Jing-Qiong Kang

TRANSFORMATION INTO TREATMENT: NOVEL THERAPEUTICS THAT BEGIN WITHIN THE CELL

K. Maiese, Zhao Zhong （兆忠） Chong （种）, Jing-Qiong Kang, 2003 .

Hematopoietic Factor Erythropoietin Fosters Neuroprotection through Novel Signal Transduction Cascades

K. Maiese, Zhao Zhong （兆忠） Chong （种）, Jing-Qiong Kang, 2002, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

Distinct roles of GRIN2A and GRIN2B variants in neurological conditions

Francis Chee Kuan Tan, Jing-Qiong Kang, S. Traynelis, 2019, F1000Research.

The GABAA Receptor γ2 Subunit R43Q Mutation Linked to Childhood Absence Epilepsy and Febrile Seizures Causes Retention of α1β2γ2S Receptors in the Endoplasmic Reticulum

R. Macdonald, Jing-Qiong Kang, Robert L. Macdonald, 2004, The Journal of Neuroscience.

A missense mutation in SLC6A1 associated with Lennox-Gastaut syndrome impairs GABA transporter 1 protein trafficking and function

Dong Xu, E. Delpire, Jing-Qiong Kang, 2019, Experimental Neurology.

A de novo missense mutation of GABRB2 causes early myoclonic encephalopathy

Joseph Watkins, R. Macdonald, Jing-Qiong Kang, 2016, Journal of Medical Genetics.

Mutations in GABAA receptor subunits associated with genetic epilepsies

Jing-Qiong Kang, M. Gallagher, R. L. Macdonald, 2010, The Journal of physiology.

Altered GABAA receptor expression in brainstem nuclei and SUDEP in Gabrg2+/Q390X mice associated with epileptic encephalopathy

R. Macdonald, Jing-Qiong Kang, Geqing Xia, 2016, Epilepsy Research.

The Human Epilepsy Mutation GABRG2(Q390X) Causes Chronic Subunit Accumulation and Neurodegeneration

Dong Xu, R. Macdonald, Jing-Qiong Kang, 2015, Nature Neuroscience.

Maternal transmission of a rare GABRB3 signal peptide variant is associated with autism

Nancy J. Cox, Eric Courchesne, Edwin H. Cook, 2009, Molecular Psychiatry.

Endoplasmic reticulum retention and degradation of a mutation in SLC6A1 associated with epilepsy and autism

E. Delpire, Jing-Qiong Kang, Juexin Wang, 2020, Molecular Brain.

The GABAA receptor gamma2 subunit R43Q mutation linked to childhood absence epilepsy and febrile seizures causes retention of alpha1beta2gamma2S receptors in the endoplasmic reticulum.

R. Macdonald, Jing-Qiong Kang, Jing-Qiong Kang, 2004, The Journal of neuroscience : the official journal of the Society for Neuroscience.

δ Subunit Susceptibility Variants E177A and R220H Associated with Complex Epilepsy Alter Channel Gating and Surface Expression of α4β2δ GABAA Receptors

R. Macdonald, J. Mulley, Jing-Qiong Kang, 2006, The Journal of Neuroscience.

GABA | Molecular Pathology of Genetic Epilepsy Associated with GABA A Receptor Subunit Gene Mutations

R. Macdonald, Jing-Qiong Kang, 2009 .