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Results: 1 to 20 of 155

1.

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]
2.

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]
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.

Microarray analysis of the Df1 mouse model of the 22q11 deletion syndrome.

Prescott K, Ivins S, Hubank M, Lindsay E, Baldini A, Scambler P.

Hum Genet. 2005 May;116(6):486-96. Epub 2005 Mar 19.

PMID:
15778864
[PubMed - indexed for MEDLINE]
5.

Goosecoid-like, a gene deleted in DiGeorge and velocardiofacial syndromes, recognizes DNA with a bicoid-like specificity and is expressed in the developing mouse brain.

Gottlieb S, Hanes SD, Golden JA, Oakey RJ, Budarf ML.

Hum Mol Genet. 1998 Sep;7(9):1497-505.

PMID:
9700206
[PubMed - indexed for MEDLINE]
Free Article
6.

Goosecoid-like (Gscl), a candidate gene for velocardiofacial syndrome, is not essential for normal mouse development.

Saint-Jore B, Puech A, Heyer J, Lin Q, Raine C, Kucherlapati R, Skoultchi AI.

Hum Mol Genet. 1998 Nov;7(12):1841-9.

PMID:
9811927
[PubMed - indexed for MEDLINE]
Free Article
7.

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]
8.

The murine homologue of HIRA, a DiGeorge syndrome candidate gene, is expressed in embryonic structures affected in human CATCH22 patients.

Wilming LG, Snoeren CA, van Rijswijk A, Grosveld F, Meijers C.

Hum Mol Genet. 1997 Feb;6(2):247-58.

PMID:
9063745
[PubMed - indexed for MEDLINE]
Free Article
9.

Dynamic changes in gene expression profiles of 22q11 and related orthologous genes during mouse development.

Amati F, Biancolella M, Farcomeni A, Giallonardi S, Bueno S, Minella D, Vecchione L, Chillemi G, Desideri A, Novelli G.

Gene. 2007 Apr 15;391(1-2):91-102. Epub 2007 Jan 19.

PMID:
17321697
[PubMed - indexed for MEDLINE]
10.

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
11.

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]
12.

Functional analysis of Gscl in the pathogenesis of the DiGeorge and velocardiofacial syndromes.

Wakamiya M, Lindsay EA, Rivera-PĂ©rez JA, Baldini A, Behringer RR.

Hum Mol Genet. 1998 Nov;7(12):1835-40.

PMID:
9811926
[PubMed - indexed for MEDLINE]
Free Article
13.

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
14.

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
15.

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]
16.

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
17.

Recovery from arterial growth delay reduces penetrance of cardiovascular defects in mice deleted for the DiGeorge syndrome region.

Lindsay EA, Baldini A.

Hum Mol Genet. 2001 Apr 15;10(9):997-1002.

PMID:
11309372
[PubMed - indexed for MEDLINE]
Free Article
18.

Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome.

Guris DL, Fantes J, Tara D, Druker BJ, Imamoto A.

Nat Genet. 2001 Mar;27(3):293-8.

PMID:
11242111
[PubMed - indexed for MEDLINE]
19.

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]
20.

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]

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