Torthaí cuardaigh - Anna Matynia

  • 1 - 14 toradh as 14 á dtaispeáint
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  1. 1
    Ran-binding Protein-1 Is an Essential Component of the Ran/RCC1 Molecular Switch System in Budding Yeast

    Ran-binding Protein-1 Is an Essential Component of the Ran/RCC1 Molecular Switch System in Budding Yeast de réir Ilia I. Ouspenski, Ulrich Mueller, Anna Matynia, Shelley Sazer, Stephen J. Elledge, B. R. Brinkley

    Foilsithe / Cruthaithe 1995
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    Artigo
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  2. 2
    Melanopsin-Positive Intrinsically Photosensitive Retinal Ganglion Cells: From Form to Function

    Melanopsin-Positive Intrinsically Photosensitive Retinal Ganglion Cells: From Form to Function de réir Tiffany M. Schmidt, Michael Tri H., Dennis M. Dacey, Robert J. Lucas, Samer Hattar, Anna Matynia

    Foilsithe / Cruthaithe 2011
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    Revisão
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  3. 3
    DNA hypomethylation restricted to the murine forebrain induces cortical degeneration and impairs postnatal neuronal maturation

    DNA hypomethylation restricted to the murine forebrain induces cortical degeneration and impairs postnatal neuronal maturation de réir Leah Hutnick, Peyman Golshani, Masakazu Namihira, Zhigang Xue, Anna Matynia, Xiaojun Yang, Alcino J. Silva, Felix E. Schweizer, Guoping Fan

    Foilsithe / Cruthaithe 2009
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  4. 4
    Matrix Metalloproteinase-9 Is Required for Hippocampal Late-Phase Long-Term Potentiation and Memory

    Matrix Metalloproteinase-9 Is Required for Hippocampal Late-Phase Long-Term Potentiation and Memory de réir Vanja Nagy, Ozlem Bozdagi, Anna Matynia, Marcin Balcerzyk, Pawel Okulski, Joanna Dzwonek, Rui M. Costa, Alcino J. Silva, Leszek Kaczmarek, George W. Huntley

    Foilsithe / Cruthaithe 2006
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  5. 5
    De Novo Occurrence of a Variant in ARL3 and Apparent Autosomal Dominant Transmission of Retinitis Pigmentosa

    De Novo Occurrence of a Variant in ARL3 and Apparent Autosomal Dominant Transmission of Retinitis Pigmentosa de réir Samuel P. Strom, Michael J. Clark, Ariadna Martinez, Sarah Garcia, Amira A. Abelazeem, Anna Matynia, Sachin Parikh, Lori S. Sullivan, Sara J. Bowne, Stephen P. Daiger, Michael B. Gorin

    Foilsithe / Cruthaithe 2016
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  6. 6
    High‐resolution characterization of a PACAP‐EGFP transgenic mouse model for mapping PACAP‐expressing neurons

    High‐resolution characterization of a PACAP‐EGFP transgenic mouse model for mapping PACAP‐expressing neurons de réir Michael Condro, Anna Matynia, Nicholas N. Foster, Yukio Ago, Abha K. Rajbhandari, Christina Van, Bhavaani Jayaram, Sachin Parikh, Anna L. Diep, Eileen Nguyen, Víctor May, Hong‐Wei Dong, James A. Waschek

    Foilsithe / Cruthaithe 2016
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  7. 7
    Peripheral Sensory Neurons Expressing Melanopsin Respond to Light

    Peripheral Sensory Neurons Expressing Melanopsin Respond to Light de réir Anna Matynia, Eileen Nguyen, Xiaoping Sun, Frank W. Blixt, Sachin Parikh, Jason Kessler, Luis Pérez de Sevilla Müller, Samer Habib, Paul Kim, Zhe Z. Wang, Allen Rodriguez, Andrew Charles, Steven Nusinowitz, Lars Edvinsson, Steven Barnes, Nicholas C. Brecha, Michael B. Gorin

    Foilsithe / Cruthaithe 2016
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  8. 8
    Systematic assessment of the contribution of structural variants to inherited retinal diseases

    Systematic assessment of the contribution of structural variants to inherited retinal diseases de réir Shu Wen, Meng C. Wang, Xinye Qian, Yumei Li, Keqing Wang, Jongsu Choi, Mark E. Pennesi, Paul Yang, Molly Marra, Robert K. Koenekoop, Irma López, Anna Matynia, Michael B. Gorin, Ruifang Sui, Fengxia Yao, Kerry Goetz, Fernanda Belga Ottoni Porto, Rui Chen

