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Items: 18

1.

CHD7 represses the retinoic acid synthesis enzyme ALDH1A3 during inner ear development.

Yao H, Hill SF, Skidmore JM, Sperry ED, Swiderski DL, Sanchez GJ, Bartels CF, Raphael Y, Scacheri PC, Iwase S, Martin DM.

JCI Insight. 2018 Feb 22;3(4). pii: 97440. doi: 10.1172/jci.insight.97440. eCollection 2018 Feb 22.

2.

Genetic analysis of CHARGE syndrome identifies overlapping molecular biology.

Moccia A, Srivastava A, Skidmore JM, Bernat JA, Wheeler M, Chong JX, Nickerson D, Bamshad M, Hefner MA, Martin DM, Bielas SL.

Genet Med. 2018 Sep;20(9):1022-1029. doi: 10.1038/gim.2017.233. Epub 2018 Jan 4.

3.

Genetic specification of left-right asymmetry in the diaphragm muscles and their motor innervation.

Charoy C, Dinvaut S, Chaix Y, Morlé L, Sanyas I, Bozon M, Kindbeiter K, Durand B, Skidmore JM, De Groef L, Seki M, Moons L, Ruhrberg C, Martin JF, Martin DM, Falk J, Castellani V.

Elife. 2017 Jun 22;6. pii: e18481. doi: 10.7554/eLife.18481.

4.

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.

Hum Mol Genet. 2014 Jan 15;23(2):434-48. doi: 10.1093/hmg/ddt435. Epub 2013 Sep 10.

5.

Pleiotropic and isoform-specific functions for Pitx2 in superior colliculus and hypothalamic neuronal development.

Waite MR, Skidmore JM, Micucci JA, Shiratori H, Hamada H, Martin JF, Martin DM.

Mol Cell Neurosci. 2013 Jan;52:128-39. doi: 10.1016/j.mcn.2012.11.007. Epub 2012 Nov 10.

6.

Disruption of RAB40AL function leads to Martin--Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorder.

Bedoyan JK, Schaibley VM, Peng W, Bai Y, Mondal K, Shetty AC, Durham M, Micucci JA, Dhiraaj A, Skidmore JM, Kaplan JB, Skinner C, Schwartz CE, Antonellis A, Zwick ME, Cavalcoli JD, Li JZ, Martin DM.

J Med Genet. 2012 May;49(5):332-40. doi: 10.1136/jmedgenet-2011-100575.

7.

Distinct populations of GABAergic neurons in mouse rhombomere 1 express but do not require the homeodomain transcription factor PITX2.

Waite MR, Skaggs K, Kaviany P, Skidmore JM, Causeret F, Martin JF, Martin DM.

Mol Cell Neurosci. 2012 Jan;49(1):32-43. doi: 10.1016/j.mcn.2011.08.011. Epub 2011 Sep 10.

8.

A novel TaulacZ allele reveals a requirement for Pitx2 in formation of the mammillothalamic tract.

Skidmore JM, Waite MR, Alvarez-Bolado G, Puelles L, Martin DM.

Genesis. 2012 Jan;50(1):67-73. doi: 10.1002/dvg.20793. Epub 2012 Jan 6.

9.

GABAergic and glutamatergic identities of developing midbrain Pitx2 neurons.

Waite MR, Skidmore JM, Billi AC, Martin JF, Martin DM.

Dev Dyn. 2011 Feb;240(2):333-46. doi: 10.1002/dvdy.22532. Epub 2011 Jan 11.

10.

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.

Mol Cell Neurosci. 2008 Apr;37(4):696-707. doi: 10.1016/j.mcn.2007.12.015. Epub 2007 Dec 15.

11.

Characterization of progenitor domains in the developing mouse thalamus.

Vue TY, Aaker J, Taniguchi A, Kazemzadeh C, Skidmore JM, Martin DM, Martin JF, Treier M, Nakagawa Y.

J Comp Neurol. 2007 Nov 1;505(1):73-91.

12.

Nestin-Cre mediated deletion of Pitx2 in the mouse.

Sclafani AM, Skidmore JM, Ramaprakash H, Trumpp A, Gage PJ, Martin DM.

Genesis. 2006 Jul;44(7):336-44.

13.
14.

PITX2 is required for normal development of neurons in the mouse subthalamic nucleus and midbrain.

Martin DM, Skidmore JM, Philips ST, Vieira C, Gage PJ, Condie BG, Raphael Y, Martinez S, Camper SA.

Dev Biol. 2004 Mar 1;267(1):93-108.

15.

Nestin-lineage cells contribute to the microvasculature but not endocrine cells of the islet.

Treutelaar MK, Skidmore JM, Dias-Leme CL, Hara M, Zhang L, Simeone D, Martin DM, Burant CF.

Diabetes. 2003 Oct;52(10):2503-12.

16.

Pitx2 distinguishes subtypes of terminally differentiated neurons in the developing mouse neuroepithelium.

Martin DM, Skidmore JM, Fox SE, Gage PJ, Camper SA.

Dev Biol. 2002 Dec 1;252(1):84-99.

17.
18.

Polar clustering of the chemoreceptor complex in Escherichia coli occurs in the absence of complete CheA function.

Skidmore JM, Ellefson DD, McNamara BP, Couto MM, Wolfe AJ, Maddock JR.

J Bacteriol. 2000 Feb;182(4):967-73.

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