Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 113

1.

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. Epub 2010 Sep 15. Review.

PMID:
20833244
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

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. Epub 2009 Sep 10.

PMID:
19805316
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

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. Epub 2008 Aug 15.

PMID:
18775783
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

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

Meechan DW, Maynard TM, Gopalakrishna D, Wu Y, LaMantia AS.

Gene Expr. 2007;13(6):299-310. Review.

PMID:
17708416
[PubMed - indexed for MEDLINE]
5.

Gene dosage in the developing and adult brain in a mouse model of 22q11 deletion syndrome.

Meechan DW, Maynard TM, Wu Y, Gopalakrishna D, Lieberman JA, LaMantia AS.

Mol Cell Neurosci. 2006 Dec;33(4):412-28. Epub 2006 Nov 13.

PMID:
17097888
[PubMed - indexed for MEDLINE]
6.

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. Epub 2012 Oct 16.

PMID:
23077214
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients.

Guo T, McDonald-McGinn D, Blonska A, Shanske A, Bassett AS, Chow E, Bowser M, Sheridan M, Beemer F, Devriendt K, Swillen A, Breckpot J, Digilio MC, Marino B, Dallapiccola B, Carpenter C, Zheng X, Johnson J, Chung J, Higgins AM, Philip N, Simon TJ, Coleman K, Heine-Suner D, Rosell J, Kates W, Devoto M, Goldmuntz E, Zackai E, Wang T, Shprintzen R, Emanuel B, Morrow B; International Chromosome 22q11.2 Consortium.

Hum Mutat. 2011 Nov;32(11):1278-89. doi: 10.1002/humu.21568. Epub 2011 Sep 16.

PMID:
21796729
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Altered expression of hippocampal dentate granule neuron genes in a mouse model of human 22q11 deletion syndrome.

Jurata LW, Gallagher P, Lemire AL, Charles V, Brockman JA, Illingworth EL, Altar CA.

Schizophr Res. 2006 Dec;88(1-3):251-9. Epub 2006 Sep 26.

PMID:
17008057
[PubMed - indexed for MEDLINE]
9.

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

Maynard TM, Haskell GT, Lieberman JA, LaMantia AS.

Int J Dev Neurosci. 2002 Jun-Aug;20(3-5):407-19. Review.

PMID:
12175881
[PubMed - indexed for MEDLINE]
10.

The 22q11 deletion: DiGeorge and velocardiofacial syndromes and the role of TBX1.

Papangeli I, Scambler P.

Wiley Interdiscip Rev Dev Biol. 2013 May-Jun;2(3):393-403. doi: 10.1002/wdev.75. Epub 2012 Jun 19.

PMID:
23799583
[PubMed - indexed for MEDLINE]
11.

The 22q11.2 deletion syndrome: a gene dosage perspective.

Baldini A.

ScientificWorldJournal. 2006 May 1;6:1881-7. Review.

PMID:
17205194
[PubMed - indexed for MEDLINE]
Free Article
12.

Refining the 22q11.2 deletion breakpoints in DiGeorge syndrome by aCGH.

Bittel DC, Yu S, Newkirk H, Kibiryeva N, Holt A 3rd, Butler MG, Cooley LD.

Cytogenet Genome Res. 2009;124(2):113-20. doi: 10.1159/000207515. Epub 2009 May 5.

PMID:
19420922
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

[Cerebral polymicrogyria and 22q11 deletion syndrome].

Arriola-Pereda G, Verdú-Pérez A, de Castro-De Castro P.

Rev Neurol. 2009 Feb 16-28;48(4):188-90. Spanish.

PMID:
19226486
[PubMed - indexed for MEDLINE]
Free Article
14.

Analyses of the associations between the genes of 22q11 deletion syndrome and schizophrenia.

Arinami T.

J Hum Genet. 2006;51(12):1037-45. Epub 2006 Sep 13. Review.

PMID:
16969581
[PubMed - indexed for MEDLINE]
15.

22q11.2 deletion syndrome: genetics, neuroanatomy and cognitive/behavioral features keywords.

Antshel KM, Kates WR, Roizen N, Fremont W, Shprintzen RJ.

Child Neuropsychol. 2005 Feb;11(1):5-19. Review.

PMID:
15823980
[PubMed - indexed for MEDLINE]
16.

Molecular mechanisms in 22q11 deletion syndrome.

Williams NM.

Schizophr Bull. 2011 Sep;37(5):882-9. doi: 10.1093/schbul/sbr095. Review.

PMID:
21860033
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

[Scoliosis in children with chromosome 22q11.2 deletion syndrome].

Colo D, Kruyt MC, Timmers-Raaijmaakers BC, Castelein RM.

Ned Tijdschr Geneeskd. 2012;156(4):A4298. Dutch.

PMID:
22278037
[PubMed - indexed for MEDLINE]
18.

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. Epub 2013 Dec 19.

PMID:
24357327
[PubMed - in process]
Free PMC Article
19.

22q11 deletion syndrome: is that what they used to call . . . ?

Umlauf MG.

Perspect Psychiatr Care. 2008 Oct;44(4):259-66. doi: 10.1111/j.1744-6163.2008.00185.x.

PMID:
18826464
[PubMed - indexed for MEDLINE]
20.

Phenotypic variability of atypical 22q11.2 deletions not including TBX1.

Verhagen JM, Diderich KE, Oudesluijs G, Mancini GM, Eggink AJ, Verkleij-Hagoort AC, Groenenberg IA, Willems PJ, du Plessis FA, de Man SA, Srebniak MI, van Opstal D, Hulsman LO, van Zutven LJ, Wessels MW.

Am J Med Genet A. 2012 Oct;158A(10):2412-20. doi: 10.1002/ajmg.a.35517. Epub 2012 Aug 14.

PMID:
22893440
[PubMed - indexed for MEDLINE]

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk