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Found 37769 matches. Displaying 9351-9360
Kong XF, Ciancanelli M, Al-Hajjar S, Alsina L, Zumwalt T, Bustamante J, Feinberg J, Audry M, Prando C, Bryant V, Kreins A, Bogunovic D, Halwani R, Zhang XX, Abel L, Chaussabel D, Al-Muhsen S, Casanova JL, Boisson-Dupuis S
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A novel form of human STAT1 deficiency impairing early but not late responses to interferons
BLOOD 2010 DEC 23; 116(26):5895-5906
Autosomal recessive STAT1 deficiency is associated with impaired cellular responses to interferons and susceptibility to intracellular bacterial and viral infections. We report here a new form of partial STAT1 deficiency in 2 siblings presenting mycobacterial and viral diseases. Both carried a homozygous missense mutation replacing a lysine with an asparagine residue at position 201 (K201N) of STAT1. This mutation causes the abnormal splicing out of exon 8 from most STAT1 mRNAs, thereby decreasing (by similar to 70%) STAT1 protein levels. The mutant STAT1 proteins are not intrinsically deleterious, in terms of tyrosine phosphorylation, dephosphorylation, homodimerization into gamma-activating factor and heterotrimerization into ISGF-3, binding to specific DNA elements, and activation of the transcription. Interestingly, the activation of gamma-activating factor and ISGF3 was impaired only at early time points in the various cells from patient (within 1 hour of stimulation), whereas sustained impairment occurs in other known forms of complete and partial recessive STAT1 deficiency. Consequently, delayed responses were normal; however, the early induction of interferon-stimulated genes was selectively and severely impaired. Thus, the early cellular responses to human interferons are critically dependent on the amount of STAT1 and are essential for the appropriate control of mycobacterial and viral infections. (Blood. 2010;116(26):5895-5906)
Ionescu R, Mediavilla JR, Chen LA, Grigorescu DO, Idomir M, Kreiswirth BN, Roberts RB
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Molecular Characterization and Antibiotic Susceptibility of Staphylococcus aureus from a Multidisciplinary Hospital in Romania
MICROBIAL DRUG RESISTANCE 2010 DEC; 16(4):263-272
From 2004 to 2005, 60%-72% of invasive Staphylococcus aureus isolates from Romanian hospitals were resistant to methicillin (methicillin-resistant S. aureus [MRSA]), the highest frequency for any European nation. Few reports, however, have addressed the molecular characteristics of S. aureus in Romania. In this study, we utilized spa typing, multilocus sequence typing, staphylococcal cassette chromosome mec (SCCmec) typing, dru typing, pulsed-field gel electrophoresis, and detection of virulence factors to characterize 146 S. aureus strains isolated from 2004 to 2005 at the Clinic County Hospital in Brasov. Antibiotic susceptibility patterns for all MRSA isolates and patient demographic data were also obtained. Fifty-six strains (38.4%) were determined to be MRSA by susceptibility testing and SCCmec typing. All MRSA strains were resistant to beta-lactams and tetracycline, but susceptible to nitrofurans, vancomycin, and clindamycin, with inducible clindamycin resistance in 23/28 clindamycin-sensitive/erythromycin-resistant isolates. Molecular typing identified 15 clonal backgrounds (CC 1, 5, 8, 8/239, 9, 15, 20, 22, 25, 30, 45, 80, 97, 101, and 121), only 4 of which were associated with MRSA (CC 1, 8/239, 30, and 80). Spa types 35 (t127, CC 1) and 351 (t030, CC 8/239) accounted for 27.4% and 21.9% of all S. aureus strains, respectively, and 19.6% and 57.1% of all MRSA strains. Both hospital-associated (SCCmec type III) and community-associated (SCCmec type IV) elements were identified within MRSA strains, whereas Panton-Valentine leukocidin was detected in 10 MRSA and 12 methicillin-sensitive S. aureus strains. These results demonstrate the presence of various endemic S. aureus clones within the Clinic County Hospital in Brasov, suggestive of ongoing nosocomial and community transmission.