    Foilsithe / Cruthaithe 2023
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  9. 9
    Systematic assessment of the contribution of structural variants to inherited retinal diseases

    Systematic assessment of the contribution of structural variants to inherited retinal diseases de réir Shu Wen, Meng C. Wang, Xinye Qian, Yumei Li, Keqing Wang, Jongsu Choi, Mark E. Pennesi, Paul Yang, Molly Marra, Robert K. Koenekoop, Irma López, Anna Matynia, Michael B. Gorin, Ruifang Sui, Fengxia Yao, Kerry Goetz, Fernanda Belga Ottoni Porto, Rui Chen

    Foilsithe / Cruthaithe 2023
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  10. 10
    Epigenetic alterations in longevity regulators, reduced life span, and exacerbated aging-related pathology in old father offspring mice

    Epigenetic alterations in longevity regulators, reduced life span, and exacerbated aging-related pathology in old father offspring mice de réir Kan Xie, Devon Ryan, Brandon L. Pearson, Kristin S. Henzel, Frauke Neff, Ramón Vidal, Magali Hennion, Isabelle Lehmann, Melvin Schleif, Susanne Schröder, Thure Adler, Birgit Rathkolb, Jan Rozman, Anna‐Lena Schütz, Cornelia Prehn, Michel‐Edwar Mickael, Marco Weiergräber, Jerzy Adamski, Dirk H. Busch, Gerhard Ehninger, Anna Matynia, Walker S. Jackson, Eckhard Wolf, Helmut Fuchs, Valérie Gailus‐Durner, Stefan Bonn, Martin Hrabě de Angelis, Dan Ehninger

    Foilsithe / Cruthaithe 2018
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  11. 11
    Association of Sex With Frequent and Mild <i>ABCA4</i> Alleles in Stargardt Disease

    Association of Sex With Frequent and Mild <i>ABCA4</i> Alleles in Stargardt Disease de réir Esmee H. Runhart, Mubeen Khan, Stéphanie S. Cornelis, Susanne Roosing, Marta Del Pozo‐Valero, Tina M. Lamey, Petra Lišková, Lisa Roberts, Heidi Stöhr, Caroline C. W. Klaver, Carel B. Hoyng, Frans P.M. Cremers, Claire‐Marie Dhaenens, Alaa AlTabishi, Carmen Ayuso, Sandro Banfi, Tamar Ben‐Yosef, L. Ingeborgh van den Born, Ana Fakin, G. Jane Farrar, Juliana Maria Ferraz Sallum, Kaoru Fujinami, Michael B. Gorin, L Hlavatá, Smaragda Kamakari, Bohdan Kousal, Ian M. MacDonald, Terri L. McLaren, Anna Matynia, Monika Ołdak, Osvaldo L. Podhajcer, Raj Ramesar, John N. De Roach, Dror Sharon, Francesca Simonelli, Francesco Testa, Jennifer A. Thompson, Anna M. Tracewska, Andrea L. Vincent, Bernhard H. F. Weber

    Foilsithe / Cruthaithe 2020
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  12. 12
    Towards Uncovering the Role of Incomplete Penetrance in Maculopathies through Sequencing of 105 Disease-Associated Genes

    Towards Uncovering the Role of Incomplete Penetrance in Maculopathies through Sequencing of 105 Disease-Associated Genes de réir Rebekkah J. Hitti‐Malin, Daan M. Panneman, Zelia Corradi, Erica G. M. Boonen, Galuh Astuti, Claire‐Marie Dhaenens, Heidi Stöhr, Bernhard H. F. Weber, Dror Sharon, Eyal Banin, Marianthi Karali, Sandro Banfi, Tamar Ben‐Yosef, Damjan Glavač, G. Jane Farrar, Carmen Ayuso, Petra Lišková, Ľubica Ďuďáková, Marie Vajter, Monika Ołdak, Jacek P. Szaflik, Anna Matynia, Michael B. Gorin, Kati Kämpjärvi, Miriam Bauwens, Elfride De Baere, Carel B. Hoyng, Catherina H. Z. Li, Caroline C. W. Klaver, Chris F. Inglehearn, Kaoru Fujinami, Carlo Rivolta, Rando Allikmets, Jana Zernant, Winston Lee, Osvaldo L. Podhajcer, Ana Fakin, Jana Sajovic, Alaa AlTalbishi, Sandra Valeiņa, Gita Tauriņa, Andrea L. Vincent, Lisa Roberts, Raj Ramesar, Giovanna Sartor, Elena Luppi, Susan M. Downes, L. Ingeborgh van den Born, Terri L. McLaren, John N. De Roach, Tina M. Lamey, Jennifer A. Thompson, Fred K. Chen, Anna M. Tracewska, Smaragda Kamakari, Juliana Maria Ferraz Sallum, Hanno J. Bolz, Hülya Kayserili, Susanne Roosing, Frans P.M. Cremers

