Hasil Pencarian - Heather Flanagan-Steet

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  1. 1
    A Biochemical Platform to Define the Relative Specific Activity of <i>IDUA</i> Variants Identified by Newborn Screening

    A Biochemical Platform to Define the Relative Specific Activity of <i>IDUA</i> Variants Identified by Newborn Screening oleh Seok-Ho Yu, Laura Pollard, Tim Wood, Heather Flanagan-Steet, Richard Steet

    Diterbitkan 2020-11-01
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  2. 2
    Upregulation of Sortilin, a Lysosomal Sorting Receptor, Corresponds with Reduced Bioavailability of Latent TGFβ in Mucolipidosis II Cells

    Upregulation of Sortilin, a Lysosomal Sorting Receptor, Corresponds with Reduced Bioavailability of Latent TGFβ in Mucolipidosis II Cells oleh Jarrod W. Barnes, Megan Aarnio-Peterson, Joy Norris, Mark Haskins, Heather Flanagan-Steet, Richard Steet

    Diterbitkan 2020-04-01
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  3. 3
    Inappropriate cathepsin K secretion promotes its enzymatic activation driving heart and valve malformation

    Inappropriate cathepsin K secretion promotes its enzymatic activation driving heart and valve malformation oleh Po-Nien Lu, Trevor Moreland, Courtney J. Christian, Troy C. Lund, Richard A. Steet, Heather Flanagan-Steet

    Diterbitkan 2020-10-01
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  4. 4
    The Role of Hematopoietic Cell Transplant in the Glycoprotein Diseases

    The Role of Hematopoietic Cell Transplant in the Glycoprotein Diseases oleh Brianna M. Naumchik, Ashish Gupta, Heather Flanagan-Steet, Richard A. Steet, Sara S. Cathey, Paul J. Orchard, Troy C. Lund

    Diterbitkan 2020-06-01
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  5. 5
    Selective inhibition of N-linked glycosylation impairs receptor tyrosine kinase processing

    Selective inhibition of N-linked glycosylation impairs receptor tyrosine kinase processing oleh Elsenoor Klaver, Peng Zhao, Melanie May, Heather Flanagan-Steet, Hudson H. Freeze, Reid Gilmore, Lance Wells, Joseph Contessa, Richard Steet

    Diterbitkan 2019-06-01
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  6. 6
    TGF-ß Regulates Cathepsin Activation during Normal and Pathogenic Development

    TGF-ß Regulates Cathepsin Activation during Normal and Pathogenic Development oleh Heather Flanagan-Steet, Courtney Christian, Po-Nien Lu, Megan Aarnio-Peterson, Laura Sanman, Stephanie Archer-Hartmann, Parastoo Azadi, Matthew Bogyo, Richard A. Steet

    Diterbitkan 2018-03-01
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  7. 7
    Dysregulated lysosomal exocytosis drives protease-mediated cartilage pathogenesis in multiple lysosomal disorders

    Dysregulated lysosomal exocytosis drives protease-mediated cartilage pathogenesis in multiple lysosomal disorders oleh Jen-Jie Lee, Tong Wang, Kali Wiggins, Po Nien Lu, Christina Underwood, Katarzyna Ochenkowska, Eric Samarut, Laura M. Pollard, Heather Flanagan-Steet, Richard Steet

    Diterbitkan 2024-04-01
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  8. 8
    Excessive activity of cathepsin K is associated with cartilage defects in a zebrafish model of mucolipidosis II

    Excessive activity of cathepsin K is associated with cartilage defects in a zebrafish model of mucolipidosis II oleh Aaron C. Petrey, Heather Flanagan-Steet, Steven Johnson, Xiang Fan, Mitche De la Rosa, Mark E. Haskins, Alison V. Nairn, Kelley W. Moremen, Richard Steet

    Diterbitkan 2012-03-01
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  9. 9
    Protease-dependent defects in N-cadherin processing drive PMM2-CDG pathogenesis

    Protease-dependent defects in N-cadherin processing drive PMM2-CDG pathogenesis oleh Elsenoor J. Klaver, Lynn Dukes-Rimsky, Brijesh Kumar, Zhi-Jie Xia, Tammie Dang, Mark A. Lehrman, Peggi Angel, Richard R. Drake, Hudson H. Freeze, Richard Steet, Heather Flanagan-Steet

    Diterbitkan 2021-12-01
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  10. 10
    PRDM1 DNA-binding zinc finger domain is required for normal limb development and is disrupted in split hand/foot malformation

    PRDM1 DNA-binding zinc finger domain is required for normal limb development and is disrupted in split hand/foot malformation oleh Brittany T. Truong, Lomeli C. Shull, Ezra Lencer, Eric G. Bend, Michael Field, Elizabeth E. Blue, Michael J. Bamshad, Cindy Skinner, David Everman, Charles E. Schwartz, Heather Flanagan-Steet, Kristin B. Artinger

    Diterbitkan 2023-04-01
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  11. 11
    Deficiency in the endocytic adaptor proteins PHETA1/2 impairs renal and craniofacial development

    Deficiency in the endocytic adaptor proteins PHETA1/2 impairs renal and craniofacial development oleh Kristin M. Ates, Tong Wang, Trevor Moreland, Rajalakshmi Veeranan-Karmegam, Manxiu Ma, Chelsi Jeter, Priya Anand, Wolfgang Wenzel, Hyung-Goo Kim, Lynne A. Wolfe, Joshi Stephen, David R. Adams, Thomas Markello, Cynthia J. Tifft, Robert Settlage, William A. Gahl, Graydon B. Gonsalvez, May Christine Malicdan, Heather Flanagan-Steet, Y. Albert Pan

    Diterbitkan 2020-05-01
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