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Chemical Modification of Cellulose Nanofibers for the Production of Highly Thermal Resistant and Optically Transparent Nanopaper for Paper Devices.

ACS applied materials & interfaces

Yagyu H, Saito T, Isogai A, Koga H, Nogi M.
PMID: 26402324
ACS Appl Mater Interfaces. 2015 Oct 07;7(39):22012-7. doi: 10.1021/acsami.5b06915. Epub 2015 Sep 24.

Optically transparent cellulose nanopaper is one of the best candidate substrates for flexible electronics. Some types of cellulose nanopaper are made of mechanically or chemically modified cellulose nanofibers. Among these, nanopapers produced from chemically modified cellulose nanofibers are the...

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Yagyu H, Saito T, Isogai A, et al. Chemical Modification of Cellulose Nanofibers for the Production of Highly Thermal Resistant and Optically Transparent Nanopaper for Paper Devices. ACS Appl Mater Interfaces. 2015;7(39):22012-7doi: 10.1021/acsami.5b06915.
Yagyu, H., Saito, T., Isogai, A., Koga, H., & Nogi, M. (2015). Chemical Modification of Cellulose Nanofibers for the Production of Highly Thermal Resistant and Optically Transparent Nanopaper for Paper Devices. ACS applied materials & interfaces, 7(39), 22012-7. https://doi.org/10.1021/acsami.5b06915
Yagyu, Hitomi, et al. "Chemical Modification of Cellulose Nanofibers for the Production of Highly Thermal Resistant and Optically Transparent Nanopaper for Paper Devices." ACS applied materials & interfaces vol. 7,39 (2015): 22012-7. doi: https://doi.org/10.1021/acsami.5b06915
Yagyu H, Saito T, Isogai A, Koga H, Nogi M. Chemical Modification of Cellulose Nanofibers for the Production of Highly Thermal Resistant and Optically Transparent Nanopaper for Paper Devices. ACS Appl Mater Interfaces. 2015 Oct 07;7(39):22012-7. doi: 10.1021/acsami.5b06915. Epub 2015 Sep 24. PMID: 26402324.
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Five-Year PROSE Treatment for Aniridic Keratopathy.

Optometry and vision science : official publication of the American Academy of Optometry

Kojima T, Hasegawa A, Nakamura T, Isogai N, Kataoka T, Ichikawa K.
PMID: 27668496
Optom Vis Sci. 2016 Oct;93(10):1328-1332. doi: 10.1097/OPX.0000000000000942.

PURPOSE: Aniridic keratopathy is vision-threatening condition in patients with aniridia. The keratopathy occurs due to limbal stem cell deficiency. When conventional treatments fail, surgical treatments such as corneal limbal transplantation or cultivated oral mucosal epithelium transplantation are the alternatives....

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Kojima T, Hasegawa A, Nakamura T, et al. Five-Year PROSE Treatment for Aniridic Keratopathy. Optom Vis Sci. 2016;93(10):1328-1332doi: 10.1097/OPX.0000000000000942.
Kojima, T., Hasegawa, A., Nakamura, T., Isogai, N., Kataoka, T., & Ichikawa, K. (2016). Five-Year PROSE Treatment for Aniridic Keratopathy. Optometry and vision science : official publication of the American Academy of Optometry, 93(10), 1328-1332. https://doi.org/10.1097/OPX.0000000000000942
Kojima, Takashi, et al. "Five-Year PROSE Treatment for Aniridic Keratopathy." Optometry and vision science : official publication of the American Academy of Optometry vol. 93,10 (2016): 1328-1332. doi: https://doi.org/10.1097/OPX.0000000000000942
Kojima T, Hasegawa A, Nakamura T, Isogai N, Kataoka T, Ichikawa K. Five-Year PROSE Treatment for Aniridic Keratopathy. Optom Vis Sci. 2016 Oct;93(10):1328-1332. doi: 10.1097/OPX.0000000000000942. PMID: 27668496.
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Search for gravitational waves associated with γ-ray bursts detected by the interplanetary network.

