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Items: 1 to 20 of 37

1.

Neural transcription factors bias cleavage stage blastomeres to give rise to neural ectoderm.

Gaur S, Mandelbaum M, Herold M, Majumdar HD, Neilson KM, Maynard TM, Mood K, Daar IO, Moody SA.

Genesis. 2016 Jun;54(6):334-49. doi: 10.1002/dvg.22943.

PMID:
27092474
2.

Functional Divergence of the Nuclear Receptor NR2C1 as a Modulator of Pluripotentiality During Hominid Evolution.

Baker JL, Dunn KA, Mingrone J, Wood BA, Karpinski BA, Sherwood CC, Wildman DE, Maynard TM, Bielawski JP.

Genetics. 2016 Jun;203(2):905-22. doi: 10.1534/genetics.115.183889.

PMID:
27075724
3.

MicroRNAs Are Involved in the Development of Morphine-Induced Analgesic Tolerance and Regulate Functionally Relevant Changes in Serpini1.

Tapocik JD, Ceniccola K, Mayo CL, Schwandt ML, Solomon M, Wang BD, Luu TV, Olender J, Harrigan T, Maynard TM, Elmer GI, Lee NH.

Front Mol Neurosci. 2016 Mar 24;9:20. doi: 10.3389/fnmol.2016.00020.

4.

A cellular and molecular mosaic establishes growth and differentiation states for cranial sensory neurons.

Karpinski BA, A Bryan C, Paronett EM, Baker JL, Fernandez A, Horvath A, Maynard TM, Moody SA, LaMantia AS.

Dev Biol. 2016 Jul 15;415(2):228-41. doi: 10.1016/j.ydbio.2016.03.015.

PMID:
26988119
5.

Testicular receptor 2, Nr2c1, is associated with stem cells in the developing olfactory epithelium and other cranial sensory and skeletal structures.

Baker JL, Wood B, Karpinski BA, LaMantia AS, Maynard TM.

Gene Expr Patterns. 2016 Jan;20(1):71-9. doi: 10.1016/j.gep.2015.12.002.

6.

Hard to swallow: Developmental biological insights into pediatric dysphagia.

LaMantia AS, Moody SA, Maynard TM, Karpinski BA, Zohn IE, Mendelowitz D, Lee NH, Popratiloff A.

Dev Biol. 2016 Jan 15;409(2):329-42. doi: 10.1016/j.ydbio.2015.09.024. Review.

7.

Modeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit development.

Meechan DW, Maynard TM, Tucker ES, Fernandez A, Karpinski BA, Rothblat LA, LaMantia AS.

Prog Neurobiol. 2015 Jul;130:1-28. doi: 10.1016/j.pneurobio.2015.03.004. Review.

8.

Ranbp1, Deleted in DiGeorge/22q11.2 Deletion Syndrome, is a Microcephaly Gene That Selectively Disrupts Layer 2/3 Cortical Projection Neuron Generation.

Paronett EM, Meechan DW, Karpinski BA, LaMantia AS, Maynard TM.

Cereb Cortex. 2015 Oct;25(10):3977-93. doi: 10.1093/cercor/bhu285.

9.

Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome.

Karpinski BA, Maynard TM, Fralish MS, Nuwayhid S, Zohn IE, Moody SA, LaMantia AS.

Dis Model Mech. 2014 Feb;7(2):245-57. doi: 10.1242/dmm.012484.

10.

Cognitive ability is associated with altered medial frontal cortical circuits in the LgDel mouse model of 22q11.2DS.

Meechan DW, Rutz HL, Fralish MS, Maynard TM, Rothblat LA, LaMantia AS.

Cereb Cortex. 2015 May;25(5):1143-51. doi: 10.1093/cercor/bht308.

11.

On becoming neural: what the embryo can tell us about differentiating neural stem cells.

Moody SA, Klein SL, Karpinski BA, Maynard TM, Lamantia AS.

Am J Stem Cells. 2013 Jun 30;2(2):74-94.

12.

Cxcr4 regulation of interneuron migration is disrupted in 22q11.2 deletion syndrome.

Meechan DW, Tucker ES, Maynard TM, LaMantia AS.

Proc Natl Acad Sci U S A. 2012 Nov 6;109(45):18601-6. doi: 10.1073/pnas.1211507109.

13.

22q11 Gene dosage establishes an adaptive range for sonic hedgehog and retinoic acid signaling during early development.

Maynard TM, Gopalakrishna D, Meechan DW, Paronett EM, Newbern JM, LaMantia AS.

Hum Mol Genet. 2013 Jan 15;22(2):300-12. doi: 10.1093/hmg/dds429.

14.

Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome.

Manzini MC, Tambunan DE, Hill RS, Yu TW, Maynard TM, Heinzen EL, Shianna KV, Stevens CR, Partlow JN, Barry BJ, Rodriguez J, Gupta VA, Al-Qudah AK, Eyaid WM, Friedman JM, Salih MA, Clark R, Moroni I, Mora M, Beggs AH, Gabriel SB, Walsh CA.

Am J Hum Genet. 2012 Sep 7;91(3):541-7. doi: 10.1016/j.ajhg.2012.07.009.

15.

Three phases of DiGeorge/22q11 deletion syndrome pathogenesis during brain development: patterning, proliferation, and mitochondrial functions of 22q11 genes.

Meechan DW, Maynard TM, Tucker ES, LaMantia AS.

Int J Dev Neurosci. 2011 May;29(3):283-94. doi: 10.1016/j.ijdevneu.2010.08.005. Review.

16.

Comt1 genotype and expression predicts anxiety and nociceptive sensitivity in inbred strains of mice.

Segall SK, Nackley AG, Diatchenko L, Lariviere WR, Lu X, Marron JS, Grabowski-Boase L, Walker JR, Slade G, Gauthier J, Bailey JS, Steffy BM, Maynard TM, Tarantino LM, Wiltshire T.

Genes Brain Behav. 2010 Nov;9(8):933-46. doi: 10.1111/j.1601-183X.2010.00633.x.

17.

Specific mesenchymal/epithelial induction of olfactory receptor, vomeronasal, and gonadotropin-releasing hormone (GnRH) neurons.

Rawson NE, Lischka FW, Yee KK, Peters AZ, Tucker ES, Meechan DW, Zirlinger M, Maynard TM, Burd GB, Dulac C, Pevny L, LaMantia AS.

Dev Dyn. 2010 Jun;239(6):1723-38. doi: 10.1002/dvdy.22315.

18.

Developmental and degenerative features in a complicated spastic paraplegia.

Manzini MC, Rajab A, Maynard TM, Mochida GH, Tan WH, Nasir R, Hill RS, Gleason D, Al Saffar M, Partlow JN, Barry BJ, Vernon M, LaMantia AS, Walsh CA.

Ann Neurol. 2010 Apr;67(4):516-25. doi: 10.1002/ana.21923.

19.

Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome.

Meechan DW, Tucker ES, Maynard TM, LaMantia AS.

Proc Natl Acad Sci U S A. 2009 Sep 22;106(38):16434-45. doi: 10.1073/pnas.0905696106.

20.

Mitochondrial localization and function of a subset of 22q11 deletion syndrome candidate genes.

Maynard TM, Meechan DW, Dudevoir ML, Gopalakrishna D, Peters AZ, Heindel CC, Sugimoto TJ, Wu Y, Lieberman JA, Lamantia AS.

Mol Cell Neurosci. 2008 Nov;39(3):439-51. doi: 10.1016/j.mcn.2008.07.027.

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