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Arthur Wuster

Showing results (21-30 of 28) with videos related to

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Immunohorizons|April 26, 2019
Inflammatory Bowel Disease Susceptibility Gene <i>C1ORF106</i> Regulates Intestinal Epithelial PermeabilityPaolo Manzanillo, Maria Mouchess, Naruhisa Ota, et al.
Nature Communications|April 14, 2021
Identifying therapeutic drug targets using bidirectional effect genesKarol Estrada, Steven Froelich, Arthur Wuster, et al.
Molecular Genetics and Metabolism Reports|April 19, 2019
Influence of genetic copy number variants of the human GLUT3 glucose transporter gene <i>SLC2A3</i> on protein expression, glycolysis and rheumatoid arthritis risk: A genetic replication studyKim R Simpfendorfer, Wentian Li, Andrew Shih, et al.
Genes and Immunity|March 19, 2018
Previously reported placebo-response-associated variants do not predict patient outcomes in inflammatory disease Phase III trial placebo armsAsher Haug-Baltzell, Tushar R Bhangale, Diana Chang, et al.
American Journal of Human Genetics|May 23, 2024
Haploinsufficiency underlies the neurodevelopmental consequences of SLC6A1 variantsDina Buitrago Silva, Marena Trinidad, Alicia Ljungdahl, et al.
Cell|February 25, 2017
An Organismal CNV Mutator Phenotype Restricted to Early Human DevelopmentPengfei Liu, Bo Yuan, Claudia M B Carvalho, et al.
Brain : a Journal of Neurology|August 30, 2023
SLC6A1 variant pathogenicity, molecular function and phenotype: a genetic and clinical analysisArthur Stefanski, Eduardo Pérez-Palma, Tobias Brünger, et al.
Medrxiv : the Preprint Server for Health Sciences|March 13, 2026
Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant ClassificationTobias Brünger, Ilona Krey, Suyeon Kim, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Immunohorizons|April 26, 2019
Inflammatory Bowel Disease Susceptibility Gene <i>C1ORF106</i> Regulates Intestinal Epithelial PermeabilityPaolo Manzanillo, Maria Mouchess, Naruhisa Ota, et al.
Nature Communications|April 14, 2021
Identifying therapeutic drug targets using bidirectional effect genesKarol Estrada, Steven Froelich, Arthur Wuster, et al.
Molecular Genetics and Metabolism Reports|April 19, 2019
Influence of genetic copy number variants of the human GLUT3 glucose transporter gene <i>SLC2A3</i> on protein expression, glycolysis and rheumatoid arthritis risk: A genetic replication studyKim R Simpfendorfer, Wentian Li, Andrew Shih, et al.
Genes and Immunity|March 19, 2018
Previously reported placebo-response-associated variants do not predict patient outcomes in inflammatory disease Phase III trial placebo armsAsher Haug-Baltzell, Tushar R Bhangale, Diana Chang, et al.
American Journal of Human Genetics|May 23, 2024
Haploinsufficiency underlies the neurodevelopmental consequences of SLC6A1 variantsDina Buitrago Silva, Marena Trinidad, Alicia Ljungdahl, et al.
Cell|February 25, 2017
An Organismal CNV Mutator Phenotype Restricted to Early Human DevelopmentPengfei Liu, Bo Yuan, Claudia M B Carvalho, et al.
Brain : a Journal of Neurology|August 30, 2023
SLC6A1 variant pathogenicity, molecular function and phenotype: a genetic and clinical analysisArthur Stefanski, Eduardo Pérez-Palma, Tobias Brünger, et al.
Medrxiv : the Preprint Server for Health Sciences|March 13, 2026
Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant ClassificationTobias Brünger, Ilona Krey, Suyeon Kim, et al.
Pageof 3