Transcriptome Profiling of NIH3T3 Cell Lines Expressing Opsin and the P23H Opsin Mutant Identifies Candidate Drugs for the Treatment of Retinitis Pigmentosa

Por Chen, Yuanyuan, Brooks, Matthew J, Gieser, Linn, Swaroop, Anand, Palczewski, Krzysztof
Publicado no Pharmacol Res (2016)

Gene expression changes in aging retinal microglia: relationship to microglial support functions and regulation of activation

Por Ma, Wenxin, Cojocaru, Radu, Gotoh, Norimoto, Gieser, Linn, Villasmil, Rafael, Cogliati, Tiziana, Swaroop, Anand, Wong, Wai T.
Publicado em 2013

Oligodeoxyribonucleotide probe accessibility on a three-dimensional DNA microarray surface and the effect of hybridization time on the accuracy of expression ratios

Por Dorris, David R, Nguyen, Allen, Gieser, Linn, Lockner, Randall, Lublinsky, Anna, Patterson, Marcus, Touma, Edward, Sendera, Timothy J, Elghanian, Robert, Mazumder, Abhijit
Publicado em 2003

Remapping of the RP15 Locus for X-Linked Cone-Rod Degeneration to Xp11.4-p21.1, and Identification of a De Novo Insertion in the RPGR Exon ORF15

Por Mears, Alan J., Hiriyanna, Suja, Vervoort, Raf, Yashar, Beverly, Gieser, Linn, Fahrner, Stacey, Daiger, Stephen P., Heckenlively, John R., Sieving, Paul A., Wright, Alan F., Swaroop, Anand
Publicado em 2000

Transcriptional Regulation of Rod Photoreceptor Homeostasis Revealed by In Vivo NRL Targetome Analysis

Por Hao, Hong, Kim, Douglas S., Klocke, Bernward, Johnson, Kory R., Cui, Kairong, Gotoh, Norimoto, Zang, Chongzhi, Gregorski, Janina, Gieser, Linn, Peng, Weiqun, Fann, Yang, Seifert, Martin, Zhao, Keji, Swaroop, Anand
Publicado em 2012

Synergistically acting agonists and antagonists of G protein–coupled receptors prevent photoreceptor cell degeneration

Por Chen, Yu, Palczewska, Grazyna, Masuho, Ikuo, Gao, Songqi, Jin, Hui, Dong, Zhiqian, Gieser, Linn, Brooks, Matthew J., Kiser, Philip D., Kern, Timothy S., Martemyanov, Kirill A., Swaroop, Anand, Palczewski, Krzysztof
Publicado no Sci Signal (2016)

An assessment of Motorola CodeLink™ microarray performance for gene expression profiling applications

Por Ramakrishnan, Ramesh, Dorris, David, Lublinsky, Anna, Nguyen, Allen, Domanus, Marc, Prokhorova, Anna, Gieser, Linn, Touma, Edward, Lockner, Randall, Tata, Murthy, Zhu, Xiaomei, Patterson, Marcus, Shippy, Richard, Sendera, Timothy J., Mazumder, Abhijit
Publicado em 2002

NRL-Regulated Transcriptome Dynamics of Developing Rod Photoreceptors

Por Kim, Jung-Woong, Yang, Hyun-Jin, Brooks, Matthew John, Zelinger, Lina, Karakülah, Gökhan, Gotoh, Norimoto, Boleda, Alexis, Gieser, Linn, Giuste, Felipe, Whitaker, Dustin Thad, Walton, Ashley, Villasmil, Rafael, Barb, Jennifer J., Munson, Peter Jonathan, Kaya, Koray Dogan, Chaitankar, Vijender, Cogliati, Tiziana, Swaroop, Anand
Publicado no Cell Rep (2016)

Whole Exome Sequencing Reveals Mutations in Known Retinal Disease Genes in 33 out of 68 Israeli Families with Inherited Retinopathies

Por Beryozkin, Avigail, Shevah, Elia, Kimchi, Adva, Mizrahi-Meissonnier, Liliana, Khateb, Samer, Ratnapriya, Rinki, Lazar, Csilla H., Blumenfeld, Anat, Ben-Yosef, Tamar, Hemo, Yitzhak, Pe’er, Jacob, Averbuch, Eduard, Sagi, Michal, Boleda, Alexis, Gieser, Linn, Zlotogorski, Abraham, Falik-Zaccai, Tzipora, Alimi-Kasem, Ola, Jacobson, Samuel G., Chowers, Itay, Swaroop, Anand, Banin, Eyal, Sharon, Dror
Publicado no Sci Rep (2015)

Mutations in a BTB-Kelch Protein, KLHL7, Cause Autosomal-Dominant Retinitis Pigmentosa

