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Mutations in the BMP pathway in mice support the existence of two molecular classes of holoprosencephaly.

Mutations in the BMP pathway in mice support the existence of two molecular classes of holoprosencephaly. Research Abstract Details 

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  • Mutations in the BMP pathway in mice support the existence of two molecular classes of holoprosencephaly. Abstract Text:

    marie fernandesMarie Fernandes,grigoriy gutinGrigoriy Gutin,heather alcornHeather Alcorn,susan k mcconnellSusan K McConnell,jean m Jean M ,marie fernandesMarie Fernandes,grigoriy gutinGrigoriy Gutin,heather alcornHeather Alcorn,susan k mcconnellSusan K McConnell,jean m Jean M ,marie fernandesMarie Fernandes,grigoriy gutinGrigoriy Gutin,heather alcornHeather Alcorn,susan k mcconnellSusan K McConnell,jean m Jean M ,

    Holoprosencephaly (HPE) is a devastating forebrain abnormality with a range of morphological defects characterized by loss of midline tissue. In the telencephalon, the embryonic precursor of the cerebral hemispheres, specialized cell types form a midline that separates the hemispheres. In the present study, deletion of the BMP receptor genes, Bmpr1b and Bmpr1a, in the mouse telencephalon results in a loss of all dorsal midline cell types without affecting the specification of cortical and ventral precursors. In the holoprosencephalic Shh(-/-) mutant, by contrast, ventral patterning is disrupted, whereas the dorsal midline initially forms. This suggests that two separate developmental mechanisms can underlie the ontogeny of HPE. The Bmpr1a;Bmpr1b mutant provides a model for a subclass of HPE in humans: midline inter-hemispheric HPE.

    Mutations in the BMP pathway in mice support the existence of two molecular classes of holoprosencephaly. Publishing Authors By Initials

    m fernandesM Fernandes,g gutinG Gutin,h alcornH Alcorn,sk mcconnellSK McConnell,jm JM ,m fernandesM Fernandes,g gutinG Gutin,h alcornH Alcorn,sk mcconnellSK McConnell,jm JM ,m fernandesM Fernandes,g gutinG Gutin,h alcornH Alcorn,sk mcconnellSK McConnell,jm JM ,

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    Mutations in the BMP pathway in mice support the existence of two molecular classes of holoprosencephaly. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Development (Cambridge, England)

    VOLUME: 134

    Page Numbers: 3789-94

    Journal Abbreviation: Development

    ISSN: 0950-1991

    DAY: 3

    MONTH: 10

    YEAR: 2007

    Mutations in the BMP pathway in mice support the existence of two molecular classes of holoprosencephaly. Information

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    LANGUAGE: eng

    NlmUniqueID: 8701744

    Mutations in the BMP pathway in mice support the existence of two molecular classes of holoprosencephaly. Keywords Mesh Terms:

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    Grant and Affiliation Information for Mutations in the BMP pathway in mice support the existence of two molecular classes of holoprosencephaly.

    AFFILIATION: Departments of Neuroscience and Molecular Genetics, Albert Einstein College of Medicine, Bronx, NY 10461, USA.

    Country: England

    England Research PublicationEngland Research Publication

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    MEDLINETA: Development

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