Long-term effects of etelcalcetide as intravenous calcimimetic therapy in hemodialysis patients with secondary hyperparathyroidism by Shigematsu, Takashi, Fukagawa, Masafumi, Yokoyama, Keitaro, Akiba, Takashi, Fujii, Akifumi, Odani, Motoi, Akizawa, Tadao

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Characterization of Werner syndrome protein DNA helicase activity: Directionality, substrate dependence and stimulation by replication protein A by Shen, Jiang-Cheng, Gray, Matthew D, Oshima, Junko, Loeb, Lawrence A

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Fabrication of Self-Organized Optical Waveguides in Photo-induced Refractive Index Variation Sol-Gel Materials With High-Index Contrast by Ono, S., Yoshimura, T., Sato, T., Oshima, J.

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Fabrication and Evaluation of Nano-Scale Optical Circuits Using Sol-Gel Materials With Photo-Induced Refractive Index Variation Characteristics by Ono, S., Yoshimura, T., Sato, T., Oshima, J.

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Werner syndrome. A prototypical form of segmental progeria. by Lessel, D, Oshima, J, Kubisch, C

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Right on track? Performance of satellite telemetry in terrestrial wildlife research by Hofman, M P G, Hayward, M W, Heim, M, Marchand, P, Rolandsen, C M, Mattisson, J, Urbano, F, Heurich, M, Mysterud, A, Melzheimer, J, Morellet, N, Voigt, U, Allen, B L, Gehr, B, Rouco, C, Ullmann, W, Holand, Ø, Jørgensen, N H, Steinheim, G, Cagnacci, F, Kroeschel, M, Kaczensky, P, Buuveibaatar, B, Payne, J C, Palmegiani, I, Jerina, K, Kjellander, P, Johansson, Ö, LaPoint, S, Bayrakcismith, R, Linnell, J D C, Zaccaroni, M, Jorge, M L S, Oshima, J E F, Songhurst, A, Fischer, C, Mc Bride, Jr, R T, Thompson, J J, Streif, S, Sandfort, R, Bonenfant, C, Drouilly, M, Klapproth, M, Zinner, D, Yarnell, R, Stronza, A, Wilmott, L, Meisingset, E, Thaker, M, Vanak, A T, Nicoloso, S, Graeber, R, Said, S, Boudreau, M R, Devlin, A, Hoogesteijn, R, May-Junior, J A, Nifong, J C, Odden, J, Quigley, H B, Tortato, F, Parker, D M, Caso, A, Perrine, J, Tellaeche, C, Zieba, F, Zwijacz-Kozica, T, Appel, C L, Axsom, I, Bean, W T, Cristescu, B, Périquet, S, Teichman, K J, Karpanty, S, Licoppe, A, Menges, V, Black, K, Scheppers, T L, Schai-Braun, S C, Azevedo, F C, Lemos, F G, Payne, A, Swanepoel, L H, Weckworth, B V, Berger, A, Bertassoni, A, McCulloch, G, Šustr, P, Athreya, V, Bockmuhl, D, Casaer, J, Ekori, A, Melovski, D, Richard-Hansen, C, van de Vyver, D, Reyna-Hurtado, R, Robardet, E, Selva, N, Sergiel, A, Farhadinia, M S

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Group size and composition of Guiana dolphins (Sotalia guianensis) (Van Bénèden, 1864) in the Paranaguá Estuarine Complex, Brazil by Santos, M C O, Oshima, J E F, Pacífico, E S, Silva, E

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P760 Post-marketing surveillance of tofacitinib in patients with ulcerative colitis in Japan: A final report of effectiveness and safety data by Matsuoka, K, Motoya, S, Yamamoto, T, Matsuura, M, Fujii, T, Shinzaki, S, Mikami, Y, Arai, S, Oshima, J, Endo, Y, Yuasa, H, Hoshi, M, Sato, K, Hisamatsu, T

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Feeding associations between Guiana dolphins, Sotalia guianensis (Van Bénèden, 1864) and seabirds in the Lagamar estuary, Brazil by Santos, M C O, Oshima, J E F, Pacífico, E S, Silva, E

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The Werner syndrome protein: an update by Oshima, Junko

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Design experiments in Japanese elementary science education with computer support for collaborative learning: hypothesis testing and collaborative construction by Oshima, Jun, Oshima, Ritsuko, Murayama, Isao, Inagaki, Shigenori, Takenaka, Makiko, Nakayama, Hayashi, Yamaguchi, Etsuji

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LMNA mutations in atypical Werner's syndrome by Chen, Lishan, Lee, Lin, Kudlow, Brian A, Dos Santos, Heloisa G, Sletvold, Olav, Shafeghati, Yousef, Botha, Eleanor G, Garg, Abhimanyu, Hanson, Nancy B, Martin, George M, Mian, I Saira, Kennedy, Brian K, Oshima, Junko

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Atypical progeroid syndrome: An unknown helicase gene defect? by Ruijs, M.W.G., van Andel, R.N.J., Oshima, J., Madan, K., Nieuwint, A.W.M., Aalfs, C.M.

