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DLX6 gene

Known as: DISTAL-LESS HOMEOBOX 6, DLX6 
National Institutes of Health

Related topics

Related topics

5 relations
DLX1 geneDLX2 geneDLX3 geneDLX4 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Altered expression of developmental regulators of parvalbumin and somatostatin neurons in the prefrontal cortex in schizophrenia
Highly Cited
2011
Highly Cited
2011
Downregulation of Dlx5 and Dlx6 expression by Hand2 is essential for initiation of tongue morphogenesis
Lower jaw development is a complex process in which multiple signaling cascades establish a proximal-distal organization. These… 
2010
2010
Expression analysis and mutation detection of DLX5 and DLX6 in autism
2009
2009
Deletion of an enhancer near DLX5 and DLX6 in a family with hearing loss, craniofacial defects, and an inv(7)(q21.3q35)
Precisely regulated temporal and spatial patterns of gene expression are essential for proper human development. Cis-acting… 
Highly Cited
2007
Highly Cited
2007
DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency.
Mutations in MECP2 and Mecp2 (encoding methyl-CpG binding protein 2 [MeCP2]) cause distinct neurological phenotypes in humans and… 
Highly Cited
2006
Highly Cited
2006
Dlx5 and Dlx6 homeobox genes are required for specification of the mammalian vestibular apparatus
The mammalian inner ear is a complex organ that develops from a surface ectoderm into distinct auditory and vestibular components… 
2004
2004
Temporal requirement of signaling cascade involving endothelin-1/endothelin receptor type A in branchial arch development
Highly Cited
2000
Highly Cited
2000
A Highly Conserved Enhancer in the Dlx5/Dlx6Intergenic Region is the Site of Cross-Regulatory Interactions betweenDlx Genes in the Embryonic Forebrain
Four Dlx homeobox genes, Dlx1,Dlx2, Dlx5, and Dlx6 are expressed in the same primordia of the mouse forebrain with temporally… 
Highly Cited
1996
Highly Cited
1996
Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development.
Split hand/split foot malformation (SHFM) is a heterogeneous limb developmental disorder, characterized by missing digits and… 
Highly Cited
1994
Highly Cited
1994
Cloning and characterization of two members of the vertebrate Dlx gene family.
A number of vertebrate genes of the Dlx gene family have been cloned in mouse, frog, and zebrafish. These genes contain a… 
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