Showing results (1-10 of 19) with videos related to
Sort By:
Pageof 2
Molecular Vision|October 10, 2009
Apoptosis of lens epithelial cells induced by high concentration of glucose is associated with a decrease in caveolin-1 levelsZhiyong Zhang, Ke Yao, Chongfei JinJapanese Journal of Ophthalmology|December 18, 2008
Correlation of the recurrent FBN1 mutation (c.364C>T) with a unique phenotype in a Chinese patient with Marfan syndromeChongfei Jin, Ke Yao, Zhaohui Sun, et al.Molecular Vision|December 9, 2010
Identification of a MIP mutation that activates a cryptic acceptor splice site in the 3' untranslated regionChongfei Jin, Jin Jiang, Wei Wang, et al.The American Journal of Case Reports|September 11, 2018
A Case of Ocular Kaposi's Sarcoma Successfully Treated with Highly Active Antiretroviral Therapy (HAART) Combined with DocetaxelChongfei Jin, Hamza Minhas, Amandeep Kaur, et al.The American Journal of Case Reports|May 4, 2019
Cardiac Arrest Due to Benzonatate OverdoseChongfei Jin, Erum Zahid, Andleed Sherazi, et al.Molecular Vision|March 7, 2012
A recurrent PAX6 mutation is associated with aniridia and congenital progressive cataract in a Chinese familyChongfei Jin, Qiwei Wang, Jinyu Li, et al.Molecular Vision|December 9, 2010
A Chinese family with progressive childhood cataracts and IVS3+1G>A CRYBA3/A1 mutationsYanan Zhu, Xingchao Shentu, Wei Wang, et al.Molecular Vision|August 8, 2007
Novel FBN1 mutations associated with predominant ectopia lentis and marfanoid habitus in Chinese patientsChongfei Jin, Ke Yao, Jin Jiang, et al.Molecular Vision|July 12, 2008
A nonsense mutation in CRYGC associated with autosomal dominant congenital nuclear cataract in a Chinese familyKe Yao, Chongfei Jin, Ning Zhu, et al.Molecular Vision|January 20, 2011
Characterization of a novel mutation in the CRYBB2 gene associated with autosomal dominant congenital posterior subcapsular cataract in a Chinese familyKe Yao, Jinyu Li, Chongfei Jin, et al.Pageof 2