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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
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Papers overview

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2015
2015
Expression of long non-coding RNA DLX6-AS1 in lung adenocarcinoma
BackgroundLung adenocarcinoma (LAC), the primary histological type of non-small cell lung cancer (NSCLC), has displayed an… Expand
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2011
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… Expand
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2011
2011
Allelic reduction of Dlx5 and Dlx6 results in early follicular depletion: a new mouse model of primary ovarian insufficiency.
Primary ovarian insufficiency (POI) is characterized by the loss of ovarian function before the age of 40 in humans. Although… Expand
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2010
2010
Expression analysis and mutation detection of DLX5 and DLX6 in autism
Linkage analysis has reported the chromosomal region 7q21 to be related with autism. This region contains an imprinting region… Expand
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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… Expand
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2007
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… Expand
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2006
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… Expand
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Highly Cited
2000
Highly Cited
2000
A highly conserved enhancer in the Dlx5/Dlx6 intergenic region is the site of cross-regulatory interactions between Dlx 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… Expand
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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… Expand
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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… Expand
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