Guoliang Chai Selected Research

ADP-ribosylarginine hydrolase

12/2021	Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome.
11/2018	Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome.
1/2018	Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome.

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Guoliang Chai Research Topics

Disease

3	Ataxia (Dyssynergia) 12/2021 - 01/2018
1	Alopecia (Baldness) 01/2021
1	Leukoencephalopathies 01/2021
1	Hereditary renal agenesis 01/2021
1	Pontocerebellar Hypoplasia 01/2021
1	Brain Diseases (Brain Disorder) 01/2021
1	Coloboma (Colobomas) 01/2021
1	Microcephaly 01/2021
1	Seizures (Absence Seizure) 01/2021
1	Syndactyly (Polysyndactyly) 01/2021
1	Hypoxia (Hypoxemia) 10/2020
1	Atrophy 11/2017
1	Metabolic Bone Diseases (Osteopenia) 11/2017
1	Epilepsy (Aura) 11/2017
1	Infections 11/2016

Drug/Important Bio-Agent (IBA)

3	ADP-ribosylarginine hydrolaseIBA 12/2021 - 01/2018
3	Proteins (Proteins, Gene)FDA Link 01/2021 - 11/2017
1	DNA (Deoxyribonucleic Acid)IBA 01/2021
1	LigandsIBA 01/2021
1	Wnt ProteinsIBA 01/2021
1	VanadiumIBA 10/2020
1	COOH-terminal signal transamidaseIBA 11/2017
1	Interferon Regulatory FactorsIBA 11/2016

Therapy/Procedure

1	Electrodes (Electrode) 10/2020