Physical review letters

Aasi J, Abbott BP, Abbott R, Abbott T, Abernathy MR, Acernese F, Ackley K, Adams C, Adams T, Addesso P, Adhikari RX, Affeldt C, Agathos M, Aggarwal N, Aguiar OD, Ajith P, Alemic A, Allen B, Allocca A, Amariutei D, Andersen M, Anderson RA, Anderson SB, Anderson WG, Arai K, Araya MC, Arceneaux C, Areeda JS, Ast S, Aston SM, Astone P, Aufmuth P, Augustus H, Aulbert C, Aylott BE, Babak S, Baker PT, Ballardin G, Ballmer SW, Barayoga JC, Barbet M, Barish BC, Barker D, Barone F, Barr B, Barsotti L, Barsuglia M, Barton MA, Bartos I, Bassiri R, Basti A, Batch JC, Bauchrowitz J, Bauer TS, Baune C, Bavigadda V, Behnke B, Bejger M, Beker MG, Belczynski C, Bell AS, Bell C, Bergmann G, Bersanetti D, Bertolini A, Betzwieser J, Bilenko IA, Billingsley G, Birch J, Biscans S, Bitossi M, Biwer C, Bizouard MA, Black E, Blackburn JK, Blackburn L, Blair D, Bloemen S, Bock O, Bodiya TP, Boer M, Bogaert G, Bogan C, Bond C, Bondu F, Bonelli L, Bonnand R, Bork R, Born M, Boschi V, Bose S, Bosi L, Bradaschia C, Brady PR, Braginsky VB, Branchesi M, Brau JE, Briant T, Bridges DO, Brillet A, Brinkmann M, Brisson V, Brooks AF, Brown DA, Brown DD, Brückner F, Buchman S, Buikema A, Bulik T, Bulten HJ, Buonanno A, Burman R, Buskulic D, Buy C, Cadonati L, Cagnoli G, Calderón Bustillo J, Calloni E, Camp JB, Campsie P, Cannon KC, Canuel B, Cao J, Capano CD, Carbognani F, Carbone L, Caride S, Castaldi G, Caudill S, Cavaglià M, Cavalier F, Cavalieri R, Celerier C, Cella G, Cepeda C, Cesarini E, Chakraborty R, Chalermsongsak T, Chamberlin SJ, Chao S, Charlton P, Chassande-Mottin E, Chen X, Chen Y, Chincarini A, Chiummo A, Cho HS, Cho M, Chow JH, Christensen N, Chu Q, Chua SS, Chung S, Ciani G, Clara F, Clark DE, Clark JA, Clayton JH, Cleva F, Coccia E, Cohadon PF, Colla A, Collette C, Colombini M, Cominsky L, Constancio M, Conte A, Cook D, Corbitt TR, Cornish N, Corsi A, Costa CA, Coughlin MW, Coulon JP, Countryman S, Couvares P, Coward DM, Cowart MJ, Coyne DC, Coyne R, Craig K, Creighton JD, Croce RP, Crowder SG, Cumming A, Cunningham L, Cuoco E, Cutler C, Dahl K, Dal Canton T, Damjanic M, Danilishin SL, D'Antonio S, Danzmann K, Dattilo V, Daveloza H, Davier M, Davies GS, Daw EJ, Day R, Dayanga T, DeBra D, Debreczeni G, Degallaix J, Deléglise S, Del Pozzo W, Denker T, Dent T, Dereli H, Dergachev V, De Rosa R, DeRosa RT, DeSalvo R, Dhurandhar S, Díaz M, Dickson J, Di Fiore L, Di Lieto A, Di Palma I, Di Virgilio A, Dolique V, Dominguez E, Donovan F, Dooley KL, Doravari S, Douglas R, Downes TP, Drago M, Drever RW, Driggers JC, Du Z, Ducrot M, Dwyer S, Eberle T, Edo T, Edwards M, Effler A, Eggenstein HB, Ehrens P, Eichholz J, Eikenberry SS, Endrőczi G, Essick R, Etzel T, Evans M, Evans T, Factourovich M, Fafone V, Fairhurst S, Fan X, Fang Q, Farinon S, Farr B, Farr WM, Favata M, Fazi D, Fehrmann H, Fejer MM, Feldbaum D, Feroz F, Ferrante I, Ferreira EC, Ferrini F, Fidecaro F, Finn LS, Fiori I, Fisher RP, Flaminio R, Fournier JD, Franco S, Frasca S, Frasconi F, Frede M, Frei Z, Freise A, Frey R, Fricke TT, Fritschel P, Frolov VV, Fulda P, Fyffe M, Gair JR, Gammaitoni L, Gaonkar S, Garufi F, Gehrels N, Gemme G, Gendre B, Genin E, Gennai A, Ghosh S, Giaime JA, Giardina KD, Giazotto A, Gleason J, Goetz E, Goetz R, Gondan L, González G, Gordon N, Gorodetsky ML, Gossan S, Goßler S, Gouaty R, Gräf C, Graff PB, Granata M, Grant A, Gras S, Gray C, Greenhalgh RJ, Gretarsson AM, Groot P, Grote H, Grover K, Grunewald S, Guidi GM, Guido CJ, Gushwa K, Gustafson EK, Gustafson R, Ha J, Hall ED, Hamilton W, Hammer D, Hammond G, Hanke M, Hanks J, Hanna C, Hannam MD, Hanson J, Harms J, Harry GM, Harry IW, Harstad ED, Hart M, Hartman MT, Haster CJ, Haughian K, Heidmann A, Heintze M, Heitmann H, Hello P, Hemming G, Hendry M, Heng IS, Heptonstall AW, Heurs M, Hewitson M, Hild S, Hoak D, Hodge KA, Hofman D, Holt K, Hopkins P, Horrom T, Hoske D, Hosken DJ, Hough J, Howell EJ, Hu Y, Huerta E, Hughey B, Husa S, Huttner SH, Huynh M, Huynh-Dinh T, Idrisy A, Ingram DR, Inta R, Islas G, Isogai T, Ivanov A, Iyer BR, Izumi K, Jacobson M, Jang H, Jaranowski P, Ji Y, Jiménez-Forteza F, Johnson WW, Jones DI, Jones R, Jonker RJ, Ju L, Haris K, Kalmus P, Kalogera V, Kandhasamy S, Kang G, Kanner JB, Karlen J, Kasprzack M, Katsavounidis E, Katzman W, Kaufer H, Kaufer S, Kaur T, Kawabe K, Kawazoe F, Kéfélian F, Keiser GM, Keitel D, Kelley DB, Kells W, Keppel DG, Khalaidovski A, Khalili FY, Khazanov EA, Kim C, Kim K, Kim NG, Kim N, Kim S, Kim YM, King EJ, King PJ, Kinzel DL, Kissel JS, Klimenko S, Kline J, Koehlenbeck S, Kokeyama K, Kondrashov V, Koranda S, Korth WZ, Kowalska I, Kozak DB, Kringel V, Krishnan B, Królak A, Kuehn G, Kumar A, Kumar DN, Kumar P, Kumar R, Kuo L, Kutynia A, Lam PK, Landry M, Lantz B, Larson S, Lasky PD, Lazzarini A, Lazzaro C, Leaci P, Leavey S, Lebigot EO, Lee CH, Lee HK, Lee HM, Lee J, Lee PJ, Leonardi M, Leong JR, Leonor I, Le Roux A, Leroy N, Letendre N, Levin Y, Levine B, Lewis J, Li TG, Libbrecht