Neena B. Haider
Affiliations: | University of Nebraska Medical Center, Omaha, NE, United States |
Area:
Cell Biology, Genetics, Neuroscience BiologyGoogle:
"Neena Haider"Mean distance: 26716.5
Children
Sign in to add trainee| Nissa J. Mollema | grad student | 2010 | University of Nebraska Medical Center |
| Austin Jelcick | grad student | 2011 | University of Nebraska Medical Center |
| Andy W. Yang | grad student | 2011 | University of Nebraska Medical Center |
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Publications
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| McNamee SM, Chan NP, Akula M, et al. (2024) Preclinical dose response study shows NR2E3 can attenuate retinal degeneration in the retinitis pigmentosa mouse model Rho. Gene Therapy |
| Li S, Datta S, Brabbit E, et al. (2020) Nr2e3 is a genetic modifier that rescues retinal degeneration and promotes homeostasis in multiple models of retinitis pigmentosa. Gene Therapy |
| Olivares AM, Han Y, Soto D, et al. (2017) Corrigendum to "The Nuclear Hormone Receptor Nr2c1 (Tr2) is a critical regulator of early retina cell pattering" [Dev. Biol. 16 (2017) 30797-7]. Developmental Biology |
| Olivares AM, Han Y, Soto D, et al. (2017) The Nuclear Hormone Receptor Gene Nr2c1 (Tr2) is a Critical Regulator of Early Retina Cell Patterning. Developmental Biology |
| Olivares AM, Jelcick AS, Reinecke J, et al. (2017) Multimodal Regulation Orchestrates Normal and Complex Disease States in the Retina. Scientific Reports. 7: 690 |
| Olivares AM, Moreno-Ramos OA, Haider NB. (2015) Role of Nuclear Receptors in Central Nervous System Development and Associated Diseases. Journal of Experimental Neuroscience. 9: 93-121 |
| Grishchuk Y, Stember KG, Matsunaga A, et al. (2015) Retinal Dystrophy and Optic Nerve Pathology in the Mouse Model of Mucolipidosis IV. The American Journal of Pathology |
| Moreno-Ramos OA, Olivares AM, Haider NB, et al. (2015) Whole-Exome Sequencing in a South American Cohort Links ALDH1A3, FOXN1 and Retinoic Acid Regulation Pathways to Autism Spectrum Disorders. Plos One. 10: e0135927 |
| von Alpen D, Tran HV, Guex N, et al. (2015) Differential dimerization of variants linked to enhanced S-cone sensitivity syndrome (ESCS) located in the NR2E3 ligand-binding domain. Human Mutation. 36: 599-610 |
| Hasegawa E, Sweigard H, Husain D, et al. (2014) Characterization of a spontaneous retinal neovascular mouse model. Plos One. 9: e106507 |