Resultados da busca - Netta Mäkinen

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  1. 1
    Characterization of MED12, HMGA2, and FH alterations reveals molecular variability in uterine smooth muscle tumors

    Characterization of MED12, HMGA2, and FH alterations reveals molecular variability in uterine smooth muscle tumors por Netta Mäkinen, Kati Kämpjärvi, Norma Frizzell, Ralf Bützow, Pia Vahteristo

    Publicado em 2017
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  2. 2
    Genomics of uterine leiomyomas: insights from high-throughput sequencing

    Genomics of uterine leiomyomas: insights from high-throughput sequencing por Miika Mehine, Netta Mäkinen, Hanna-Riikka Heinonen, Lauri A. Aaltonen, Pia Vahteristo

    Publicado em 2014
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  3. 3
    MED12 exon 2 mutations in histopathological uterine leiomyoma variants

    MED12 exon 2 mutations in histopathological uterine leiomyoma variants por Netta Mäkinen, Pia Vahteristo, Kati Kämpjärvi, Johanna Arola, Ralf Bützow, Lauri A. Aaltonen

    Publicado em 2013
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  4. 4
    MED12 exon 2 mutations are common in uterine leiomyomas from South African patients

    MED12 exon 2 mutations are common in uterine leiomyomas from South African patients por Netta Mäkinen, Hanna-Riikka Heinonen, Shane Moore, Ian Tomlinson, Zephne M. van der Spuy, Lauri A. Aaltonen

    Publicado em 2011
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  5. 5
    Exome Sequencing of Uterine Leiomyosarcomas Identifies Frequent Mutations in TP53, ATRX, and MED12

    Exome Sequencing of Uterine Leiomyosarcomas Identifies Frequent Mutations in TP53, ATRX, and MED12 por Netta Mäkinen, Mervi Aavikko, Tuomas Heikkinen, Minna Taipale, Jussi Taipale, Riitta Koivisto-Korander, Ralf Bützow, Pia Vahteristo

    Publicado em 2016
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  6. 6
    MED12 mutation frequency in unselected sporadic uterine leiomyomas

    MED12 mutation frequency in unselected sporadic uterine leiomyomas por Hanna-Riikka Heinonen, Nanna Sarvilinna, Jari Sjöberg, Kati Kämpjärvi, Esa Pitkänen, Pia Vahteristo, Netta Mäkinen, Lauri A. Aaltonen

    Publicado em 2014
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  7. 7
    Multiple clinical characteristics separate MED12-mutation-positive and -negative uterine leiomyomas

    Multiple clinical characteristics separate MED12-mutation-positive and -negative uterine leiomyomas por Hanna-Riikka Heinonen, Annukka Pasanen, Oskari Heikinheimo, Tomas Tanskanen, Kimmo Palin, Jaana Tolvanen, Pia Vahteristo, Jari Sjöberg, Esa Pitkänen, Ralf Bützow, Netta Mäkinen, Lauri A. Aaltonen

    Publicado em 2017
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  8. 8
    Characterization of Uterine Leiomyomas by Whole-Genome Sequencing

    Characterization of Uterine Leiomyomas by Whole-Genome Sequencing por Miika Mehine, Eevi Kaasinen, Netta Mäkinen, Riku Katainen, Kati Kämpjärvi, Esa Pitkänen, Hanna-Riikka Heinonen, Ralf Bützow, Outi Kilpivaara, Anna Kuosmanen, Heikki Ristolainen, Massimiliano Gentile, Jari Sjöberg, Pia Vahteristo, Lauri A. Aaltonen

    Publicado em 2013
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  9. 9
    Integrated data analysis reveals uterine leiomyoma subtypes with distinct driver pathways and biomarkers

    Integrated data analysis reveals uterine leiomyoma subtypes with distinct driver pathways and biomarkers por Miika Mehine, Eevi Kaasinen, Hanna-Riikka Heinonen, Netta Mäkinen, Kati Kämpjärvi, Nanna Sarvilinna, Mervi Aavikko, Anna Vähärautio, Annukka Pasanen, Ralf Bützow, Oskari Heikinheimo, Jari Sjöberg, Esa Pitkänen, Pia Vahteristo, Lauri A. Aaltonen

    Publicado em 2016
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  10. 10
    MED12 mutations and FH inactivation are mutually exclusive in uterine leiomyomas

    MED12 mutations and FH inactivation are mutually exclusive in uterine leiomyomas por Kati Kämpjärvi, Netta Mäkinen, Miika Mehine, Salla Välipakka, Outi Uimari, Esa Pitkänen, Hanna-Riikka Heinonen, Tuomas Heikkinen, Jaana Tolvanen, Anne Ahtikoski, Norma Frizzell, Nanna Sarvilinna, Jari Sjöberg, Ralf Bützow, Lauri A. Aaltonen, Pia Vahteristo