Aaltonen T, Gonzalez BA, Amerio S, Amidei D, Anastassov A, Annovi A, Antos J, Apollinari G, Appel JA, Apresyan A, Arisawa T, Artikov A, Asaadi J, Ashmanskas W, Auerbach B, Aurisano A, Azfar F, Badgett W, Barbaro-Galtieri A, Barnes VE, Barnett BA, Barria P, Bartos P, Bauce M, Bauer G, Bedeschi F, Beecher D, Behari S, Bellettini G, Bellinger J, Benjamin D, Beretvas A, Bhatti A, Binkley M, Bisello D, Bizjak I, Bland KR, Blocker C, Blumenfeld B, Bocci A, Bodek A, Bortoletto D, Boudreau J, Boveia A, Brau B, Brigliadori L, Brisuda A, Bromberg C, Brucken E, Bucciantonio M, Budagov J, Budd HS, Budd S, Burkett K, Busetto G, Bussey P, Buzatu A, Cabrera S, Calancha C, Camarda S, Campanelli M, Campbell M, Canelli F, Canepa A, Carls B, Carlsmith D, Carosi R, Carrillo S, Carron S, Casal B, Casarsa M, Castro A, Catastini P, Cauz D, Cavaliere V, Cavalli-Sforza M, Cerri A, Cerrito L, Chen YC, Chertok M, Chiarelli G, Chlachidze G, Chlebana F, Cho K, Chokheli D, Chou JP, Chung WH, Chung YS, Ciobanu CI, Ciocci MA, Clark A, Clark D, Compostella G, Convery ME, Conway J, Corbo M, Cordelli M, Cox CA, Cox DJ, Crescioli F, Almenar CC, Cuevas J, Culbertson R, Dagenhart D, d'Ascenzo N, Datta M, de Barbaro P, De Cecco S, De Lorenzo G, Dell'Orso M, Deluca C, Demortier L, Deng J, Deninno M, Devoto F, d'Errico M, Di Canto A, Di Ruzza B, Dittmann JR, D'Onofrio M, Donati S, Dong P, Dorigo T, Ebina K, Elagin A, Eppig A, Erbacher R, Errede D, Errede S, Ershaidat N, Eusebi R, Fang HC, Farrington S, Feindt M, Fernandez JP, Ferrazza C, Field R, Flanagan G, Forrest R, Frank MJ, Franklin M, Freeman JC, Furic I, Gallinaro M, Galyardt J, Garcia JE, Garfinkel AF, Garosi P, Gerberich H, Gerchtein E, Giagu S, Giakoumopoulou V, Giannetti P, Gibson K, Ginsburg CM, Giokaris N, Giromini P, Giunta M, Giurgiu G, Glagolev V, Glenzinski D, Gold M, Goldin D, Goldschmidt N, Golossanov A, Gomez G, Gomez-Ceballos G, Goncharov M, Gonzalez O, Gorelov I, Goshaw AT, Goulianos K, Gresele A, Grinstein S, Grosso-Pilcher C, Group RC, da Costa JG, Gunay-Unalan Z, Haber C, Hahn SR, Halkiadakis E, Hamaguchi A, Han JY, Happacher F, Hara K, Hare D, Hare M, Harr RF, Hatakeyama K, Hays C, Heck M, Heinrich J, Herndon M, Hewamanage S, Hidas D, Hocker A, Hopkins W, Horn D, Hou S, Hughes RE, Hurwitz M, Husemann U, Hussain N, Hussein M, Huston J, Introzzi G, Iori M, Ivanov A, James E, Jang D, Jayatilaka B, Jeon EJ, Jha MK, Jindariani S, Johnson W, Jones M, Joo KK, Jun SY, Junk TR, Kamon T, Karchin PE, Kato Y, Ketchum W, Keung J, Khotilovich V, Kilminster B, Kim DH, Kim HS, Kim HW, Kim JE, Kim MJ, Kim SB, Kim SH, Kim YK, Kimura N, Klimenko S, Kondo K, Kong DJ, Konigsberg J, Korytov A, Kotwal AV, Kreps M, Kroll J, Krop D, Krumnack N, Kruse M, Krutelyov V, Kuhr T, Kurata M, Kwang S, Laasanen AT, Lami S, Lammel S, Lancaster M, Lander RL, Lannon K, Lath A, Latino G, Lazzizzera I, LeCompte T, Lee E, Lee HS, Lee JS, Lee SW, Leo S, Leone S, Lewis JD, Lin CJ, Linacre J, Lindgren M, Lipeles E, Lister A, Litvintsev DO, Liu C, Liu Q, Liu T, Lockwitz S, Lockyer NS, Loginov A, Lucchesi D, Lueck J, Lujan P, Lukens P, Lungu G, Lys J, Lysak R, Madrak R, Maeshima K, Makhoul K, Maksimovic P, Malik S, Manca G, Manousakis-Katsikakis A, Margaroli