Found: 13
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Satb2, modularity, and the evolvability of the vertebrate jaw.
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- Evolution & Development, 2011, v. 13, n. 6, p. 549, doi. 10.1111/j.1525-142X.2011.00511.x
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- Article
Evolution of the Alx homeobox gene family: parallel retention and independent loss of the vertebrate Alx3 gene.
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- Evolution & Development, 2011, v. 13, n. 4, p. 343, doi. 10.1111/j.1525-142X.2011.00489.x
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- Article
OSVZ progenitors of human and ferret neocortex are epithelial-like and expand by integrin signaling.
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- Nature Neuroscience, 2010, v. 13, n. 6, p. 690, doi. 10.1038/nn.2553
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- Article
Developmental nonlinearity drives phenotypic robustness.
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- Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-02037-7
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- Article
Fgf8 dosage regulates jaw shape and symmetry through pharyngeal‐cardiac tissue relationships.
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- Developmental Dynamics, 2022, v. 251, n. 10, p. 1711, doi. 10.1002/dvdy.501
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- Article
Developmental processes regulate craniofacial variation in disease and evolution.
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- Genesis: The Journal of Genetics & Development, 2019, v. 57, n. 1, p. N.PAG, doi. 10.1002/dvg.23249
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- Article
Pax6 regulates craniofacial form through its control of an essential cephalic ectodermal patterning center.
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- Genesis: The Journal of Genetics & Development, 2011, v. 49, n. 4, p. 307, doi. 10.1002/dvg.20724
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- Article
Bone health in SATB2‐associated syndrome: Results from a large prospective cohort and recommendations for surveillance.
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- American Journal of Medical Genetics. Part A, 2024, v. 194, n. 2, p. 203, doi. 10.1002/ajmg.a.63421
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- Article
The society for craniofacial genetics and developmental biology 39th annual meeting.
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- American Journal of Medical Genetics. Part A, 2017, v. 173, n. 4, p. 985, doi. 10.1002/ajmg.a.38096
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- Article
SATB2-associated syndrome: Mechanisms, phenotype, and practical recommendations.
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- American Journal of Medical Genetics. Part A, 2017, v. 173, n. 2, p. 327, doi. 10.1002/ajmg.a.38022
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- Article
Mutation in Eftud2 causes craniofacial defects in mice via mis-splicing of Mdm2 and increased P53.
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- Human Molecular Genetics, 2021, v. 30, n. 9, p. 739, doi. 10.1093/hmg/ddab051
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- Article
Abnormalities in pharyngeal arch‐derived structures in SATB2‐associated syndrome.
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- Clinical Genetics, 2024, v. 106, n. 2, p. 209, doi. 10.1111/cge.14540
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- Article
Growth, development, and phenotypic spectrum of individuals with deletions of 2q33.1 involving SATB2.
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- Clinical Genetics, 2021, v. 99, n. 4, p. 547, doi. 10.1111/cge.13912
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- Article