Rezultati pretrage - Cherry, Timothy

Development and diversification of retinal amacrine interneurons at single cell resolution od Cherry, Timothy J., Trimarchi, Jeffrey M., Stadler, Michael B., Cepko, Constance L.

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Distinct features of brain perivascular fibroblasts and mural cells revealed by in vivo two-photon imaging od Bonney, Stephanie K, Sullivan, Liam T, Cherry, Timothy J, Daneman, Richard, Shih, Andy Y

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NeuroD Factors Regulate Cell Fate and Neurite Stratification in the Developing Retina od Cherry, Timothy J., Wang, Sui, Bormuth, Ingo, Schwab, Markus, Olson, James, Cepko, Constance L.

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Monocarboxylate Transporter 1 (MCT1) Mediates Succinate Export in the Retina od Bisbach, Celia M., Hass, Daniel T., Thomas, Eric D., Cherry, Timothy J., Hurley, James B.

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Machine Learning Prediction of Non-Coding Variant Impact in Human Retinal cis-Regulatory Elements od VandenBosch, Leah S., Luu, Kelsey, Timms, Andrew E., Challam, Shriya, Wu, Yue, Lee, Aaron Y., Cherry, Timothy J.

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Early asymmetry of gene transcription between embryonic human left and right cerebral cortex od Sun, Tao, Patoine, Christina, Abu-Khalil, Amir, Visvader, Jane, Sum, Eleanor, Cherry, Timothy J., Orkin, Stuart H., Geschwind, Daniel H., Walsh, Christopher A.

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Transient expression of a GABA receptor subunit during early development is critical for inhibitory synapse maturation and function od Sinha, Raunak, Grimes, William N, Wallin, Julie, Ebbinghaus, Briana N, Luu, Kelsey, Cherry, Timothy, Rieke, Fred, Rudolph, Uwe, Wong, Rachel O, Hoon, Mrinalini

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Chromatin Environment and Cellular Context Specify Compensatory Activity of Paralogous MEF2 Transcription Factors od Majidi, Shahriyar P., Reddy, Naveen C., Moore, Michael J., Chen, Hao, Yamada, Tomoko, Andzelm, Milena M., Cherry, Timothy J., Hu, Linda S., Greenberg, Michael E., Bonni, Azad

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Mapping the cis-regulatory architecture of the human retina reveals noncoding genetic variation in disease od Cherry, Timothy J., Yang, Marty G., Harmin, David A., Tao, Peter, Timms, Andrew E., Bauwens, Miriam, Allikmets, Rando, Jones, Evan M., Chen, Rui, De Baere, Elfride, Greenberg, Michael E.

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Contribution of non-coding mutations to RPGRIP1-mediated inherited retinal degeneration od Jamshidi, Farzad, Place, Emily M., Mehrotra, Sudeep, Navarro-Gomez, Daniel, Maher, Mathew, Branham, Kari E., Valkanas, Elise, Cherry, Timothy J., Lek, Monkol, MacArthur, Daniel, Pierce, Eric A., Bujakowska, Kinga M.

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Cell-Specific Cis-Regulatory Elements and Mechanisms of Non-Coding Genetic Disease in Human Retina and Retinal Organoids od Thomas, Eric D., Timms, Andrew E., Giles, Sarah, Harkins-Perry, Sarah, Lyu, Pin, Hoang, Thanh, Qian, Jiang, Jackson, Victoria E., Bahlo, Melanie, Blackshaw, Seth, Friedlander, Martin, Eade, Kevin, Cherry, Timothy J.

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MEF2D drives photoreceptor development through a genome-wide competition for tissue-specific enhancers od Andzelm, Milena M., Cherry, Timothy J., Harmin, David A., Boeke, Annabel C., Lee, Charlotte, Hemberg, Martin, Pawlyk, Basil, Malik, Athar N., Flavell, Steven W., Sandberg, Michael A., Raviola, Elio, Greenberg, Michael E.

