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[会议论文] 作者：Tang Xiajing,Yao Ke,
来源：the 6th Asian Cataract Research Conference(第六届亚洲白内障研究会议) 年份：2006
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β B2-crystallin gene mutation causes dominant progressive congenital cataract in a five generation f
[会议论文] 作者：Tang Xiajing,Yao Ke,
来源：the 6th Asian Cataract Research Conference(第六届亚洲白内障研究会议) 年份：2006
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Parthenolide protects human lens epithelial cells from oxidative stress-induced apoptosis via inhibi
[会议论文] 作者：Tang Xiajing,Yao Ke,
来源：the 6th Asian Cataract Research Conference(第六届亚洲白内障研究会议) 年份：2006
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p53-dependent mitochondrial dysfunction mediates Adriamycin-induced ARPE-19 cells apoptosis for prol
[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
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Adriamycin induced DNA damage,p53-regulated mitochondrial dysfunction and caspase-dependent apoptosi
[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...
Unsatisfactory outcomes of prolonged ischemic priapism without early surgical~shunts： our clinical e
[期刊论文] 作者：Da-Chao Zheng Hai-Iun Yao Ke Z,
来源：亚洲男性学杂志：英文版 年份：2013
Ischemic 持续勃起症是没有及时治疗，能引起严重可勃起的机能障碍(编辑) 的稀罕出现。这回顾的研究报导我们在对待的经验延长了 ischemic 持续勃起症并且建议我们的进一步的考...
[期刊论文] 作者：LIU Zhe,SUN Chuan-bin,YAO Ke,
来源：中华医学杂志（英文版） 年份：2004
Internal lenticonus is a very rare morphologic abnormality of crystalline lens which has been reported in only several cases in the literature.We herein reporte...
[期刊论文] 作者：Wenqi Yao,Ke Li,Kan Liao,
来源：生物化学与生物物理学报（英文版） 年份：2009
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[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...
Characterization of a CRYBB2 nonsense mutation associated with autosomal dominant congenital catarac
[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...
A Novel Single-Base Deletional Mutation in Major Intrinsic Protein(MIP)in Autosomal Dominant Catarac
[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...
Bilateral Congenital Cataract in Colobomatous Macrophthalmos with Microcornea Syndrome:a case report
[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...
A novel splice site mutation of CRYBA3/A1 gene associated with congenital cataract in a Chinese fami
[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...
Another evidence for an A2V mutation in the CRYBB2gene associated with autosomal dominant congenital
[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...
Identification and functional analysis of a novel connexin 50 mutation associated with autosome domi
[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...
[期刊论文] 作者：LIU Ya-Feng,YAO Ke,Roger Hutton,ZOU Ya-Ming,
来源：中国物理快报（英文版） 年份：2005
We present a calculation scheme with significant modifications and improvements for determining the ionization balance and the ion temperature evolution in an e...
A New Silicone Polymeric Artificial Cornea Based on Spherically Templated Angiogenic Regenerative Bi
[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...
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