檢索結果 - Alison Homstad

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  1. 1
    Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis

    Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis 由 Rasheed Gbadegesin, Peter Lavin, Gentzon Hall, Bartlomiej Bartkowiak, Alison Homstad, Ruiji Jiang, Guanghong Wu, Alison Byrd, Kelvin L. Lynn, Norman M. Wolfish, Carolina Ottati, Paul E. Stevens, David N. Howell, Peter J. Conlon, Michelle P. Winn

    出版 2011
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  2. 2
    TRPC6 Enhances Angiotensin II-induced Albuminuria

    TRPC6 Enhances Angiotensin II-induced Albuminuria 由 Jason Eckel, Peter Lavin, Elizabeth Finch, Nirvan Mukerji, Jarrett Burch, Rasheed Gbadegesin, Guanghong Wu, Brandy L. Bowling, Alison Byrd, Gentzon Hall, Matthew A. Sparks, Zhu Shan Zhang, Alison Homstad, Laura Barisoni, Lutz Birbaumer, Paul B. Rosenberg, Michelle P. Winn

    出版 2011
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  3. 3
    A Novel Missense Mutation of Wilms’ Tumor 1 Causes Autosomal Dominant FSGS

    A Novel Missense Mutation of Wilms’ Tumor 1 Causes Autosomal Dominant FSGS 由 Gentzon Hall, Rasheed Gbadegesin, Peter Lavin, Guanghong Wu, Yangfan Liu, Edwin C. Oh, Liming Wang, Robert F. Spurney, Jason Eckel, Thomas Lindsey, Alison Homstad, Andrew F. Malone, Paul J. Phelan, Andréy S. Shaw, David N. Howell, Peter J. Conlon, Nicholas Katsanis, Michelle P. Winn

    出版 2014
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  4. 4
    Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis

    Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis 由 Andrew F. Malone, Paul J. Phelan, Gentzon Hall, Ümran Çetinçelik, Alison Homstad, Andrea Alonso, Ruiji Jiang, Thomas Lindsey, Guanghong Wu, Matthew A. Sparks, Stephen R. Smith, Nicholas J.A. Webb, Philip A. Kalra, Adebowale Adeyemo, Andréy S. Shaw, Peter J. Conlon, J. Charles Jennette, David N. Howell, Michelle P. Winn, Rasheed Gbadegesin

    出版 2014
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  5. 5
    TNXB Mutations Can Cause Vesicoureteral Reflux

    TNXB Mutations Can Cause Vesicoureteral Reflux 由 Rasheed Gbadegesin, Patrick D. Brophy, Adebowale Adeyemo, Gentzon Hall, Indra R. Gupta, David S. Hains, Bartlomeij Bartkowiak, C. Egla Rabinovich, Settara C. Chandrasekharappa, Alison Homstad, Katherine D. Westreich, Guanghong Wu, Yutao Liu, Danniele G. Holanda, Jason Clarke, Peter Lavin, Angelica Selim, Sara Miller, John S. Wiener, Sherry S. Ross, John W. Foreman, Charles N. Rotimi, Michelle P. Winn

    出版 2013
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  6. 6
    Mutations in the Gene That Encodes the F-Actin Binding Protein Anillin Cause FSGS

    Mutations in the Gene That Encodes the F-Actin Binding Protein Anillin Cause FSGS 由 Rasheed Gbadegesin, Gentzon Hall, Adebowale Adeyemo, Nils Hanke, Irini Tossidou, James L. Burchette, Guanghong Wu, Alison Homstad, Matthew A. Sparks, José A. Gómez, Ruiji Jiang, Andrea Alonso, Peter Lavin, Peter J. Conlon, Ron Korstanje, M. Ständer, Ghaidan A. Shamsan, Moumita Barua, Robert F. Spurney, Pravin C. Singhal, Jeffrey B. Kopp, Hermann Haller, David N. Howell, Martin R. Pollak, Andréy S. Shaw, Mario Schiffer, Michelle P. Winn

    出版 2014
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  7. 7
    HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome

    HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome 由 Rasheed Gbadegesin, Adebowale Adeyemo, Nicholas J.A. Webb, Larry A. Greenbaum, Asiri Abeyagunawardena, Shenal Thalgahagoda, Arundhati S. Kale, Debbie S. Gipson, Tarak Srivastava, Jen-Jar Lin, Deepa H. Chand, Tracy E. Hunley, Patrick D. Brophy, Arvind Bagga, Aditi Sinha, Michelle N. Rheault, Joanna R. Ghali, Kathy Nicholls, Elizabeth Abraham, Halima S. Janjua, Abiodun Omoloja, Gina-Marie Barletta, Yi Cai, David Milford, Catherine O’Brien, Atif Awan, Vladimir Belostotsky, William E. Smoyer, Alison Homstad, Gentzon Hall, Guanghong Wu, Shashi Nagaraj, Delbert R. Wigfall, John W. Foreman, Michelle P. Winn

    出版 2014
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