Martin DM - Search Results

1

Inappropriate p53 activation during development induces features of CHARGE syndrome.

Van Nostrand JL, Brady CA, Jung H, Fuentes DR, Kozak MM, Johnson TM, Lin CY, Lin CJ, Swiderski DL, Vogel H, Bernstein JA, Attié-Bitach T, Chang CP, Wysocka J, Martin DM, Attardi LD. Van Nostrand JL, et al. Among authors: martin dm. Nature. 2014 Oct 9;514(7521):228-32. doi: 10.1038/nature13585. Epub 2014 Aug 3. Nature. 2014. PMID: 25119037 Free PMC article.

2

Defects in vestibular sensory epithelia and innervation in mice with loss of Chd7 function: implications for human CHARGE syndrome.

Adams ME, Hurd EA, Beyer LA, Swiderski DL, Raphael Y, Martin DM. Adams ME, et al. Among authors: martin dm. J Comp Neurol. 2007 Oct 10;504(5):519-32. doi: 10.1002/cne.21460. J Comp Neurol. 2007. PMID: 17701983 Free article.

3

Defects in neural stem cell proliferation and olfaction in Chd7 deficient mice indicate a mechanism for hyposmia in human CHARGE syndrome.

Layman WS, McEwen DP, Beyer LA, Lalani SR, Fernbach SD, Oh E, Swaroop A, Hegg CC, Raphael Y, Martens JR, Martin DM. Layman WS, et al. Among authors: martin dm. Hum Mol Genet. 2009 Jun 1;18(11):1909-23. doi: 10.1093/hmg/ddp112. Epub 2009 Mar 11. Hum Mol Genet. 2009. PMID: 19279158 Free PMC article.

4

Chromodomain proteins in development: lessons from CHARGE syndrome.

Layman WS, Hurd EA, Martin DM. Layman WS, et al. Among authors: martin dm. Clin Genet. 2010 Jul;78(1):11-20. doi: 10.1111/j.1399-0004.2010.01446.x. Epub 2010 Apr 8. Clin Genet. 2010. PMID: 20507341 Free PMC article. Review.

5

Reproductive dysfunction and decreased GnRH neurogenesis in a mouse model of CHARGE syndrome.

Layman WS, Hurd EA, Martin DM. Layman WS, et al. Among authors: martin dm. Hum Mol Genet. 2011 Aug 15;20(16):3138-50. doi: 10.1093/hmg/ddr216. Epub 2011 May 19. Hum Mol Genet. 2011. PMID: 21596839 Free PMC article.

6

Mature middle and inner ears express Chd7 and exhibit distinctive pathologies in a mouse model of CHARGE syndrome.

Hurd EA, Adams ME, Layman WS, Swiderski DL, Beyer LA, Halsey KE, Benson JM, Gong TW, Dolan DF, Raphael Y, Martin DM. Hurd EA, et al. Among authors: martin dm. Hear Res. 2011 Dec;282(1-2):184-95. doi: 10.1016/j.heares.2011.08.005. Epub 2011 Aug 23. Hear Res. 2011. PMID: 21875659 Free PMC article.

7

Delayed fusion and altered gene expression contribute to semicircular canal defects in Chd7 deficient mice.

Hurd EA, Micucci JA, Reamer EN, Martin DM. Hurd EA, et al. Among authors: martin dm. Mech Dev. 2012 Sep-Dec;129(9-12):308-23. doi: 10.1016/j.mod.2012.06.002. Epub 2012 Jun 15. Mech Dev. 2012. PMID: 22705977 Free PMC article.

8

CHD7 and retinoic acid signaling cooperate to regulate neural stem cell and inner ear development in mouse models of CHARGE syndrome.

Micucci JA, Layman WS, Hurd EA, Sperry ED, Frank SF, Durham MA, Swiderski DL, Skidmore JM, Scacheri PC, Raphael Y, Martin DM. Micucci JA, et al. Among authors: martin dm. Hum Mol Genet. 2014 Jan 15;23(2):434-48. doi: 10.1093/hmg/ddt435. Epub 2013 Sep 10. Hum Mol Genet. 2014. PMID: 24026680 Free PMC article.

9

The chromatin remodeling protein CHD7, mutated in CHARGE syndrome, is necessary for proper craniofacial and tracheal development.

Sperry ED, Hurd EA, Durham MA, Reamer EN, Stein AB, Martin DM. Sperry ED, et al. Among authors: martin dm. Dev Dyn. 2014 Sep;243(9):1055-66. doi: 10.1002/dvdy.24156. Epub 2014 Jul 10. Dev Dyn. 2014. PMID: 24975120 Free PMC article.

10

CHD7 mutations and CHARGE syndrome in semicircular canal dysplasia.

Green GE, Huq FS, Emery SB, Mukherji SK, Martin DM. Green GE, et al. Among authors: martin dm. Otol Neurotol. 2014 Sep;35(8):1466-70. doi: 10.1097/MAO.0000000000000260. Otol Neurotol. 2014. PMID: 24979395 Free PMC article.

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