Publications by authors named "Anel Tankovic"

Claim this Profile
D
De novo GRIN variants in M3 helix associated with neurological disorders control channel gating of NMDA receptor.
Yuchen Xu, Rui Song, Riley E Perszyk, Wenjuan Chen, Sukhan Kim, Anel Tankovic

Cell Mol Life Sci· March 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A de novo loss-of-function GRIN2A mutation associated with childhood focal epilepsy and acquired epileptic aphasia.
Kai Gao, Anel Tankovic, Yujia Zhang, Hirofumi Kusumoto, Jin Zhang

PLoS One· August 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
GRIN1 mutation associated with intellectual disability alters NMDA receptor trafficking and function.
Wenjuan Chen, Christine Shieh, Sharon A Swanger, Anel Tankovic, Margaret Au

J Hum Genet· June 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Functional Evaluation of a De Novo Mutation Identified in a Patient with Profound Global Developmental Delay and Refractory Epilepsy.
Wenjuan Chen, Anel Tankovic, Pieter B Burger, Hirofumi Kusumoto, Stephen F Traynelis

Mol Pharmacol· April 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Molecular Mechanism of Disease-Associated Mutations in the Pre-M1 Helix of NMDA Receptors and Potential Rescue Pharmacology.
Kevin K Ogden, Wenjuan Chen, Sharon A Swanger, Miranda J McDaniel, Linlin Z Fan, Anel Tankovic

PLoS Genet· January 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mechanistic Insight into NMDA Receptor Dysregulation by Rare Variants in the GluN2A and GluN2B Agonist Binding Domains.
Sharon A Swanger, Wenjuan Chen, Gordon Wells, Pieter B Burger, Anel Tankovic

Am J Hum Genet· December 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers.
Dong Li, Hongjie Yuan, Xilma R Ortiz-Gonzalez, Eric D Marsh, Lifeng Tian, Anel Tankovic

Am J Hum Genet· October 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
mutation and early-onset epileptic encephalopathy: personalized therapy with memantine.
Tyler Mark Pierson, Hongjie Yuan, Eric D Marsh, Karin Fuentes-Fajardo, David R Adams, Anel Tankovic

Ann Clin Transl Neurol· March 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis