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187 results on '"Winther B"'

13. Measurement of cell volume changes by fluorescence self-quenching

Author

Hamann, Steffen, Kiilgaard, J.F., Litman, Thomas, Alvarez-Leefmans, F.J., Winther, B. R., Zeuthen, Thomas, Hamann, Steffen, Kiilgaard, J.F., Litman, Thomas, Alvarez-Leefmans, F.J., Winther, B. R., and Zeuthen, Thomas

Abstract

At high concentrations, certain fluorophores undergo self-quenching, i.e., fluorescence intensity decreases with increasing fluorophore concentration. Accordingly, the self-quenching properties can be used for measuring water volume changes in lipid vesicles. In cells, quantitative determination of water transport using fluorescence self-quenching has been complicated by the requirement of relatively high (mM) and often toxic loading concentrations. Here we report a simple method that uses low (muM) loading concentrations of calcein-acetoxymethyl ester (calcein-AM) to obtain intracellular concentrations of the fluorophore calcein suitable for measurement of changes in cell water volume by self-quenching. The relationship between calcein fluorescence intensity, when excited at 490 nm (its excitation maximum), and calcein concentration was investigated in vitro and in various cultured cell types. The relationship was bell-shaped, with the negative slope in the concentration range where the fluorophore undergoes fluorescence self-quenching. In cultured retinal pigment epithelial cells, calcein fluorescence and extracellular osmolarity were linearly related. A 25-mOsm hypertonic challenge corresponded to a decrease in calcein fluorescence with high signal-to-noise ratio (>15). Similar results were obtained with the fluorophore BCECF when excited at its isosbestic wavelength (436 nm). The present results demonstrate the usefulness of fluorescence self-quenching to measure rapid changes in cell water volume.

Published
2002

16. Wind tunnel investigation of active controls technology applied to a DC-10 derivative

Author

Winther, B. A, Shirley, W. A, and Heimbaugh, R. M

Subjects
Aircraft Stability And Control
Abstract

Application of active controls technology to reduce aeroelastic response offers a potential for significant payoffs in terms of aerodynamic efficiency and structural weight. As part of the NASA Energy Efficient Transport program, the impact upon flutter and gust load characteristics has been investigated by means of analysis and low-speed wind tunnel tests of a semispan model. The model represents a DC-10 derivative with increased wing span and an active aileron surface, responding to vertical acceleration at the wing tip. A control law satisfying both flutter and gust load constraints is presented and evaluated. In general, the beneficial effects predicted by analysis are in good agreement with experimental data.

Published
1980

17. Demonstration of aircraft wing/store flutter suppression systems

Author

Hwang, C, Winther, B. A, Mills, G. R, Noll, T. E, and Farmer, M. G

Subjects
Aircraft Design, Testing And Performance
Abstract

A wind tunnel test program was conducted to demonstrate the active wing/store flutter suppression systems on a lightweight fighter aircraft. The program, completed in mid-1978, included the design, analysis, fabrication, and testing of a scale model. The tests were conducted at the NASA Langley 16-ft Transonic Dynamics Tunnel. Three store configurations were selected for testing. Two of these configurations were deliberately designed to exhibit low flutter speeds with rapid reductions in damping at the incipient flutter condition. After initial tunnel entries, which showed the need for certain improvements in the model and the control system design, substantial increases in the flutter speeds were achieved using both leading- and trailing-edge control surfaces, separately. For the most critical configuration, a demonstrated improvement of 18% and a projected improvement of 29% in the dynamic pressure were achieved.

Published
1979

18. Demonstration of aircraft wing/store flutter suppression systems

Author

Hwang, C, Winther, B. A, Noll, T. E, and Farmer, M. G

Subjects
Aircraft Stability And Control
Abstract

Preliminary results are presented of the design analysis and the test progress of active wing/store flutter suppression systems on a lightweight fighter aircraft. Three configurations were selected for final testing. Two of these configurations were deliberately designed to exhibit low flutter speeds with rapid reduction in damping at the incipient flutter condition. After initial tunnel entries, which showed the need for certain improvements in the model and the control system design, substantial increases in the flutter speeds were achieved using both leading and trailing edge control surfaces separately. For the most critical configuration, a demonstrated improvement of 18% and a projected improvement of 29% in the dynamic pressure were accomplished.

