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[会议论文] 作者：KunXia;,
来源：Symposium for Chinese Neuroscientists Worldwide 2014(第八届海内外华 年份：2014
Autism is a highly heritable neurodevelopmental disorder,known genetic variants,mostly rare,only account for a small proportion of cases.We performed genome...
[会议论文] 作者：zengjunzhang,mingxiahuang,dongwang,chaochen,kunxia,
来源：中华放射学学术大会2016、中华医学会第23次全国放射学学术大会暨中华医学会第24次全国影像技术学术大会 年份：2016
Objective To study CT scan finding of retroperitoneal neuroblastom.Methods 32 cases confirmed by surgery and pathology were retrospectively analyzed.Results In 15 cases of neuroblastom ,round mass was...
[会议论文] 作者：zengjunzhang,mingxiahuang,dongwang,huachen,chaochen,xinhou,kunxia,
来源：中华放射学学术大会2016、中华医学会第23次全国放射学学术大会暨中华医学会第24次全国影像技术学术大会 年份：2016
Objective To investigate the white matter microstructure changes by using DTI in children with congenital hypothyroidism(CH). Methods 20 children with CH and 20 normal children matched in terms of age...
[会议论文] 作者：YaweiLi[1]WeiLi[2]KunXia[2]BingWang[1],
来源：第十四次全国医学遗传学学术会议 年份：2015
Purpose: The aim of this study was to identify a novel causative gene in a ChineseHan origin family with autosomal-dominant adolescent idiopathic scoliosis,...
[会议论文] 作者：Bao-RongZHANG[1]JunTIAN[1]Xin-ZhenYIN[1]WeiLUO[1]KunXIA[2],
来源：中国神经科学学会第四次会员代表大会暨第七届全国学术会议(The 7th Biennial Meeting and the 年份：2007
This study aimed to develop a cell culture model of Huntington disease and observe the effect of sodium butyrate on this cell culture model.Exon 1 of both a...
[期刊论文] 作者：YePU，HongboLIU，RuojingYAN，HaoYANG，KunXIA，YiyuanLI，LiDONG，LijuanLI，HeWANG，YanNIE，MirongSONG，JinboXIE，ShuwenZHAO，KangjunCHEN，BinWANG，JianghaoLI，LingZUO，YePU，HongboLIU，RuojingYAN，HaoYANG，KunXIA，YiyuanLI，,
来源：大气科学进展（英文版） 年份：2020
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[会议论文] 作者：ChangbeiMa[1]KeminWang[2]KunXia[1]HanchunChen[1]HailunHe[1]WeiminZeng[1],
来源：湖南省生理科学会2013年度学术年会 年份：2013
DNA strand break repair plays a key role in protecting the genome from endogenous and exogenous DNA damage.Traditionally, it is assayed by denaturing gel el...
A novel PLA2G6 gene mutation causes autosomal recessive early-onset parkinsonism with typical clinic
[会议论文] 作者：Ji-FengGUO[1]QianPAN[2]KunXIA[2]Bei-ShaTANG[3]Chang-HeSHI[4]LeiWANG[4]Zhan-YunLV[4]JianWANG[5]Lin-ZiLUO,
来源：中国神经科学学会第九届全国学术会议暨第五届会员代表大会 年份：2011
Objective Mutations in the PLA2G6 gene at the PARK14 locus have been reported in complicated parkinsonism patients.To assess the prevalence of and phenotype...
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