Skip to main content
Stanford University
Mahajan Laboratories
Department of Ophthalmology
Search
Menu
Toggle menu visibility
About
Mission
For Patients
Contact
People
Graduate Students
Postdoctoral Fellows
Surgical Fellows
Medical Students
Undergraduate Students
Scientists and Technicians
Affiliated Faculty
Alumni
Collaborative Science Systems
Publications
Make a Gift
20 / 20 Blog Archive
Education Links
Grants and Funding
National Institutes of Health
Training Grants
Foundations
Institutional
Press
Gallery
Precision Health
OMICS Lab
Overview
Proteomics
Genomics
Phenomics
ADNIV
Structure
Gene Therapy
Drug Design
Molecular Surgery
Overview
YouTube channel
Human Molecular Surgery
Mouse Molecular Surgery
Instrumentation
Education
Publications
Search by Title OR Author(s) OR Year OR keywords
Items per page
5
10
20
50
100
2020
Sex Does Not Influence Visual Outcomes After Blast-Mediated Traumatic Brain Injury but IL-1 Pathway Mutations Confer Partial Rescue.
|
L.P. Evans; N. Boehme; S. Wu; E.L. Burghardt; A. Akurathi; B.P. Todd; E.A. Newell; P.J. Ferguson; V.B. Mahajan; L.M. Dutca; M.M. Harper; A.G. Bassuk
|
Details
Retinal Manifestations of Mitochondrial Oxidative Phosphorylation Disorders.
|
J.Kyun Oh; J.Ronaldo Li de Carvalho; Y. Nuzbrokh; J. Ryu; T. Chemudupati; V.B. Mahajan; J.R. Sparrow; S.H. Tsang
|
Details
Molecular Surgery: Proteomics of a Rare Genetic Disease Gives Insight into Common Causes of Blindness.
|
G. Velez; V.B. Mahajan
|
Details
Fundoscopy-directed genetic testing to re-evaluate negative whole exome sequencing results.
|
A. Cho; J.Ronaldo Li de Carvalho; A.J. Tanaka; R. Jauregui; S.R. Levi; A.G. Bassuk; V.B. Mahajan; S.H. Tsang
|
Details
Reply to Comment on: Sex Differences in the Repair of Retinal Detachments in the United States.
|
N.F. Callaway; D. Vail; A. Al-Moujahed; C. Ludwig; M.H. Ji; V.B. Mahajan; S. Pershing; D.M. Moshfeghi
|
Details
Structural Insights into the Unique Activation Mechanisms of a Non-classical Calpain and Its Disease-Causing Variants.
|
G. Velez; Y.Joo Sun; S. Khan; J. Yang; J. Herrmann; T. Chemudupati; R.E. MacLaren; L. Gakhar; S. Wakatsuki; A.G. Bassuk; V.B. Mahajan
|
Details
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
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
Pages
« first
‹ previous
1
2
3
4
5
6
7
8
9
…
next ›
last »
Menu
Toggle menu visibility
Mission
For Patients
Contact
People
Collaborative Science Systems
Publications
Make a Gift
20 / 20 Blog Archive
Education Links
Grants and Funding
Press
Gallery