K, Libson A, Lin AC, Littenberg TB, Lockerbie NA, Lockett V, Lodhia D, Loew K, Logue J, Lombardi AL, Lopez E, Lorenzini M, Loriette V, Lormand M, Losurdo G, Lough J, Lubinski MJ, Lück H, Lundgren AP, Ma Y, Macdonald EP, MacDonald T, Machenschalk B, MacInnis M, Macleod DM, Magaña-Sandoval F, Magee R, Mageswaran M, Maglione C, Mailand K, Majorana E, Maksimovic I, Malvezzi V, Man N, Manca GM, Mandel I, Mandic V, Mangano V, Mangini NM, Mansell G, Mantovani M, Marchesoni F, Marion F, Márka S, Márka Z, Markosyan A, Maros E, Marque J, Martelli F, Martin IW, Martin RM, Martinelli L, Martynov D, Marx JN, Mason K, Masserot A, Massinger TJ, Matichard F, Matone L, Mavalvala N, May G, Mazumder N, Mazzolo G, McCarthy R, McClelland DE, McGuire SC, McIntyre G, McIver J, McLin K, Meacher D, Meadors GD, Mehmet M, Meidam J, Meinders M, Melatos A, Mendell G, Mercer RA, Meshkov S, Messenger C, Meyer MS, Meyers PM, Mezzani F, Miao H, Michel C, Mikhailov EE, Milano L, Miller J, Minenkov Y, Mingarelli CM, Mishra C, Mitra S, Mitrofanov VP, Mitselmakher G, Mittleman R, Moe B, Moggi A, Mohan M, Mohapatra SR, Moraru D, Moreno G, Morgado N, Morriss SR, Mossavi K, Mours B, Mow-Lowry CM, Mueller CL, Mueller G, Mukherjee S, Mullavey A, Munch J, Murphy D, Murray PG, Mytidis A, Nagy MF, Nardecchia I, Naticchioni L, Nayak RK, Necula V, Nelemans G, Neri I, Neri M, Newton G, Nguyen T, Nielsen AB, Nissanke S, Nitz AH, Nocera F, Nolting D, Normandin ME, Nuttall LK, Ochsner E, O'Dell J, Oelker E, Oh JJ, Oh SH, Ohme F, Omar S, Oppermann P, Oram R, O'Reilly B, Ortega W, O'Shaughnessy R, Osthelder C, Ottaway DJ, Ottens RS, Overmier H, Owen BJ, Padilla C, Pai A, Palashov O, Palomba C, Pan H, Pan Y, Pankow C, Paoletti F, Papa MA, Paris H, Pasqualetti A, Passaquieti R, Passuello D, Pedraza M, Pele A, Penn S, Perreca A, Phelps M, Pichot M, Pickenpack M, Piergiovanni F, Pierro V, Pinard L, Pinto IM, Pitkin M, Poeld J, Poggiani R, Poteomkin A, Powell J, Prasad J, Predoi V, Premachandra S, Prestegard T, Price LR, Prijatelj M, Privitera S, Prodi GA, Prokhorov L, Puncken O, Punturo M, Puppo P, Pürrer M, Qin J, Quetschke V, Quintero E, Quitzow-James R, Raab FJ, Rabeling DS, Rácz I, Radkins H, Raffai P, Raja S, Rajalakshmi G, Rakhmanov M, Ramet C, Ramirez K, Rapagnani P, Raymond V, Razzano M, Re V, Recchia S, Reed CM, Regimbau T, Reid S, Reitze DH, Reula O, Rhoades E, Ricci F, Riesen R, Riles K, Robertson NA, Robinet F, Rocchi A, Roddy SB, Rolland L, Rollins JG, Romano R, Romanov G, Romie JH, Rosińska D, Rowan S, Rüdiger A, Ruggi P, Ryan K, Salemi F, Sammut L, Sandberg V, Sanders JR, Sankar S, Sannibale V, Santiago-Prieto I, Saracco E, Sassolas B, Sathyaprakash BS, Saulson PR, Savage R, Scheuer J, Schilling R, Schilman M, Schmidt P, Schnabel R, Schofield RM, Schreiber E, Schuette D, Schutz BF, Scott J, Scott SM, Sellers D, Sengupta AS, Sentenac D, Sequino V, Sergeev A, Shaddock DA, Shah S, Shahriar MS, Shaltev M, Shao Z, Shapiro B, Shawhan P, Shoemaker DH, Sidery TL, Siellez K, Siemens X, Sigg D, Simakov D, Singer A, Singer L, Singh R, Sintes AM, Slagmolen BJ, Slutsky J, Smith JR, Smith MR, Smith RJ, Smith-Lefebvre ND, Son EJ, Sorazu B, Souradeep T, Staley A, Stebbins J, Steinke M, Steinlechner J, Steinlechner S, Stephens BC, Steplewski S, Stevenson S, Stone R, Stops D, Strain KA, Straniero N, Strigin S, Sturani R, Stuver AL, Summerscales TZ, Susmithan S, Sutton PJ, Swinkels B, Tacca M, Talukder D, Tanner DB, Tao J, Tarabrin SP, Taylor R, Tellez G, Thirugnanasambandam MP, Thomas M, Thomas P, Thorne KA, Thorne KS, Thrane E, Tiwari V, Tokmakov KV, Tomlinson C, Tonelli M, Torres CV, Torrie CI, Travasso F, Traylor G, Tse M, Tshilumba D, Tuennermann H, Ugolini D, Unnikrishnan CS, Urban AL, Usman SA, Vahlbruch H, Vajente G, Valdes G, Vallisneri M, van Beuzekom M, van den Brand JF, Van Den Broeck C, van der Sluys MV, van Heijningen J, van Veggel AA, Vass S, Vasúth M, Vaulin R, Vecchio A, Vedovato G, Veitch J, Veitch PJ, Venkateswara K, Verkindt D, Vetrano F, Viceré A, Vincent-Finley R, Vinet JY, Vitale S, Vo T, Vocca H, Vorvick C, Vousden WD, Vyachanin SP, Wade AR, Wade L, Wade M, Walker M, Wallace L, Walsh S, Wang M, Wang X, Ward RL, Was M, Weaver B, Wei LW, Weinert M, Weinstein AJ, Weiss R, Welborn T, Wen L, Wessels P, West M, Westphal T, Wette K, Whelan JT, White DJ, Whiting BF, Wiesner K, Wilkinson C, Williams K, Williams L, Williams R, Williams TD, Williamson AR, Willis JL, Willke B, Wimmer M, Winkler W, Wipf CC, Wiseman AG, Wittel H, Woan G, Wolovick N, Worden J, Wu Y, Yablon J, Yakushin I, Yam W, Yamamoto H, Yancey CC, Yang H, Yoshida S, Yvert M, Zadrożny A, Zanolin M, Zendri JP, Zhang F, Zhang L, Zhao C, Zhu H, Zhu XJ, Zucker ME, Zuraw S, Zweizig J, Aptekar RL, Atteia JL, Cline T, Connaughton V, Frederiks DD, Golenetskii SV, Hurley K, Krimm HA, Marisaldi M, Pal'shin VD, Palmer D, Svinkin DS, Terada Y, von Kienlin A.
PMID: 25032916
Phys Rev Lett. 2014 Jul 04;113(1):011102. doi: 10.1103/PhysRevLett.113.011102. Epub 2014 Jun 30.

