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Results: 1 to 20 of 101

1.

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
2.

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
3.

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
4.

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]
5.

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
6.

Palmitoylation-dependent neurodevelopmental deficits in a mouse model of 22q11 microdeletion.

Mukai J, Dhilla A, Drew LJ, Stark KL, Cao L, MacDermott AB, Karayiorgou M, Gogos JA.

Nat Neurosci. 2008 Nov;11(11):1302-10. doi: 10.1038/nn.2204. Epub 2008 Oct 5.

PMID:
18836441
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome.

Prasad SE, Howley S, Murphy KC.

Dev Disabil Res Rev. 2008;14(1):26-34. doi: 10.1002/ddrr.5. Review.

PMID:
18636634
[PubMed - indexed for MEDLINE]
8.

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
9.

A comprehensive analysis of 22q11 gene expression in the developing and adult brain.

Maynard TM, Haskell GT, Peters AZ, Sikich L, Lieberman JA, LaMantia AS.

Proc Natl Acad Sci U S A. 2003 Nov 25;100(24):14433-8. Epub 2003 Nov 12.

PMID:
14614146
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Patient with a 22q11.2 deletion with no overlap of the minimal DiGeorge syndrome critical region (MDGCR).

McQuade L, Christodoulou J, Budarf M, Sachdev R, Wilson M, Emanuel B, Colley A.

Am J Med Genet. 1999 Sep 3;86(1):27-33.

PMID:
10440825
[PubMed - indexed for MEDLINE]
11.

Unraveling the genetic and developmental mysteries of 22q11 deletion syndrome.

Yamagishi H, Srivastava D.

Trends Mol Med. 2003 Sep;9(9):383-9. Review.

PMID:
13129704
[PubMed - indexed for MEDLINE]
12.

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]
13.

Der(22) syndrome and velo-cardio-facial syndrome/DiGeorge syndrome share a 1.5-Mb region of overlap on chromosome 22q11.

Funke B, Edelmann L, McCain N, Pandita RK, Ferreira J, Merscher S, Zohouri M, Cannizzaro L, Shanske A, Morrow BE.

Am J Hum Genet. 1999 Mar;64(3):747-58.

PMID:
10053009
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

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]
15.
16.

Isolation and characterization of a gene from the DiGeorge chromosomal region homologous to the mouse Tbx1 gene.

Chieffo C, Garvey N, Gong W, Roe B, Zhang G, Silver L, Emanuel BS, Budarf ML.

Genomics. 1997 Aug 1;43(3):267-77.

PMID:
9268629
[PubMed - indexed for MEDLINE]
17.

Deletion of 22q11 in two brothers with different phenotype.

Kasprzak L, Der Kaloustian VM, Elliott AM, Shevell M, Lejtenyi C, Eydoux P.

Am J Med Genet. 1998 Jan 23;75(3):288-91.

PMID:
9475599
[PubMed - indexed for MEDLINE]
18.

The clinical, immunological, and molecular spectrum of chromosome 22q11.2 deletion syndrome and DiGeorge syndrome.

Sullivan KE.

Curr Opin Allergy Clin Immunol. 2004 Dec;4(6):505-12. Review.

PMID:
15640691
[PubMed - indexed for MEDLINE]
19.

Differential gene expression in the hippocampus of the Df1/+ mice: a model for 22q11.2 deletion syndrome and schizophrenia.

Sivagnanasundaram S, Fletcher D, Hubank M, Illingworth E, Skuse D, Scambler P.

Brain Res. 2007 Mar 30;1139:48-59. Epub 2007 Jan 10.

PMID:
17292336
[PubMed - indexed for MEDLINE]
20.

Chromosome 22q11.2 deletion syndrome: DiGeorge syndrome/velocardiofacial Syndrome.

Sullivan KE.

Immunol Allergy Clin North Am. 2008 May;28(2):353-66. doi: 10.1016/j.iac.2008.01.003. Review.

PMID:
18424337
[PubMed - indexed for MEDLINE]

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