Mali, Raghuveer S, Peng, Guang-Hua, Zhang, Xiao, Dang, Loan, Chen, Shiming, Mitton, Kenneth P
Abstract Background FIZ1 (Flt-3 Interacting Zinc-finger) is a broadly expressed protein of unknown function. We reported previously that in the mammalian retina, FIZ1 interacts with NRL...
Peng, Guang-Hua, Chen, Shiming
The homeodomain transcription factor Crx is required for expression of many photoreceptor genes in the mammalian retina. The mechanism by which Crx activates transcription remains to be determined....
Peng, Guang-Hua, Ahmad, Omar, Ahmad, Faisel, Liu, Jianfeng, Chen, Shiming
Nr2e3 is an orphan nuclear receptor expressed specifically by retinal photoreceptor cells. Mutations in Nr2e3 result in syndromes characterized by excess blue cones and loss of rods: enhanced S-cone...
Peng, Guang-Hua, Ahmad, Omar, Ahmad, Faisel, Liu, Jianfeng, Chen, Shiming
Nr2e3 is an orphan nuclear receptor expressed specifically by retinal photoreceptor cells. Mutations in Nr2e3 result in syndromes featuring excess blue cones and loss of rods: enhanced S-cone...
QRX, a Novel Homeobox Gene, Modulates Photoreceptor Gene Expression (2004)
Wang, Qing-liang, Chen, Shiming, Esumi, Noriko, Swain, Prabodh K., Haines, Heidi S., Peng, Guanghua, ...
A novel paired-like homeobox gene, designated as Qrx, was identified by a yeast one-hybrid screen using the bovine Rhodopsin promoter Ret-1 DNA regulatory element as bait. Qrx is preferentially...
QRX, a novel homeobox gene, modulates photoreceptor gene expression (2004)
Wang, Qing-liang, Chen, Shiming, Esumi, Noriko, Swain, Prabodh K., Haines, Heidi S., Peng, Guanghua, ...
A novel paired-like homeobox gene, designated as Qrx, was identified by a yeast one-hybrid screen using the bovine Rhodopsin promoter Ret-1 DNA regulatory element as bait. Qrx is preferentially...
Chen, Shiming, Peng, Guang-Hua, Wang, Xuejiao, Smith, Annette C., Grote, Sara K., Sopher, Bryce L., ...
Spinocerebellar ataxia type 7 (SCA7) is an inherited neurodegenerative disorder caused by expansion of a polyglutamine tract in the ataxin-7 protein. A unique feature of SCA7 is degeneration of...
QRX, a Novel Homeobox Gene, Modulates Photoreceptor Gene Expression (2004)
Wang, Qing-liang, Chen, Shiming, Esumi, Noriko, Swain, Prabodh K., Haines, Heidi S., Peng, Guanghua, ...
A novel paired-like homeobox gene, designated as Qrx, was identified by a yeast one-hybrid screen using the bovine Rhodopsin promoter Ret-1 DNA regulatory element as bait. Qrx is preferentially...
Chen, Shiming, Peng, Guang-Hua, Wang, Xuejiao, Smith, Annette C., Grote, Sara K., Sopher, Bryce L., ...
Spinocerebellar ataxia type 7 (SCA7) is an inherited neurodegenerative disorder caused by expansion of a polyglutamine tract in the ataxin-7 protein. A unique feature of SCA7 is degeneration of...
Chen, Shiming, Peng, Guang-Hua, Wang, Xuejiao, Smith, Annette C., Grote, Sara K., Sopher, Bryce L., ...
Spinocerebellar ataxia type 7 (SCA7) is an inherited neurodegenerative disorder caused by expansion of a polyglutamine tract in the ataxin-7 protein. A unique feature of SCA7 is degeneration of...
Functional analysis of cone-rod homeobox (CRX) mutations associated with retinal dystrophy (2002)
Chen, Shiming, Wang, Qing-Liang, Xu, Siqun, Liu, Ivy, Li, Lili Y., Wang, Yufang, ...
Mutations in the photoreceptor transcription factor cone–rod homeobox (CRX) have been identified in patients with several forms of retinal degenerative disease. To investigate the mechanisms by...
Fei, Yijian, Matragoon, Suraporn, Smith, Sylvia B., Overbeek, Paul A., Chen, Shiming, Zack, Donald J., ...
The essential control elements in the interphotoreceptor retinoid-binding protein gene (IRBP) promoter are located between −156 and +19. The −156/−109 sequence contains a...
Thesis (Ph. D.)--State University of New York, Health Science Center at Syracuse, 1992.
Instability of composite beams in hogging bending. (1992)
Thesis (Ph. D.)--University of Warwick, 1992.
Li, Xiaodong, Chen, Shiming, Wang, Qingliang, Zack, Donald J., Snyder, Solomon H., Borjigin, Jimo
The circadian hormone melatonin is synthesized predominantly in the pineal gland by the actions of two pineal-specific enzymes: serotonin N-acetyltransferase (NAT) and...
Palhan, Vikas B., Chen, Shiming, Peng, Guang-Hua, Tjernberg, Agneta, Gamper, Armin M., Fan, Yuxin, ...
Spinocerebellar ataxia type 7 (SCA7) is characterized by cone-rod dystrophy retinal degeneration and is caused by a polyglutamine [poly(Q)] expansion within ataxin-7, a protein of previously unknown...
Li, Xiaodong, Chen, Shiming, Wang, Qingliang, Zack, Donald J., Snyder, Solomon H., Borjigin, Jimo
The circadian hormone melatonin is synthesized predominantly in the pineal gland by the actions of two pineal-specific enzymes: serotonin N-acetyltransferase (NAT) and...
Palhan, Vikas B., Chen, Shiming, Peng, Guang-Hua, Tjernberg, Agneta, Gamper, Armin M., Fan, Yuxin, ...
Spinocerebellar ataxia type 7 (SCA7) is characterized by cone-rod dystrophy retinal degeneration and is caused by a polyglutamine [poly(Q)] expansion within ataxin-7, a protein of previously unknown...