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by Aung, T and Ozaki, M and Lee, M.C and Schlotzer-Schrehardt, U and Thorleifsson, G and Mizoguchi, T and Igo, R.P., Jr and Haripriya, A and Williams, S.E and Astakhov, Y.S and Orr, A.C and Burdon, K.P and Nakano, S and Mori, K and Abu-Amero, K and Hauser, M and Li, Z and Prakadeeswari, G and Bailey, J.N and Cherecheanu, A.P and Kang, J.H and Nelson, S and Hayashi, K and Manabe, S.I and Kazama, S and Zarnowski, T and Inoue, K and Irkec, M and Coca-Prados, M and Sugiyama, K and Jarvela, I and Schlottmann, P and Lerner, S.F and Lamari, H and Nilgun, Y and Bikbov, M and Park, K.H and Cha, S.C and Yamashiro, K and Zenteno, J.C and Jonas, J.B and Kumar, R.S.S and Perera, S.A and Chan, A.S.Y and Kobakhidze, N and George, R and Vijaya, L and Do, T and Edward, D.P and Juan Marcos, L. de and Pakravan, M and Moghimi, S and Ideta, R and Bach-Holm, D and Kappelgaard, P and Wirostko, B and Thomas, S and Gaston, D and Bedard, K and Greer, W.L and Yang, Z and Chen, X and Huang, L and Sang, J and Jia, H and Jia, L and Qiao, C and Zhang, H and Liu, X and Zhao, B and Wang, Y.X and Xu, L and Leruez, S and Reynier, P and Chichua, G and Tabagari, S and Uebe, S and Zenkel, M and Berner, D and Mossbock, G and Weisschuh, N and Hoja, U and Welge-Luessen, U.C and Mardin, C and Founti, P and Chatzikyriakidou, A and Pappas, T and Anastasopoulos, E and Lambropoulos, A and Ghosh, A and Shetty, R and Porporato, N and Saravanan, V and Venkatesh, R and Shivkumar, C and Kalpana, N and Sarangapani, S and Kanavi, M.R and Beni, A.N and Yazdani, S and ...
Nature Genetics, ISSN 1061-4036, 2017, Volume 49, Issue 7, pp. 993 - 1004
Exfoliation syndrome (XFS) is the most common known risk factor for secondary glaucoma and a major cause of blindness worldwide. Variants in two genes, LOXL1... 
INDIVIDUALS | RISK LOCI | PSEUDOEXFOLIATION SYNDROME | INFLAMMATORY-BOWEL-DISEASE | METAANALYSIS | POLYMORPHISMS | COMMON SEQUENCE VARIANTS | GENETICS & HEREDITY | GLAUCOMA | BLOOD-PRESSURE | GENOME-WIDE ASSOCIATION | Haplotypes | Humans | Asian Continental Ancestry Group - genetics | Extracellular Matrix - metabolism | Male | Gene Expression Profiling | Mutation, Missense | Amino Acid Oxidoreductases - genetics | Exfoliation Syndrome - ethnology | RNA, Messenger - biosynthesis | Aged, 80 and over | Female | Spheroids, Cellular | Calcium Channels - genetics | Molecular Chaperones - biosynthesis | Eye - metabolism | Genetic Predisposition to Disease | Genome-Wide Association Study | Amino Acid Oxidoreductases - physiology | Molecular Chaperones - genetics | Cell Adhesion | Point Mutation | Alleles | Exfoliation Syndrome - genetics | Amino Acid Substitution | Exfoliatins | Disease susceptibility | Genetic aspects | Analysis | Risk factors | Glaucoma | Genes | Principal components analysis | Cardiovascular disease | Genomes | Biology | Loci | Exfoliation | Studies | Collaboration | Blindness | Alzheimers disease | Life Sciences | Populations and Evolution | Microbiology and Parasitology | Parasitology | Quantitative Methods | Computer Science | Genetics | Santé publique et épidémiologie | Bioinformatics | Human genetics | Virology
Journal Article
Science, ISSN 0036-8075, 3/2001, Volume 291, Issue 5511, pp. 2159 - 2162
RNA editing in trypanosomes occurs by a series of enzymatic steps that are catalyzed by a macromolecular complex. The TbMP52 protein is shown to be a component... 
