Resultados de búsqueda - Wilson, Nathan R
- Mostrando 1 - 12 Resultados de 12
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Response features of parvalbumin-expressing interneurons suggest precise roles for subtypes of inhibition in visual cortex por Runyan, Caroline A., Schummers, James, Wart, Audra Van, Kuhlman, Sandra J., Wilson, Nathan R., Huang, Z. Josh, Sur, Mriganka
Publicado 2010Texto -
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Presynaptic Regulation of Quantal Size by the Vesicular Glutamate Transporter VGLUT1 por Wilson, Nathan R., Kang, Jiansheng, Hueske, Emily V., Leung, Tony, Varoqui, Helene, Murnick, Jonathan G., Erickson, Jeffrey D., Liu, Guosong
Publicado 2005Texto -
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A Platform for Spatiotemporal “Matrix” Stimulation in Brain Networks Reveals Novel Forms of Circuit Plasticity por Wilson, Nathan R., Wang, Forea L., Chen, Naiyan, Yan, Sherry X., Daitch, Amy L., Shi, Bo, Sharma, Samvaran, Sur, Mriganka
Publicado 2022Texto -
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Partial reversal of Rett Syndrome-like symptoms in MeCP2 mutant mice por Tropea, Daniela, Giacometti, Emanuela, Wilson, Nathan R., Beard, Caroline, McCurry, Cortina, Fu, Dong Dong, Flannery, Ruth, Jaenisch, Rudolf, Sur, Mriganka
Publicado 2009Texto -
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SPECC1L-deficient primary mouse embryonic palatal mesenchyme cells show speed and directionality defects por Goering, Jeremy P., Isai, Dona G., Hall, Everett G., Wilson, Nathan R., Kosa, Edina, Wenger, Luke W., Umar, Zaid, Yousaf, Abdul, Czirok, Andras, Saadi, Irfan
Publicado 2021Texto -
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Exome sequencing reveals a thrombopoietin ligand mutation in a Micronesian family with autosomal recessive aplastic anemia por Dasouki, Majed J., Rafi, Syed K., Olm-Shipman, Adam J., Wilson, Nathan R., Abhyankar, Sunil, Ganter, Brigitte, Furness, L. Mike, Fang, Jianwen, Calado, Rodrigo T., Saadi, Irfan
Publicado 2013Texto -
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Anti-epileptic drug topiramate upregulates TGFβ1 and SOX9 expression in primary embryonic palatal mesenchyme cells: Implications for teratogenicity por Rafi, Syed K., Goering, Jeremy P., Olm-Shipman, Adam J., Hipp, Lauren A., Ernst, Nicholas J., Wilson, Nathan R., Hall, Everett G., Gunewardena, Sumedha, Saadi, Irfan
Publicado 2021Texto -
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Mutations in SPECC1L, encoding sperm antigen with calponin homology and coiled-coil domains 1-like, are found in some cases of autosomal dominant Opitz G/BBB syndrome por Kruszka, Paul, Li, Dong, Harr, Margaret H, Wilson, Nathan R, Swarr, Daniel, McCormick, Elizabeth M, Chiavacci, Rosetta M, Li, Mindy, Martinez, Ariel F, Hart, Rachel A, McDonald-McGinn, Donna M, Deardorff, Matthew A, Falk, Marni J, Allanson, Judith E, Hudson, Cindy, Johnson, John P, Saadi, Irfan, Hakonarson, Hakon, Muenke, Maximilian, Zackai, Elaine H
Publicado 2014Texto -
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SPECC1L regulates palate development downstream of IRF6 por Hall, Everett G, Wenger, Luke W, Wilson, Nathan R, Undurty-Akella, Sraavya S, Standley, Jennifer, Augustine-Akpan, Eno-Abasi, Kousa, Youssef A, Acevedo, Diana S, Goering, Jeremy P, Pitstick, Lenore, Natsume, Nagato, Paroya, Shahnawaz M, Busch, Tamara D, Ito, Masaaki, Mori, Akihiro, Imura, Hideto, Schultz-Rogers, Laura E, Klee, Eric W, Babovic-Vuksanovic, Dusica, Kroc, Sarah A, Adeyemo, Wasiu L, Eshete, Mekonen A, Bjork, Bryan C, Suzuki, Satoshi, Murray, Jeffrey C, Schutte, Brian C, Butali, Azeez, Saadi, Irfan
Publicado 2020Texto