Maynard TM - Search Results

1

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. LaMantia AS, et al. Among authors: maynard tm. Dev Biol. 2016 Jan 15;409(2):329-42. doi: 10.1016/j.ydbio.2015.09.024. Epub 2015 Nov 7. Dev Biol. 2016. PMID: 26554723 Free PMC article. Review.

2

Neural development, cell-cell signaling, and the "two-hit" hypothesis of schizophrenia.

Maynard TM, Sikich L, Lieberman JA, LaMantia AS. Maynard TM, et al. Schizophr Bull. 2001;27(3):457-76. doi: 10.1093/oxfordjournals.schbul.a006887. Schizophr Bull. 2001. PMID: 11596847 Review.

3

High-resolution mapping of the Gli3 mutation extra-toes reveals a 51.5-kb deletion.

Maynard TM, Jain MD, Balmer CW, LaMantia AS. Maynard TM, et al. Mamm Genome. 2002 Jan;13(1):58-61. doi: 10.1007/s00335-001-2115-x. Mamm Genome. 2002. PMID: 11773971 No abstract available.

4

RanBP1, a velocardiofacial/DiGeorge syndrome candidate gene, is expressed at sites of mesenchymal/epithelial induction.

Maynard TM, Haskell GT, Bhasin N, Lee JM, Gassman AA, Lieberman JA, LaMantia AS. Maynard TM, et al. Mech Dev. 2002 Feb;111(1-2):177-80. doi: 10.1016/s0925-4773(01)00616-5. Mech Dev. 2002. PMID: 11804793 Free article.

5

22q11 DS: genomic mechanisms and gene function in DiGeorge/velocardiofacial syndrome.

Maynard TM, Haskell GT, Lieberman JA, LaMantia AS. Maynard TM, et al. Int J Dev Neurosci. 2002 Jun-Aug;20(3-5):407-19. doi: 10.1016/s0736-5748(02)00050-3. Int J Dev Neurosci. 2002. PMID: 12175881 Review.

6

Retinoic acid signaling at sites of plasticity in the mature central nervous system.

Thompson Haskell G, Maynard TM, Shatzmiller RA, Lamantia AS. Thompson Haskell G, et al. Among authors: maynard tm. J Comp Neurol. 2002 Oct 21;452(3):228-41. doi: 10.1002/cne.10369. J Comp Neurol. 2002. PMID: 12353219

7

No evidence for parental imprinting of mouse 22q11 gene orthologs.

Maynard TM, Meechan DW, Heindel CC, Peters AZ, Hamer RM, Lieberman JA, LaMantia AS. Maynard TM, et al. Mamm Genome. 2006 Aug;17(8):822-32. doi: 10.1007/s00335-006-0011-0. Epub 2006 Aug 4. Mamm Genome. 2006. PMID: 16897343 Free PMC article.

8

When half is not enough: gene expression and dosage in the 22q11 deletion syndrome.

Meechan DW, Maynard TM, Gopalakrishna D, Wu Y, LaMantia AS. Meechan DW, et al. Among authors: maynard tm. Gene Expr. 2007;13(6):299-310. doi: 10.3727/000000006781510697. Gene Expr. 2007. PMID: 17708416 Free PMC article. Review.

9

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. Meechan DW, et al. Among authors: maynard tm. Proc Natl Acad Sci U S A. 2009 Sep 22;106(38):16434-45. doi: 10.1073/pnas.0905696106. Epub 2009 Sep 10. Proc Natl Acad Sci U S A. 2009. PMID: 19805316 Free PMC article.

10

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. Manzini MC, et al. Among authors: maynard tm. Ann Neurol. 2010 Apr;67(4):516-25. doi: 10.1002/ana.21923. Ann Neurol. 2010. PMID: 20437587 Free PMC article.

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