Search Results - Haider, Neena B.

Role of Nuclear Receptors in Central Nervous System Development and Associated Diseases by Olivares, Ana Maria, Moreno-Ramos, Oscar Andrés, Haider, Neena B.

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Patterned Neuroprotection in the Inpp4a(wbl) Mutant Mouse Cerebellum Correlates with the Expression of Eaat4 by Sachs, Andrew J., David, Samuel A., Haider, Neena B., Nystuen, Arne M.

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A novel mutation in Prph2, a gene regulated by Nr2e3, causes retinal degeneration and outer segment defects similar to Nr2e3(rd7/rd7) retinas by Nystuen, Arne M., Sachs, Andrew J., Yuan, Yang, Heuermann, Laura, Haider, Neena B.

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Interspecies Correlations between Human and Mouse NR2E3-Associated Recessive Disease by Iannaccone, Alessandro, Brabbit, Emily, Lopez-Miro, Christiaan, Love, Zoe, Griffiths, Victoria, Kedrov, Marina, Haider, Neena B.

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Whole-Exome Sequencing in a South American Cohort Links ALDH1A3, FOXN1 and Retinoic Acid Regulation Pathways to Autism Spectrum Disorders by Moreno-Ramos, Oscar A., Olivares, Ana María, Haider, Neena B., de Autismo, Liga Colombiana, Lattig, María Claudia

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Nuclear Receptor Rev-erb Alpha (Nr1d1) Functions in Concert with Nr2e3 to Regulate Transcriptional Networks in the Retina by Mollema, Nissa J., Yuan, Yang, Jelcick, Austin S., Sachs, Andrew J., von Alpen, Désirée, Schorderet, Daniel, Escher, Pascal, Haider, Neena B.

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Nr2e3-Directed Transcriptional Regulation of Genes Involved in Photoreceptor Development and Cell-Type Specific Phototransduction by Haider, Neena B., Mollema, Nissa, Gaule, Meghan, Yuan, Yang, Sachs, Andrew J., Nystuen, Arne M., Naggert, Jürgen K., Nishina, Patsy M.

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Modifier Genes as Therapeutics: The Nuclear Hormone Receptor Rev Erb Alpha (Nr1d1) Rescues Nr2e3 Associated Retinal Disease by Cruz, Nelly M., Yuan, Yang, Leehy, Barrett D., Baid, Rinku, Kompella, Uday, DeAngelis, Margaret M., Escher, Pascal, Haider, Neena B.

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Differential dimerization of variants linked to enhanced S-Cone Sensitivity Syndrome (ESCS) located in the NR2E3 ligand-binding domain by von Alpen, Désirée, Tran, H. Viet, Guex, Nicolas, Venturini, Giulia, Munier, Francis L., Schorderet, Daniel F., Haider, Neena B., Escher, Pascal

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Genetic Variations Strongly Influence Phenotypic Outcome in the Mouse Retina by Jelcick, Austin S., Yuan, Yang, Leehy, Barrett D., Cox, Lakeisha C., Silveira, Alexandra C., Qiu, Fang, Schenk, Sarah, Sachs, Andrew J., Morrison, Margaux A., Nystuen, Arne M., DeAngelis, Margaret M., Haider, Neena B.

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Correction: Genetic Variations Strongly Influence Phenotypic Outcome in the Mouse Retina by Jelcick, Austin S., Yuan, Yang, Leehy, Barrett D., Cox, Lakeisha C., Silveira, Alexandra C., Qiu, Fang, Schenk, Sarah, Sachs, Andrew J., Morrison, Margaux A., Nystuen, Arne M., DeAngelis, Margaret M., Haider, Neena B.

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Nr2e3 is a genetic modifier that rescues retinal degeneration and promotes homeostasis in multiple models of retinitis pigmentosa by Li, Sujun, Datta, Shyamtanu, Brabbit, Emily, Love, Zoe, Woytowicz, Victoria, Flattery, Kyle, Capri, Jessica, Yao, Katie, Wu, Siqi, Imboden, Michael, Upadhyay, Arun, Arumugham, Rasappa, Thoreson, Wallace B., DeAngelis, Margaret M., Haider, Neena B.