F, Marino C, Martinez M, Martinez-Ballarin R, Mastrandrea P, Mathis M, Mattson ME, Mazzanti P, McFarland KS, McIntyre P, McNulty R, Mehta A, Mehtala P, Menzione A, Mesropian C, Miao T, Mietlicki D, Mitra A, Miyake H, Moed S, Moggi N, Mondragon MN, Moon CS, Moore R, Morello MJ, Morlock J, Fernandez PM, Mukherjee A, Muller T, Murat P, Mussini M, Nachtman J, Nagai Y, Naganoma J, Nakano I, Napier A, Nett J, Neu C, Neubauer MS, Nielsen J, Nodulman L, Norniella O, Nurse E, Oakes L, Oh SH, Oh YD, Oksuzian I, Okusawa T, Orava R, Ortolan L, Griso SP, Pagliarone C, Palencia E, Papadimitriou V, Paramonov AA, Patrick J, Pauletta G, Paulini M, Paus C, Pellett DE, Penzo A, Phillips TJ, Piacentino G, Pianori E, Pilot J, Pitts K, Plager C, Pondrom L, Potamianos K, Poukhov O, Prokoshin F, Pronko A, Ptohos F, Pueschel E, Punzi G, Pursley J, Rahaman A, Ramakrishnan V, Ranjan N, Redondo I, Renton P, Rescigno M, Rimondi F, Ristori L, Robson A, Rodrigo T, Rodriguez T, Rogers E, Rolli S, Roser R, Rossi M, Ruffini F, Ruiz A, Russ J, Rusu V, Safonov A, Sakumoto WK, Santi L, Sartori L, Sato K, Saveliev V, Savoy-Navarro A, Schlabach P, Schmidt A, Schmidt EE, Schmidt MP, Schmitt M, Schwarz T, Scodellaro L, Scribano A, Scuri F, Sedov A, Seidel S, Seiya Y, Semenov A, Sforza F, Sfyrla A, Shalhout SZ, Shears T, Shekhar R, Shepard PF, Shimojima M, Shiraishi S, Shochet M, Shreyber I, Simonenko A, Sinervo P, Sissakian A, Sliwa K, Smith JR, Snider FD, Soha A, Somalwar S, Sorin V, Squillacioti P, Stanitzki M, Denis RS, Stelzer B, Stelzer-Chilton O, Stentz D, Strologas J, Strycker GL, Sudo Y, Sukhanov A, Suslov I, Takemasa K, Takeuchi Y, Tang J, Tecchio M, Teng PK, Thom J, Thome J, Thompson GA, Thomson E, Ttito-Guzman P, Tkaczyk S, Toback D, Tokar S, Tollefson K, Tomura T, Tonelli D, Torre S, Torretta D, Totaro P, Trovato M, Tu Y, Turini N, Ukegawa F, Uozumi S, Varganov A, Vataga E, Vazquez F, Velev G, Vellidis C, Vidal M, Vila I, Vilar R, Vogel M, Volpi G, Wagner P, Wagner RL, Wakisaka T, Wallny R, Wang SM, Warburton A, Waters D, Weinberger M, Wester WC, Whitehouse B, Whiteson D, Wicklund AB, Wicklund E, Wilbur S, Wick F, Williams HH, Wilson JS, Wilson P, Winer BL, Wittich P, Wolbers S, Wolfe H, Wright T, Wu X, Wu Z, Yamamoto K, Yamaoka J, Yang T, Yang UK, Yang YC, Yao WM, Yeh GP, Yi K, Yoh J, Yorita K, Yoshida T, Yu GB, Yu I, Yu SS, Yun JC, Zanetti A, Zeng Y, Zucchelli S
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Improved Search for a Higgs Boson Produced in Association with Z -> l(+)l(-) in p(p)over-bar Collisions at root s=1.96 TeV
PHYSICAL REVIEW LETTERS 2010 DEC 13; 105(25):? Article 251802
We search for the standard model Higgs boson produced with a Z boson in 4: 1 fb(-1) of integrated luminosity collected with the CDF II detector at the Tevatron. In events consistent with the decay of the Higgs boson to a bottom-quark pair and the Z boson to electrons or muons, we set 95% credibility level upper limits on the ZH production cross section multiplied by the H -> b (b) over bar branching ratio. Improved analysis methods enhance signal sensitivity by 20% relative to previous searches. At a Higgs boson mass of 115 GeV/c(2) we set a limit of 5.9 times the standard model cross section.
