1 expression in pinna and lateral facial morphogenesis and is regulated by the Hox-Pbx-Meis complex.

Rosin JM, Li W, Cox LL, Rolfe SM, Latorre V, Akiyama JA, Visel A, Kuramoto T, Bobola N, Turner EE, Cox TC. Rosin JM, et al. Among authors: cox tc, cox ll. Development. 2016 Jul 15;143(14):2582-92. doi: 10.1242/dev.133736. Epub 2016 Jun 10. Development. 2016. PMID: 27287804 Free PMC article.

7

Isolation and characterisation of the chick orthologue of the Opitz syndrome gene, Mid1, supports a conserved role in vertebrate development.

Richman JM, Fu KK, Cox LL, Sibbons JP, Cox TC. Richman JM, et al. Among authors: cox tc, cox ll. Int J Dev Biol. 2002;46(4):441-8. Int J Dev Biol. 2002. PMID: 12141430

8

Negative regulation of endothelin signaling by SIX1 is required for proper maxillary development.

Tavares ALP, Cox TC, Maxson RM, Ford HL, Clouthier DE. Tavares ALP, et al. Among authors: cox tc. Development. 2017 Jun 1;144(11):2021-2031. doi: 10.1242/dev.145144. Epub 2017 Apr 28. Development. 2017. PMID: 28455376 Free PMC article.

9

Microtomographic analysis of lower urinary tract obstruction.

Siebert JR, Smith KJ, Cox LL, Glass IA, Cox TC. Siebert JR, et al. Among authors: cox tc, cox ll. Pediatr Dev Pathol. 2013 Nov-Dec;16(6):405-14. doi: 10.2350/13-08-1359-OA.1. Epub 2013 Aug 26. Pediatr Dev Pathol. 2013. PMID: 23977847 Free PMC article.

10

SLC20A2 Deficiency in Mice Leads to Elevated Phosphate Levels in Cerbrospinal Fluid and Glymphatic Pathway-Associated Arteriolar Calcification, and Recapitulates Human Idiopathic Basal Ganglia Calcification.

Wallingford MC, Chia JJ, Leaf EM, Borgeia S, Chavkin NW, Sawangmake C, Marro K, Cox TC, Speer MY, Giachelli CM. Wallingford MC, et al. Among authors: cox tc. Brain Pathol. 2017 Jan;27(1):64-76. doi: 10.1111/bpa.12362. Epub 2016 May 6. Brain Pathol. 2017. PMID: 26822507 Free PMC article.

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