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Characterization of a Spontaneous Retinal Neovascular Mouse Model by Hasegawa, Eiichi, Sweigard, Harry, Husain, Deeba, Olivares, Ana M., Chang, Bo, Smith, Kaylee E., Birsner, Amy E., D’Amato, Robert J., Michaud, Norman A., Han, Yinan, Vavvas, Demetrios G., Miller, Joan W., Haider, Neena B., Connor, Kip M.

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Influence of ROBO1 and RORA on Risk of Age-Related Macular Degeneration Reveals Genetically Distinct Phenotypes in Disease Pathophysiology by Jun, Gyungah, Nicolaou, Michael, Morrison, Margaux A., Buros, Jacqueline, Morgan, Denise J., Radeke, Monte J., Yonekawa, Yoshihiro, Tsironi, Evangelia E., Kotoula, Maria G., Zacharaki, Fani, Mollema, Nissa, Yuan, Yang, Miller, Joan W., Haider, Neena B., Hageman, Gregory S., Kim, Ivana K., Schaumberg, Debra A., Farrer, Lindsay A., DeAngelis, Margaret M.

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Convergence of linkage, gene expression and association data demonstrates the influence of the RAR-related orphan receptor alpha (RORA) gene on neovascular AMD: A systems biology b... by Silveira, Alexandra C., Morrison, Margaux A., Ji, Fei, Xu, Haiyan, Reinecke, James B., Adams, Scott M., Arneberg, Trevor M., Janssian, Maria, Lee, Joo-Eun, Yuan, Yang, Schaumberg, Debra A., Kotoula, Maria G., Tsironi, Evangeline E., Tsiloulis, Aristoteles N., Chatzoulis, Dimitrios Z., Miller, Joan W., Kim, Ivana K., Hageman, Gregory H., Farrer, Lindsay A., Haider, Neena B., DeAngelis, Margaret M.

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FLT1 Genetic Variation Predisposes to Neovascular AMD in Ethnically Diverse Populations and Alters Systemic FLT1 Expression by Owen, Leah A., Morrison, Margaux A., Ahn, Jeeyun, Woo, Se Joon, Sato, Hajime, Robinson, Rosann, Morgan, Denise J., Zacharaki, Fani, Simeonova, Marina, Uehara, Hironori, Chakravarthy, Usha, Hogg, Ruth E., Ambati, Balamurali K., Kotoula, Maria, Baehr, Wolfgang, Haider, Neena B., Silvestri, Giuliana, Miller, Joan W., Tsironi, Evangelia E., Farrer, Lindsay A., Kim, Ivana K., Park, Kyu Hyung, DeAngelis, Margaret M.

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Systems biology-based analysis implicates a novel role for vitamin D metabolism in the pathogenesis of age-related macular degeneration by Morrison, Margaux A, Silveira, Alexandra C, Huynh, Nancy, Jun, Gyungah, Smith, Silvia E, Zacharaki, Fani, Sato, Hajime, Loomis, Stephanie, Andreoli, Michael T, Adams, Scott M, Radeke, Monte J, Jelcick, Austin S, Yuan, Yang, Tsiloulis, Aristoteles N, Chatzoulis, Dimitrios Z, Silvestri, Giuliana, Kotoula, Maria G, Tsironi, Evangelia E, Hollis, Bruce W, Chen, Rui, Haider, Neena B, Miller, Joan W, Farrer, Lindsay A, Hageman, Gregory S, Kim, Ivana K, Schaumberg, Debra A, DeAngelis, Margaret M

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ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorder by Williams, Lloyd B., Javed, Asif, Sabri, Amin, Morgan, Denise J., Huff, Chad D., Grigg, John R., Heng, Xiu Ting, Khng, Alexis J., Hollink, Iris H. I. M., Morrison, Margaux A., Owen, Leah A., Anderson, Katherine, Kinard, Krista, Greenlees, Rebecca, Novacic, Danica, Nida Sen, H., Zein, Wadih M., Rodgers, George M., Vitale, Albert T., Haider, Neena B., Hillmer, Axel M., Ng, Pauline C., Shankaracharya, Cheng, Anson, Zheng, Linda, Gillies, Mark C., van Slegtenhorst, Marjon, van Hagen, P. Martin, Missotten, Tom O. A. R., Farley, Gary L., Polo, Michael, Malatack, James, Curtin, Julie, Martin, Frank, Arbuckle, Susan, Alexander, Stephen I., Chircop, Megan, Davila, Sonia, Digre, Kathleen B., Jamieson, Robyn V., DeAngelis, Margaret M.

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