PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES (disorder)

Known as: Holoprosencephaly 9, HPE9, HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES 
 
National Institutes of Health

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Highly Cited
2010
Highly Cited
2010
Variation is an intrinsic feature of biological systems, yet developmental biology does not frequently address population-level… (More)
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2010
2010
BACKGROUND The Hedgehog (Hh) pathway provides inductive signals critical for developmental patterning of the brain and face. In… (More)
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2009
2009
Holoprosencephaly (HPE) is the most common congenital malformation of the forebrain in human. Several genes with essential roles… (More)
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2009
2009
Holoprosencephaly (HPE) is the most frequently observed human embryonic forebrain defect. Recent evidence indicates that the two… (More)
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2008
2008
The putative transcription factor ZIC2 is associated with a defect of forebrain development, known as Holoprosencephaly (HPE), in… (More)
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2008
2008
Holoprosencephaly (HPE) is the most common human congenital forebrain defect, affecting specification of forebrain tissue and… (More)
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2004
2004
Mutations of the developmental gene Sonic hedgehog (SHH) and alterations of SHH signaling have been associated with… (More)
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2003
2003
Holoprosencephaly (HPE) is a common forebrain malformation associated with mental retardation and craniofacial anomalies… (More)
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2002
2002
Holoprosencephaly (HPE) is a condition characterized by a defect in the development of the midline embryonic forebrain. When… (More)
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2000
2000
The homeodomain protein TGIF represses transcription in part by recruiting histone deacetylases. TGIF binds directly to DNA to… (More)
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