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Guoling Tian Selected Research

Lissencephaly

11/2016A patient with lissencephaly, developmental delay, and infantile spasms, due to de novo heterozygous mutation of KIF2A.
12/2012Mutations in the β-tubulin gene TUBB5 cause microcephaly with structural brain abnormalities.
3/2008A pachygyria-causing alpha-tubulin mutation results in inefficient cycling with CCT and a deficient interaction with TBCB.
1/2007Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans.

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Guoling Tian Research Topics

Disease

4Lissencephaly
11/2016 - 01/2007
2Polymicrogyria
12/2012 - 06/2009
1Hearing Loss (Hearing Impairment)
12/2017
1Neurodevelopmental Disorders
01/2017
1Neurodegenerative Diseases (Neurodegenerative Disease)
11/2016
1Malformations of Cortical Development
11/2016
1Ocular Motility Disorders (Convergence Insufficiency)
12/2012
1Microcephaly
12/2012

Drug/Important Bio-Agent (IBA)

8TubulinIBA
12/2017 - 01/2007
1Proteins (Proteins, Gene)FDA Link
11/2016