Manisha Anand

发表

RPGR isoform imbalance causes ciliary defects due to exon ORF15 mutations in X-linked retinitis pigmentosa (XLRP)

E. L. West, A. Cideciyan, S. Jacobson, 2020, Human molecular genetics.

Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degeneration.

A. J. Roman, A. Cideciyan, S. Schwartz, 2016, Human molecular genetics.

Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF 15-associated retinal degeneration

A. J. Roman, A. Cideciyan, S. Schwartz, 2018 .

Ciliary transition zone (TZ) proteins RPGR and CEP290: role in photoreceptor cilia and degenerative diseases

H. Khanna, Manisha Anand, 2012, Expert opinion on therapeutic targets.

Prenylated retinal ciliopathy protein RPGR interacts with PDE6δ and regulates ciliary localization of Joubert syndrome-associated protein INPP5E.

H. Khanna, Wei Zhang, Linjing Li, 2016, Human molecular genetics.

Prenylated retinal ciliopathy protein RPGR interacts with PDE6δ and regulates ciliary localization of Joubert syndrome-associated protein INPP5E.

H. Khanna, Wei Zhang, Linjing Li, 2016, Human molecular genetics.

Loss of Raf-1 kinase inhibitory protein delays early-onset severe retinal ciliopathy in Cep290rd16 mouse.

H. Khanna, N. Khan, Balajikarthick Subramanian, 2014, Investigative ophthalmology & visual science.

The carboxyl terminal mutational hotspot of the ciliary disease protein RPGRORF15 (retinitis pigmentosa GTPase regulator) is glutamylated in vivo

H. Khanna, K. N. Rao, Manisha Anand, 2016, Biology Open.

Ablation of retinal ciliopathy protein RPGR results in altered photoreceptor ciliary composition

H. Khanna, Linjing Li, K. N. Rao, 2015, Scientific Reports.

Photoreceptor Sensory Cilium and Associated Disorders

H. Khanna, Linjing Li, Ozge Yildiz, 2012 .

Ocular Ciliopathies: genetic and mechanistic insights into developing therapies.

H. Khanna, S. Chakrabarti, Mahesh Shivanna, 2019, Current medicinal chemistry.

The carboxyl terminal mutational hotspot of the ciliary disease protein RPGRORF15 (retinitis pigmentosa GTPase regulator) is glutamylated in vivo

H. Khanna, K. N. Rao, Manisha Anand, 2016, Biology Open.

Prenylated retinal ciliopathy protein RPGR interacts with PDE6δ and regulates ciliary localization of Joubert syndrome-associated protein INPP5E.

H. Khanna, Wei Zhang, Linjing Li, 2016, Human molecular genetics.

Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degeneration.

A. J. Roman, A. Cideciyan, S. Schwartz, 2018, Human molecular genetics.