Результаты поиска - Jonatan Halvardson

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  1. 1
    Exome RNA sequencing reveals rare and novel alternative transcripts

    Exome RNA sequencing reveals rare and novel alternative transcripts по Jonatan Halvardson, Ammar Zaghlool, Lars Feuk

    Опубликовано 2012
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    Artigo
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  2. 2
    Efficient cellular fractionation improves RNA sequencing analysis of mature and nascent transcripts from human tissues

    Efficient cellular fractionation improves RNA sequencing analysis of mature and nascent transcripts from human tissues по Ammar Zaghlool, Adam Ameur, Linnea Nyberg, Jonatan Halvardson, Manfred Grabherr, Lucia Cavelier, Lars Feuk

    Опубликовано 2013
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    Artigo
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  3. 3
    Deleterious mutation in FDX1L gene is associated with a novel mitochondrial muscle myopathy

    Deleterious mutation in FDX1L gene is associated with a novel mitochondrial muscle myopathy по Ronen Spiegel, Ann Saada, Jonatan Halvardson, Devorah Soiferman, Avraham Shaag, Simon Edvardson, Yoseph Horovitz, Morad Khayat, Stavit A. Shalev, Lars Feuk, Orly Elpeleg

    Опубликовано 2013
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    Artigo
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  4. 4
    Mutations in<i>HECW2</i>are associated with intellectual disability and epilepsy

    Mutations in<i>HECW2</i>are associated with intellectual disability and epilepsy по Jonatan Halvardson, Jin Zhao, Ammar Zaghlool, Christian Wentzel, Patrik Georgii‐Hemming, Else Månsson, Helena Ederth Sävmarker, Göran Brandberg, Cecilia Zander, Ann‐Charlotte Thuresson, Lars Feuk

    Опубликовано 2016
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    Artigo
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  5. 5
    Exome sequencing reveals <i>NAA15</i> and <i>PUF60</i> as candidate genes associated with intellectual disability

    Exome sequencing reveals <i>NAA15</i> and <i>PUF60</i> as candidate genes associated with intellectual disability по Jin Zhao, Jonatan Halvardson, Cecilia Zander, Ammar Zaghlool, Patrik Georgii‐Hemming, Else Månsson, Göran Brandberg, Helena Ederth Sävmarker, Carina Frykholm, Ekaterina Kuchinskaya, Ann‐Charlotte Thuresson, Lars Feuk

    Опубликовано 2017
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    Artigo
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  6. 6
    Loss of Y and clonal hematopoiesis in blood—two sides of the same coin?

    Loss of Y and clonal hematopoiesis in blood—two sides of the same coin? по Viktor Ljungström, Jonas Mattisson, Jonatan Halvardson, Tatjana Pandzic, Hanna Davies, Edyta Rychlicka-Buniowska, Marcus Danielsson, Paul Lacaze, Lucia Cavelier, Jan P. Dumanski, Panagiotis Baliakas, Lars A. Forsberg

    Опубликовано 2021
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    Carta
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  7. 7
    Infantile Cerebellar-Retinal Degeneration Associated with a Mutation in Mitochondrial Aconitase, ACO2

    Infantile Cerebellar-Retinal Degeneration Associated with a Mutation in Mitochondrial Aconitase, ACO2 по Ronen Spiegel, Ophry Pines, Asaf Ta‐Shma, Efrat Burak, Avraham Shaag, Jonatan Halvardson, Simon Edvardson, Muhammad Mahajna, Shamir Zenvirt, Ann Saada, Stavit A. Shalev, Lars Feuk, Orly Elpeleg

    Опубликовано 2012
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    Artigo
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  8. 8
    Loss of chromosome Y in regulatory T cells

    Loss of chromosome Y in regulatory T cells по Jonas Mattisson, Jonatan Halvardson, Hanna Davies, Bożena Bruhn‐Olszewska, Paweł Olszewski, Marcus Danielsson, Josefin Bjurling, Amanda Lindberg, Ammar Zaghlool, Edyta Rychlicka-Buniowska, Jan P. Dumanski, Lars A. Forsberg

    Опубликовано 2024
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    Artigo
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  9. 9
    Leukocytes with chromosome Y loss have reduced abundance of the cell surface immunoprotein CD99

    Leukocytes with chromosome Y loss have reduced abundance of the cell surface immunoprotein CD99 по Jonas Mattisson, Marcus Danielsson, Maria Hammond, Hanna Davies, Caroline J. Gallant, Jessica Nordlund, Amanda Raine, Malin Edén, Lena Kilander, Martin Ingelsson, Jan P. Dumanski, Jonatan Halvardson, Lars A. Forsberg

    Опубликовано 2021
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    Artigo
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  10. 10
    Longitudinal changes in the frequency of mosaic chromosome Y loss in peripheral blood cells of aging men varies profoundly between individuals

