Hasil Pencarian - Denise Perry

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  1. 1
    Empirical Studies on Effect of Low-Level Laser Treatment on Glioblastoma Multiforme in Combination with Ag-PMMA-PAA Nanoparticles: Paired Red Region Optical-Property Treatment Platform

    Empirical Studies on Effect of Low-Level Laser Treatment on Glioblastoma Multiforme in Combination with Ag-PMMA-PAA Nanoparticles: Paired Red Region Optical-Property Treatment Plat... oleh Rohini Atluri, Daniel Korir, Tae-Youl Choi, Denise Perry Simmons

    Diterbitkan 2022-06-01
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  2. 2
    P636: Lp(a) genetic risk screening using genome sequencing

    P636: Lp(a) genetic risk screening using genome sequencing oleh Samuel Strom, Laura Amendola, Aditi Chawla, Vitor Onucic, Denise Perry, Akanchha Kesari, Ryan Taft

    Diterbitkan 2024-01-01
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  3. 3
    P471: Quad whole genome sequencing detects reciprocal copy number variants in affected siblings, consistent with familial translocation

    P471: Quad whole genome sequencing detects reciprocal copy number variants in affected siblings, consistent with familial translocation oleh Katie Golden-Grant, Amanda Buchanan, Alison Coffey, Yvonne Brew, Brittany Thomas, Akanchha Kesari, Denise Perry, Ryan Taft

    Diterbitkan 2023-01-01
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  4. 4
    Single-Step Photochemical Formation of Near-Infrared-Absorbing Gold Nanomosaic within PNIPAm Microgels: Candidates for Photothermal Drug Delivery

    Single-Step Photochemical Formation of Near-Infrared-Absorbing Gold Nanomosaic within PNIPAm Microgels: Candidates for Photothermal Drug Delivery oleh Sreekar B. Marpu, Brian Leon Kamras, Nooshin MirzaNasiri, Oussama Elbjeirami, Denise Perry Simmons, Zhibing Hu, Mohammad A. Omary

    Diterbitkan 2020-06-01
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  5. 5
    P572: Detecting short tandem repeat expansions: Three-year experience with clinical whole genome sequencing (cWGS) for a rare and undiagnosed population

    P572: Detecting short tandem repeat expansions: Three-year experience with clinical whole genome sequencing (cWGS) for a rare and undiagnosed population oleh Brittany Thomas, Akanchha Kesari, Aime Lumaka, Mario Cornejo-Olivas, David Ward, Parul Jayakar, Donald Basel, Marilyn Jones, Erin Thorpe, Denise Perry, Ryan Taft

    Diterbitkan 2023-01-01
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  6. 6
    P420: Development of a comprehensive cardiovascular disease whole genome sequencing test

    P420: Development of a comprehensive cardiovascular disease whole genome sequencing test oleh Laura Amendola, Alison Coffey, Samuel Strom, Akanchha Kesari, James Avecilla, Josh Lowry, Stetson Thacker, Julie Taylor, Kathryn Golden-Grant, Matt Brown, Becky Milewski, John Belmont, Denise Perry, Ryan Taft

    Diterbitkan 2023-01-01
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  7. 7
    P507: Implementation of automated pharmacogenomics reporting for a clinically validated whole genome sequencing test

    P507: Implementation of automated pharmacogenomics reporting for a clinically validated whole genome sequencing test oleh Alka Malhotra, Rueben Hejja, James Avecilla, Andrew Walker, Phillip Medrano, Felipe Mullen, Anusha Balusu, Pratyusha Vankayala, Maren Bennett, Aditi Chawla, Subramanian Ajay, Samuel Strom, Akanchha Kesari, Denise Perry, Ryan Taft

    Diterbitkan 2023-01-01
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  8. 8
    O38: The impact of whole genome sequencing in a diverse global population of genetic disease patients*

    O38: The impact of whole genome sequencing in a diverse global population of genetic disease patients* oleh Ryan Taft, Erin Thorpe, John Belmont, Taylor Williams, Chad Shaw, Jason Button, Julia Ortega, Keisha Robinson, Marilyn Jones, Diane Masser-Frye, Donald Basel, Chester Brown, Keith Vaux, Aime Lumaka, Fabio Sirchia, Milagros Dueñas Roque, Mario Cornejo-Olivas, Jeny Bazalar-Montoya, Nora Urraca, Alejandra Salguero, Samuel Wiafe, Romina Foster-Bonds, Erin Royer, Michelle Gallas, Pilar Magoulas, Adeline Vanderver, Marwan Shinawi, Alan Taylor, Kristen Fishler, Duncan Henry, Daria Salyakina, Kate Gibson, Melissa Lah, Alka Malhotra, James Avecilla, Andrew Warren, Denise Perry, Max Arseneault

    Diterbitkan 2023-01-01
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