Publications

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2019

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

2018

Autologous stem cell therapy for inherited and acquired retinal disease   |     |   Details
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
Acute vitreoretinal trauma and inflammation after traumatic brain injury in mice.   |   L.P. Evans; E.A. Newell; M. Mahajan; S.H. Tsang; P.J. Ferguson; J. Mahoney; C.D. Hue; E.W. Vogel; B. Morrison; O. Arancio; R. Nichols; A.G. Bassuk; V.B. Mahajan   |   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
HTRA1, an age-related macular degeneration protease, processes extracellular matrix proteins EFEMP1 and TSP1   |   M.K. Lin; J. Yang; C.Wei Hsu; A. Gore; A.G. Bassuk; L.M. Brown; R. Colligan; J.D. Sengillo; V.B. Mahajan; S.H. Tsang   |   Details
Gene therapy and genome surgery in the retina.   |   J.E. DiCarlo; V.B. Mahajan; S.H. Tsang   |   Details
Deferoxamine-induced electronegative ERG responses.   |   R. Jauregui; K.Sophia Park; A.G. Bassuk; V.B. Mahajan; S.H. Tsang   |   Details
CRISPR GENOME SURGERY IN THE RETINA IN LIGHT OF OFF-TARGETING.   |   G.Y. Cho; K.A. Schaefer; A.G. Bassuk; S.H. Tsang; V.B. Mahajan   |   Details
A novel de novo CAPN5 mutation in a patient with inflammatory vitreoretinopathy, hearing loss, and developmental delay   |   G. Velez; A.G. Bassuk; K.A. Schaefer; B. Brooks; L. Gakhar; M. Mahajan; P. Kahn; S.H. Tsang; P.J. Ferguson; V.B. Mahajan   |   Details
Missense mutation in SLIT2 associated with congenital myopia, anisometropia, connective tissue abnormalities, and obesity   |   K.Y. Liu; J.D. Sengillo; G. Velez; R. Jauregui; L.Y. Sakai; I.H. Maumenee; A.G. Bassuk; V.B. Mahajan; S.H. Tsang   |   Details
Extracellular superoxide dismutase 3 (SOD3) regulates oxidative stress at the vitreoretinal interface   |   K.J. Wert; G. Velez; M.R. Cross; B.A. Wagner; M.L. Teoh-Fitzgerald; G.R. Buettner; J. McAnany; A. Olivier; S.H. Tsang; M.M. Harper;   |   Details
Quantitative progression of retinitis pigmentosa by optical coherence tomography angiography   |   R. Jauregui; K.Sophia Park; J.K. Duong; V.B. Mahajan; S.H. Tsang   |   Details

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