Martin DM - Search Results

1

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.

2

Exclusion of PITX2 mutations as a major cause of CHARGE association.

Martin DM, Probst FJ, Fox SE, Schimmenti LA, Semina EV, Hefner MA, Belmont JW, Camper SA. Martin DM, et al. Am J Med Genet. 2002 Jul 22;111(1):27-30. doi: 10.1002/ajmg.10473. Am J Med Genet. 2002. PMID: 12124729 Free article.

3

Myo15 function is distinct from Myo6, Myo7a and pirouette genes in development of cochlear stereocilia.

Karolyi IJ, Probst FJ, Beyer L, Odeh H, Dootz G, Cha KB, Martin DM, Avraham KB, Kohrman D, Dolan DF, Raphael Y, Camper SA. Karolyi IJ, et al. Among authors: martin dm. Hum Mol Genet. 2003 Nov 1;12(21):2797-805. doi: 10.1093/hmg/ddg308. Epub 2003 Sep 9. Hum Mol Genet. 2003. PMID: 12966030

4

Loss of Chd7 function in gene-trapped reporter mice is embryonic lethal and associated with severe defects in multiple developing tissues.

Hurd EA, Capers PL, Blauwkamp MN, Adams ME, Raphael Y, Poucher HK, Martin DM. Hurd EA, et al. Among authors: martin dm. Mamm Genome. 2007 Feb;18(2):94-104. doi: 10.1007/s00335-006-0107-6. Epub 2007 Feb 28. Mamm Genome. 2007. PMID: 17334657

5

The 20th International Mammalian Genome Conference meeting report.

Hurd EA, Martin DM. Hurd EA, et al. Among authors: martin dm. Mamm Genome. 2007 Mar;18(3):145-53. doi: 10.1007/s00335-007-9005-9. Epub 2007 Apr 10. Mamm Genome. 2007. PMID: 17436036 No abstract available.

6

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.

7

Cre fate mapping reveals lineage specific defects in neuronal migration with loss of Pitx2 function in the developing mouse hypothalamus and subthalamic nucleus.

Skidmore JM, Cramer JD, Martin JF, Martin DM. Skidmore JM, et al. Among authors: martin jf, martin dm. Mol Cell Neurosci. 2008 Apr;37(4):696-707. doi: 10.1016/j.mcn.2007.12.015. Epub 2007 Dec 15. Mol Cell Neurosci. 2008. PMID: 18206388 Free PMC article.

8

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.

9

Molecular and phenotypic aspects of CHD7 mutation in CHARGE syndrome.

Zentner GE, Layman WS, Martin DM, Scacheri PC. Zentner GE, et al. Among authors: martin dm. Am J Med Genet A. 2010 Mar;152A(3):674-86. doi: 10.1002/ajmg.a.33323. Am J Med Genet A. 2010. PMID: 20186815 Free PMC article. Review.

10

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.

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