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American Journal of Ophthalmology Case Reports
|
April 11, 2020
Proteomic analysis of intermediate uveitis suggests myeloid cell recruitment and implicates IL-23 as a therapeutic target
Yasir J Sepah, Gabriel Velez, Peter H Tang, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
November 28, 2022
Human Brainstem and Cerebellum Atlas: Chemoarchitecture and Cytoarchitecture Paired to MRI
Lindsay J Agostinelli, Scott C Seaman, Clifford B Saper, et al.
Brain Communications
|
October 2, 2024
Enhanced Fyn-tau and NR2B-PSD95 interactions in epileptic foci in experimental models and human epilepsy
Marson Putra, Nikhil S Rao, Cara Gardner, et al.
Human Mutation
|
March 26, 2009
Novel mutations in VANGL1 in neural tube defects
Zoha Kibar, Ciprian M Bosoi, Megan Kooistra, et al.
Journal of Proteome Research
|
January 3, 2024
Liquid Biopsy Proteomics in Ophthalmology
Julian Wolf, Joel A Franco, Rui Yip, et al.
Journal of Visualized Experiments : Jove
|
November 21, 2017
Dissection of Human Retina and RPE-Choroid for Proteomic Analysis
Thiago Cabral, Marcus A Toral, Gabriel Velez, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
May 21, 2016
CRISPR Repair Reveals Causative Mutation in a Preclinical Model of Retinitis Pigmentosa
Wen-Hsuan Wu, Yi-Ting Tsai, Sally Justus, et al.
Cold Spring Harbor Molecular Case Studies
|
February 24, 2018
A novel de novo <i>CAPN5</i> mutation in a patient with inflammatory vitreoretinopathy, hearing loss, and developmental delay
Gabriel Velez, Alexander G Bassuk, Kellie A Schaefer, et al.
Orphanet Journal of Rare Diseases
|
August 17, 2018
Missense mutation in SLIT2 associated with congenital myopia, anisometropia, connective tissue abnormalities, and obesity
Katherine Y Liu, Jesse D Sengillo, Gabriel Velez, et al.
European Journal of Human Genetics : EJHG
|
June 7, 2021
PRICKLE2 revisited-further evidence implicating PRICKLE2 in neurodevelopmental disorders
Allan Bayat, Sumaiya Iqbal, Kim Borredy, et al.
Page
of 16
Search research articles
Search
Showing results (81-90 of 156) with videos related to
Sort By:
Page
of 16
American Journal of Ophthalmology Case Reports
|
April 11, 2020
Proteomic analysis of intermediate uveitis suggests myeloid cell recruitment and implicates IL-23 as a therapeutic target
Yasir J Sepah, Gabriel Velez, Peter H Tang, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
November 28, 2022
Human Brainstem and Cerebellum Atlas: Chemoarchitecture and Cytoarchitecture Paired to MRI
Lindsay J Agostinelli, Scott C Seaman, Clifford B Saper, et al.
Brain Communications
|
October 2, 2024
Enhanced Fyn-tau and NR2B-PSD95 interactions in epileptic foci in experimental models and human epilepsy
Marson Putra, Nikhil S Rao, Cara Gardner, et al.
Human Mutation
|
March 26, 2009
Novel mutations in VANGL1 in neural tube defects
Zoha Kibar, Ciprian M Bosoi, Megan Kooistra, et al.
Journal of Proteome Research
|
January 3, 2024
Liquid Biopsy Proteomics in Ophthalmology
Julian Wolf, Joel A Franco, Rui Yip, et al.
Journal of Visualized Experiments : Jove
|
November 21, 2017
Dissection of Human Retina and RPE-Choroid for Proteomic Analysis
Thiago Cabral, Marcus A Toral, Gabriel Velez, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
May 21, 2016
CRISPR Repair Reveals Causative Mutation in a Preclinical Model of Retinitis Pigmentosa
Wen-Hsuan Wu, Yi-Ting Tsai, Sally Justus, et al.
Cold Spring Harbor Molecular Case Studies
|
February 24, 2018
A novel de novo <i>CAPN5</i> mutation in a patient with inflammatory vitreoretinopathy, hearing loss, and developmental delay
Gabriel Velez, Alexander G Bassuk, Kellie A Schaefer, et al.
Orphanet Journal of Rare Diseases
|
August 17, 2018
Missense mutation in SLIT2 associated with congenital myopia, anisometropia, connective tissue abnormalities, and obesity
Katherine Y Liu, Jesse D Sengillo, Gabriel Velez, et al.
European Journal of Human Genetics : EJHG
|
June 7, 2021
PRICKLE2 revisited-further evidence implicating PRICKLE2 in neurodevelopmental disorders
Allan Bayat, Sumaiya Iqbal, Kim Borredy, et al.
Page
of 16