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DLX6 gene

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

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Dysfunction of prefrontal cortex (PFC) inhibitory neurons that express the calcium-binding protein parvalbumin or the… Expand
Highly Cited
2015
Highly Cited
2015
BackgroundLung adenocarcinoma (LAC), the primary histological type of non-small cell lung cancer (NSCLC), has displayed an… Expand
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Highly Cited
2011
Highly Cited
2011
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
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
Linkage analysis has reported the chromosomal region 7q21 to be related with autism. This region contains an imprinting region… Expand
Highly Cited
2007
Highly Cited
2007
Mutations in MECP2 and Mecp2 (encoding methyl-CpG binding protein 2 [MeCP2]) cause distinct neurological phenotypes in humans and… Expand
2006
2006
The mammalian inner ear is a complex organ that develops from a surface ectoderm into distinct auditory and vestibular components… Expand
Highly Cited
2000
Highly Cited
2000
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
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
A number of vertebrate genes of the Dlx gene family have been cloned in mouse, frog, and zebrafish. These genes contain a… Expand