Expression of transcription factors and crystallin proteins during rat lens regeneration

por Huang, Yusen, Xie, Lixin
Publicado 2010

Neuroprotectin D1 Attenuates Laser-induced Choroidal Neovascularization in Mouse

por Sheets, Kristopher G., Zhou, Yongdong, Ertel, Monica K., Knott, Eric J., Regan, Cornelius E., Elison, Jasmine R., Gordon, William C., Gjorstrup, Per, Bazan, Nicolas G.
Publicado 2010

Novel mutations in MERTK associated with childhood onset rod-cone dystrophy

por Mackay, Donna S., Henderson, Robert H., Sergouniotis, Panagiotis I., Li, Zheng, Moradi, Phillip, Holder, Graham E., Waseem, Naushin, Bhattacharya, Shomi S., Aldahmesh, Mohammed A., Alkuraya, Fowzan S., Meyer, Brian, Webster, Andrew R., Moore, Anthony T.
Publicado 2010

A monogenic dominant mutation in Rom1 generated by N-ethyl-N-nitrosourea mutagenesis causes retinal degeneration in mice

por Sato, Hajime, Suzuki, Tomohiro, Ikeda, Kyoko, Masuya, Hiroshi, Sezutsu, Hideki, Kaneda, Hideki, Kobayashi, Kimio, Miura, Ikuo, Kurihara, Yasuyuki, Yokokura, Shunji, Nishida, Kohji, Tamai, Makoto, Gondo, Yoichi, Noda, Tetsuo, Wakana, Shigeharu
Publicado 2010

FOXO1 plays an essential role in apoptosis of retinal pericytes

por Alikhani, Mani, Roy, Sayon, Graves, Dana T.
Publicado 2010

Evaluation of the X-linked modifier loci for Leber hereditary optic neuropathy with the G11778A mutation in Chinese

por Ji, Yanli, Jia, Xiaoyun, Li, Shiqiang, Xiao, Xueshan, Guo, Xiangming, Zhang, Qingjiong
Publicado 2010

TRPM1 mutations are associated with the complete form of congenital stationary night blindness

por Nakamura, Makoto, Sanuki, Rikako, Yasuma, Tetsuhiro R., Onishi, Akishi, Nishiguchi, Koji M., Koike, Chieko, Kadowaki, Mikiko, Kondo, Mineo, Miyake, Yozo, Furukawa, Takahisa
Publicado 2010

Decreasing the homodimer interaction: a common mechanism shared by the ΔG91 mutation and deamidation in βA3-crystallin

por Xu, Jianzhen, Wong, Chiwai, Tan, Xiaorong, Jing, Hongjuan, Zhou, Guangzhou, Song, Wei
Publicado 2010

Alterations in lenticular proteins during ageing and selenite-induced cataractogenesis in Wistar rats

por Sakthivel, Muniyan, Elanchezhian, Rajan, Thomas, Philip A., Geraldine, Pitchairaj
Publicado 2010

Mitogen-activated protein kinases in the porcine retinal arteries and neuroretina following retinal ischemia-reperfusion

por Gesslein, Bodil, Håkansson, Gisela, Carpio, Ronald, Gustafsson, Lotta, Perez, Maria-Thereza, Malmsjö, Malin
Publicado 2010

Novel USH2A compound heterozygous mutations cause RP/USH2 in a Chinese family

por Liu, Xiaowen, Tang, Zhaohui, Li, Chang, Yang, Kangjuan, Gan, Guanqi, Zhang, Zibo, Liu, Jingyu, Jiang, Fagang, Wang, Qing, Liu, Mugen
Publicado 2010

Analysis of microsatellite polymorphisms within the GLC1F locus in Japanese patients with normal tension glaucoma

por Murakami, Kaori, Meguro, Akira, Ota, Masao, Shiota, Tomoko, Nomura, Naoko, Kashiwagi, Kenji, Mabuchi, Fumihiko, Iijima, Hiroyuki, Kawase, Kazuhide, Yamamoto, Tetsuya, Nakamura, Makoto, Negi, Akira, Sagara, Takeshi, Nishida, Teruo, Inatani, Masaru, Tanihara, Hidenobu, Aihara, Makoto, Araie, Makoto, Fukuchi, Takeo, Abe, Haruki, Higashide, Tomomi, Sugiyama, Kazuhisa, Kanamoto, Takashi, Kiuchi, Yoshiaki, Iwase, Aiko, Ohno, Shigeaki, Inoko, Hidetoshi, Mizuki, Nobuhisa
Publicado 2010

Variable phenotypic expressivity in a Swiss family with autosomal dominant retinitis pigmentosa due to a T494M mutation in the PRPF3 gene

por Vaclavik, Veronika, Gaillard, Marie-Claire, Tiab, L., Schorderet, Daniel F., Munier, Francis L.
Publicado 2010

Oxidative stress in lens in vivo: Inhibitory effect of caffeine. A preliminary report

por Varma, SD, Hegde, KR, Kovtun, S
Publicado 2010

Identification of crystallin modifications in the human lens cortex and nucleus using laser capture microdissection and CyDye labeling

por Asomugha, C.O., Gupta, R., Srivastava, O.P.
Publicado 2010

Smell perception in normal tension glaucoma patients

por Mozaffarieh, Maneli, Hauenstein, Daniela, Schoetzau, Andreas, Konieczka, Katarzyna, Flammer, Josef
Publicado 2010

Sequence variants of the DFNB31 gene among Usher syndrome patients of diverse origin

por Aller, Elena, Jaijo, Teresa, van Wijk, Erwin, Ebermann, Inga, Kersten, Ferry, García-García, Gema, Voesenek, Krysta, Aparisi, María José, Hoefsloot, Lies, Cremers, Cor, Díaz-Llopis, Manuel, Pennings, Ronald, Bolz, Hanno J., Kremer, Hannie, Millán, José M.
Publicado 2010

A mutation in the FOXE3 gene causes congenital primary aphakia in an autosomal recessive consanguineous Pakistani family

por Anjum, Iram, Eiberg, Hans, Baig, Shahid Mahmood, Tommerup, Niels, Hansen, Lars
Publicado 2010

Autosomal recessive congenital cataract linked to EPHA2 in a consanguineous Pakistani family

por Kaul, Haiba, Riazuddin, S. Amer, Shahid, Mariam, Kousar, Samra, Butt, Nadeem H., Zafar, Ahmad U., Khan, Shaheen N., Husnain, Tayyab, Akram, Javed, Hejtmancik, J. Fielding, Riazuddin, Sheikh
Publicado 2010

Mitochondrial DNA analysis in primary congenital glaucoma

por Tanwar, Mukesh, Dada, Tanuj, Sihota, Ramanjit, Dada, Rima
Publicado 2010