Developmental expression of three small GTPases in the mouse eye

por Mitchell, Dianne C., Bryan, Brad A., Liu, Jin-Ping, Liu, Wen-Bin, Zhang, Lan, Qu, Jia, Zhou, Xiangtian, Liu, Mingyao, Li, David W.
Publicado 2007

Math5 promotes retinal ganglion cell expression patterns in retinal progenitor cells

por Yao, Jing, Sun, Xinghuai, Wang, Yang, Xu, Gezhi, Qian, Jiang
Publicado 2007

Structure/function studies of dogfish α-crystallin, comparison with bovine α-crystallin

por Ghahghaei, A., Rekas, A., Carver, J.A., Augusteyn, R.C.
Publicado 2009

Distribution of ferritin chains in canine lenses with and without age-related nuclear cataracts

por Goralska, M., Nagar, S., Fleisher, L.N., McGahan, M.C.
Publicado 2009

Expression analysis of human pterygium shows a predominance of conjunctival and limbal markers and genes associated with cell migration

por Jaworski, C.J., Aryankalayil-John, M., Campos, M.M., Fariss, R.N., Rowsey, J., Agarwalla, N., Reid, T.W., Dushku, N., Cox, C.A., Carper, D., Wistow, G.
Publicado 2009

Glucocorticoids inhibit the innate immune system of human corneal fibroblast through their suppression of toll-like receptors

por Jin, Xiuming, Qin, Qin, Tu, Lili, Qu, Jia
Publicado 2009

Molecular characterization of retinitis pigmentosa in Saudi Arabia

por Aldahmesh, Mohammed A., Abu Safieh, Leen, Alkuraya, Hisham, Al-Rajhi, Ali, Shamseldin, Hanan, Hashem, Mais, Alzahrani, Fatemah, Khan, Arif O., Alqahtani, Faisal, Rahbeeni, Zuhair, Alowain, Mohammed, Khalak, Hanif, Al-Hazzaa, Salwa, Meyer, Brian F., Alkuraya, Fowzan S.
Publicado 2009

The membrane proteome of the mouse lens fiber cell

por Bassnett, Steven, Wilmarth, Phillip A., David, Larry L.
Publicado 2009

A novel VSX1 mutation identified in an individual with keratoconus in India

por Paliwal, Preeti, Singh, Anuradha, Tandon, Radhika, Titiyal, Jeevan S, Sharma, Arundhati
Publicado 2009

Evaluation of differentially expressed genes identified in keratoconus

por Lee, Ji-Eun, Oum, Boo Sup, Choi, Hee Young, Lee, Seung Uk, Lee, Jong Soo
Publicado 2009

A rare de novo nonsense mutation in OTX2 causes early onset retinal dystrophy and pituitary dysfunction

por Henderson, Robert H., Williamson, Kathleen A., Kennedy, Joanna S., Webster, Andrew R., Holder, Graham E., Robson, Anthony G., FitzPatrick, David R., van Heyningen, Veronica, Moore, Anthony T.
Publicado 2009

Evaluation of the CYP1B1 gene as a candidate gene in beagles with primary open-angle glaucoma (POAG)

por Kato, K., Kamida, A., Sasaki, N., Shastry, B.S.
Publicado 2009

A novel mutation I522N within the TGFBI gene caused lattice corneal dystrophy I

por Zhang, Chunmei, Zeng, Guang, Lin, Hui, Li, Dandan, Zhao, Liming, Zhou, Nan, Qi, Yanhua
Publicado 2009

Role of miR-29b on the regulation of the extracellular matrix in human trabecular meshwork cells under chronic oxidative stress

por Luna, Coralia, Li, Guorong, Qiu, Jianmimg, Epstein, David L., Gonzalez, Pedro
Publicado 2009

Effects of computer monitor-emitted radiation on oxidant/antioxidant balance in cornea and lens from rats

por Balci, Mehmet, Namuslu, Mehmet, Devrim, Erdinç, Durak, İlker
Publicado 2009

Hypoxia-altered signaling pathways of toll-like receptor 4 (TLR4) in human corneal epithelial cells

por Hara, Yuko, Shiraishi, Atsushi, Ohashi, Yuichi
Publicado 2009

A homozygous p.Glu150Lys mutation in the opsin gene of two Pakistani families with autosomal recessive retinitis pigmentosa

por Azam, Maleeha, Khan, Muhammad Imran, Gal, Andreas, Hussain, Alamdar, Shah, Syed Tahir Abbas, Khan, Muhammad Shakil, Sadeque, Ahmed, Bokhari, Habib, Collin, Rob W.J., Orth, Ulrike, van Genderen, Maria M., den Hollander, A.I., Cremers, Frans P. M., Qamar, Raheel
Publicado 2009

Gene expression and differentiation characteristics in mice E13.5 and E17.5 neural retinal progenitors

por Sun, Xuerong, Jiang, Ruzhang, Zhang, Yuehong, Chen, Mengfei, Xiang, Peng, Qi, Ying, Gao, Qianying, Huang, Bing, Ge, Jian
Publicado 2009

NADPH oxidase expression and production of superoxide by human corneal stromal cells

por O’Brien, William J, Heimann, Tom, Rizvi, Farhan
Publicado 2009

Phenotypic characterisation and ZEB1 mutational analysis in posterior polymorphous corneal dystrophy in a New Zealand population

por Vincent, Andrea L., Niederer, Rachael L., Richards, Amanda, Karolyi, Betina, Patel, Dipika V., McGhee, Charles N.J.
Publicado 2009