Hasil Pencarian - Robert A Kesterson

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  1. 1
    CRYβA3/A1-Crystallin Knockout Develops Nuclear Cataract and Causes Impaired Lysosomal Cargo Clearance and Calpain Activation.

    CRYβA3/A1-Crystallin Knockout Develops Nuclear Cataract and Causes Impaired Lysosomal Cargo Clearance and Calpain Activation. oleh Shylaja Hegde, Robert A Kesterson, Om P Srivastava

    Diterbitkan 2016-01-01
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  2. 2
    Genetic ablation of CD68 results in mice with increased bone and dysfunctional osteoclasts.

    Genetic ablation of CD68 results in mice with increased bone and dysfunctional osteoclasts. oleh Jason W Ashley, Zhenqi Shi, Haibo Zhao, Xingsheng Li, Robert A Kesterson, Xu Feng

    Diterbitkan 2011-01-01
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  3. 3
    Humanized GPRC6A KGKY is a gain-of-function polymorphism in mice

    Humanized GPRC6A KGKY is a gain-of-function polymorphism in mice oleh Min Pi, Fuyi Xu, Ruisong Ye, Satoru K. Nishimoto, Robert A. Kesterson, Robert W. Williams, Lu Lu, L. Darryl Quarles

    Diterbitkan 2020-07-01
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  4. 4
    Novel Hypomorphic Alleles of the Mouse Tyrosinase Gene Induced by CRISPR-Cas9 Nucleases Cause Non-Albino Pigmentation Phenotypes.

    Novel Hypomorphic Alleles of the Mouse Tyrosinase Gene Induced by CRISPR-Cas9 Nucleases Cause Non-Albino Pigmentation Phenotypes. oleh Anil K Challa, Evan R Boitet, Ashley N Turner, Larry W Johnson, Daniel Kennedy, Ethan R Downs, Katherine M Hymel, Alecia K Gross, Robert A Kesterson

    Diterbitkan 2016-01-01
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  5. 5
    Mice with altered serotonin 2C receptor RNA editing display characteristics of Prader–Willi syndrome

    Mice with altered serotonin 2C receptor RNA editing display characteristics of Prader–Willi syndrome oleh Michael V. Morabito, Atheir I. Abbas, Jennifer L. Hood, Robert A. Kesterson, Michelle M. Jacobs, David S. Kump, David L. Hachey, Bryan L. Roth, Ronald B. Emeson

    Diterbitkan 2010-08-01
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  6. 6
    Increased trabecular bone and improved biomechanics in an osteocalcin-null rat model created by CRISPR/Cas9 technology

    Increased trabecular bone and improved biomechanics in an osteocalcin-null rat model created by CRISPR/Cas9 technology oleh Laura J. Lambert, Anil K. Challa, Aidi Niu, Lihua Zhou, Janusz Tucholski, Maria S. Johnson, Tim R. Nagy, Alan W. Eberhardt, Patrick N. Estep, Robert A. Kesterson, Jayleen M. Grams

    Diterbitkan 2016-10-01
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  7. 7
    Aberrant regulation of a poison exon caused by a non-coding variant in a mouse model of Scn1a-associated epileptic encephalopathy.

    Aberrant regulation of a poison exon caused by a non-coding variant in a mouse model of Scn1a-associated epileptic encephalopathy. oleh Yuliya Voskobiynyk, Gopal Battu, Stephanie A Felker, J Nicholas Cochran, Megan P Newton, Laura J Lambert, Robert A Kesterson, Richard M Myers, Gregory M Cooper, Erik D Roberson, Gregory S Barsh

    Diterbitkan 2021-01-01
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  8. 8
    Mutation-Directed Therapeutics for Neurofibromatosis Type I

    Mutation-Directed Therapeutics for Neurofibromatosis Type I oleh Andre Leier, David M. Bedwell, Ann T. Chen, George Dickson, Kim M. Keeling, Robert A. Kesterson, Bruce R. Korf, Tatiana T. Marquez Lago, Ulrich F. Müller, Linda Popplewell, Jiangbing Zhou, Deeann Wallis

    Diterbitkan 2020-06-01
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  9. 9
    Mice with missense and nonsense NF1 mutations display divergent phenotypes compared with human neurofibromatosis type I

    Mice with missense and nonsense NF1 mutations display divergent phenotypes compared with human neurofibromatosis type I oleh Kairong Li, Ashley N. Turner, Min Chen, Stephanie N. Brosius, Trenton R. Schoeb, Ludwine M. Messiaen, David M. Bedwell, Kurt R. Zinn, Corina Anastasaki, David H. Gutmann, Bruce R. Korf, Robert A. Kesterson

    Diterbitkan 2016-07-01
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  10. 10
    snRNA-seq of human cutaneous neurofibromas before and after selumetinib treatment implicates role of altered Schwann cell states, inter-cellular signaling, and extracellular matrix in treatment response

    snRNA-seq of human cutaneous neurofibromas before and after selumetinib treatment implicates role of altered Schwann cell states, inter-cellular signaling, and extracellular matrix... oleh Cameron Church, Christian X. Fay, Emil Kriukov, Hui Liu, Ashley Cannon, Lauren Ashley Baldwin, David K. Crossman, Bruce Korf, Margaret R. Wallace, Andrea M. Gross, Brigitte C. Widemann, Robert A. Kesterson, Petr Baranov, Deeann Wallis

    Diterbitkan 2024-06-01
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  11. 11
    Targeted exon skipping of NF1 exon 17 as a therapeutic for neurofibromatosis type I

    Targeted exon skipping of NF1 exon 17 as a therapeutic for neurofibromatosis type I oleh André Leier, Marc Moore, Hui Liu, Michael Daniel, Alexis M. Hyde, Ludwine Messiaen, Bruce R. Korf, Jamuna Selvakumaran, Lukasz Ciszewski, Laura Lambert, Jeremy Foote, Margaret R. Wallace, Robert A. Kesterson, George Dickson, Linda Popplewell, Deeann Wallis

    Diterbitkan 2022-06-01
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  12. 12
    Cystin genetic variants cause autosomal recessive polycystic kidney disease associated with altered Myc expression

    Cystin genetic variants cause autosomal recessive polycystic kidney disease associated with altered Myc expression oleh Chaozhe Yang, Naoe Harafuji, Amber K. O’Connor, Robert A. Kesterson, Jacob A. Watts, Amar J. Majmundar, Daniela A. Braun, Monkol Lek, Kristen M. Laricchia, Hanan M. Fathy, Shrikant Mane, Shirlee Shril, Friedhelm Hildebrandt, Lisa M. Guay-Woodford

    Diterbitkan 2021-09-01
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  13. 13
    Mutation of Growth Arrest Specific 8 Reveals a Role in Motile Cilia Function and Human Disease.

    Mutation of Growth Arrest Specific 8 Reveals a Role in Motile Cilia Function and Human Disease. oleh Wesley R Lewis, Erik B Malarkey, Douglas Tritschler, Raqual Bower, Raymond C Pasek, Jonathan D Porath, Susan E Birket, Sophie Saunier, Corinne Antignac, Michael R Knowles, Margaret W Leigh, Maimoona A Zariwala, Anil K Challa, Robert A Kesterson, Steven M Rowe, Iain A Drummond, John M Parant, Friedhelm Hildebrandt, Mary E Porter, Bradley K Yoder, Nicolas F Berbari

    Diterbitkan 2016-07-01
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