SLNSW-Mouse model of Noonan syndrome reveals cell type-...-TN_cdi_proquest_miscellaneous_66763560

Mouse model of Noonan syndrome reveals cell type- and gene dosage-dependent effects of Ptpn11 mutation

Full title: Mouse model of Noonan syndrome reveals cell type- and gene dosage-dependent effects of Ptpn11 mutation

Author/creator: Araki, Toshiyuki, Mohi, M Golam, Ismat, Fraz A, Bronson, Roderick T, Williams, Ifor R, Kutok, Jeffery L, Yang, Wentian, Pao, Lily I, Gilliland, D Gary, Epstein, Jonathan A, Neel, Benjamin G.

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Record Identifier: TN_cdi_proquest_miscellaneous_66763560

Language: English

Formats: Articles

Publishers: United States: Nature Publishing Group

Permalink: https://collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_66763560

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    Record title

    Mouse model of Noonan syndrome reveals cell type- and gene dosage-dependent effects of Ptpn11 mutation

    Record identifier

    TN_cdi_proquest_miscellaneous_66763560

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    https://collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_66763560

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    Mouse model of Noonan syndrome reveals cell type- and gene dosage-dependent effects of Ptpn11 mutation

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    https://collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_66763560

    Mouse model of Noonan syndrome reveals cell type- and gene dosage-dependent effects of Ptpn11 mutation

    Full title

    Mouse model of Noonan syndrome reveals cell type- and gene dosage-dependent effects of Ptpn11 mutation

    Author / Creator

    Araki, Toshiyuki ; Mohi, M Golam ; Ismat, Fraz A ; Bronson, Roderick T ; Williams, Ifor R ; Kutok, Jeffery L ; Yang, Wentian ; Pao, Lily I ; Gilliland, D Gary ; Epstein, Jonathan A ; Neel, Benjamin G

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    United States: Nature Publishing Group

    Journal title

    Nature medicine, 2004, Vol.10 (8), p.849-857

    Record Identifier

    TN_cdi_proquest_miscellaneous_66763560

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    English

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    Articles

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    Animals Cell Lineage - genetics Craniofacial Abnormalities - genetics Disease Models, Animal Endocardial Cushion Defects - genetics Endocardial Cushion Defects - metabolism Flow Cytometry Gene Dosage Genes, Dominant Heart Defects, Congenital - genetics Immunohistochemistry Intracellular Signaling Peptides and Proteins Mice Mice, Mutant Strains Mitogen-Activated Protein Kinases - metabolism Mutation - genetics Myeloproliferative Disorders - genetics Noonan Syndrome - genetics Precipitin Tests Protein Tyrosine Phosphatase, Non-Receptor Type 11 Protein Tyrosine Phosphatases - genetics Protein Tyrosine Phosphatases - metabolism

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    TN_cdi_proquest_miscellaneous_66763560

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    https://collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_66763560

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