Advanced search    

Search: authors:"Xiong-jian Luo"

6 papers found.
Use AND, OR, NOT, +word, -word, "long phrase", (parentheses) to fine-tune your search.

Further evidence for the genetic association between CACNA1I and schizophrenia

Background Recent large-scale genome-wide association studies (GWAS) have showed that the neuronal calcium signaling has pivotal roles in schizophrenia (SCZ) in populations of European of ancestry. However, it is not known if calcium signaling pathway genes are also associated with SCZ in Han Chinese population. Methods Here we investigated the association between genetic...

Do nuclear-encoded core subunits of mitochondrial complex I confer genetic susceptibility to schizophrenia in Han Chinese populations?

Province, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming 650223, ChinaXiao Li, Wen Zhang, Xiong-jian Luo & Yong-Gang YaoInstitute of Mental Health, the Second Xiangya Hospital, Central ... Xiong-jian Luo in:Nature Research journals • PubMed • Google ScholarSearch for Xiaogang Chen in:Nature Research journals • PubMed • Google ScholarSearch for Yong-Gang Yao in:Nature Research journals

Meta-Analysis Indicates That the European GWAS-Identified Risk SNP rs1344706 within ZNF804A Is Not Associated with Schizophrenia in Han Chinese Population

Recent genetic association studies have implicated several candidate susceptibility variants for schizophrenia among general populations. Rs1344706, an intronic SNP within ZNF804A, was identified as one of the most compelling candidate risk SNPs for schizophrenia in Europeans through genome-wide association studies (GWASs) and replications as well as large-scale meta-analyses...

GATA3 controls the specification of prosensory domain and neuronal survival in the mouse cochlea

HDR syndrome (also known as Barakat syndrome) is a developmental disorder characterized by hypoparathyroidism, sensorineural deafness and renal disease. Although genetic mapping and subsequent functional studies indicate that GATA3 haplo-insufficiency causes human HDR syndrome, the role of Gata3 in sensorineural deafness and auditory system development is largely unknown. In this...

The Interleukin 3 Gene (IL3) Contributes to Human Brain Volume Variation by Regulating Proliferation and Survival of Neural Progenitors

One of the most significant evolutionary changes underlying the highly developed cognitive abilities of humans is the greatly enlarged brain volume. In addition to being far greater than in most other species, the volume of the human brain exhibits extensive variation and distinct sexual dimorphism in the general population. However, little is known about the genetic mechanisms...

Apoptotic Engulfment Pathway and Schizophrenia

V. Chowdari Vishwajit L. Nimgaonkar Adrian Scott Sibylle G. Schwab Dieter B. Wildenauer Ronglin Che Wei Tang Yongyong Shi Lin He Xiong-jian Luo Bing Su Todd L. Edwards Zhongming Zhao Kenneth S