Khachatryan V, Sirunyan AM, Tumasyan A, Adam W, Bergauer T, Dragicevic M, Ero J, Fabjan C, Friedl M, Fruhwirth R, Ghete VM, Hammer J, Hansel S, Hoch M, Hormann N, Hrubec J, Jeitler M, Kasieczka G, Kiesenhofer W, Krammer M, Liko D, Mikulec I, Pernicka M, Rohringer H, Schofbeck R, Strauss J, Taurok A, Teischinger F, Waltenberger W, Walzel G, Widl E, Wulz CE, Mossolov V, Shumeiko N, Gonzalez JS, Benucci L, Ceard L, De Wolf EA, Hashemi M, Janssen X, Maes T, Mucibello L, Ochesanu S, Roland B, Rougny R, Selvaggi M, Van Haevermaet H, Van Mechelen P, Van Remortel N, Adler V, Beauceron S, Blyweert S, D'Hondt J, Devroede O, Kalogeropoulos A, Maes J, Maes M, Tavernier S, Van Doninck W, Van Mulders P, Villella I, Chabert EC, Charaf O, Clerbaux B, De Lentdecker G, Dero V, Gay APR, Hammad GH, Marage PE, Vander Velde C, Vanlaer P, Wickens J, Costantini S, Grunewald M, Klein B, Marinov A, Ryckbosch D, Thyssen F, Tytgat M, Vanelderen L, Verwilligen P, Walsh S, Zaganidis N, Basegmez S, Bruno G, Caudron J, De Jeneret JD, Delaere C, Demin P, Favart D, Giammanco A, Gregorie G, Hollar J, Lemaitre V, Militaru O, Ovyn S, Pagano D, Pin A, Piotrzkowski K, Quertenmont L, Schul N, Beliy N, Caebergs T, Daubie E, Alves GA, Carneiro M, Pol ME, Souza MHG, Carvalho W, Da Costa EM, Damiao DD, Martins CD, De Souza SF, Mundim L, Nogima H, Oguri V, Santoro A, Do Amaral SMS, Sznajder A, De Araujo FTD, Dias FA, Dias MAF, Tomei TRFP, Gregores EM, Marinho F, Novaes SF, Padula SS, Darmenov N, Dimitrov L, Genchev V, Iaydjiev P, Piperov S, Stoykova S, Sultanov G, Trayanov R, Vankov I, Dyulendarova M, Hadjiiska R, Kozhuharov V, Litov L, Marinova E, Mateev M, Pavlov B, Petkov P, Bian JG, Chen GM, Chen HS, Jiang CH, Liang D, Liang S, Wang J, Wang J, Wang X, Wang Z, Yang M, Zang J, Zhang Z, Ban Y, Guo S, Hu Z, Mao Y, Qian SJ, Teng H, Zhu B, Cabrera A, Montoya CAC, Moreno BG, Rios AAO, Oliveros AFO, Sanabria JC, Godinovic N, Lelas D, Lelas K, Plestina R, Polic D, Puljak I, Antunovic Z, Dzelalija M, Brigljevic V, Duric S, Kadija K, Morovic S, Attikis A, Fereos R, Galanti M, Mousa J, Nicolaou C, Ptochos F, Razis PA, Rykaczewski H, Mahmoud MA, Hektor A, Kadastik M, Kannike K, Muntel M, Raidal M, Rebane L, Azzolini V, Eerola P, Czellar S, Harkonen J, Heikkinen A, Karimaki V, Kinnunen R, Klem J, Kortelainen MJ, Lampen T, Lasila-Perini K, Lehti S, Linden T, Luukka P, Maenpaa T, Tuominen E, Tuominiemi J, Tuovinen E, Ungaro D, Wendland L, Banzuzi K, Korpela A, Tuuva T, Sillou D, Besancon M, Dejardin M, Denegri D, Descamps J, Fabbro B, Faure JL, Ferri F, Ganjour S, Gentit FX, Givernaud A, Gras P, de Monchenault GH, Jarry P, Locci E, Malcles J, Marionneau M, Millischer L, Rander J, Rosowsky A, Rousseau D, Titov M, Verrecchia P, Baffioni S, Bianchini L, Bluj M, Broutin C, Busson P, Charlot