Por Friedman, James S., Ray, Joseph W., Waseem, Naushin, Johnson, Kory, Brooks, Matthew J., Hugosson, Therése, Breuer, Debra, Branham, Kari E., Krauth, Daniel S., Bowne, Sara J., Sullivan, Lori S., Ponjavic, Vesna, Gränse, Lotta, Khanna, Ritu, Trager, Edward H., Gieser, Linn M., Hughbanks-Wheaton, Dianna, Cojocaru, Radu I., Ghiasvand, Noor M., Chakarova, Christina F., Abrahamson, Magnus, Göring, Harald H.H., Webster, Andrew R., Birch, David G., Abecasis, Goncalo R., Fann, Yang, Bhattacharya, Shomi S., Daiger, Stephen P., Heckenlively, John R., Andréasson, Sten, Swaroop, Anand
Publicado em 2009

A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants

Por Fritsche, Lars G., Igl, Wilmar, Cooke Bailey, Jessica N., Grassmann, Felix, Sengupta, Sebanti, Bragg-Gresham, Jennifer L., Burdon, Kathryn P., Hebbring, Scott J., Wen, Cindy, Gorski, Mathias, Kim, Ivana K., Cho, David, Zack, Donald, Souied, Eric, Scholl, Hendrik P. N., Bala, Elisa, Lee, Kristine E., Hunter, David J., Sardell, Rebecca J., Mitchell, Paul, Merriam, Joanna E., Cipriani, Valentina, Hoffman, Joshua D., Schick, Tina, Lechanteur, Yara T. E., Guymer, Robyn H., Johnson, Matthew P., Jiang, Yingda, Stanton, Chloe M., Buitendijk, Gabriëlle H. S., Zhan, Xiaowei, Kwong, Alan M., Boleda, Alexis, Brooks, Matthew, Gieser, Linn, Ratnapriya, Rinki, Branham, Kari E., Foerster, Johanna R., Heckenlively, John R., Othman, Mohammad I., Vote, Brendan J., Liang, Helena Hai, Souzeau, Emmanuelle, McAllister, Ian L., Isaacs, Timothy, Hall, Janette, Lake, Stewart, Mackey, David A., Constable, Ian J., Craig, Jamie E., Kitchner, Terrie E., Yang, Zhenglin, Su, Zhiguang, Luo, Hongrong, Chen, Daniel, Ouyang, Hong, Flagg, Ken, Lin, Danni, Mao, Guanping, Ferreyra, Henry, Stark, Klaus, von Strachwitz, Claudia N., Wolf, Armin, Brandl, Caroline, Rudolph, Guenther, Olden, Matthias, Morrison, Margaux A., Morgan, Denise J., Schu, Matthew, Ahn, Jeeyun, Silvestri, Giuliana, Tsironi, Evangelia E., Park, Kyu Hyung, Farrer, Lindsay A., Orlin, Anton, Brucker, Alexander, Li, Mingyao, Curcio, Christine, Mohand-Saïd, Saddek, Sahel, José-Alain, Audo, Isabelle, Benchaboune, Mustapha, Cree, Angela J., Rennie, Christina A., Goverdhan, Srinivas V., Grunin, Michelle, Hagbi-Levi, Shira, Campochiaro, Peter, Katsanis, Nicholas, Holz, Frank G., Blond, Frédéric, Blanché, Hélène, Deleuze, Jean-François, Igo, Robert P., Truitt, Barbara, Peachey, Neal S., Meuer, Stacy M., Myers, Chelsea E., Moore, Emily L., Klein, Ronald, Hauser, Michael A., Postel, Eric A., Courtenay, Monique D., Schwartz, Stephen G., Kovach, Jaclyn L., Scott, William K., Liew, Gerald, Tƒan, Ava G., Gopinath, Bamini, Merriam, John C., Smith, R. Theodore, Khan, Jane C., Shahid, Humma, Moore, Anthony T., McGrath, J. Allie, Laux, Reneé, Brantley, Milam A., Agarwal, Anita, Ersoy, Lebriz, Caramoy, Albert, Langmann, Thomas, Saksens, Nicole T. M., de Jong, Eiko K., Hoyng, Carel B., Cain, Melinda S., Richardson, Andrea J., Martin, Tammy M., Blangero, John, Weeks, Daniel E., Dhillon, Bal, van Duijn, Cornelia M., Doheny, Kimberly F., Romm, Jane, Klaver, Caroline C. W., Hayward, Caroline, Gorin, Michael B., Klein, Michael L., Baird, Paul N., den Hollander, Anneke I., Fauser, Sascha, Yates, John R. W., Allikmets, Rando, Wang, Jie Jin, Schaumberg, Debra A., Klein, Barbara E. K., Hagstrom, Stephanie A., Chowers, Itay, Lotery, Andrew J., Léveillard, Thierry, Zhang, Kang, Brilliant, Murray H., Hewitt, Alex W., Swaroop, Anand, Chew, Emily Y., Pericak-Vance, Margaret A., DeAngelis, Margaret, Stambolian, Dwight, Haines, Jonathan L., Iyengar, Sudha K., Weber, Bernhard H. F., Abecasis, Gonçalo R., Heid, Iris M.
Publicado no Nat Genet (2015)