RNA editing | Cell growth | Messenger RNA | RNA | DNA | Alleles | Reports | Infections | Mitochondrial DNA | Parasites | Transfer RNA | SITE | ENZYME | MESSENGER-RNA | GENE | NADH DEHYDROGENASE | MULTIDISCIPLINARY SCIENCES | MITOCHONDRIA | EXPRESSION | Trypanosoma brucei | Research | Proteins | Enzymes | Ribonucleic acid--RNA | Ribonucleic acid
Journal Article
by Fritsche, L.G and Igl, W and Bailey, J.N and Grassmann, F and Sengupta, S and Bragg-Gresham, J.L and Burdon, K.P and Hebbring, S.J and Wen, C and Gorski, M and Kim, I.K and Cho, D and Zack, D and Souied, E and Scholl, H.P and Bala, E and Lee, K.E and Hunter, D.J and Sardell, R.J and Mitchell, P and Merriam, J.E and Cipriani, V and Hoffman, J.D and Schick, T and Lechanteur, Y.T and Guymer, R.H and Johnson, M.P and Jiang, Y and Stanton, C.M and Buitendijk, G.H and Zhan, X and Kwong, A.M and Boleda, A and Brooks, M and Gieser, L and Ratnapriya, R and Branham, K.E and Foerster, J.R and Heckenlively, J.R and Othman, M.I and Vote, B.J and Liang, H.H and Souzeau, E and McAllister, I.L and Isaacs, T and Hall, J and Lake, S and Mackey, D.A and Constable, I.J and Craig, J.E and Kitchner, T.E and Yang, Z and Su, Z and Luo, H and Chen, D and Ouyang, H and Flagg, K and Lin, D and Mao, G and Ferreyra, H and Stark, K and Strachwitz, C.N. von and Wolf, A and Brandl, C and Rudolph, G and Olden, M and Morrison, M.A and Morgan, D.J and Schu, M and Ahn, J and Silvestri, G and Tsironi, E.E and Park, K.H and Farrer, L.A and Orlin, A and Brucker, A and Li, M and Curcio, C.A and Mohand-Said, S and Sahel, J.A and Audo, I and Benchaboune, M and Cree, A.J and Rennie, C.A and Goverdhan, S.V and Grunin, M and Hagbi-Levi, S and Campochiaro, P and Katsanis, N and Holz, F.G and Blond, F and Blanche, H and Deleuze, J.F and Igo, R.P., Jr and Truitt, B and Peachey, N.S and Meuer, S.M and Myers, C.E and Moore, E.L and Klein, R and ...
Nature Genetics, ISSN 1061-4036, 2016, Volume 48, pp. 134 - 143
Advanced age-related macular degeneration (AMD) is the leading cause of blindness in the elderly, with limited therapeutic options. Here we report on a study... 
Journal Article
by Fan, Q and Verhoeven, V.J and Wojciechowski, R and Barathi, V.A and Hysi, P.G and Guggenheim, J.A and Hohn, R and Vitart, V and Khawaja, A.P and Yamashiro, K and Hosseini, S.M and Lehtimaki, T and Lu, Y and Haller, T and Xie, J and Delcourt, C and Pirastu, M and Wedenoja, J and Gharahkhani, P and Venturini, C and Miyake, M and Hewitt, A.W and Guo, X and Mazur, J and Huffman, J.E and Williams, K.M and Polasek, O and Campbell, H and Rudan, I and Vatavuk, Z and Wilson, J.F and Joshi, P.K and McMahon, G and St Pourcain, B and Evans, D.M and Simpson, C.L and Schwantes-An, T.H and Igo, R.P., Jr and Mirshahi, A and Cougnard-Gregoire, A and Bellenguez, C and Blettner, M and Raitakari, O and Kahonen, M and Seppala, I and Zeller, T and Meitinger, T and Ried, J.S and Gieger, C and Portas, L and Leeuwen, E.M. van and Amin, N and Uitterlinden, A.G and Rivadeneira, F and Hofman, A and Vingerling, J.R and Wang, Y.X and Wang, X and Boh, E.T.H and Ikram, M.K and Sabanayagam, C and Gupta, P and Tan, V and Zhou, L and Ho, C.E and Lim, W and Beuerman, R.W and Siantar, R and Tai, E.S and Vithana, E and Mihailov, E and Khor, C.C and Hayward, C and Luben, R.N and Foster, P.J and Klein, B.E and Klein, R and Wong, H.S and Mitchell, P and Metspalu, A and Aung, T and Young, T.L and He, M and Parssinen, O and Duijn, C.M. van and Wang, J.J and Williams, C and Jonas, J.B and Teo, Y.Y and Mackey, D.A and Oexle, K and Yoshimura, N and Paterson, A.D and Pfeiffer, N and Wong, T.Y and Baird, P.N and Stambolian, D and Wilson, J.E and Cheng, C.Y and Hammond, C.J and ...
Nature Communications, ISSN 2041-1723, 2016, Volume 7, p. 11008
Myopia is the most common human eye disorder and it results from complex genetic and environmental causes. The rapidly increasing prevalence of myopia poses a... 
Journal Article
Journal Article
Molecular and Cellular Biology, ISSN 0270-7306, 11/2000, Volume 20, Issue 22, pp. 8447 - 8457
Journal Article
Human Heredity, ISSN 0001-5652, 12/2011, Volume 72, Issue 4, pp. 298 - 298
Journal Article
Human Heredity, ISSN 0001-5652, 12/2011, Volume 72, Issue 4, pp. I - IV
Journal Article
Physics Reports, ISSN 0370-1573, 2006, Volume 427, Issue 5, pp. 257 - 454
Journal Article