C, Dobrzynski L, Elgammal S, de Cassagnac RG, Haguenauer M, Kalinowski A, Mine P, Paganini P, Sabes D, Sirois Y, Thiebaux C, Zabi A, Agram JL, Besson A, Bloch D, Bodin D, Brom JM, Cardaci M, Conte E, Drouhin F, Ferro C, Fontaine JC, Gele D, Goerlach U, Greder S, Juillot P, Karim M, Le Bihan AC, Mikami Y, Speck J, Van Hove P, Fassi F, Mercier D, Baty C, Beaupere N, Bedjidian M, Bondu O, Boudoul G, Boumediene D, Brun H, Chanon N, Chierici R, Contardo D, Depasse P, El Mamouni H, Fay J, Gascon S, Ille B, Kurca T, Le Grand T, Lethuillier M, Mirabito L, Perries S, Sordini V, Tosi S, Tschudi Y, Verdier P, Xiao H, Roinishvili V, Anagnostou G, Edelhoff M, Feld L, Heracleous N, Hindrichs O, Jussen R, Klein K, Merz J, Mohr N, Ostapchuk A, Perieanu A, Raupach F, Sammet J, Schael S, Sprenger D, Weber H, Weber M, Wittmer B, Actis O, Ata M, Bender W, Biallass P, Erdmann M, Frangenheim J, Hebbeker T, Hinzmann A, Hoepfner K, Hof C, Kirsch M, Klimkovich T, Kreuzer P, Lanske D, Magass C, Merschmeyer M, Meyer A, Papacz P, Pieta H, Reithler H, Schmitz SA, Sonnenschein L, Sowa M, Steggemann J, Teyssier D, Zeidler C, Bontenackels M, Davids M, Duda M, Flugge G, Geenen H, Giffels M, Ahmad WH, Heydhausen D, Kress T, Kuessel Y, Linn A, Nowack A, Perchalla L, Pooth O, Sauerland P, Stahl A, Thomas M, Tornier D, Zoeller MH, Martin MA, Behrenhoff W, Behrens U, Bergholz M, Borras K, Campbell A, Castro E, Dammann D, Eckerlin G, Flossdorf A, Flucke G, Geiser A, Hauk J, Jung H, Kasemann M, Katkov I, Kleinwort C, Kluge H, Knutsson A, Kuznetsova E, Lange W, Lohmann W, Mankel R, Marienfeld M, Melzer-Pellmann IA, Meyer AB, Mnich J, Mussgiller A, Olzem J, Parenti A, Raspereza A, Schmidt R, Schoerner-Sadenius T, Sen N, Stein M, Tomaszewska J, Volyanskyy D, Wissing C, Autermann C, Draeger J, Eckstein D, Enderle H, Gebbert U, Kaschube K, Kaussen G, Klanner R, Mura B, Naumann-Emme S, Nowak F, Sander C, Schettler H, Schleper P, Schroder M, Schum T, Schwandt J, Srivastava AK, Stadie H, Steinbruck G, Thomsen J, Wolf R, Bauer J, Buege V, Cakir A, Chwalek T, Daeuwel D, De Boer W, Dierlamm A, Dirkes G, Feindt M, Gruschke J, Hackstein C, Hartmann F, Heinrich M, Held H, Hoffmann KH, Honc S, Kuhr T, Martschei D, Mueller S, Muller T, Niegel M, Oberst O, Oehler A, Ott J, Peiffer T, Piparo D, Quast G, Rabbertz K, Ratnikov F, Renz M, Sabellek A, Saout C, Scheurer A, Schieferdecker P, Schilling FP, Schott G, Simonis HJ, Stober FM, Troendle D, Wagner-Kuhr J, Zeise M, Zhukovh V, Ziebarth EB, Daskalakis G, Geralis T, Kyriakis A, Loukas D, Manolakos I, Markou A, Markou C, Mavrommatis C, Petrakou E, Gouskos L, Katsas P, Panagiotou A, Evangelou I, Kokkas P, Manthos N, Papadopoulos I, Patras V, Triantis FA, Aranyi A, Bencze G, Boldizsar L, Debreczeni G, Hajdu C, Horvath D, Kapusi A, Krajczar K, Laszlo