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Gabriel Velez
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Recessive coding and regulatory mutations in FBLIM1 underlie the pathogenesis of chronic recurrent multifocal osteomyelitis (CRMO)
AJ Cox, BW Darbro, RM Laxer, G Velez, X Bing, AL Finer, A Erives, ...
PloS one 12 (3), e0169687, 2017
742017
Precision medicine: personalized proteomics for the diagnosis and treatment of idiopathic inflammatory disease
G Velez, CN Roybal, D Colgan, SH Tsang, AG Bassuk, VB Mahajan
JAMA ophthalmology 134 (4), 444-448, 2016
732016
Paracrine WNT5A signaling inhibits expansion of tumor-initiating cells
N Borcherding, D Kusner, R Kolb, Q Xie, W Li, F Yuan, G Velez, ...
Cancer research 75 (10), 1972-1982, 2015
712015
BESTROPHIN1 mutations cause defective chloride conductance in patient stem cell-derived RPE
Y Moshfegh, G Velez, Y Li, AG Bassuk, VB Mahajan, SH Tsang
Human molecular genetics 25 (13), 2672-2680, 2016
522016
Ocular hypertension after intravitreal dexamethasone (ozurdex) sustained-release implant
EK Chin, DRP Almeida, G Velez, K Xu, M Peraire, M Corbella, ...
Retina 37 (7), 1345-1351, 2017
492017
Personalized proteomics in proliferative vitreoretinopathy implicate hematopoietic cell recruitment and mTOR as a therapeutic target
CN Roybal, G Velez, MA Toral, SH Tsang, AG Bassuk, VB Mahajan
American journal of ophthalmology 186, 152-163, 2018
482018
Extracellular superoxide dismutase (SOD3) regulates oxidative stress at the vitreoretinal interface
KJ Wert, G Velez, MR Cross, BA Wagner, ML Teoh-Fitzgerald, ...
Free Radical Biology and Medicine 124, 408-419, 2018
462018
Metabolite therapy guided by liquid biopsy proteomics delays retinal neurodegeneration
KJ Wert, G Velez, VL Kanchustambham, V Shankar, LP Evans, ...
EBioMedicine 52, 2020
422020
Proteomic analysis of the human retina reveals region-specific susceptibilities to metabolic-and oxidative stress-related diseases
G Velez, DA Machlab, PH Tang, Y Sun, SH Tsang, AG Bassuk, ...
PLoS One 13 (2), e0193250, 2018
422018
Personalized proteomics for precision health: identifying biomarkers of vitreoretinal disease
G Velez, PH Tang, T Cabral, GY Cho, DA Machlab, SH Tsang, AG Bassuk, ...
Translational vision science & technology 7 (5), 12-12, 2018
412018
Gene Therapy Restores Mfrp and Corrects Axial Eye Length
G Velez, SH Tsang, YT Tsai, CW Hsu, A Gore, AH Abdelhakim, ...
Scientific Reports 7 (1), 16151, 2017
382017
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, RM Laxer, SML Tse, VB Mahajan, ...
Proceedings of the National Academy of Sciences 116 (24), 11872-11877, 2019
352019
Calpain-5 expression in the retina localizes to photoreceptor synapses
KA Schaefer, MA Toral, G Velez, AJ Cox, SA Baker, NC Borcherding, ...
Investigative ophthalmology & visual science 57 (6), 2509-2521, 2016
342016
Therapeutic drug repositioning using personalized proteomics of liquid biopsies
G Velez, AG Bassuk, D Colgan, SH Tsang, VB Mahajan
JCI insight 2 (24), 2017
322017
Liquid biopsy proteomics of uveal melanoma reveals biomarkers associated with metastatic risk
G Velez, HV Nguyen, T Chemudupati, CA Ludwig, M Toral, S Reddy, ...
Molecular Cancer 20, 1-5, 2021
282021
Role for Krüppel-like transcription factor 11 in mesenchymal cell function and fibrosis
A Mathison, A Grzenda, G Lomberk, G Velez, N Buttar, P Tietz, ...
PloS one 8 (9), e75311, 2013
272013
A novel de novo CAPN5 mutation in a patient with inflammatory vitreoretinopathy, hearing loss, and developmental delay
G Velez, AG Bassuk, KA Schaefer, B Brooks, L Gakhar, MA Mahajan, ...
Molecular Case Studies 4 (3), a002519, 2018
252018
Structure-based phylogeny identifies avoralstat as a TMPRSS2 inhibitor that prevents SARS-CoV-2 infection in mice
YJ Sun, G Velez, DE Parsons, K Li, ME Ortiz, S Sharma, PB McCray, ...
The Journal of clinical investigation 131 (10), 2021
242021
Evidence supporting the existence of a NUPR1-like family of helix-loop-helix chromatin proteins related to, yet distinct from, AT hook-containing HMG proteins
R Urrutia, G Velez, M Lin, G Lomberk, JL Neira, J Iovanna
Journal of molecular modeling 20, 1-20, 2014
242014
Structural modeling of a novel SLC38A8 mutation that causes foveal hypoplasia
MA Toral, G Velez, K Boudreault, KA Schaefer, Y Xu, N Saffra, AG Bassuk, ...
Molecular genetics & genomic medicine 5 (3), 202-209, 2017
232017
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