Regulation of a remote Shh forebrain enhancer by the Six3 homeoprotein

Regulation of a remote Shh forebrain enhancer by the Six3 homeoprotein

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Bibliografiske detaljer
Main Authors:	Yongsu Jeong, Federico Coluccio Leskow, Kênia Balbi El-Jaick, Erich Roessler, Maximilian Muenke, Anastasia K. Yocum, Christèle Dubourg, Xue Li, Xin Geng, Guillermo Oliver, Douglas J. Epstein
Format:	Artigo
Sprog:	engelsk
Udgivet:	2008
Online adgang:	https://doi.org/10.1038/ng.230
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Lignende værker

Regulation of a remote Sonic hedgehog forebrain enhancer by the Six3 homeoprotein
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A functional screen for sonic hedgehog regulatory elements across a 1 Mb interval identifies long-range ventral forebrain enhancers
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The mutational spectrum of holoprosencephaly-associated changes within the<i>SHH</i>gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis
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Utilizing prospective sequence analysis of SHH, ZIC2, SIX3 and TGIF in holoprosencephaly probands to describe the parameters limiting the observed frequency of mutant gene × gene interactions
af: Erich Roessler, et al.
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Utilizing prospective sequence analysis of SHH, ZIC2, SIX3 and TGIF in holoprosencephaly probands to describe the parameters limiting the observed frequency of mutant gene x gene interactions
af: Roessler, Erich, et al.
Udgivet: (2012)

The Mutational Spectrum of Holoprosencephaly-Associated Changes within the SHH Gene in Humans Predicts Loss-of-Function Through Either Key Structural Alterations of the Ligand or Its Altered Synthesis
af: Roessler, Erich, et al.
Udgivet: (2009)

Current recommendations for the molecular evaluation of newly diagnosed holoprosencephaly patients
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Current recommendations for the molecular evaluation of newly diagnosed holoprosencephaly patients
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Mutations in the human SIX3 gene in holoprosencephaly are loss of function
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Evidence for SHH as a candidate gene for encephalocele
af: Bear, Kelly A., et al.
Udgivet: (2012)

Heterozygous mutations in SIX3 and SHH are associated with schizencephaly and further expand the clinical spectrum of holoprosencephaly
af: Ute Hehr, et al.
Udgivet: (2010)

Heterozygous mutations in SIX3 and SHH are associated with schizencephaly and further expand the clinical spectrum of holoprosencephaly
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Direct transcriptional regulation of Six6 is controlled by SoxB1 binding to a remote forebrain enhancer
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Udgivet: (2012)

Truncating loss-of-function mutations of DISP1 contribute to holoprosencephaly-like microform features in humans
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Clinical utility gene card for: Holoprosencephaly
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Truncating loss-of-function mutations of DISP1 contribute to holoprosencephaly-like microform features in humans
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Functional analysis of mutations in TGIF associated with holoprosencephaly
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Udgivet: (2006)

Missense substitutions in the GAS1 protein present in holoprosencephaly patients reduce the affinity for its ligand, SHH
af: Daniel Pineda‐Alvarez, et al.
Udgivet: (2011)

Missense substitutions in the GAS1 protein present in holoprosencephaly patients reduce the affinity for its ligand, SHH
af: Pineda-Alvarez, Daniel E., et al.
Udgivet: (2011)

Genetics of ventral forebrain development and holoprosencephaly
af: Maximilian Muenke
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Clinicopathological significance of homeoprotein Six1 in hepatocellular carcinoma
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Clinicopathological significance of homeoprotein Six1 in hepatocellular carcinoma
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Distinct regulators of<i>Shh</i>transcription in the floor plate and notochord indicate separate origins for these tissues in the mouse node
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The molecular genetics of holoprosencephaly
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The molecular genetics of holoprosencephaly
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Haploinsufficiency of Six3 fails to activate Sonic hedgehog expression in the ventral forebrain and causes holoprosencephaly
af: Geng, Xin, et al.
Udgivet: (2008)

Haploinsufficiency of Six3 Fails to Activate Sonic hedgehog Expression in the Ventral Forebrain and Causes Holoprosencephaly
af: Xin Geng, et al.
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The Six1 homeoprotein stimulates tumorigenesis by reactivation of cyclin A1
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Defining a role for the homeoprotein Six1 in EMT and mammary tumorigenesis
af: Radisky, Derek C.
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The Six1 homeoprotein stimulates tumorigenesis by reactivation of cyclin A1
af: Ricardo D. Coletta, et al.
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Homeoproteins Six1 and Six4 Regulate Male Sex Determination and Mouse Gonadal Development
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Cartilage homeoprotein 1, a homeoprotein selectively expressed in chondrocytes.
af: Zhao, G Q, et al.
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Cartilage homeoprotein 1, a homeoprotein selectively expressed in chondrocytes.
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Six1 homeoprotein drives myofiber type IIA specialization in soleus muscle
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Analysis of genotype–phenotype correlations in human holoprosencephaly
af: Benjamin D. Solomon, et al.
Udgivet: (2010)

Functional analysis of mutations in TGIF associated with holoprosencephaly
af: El-Jaick, Kenia B., et al.
Udgivet: (2006)

A Novel SIX3 Mutation Segregates With Holoprosencephaly in a Large Family
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The Physiology of Homeoprotein Transduction
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Analysis of Genotype-Phenotype Correlations in Human Holoprosencephaly
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The Full Spectrum of Holoprosencephaly-Associated Mutations within the ZIC2 Gene in Humans Predicts Loss-of-Function as the Predominant Disease Mechanism
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