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Annarita Giliberti et al.
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Heterozygous loss-of-function variants of MEIS2 cause a triad of palatal defects, congenital heart defects, and intellectual disability
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EUROPEAN JOURNAL OF HUMAN GENETICS (2019)
Pbx loss in cranial neural crest, unlike in epithelium, results in cleft palate only and a broader midface
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Genes and microRNAs associated with mouse cleft palate: A systematic review and bioinformatics analysis
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A unique stylopod patterning mechanism by Shox2-controlled osteogenesis
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Constitutively active mutation of ACVR1 in oral epithelium causes submucous cleft palate in mice
Kazuo Noda et al.
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Retinoic acid signalling in the development of the epidermis, the limbs and the secondary palate
Aysel Mammadova et al.
DIFFERENTIATION (2016)
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Meis2 is essential for cranial and cardiac neural crest development
Ondrej Machon et al.
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Hoxa2 Selectively Enhances Meis Binding to Change a Branchial Arch Ground State
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HISAT: a fast spliced aligner with low memory requirements
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Haploinsufficiency of MEIS2 is associated with orofacial clefting and learning disability
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PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2014)
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Generation of Shox2-Cre allele for tissue specific manipulation of genes in the developing heart, palate, and limb
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Tbx22null mice have a submucous cleft palate due to reduced palatal bone formation and also display ankyloglossia and choanal atresia phenotypes
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HUMAN MOLECULAR GENETICS (2009)
Mice with an anterior cleft of the palate survive neonatal lethality
Shuping Gu et al.
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GENOME BIOLOGY (2008)
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Shox2-deficient mice exhibit a rare type of incomplete clefting of the secondary palate
L Yu et al.
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Runx2 regulates FGF2-induced Bmp2 expression during cranial bone development
KY Choi et al.
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MEIS C termini harbor transcriptional activation domains that respond to cell signaling
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