Published
1978

19. Prediction of unsteady aerodynamic loadings caused by trailing edge control surface motions in subsonic compressible flow: Computer program description

Author

Redman, M. C, Rowe, W. S, and Winther, B. A

Subjects
Fluid Mechanics
Abstract

A digital computer program has been developed to calculate unsteady loadings caused by motions of lifting surfaces with trailing edge control based on the subsonic kernal function approach. The pressure singularities at hinge line and side edges have been extracted analytically as a preliminary step to solving the integral by collocation. The program calculates generalized aerodynamic forces for user supplied deflection modes. Optional intermediate output includes pressure at an array of points, and sectional generalized forces. From one to four controls on the half span can be accommodated.

Published
1972

21. Prediction of unsteady aerodynamic loadings caused by trailing edge control surface motions in subsonic compressible flow: Analysis and results

Author

Rowe, W. S, Winther, B. A, and Redman, M. C

Subjects
Aerodynamics
Abstract

A theoretical analysis and a computer program have been developed for the prediction of unsteady lifting surface loadings caused by motions of trailing edge control surfaces having sealed gaps. The final form of the downwash integral equation has been formulated by isolating the singularities from the non-singular terms and establishing a preferred solution process to remove and evaluate the downwash discontinuities in a systematic manner. Comparisons of theoretical and experimental pressure data are made for several control surface configurations. The comparisons indicate that reasonably accurate theoretical pressure distributions and generalized forces may be obtained for a wide variety of control surface configurations. Spanwise symmetry or antisymmetry of motion, and up to four control surfaces on each half span can be accommodated.

Published
1972

23. Efficacy of tremacamra, a soluble intercellular adhesion molecule 1, for experimental rhinovirus infection: a randomized clinical trial.

Author

Turner RB, Wecker MT, Pohl G, Witek TJ, McNally E, St. George R, Winther B, Hayden FG, Turner, R B, Wecker, M T, Pohl, G, Witek, T J, McNally, E, St George, R, Winther, B, and Hayden, F G

Abstract

Context: Attachment of most rhinovirus subtypes to cells depends on a cellular receptor, the intercellular adhesion molecule 1 (ICAM-1). A recombinant soluble ICAM-1 (tremacamra, formerly BIRR 4) has shown possible efficacy in early studies.Objective: To determine the efficacy and safety of intranasal administration of tremacamra in experimental rhinovirus colds in humans.Design: Four randomized, double-blind, placebo-controlled trials conducted in January to March 1996.Setting and Subjects: Volunteers between the ages of 18 and 60 years who had an antibody titer of 1:4 or less to the challenge virus. Subjects were isolated in a hotel room during study days 0 to 8; symptoms were recorded through day 14. A total of 198 subjects were randomized, of whom 196 received drug or placebo and were included in the safety analysis. A total of 177 subjects were included in the efficacy analysis.Interventions: Tremacamra or placebo was given beginning 7 hours before inoculation with rhinovirus type 39 (preinoculation studies) or 12 hours after (postinoculation studies). Tremacamra as an inhaled solution or as a powder (each given preinoculation and postinoculation for a total of 4 studies) and placebo were given in 6 doses at 3-hour intervals daily during days 1 through 7. Recipients of active treatment received 367 microg of tremacamra per nostril per dose for a total of 4.4 mg/d.Main Outcome Measures: Effect of tremacamra on infection, as determined by virus isolation and seroconversion, and on illness, as determined by symptom scores, clinical colds, and nasal mucus weights. Treatment-by-study interaction was not significant, so results were pooled for the main analysis.Results: A total of 88 (92%) of the 96 subjects in the placebo groups and 69 (85%) of the 81 subjects in the active treatment groups were infected (P=.19). For placebo vs tremacamra, respectively, the total symptom score (+/- 95% confidence interval [CI]) was 17.6 (+/- 2.7) vs 9.6 (+/- 2.9), the proportion of clinical colds was 64/96 (67% +/- 9%) vs 36/81 (44% +/- 11%), and the nasal mucus weight was 32.9 (+/- 8.8) g vs 14.5 (+/- 9.4) g (P<.001 for all comparisons). Tremacamra was not associated with adverse effects or evidence of absorption through the nasal mucosa and did not interfere with development of neutralizing antibody.Conclusion: Tremacamra reduced the severity of experimental rhinovirus colds. Whether tremacamra will be useful clinically will require further study. [ABSTRACT FROM AUTHOR]

