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[会议论文] 作者:Lin Yuchen,Yao Ke, 来源:2016年第十届中国医师协会眼科医师分会年会 年份:2016
[会议论文] 作者:Lin Yuchen,Yao Ke, 来源:第八届中国眼科学和视觉科学研究大会 年份:2016
Purpose To investigate the mechanisms of adriamycin(ADR)for proliferative vitreoretinopathy(PVR)treatment by using human retinal pigment epithelial(RPE)-derived(ARPE-19)cells.Methods Cultured ARPE-19...
[会议论文] 作者:Yu Yinhui,Wu Menghan,Yao Ke, 来源:第八届中国眼科学和视觉科学研究大会 年份:2016
Purpose To identify the pathogenic mutation responsible for autosomal dominan congenital cataract(ADCC)in a Chinese pedigree with bilateral zonular pulverulent cataract and characterize the functional...
[会议论文] 作者:Yu Yinhui,Wu Menghan,Yao Ke, 来源:第八届中国眼科学和视觉科学研究大会 年份:2016
Purpose We sought to identify the genetic defect in a three-generations of a Chinese family affected with bilateral punctuate congenital cataract and to examine the clinical features in detail.Methods...
[会议论文] 作者:Wu Menghan,Yu Yinhui,Yao Ke, 来源:第八届中国眼科学和视觉科学研究大会 年份:2016
Background Marfans syndrome is an important cause of visual impairment.The most important causative gene of it is FBN1 gene.The study aimed to identify the disease-causing mutation which is responsibl...
[会议论文] 作者:Wu Menghan,Yu Yinhui,Yao Ke, 来源:第八届中国眼科学和视觉科学研究大会 年份:2016
Objective To identify the cataract-causing mutations in a Chinese family and primitively determine themechanism underlying cataracts formation.Methods All patients in this family who participated in t...
[会议论文] 作者:Yu Yinhui,Wu Menghan,Yao Ke, 来源:第八届中国眼科学和视觉科学研究大会 年份:2016
Purpose To identify the underlying genetic defect and the molecular phenotype in a Chinese family affected with autosomal dominant congenital punctate cataract.Methods Detailed clinical and ophthalmol...
[会议论文] 作者:Yu Yinhui,Wu Menghan,Yao Ke, 来源:第八届中国眼科学和视觉科学研究大会 年份:2016
Aim To report a rare case of bilateral congenital cataract in colobomatous macrophthalmos with microcornea syndrome.Methods A 16-year-old female with bilateral congenital cataract was referred to our...
[会议论文] 作者:Wu Menghan,Yu Yinhui,Yao Ke, 来源:第八届中国眼科学和视觉科学研究大会 年份:2016
Aim To identify the mutations associated with congenital cataract in a Chinese family and study the functional effects of the mutant connexin50.Methods Each family member participating in this study u...
[会议论文] 作者:Wu Menghan,Yu Yinhui,Yao Ke, 来源:第八届中国眼科学和视觉科学研究大会 年份:2016
AIM Congenital cataracts are a major cause of visual impairment in children[1,2].The study aimed to identify the disease-causing mutation which is responsible for the presence of congenital cataract i...
[会议论文] 作者:Yu Yinhui,Wu Menghan,Yao Ke, 来源:第八届中国眼科学和视觉科学研究大会 年份:2016
Purpose To identify the pathogenic gene mutation in a Chinese family with autosomal dominant inherited posterior subcapsular cataracts.Methods After obtained informed consent,detailed ophthalmic exami...
[会议论文] 作者:Yu Yinhui,Wu Menghan,Yao Ke, 来源:第八届中国眼科学和视觉科学研究大会 年份:2016
Purpose To identify the potential pathogenic mutation responsible for autosomal dominan congenital cataract(ADCC)in a Chinese pedigree and characterize the functional and cellular consequences of the...
[会议论文] 作者:Teng Wenqi,Yao ke,Shen Tueng,Ratner Buddy, 来源:第八届中国眼科学和视觉科学研究大会 年份:2016
Purpose: To develop a novel silicone polymeric artificial cornea using spherically template angiogenic regenerative(STAR)biomaterial technology with a one-piece mold design for fighting treatable corn...
[会议论文] 作者:yang dongliang,shen yao,ke lu,zhang jingzhu,tong zhihui,li weiqin, 来源:中华医学会第10次全国重症医学大会 年份:2016
Objective The aim of this study was to describe the clinical features of acute pancreatitis(AP) patients who developed acute cholecystitis in the late phase(late AC) and to facilitate the clinicians f...
[会议论文] 作者:Yao Ke,Liu Ying,Xu Shaobo,Zuo Feifei,Xu Xiaoyang,Wei Shuangyan,Xu Xia, 来源:第34届(2016)中国质谱学会学术年会 年份:2016
  ABSTGRACT: Aim: To analyze the metabolic profiles in the plasma samples of lymphoma patients as well as healthy controls and further explore potential bioma...
[会议论文] 作者:Liu Huifang,Liu Chuan,Yang Xiao-Tian,Fu Xin-Yu,Lu Chun-Lan,Ji Qiao-Dan,Yang Zhou-Yuan,Yao Ke,Luo Huan-Yuan, 来源:中华医学会第十七次全国物理医学与康复学学术会议 年份:2016
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