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Expert Opinion on Therapeutic Targets|May 9, 2012
Ciliary transition zone (TZ) proteins RPGR and CEP290: role in photoreceptor cilia and degenerative diseasesManisha Anand, Hemant KhannaBiology Open|March 5, 2016
The carboxyl terminal mutational hotspot of the ciliary disease protein RPGRORF15 (retinitis pigmentosa GTPase regulator) is glutamylated in vivoKollu N Rao, Manisha Anand, Hemant KhannaCurrent Medicinal Chemistry|September 18, 2018
Ocular Ciliopathies: Genetic and Mechanistic Insights into Developing TherapiesMahesh Shivanna, Manisha Anand, Subhabrata Chakrabarti, et al.Scientific Reports|June 13, 2015
Ablation of retinal ciliopathy protein RPGR results in altered photoreceptor ciliary compositionKollu N Rao, Linjing Li, Manisha Anand, et al.Methods in Cell Biology|April 4, 2015
Cilia in photoreceptorsLinjing Li, Manisha Anand, Kollu Nageswara Rao, et al.Investigative Ophthalmology & Visual Science|August 16, 2014
Loss of Raf-1 kinase inhibitory protein delays early-onset severe retinal ciliopathy in Cep290rd16 mouseBalajikarthick Subramanian, Manisha Anand, Naheed W Khan, et al.Human Molecular Genetics|February 8, 2017
Prenylated retinal ciliopathy protein RPGR interacts with PDE6δ and regulates ciliary localization of Joubert syndrome-associated protein INPP5EKollu N Rao, Wei Zhang, Linjing Li, et al.Human Molecular Genetics|November 1, 2016
Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degenerationJason Charng, Artur V Cideciyan, Samuel G Jacobson, et al.Human Molecular Genetics|December 23, 2020
RPGR isoform imbalance causes ciliary defects due to exon ORF15 mutations in X-linked retinitis pigmentosa (XLRP)Laura Moreno-Leon, Emma L West, Michelle O'Hara-Wright, et al.Pageof 1