    Publicado em 2016
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  11. 11
    Exome-wide somatic mutation characterization of small bowel adenocarcinoma

    Exome-wide somatic mutation characterization of small bowel adenocarcinoma por Ulrika A. Hänninen, Riku Katainen, Tomas Tanskanen, Roosa‐Maria Plaketti, Riku Laine, Jiri Hamberg, Ari Ristimäki, ­Eero Pukkala, Minna Taipale, Jukka‐Pekka Mecklin, Linda Forsström, Esa Pitkänen, Kimmo Palin, Niko Välimäki, Netta Mäkinen, Lauri A. Aaltonen

    Publicado em 2018
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  12. 12
    <i>MED12</i> , the <i>Mediator Complex Subunit 12</i> Gene, Is Mutated at High Frequency in Uterine Leiomyomas

    <i>MED12</i> , the <i>Mediator Complex Subunit 12</i> Gene, Is Mutated at High Frequency in Uterine Leiomyomas por Netta Mäkinen, Miika Mehine, Jaana Tolvanen, Eevi Kaasinen, Yilong Li, Heli Lehtonen, Massimiliano Gentile, Jian Yan, Martin Enge, Minna Taipale, Mervi Aavikko, Riku Katainen, Elina Virolainen, Tom Böhling, Taru A. Koski, Virpi Launonen, Jari Sjöberg, Jussi Taipale, Pia Vahteristo, Lauri A. Aaltonen

    Publicado em 2011
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  13. 13
    Uterine Leiomyoma-Linked MED12 Mutations Disrupt Mediator-Associated CDK Activity

    Uterine Leiomyoma-Linked MED12 Mutations Disrupt Mediator-Associated CDK Activity por Mikko Turunen, Jason M. Spaeth, Salla Keskitalo, Min Ju Park, Teemu Kivioja, Alison D. Clark, Netta Mäkinen, Fangjian Gao, Kimmo Palin, Helka Nurkkala, Anna Vähärautio, Mervi Aavikko, Kati Kämpjärvi, Pia Vahteristo, Chongwoo A. Kim, Lauri A. Aaltonen, Markku Varjosalo, Jussi Taipale, Thomas G. Boyer

    Publicado em 2014
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  14. 14
    Somatic MED12 mutations in uterine leiomyosarcoma and colorectal cancer

    Somatic MED12 mutations in uterine leiomyosarcoma and colorectal cancer por Kati Kämpjärvi, Netta Mäkinen, Outi Kilpivaara, Johanna Arola, Hanna-Riikka Heinonen, Jan Böhm, Omar Abdel‐Wahab, Heli Lehtonen, Liisa M. Pelttari, Miika Mehine, Heinrich Schrewe, Heli Nevanlinna, Ross L. Levine, Peter Hokland, Tom Böhling, Jukka‐Pekka Mecklin, Ralf Bützow, Lauri A. Aaltonen, Pia Vahteristo

    Publicado em 2012
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  15. 15
    Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis

    Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis por C. Scott Gallagher, Netta Mäkinen, Holly R. Harris, Nilüfer Rahmioğlu, Outi Uimari, James P. Cook, Nina Shigesi, Teresa Ferreira, Digna Velez-Edwards, Todd L. Edwards, Sally Mortlock, Z. Ruhioglu, Felix R. Day, Christian M. Becker, Ville Karhunen, Hannu Martikainen, Marjo‐Riitta Järvelin, Rita M. Cantor, Paul M. Ridker, Kathryn L. Terry, Julie E. Buring, Scott D. Gordon, Sarah E. Medland, Grant W. Montgomery, Dale R. Nyholt, David A. Hinds, Joyce Y. Tung, Michelle Agee, Babak Alipanahi, Adam Auton, Robert K. Bell, Katarzyna Bryc, Sarah L. Elson, Pierre Fontanillas, Nicholas A. Furlotte, Karen E. Huber, Aaron Kleinman, Nadia K. Litterman, Matthew H. McIntyre, Joanna L. Mountain, Elizabeth S. Noblin, Carrie A. M. Northover, Steven J. Pitts, J. Fah Sathirapongsasuti, Olga V. Sazonova, Janie F. Shelton, Suyash Shringarpure, Chao Tian, Vladimir Vacic, Catherine H. Wilson, John R. B. Perry, Penelope A. Lind, Jodie N. Painter, Nicholas G. Martin, Andrew P. Morris, Daniel I. Chasman, Stacey A. Missmer, Krina T. Zondervan, Cynthia C. Morton

    Publicado em 2019
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