    Longitudinal changes in the frequency of mosaic chromosome Y loss in peripheral blood cells of aging men varies profoundly between individuals по Marcus Danielsson, Jonatan Halvardson, Hanna Davies, Behrooz Torabi Moghadam, Jonas Mattisson, Edyta Rychlicka-Buniowska, Janusz Jaszczyński, Julia Heintz, Lars Lannfelt, Vilmantas Giedraitis, Martin Ingelsson, Jan P. Dumanski, Lars A. Forsberg

    Опубликовано 2019
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    Artigo
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  11. 11
    Mosaic loss of chromosome Y in blood is associated with male susceptibility for idiopathic pulmonary fibrosis

    Mosaic loss of chromosome Y in blood is associated with male susceptibility for idiopathic pulmonary fibrosis по Josefin Bjurling, Nicholas W. Chavkin, Jonatan Halvardson, Mark C. Thel, Jonas Mattisson, John S. Kim, Ammar Zaghlool, Shwu‐Fan Ma, Fernando J. Martínez, Kevin J. Anstrom, Imre Noth, Kenneth Walsh, Lars A. Forsberg

    Опубликовано 2025
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    Artigo
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  12. 12
    Hematopoietic loss of Y chromosome leads to cardiac fibrosis and heart failure mortality

    Hematopoietic loss of Y chromosome leads to cardiac fibrosis and heart failure mortality по Soichi Sano, Keita Horitani, Hayato Ogawa, Jonatan Halvardson, Nicholas W. Chavkin, Ying Wang, Miho Sano, Jonas Mattisson, Atsushi Hata, Marcus Danielsson, Emiri Miura‐Yura, Ammar Zaghlool, Megan A. Evans, Tove Fall, Henry N. De Hoyos, Johan Sundström, Yoshimitsu Yura, Anupreet Kour, Yohei Arai, Mark C. Thel, Yuka Arai, Josyf C. Mychaleckyj, Karen K. Hirschi, Lars A. Forsberg, Kenneth Walsh

    Опубликовано 2022
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    Artigo
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  13. 13
    Immune cells lacking Y chromosome show dysregulation of autosomal gene expression

    Immune cells lacking Y chromosome show dysregulation of autosomal gene expression по Jan P. Dumanski, Jonatan Halvardson, Hanna Davies, Edyta Rychlicka-Buniowska, Jonas Mattisson, Behrooz Torabi Moghadam, Noémi Nagy, Kazimierz Węglarczyk, Karolina Bukowska-Straková, Marcus Danielsson, Paweł Olszewski, Arkadiusz Piotrowski, Erin Oerton, Aleksandra Ambicka, Marcin Przewoźnik, Łukasz Bełch, Tomasz Grodzicki, Piotr Chłosta, Stefan Imreh, Vilmantas Giedraitis, Lena Kilander, Jessica Nordlund, Adam Ameur, Ulf Gyllensten, Åsa Johansson, Alicja Józkowicz, Maciej Siedlar, Alicja Klich‐Rączka, Janusz Jaszczyński, Stefan Enroth, Jarosław Baran, Martin Ingelsson, John R. B. Perry, Janusz Ryś, Lars A. Forsberg

    Опубликовано 2021
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    Artigo
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  14. 14
    Genetic predisposition to mosaic Y chromosome loss in blood

    Genetic predisposition to mosaic Y chromosome loss in blood по Deborah J. Thompson, Giulio Genovese, Jonatan Halvardson, Jacob C. Ulirsch, Daniel J. Wright, Chikashi Terao, Olafur B. Davidsson, Felix R. Day, Patrick Sulem, Yunxuan Jiang, Marcus Danielsson, Hanna Davies, Joe Dennis, Malcolm G. Dunlop, Douglas F. Easton, Victoria A. Fisher, Florian Zink, Richard S. Houlston, Martin Ingelsson, Siddhartha Kar, Nicola D. Kerrison, Ben Kinnersley, Ragnar P. Kristjansson, Philip Law, Rong Li, Chey Loveday, Jonas Mattisson, Steven A. McCarroll, Yoshinori Murakami, Anna Murray, Paweł Olszewski, Edyta Rychlicka-Buniowska, Robert A. Scott, Unnur Þorsteinsdóttir, Ian Tomlinson, Behrooz Torabi Moghadam, Clare Turnbull, Nicholas J. Wareham, Daníel F. Guðbjartsson, Yoichiro Kamatani, Eva R. Hoffmann, Stephen P. Jackson, Kāri Stefánsson, Adam Auton, Ken K. Ong, Mitchell J. Machiela, Po‐Ru Loh, Jan P. Dumanski, Stephen J. Chanock, Lars A. Forsberg, John R. B. Perry

    Опубликовано 2019
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    Artigo
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