We present the results of a search for gravitational waves associated with 223 γ-ray bursts (GRBs) detected by the InterPlanetary Network (IPN) in 2005-2010 during LIGO's fifth and sixth science runs and Virgo's first, second, and third science runs....

Cite
Aasi J, Abbott BP, Abbott R, et al. Search for gravitational waves associated with γ-ray bursts detected by the interplanetary network. Phys Rev Lett. 2014;113(1):011102doi: 10.1103/PhysRevLett.113.011102.
Aasi, J., Abbott, B. P., Abbott, R., Abbott, T., Abernathy, M. R., Acernese, F., Ackley, K., Adams, C., Adams, T., Addesso, P., Adhikari, R. X., Affeldt, C., Agathos, M., Aggarwal, N., Aguiar, O. D., Ajith, P., Alemic, A., Allen, B., Allocca, A., Amariutei, D., Andersen, M., Anderson, R. A., Anderson, S. B., Anderson, W. G., Arai, K., Araya, M. C., Arceneaux, C., Areeda, J. S., Ast, S., Aston, S. M., Astone, P., Aufmuth, P., Augustus, H., Aulbert, C., Aylott, B. E., Babak, S., Baker, P. T., Ballardin, G., Ballmer, S. W., Barayoga, J. C., Barbet, M., Barish, B. C., Barker, D., Barone, F., Barr, B., Barsotti, L., Barsuglia, M., Barton, M. A., Bartos, I., Bassiri, R., Basti, A., Batch, J. C., Bauchrowitz, J., Bauer, T. S., Baune, C., Bavigadda, V., Behnke, B., Bejger, M., Beker, M. G., Belczynski, C., Bell, A. S., Bell, C., Bergmann, G., Bersanetti, D., Bertolini, A., Betzwieser, J., Bilenko, I. A., Billingsley, G., Birch, J., Biscans, S., Bitossi, M., Biwer, C., Bizouard, M. A., Black, E., Blackburn, J. K., Blackburn, L., Blair, D., Bloemen, S., Bock, O., Bodiya, T. P., Boer, M., Bogaert, G., Bogan, C., Bond, C., Bondu, F., Bonelli, L., Bonnand, R., Bork, R., Born, M., Boschi, V., Bose, S., Bosi, L., Bradaschia, C., Brady, P. R., Braginsky, V. B., Branchesi, M., Brau, J. E., Briant, T., Bridges, D. O., Brillet, A., Brinkmann, M., Brisson, V., Brooks, A. F., Brown, D. A., Brown, D. D., Brückner, F., Buchman, S., Buikema, A., Bulik, T., Bulten, H. J., Buonanno, A., Burman, R., Buskulic, D., Buy, C., Cadonati, L., Cagnoli, G., Calderón Bustillo, J., Calloni, E., Camp, J. B., Campsie, P., Cannon, K. C., Canuel, B., Cao, J., Capano, C. D., Carbognani, F., Carbone, L., Caride, S., Castaldi, G., Caudill, S., Cavaglià, M., Cavalier, F., Cavalieri, R., Celerier, C., Cella, G., Cepeda, C., Cesarini, E., Chakraborty, R., Chalermsongsak, T., Chamberlin, S. J., Chao, S., Charlton, P., Chassande-Mottin, E., Chen, X., Chen, Y., Chincarini, A., Chiummo, A., Cho, H. S., Cho, M., Chow, J. H., Christensen, N., Chu, Q., Chua, S. S., Chung, S., Ciani, G., Clara, F., Clark, D. E., Clark, J. A., Clayton, J. H., Cleva, F., Coccia, E., Cohadon, P. F., Colla, A., Collette, C., Colombini, M., Cominsky, L., Constancio, M., Conte, A., Cook, D., Corbitt, T. R., Cornish, N., Corsi, A., Costa, C. A., Coughlin, M. W., Coulon, J. P., Countryman, S., Couvares, P., Coward, D. M., Cowart, M. J., Coyne, D. C., Coyne, R., Craig, K., Creighton, J. D., Croce, R. P., Crowder, S. G., Cumming, A., Cunningham, L., Cuoco, E., Cutler, C., Dahl, K., Dal Canton, T., Damjanic, M., Danilishin, S. L., D'Antonio, S., Danzmann, K., Dattilo, V., Daveloza, H., Davier, M., Davies, G. S., Daw, E. J., Day, R., Dayanga, T., DeBra, D., Debreczeni, G., Degallaix, J., Deléglise, S., Del Pozzo, W., Denker, T., Dent, T., Dereli, H., Dergachev, V., De Rosa, R., DeRosa, R. T., DeSalvo, R., Dhurandhar, S., Díaz, M., Dickson, J., Di Fiore, L., Di Lieto, A., Di Palma, I., Di