    Foilsithe / Cruthaithe 2024
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  13. 13
    Resolving the dark matter of <i>ABCA4</i> for 1,054 Stargardt disease probands through integrated genomics and transcriptomics

    Resolving the dark matter of <i>ABCA4</i> for 1,054 Stargardt disease probands through integrated genomics and transcriptomics de réir Mubeen Khan, Stéphanie S. Cornelis, Marta Del Pozo‐Valero, Laura Whelan, Esmee H. Runhart, Ketan Mishra, Femke Bults, Yahya AlSwaiti, Alaa AlTabishi, Elfride De Baere, Sandro Banfi, Eyal Banin, Miriam Bauwens, Tamar Ben‐Yosef, Camiel J. F. Boon, L. Ingeborgh van den Born, Sabine Defoort, Aurore Devos, Adrian Dockery, Ľubica Ďuďáková, Ana Fakin, G. Jane Farrar, Juliana Maria Ferraz Sallum, Kaoru Fujinami, Christian Gilissen, Damjan Glavač, Michael B. Gorin, Jacquie Greenberg, Takaaki Hayashi, Ymkje M. Hettinga, Alexander Hoischen, Carel B. Hoyng, Karsten Hufendiek, Herbert Jägle, Smaragda Kamakari, Marianthi Karali, Ulrich Kellner, Caroline C. W. Klaver, Bohdan Kousal, Tina M. Lamey, Ian M. MacDonald, Anna Matynia, Terri L. McLaren, Marcela Mena, Isabelle Meunier, Rianne Miller, Hadas Newman, Buhle Ntozini, Monika Ołdak, Marc Pieterse, Osvaldo L. Podhajcer, Bernard Puech, Raj Ramesar, Klaus Rüther, Manar Salameh, Mariana Vallim Salles, Dror Sharon, Francesca Simonelli, Georg Spital, Marloes Steehouwer, Jacek P. Szaflik, Jennifer A. Thompson, C. Thuillier, Anna M. Tracewska, Martine van Zweeden, Andrea L. Vincent, Xavier Zanlonghi, Petra Lišková, Heidi Stöhr, John N. De Roach, Carmen Ayuso, Lisa Roberts, Bernhard H. F. Weber, Claire‐Marie Dhaenens, Frans P.M. Cremers

    Foilsithe / Cruthaithe 2019
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  14. 14
    Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics

    Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics de réir Mubeen Khan, Stéphanie S. Cornelis, Marta Del Pozo‐Valero, Laura Whelan, Esmee H. Runhart, Ketan Mishra, Femke Bults, Yahya AlSwaiti, Alaa AlTalbishi, Elfride De Baere, Sandro Banfi, Eyal Banin, Miriam Bauwens, Tamar Ben‐Yosef, Camiel J. F. Boon, L. Ingeborgh van den Born, Sabine Defoort, Aurore Devos, Adrian Dockery, Ľubica Ďuďáková, Ana Fakin, G. Jane Farrar, Juliana Maria Ferraz Sallum, Kaoru Fujinami, Christian Gilissen, Damjan Glavač, Michael B. Gorin, Jacquie Greenberg, Takaaki Hayashi, Ymkje M. Hettinga, Alexander Hoischen, Carel B. Hoyng, Karsten Hufendiek, Herbert Jägle, Smaragda Kamakari, Marianthi Karali, Ulrich Kellner, Caroline C. W. Klaver, Bohdan Kousal, Tina M. Lamey, Ian M. MacDonald, Anna Matynia, Terri L. McLaren, Marcela Mena, Isabelle Meunier, Rianne Miller, Hadas Newman, Buhle Ntozini, Monika Ołdak, Marc Pieterse, Osvaldo L. Podhajcer, Bernard Puech, Raj Ramesar, Klaus Rüther, Manar Salameh, Mariana Vallim Salles, Dror Sharon, Francesca Simonelli, Georg Spital, Marloes Steehouwer, Jacek P. Szaflik, Jennifer A. Thompson, C. Thuillier, Anna M. Tracewska, Martine van Zweeden, Andrea L. Vincent, Xavier Zanlonghi, Petra Lišková, Heidi Stöhr, John N. De Roach, Carmen Ayuso, Lisa Roberts, Bernhard H. F. Weber, Claire‐Marie Dhaenens, Frans P.M. Cremers

    Foilsithe / Cruthaithe 2020
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