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A Novel LMNA Mutation Causes Altered Nuclear Morphology and Symptoms of Familial Partial Lipodystrophy (Dunnigan Variety) with Progeroid Features by Saha, B., Lessel, D., Hisama, F.M., Leistritz, D.F., Friedrich, K., Martin, G.M., Kubisch, C., Oshima, J.

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Homozygous and Compound Heterozygous Mutations at the Werner Syndrome Locus by Oshima, Junko, Yu, Chang-En, Piussan, Charles, Klein, Georg, Jabkowski, Jörg, Balci, Sevim, Miki, Tetsuro, Nakura, Jun, Ogihara, Toshio, Ells, James, Smith, Marilia de A. C., Melaragno, Maria I., Fraccaro, Marco, Scappaticci, Susi, Matthews, John, Ouais, Samir, Jarzebowicz, Amy, Schellenberg, Gerard D., Martin, George M.

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Identification of a transcript that is down-regulated in senescent human fibroblasts. Cloning, sequence analysis, and regulation of the human L7 ribosomal protein gene by Seshadri, T., Uzman, J.A., Oshima, J., Campisi, J.

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Werner syndrome protein limits MYC-induced cellular senescence by Grandori, Carla, Wu, Kou-Juey, Fernandez, Paula, Ngouenet, Celine, Grim, Jonathan, Clurman, Bruce E, Moser, Michael J, Oshima, Junko, Russell, David W, Swisshelm, Karen, Frank, Scott, Amati, Bruno, Dalla-Favera, Riccardo, Monnat, Jr, Raymond J

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Lessons from human progeroid syndromes by Martin, George M, Oshima, Junko

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Right on track? Performance of satellite telemetry in terrestrial wildlife research by Hofman, M P G, Hayward, M W, Heim, M, Marchand, P, Rolandsen, C M, Mattisson, J, Urbano, F, Heurich, M, Mysterud, A, Melzheimer, J, Morellet, N, Voigt, U, Allen, B L, Gehr, B, Rouco, C, Ullmann, W, Holand, Ø, Jørgensen, N H, Steinheim, G, Cagnacci, F, Kroeschel, M, Kaczensky, P, Buuveibaatar, B, Payne, J C, Palmegiani, I, Jerina, K, Kjellander, P, Johansson, Ö, Lapoint, S, Bayrakcismith, R, Linnell, J D C, Zaccaroni, M, Jorge, M L S, Oshima, J E F, Songhurst, A, Fischer, C, Mc Bride, R T, Thompson, J J, Streif, S, Sandfort, R, Bonenfant, C, Drouilly, M, Klapproth, M, Zinner, D, Yarnell, R, Stronza, A, Wilmott, L, Meisingset, E, Thaker, M, Vanak, A T, Nicoloso, S, Graeber, R, Said, S, Boudreau, M R, Devlin, A, Hoogesteijn, R, May-Junior, J A, Nifong, J C, Odden, J, Quigley, H B, Tortato, F, Parker, D M, Caso, A, Perrine, J, Tellaeche, C, Zieba, F, Zwijacz-Kozica, T, Appel, C L, Axsom, I, Bean, W T, Cristescu, B, Périquet, S, Teichman, K J, Karpanty, S, Licoppe, A, Menges, V, Black, K, Scheppers, T L, Schai-Braun, S C, Azevedo, F C, Lemos, F G, Payne, A, Swanepoel, L H, Weckworth, B V, Berger, A, Bertassoni, A, Mcculloch, G, Šustr, P, Athreya, V, Bockmuhl, D, Casaer, J, Ekori, A, Melovski, D, Richard-Hansen, Cecile, van de Vyver, D, Reyna-Hurtado, R, Robardet, E, Selva, N, Sergiel, A, Farhadinia, M S

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Positional Cloning of the Werner's Syndrome Gene by Yu, Chang-En, Oshima, Junko, Fu, Ying-Hui, Wijsman, Ellen M., Hisama, Fuki, Alisch, Reid, Matthews, Shellie, Nakura, Jun, Miki, Tetsuro, Ouais, Samir, Martin, George M., Mulligan, John, Schellenberg, Gerard D.

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