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Gene regulatory networks controlling temporal patterning, neurogenesis, and cell-fate specification in mammalian retina od Lyu, Pin, Hoang, Thanh, Santiago, Clayton P., Thomas, Eric D., Timms, Andrew E., Appel, Haley, Gimmen, Megan, Le, Nguyet, Jiang, Lizhi, Kim, Dong Won, Chen, Siqi, Espinoza, David F., Telger, Ariel E., Weir, Kurt, Clark, Brian S., Cherry, Timothy J., Qian, Jiang, Blackshaw, Seth

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Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations od Van Schil, Kristof, Naessens, Sarah, Van de Sompele, Stijn, Carron, Marjolein, Aslanidis, Alexander, Van Cauwenbergh, Caroline, Kathrin Mayer, Anja, Van Heetvelde, Mattias, Bauwens, Miriam, Verdin, Hannah, Coppieters, Frauke, Greenberg, Michael E, Yang, Marty G, Karlstetter, Marcus, Langmann, Thomas, De Preter, Katleen, Kohl, Susanne, Cherry, Timothy J, Leroy, Bart P, De Baere, Elfride

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Correction: Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations od Van Schil, Kristof, Naessens, Sarah, Van de Sompele, Stijn, Carron, Marjolein, Aslanidis, Alexander, Van Cauwenbergh, Caroline, Mayer, Anja K., Van Heetvelde, Mattias, Bauwens, Miriam, Verdin, Hannah, Coppieters, Frauke, Greenberg, Michael E., Yang, Marty G., Karlstetter, Marcus, Langmann, Thomas, De Preter, Katleen, Kohl, Susanne, Cherry, Timothy J., Leroy, Bart P., De Baere, Elfride

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Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease od Van de Sompele, Stijn, Smith, Claire, Karali, Marianthi, Corton, Marta, Van Schil, Kristof, Peelman, Frank, Cherry, Timothy, Rosseel, Toon, Verdin, Hannah, Derolez, Julien, Van Laethem, Thalia, Khan, Kamron N., McKibbin, Martin, Toomes, Carmel, Ali, Manir, Torella, Annalaura, Testa, Francesco, Jimenez, Belen, Simonelli, Francesca, De Zaeytijd, Julie, Van den Ende, Jenneke, Leroy, Bart P., Coppieters, Frauke, Ayuso, Carmen, Inglehearn, Chris F., Banfi, Sandro, De Baere, Elfride

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Correction: Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease od Van de Sompele, Stijn, Smith, Claire, Karali, Marianthi, Corton, Marta, Van Schil, Kristof, Peelman, Frank, Cherry, Timothy, Rosseel, Toon, Verdin, Hannah, Derolez, Julien, Van Laethem, Thalia, Khan, Kamron N., McKibbin, Martin, Toomes, Carmel, Ali, Manir, Torella, Annalaura, Testa, Francesco, Jimenez, Belen, Simonelli, Francesca, De Zaeytijd, Julie, Van den Ende, Jenneke, Leroy, Bart P., Coppieters, Frauke, Ayuso, Carmen, Inglehearn, Chris F., Banfi, Sandro, De Baere, Elfride

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ABCA4-associated disease as a model for missing heritability in autosomal recessive disorders: novel noncoding splice, cis-regulatory, structural, and recurrent hypomorphic variant... od Bauwens, Miriam, Garanto, Alejandro, Sangermano, Riccardo, Naessens, Sarah, Weisschuh, Nicole, De Zaeytijd, Julie, Khan, Mubeen, Sadler, Françoise, Balikova, Irina, Van Cauwenbergh, Caroline, Rosseel, Toon, Bauwens, Jim, De Leeneer, Kim, De Jaegere, Sarah, Van Laethem, Thalia, De Vries, Meindert, Carss, Keren, Arno, Gavin, Fakin, Ana, Webster, Andrew R., de Ravel de l’Argentière, Thomy J. L., Sznajer, Yves, Vuylsteke, Marnik, Kohl, Susanne, Wissinger, Bernd, Cherry, Timothy, Collin, Rob W. J., Cremers, Frans P. M., Leroy, Bart P., De Baere, Elfride

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