Virgilio, A., Dolique, V., Dominguez, E., Donovan, F., Dooley, K. L., Doravari, S., Douglas, R., Downes, T. P., Drago, M., Drever, R. W., Driggers, J. C., Du, Z., Ducrot, M., Dwyer, S., Eberle, T., Edo, T., Edwards, M., Effler, A., Eggenstein, H. B., Ehrens, P., Eichholz, J., Eikenberry, S. S., Endrőczi, G., Essick, R., Etzel, T., Evans, M., Evans, T., Factourovich, M., Fafone, V., Fairhurst, S., Fan, X., Fang, Q., Farinon, S., Farr, B., Farr, W. M., Favata, M., Fazi, D., Fehrmann, H., Fejer, M. M., Feldbaum, D., Feroz, F., Ferrante, I., Ferreira, E. C., Ferrini, F., Fidecaro, F., Finn, L. S., Fiori, I., Fisher, R. P., Flaminio, R., Fournier, J. D., Franco, S., Frasca, S., Frasconi, F., Frede, M., Frei, Z., Freise, A., Frey, R., Fricke, T. T., Fritschel, P., Frolov, V. V., Fulda, P., Fyffe, M., Gair, J. R., Gammaitoni, L., Gaonkar, S., Garufi, F., Gehrels, N., Gemme, G., Gendre, B., Genin, E., Gennai, A., Ghosh, S., Giaime, J. A., Giardina, K. D., Giazotto, A., Gleason, J., Goetz, E., Goetz, R., Gondan, L., González, G., Gordon, N., Gorodetsky, M. L., Gossan, S., Goßler, S., Gouaty, R., Gräf, C., Graff, P. B., Granata, M., Grant, A., Gras, S., Gray, C., Greenhalgh, R. J., Gretarsson, A. M., Groot, P., Grote, H., Grover, K., Grunewald, S., Guidi, G. M., Guido, C. J., Gushwa, K., Gustafson, E. K., Gustafson, R., Ha, J., Hall, E. D., Hamilton, W., Hammer, D., Hammond, G., Hanke, M., Hanks, J., Hanna, C., Hannam, M. D., Hanson, J., Harms, J., Harry, G. M., Harry, I. W., Harstad, E. D., Hart, M., Hartman, M. T., Haster, C. J., Haughian, K., Heidmann, A., Heintze, M., Heitmann, H., Hello, P., Hemming, G., Hendry, M., Heng, I. S., Heptonstall, A. W., Heurs, M., Hewitson, M., Hild, S., Hoak, D., Hodge, K. A., Hofman, D., Holt, K., Hopkins, P., Horrom, T., Hoske, D., Hosken, D. J., Hough, J., Howell, E. J., Hu, Y., Huerta, E., Hughey, B., Husa, S., Huttner, S. H., Huynh, M., Huynh-Dinh, T., Idrisy, A., Ingram, D. R., Inta, R., Islas, G., Isogai, T., Ivanov, A., Iyer, B. R., Izumi, K., Jacobson, M., Jang, H., Jaranowski, P., Ji, Y., Jiménez-Forteza, F., Johnson, W. W., Jones, D. I., Jones, R., Jonker, R. J., Ju, L., Haris, K., Kalmus, P., Kalogera, V., Kandhasamy, S., Kang, G., Kanner, J. B., Karlen, J., Kasprzack, M., Katsavounidis, E., Katzman, W., Kaufer, H., Kaufer, S., Kaur, T., Kawabe, K., Kawazoe, F., Kéfélian, F., Keiser, G. M., Keitel, D., Kelley, D. B., Kells, W., Keppel, D. G., Khalaidovski, A., Khalili, F. Y., Khazanov, E. A., Kim, C., Kim, K., Kim, N. G., Kim, N., Kim, S., Kim, Y. M., King, E. J., King, P. J., Kinzel, D. L., Kissel, J. S., Klimenko, S., Kline, J., Koehlenbeck, S., Kokeyama, K., Kondrashov, V., Koranda, S., Korth, W. Z., Kowalska, I., Kozak, D. B., Kringel, V., Krishnan, B., Królak, A., Kuehn, G., Kumar, A., Kumar, D. 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Early Steps of Dauricine Biosynthesis in Cultured Roots of Menispermum dauricum.

Bioscience, biotechnology, and biochemistry

Sugimoto Y, Uchida S, Inanaga S, Kimura Y, Hashimoto M, Isogai A.
PMID: 27299554
Biosci Biotechnol Biochem. 1996 Jan;60(3):503-5. doi: 10.1271/bbb.60.503.

Cultured roots of Menispermum dauricum, a rich source of the bisbenzylisoquinoline alkaloid dauricine (1), were fed with l-[U-(14)C] tyrosine, L-[3-(13)C] tyrosine, and [2-(13)C] tvramine independently, and the incorporation of possible early precursors into 1 was studied. The results demonstrated...

