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H. Kondo

Investigative Ophthalmology and Visual Science, American Journal of Human Genetics, Proceedings of the National Academy of Sciences of the United States of America, Human Mutation, Molecular Vision
9
Role
Title
Level Year L/R
🐜 Mutations in TSPAN12 cause autosomal-dominant familial exudative vitreoretinopathy.
16 auth. J. Poulter, Manir Ali, D. Gilmour, A. Rice, H. Kondo, K. Hayashi, D. Mackey, L. Kearns, J. Ruddle, J. Craig, ... E. Pierce, L. Downey, M. Mohamed, A. Markham, C. Inglehearn, C. Toomes 		7 2010
7
🐜
🐜 ZNF408 is mutated in familial exudative vitreoretinopathy and is crucial for the development of zebrafish retinal vasculature
26 auth. R. Collin, K. Nikopoulos, Margo Dona, C. Gilissen, A. Hoischen, F. N. Boonstra, J. Poulter, H. Kondo, W. Berger, C. Toomes, T. Tahira, Lucas Mohn, E. Blokland, L. Hetterschijt, Manir Ali, ... J. Groothuismink, Lonneke Duijkers, C. Inglehearn, Lea Sollfrank, T. Strom, E. Uchio, C. E. van Nouhuys, H. Kremer, J. Veltman, E. van Wijk, F. Cremers 		7 2013
7
🐜
🐒 Complexity of the genotype–phenotype correlation in familial exudative vitreoretinopathy with mutations in the LRP5 and/or FZD4 genes
Minghui Qin, H. Hayashi, K. Oshima, T. Tahira, K. Hayashi, H. Kondo 		7 2005
7
🐒
🐜 Quercetin induces the expression of peroxiredoxins 3 and 5 via the Nrf2/NRF1 transcription pathway.
7 auth. Naoya Miyamoto, H. Izumi, R. Miyamoto, H. Kondo, A. Tawara, Y. Sasaguri, ... K. Kohno 		6 2011
6
🐜
🐜 Defects in the Cell Signaling Mediator β-Catenin Cause the Retinal Vascular Condition FEVR.
18 auth. Evangelia S Panagiotou, Carla Sanjurjo Soriano, J. Poulter, Emma C. Lord, Denisa DΕΎulovΓ‘, H. Kondo, Atsushi Hiyoshi, B. Chung, Y. W. Chu, C. Lai, ... Mark E. Tafoya, D. Karjosukarso, R. Collin, J. Topping, L. Downey, Manir Ali, C. Inglehearn, C. Toomes 		6 2017
6
🐜
🦁 A homozygosity-based search for mutations in patients with autosomal recessive retinitis pigmentosa, using microsatellite markers.
9 auth. H. Kondo, Minghui Qin, A. Mizota, M. Kondo, H. Hayashi, K. Hayashi, ... K. Oshima, T. Tahira, K. Hayashi 		6 2004
6
🦁
🐜 Transcriptional regulation of activating transcription factor 4 under oxidative stress in retinal pigment epithelial ARPE-19/HPV-16 cells.
8 auth. Naoya Miyamoto, H. Izumi, R. Miyamoto, Hang Bin, H. Kondo, A. Tawara, ... Y. Sasaguri, K. Kohno 		5 2011
5
🐜
🦁 Genetic variants of FZD4 and LRP5 genes in patients with advanced retinopathy of prematurity
H. Kondo, S. Kusaka, Aki Yoshinaga, E. Uchio, A. Tawara, T. Tahira 		5 2013
5
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🦁 Novel mutations in Norrie disease gene in Japanese patients with Norrie disease and familial exudative vitreoretinopathy.
8 auth. H. Kondo, Minghui Qin, S. Kusaka, T. Tahira, H. Hasebe, H. Hayashi, ... E. Uchio, K. Hayashi 		5 2007
5
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