Zobrazeno 1 - 10
of 97
pro vyhledávání: '"Neena B. Haider"'
Autor:
Shannon M. McNamee, Monica Akula, Zoe Love, Neelaab Nasraty, Kaden Nystuen, Pushpendra Singh, Arun K. Upadhyay, Margaret M. DeAngelis, Neena B. Haider
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-14 (2024)
Abstract Retinitis Pigmentosa is a leading cause of severe vision loss. Retinitis Pigmentosa can present with a broad range of phenotypes impacted by disease age of onset, severity, and progression. This variation is influenced both by different gene
Externí odkaz:
https://doaj.org/article/760fb0df93694cf99cd9a1e2ee8b751e
Publikováno v:
Bioengineering, Vol 11, Iss 2, p 179 (2024)
Ocular diseases present a unique challenge and opportunity for therapeutic development. The eye has distinct advantages as a therapy target given its accessibility, compartmentalization, immune privilege, and size. Various methodologies for therapeut
Externí odkaz:
https://doaj.org/article/fd56c8305f874fadb70a162095cc027e
Autor:
Kaden L. Nystuen, Shannon M. McNamee, Monica Akula, Kristina M. Holton, Margaret M. DeAngelis, Neena B. Haider
Publikováno v:
Bioengineering, Vol 11, Iss 1, p 45 (2024)
Alzheimer’s Disease (AD) is a complex neurodegenerative disease resulting in progressive loss of memory, language and motor abilities caused by cortical and hippocampal degeneration. This review captures the landscape of understanding of AD patholo
Externí odkaz:
https://doaj.org/article/bf3971ef913347aeafe2a1c4a2737b76
Publikováno v:
Journal of Experimental Neuroscience, Vol 2015, Iss Suppl. 2, Pp 93-121 (2016)
Externí odkaz:
https://doaj.org/article/7a82cffbc17f4cf98be6756916090646
Publikováno v:
Journal of Experimental Neuroscience, Vol 9s2 (2015)
The nuclear hormone receptor (NHR) superfamily is composed of a wide range of receptors involved in a myriad of important biological processes, including development, growth, metabolism, and maintenance. Regulation of such wide variety of functions r
Externí odkaz:
https://doaj.org/article/51e09eb2d02445c1a7878a63d2209f32
Autor:
Austin S. Jelcick, Yang Yuan, Barrett D. Leehy, Lakeisha C. Cox, Alexandra C. Silveira, Fang Qiu, Sarah Schenk, Andrew J. Sachs, Margaux A. Morrison, Arne M. Nystuen, Margaret M. DeAngelis, Neena B. Haider
Publikováno v:
PLoS ONE, Vol 6, Iss 10 (2011)
Externí odkaz:
https://doaj.org/article/fb23f87577384cd0aad77c82aaaad8c4
Autor:
Nakul, Singh, Neena B, Haider
Publikováno v:
International Ophthalmology Clinics. 62:197-214
Autor:
Charles Zhang, Julie L. Barr, Leah A. Owen, Akbar Shakoor, Albert T. Vitale, John H Lillvis, Parker Cromwell, Nadine Husami, Robert Finley, Davis Ammar, Elizabeth Au, Neena B. Haider, Rylee A. Zavala, Elijah C. Graves, Mingyao Li, Amany Tawfik, Sarah X. Zhang, Dwight Stambolian, Michael H. Farkas, Ivana K. Kim, Richard M. Sherva, Lindsay A. Farrer, Margaret M. DeAngelis
Age-related macular degeneration (AMD) is a complex neurodegenerative disease and is the leading cause of blindness in the aging population. Early AMD is characterized by drusen in the macula and causes minimal changes in visual function. The later s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::04d715b61a9c8d6d2fab8fac8e322c60
https://doi.org/10.1101/2022.12.19.521092
https://doi.org/10.1101/2022.12.19.521092
Autor:
Jessica Capri, Neena B. Haider, Sujun Li, Victoria Woytowicz, Rasappa Arumugham, Arun K. Upadhyay, Siqi Wu, Margaret M. DeAngelis, Shyamtanu Datta, Michael Imboden, Katie Yao, Emily Brabbit, Zoe Love, Wallace B. Thoreson, Kyle Flattery
Publikováno v:
Gene therapy
Recent advances in viral vector engineering, as well as an increased understanding of the cellular and molecular mechanism of retinal diseases, have led to the development of novel gene therapy approaches. Furthermore, ease of accessibility and ocula
Autor:
Christiaan Lopez-Miro, Victoria Griffiths, Neena B. Haider, Alessandro Iannaccone, Zoe Love, Emily Brabbit, Marina Kedrov
Publikováno v:
Journal of Clinical Medicine
Volume 10
Issue 3
Journal of Clinical Medicine, Vol 10, Iss 475, p 475 (2021)
Volume 10
Issue 3
Journal of Clinical Medicine, Vol 10, Iss 475, p 475 (2021)
NR2E3-associated recessive disease in humans is historically defined by congenital night blinding retinopathy, characterized by an initial increase in short-wavelength (S)-cone sensitivity and progressive loss of rod and cone function. The retinal de