Published
1999
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38. Gene expression profiles during in vivo human rhinovirus infection: insights into the host response.

Author

Proud D, Turner RB, Winther B, Wiehler S, Tiesman JP, Reichling TD, Juhlin KD, Fulmer AW, Ho BY, Walanski AA, Poore CL, Mizoguchi H, Jump L, Moore ML, Zukowski CK, Clymer JW, Proud, David, Turner, Ronald B, Winther, Birgit, and Wiehler, Shahina

Abstract

Rationale: Human rhinovirus infections cause colds and trigger exacerbations of lower airway diseases.Objectives: To define changes in gene expression profiles during in vivo rhinovirus infections.Methods: Nasal epithelial scrapings were obtained before and during experimental rhinovirus infection, and gene expression was evaluated by microarray. Naturally acquired rhinovirus infections, cultured human epithelial cells, and short interfering RNA knockdown were used to further evaluate the role of viperin in rhinovirus infections.Measurements and Main Results: Symptom scores and viral titers were measured in subjects inoculated with rhinovirus or sham control, and changes in gene expression were assessed 8 and 48 hours after inoculation. Real-time reverse transcription-polymerase chain reaction for viperin and rhinoviruses was used in naturally acquired infections, and viperin mRNA levels and viral titers were measured in cultured cells. Rhinovirus-induced changes in gene expression were not observed 8 hours after viral infection, but 11,887 gene transcripts were significantly altered in scrapings obtained 2 days postinoculation. Major groups of up-regulated genes included chemokines, signaling molecules, interferon-responsive genes, and antivirals. Viperin expression was further examined and also was increased in naturally acquired rhinovirus infections, as well as in cultured human epithelial cells infected with intact, but not replication-deficient, rhinovirus. Knockdown of viperin with short interfering RNA increased rhinovirus replication in infected epithelial cells.Conclusions: Rhinovirus infection significantly alters the expression of many genes associated with the immune response, including chemokines and antivirals. The data obtained provide insights into the host response to rhinovirus infection and identify potential novel targets for further evaluation. [ABSTRACT FROM AUTHOR]

Published
2008
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43. Light and Scanning Electron Microscopy of Nasal Biopsy Material from Patients with Naturally Acquired Common Colds

Author

Niels Mygind, Winther B, B. Christensen And, and Brofeldt S

Subjects
Adult, Male, medicine.medical_specialty, Nasal biopsy, Pathology, Scanning electron microscope, Biopsy, Common Cold, General Medicine, Biology, Epithelium, Nasal Mucosa, Otorhinolaryngology, Microscopy, Microscopy, Electron, Scanning, medicine, Humans, Female, Histopathology, Cilia
Abstract

As our knowledge of the histopathology of common colds is very limited, we have undertaken a blind quantitative examination by scanning electron microscopy and light microscopy of 56 nasal biopsies, taken from 29 volunteers with naturally acquired colds. In agreement with earlier reports we found evidence of sloughing of epithelial cells, but in contrast to in vitro experiments, this did not result in a destruction of the epithelial lining, which by and large remained continuous, with structurally normal cell borders. There was a significant increase in the number of neutrophils, both in epithelium and in lamina propria, already on the 2nd day of the disease, and the hypothesis is advanced that the virus infection itself is the cause of the local neutrophilia. The only other abnormality demonstrated was an increased number of extracellular erythrocytes in the acute stage. The histological picture was not suggestive of an involvement of epithelial mast cells in the inflammation.

