Výsledky vyhledávání - Melissa Kelly

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  1. 1
    Signaling Hierarchy Regulating Human Endothelial Cell Development

    Signaling Hierarchy Regulating Human Endothelial Cell Development Autor Melissa Kelly, Karen K. Hirschi

    Vydáno 2009
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  2. 2
    Job Stress, Burnout, Work-Life Balance, Well-Being, and Job Satisfaction Among Pathology Residents and Fellows

    Job Stress, Burnout, Work-Life Balance, Well-Being, and Job Satisfaction Among Pathology Residents and Fellows Autor Melissa Kelly, Ryan Soles, Edna Garcia, Iman Kundu

    Vydáno 2020
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  3. 3
    The American Society for Clinical Pathology’s 2018 Vacancy Survey of Medical Laboratories in the United States

    The American Society for Clinical Pathology’s 2018 Vacancy Survey of Medical Laboratories in the United States Autor Edna Garcia, Iman Kundu, Melissa Kelly, Ryan Soles

    Vydáno 2019
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  4. 4
    The American Society for Clinical Pathology 2022 Vacancy Survey of medical laboratories in the United States

    The American Society for Clinical Pathology 2022 Vacancy Survey of medical laboratories in the United States Autor Edna Garcia, Iman Kundu, Melissa Kelly, Ryan Soles

    Vydáno 2023
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  5. 5
    Reactive Oxygen Species: Stuck in the Middle of Neurodegeneration

    Reactive Oxygen Species: Stuck in the Middle of Neurodegeneration Autor David A. Patten, Marc Germain, Melissa Kelly, Ruth S. Slack

    Vydáno 2010
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  6. 6
    Inherited Cardiomyopathies

    Inherited Cardiomyopathies Autor Polakit Teekakirikul, Melissa Kelly, Heidi L. Rehm, Neal K. Lakdawala, Birgit H. Funke

    Vydáno 2012
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  7. 7
    Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders

    Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders Autor Matthew T. Oetjens, Melissa Kelly, Amy C. Sturm, C. L. Martin, David H. Ledbetter

    Vydáno 2019
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  8. 8
    The American Society for Clinical Pathology’s Job Satisfaction, Well-Being, and Burnout Survey of Laboratory Professionals

    The American Society for Clinical Pathology’s Job Satisfaction, Well-Being, and Burnout Survey of Laboratory Professionals Autor Edna Garcia, Iman Kundu, Melissa Kelly, Ryan Soles, Lotte Mulder, Geoffrey A. Talmon

    Vydáno 2020
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  9. 9
    How low can you go? Titrating the lowest effective dose of cyproterone acetate for transgender and gender diverse people who request feminizing hormones

    How low can you go? Titrating the lowest effective dose of cyproterone acetate for transgender and gender diverse people who request feminizing hormones Autor Sarah Warzywoda, James A. Fowler, Penny Wood, Fiona Bisshop, Darren Russell, Hemming Luu, Melissa Kelly, Victoria Featherstone, Judith Dean

    Vydáno 2024
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  10. 10
    Imetelstat, a novel, first‐in‐class telomerase inhibitor: Mechanism of action, clinical, and translational science

    Imetelstat, a novel, first‐in‐class telomerase inhibitor: Mechanism of action, clinical, and translational science Autor Ashley L. Lennox, Fei Huang, Melissa Kelly Behrs, Mario González‐Sales, Neha Bhise, Ying Wan, Libo Sun, Tymara Berry, Faye Feller, Peter N. Morcos

    Vydáno 2024
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  11. 11
    Mcl-1 Is a Key Regulator of Apoptosis during CNS Development and after DNA Damage

    Mcl-1 Is a Key Regulator of Apoptosis during CNS Development and after DNA Damage Autor Nicole Arbour, Jacqueline L. Vanderluit, Jaclyn Nicole Le Grand, Arezu Jahani‐Asl, Vladimir Ruzhynsky, Eric C. Cheung, Melissa Kelly, Alex MacKenzie, David S. Park, Joseph T. Opferman, Ruth S. Slack

    Vydáno 2008
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  12. 12
    The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing

    The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing Autor Trevor J. Pugh, Melissa Kelly, Sivakumar Gowrisankar, Elizabeth Hynes, Michael A. Seidman, Samantha Baxter, Mark Bowser, Bryan D. Harrison, Daniel Aaron, Lisa Mahanta, Neal K. Lakdawala, Gregory McDermott, Emily White, Heidi L. Rehm, Matthew S. Lebo, Birgit Funke

    Vydáno 2014
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  13. 13
    Genomic Screening at a Single Health System

    Genomic Screening at a Single Health System Autor Juliann M. Savatt, Melissa Kelly, Amy C. Sturm, Cara Z. McCormick, Marc S. Williams, Michelle Pistner Nixon, David D.K. Rolston, Natasha T. Strande, Karen E. Wain, Huntington F. Willard, W. Andrew Faucett, David H. Ledbetter, Adam H. Buchanan, Alastair J. Martin

    Vydáno 2025
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  14. 14
    Prevalence and Electronic Health Record-Based Phenotype of Loss-of-Function Genetic Variants in Arrhythmogenic Right Ventricular Cardiomyopathy-Associated Genes

    Prevalence and Electronic Health Record-Based Phenotype of Loss-of-Function Genetic Variants in Arrhythmogenic Right Ventricular Cardiomyopathy-Associated Genes Autor Eric Carruth, W. Glenn Young, Dominik Beer, Cynthia A. James, Hugh Calkins, Linyuan Jing, Sushravya Raghunath, Dustin N. Hartzel, Joseph B. Leader, H. Lester Kirchner, Diane T. Smelser, David J. Carey, Melissa Kelly, Amy C. Sturm, Amro Alsaid, Brandon K. Fornwalt, Christopher M. Haggerty

    Vydáno 2019
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  15. 15
    Clinical outcomes of a genomic screening program for actionable genetic conditions

    Clinical outcomes of a genomic screening program for actionable genetic conditions Autor Adam H. Buchanan, H. Lester Kirchner, M. Schwartz, Melissa Kelly, Tara Schmidlen, Laney K. Jones, Miranda L. G. Hallquist, Heather Rocha, Megan Betts, Rachel Schwiter, Loren Butry, Amanda L. Lazzeri, Lauren R. Frisbie, Alanna Kulchak Rahm, Jing Hao, Huntington F. Willard, Christa Lese Martin, David H. Ledbetter, Marc S. Williams, Amy C. Sturm

    Vydáno 2020
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  16. 16
    Activating<i>RAC1</i>variants in the switch II region cause a developmental syndrome and alter neuronal morphology

    Activating<i>RAC1</i>variants in the switch II region cause a developmental syndrome and alter neuronal morphology Autor Siddharth Banka, Abigail Bennington, Martin J. Baker, Ellen Rijckmans, Giuliana Clemente, Nurhuda Mohamad Ansor, Hilary Sito, P. Phaniram Prasad, Kwame Anyane‐Yeboa, Lauren Badalato, Boyan Dimitrov, David Fitzpatrick, Anna Hurst, Anna Jansen, Melissa Kelly, Ian D. Krantz, Claudine Rieubland, Meredith J. Ross, Natasha L. Rudy, Javier Sanz, Katrien Stouffs, Zhuo Luan Xu, Angeliki Malliri, Marcelo G. Kazanietz, Tom H. Millard

    Vydáno 2022
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  17. 17
    Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen’s Inherited Cardiomyopathy Expert Panel

    Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen’s Inherited Cardiomyopathy Exp... Autor Melissa Kelly, Colleen Caleshu, Ana Morales, Jillian G. Buchan, Zena Wolf, Steven M. Harrison, Stuart A. Cook, Mitchell W. Dillon, John Garcia, Eden Haverfield, Jan D.H. Jongbloed, Daniela Macaya, Arjun K. Manrai, Kate M. Orland, Gabriele Richard, Katherine G. Spoonamore, Matthew Thomas, Kate Thomson, Lisa M. Vincent, Roddy Walsh, Hugh Watkins, Nicola Whiffin, Jodie Ingles, J. Peter van Tintelen, Christopher Semsarian, James S. Ware, Ray E. Hershberger, Birgit Funke

