Canlyniadau Chwilio - Anna Matynia
- Dangos 1 - 13 canlyniadau o 13
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DNA hypomethylation restricted to the murine forebrain induces cortical degeneration and impairs postnatal neuronal maturation gan Leah Hutnick, Peyman Golshani, Masakazu Namihira, Zhigang Xue, Anna Matynia, Xiaojun Yang, Alcino J. Silva, Felix E. Schweizer, Guoping Fan
Cyhoeddwyd 2009Artigo -
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Matrix Metalloproteinase-9 Is Required for Hippocampal Late-Phase Long-Term Potentiation and Memory gan Vanja Nagy, Ozlem Bozdagi, Anna Matynia, Marcin Balcerzyk, Pawel Okulski, Joanna Dzwonek, Rui M. Costa, Alcino J. Silva, Leszek Kaczmarek, George W. Huntley
Cyhoeddwyd 2006Artigo -
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De Novo Occurrence of a Variant in ARL3 and Apparent Autosomal Dominant Transmission of Retinitis Pigmentosa gan 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
Cyhoeddwyd 2016Artigo -
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High‐resolution characterization of a PACAP‐EGFP transgenic mouse model for mapping PACAP‐expressing neurons gan 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
Cyhoeddwyd 2016Artigo -
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Peripheral Sensory Neurons Expressing Melanopsin Respond to Light gan 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
Cyhoeddwyd 2016Artigo -
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Systematic assessment of the contribution of structural variants to inherited retinal diseases gan 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
Cyhoeddwyd 2023Pré-impressão -
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Systematic assessment of the contribution of structural variants to inherited retinal diseases gan 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
Cyhoeddwyd 2023Artigo -
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Epigenetic alterations in longevity regulators, reduced life span, and exacerbated aging-related pathology in old father offspring mice gan 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
Cyhoeddwyd 2018Artigo -
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Towards Uncovering the Role of Incomplete Penetrance in Maculopathies through Sequencing of 105 Disease-Associated Genes gan 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
Cyhoeddwyd 2024Artigo -
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Resolving the dark matter of <i>ABCA4</i> for 1,054 Stargardt disease probands through integrated genomics and transcriptomics gan 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
Cyhoeddwyd 2019Pré-impressão -
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Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics gan 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
Cyhoeddwyd 2020Artigo
Offerynnau Chwilio:
Pynciau Perthynol
Biology
Gene
Genetics
Neuroscience
Computational biology
Mutation
Phenotype
ABCA4
Biochemistry
Cell biology
DNA sequencing
Disease gene identification
Exome
Exome sequencing
Genome
Sanger sequencing
Candidate gene
Copy-number variation
DNA methylation
Epigenetics
Gene expression
Genetic heterogeneity
Hippocampal formation
Intrinsically photosensitive retinal ganglion cells
Medicine
Melanopsin
Photopigment
Proband
Receptor
Retina