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DLX6 gene
Known as:
DISTAL-LESS HOMEOBOX 6
, DLX6
National Institutes of Health
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Related topics
Related topics
5 relations
DLX1 gene
DLX2 gene
DLX3 gene
DLX4 gene
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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
D. Volk
,
J. R. Edelson
,
D. Lewis
Schizophrenia Research
2016
Corpus ID: 33154223
Dysfunction of prefrontal cortex (PFC) inhibitory neurons that express the calcium-binding protein parvalbumin or the…
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Highly Cited
2015
Highly Cited
2015
Expression of long non-coding RNA DLX6-AS1 in lung adenocarcinoma
Juan Li
,
P. Li
,
+10 authors
G. Zhang
Cancer Cell International
2015
Corpus ID: 590853
BackgroundLung adenocarcinoma (LAC), the primary histological type of non-small cell lung cancer (NSCLC), has displayed an…
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Highly Cited
2011
Highly Cited
2011
Downregulation of Dlx5 and Dlx6 expression by Hand2 is essential for initiation of tongue morphogenesis
F. Barron
,
Crystal Woods
,
K. Kuhn
,
Jonathan Bishop
,
M. Howard
,
D. Clouthier
Development
2011
Corpus ID: 15529569
Lower jaw development is a complex process in which multiple signaling cascades establish a proximal-distal organization. These…
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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.
Kamal Bouhali
,
A. Dipietromaria
,
+6 authors
G. Levi
Human molecular genetics
2011
Corpus ID: 14631577
Primary ovarian insufficiency (POI) is characterized by the loss of ovarian function before the age of 40 in humans. Although…
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2010
2010
Expression analysis and mutation detection of DLX5 and DLX6 in autism
N. Nakashima
,
T. Yamagata
,
M. Mori
,
M. Kuwajima
,
M. Momoi
Brain and Development
2010
Corpus ID: 140205274
Linkage analysis has reported the chromosomal region 7q21 to be related with autism. This region contains an imprinting region…
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Highly Cited
2007
Highly Cited
2007
DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency.
B. Schüle
,
H. Li
,
C. Fisch-Kohl
,
C. Purmann
,
U. Francke
American journal of human genetics
2007
Corpus ID: 41333870
Mutations in MECP2 and Mecp2 (encoding methyl-CpG binding protein 2 [MeCP2]) cause distinct neurological phenotypes in humans and…
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2006
2006
Dlx5 and Dlx6 homeobox genes are required for specification of the mammalian vestibular apparatus
R. F. Robledo
,
T. Lufkin
Genesis
2006
Corpus ID: 24495075
The mammalian inner ear is a complex organ that develops from a surface ectoderm into distinct auditory and vestibular components…
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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
T. Zerucha
,
T. Stühmer
,
+7 authors
M. Ekker
The Journal of Neuroscience
2000
Corpus ID: 17675513
Four Dlx homeobox genes, Dlx1,Dlx2, Dlx5, and Dlx6 are expressed in the same primordia of the mouse forebrain with temporally…
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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.
M. Crackower
,
S. Scherer
,
+7 authors
L. Tsui
Human molecular genetics
1996
Corpus ID: 14434330
Split hand/split foot malformation (SHFM) is a heterogeneous limb developmental disorder, characterized by missing digits and…
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Highly Cited
1994
Highly Cited
1994
Cloning and characterization of two members of the vertebrate Dlx gene family.
A. Simeone
,
D. Acampora
,
+7 authors
K. Huebner
Proceedings of the National Academy of Sciences…
1994
Corpus ID: 11520164
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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