    Vydáno 2018
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  18. 18
    Developing and Optimizing Innovative Tools to Address Familial Hypercholesterolemia Underdiagnosis

    Developing and Optimizing Innovative Tools to Address Familial Hypercholesterolemia Underdiagnosis Autor Gemme Campbell‐Salome, Laney K. Jones, Max Masnick, Nephi Walton, Catherine D. Ahmed, Adam H. Buchanan, Andrew Brangan, Edward D. Esplin, David Kann, Ilene Ladd, Melissa Kelly, Iris Kindt, H. Lester Kirchner, Mary P. McGowan, Megan McMinn, Ana Morales, Kelly D. Myers, Matthew T. Oetjens, Alanna Kulchak Rahm, Tara Schmidlen, Amanda Sheldon, Emilie Simmons, Moran Snir, Natasha T. Strande, Nicole L. Walters, Katherine Wilemon, Marc S. Williams, Samuel S. Gidding, Amy C. Sturm

    Vydáno 2021
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  19. 19
    Genomics-First Evaluation of Heart Disease Associated With Titin-Truncating Variants

    Genomics-First Evaluation of Heart Disease Associated With Titin-Truncating Variants Autor Christopher M. Haggerty, Scott M. Damrauer, Michael G. Levin, David Birtwell, David J. Carey, Alicia Golden, Dustin N. Hartzel, Yirui Hu, Renae Judy, Melissa Kelly, Rachel L. Kember, H. Lester Kirchner, Joseph B. Leader, Lusha W. Liang, Chris McDermott‐Roe, Apoorva Babu, Michael P. Morley, Zachariah Nealy, Thomas N. Person, Arichanah Pulenthiran, Aeron Small, Diane T. Smelser, Richard C. Stahl, Amy C. Sturm, Heather Williams, Aris Baras, Kenneth B. Margulies, Thomas P. Cappola, Frederick E. Dewey, Anurag Verma, Xinyuan Zhang, Adolfo Correa, Michael E. Hall, James Wilson, Marylyn D. Ritchie, Daniel J. Rader, Michael F. Murray, Brandon K. Fornwalt, Zoltàn Arany

    Vydáno 2019
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  20. 20
    The landscape of reported VUS in multi-gene panel and genomic testing: Time for a change

    The landscape of reported VUS in multi-gene panel and genomic testing: Time for a change Autor Heidi L. Rehm, Joseph T. Alaimo, Swaroop Aradhya, Pınar Bayrak‐Toydemir, Hunter Best, Rhonda Brandon, Jillian G. Buchan, Elizabeth Chao, Elaine Chen, Jacob Clifford, Ana S.A. Cohen, Laura K. Conlin, Soma Das, Kyle Davis, Daniela del Gaudio, Florencia Del Viso, Christina DiVincenzo, Marcia Eisenberg, Lucia Guidugli, Monia Hammer, Steven M. Harrison, Kathryn E. Hatchell, Lindsay Havens Dyer, Lily Hoang, James Holt, Vaidehi Jobanputra, Izabela Karbassi, Hutton M. Kearney, Melissa Kelly, Jacob M. Kelly, Michelle L. Kluge, Timothy Komala, Paul Kruszka, Lynette Lau, Matthew S. Lebo, Christian R. Marshall, Dianalee McKnight, Kirsty McWalter, Yan Meng, Narasimhan Nagan, Christian S. Neckelmann, Nir Neerman, Zhiyv Niu, Vitoria Paolillo, Sarah A Paolucci, Denise Perry, Tina Pesaran, Kelly Radtke, Kristen Rasmussen, Kyle Retterer, Carol Saunders, Elizabeth Spiteri, Christine M. Stanley, Anna Szuto, Ryan J. Taft, Isabelle Thiffault, Brittany C. Thomas, Amanda Thomas‐Wilson, Erin Thorpe, Timothy Tidwell, Meghan C. Towne, Hana Zouk, Christian Marshall, Linyan Meng, Vaidehi Jobanputra, Ryan J. Taft, Euan A. Ashley, Ghunwa Nakouzi, Wei Shen, Stephen F. Kingsmore, Heidi L. Rehm

    Vydáno 2023
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