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Sugimoto Y, Uchida S, Inanaga S, et al. Early Steps of Dauricine Biosynthesis in Cultured Roots of Menispermum dauricum. Biosci Biotechnol Biochem. 1996;60(3):503-5doi: 10.1271/bbb.60.503.
Sugimoto, Y., Uchida, S., Inanaga, S., Kimura, Y., Hashimoto, M., & Isogai, A. (1996). Early Steps of Dauricine Biosynthesis in Cultured Roots of Menispermum dauricum. Bioscience, biotechnology, and biochemistry, 60(3), 503-5. https://doi.org/10.1271/bbb.60.503
Sugimoto, Y, et al. "Early Steps of Dauricine Biosynthesis in Cultured Roots of Menispermum dauricum." Bioscience, biotechnology, and biochemistry vol. 60,3 (1996): 503-5. doi: https://doi.org/10.1271/bbb.60.503
Sugimoto Y, Uchida S, Inanaga S, Kimura Y, Hashimoto M, Isogai A. Early Steps of Dauricine Biosynthesis in Cultured Roots of Menispermum dauricum. Biosci Biotechnol Biochem. 1996 Jan;60(3):503-5. doi: 10.1271/bbb.60.503. PMID: 27299554.
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CASE REPORT How to Repair the Lower Eyelid Retraction, Resulting From the Primary Surgery for Epiblepharon?.

Eplasty

Asamura S, Kakizaki H, Matsushima S, Morotomi T, Isogai N.
PMID: 24324846
Eplasty. 2013 Oct 31;13:e55. eCollection 2013.

OBJECTIVE: Among the surgical procedures used to correct the positions of the eyelids or improve their cosmetic appearance, procedures for treating eyelid retraction are some of the most challenging. Lower eyelid retraction can occur iatrogenically after various surgical procedures....

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Asamura S, Kakizaki H, Matsushima S, et al. CASE REPORT How to Repair the Lower Eyelid Retraction, Resulting From the Primary Surgery for Epiblepharon?. Eplasty. 2013;13:e55
Asamura, S., Kakizaki, H., Matsushima, S., Morotomi, T., & Isogai, N. (2013). CASE REPORT How to Repair the Lower Eyelid Retraction, Resulting From the Primary Surgery for Epiblepharon?. Eplasty, 13e55.
Asamura, Shinichi, et al. "CASE REPORT How to Repair the Lower Eyelid Retraction, Resulting From the Primary Surgery for Epiblepharon?." Eplasty vol. 13 (2013): e55.
Asamura S, Kakizaki H, Matsushima S, Morotomi T, Isogai N. CASE REPORT How to Repair the Lower Eyelid Retraction, Resulting From the Primary Surgery for Epiblepharon?. Eplasty. 2013 Oct 31;13:e55. eCollection 2013. PMID: 24324846; PMCID: PMC3819113.
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In Silico Risk Assessment of HLA-A*02:06-Associated Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Caused by Cold Medicine Ingredients.

Journal of toxicology

Isogai H, Miyadera H, Ueta M, Sotozono C, Kinoshita S, Tokunaga K, Hirayama N.
PMID: 24285954
J Toxicol. 2013;2013:514068. doi: 10.1155/2013/514068. Epub 2013 Oct 12.

Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are severe drug hypersensitivities with high mortality. Typical over-the-counter drugs of cold medicines are suggested to be causative. As multiple ingredients are generally contained in cold medicines, it is of particular...

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Isogai H, Miyadera H, Ueta M, et al. In Silico Risk Assessment of HLA-A*02:06-Associated Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Caused by Cold Medicine Ingredients. J Toxicol. 2013;2013:514068doi: 10.1155/2013/514068.
Isogai, H., Miyadera, H., Ueta, M., Sotozono, C., Kinoshita, S., Tokunaga, K., & Hirayama, N. (2013). In Silico Risk Assessment of HLA-A*02:06-Associated Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Caused by Cold Medicine Ingredients. Journal of toxicology, 2013514068. https://doi.org/10.1155/2013/514068
Isogai, Hideto, et al. "In Silico Risk Assessment of HLA-A*02:06-Associated Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Caused by Cold Medicine Ingredients." Journal of toxicology vol. 2013 (2013): 514068. doi: https://doi.org/10.1155/2013/514068
Isogai H, Miyadera H, Ueta M, Sotozono C, Kinoshita S, Tokunaga K, Hirayama N. In Silico Risk Assessment of HLA-A*02:06-Associated Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Caused by Cold Medicine Ingredients. J Toxicol. 2013;2013:514068. doi: 10.1155/2013/514068. Epub 2013 Oct 12. PMID: 24285954; PMCID: PMC3810500.
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Peptidal Sex Hormones Inducing Conjugation Tube Formation in Compatible Mating-Type Cells of Tremella mesenterica.

Science (New York, N.Y.)

Sakagami Y, Yoshida M, Isogai A, Suzuki A.
PMID: 17790543
Science. 1981 Jun 26;212(4502):1525-7. doi: 10.1126/science.212.4502.1525.

The pair of peptidal sex hormones (tremerogen A-10 and tremerogen a-13) that induce conjugation tube formation in compatible type cells (A and a types) of Tremella mesenterica were isolated. Tremerogen A-10 is a dodecapeptide and tremerogen a-13, a tridecapeptide....

