S. Hiriyanna

发表

Molecular codes for cell type specification in Brn3 retinal ganglion cells

T. Badea, Zhijian Wu, M. Brooks, 2017, Proceedings of the National Academy of Sciences.

Retinal Structure and Gene Therapy Outcome in Retinoschisin-Deficient Mice Assessed by Spectral-Domain Optical Coherence Tomography

P. Sieving, R. Petralia, Zhijian Wu, 2016, Investigative ophthalmology & visual science.

Potent immune responses and in vitro pro-inflammatory cytokine suppression by a novel adenovirus vaccine vector based on rare human serotype 28.

J. Gall, Ping Chen, C. King, 2010, Vaccine.

Clinical and immunohistochemical evidence for an X linked retinitis pigmentosa syndrome with recurrent infections and hearing loss in association with an RPGR mutation

A. Swaroop, C. Morton, D. Breuer, 2003, Journal of medical genetics.

Phenotype correction of hemophilia A mice by spliceosome-mediated RNA trans-splicing

M. Garcia-Blanco, L. Mitchell, S. Mansfield, 2003, Nature Medicine.

Retinal AAV8-RS1 Gene Therapy for X-Linked Retinoschisis: Initial Findings from a Phase I/IIa Trial by Intravitreal Delivery.

P. Sieving, B. Jeffrey, C. Cukras, 2018, Molecular therapy : the journal of the American Society of Gene Therapy.

In vitro modeling and rescue of ciliopathy associated with IQCB1/NPHP5 mutations using patient-derived cells

A. Swaroop, W. Zein, Emily Welby, 2022, Stem cell reports.

Gene therapy of dominant CRX-Leber congenital amaurosis using patient stem cell-derived retinal organoids.

A. Swaroop, Zhijian Wu, Z. Batz, 2021, Stem cell reports.

Preclinical safety evaluation of a recombinant AAV8 vector for X-linked retinoschisis after intravitreal administration in rabbits.

P. Sieving, C. Zeiss, Zhijian Wu, 2014, Human gene therapy. Clinical development.

Nrl knockdown by AAV-delivered CRISPR/Cas9 prevents retinal degeneration in mice

Vijender Chaitankar, Anand Swaroop, Suja Hiriyanna, 2017, Nature Communications.

A visual circuit uses complementary mechanisms to support transient and sustained pupil constriction

William Thomas Keenan, Alan C. Rupp, Preethi Somasundaram, 2016, eLife.

Microarray analysis of gene expression in the aging human retina.

A. Swaroop, S. Yoshida, B. Yashar, 2002, Investigative ophthalmology & visual science.

Rd9 Is a Naturally Occurring Mouse Model of a Common Form of Retinitis Pigmentosa Caused by Mutations in RPGR-ORF15

A. Swaroop, Tiansen Li, H. Khanna, 2012, PloS one.

A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosa.

P. Sieving, S. Jacobson, A. Swaroop, 2002, American journal of human genetics.

Preclinical Dose-Escalation Study of Intravitreal AAV-RS1 Gene Therapy in a Mouse Model of X-linked Retinoschisis: Dose-Dependent Expression and Improved Retinal Structure and Function.

P. Sieving, Zhijian Wu, P. Colosi, 2016, Human gene therapy.

Ocular and systemic safety of a recombinant AAV8 vector for X-linked retinoschisis gene therapy: GLP studies in rabbits and Rs1-KO mice

P. Sieving, Zhijian Wu, L. Wei, 2016, Molecular therapy. Methods & clinical development.

Retinal histopathology of an XLRP carrier with a mutation in the RPGR exon ORF15.

A. Milam, G. Aguirre, A. Swaroop, 2002, Experimental eye research.

Clinical studies of X-linked retinitis pigmentosa in three Swedish families with newly identified mutations in the RP2 and RPGR-ORF15 genes

A. Swaroop, D. Breuer, B. Yashar, 2003, Ophthalmic genetics.

X-Linked Retinitis Pigmentosa: Current Status

P. Sieving, S. Jacobson, A. Swaroop, 2001 .

Long-term rescue of cone photoreceptor degeneration in retinitis pigmentosa 2 (RP2)-knockout mice by gene replacement therapy.

Wei Li, A. Swaroop, Tiansen Li, 2015, Human molecular genetics.

Protein-truncation mutations in the RP2 gene in a North American cohort of families with X-linked retinitis pigmentosa.

P. Sieving, S. Jacobson, A. Swaroop, 1999, American journal of human genetics.

A Common Outer Retina Change in Retinal Degeneration by Optical Coherence Tomography Can Be Used to Assess Outcomes of Gene Therapy.

M. Abu-Asab, Zhijian Wu, S. Hiriyanna, 2019, Human gene therapy.

A CEP290 C-Terminal Domain Complements the Mutant CEP290 of Rd16 Mice In Trans and Rescues Retinal Degeneration.

A. Swaroop, Tiansen Li, Zhijian Wu, 2018, Cell reports.

Remapping of the RP15 locus for X-linked cone-rod degeneration to Xp11.4-p21.1, and identification of a de novo insertion in the RPGR exon ORF15.

P. Sieving, A. Swaroop, A. Wright, 2000, American journal of human genetics.

A long-term efficacy study of gene replacement therapy for RPGR-associated retinal degeneration.

P. Sieving, A. Swaroop, Tiansen Li, 2015, Human molecular genetics.

Remapping of the RP 15 Locus for X-Linked Cone-Rod Degeneration to Xp 11 . 4p 21 . 1 , and Identification of a De Novo Insertion in the RPGR Exon ORF 15

P. Sieving, A. Swaroop, R. Vervoort, 2022 .

Ocular and systemic safety of a recombinant AAV8 vector for X-linked retinoschisis gene therapy: GLP studies in rabbits and Rs1-KO mice

P. Sieving, Zhijian Wu, L. Wei, 2016, Molecular therapy. Methods & clinical development.