Published
1984

44. «Lindrende Sygepleje» – en begrebsafklaring.

Author

Winther B and Madsen KH

Abstract

Copyright of Nordic Journal of Nursing Research & Clinical Studies / Vård i Norden is the property of Sage Publications, Ltd. and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Published
2006
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45. Study of bacteria in the nasal cavity and nasopharynx during naturally acquired common colds

Author

Grønborg H, Niels Mygind, Winther B, Brofeldt S, R Vejlsgaard, and Pedersen M

Subjects
Nasal cavity, Adult, Time Factors, Common Cold, Mucous membrane of nose, medicine.disease_cause, Nasopharynx, otorhinolaryngologic diseases, medicine, Humans, Nose, Bacteriological Techniques, biology, Adult patients, Bacteria, business.industry, Common cold, Pathogenic bacteria, General Medicine, respiratory system, medicine.disease, biology.organism_classification, Nasal Mucosa, medicine.anatomical_structure, Otorhinolaryngology, Immunology, Nasal Cavity, business, Nasal symptoms
Abstract

It was the purpose of this study to examine whether the number of bacteria in the nose and nasopharynx changes during a common cold. Samples for bacteriological culture were taken from the nasal cavity of 29 and from the nasopharynx of 26 adult patients with naturally acquired colds. The bacteriological samples were taken on days 2, 4, 8 16, 32 and 64 after the first nasal symptoms. The results showed that there were few pathogenic bacteria in the nasal cavity and nasopharynx. There was no tendency to an increase in the number of positive cultures during the cold, although most patients had macroscopically purulent discharge on days 3-5. In conclusion, the study indicates that during an uncomplicated common cold, a bacterial infection is not responsible for the occurrence of purulent nasal discharge which may be a direct consequence of the viral infection.

Published
1984

46. The HOPE (Heart Outcomes Prevention Evaluation) Study: The design of a large, simple randomized trial of an angiotensin converting enzyme inhibitor (ramipril) and vitamin E in patients at high risk of cardiovascular events