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Sakagami Y, Yoshida M, Isogai A, et al. Peptidal Sex Hormones Inducing Conjugation Tube Formation in Compatible Mating-Type Cells of Tremella mesenterica. Science. 1981;212(4502):1525-7doi: 10.1126/science.212.4502.1525.
Sakagami, Y., Yoshida, M., Isogai, A., & Suzuki, A. (1981). Peptidal Sex Hormones Inducing Conjugation Tube Formation in Compatible Mating-Type Cells of Tremella mesenterica. Science (New York, N.Y.), 212(4502), 1525-7. https://doi.org/10.1126/science.212.4502.1525
Sakagami, Y, et al. "Peptidal Sex Hormones Inducing Conjugation Tube Formation in Compatible Mating-Type Cells of Tremella mesenterica." Science (New York, N.Y.) vol. 212,4502 (1981): 1525-7. doi: https://doi.org/10.1126/science.212.4502.1525
Sakagami Y, Yoshida M, Isogai A, Suzuki A. Peptidal Sex Hormones Inducing Conjugation Tube Formation in Compatible Mating-Type Cells of Tremella mesenterica. Science. 1981 Jun 26;212(4502):1525-7. doi: 10.1126/science.212.4502.1525. PMID: 17790543.
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Analysis of cationic structure in some room-temperature molten fluorides and dependence of their ionic conductivity and viscosity on hydrofluoric acid concentration.

The journal of physical chemistry. B

Isogai T, Nakai T, Inoue H, Nakanishi K, Kohara S, Saito M, Inaba M, Tasaka A.
PMID: 21714521
J Phys Chem B. 2011 Aug 11;115(31):9593-603. doi: 10.1021/jp110867k. Epub 2011 Jul 20.

To understand the ionic and nonionic species in (CH(3))(4)NF·mHF, (CH(3))(3)N·mHF, (C(2)H(5))(4)NF·mHF, and (C(2)H(5))(3)N·mHF melts, the structures of these melts were investigated by infrared spectroscopy, NMR, and high-energy X-ray diffraction. Infrared spectra revealed that three kinds of fluorohydrogenate anions, (FH)(n)F(-)...

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Isogai T, Nakai T, Inoue H, et al. Analysis of cationic structure in some room-temperature molten fluorides and dependence of their ionic conductivity and viscosity on hydrofluoric acid concentration. J Phys Chem B. 2011;115(31):9593-603doi: 10.1021/jp110867k.
Isogai, T., Nakai, T., Inoue, H., Nakanishi, K., Kohara, S., Saito, M., Inaba, M., & Tasaka, A. (2011). Analysis of cationic structure in some room-temperature molten fluorides and dependence of their ionic conductivity and viscosity on hydrofluoric acid concentration. The journal of physical chemistry. B, 115(31), 9593-603. https://doi.org/10.1021/jp110867k
Isogai, Tomohiro, et al. "Analysis of cationic structure in some room-temperature molten fluorides and dependence of their ionic conductivity and viscosity on hydrofluoric acid concentration." The journal of physical chemistry. B vol. 115,31 (2011): 9593-603. doi: https://doi.org/10.1021/jp110867k
Isogai T, Nakai T, Inoue H, Nakanishi K, Kohara S, Saito M, Inaba M, Tasaka A. Analysis of cationic structure in some room-temperature molten fluorides and dependence of their ionic conductivity and viscosity on hydrofluoric acid concentration. J Phys Chem B. 2011 Aug 11;115(31):9593-603. doi: 10.1021/jp110867k. Epub 2011 Jul 20. PMID: 21714521.
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4-[(3-Formyl-4-hydroxy-phen-yl)diazen-yl]-N-(pyrimidin-2-yl)benzene-sulfonamide.

Acta crystallographica. Section E, Structure reports online

El-Ghamry H, Issa R, El-Baradie K, Isagai K, Masaoka S, Sakai K.
PMID: 21201664
Acta Crystallogr Sect E Struct Rep Online. 2008 Aug 06;64:o1673-4. doi: 10.1107/S1600536808024239.

The title mol-ecule, C(17)H(13)N(5)O(4)S, has a trans configuration with respect to the diazenyl (azo) group. The pyrimidine ring and the terminal benzene ring are inclined at angles of 89.38 (4) and 1.6 (6)°, respectively, with respect to the central...

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El-Ghamry H, Issa R, El-Baradie K, et al. 4-[(3-Formyl-4-hydroxy-phen-yl)diazen-yl]-N-(pyrimidin-2-yl)benzene-sulfonamide. Acta Crystallogr Sect E Struct Rep Online. 2008;64:o1673-4doi: 10.1107/S1600536808024239.
El-Ghamry, H., Issa, R., El-Baradie, K., Isagai, K., Masaoka, S., & Sakai, K. (2008). 4-[(3-Formyl-4-hydroxy-phen-yl)diazen-yl]-N-(pyrimidin-2-yl)benzene-sulfonamide. Acta crystallographica. Section E, Structure reports online, 64o1673-4. https://doi.org/10.1107/S1600536808024239
El-Ghamry, Hoda, et al. "4-[(3-Formyl-4-hydroxy-phen-yl)diazen-yl]-N-(pyrimidin-2-yl)benzene-sulfonamide." Acta crystallographica. Section E, Structure reports online vol. 64 (2008): o1673-4. doi: https://doi.org/10.1107/S1600536808024239
El-Ghamry H, Issa R, El-Baradie K, Isagai K, Masaoka S, Sakai K. 4-[(3-Formyl-4-hydroxy-phen-yl)diazen-yl]-N-(pyrimidin-2-yl)benzene-sulfonamide. Acta Crystallogr Sect E Struct Rep Online. 2008 Aug 06;64:o1673-4. doi: 10.1107/S1600536808024239. PMID: 21201664; PMCID: PMC2960714.
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Structure-dependent induction of CYP2B1/2 by 3-methylsulfonyl metabolites of polychlorinated biphenyl congeners in rats.

Environmental toxicology and pharmacology

Kato Y, Haraguchi K, Tomiyasu K, Hiroyuki Saito, Isogai M, Masuda Y, Kimura R.
PMID: 21781771
Environ Toxicol Pharmacol. 1997 Jun 06;3(2):137-44. doi: 10.1016/s1382-6689(97)00150-6.

