Publications

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2019

Hypoxic drive caused type 3 neovascularization in a preclinical model of exudative age-related macular degeneration.   |   L. Zhang; X. Cui; Y. Han; K.Sophia Park; X. Gao; X. Zhang; Z. Yuan; Y. Hu; C.W. Hsu; X. Li; A.G. Bassuk; V.B. Mahajan; N.K. Wang; S.H. Tsang   |   Details
Comparison of structural progression between ciliopathy and non-ciliopathy associated with autosomal recessive retinitis pigmentosa.   |     |   Details
Novel mutations in the 3-box motif of the BACK domain of KLHL7 associated with nonsyndromic autosomal dominant retinitis pigmentosa.   |     |   Details
Mechanisms of neurodegeneration in a preclinical autosomal dominant retinitis pigmentosa knock-in model with a RhoD190N mutation.   |   S.P. J; L.W.Cui X; T. YT; W. WH; J. S; W. I; H. CW; P. KS; K. S; V. G; B. AG; M. VB; L. CS; T. SH   |   Details
Traumatic chorioretinitis sclopetaria: Risk factors, management, and prognosis.   |   C.A. Ludwig; R.A. Shields; D.V. Do; D.M. Moshfeghi; V.B. Mahajan   |   Details
Optical Coherence Tomography Angiography of RPGR-Associated Retinitis Pigmentosa Suggests Foveal Avascular Zone is a Biomarker for Vision Loss.   |   P.H. Tang; R. Jauregui; S.H. Tsang; A.G. Bassuk; V.B. Mahajan   |   Details
VCAN Canonical Splice Site Mutation is Associated With Vitreoretinal Degeneration and Disrupts an MMP Proteolytic Site.   |   P.H. Tang; G. Velez; S.H. Tsang; A.G. Bassuk; V.B. Mahajan   |   Details
Fundus autofluorescence and ellipsoid zone (EZ) line width can be an outcome measurement in RHO-associated autosomal dominant retinitis pigmentosa.   |   V.K.L. Takahashi; J.T. Takiuti; J.R.L. Carvalho-Jr; C.L. Xu; J.K. Duong; V.B. Mahajan; S.H. Tsang   |   Details
Viral Delivery Systems for CRISPR.   |   C.L. Xu; M.Z.C. Ruan; V.B. Mahajan; S.H. Tsang   |   Details
In Vivo Expression of Mutant Calpains in the Eye Using Lentivirus.   |   K.J. Wert; V.B. Mahajan   |   Details
CRISPR Base Editing in Induced Pluripotent Stem Cells.   |   Y.J. Chang; C.L. Xu; X. Cui; A.G. Bassuk; V.B. Mahajan; Y.T. Tsai; S.H. Tsang   |   Details
In trans variant calling reveals enrichment for compound heterozygous variants in genes involved in neuronal development and growth.   |   A.J. Cox; F. Grady; G. Velez; V.B. Mahajan; P.J. Ferguson; A. Kitchen; B.W. Darbro; A.G. Bassuk   |   Details
Bilateral Endophthalmitis after Immediately Sequential Bilateral Cataract Surgery.   |   N.F. Callaway; M.H. Ji; V.B. Mahajan; D.M. Moshfeghi   |   Details
Gain-of-function mutations in a member of the Src family kinases cause autoinflammatory bone disease in mice and humans.   |   K. Abe; A. Cox; N. Takamatsu; G. Velez; R.M. Laxer; S.M.L. Tse; V.B. Mahajan; A.G. Bassuk; H. Fuchs; P.J. Ferguson; M.Hrabe de Angelis   |   Details
Proteomic insight into the pathogenesis of CAPN5-vitreoretinopathy.   |   G. Velez; J. Yang; A.S. Li; S.H. Tsang; A.G. Bassuk; V.B. Mahajan   |   Details
Insights into Retinal Development Using Live Imaging in Female Carriers of Choroideremia.   |   K.J. Wert; B. Bakall; A.G. Bassuk; S.H. Tsang; V.B. Mahajan   |   Details
Silicone oil-induced ocular hypertension and glaucomatous neurodegeneration in mouse.   |   J. Zhang; L. Li; H. Huang; F. Fang; H.C. Webber; P. Zhuang; L. Liu; R. Dalal; P.H. Tang; V.B. Mahajan; Y. Sun; S. Li; M. Zhang; J.L. Goldberg; Y. Hu   |   Details

2018

Proteomic analysis of the human retina reveals region-specific susceptibilities to metabolic-and oxidative stress-related diseases   |   G. Velez; D.A. Machlab; P.H. Tang; Y. Sun; S.H. Tsang; A.G. Bassuk; V.B. Mahajan   |   Details
Caring for Hereditary Childhood Retinal Blindness.   |   R. Jauregui; G.Y. Cho; V.K.L. Takahashi; J.T. Takiuti; A.G. Bassuk; V.B. Mahajan; S.H. Tsang   |   Details
CRISPR Repair Reveals Causative Mutation in a Preclinical Model of Retinitis Pigmentosa: A Brief Methodology   |   Wu, W. H., Tsai, Y. T., Justus, S., Cho, G. Y., Sengillo, J. D., Xu, Y., Cabral, T., Lin, C. S., Bassuk, A. G., Mahajan, V. B., & Tsang, S. H.   |   Details

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