Role of Nuclear Receptors in Central Nervous System Development and Associated Diseases

Por Olivares, Ana Maria, Moreno-Ramos, Oscar Andrés, Haider, Neena B.
Publicado no J Exp Neurosci (2016)

Patterned Neuroprotection in the Inpp4a(wbl) Mutant Mouse Cerebellum Correlates with the Expression of Eaat4

Por Sachs, Andrew J., David, Samuel A., Haider, Neena B., Nystuen, Arne M.
Publicado em 2009

A novel mutation in Prph2, a gene regulated by Nr2e3, causes retinal degeneration and outer segment defects similar to Nr2e3(rd7/rd7) retinas

Por Nystuen, Arne M., Sachs, Andrew J., Yuan, Yang, Heuermann, Laura, Haider, Neena B.
Publicado no Mamm Genome (2008)

Orally Active Multi-Functional Antioxidants Are Neuroprotective in a Rat Model of Light-Induced Retinal Damage

Por Randazzo, James, Zhang, Zifeng, Hoff, Michael, Kawada, Hiroyoshi, Sachs, Andrew, Yuan, Yang, Haider, Neena, Kador, Peter
Publicado em 2011

Whole-Exome Sequencing in a South American Cohort Links ALDH1A3, FOXN1 and Retinoic Acid Regulation Pathways to Autism Spectrum Disorders

Por Moreno-Ramos, Oscar A., Olivares, Ana María, Haider, Neena B., de Autismo, Liga Colombiana, Lattig, María Claudia
Publicado no PLoS One (2015)

Complement Factor H Gene Mutation Associated with Autosomal Recessive Atypical Hemolytic Uremic Syndrome

Por Ying, Lihua, Katz, Yitzhak, Schlesinger, Menachem, Carmi, Rivka, Shalev, Hanna, Haider, Neena, Beck, Gretel, Sheffield, Val C., Landau, Daniel
Publicado em 1999

Novel Diabetic Mouse Models as Tools for Investigating Diabetic Retinopathy

Por Kador, Peter F., Zhang, Peng, Makita, Jun, Zhang, Zifeng, Guo, Changmei, Randazzo, James, Kawada, Hiroyoshi, Haider, Neena, Blessing, Karen
Publicado em 2012

Animal Models of Diabetic Retinopathy

Por Olivares, Ana Maria, Althoff, Kristen, Chen, Gloria Fanghua, Wu, Siqi, Morrisson, Margaux A., DeAngelis, Margaret M., Haider, Neena
Publicado no Curr Diab Rep (2017)

Nuclear Receptor Rev-erb Alpha (Nr1d1) Functions in Concert with Nr2e3 to Regulate Transcriptional Networks in the Retina

Por Mollema, Nissa J., Yuan, Yang, Jelcick, Austin S., Sachs, Andrew J., von Alpen, Désirée, Schorderet, Daniel, Escher, Pascal, Haider, Neena B.
Publicado em 2011

Nr2e3-Directed Transcriptional Regulation of Genes Involved in Photoreceptor Development and Cell-Type Specific Phototransduction

Por Haider, Neena B., Mollema, Nissa, Gaule, Meghan, Yuan, Yang, Sachs, Andrew J., Nystuen, Arne M., Naggert, Jürgen K., Nishina, Patsy M.
Publicado em 2009

Modifier Genes as Therapeutics: The Nuclear Hormone Receptor Rev Erb Alpha (Nr1d1) Rescues Nr2e3 Associated Retinal Disease

Por Cruz, Nelly M., Yuan, Yang, Leehy, Barrett D., Baid, Rinku, Kompella, Uday, DeAngelis, Margaret M., Escher, Pascal, Haider, Neena B.
Publicado em 2014

Differential dimerization of variants linked to enhanced S-Cone Sensitivity Syndrome (ESCS) located in the NR2E3 ligand-binding domain

Por von Alpen, Désirée, Tran, H. Viet, Guex, Nicolas, Venturini, Giulia, Munier, Francis L., Schorderet, Daniel F., Haider, Neena B., Escher, Pascal
Publicado no Hum Mutat (2015)

Pitfalls in Homozygosity Mapping

Por Miano, Maria G., Jacobson, Samuel G., Carothers, Andrew, Hanson, Isabel, Teague, Peter, Lovell, Jill, Cideciyan, Artur V., Haider, Neena, Stone, Edwin M., Sheffield, Val C., Wright, Alan F.
Publicado em 2000

Genetic Variations Strongly Influence Phenotypic Outcome in the Mouse Retina

Por 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.
Publicado em 2011

Correction: Genetic Variations Strongly Influence Phenotypic Outcome in the Mouse Retina

Por 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.
Publicado em 2011

Nr2e3 is a genetic modifier that rescues retinal degeneration and promotes homeostasis in multiple models of retinitis pigmentosa

Por 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.
Publicado no Gene Ther (2020)

Retinal Dystrophy and Optic Nerve Pathology in the Mouse Model of Mucolipidosis IV

Por Grishchuk, Yulia, Stember, Katherine G., Matsunaga, Aya, Olivares, Ana M., Cruz, Nelly M., King, Victoria E., Humphrey, Daniel M., Wang, Shirley L., Muzikansky, Alona, Betensky, Rebecca A., Thoreson, Wallace B., Haider, Neena, Slaugenhaupt, Susan A.
Publicado no Am J Pathol (2016)

Characterization of a Spontaneous Retinal Neovascular Mouse Model

Por 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.
Publicado em 2014

Influence of ROBO1 and RORA on Risk of Age-Related Macular Degeneration Reveals Genetically Distinct Phenotypes in Disease Pathophysiology

Por 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.
Publicado em 2011

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...

Por 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.
Publicado em 2009