Hasil Pencarian - Peer Arts

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  1. 1
    Transcription factor genetics and biology in predisposition to bone marrow failure and hematological malignancy

    Transcription factor genetics and biology in predisposition to bone marrow failure and hematological malignancy oleh Jiarna R. Zerella, Jiarna R. Zerella, Claire C. Homan, Claire C. Homan, Peer Arts, Peer Arts, Anna L. Brown, Anna L. Brown, Anna L. Brown, Hamish S. Scott, Hamish S. Scott, Hamish S. Scott, Christopher N. Hahn, Christopher N. Hahn, Christopher N. Hahn

    Diterbitkan 2023-06-01
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  2. 2
    Quantification of differential gene expression by multiplexed targeted resequencing of cDNA

    Quantification of differential gene expression by multiplexed targeted resequencing of cDNA oleh Peer Arts, Jori van der Raadt, Sebastianus H.C. van Gestel, Marloes Steehouwer, Jay Shendure, Alexander Hoischen, Cornelis A. Albers

    Diterbitkan 2017-05-01
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  3. 3
    Compound heterozygous variants in LAMC3 in association with posterior periventricular nodular heterotopia

    Compound heterozygous variants in LAMC3 in association with posterior periventricular nodular heterotopia oleh Carla De Angelis, Alicia B. Byrne, Rebecca Morrow, Jinghua Feng, Thuong Ha, Paul Wang, Andreas W. Schreiber, Milena Babic, Ajay Taranath, Nick Manton, Sarah L. King-Smith, Quenten Schwarz, Peer Arts, Hamish S. Scott, Christopher Barnett

    Diterbitkan 2021-02-01
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  4. 4
    Impact of rare and common genetic variation in the interleukin-1 pathway on human cytokine responses

    Impact of rare and common genetic variation in the interleukin-1 pathway on human cytokine responses oleh Rosanne C. van Deuren, Peer Arts, Giulio Cavalli, Martin Jaeger, Marloes Steehouwer, Maartje van de Vorst, Christian Gilissen, Leo A. B. Joosten, Charles A. Dinarello, Musa M. Mhlanga, Vinod Kumar, Mihai G. Netea, Frank L. van de Veerdonk, Alexander Hoischen

    Diterbitkan 2021-05-01
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  5. 5
    Introme accurately predicts the impact of coding and noncoding variants on gene splicing, with clinical applications

    Introme accurately predicts the impact of coding and noncoding variants on gene splicing, with clinical applications oleh Patricia J. Sullivan, Velimir Gayevskiy, Ryan L. Davis, Marie Wong, Chelsea Mayoh, Amali Mallawaarachchi, Yvonne Hort, Mark J. McCabe, Sarah Beecroft, Matilda R. Jackson, Peer Arts, Andrew Dubowsky, Nigel Laing, Marcel E. Dinger, Hamish S. Scott, Emily Oates, Mark Pinese, Mark J. Cowley

    Diterbitkan 2023-05-01
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  6. 6
    Human variation in population-wide gene expression data predicts gene perturbation phenotype

    Human variation in population-wide gene expression data predicts gene perturbation phenotype oleh Lorenzo Bonaguro, Jonas Schulte-Schrepping, Caterina Carraro, Laura L. Sun, Benedikt Reiz, Ioanna Gemünd, Adem Saglam, Souad Rahmouni, Michel Georges, Peer Arts, Alexander Hoischen, Leo A.B. Joosten, Frank L. van de Veerdonk, Mihai G. Netea, Kristian Händler, Sach Mukherjee, Thomas Ulas, Joachim L. Schultze, Anna C. Aschenbrenner

    Diterbitkan 2022-11-01
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  7. 7
    The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy

    The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy oleh Claire C. Homan, Sarah L. King-Smith, David M. Lawrence, Peer Arts, Jinghua Feng, James Andrews, Mark Armstrong, Thuong Ha, Julia Dobbins, Michael W. Drazer, Kai Yu, Csaba Bödör, Alan Cantor, Mario Cazzola, Erin Degelman, Courtney D. DiNardo, Nicolas Duployez, Remi Favier, Stefan Fröhling, Jude Fitzgibbon, Jeffery M. Klco, Alwin Krämer, Mineo Kurokawa, Joanne Lee, Luca Malcovati, Neil V. Morgan, Georges Natsoulis, Carolyn Owen, Keyur P. Patel, Claude Preudhomme, Hana Raslova, Hugh Rienhoff, Tim Ripperger, Rachael Schulte, Kiran Tawana, Elvira Velloso, Benedict Yan, Paul Liu, Lucy A. Godley, Andreas W. Schreiber, Christopher N. Hahn, Hamish S. Scott, Anna L. Brown

    Diterbitkan 2021-07-01
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  8. 8
    Exome sequencing in routine diagnostics: a generic test for 254 patients with primary immunodeficiencies

    Exome sequencing in routine diagnostics: a generic test for 254 patients with primary immunodeficiencies oleh Peer Arts, Annet Simons, Mofareh S. AlZahrani, Elanur Yilmaz, Eman AlIdrissi, Koen J. van Aerde, Njood Alenezi, Hamza A. AlGhamdi, Hadeel A. AlJubab, Abdulrahman A. Al-Hussaini, Fahad AlManjomi, Alaa B. Alsaad, Badr Alsaleem, Abdulrahman A. Andijani, Ali Asery, Walid Ballourah, Chantal P. Bleeker-Rovers, Marcel van Deuren, Michiel van der Flier, Erica H. Gerkes, Christian Gilissen, Murad K. Habazi, Jayne Y. Hehir-Kwa, Stefanie S. Henriet, Esther P. Hoppenreijs, Sarah Hortillosa, Chantal H. Kerkhofs, Riikka Keski-Filppula, Stefan H. Lelieveld, Khurram Lone, Marius A. MacKenzie, Arjen R. Mensenkamp, Jukka Moilanen, Marcel Nelen, Jaap ten Oever, Judith Potjewijd, Pieter van Paassen, Janneke H. M. Schuurs-Hoeijmakers, Anna Simon, Tomasz Stokowy, Maartje van de Vorst, Maaike Vreeburg, Anja Wagner, Gijs T. J. van Well, Dimitra Zafeiropoulou, Evelien Zonneveld-Huijssoon, Joris A. Veltman, Wendy A. G. van Zelst-Stams, Eissa A. Faqeih, Frank L. van de Veerdonk, Mihai G. Netea, Alexander Hoischen

    Diterbitkan 2019-06-01
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