Publications

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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
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
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
Autologous stem cell therapy for inherited and acquired retinal disease   |     |   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
Personalized Proteomics for Precision Health: Identifying Biomarkers of Vitreoretinal Disease.   |   G. Velez; P.H. Tang; T. Cabral; G.Y. Cho; D.A. Machlab; S.H. Tsang; 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
Rates of Bone Spicule Pigment Appearance in patients with Retinitis Pigmentosa Sine Pigmento.   |   V.K.L. Takahashi; J.T. Takiuti; R. Jauregui; V.B. Mahajan; S.H. Tsang   |   Details
Translation of CRISPR Genome Surgery to the Bedside for Retinal Diseases.   |   C.L. Xu; G.Y. Cho; J.D. Sengillo; K.S. Park; V.B. Mahajan; S.H. Tsang   |   Details
PROGRESSION OF SCOTOPIC SINGLE-FLASH ELECTRORETINOGRAPHY IN THE STAGES OF CAPN5 VITREORETINOPATHY.   |   P.H. Tang; T.R. Kinnick; J.C. Folk; M. Mahajan; A.G. Bassuk; S.H. Tsang; V.B. Mahajan   |   Details
Fibrin Glue and Internal Limiting Membrane Abrasion for Optic Disc Pit Maculopathy.   |   D.R.P. Almeida; E.K. Chin; P. Arjmand; G. Velez; L.P. Evans; 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
SCAPER-associated nonsyndromic autosomal recessive retinitis pigmentosa.   |   R. Jauregui; A.L. Thomas; B. Liechty; G. Velez; V.B. Mahajan; L. Clark; S.H. Tsang   |   Details
Review of Ocular Manifestations of Joubert Syndrome.   |   S.F. Wang; T.J. Kowal; K. Ning; E.B. Koo; A.Y. Wu; V.B. Mahajan; Y. Sun   |   Details

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