S. He

发表

RPGR-ORF15, Which Is Mutated in Retinitis Pigmentosa, Associates with SMC1, SMC3, and Microtubule Transport Proteins*

A. Swaroop, A. Wright, H. Khanna, 2005, Journal of Biological Chemistry.

A variant of mitochondrial protein LOC387715/ARMS2, not HTRA1, is strongly associated with age-related macular degeneration

Gonçalo R. Abecasis, Anand Swaroop, Wei Chen, 2007, Proceedings of the National Academy of Sciences.

Management of autoimmune retinopathies with immunosuppression.

S. He, J. Heckenlively, N. Khan, 2009, Archives of ophthalmology.

Anti-retinal pigment epithelium antibodies in acute exudative polymorphous vitelliform maculopathy: a new hypothesis about disease pathogenesis.

S. He, J. Heckenlively, N. Khan, 2009, Archives of ophthalmology.

Two mouse models for recoverin-associated autoimmune retinopathy

S. He, J. Heckenlively, N. Khan, 2010, Molecular vision.

Expression profiling of the developing and mature Nrl-/- mouse retina: identification of retinal disease candidates and transcriptional regulatory targets of Nrl.

Shigeo Yoshida, Alfred O Hero, Anand Swaroop, 2004, Human molecular genetics.

Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulin

R. Reinhardt, J. Hellemans, A. Swaroop, 2005, Nature Genetics.

In-frame deletion in a novel centrosomal/ciliary protein CEP290/NPHP6 perturbs its interaction with RPGR and results in early-onset retinal degeneration in the rd16 mouse.

A. Swaroop, H. Khanna, C. Lillo, 2006, Human molecular genetics.

Melanoma-associated retinopathy: a paraneoplastic autoimmune complication.

S. He, J. Heckenlively, T. Jayasundera, 2009, Archives of ophthalmology.

Retinitis Pigmentosa GTPase Regulator (RPGR) protein isoforms in mammalian retina: Insights into X-linked Retinitis Pigmentosa and associated ciliopathies

Hemant Khanna, Anand Swaroop, A. Swaroop, 2008, Vision Research.

Altered Expression of Genes of the Bmp/Smad and Wnt/Calcium Signaling Pathways in the Cone-only Nrl-/- Mouse Retina, Revealed by Gene Profiling Using Custom cDNA Microarrays*

Jindan Yu, Masayuki Akimoto, Anand Swaroop, 2004, Journal of Biological Chemistry.

Centrosomal‐ciliary gene CEP290/NPHP6 mutations result in blindness with unexpected sparing of photoreceptors and visual brain: implications for therapy of Leber congenital amaurosis

T. Aleman, A. Cideciyan, S. Schwartz, 2007, Human mutation.

RPGR Interacts With a Novel Ciliary IQ Domain Protein Nephrocystin 5, Mutated in Senior–Loken Syndrome (Nephronophthisis With Retinitis Pigmentosa)

A. Swaroop, H. Khanna, C. Lillo, 2005 .