Author

Mindlen, F., Nordaby, R., Ruiz, M., Zavala, A., Guzman, L., Martinez, F., Diaz, Rr, Mackey, C., Marino, M., Romero, G., Zapata, G., Cuneo, C., Kawamura, T., Coelho, O., Massayochi, O., Braga, J., Labrunie, A., Bodanese, L., Manenti, E., Vitola, D., Nicolau, J., Amodeo, C., Armaganijan, D., Bertolami, M., Caramelli, B., Carvalho, A., Cirenza, C., Fichino, M., Franken, R., Ghorayeb, N., Kadri, T., Leao, P., Malheiros, F., Pavanello, R., Ramires, F., Ramires, J., Savioli, F., Sousa, A., Tanajura, L., Topps, D., Korner, L., Martinez, V., Baptie, B., Basinger, M., Baylis, B., Beresford, P., Edwards, A., Giannaccaro, P., Groenewoud, Y., Grose, M., Kellen, J., Lam, S., Lesoway, R., Ma, P., Meldrum, D., Mitchell, D., Mitchell, Lb, Roth, D., Shumak, S., Simon, M., Stone, J., Warnica, W., Wyse, D., Neffgen, C., Neffgen, J., Armstrong, F., Armstrong, W., Bell, N., Black, W., Brass, N., Brenneis, F., Brownoff, R., Chaytors, G., Debanne, D., Derksen, C., Donoff, M., Dzavik, V., Goeres, M., Greenwood, P., Gulamhusein, S., Hui, W., Hutchison, K., Kasian, L., Kasza, L., Krikke, E., Kvill, L., Lakhani, Z., Linklater, D., Mackel, J., Martin, S., Montague, T., Moores, D., Musseau, A., Muzyka, T., Paradis, J., Prosser, A., Ryan, E., Senaratne, M., Stenerson, P., Talibi, T., Teo, K., Young, C., Zuk, V., White, R., Browne, K., Browne, M., Happel, K., Irving, A., Plesko, A., Donnelly, R., Radomsky, N., Felker, P., Larsen, D., Morse, J., Rowntree, C., Thompson, J., Wedel, R., Bloomberg, G., Chomin, G., Dahl, M., Leong, W., Moy, V., Heath, J., Marshall, J., Terwiel, M., Kenefick, G., Kuritzky, R., Stevens, K., Weddings, K., Barban, K., Imrie, J., Woo, K., Ashton, T., Calvert, K., Bishop, W., Sweeney, R., Breakwell, L., Kornder, J., Pearce, S., Polasek, P., Richardson, P., Ghosh, S., Rielly, M., Wagner, K., Bemstein, V., Dawson, K., Lee, P., Lewis, J., Macdonald, K., Mcgee, L., Thompson, C., Hilton, D., Illott, K., Klinke, P., Mcconnell, J., Rabkin, S., Ong, A., Ong, G., Bedard, D., Hoeschen, R., Mehta, P., Mohammad, I., Morris, A., Bessoudo, R., Dobbins, N., Mclellan, L., Milton, J., Davis, R., Okeefe, D., Smith, R., Joyce, C., Parsons, M., Skanes, J., Sussex, B., Tobini, M., Ravalia, M., Sherman, G., Worrall, G., Atkinson, A., Hatheway, R., Johnson, B., Barnhill, S., Bata, I., Cosseet, J., Johnstone, D., Macfarlane, M., Sheridan, W., Crossman, L., Folkins, D., Shirley, M., Machel, T., Morash, J., Gupta, M., Mayich, M., Vakani, T., Baitz, T., Macphee, E., Turton, E., Turton, M., Chan, N., Misterski, J., Raco, D., Curnew, G., Fallen, E., Finkelstein, L., Gerstein, H., Hardman, P., Lawand, S., Lonn, E., Magi, W., Mcqueen, M., Panju, A., Patterson, R., Sullivan, B., Sullivan, H., Sullivan, M., Taylor, K., Worron, I., Yusuf, S., Cameron, W., Noseworthy, C., Houlden, R., Lavalle, T., Fowlis, R., Janzen, I., Arnold, M., Cann, M., Carroll, S., Dumaresq, S., Edmonds, M., Furlong, P., Geddes, C., Graham, E., Harris, K., Hramiak, I., Kennedy, R., Kostuk, W., Krupa, M., Lent, B., Lovell, M., Maclean, C., Massel, D., Mcmanus, R., Mcsherry, J., Munoz, C., Occhipinti, J., Oosterveld, L., Pflugfelder, P., Powers, S., Southern, R., Spence, D., Squires, P., Wetmore, S., Willing, J., Wisenberg, G., Wolfe, B., Kannampuzha, P., Rebane, T., Sluzar, V., Hess, A., Chan, Y., Thomson, D., Baigrie, R., Dubbin, J., Liuni, C., Tan, Kw, Brankston, E., Hewson, P., Hrycyshyn, B., Kapusta, W., Knox, L., Lockner, C., Whitsitt, P., Baird, M., Conroy, D., Davies, Ra, Davies, Rf, Fraser, M., Hagar, S., Hierlihy, P., Keely, E., Khan, S., Lau, Dgw, Marois, L., Nemeth, K., Reeves, E., Turek, M., Vexler, R., Young, D., Kumar, G., Kuruvilla, G., Kuruvilla, P., Lowe, D., Kwok, K., Blakely, J., Styling, S., Bozek, B., Charles, J., Fell, D., Fell, Da, Goode, E., Grossman, Ld, Matthews, E., Nitkin, R., Ricci, J., Selby, A., Singh, N., Swan, J., Emmett, J., Weingert, M., Ganjavi, F., Hill, D., Nawaz, S., Hessian, R., Kwiatkowski, K., Lai, C., Mulaisho, C., Okeefe, H., Smith, H., Weeks, A., Andrews, J., Barnie, A., Drobac, M., Hacker, P., Hanna, A., Iwanochko, M., Kenshole, A., Langer, A., Liu, P., Maclean, S., Moe, G., Sasson, Z., Sternberg, L., Trachuk, C., Walters, J., Zinman, B., Cheung, M., Cina, C., Yao, L., Man, K., Fulop, J., Glanz, A., Sibbick, M., Carter, P., Hickey, J., Mcmillian, E., Dion, D., Sthilaire, R., Coutu, D., Damours, G., Starra, R., Brooks, J., Dechamps, P., Kiwan, G., Kouz, S., Laforest, M., Remillard, C., Bellamy, D., Brossoit, R., Carrier, S., Houde, A., Labonte, I., Belanger, A., Kandalaft, N., Quenneville, L., Sandi, M., Auger, P., Bilodeau, N., Delage, F., Dumont, F., Giroux, R., Loisel, R., Poirier, C., Saulnier, D., Carmichael, P., Lemay, C., Lenis, J., Arisjilwan, N., Bedard, H., Casavant, C., Chiasson, J., Dagenais, D., Fitchett, D., Gossard, D., Halle, H., Hamel, N., Joyal, M., Magnan, O., Methe, M., Pedneault, L., Pilon, C., Poisson, D., Primeau, L., Rondeau, C., Roy, C., Ruel, M., Serpa, A., Sestier, F., Smilovitch, M., Theroux, P., Beaudoin, J., Boudreault, Jr, D Amours, D., Douville, T., Giguere, G., Houde, G., Labbe, R., Lachance, S., Lessard, L., Mercier, G., Noel, Hp, Talbot, P., Tremblay, J., Karabatsos, A., Maclellan, K., Wilson, P., Bogaty, P., Laforge, D., Langlais, M., Leblanc, M., Samson, M., Turcotte, J., Campeau, J., Dupuis, R., Lauzon, C., Ouimet, F., Pruneau, G., Desmaris, C., Frechetto, I., Gervais, P., James Brophy, Leroux, S., Bester, S., Meunier, L., Sayeed, M., Hart, M., Moumne, I., Thomasse, G., Walker, J., Walker, M., Ahmed, S., Habib, Nm, Kuny, P., Lopez, J., Klein, W., Grisold, M., Heyndrickx, L., Fiasse, A., Degaute, Jp, Mockel, J., Duprez, D., Chaudron, Jm, Bodson, A., Krzentowski, G., Boland, J., Kolendorf, K., Winther, B., Juhl, H., Hamalainen, T., Siitonen, O., Gin, H., Rigalleau, V., Hensen, J., Riel, R., Oehmenbritsch, R., Schulzeschleppinghoff, B., Hopf, R., Moller, A., Rosak, C., Wetzel, H., Hasslacher, C., Martin, T., Stein, J., Erdmann, E., Bohm, M., Hartmann, D., Breidert, M., Fritzen, R., Scherbaum, W., Mann, J., Maus, J., Schroeder, C., Henrichs, H., Unger, H., Ickenstein, G., Kromer, E., Riegger, G., Schunkert, H., Basan, B., Hampel, R., Crean, P., Garadah, T., White, U., Marini, N., Paciaroni, E., Saccomano, G., Diluzio, S., Magnani, B., Mantovani, B., Pareschi, P., Stucchi, N., Nanni, D., Rusticali, F., Simoni, C., Brunelli, C., Caponnetto, S., Gatto, E., Mazzantini, A., Molinari, O., Morello, R., Degiorgio, L., Imparato, C., Barbaresi, F., Cotogni, A., Pasqualini, M., Frigeni, G., Landoni, M., Polese, A., Cernigoi, A., Merni, M., Tortul, C., Velussi, M., Aina, F., Cernigliaro, C., Dellavesa, P., Dejoannon, U., Pierfranceschi, G., Zavaroni, D., Emilia, R., Manicardi, E., Minelli, E., Penazzoli, F., Portioli, I., Rossi, E., Giani, P., Roccaforte, R., Casaccia, M., Larovere, R., Miglierina, E., Repetto, S., Centofante, P., Vincenzi, M., Nieuwenhuijzen, Ac, Sels, J., Wolffenbuttel, Bhr, Kip, J., Mantingh, L., Mulder, H., Vandoorn, Lg, Hjerkinn, E., Reikvam, A., Cardona, M., Sanz, G., Karoni, A., Bescos, Ll, Albert, X., Masia, R., Alvarez, A., Saenz, L., Astrom, L., Press, R., Sjostedt, P., Tabrizi, F., Bergbom, I., Hansson, P., Held, C., Kahan, T., Ryden, B., Andersson, O., Wysocki, M., Karlsson, E., Sartor, G., Smith, L., Katzman, P., Ljungdahl, L., Noren, P., Hallberg, A., Olsson, Po, Asbrink, S., Molgaard, J., Nilsson, V., Nystrom, F., Ohman, P., Andersson, C., Ekholm, L., Svensson, Ka, Torebo, E., Fagher, B., Svenstam, I., Thulin, T., Ericsson, Ub, Ahnberg, K., Henning, R., Jacobsson, L., Taghavi, A., Ahlstrom, P., Rosenqvist, U., Ericson, C., Gertow, O., Kristensson, Be, Stahl, L., Bergsten, L., Harden, R., Jagren, C., Leijd, B., Lennerhagen, P., Ostergrens, J., Sandstrom, V., Sundelin, R., Hagg, A., Morlin, C., Pettersson, F., Wanders, A., Bjorkman, H., Karlsson, G., Larsson, H., Lonndahl, Y., Weber, P., Cozzi, R., Gerber, P., Moccetti, T., Safwan, E., Sessa, F., Binder, T., Boman, P., Kiowski, W., Lehman, R., Lull, B., Spinas, G., Jamieson, A., Kennedy, Ja, Kesson, C., Gryczka, R., Parker, P., Sidiki, S., Small, M., Struthers, S., Manns, J., Smithurst, H., Begg, A., Fisher, Bm, Bedford, C., Heller, S., Marlow, S., Munoz, Ec, Garcia, Hh, Ruiz, Ro, Meaney, E., Flores, Mi, Brown, E., Perry, G., Patel, G., Sarma, R., Szlachcic, Y., Dorman, J., Singh, B., Bailey, G., Clegg, L., Horwitz, L., Leahy, J., Rashkow, A., Hudson, M., Miller, A., Umberger, J., Zoble, R., Orander, P., Sridharan, M., Defrancisco, G., Davidson, M., Islam, N., Mathew, J., Rajanahally, R., French, D., Wickemeyer, W., Effron, M., Goldstein, M., Utley, K., Pierpont, G., Weigenant, J., Farkouh, M., Kubly, V., Rich, M., Wisneski, L., Abrams, J., Garcia, D., Bonora, M., Kohn, R., Muffoletto, E., Brink, D., Lader, E., Singler, A., Pande, P., Powers, J., Hoogwerf, B., Moore, J., Yanak, F., Gupta, S., Williams, D., Danisa, K., Kirk, C., Wescott, B., Grover, J., Mackenzie, M., Amidi, M., Bell, M., Farmer, J., Kingry, C., Young, J., Harms, V., Kennedy, Jw, Letterer, R., Heller, C., and Mack, R.

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