A, Sikler F, Vesztergombi G, Beni N, Molnar J, Palinkas J, Szillasi Z, Veszpremi V, Raics P, Trocsanyi ZL, Ujvari B, Bansal S, Beri SB, Bhatnagar V, Jindal M, Kaur M, Kohli JM, Mehta MZ, Nishu N, Saini LK, Sharma A, Sharma R, Singh AP, Singh JB, Singh SP, Ahuja S, Bhattacharya S, Chauhan S, Choudhary BC, Gupta P, Jain S, Jain S, Kumar A, Ranjan K, Shivpuri RK, Choudhury RK, Dutta D, Kailas S, Kataria SK, Mohanty AK, Pant LM, Shukla P, Suggisetti P, Aziz T, Guchait M, Gurtu A, Maity M, Majumder D, Majumder G, Mazumdar K, Mohanty GB, Saha A, Sudhakar K, Wickramage N, Banerjee S, Dugad S, Mondal NK, Arfaei H, Bakhshiansohi H, Fahim A, Jafari A, Najafabadi MM, Mehdiabadi SP, Safarzadeh B, Zeinali M, Abbrescia M, Barbone L, Colaleo A, Creanza D, De Filippis N, De Palma M, Dimitrov A, Fedele F, Fiore L, Iaselli G, Lusito L, Maggi G, Maggi M, Manna N, Marangelli B, My S, Nuzzo S, Pierro GA, Pompili A, Pugliese G, Romano F, Roselli G, Selvaggi G, Silvestris L, Trentadue R, Tupputi S, Zito G, Abbiendi G, Benvenuti AC, Bonacorsi D, Braibant-Giacomelli S, Capiluppi P, Castro A, Cavallo FR, Codispoti G, Cuffiani M, Dallavalle GM, Fabbri F, Fanfani A, Fasanella D, Giacomelli P, Giunta M, Marcellini S, Masetti G, Montanari A, Navarria FL, Odorici F, Perrotta A, Rovelli T, Siroli G, Travaglini R, Albergo S, Cappello G, Chiorboli M, Costa S, Tricomi A, Tuve C, Barbagli G, Broccolo G, Ciulli V, Civinini C, D'Alessandro R, Focardi E, Frosali S, Gallo E, Genta C, Lenzi P, Meschini M, Paoletti S, Sguazzoni G, Tropiano A, Benussi L, Bianco S, Colafranceschi S, Fabbri F, Piccolo D, Fabbricatore P, Musenich R, Benaglia A, Cerati GB, De Guio F, Di Matteo L, Ghezzi A, Govoni P, Malberti M, Malvezzi S, Martelli A, Massironi A, Menasce D, Miccio V, Moroni L, Negri P, Paganoni M, Pedrini D, Ragazzi S, Redaelli N, Sala S, Salerno R, de Fatis TT, Tancini V, Taroni S, Buontempo S, Cimmino A, De Cosa A, De Gruttola M, Fabozzi F, Iorio AOM, Lista L, Noli P, Paolucci P, Azzi P, Bacchetta N, Bellan P, Bisello D, Carlin R, Checchia P, De Mattia M, Dorigo T, Dosselli U, Gasparini F, Giubilato P, Gresele A, Gulmini M, Lacaprara S, Lazzizzera I, Margoni M, Mazzucato M, Meneguzzo AT, Passaseo M, Perrozzi L, Pozzobon N, Ronchese P, Simonetto F, Torassa E, Tosi M, Triossi A, Vanini S, Ventura S, Zotto P, Baesso P, Berzano U, Riccardi C, Torre P, Vitulo P, Viviani C, Biasini M, Bilei GM, Caponeri B, Fano L, Lariccia P, Lucaroni A, Mantovani G, Menichelli M, Nappi A, Santocchia A, Servoli L, Valdata M, Volpe R, Azzurri P, Bagliesi G, Bernardini J, Boccali T, Castaldi R, Dagnolo RT, Dell'Orso R, Fiori F, Foa L, Giassi A, Kraan A, Ligabue F, Lomtadze T, Martini L, Messineo A, Palla F, Palmonari F, Segneri G, Serban AT, Spagnolo P, Tenchini R, Tonelli G, Venturi A, Verdini PG, Barone