The effects of eleven 3-methylsulfonyl (3-MeSO(2))-metabolites of polychlorinated biphenyl (PCB) congeners (which were reported to remain in Swedish mother's milk and Japanese Yusho patient's tissues) and their two structurally similar 3-MeSO(2)-PCBs on the hepatic drug-metabolizing enzyme activities were compared...

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Kato Y, Haraguchi K, Tomiyasu K, et al. Structure-dependent induction of CYP2B1/2 by 3-methylsulfonyl metabolites of polychlorinated biphenyl congeners in rats. Environ Toxicol Pharmacol. 1997;3(2):137-44doi: 10.1016/s1382-6689(97)00150-6.
Kato, Y., Haraguchi, K., Tomiyasu, K., Hiroyuki Saito, Isogai, M., Masuda, Y., & Kimura, R. (1997). Structure-dependent induction of CYP2B1/2 by 3-methylsulfonyl metabolites of polychlorinated biphenyl congeners in rats. Environmental toxicology and pharmacology, 3(2), 137-44. https://doi.org/10.1016/s1382-6689(97)00150-6
Kato, Y, et al. "Structure-dependent induction of CYP2B1/2 by 3-methylsulfonyl metabolites of polychlorinated biphenyl congeners in rats." Environmental toxicology and pharmacology vol. 3,2 (1997): 137-44. doi: https://doi.org/10.1016/s1382-6689(97)00150-6
Kato Y, Haraguchi K, Tomiyasu K, Hiroyuki Saito, Isogai M, Masuda Y, Kimura R. Structure-dependent induction of CYP2B1/2 by 3-methylsulfonyl metabolites of polychlorinated biphenyl congeners in rats. Environ Toxicol Pharmacol. 1997 Jun 06;3(2):137-44. doi: 10.1016/s1382-6689(97)00150-6. PMID: 21781771.
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Ultrashort pulse-generation by saturable absorber mirrors based on polymer-embedded carbon nanotubes.

Optics express

Schibli T, Minoshima K, Kataura H, Itoga E, Minami N, Kazaoui S, Miyashita K, Tokumoto M, Sakakibara Y.
PMID: 19498832
Opt Express. 2005 Oct 03;13(20):8025-31. doi: 10.1364/opex.13.008025.

We demonstrate passive mode locking of solid-state lasers by saturable absorbers based on carbon nanotubes (CNT). These novel absorbers are fabricated by spin-coating a polymer doped with CNTs onto commercial dielectric laser-mirrors. We obtain broadband artificial saturable absorber mirrors...

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Schibli T, Minoshima K, Kataura H, et al. Ultrashort pulse-generation by saturable absorber mirrors based on polymer-embedded carbon nanotubes. Opt Express. 2005;13(20):8025-31doi: 10.1364/opex.13.008025.
Schibli, T., Minoshima, K., Kataura, H., Itoga, E., Minami, N., Kazaoui, S., Miyashita, K., Tokumoto, M., & Sakakibara, Y. (2005). Ultrashort pulse-generation by saturable absorber mirrors based on polymer-embedded carbon nanotubes. Optics express, 13(20), 8025-31. https://doi.org/10.1364/opex.13.008025
Schibli, T, et al. "Ultrashort pulse-generation by saturable absorber mirrors based on polymer-embedded carbon nanotubes." Optics express vol. 13,20 (2005): 8025-31. doi: https://doi.org/10.1364/opex.13.008025
Schibli T, Minoshima K, Kataura H, Itoga E, Minami N, Kazaoui S, Miyashita K, Tokumoto M, Sakakibara Y. Ultrashort pulse-generation by saturable absorber mirrors based on polymer-embedded carbon nanotubes. Opt Express. 2005 Oct 03;13(20):8025-31. doi: 10.1364/opex.13.008025. PMID: 19498832.
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Dispersion-managed, high-power, Er-doped ultrashort-pulse fiber laser using carbon-nanotube polyimide film.

Optics express

Nishizawa N, Nozaki Y, Itoga E, Kataura H, Sakakibara Y.
PMID: 22109039
Opt Express. 2011 Oct 24;19(22):21874-9. doi: 10.1364/OE.19.021874.

We investigated a dispersion-managed, passively mode-locked, ultrashort-pulse, Er-doped fiber laser using a polyimide film containing dispersed single-wall carbon nanotubes (SWNTs) and examined the dependence on net cavity dispersion and output coupling ratio using normal-dispersion fibers and a variable output...

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Nishizawa N, Nozaki Y, Itoga E, et al. Dispersion-managed, high-power, Er-doped ultrashort-pulse fiber laser using carbon-nanotube polyimide film. Opt Express. 2011;19(22):21874-9doi: 10.1364/OE.19.021874.
Nishizawa, N., Nozaki, Y., Itoga, E., Kataura, H., & Sakakibara, Y. (2011). Dispersion-managed, high-power, Er-doped ultrashort-pulse fiber laser using carbon-nanotube polyimide film. Optics express, 19(22), 21874-9. https://doi.org/10.1364/OE.19.021874
Nishizawa, N, et al. "Dispersion-managed, high-power, Er-doped ultrashort-pulse fiber laser using carbon-nanotube polyimide film." Optics express vol. 19,22 (2011): 21874-9. doi: https://doi.org/10.1364/OE.19.021874
Nishizawa N, Nozaki Y, Itoga E, Kataura H, Sakakibara Y. Dispersion-managed, high-power, Er-doped ultrashort-pulse fiber laser using carbon-nanotube polyimide film. Opt Express. 2011 Oct 24;19(22):21874-9. doi: 10.1364/OE.19.021874. PMID: 22109039.
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