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Kollu N Rao

Showing results (1-10 of 10) with videos related to

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Indian Journal of Ophthalmology|December 15, 2010
Complex genetic mechanisms in glaucoma: an overviewKollu N Rao, Srujana Nagireddy, Subhabrata Chakrabarti
Frontiers in Genetics|April 27, 2019
Structural but Not Functional Alterations in Cones in the Absence of the Retinal Disease Protein Retinitis Pigmentosa 2 (RP2) in a Cone-Only RetinaLinjing Li, Kollu N Rao, Hemant Khanna
Proceedings of the National Academy of Sciences of the United States of America|October 23, 2009
Lack of association of three primary open-angle glaucoma-susceptible loci with primary glaucomas in an Indian populationKollu N Rao, Inderjeet Kaur, Subhabrata Chakrabarti
Biology 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 Khanna
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.
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|March 4, 2016
Ciliopathy-associated protein CEP290 modifies the severity of retinal degeneration due to loss of RPGRKollu N Rao, Wei Zhang, Linjing Li, et al.
Human Molecular Genetics|February 25, 2016
Loss of human disease protein retinitis pigmentosa GTPase regulator (RPGR) differentially affects rod or cone-enriched retinaKollu N Rao, Linjing Li, Wei Zhang, et al.
Investigative Ophthalmology & Visual Science|May 14, 2010
Variations in NTF4, VAV2, and VAV3 genes are not involved with primary open-angle and primary angle-closure glaucomas in an indian populationKollu N Rao, Inderjeet Kaur, Rajul S Parikh, et al.
Human Molecular Genetics|July 28, 2010
A polymorphism in the CYP1B1 promoter is functionally associated with primary congenital glaucomaSubhabrata Chakrabarti, Yashoda Ghanekar, Kiranpreet Kaur, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Indian Journal of Ophthalmology|December 15, 2010
Complex genetic mechanisms in glaucoma: an overviewKollu N Rao, Srujana Nagireddy, Subhabrata Chakrabarti
Frontiers in Genetics|April 27, 2019
Structural but Not Functional Alterations in Cones in the Absence of the Retinal Disease Protein Retinitis Pigmentosa 2 (RP2) in a Cone-Only RetinaLinjing Li, Kollu N Rao, Hemant Khanna
Proceedings of the National Academy of Sciences of the United States of America|October 23, 2009
Lack of association of three primary open-angle glaucoma-susceptible loci with primary glaucomas in an Indian populationKollu N Rao, Inderjeet Kaur, Subhabrata Chakrabarti
Biology 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 Khanna
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.
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|March 4, 2016
Ciliopathy-associated protein CEP290 modifies the severity of retinal degeneration due to loss of RPGRKollu N Rao, Wei Zhang, Linjing Li, et al.
Human Molecular Genetics|February 25, 2016
Loss of human disease protein retinitis pigmentosa GTPase regulator (RPGR) differentially affects rod or cone-enriched retinaKollu N Rao, Linjing Li, Wei Zhang, et al.
Investigative Ophthalmology & Visual Science|May 14, 2010
Variations in NTF4, VAV2, and VAV3 genes are not involved with primary open-angle and primary angle-closure glaucomas in an indian populationKollu N Rao, Inderjeet Kaur, Rajul S Parikh, et al.
Human Molecular Genetics|July 28, 2010
A polymorphism in the CYP1B1 promoter is functionally associated with primary congenital glaucomaSubhabrata Chakrabarti, Yashoda Ghanekar, Kiranpreet Kaur, et al.
Pageof 1