L, Cavallari F, Del Re D, Di Marco E, Diemoz M, Franci D, Grassi M, Longo E, Organtini G, Palma A, Pandolfi F, Paramatti R, Rahatlou S, Amapane N, Arcidiacono R, Argiro S, Arneodo M, Biino C, Botta C, Cartiglia N, Castello R, Costa M, Demaria N, Graziano A, Mariotti C, Marone M, Maselli S, Migliore E, Mila G, Monaco V, Musich M, Obertino MM, Pastrone N, Pelliccioni M, Romero A, Ruspa M, Sacchi R, Solano A, Staiano A, Trocino D, Pereira AV, Ambroglini F, Belforte S, Cossutti F, Della Ricca G, Gobbo B, Montanino D, Penzo A, Chang S, Chung J, Kim DH, Kim GN, Kim JE, Kong DJ, Park H, Son D, Son DC, Kim Z, Kim JY, Song S, Hong B, Kim H, Kim JH, Kim TJ, Lee KS, Moon DH, Park SK, Rhee HB, Sim KS, Choi M, Kang S, Kim H, Park C, Park IC, Park S, Choi S, Choi Y, Choi YK, Goh J, Lee J, Lee S, Seo H, Yu I, Janulis M, Martisiute D, Petrov P, Sabonis T, Valdez HC, Burelo ED, Lopez-Fernandez R, Hernandez AS, Villasenor-Cendejas LM, Moreno SC, Ibarguen HAS, Linares EC, Pineda AM, Reyes-Santos MA, Allfrey P, Krofcheck D, Tam J, Butler PH, Signal T, Williams JC, Ahmad M, Ahmed I, Asghar MI, Hoorani HR, Khan WA, Khurshid T, Qazi S, Cwiok M, Dominik W, Doroba K, Konecki M, Krolikowski J, Frueboes T, Gokieli R, Gorski M, Kazana M, Nawrocki K, Szleper M, Wrochna G, Zalewski P, Almeida N, David A, Faccioli P, Parracho PGF, Gallinaro M, Mini G, Musella P, Nayak A, Raposo L, Ribeiro PQ, Seixas J, Silva P, Soares D, Varelab J, Wohri HK, Belotelov I, Bunin P, Finger M, Finger M, Golutvin I, Kamenev A, Karjavin V, Kozlov G, Lanev A, Moisenz P, Palichik V, Perelygin V, Shmatov S, Smirnov V, Volodko A, Zarubin A, Bondar N, Golovtsov V, Ivanov Y, Kim V, Levchenko P, Smirnov I, Sulimov V, Uvarov L, Vavilov S, Vorobyev A, Andreev Y, Gninenko S, Golubev N, Kirsanov M, Krasnikov N, Matveev V, Pashenkov A, Toropin A, Troitsky S, Epshteyn V, Gavrilov V, Ilina N, Kaftanov V, Kossov M, Krokhotin A, Kuleshov S, Oulianov A, Safronov G, Semenov S, Shreyber I, Stolin V, Vlasov E, Zhokin A, Boos E, Dubinin M, Dudko L, Ershov A, Gribushin A, Kodolova O, Lokhtin I, Obraztsov S, Petrushanko S, Sarycheva L, Savrin V, Snigirev A, Andreev V, Dremin I, Kirakosyan M, Rusakov SV, Vinogradov A, Azhgirey I, Bitioukov S, Datsko K, Grishin V, Kachanov V, Konstantinov D, Krychkine V, Petrov V, Ryutin R, Slabospitsky S, Sobol A, Sytine A, Tourtchanovitch L, Troshin S, Tyurin N, Uzunian A, Volkov A, Adzic P, Djordjevic M, Krpic D, Maletic D, Milosevic J, Puzovic J, Aguilar-Benitez M, Maestre JA, Arce P, Battilana C, Calvo E, Cepeda M, Cerrada M, Llatas MC, Colino N, De La Cruz B, Pardos CD, Bedoya CF, Ramos JPF, Ferrando A, Flix J, Fouz MC, Garcia-Abia 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First measurement of the underlying event activity at the LHC with root s=0.9 TeV
EUROPEAN PHYSICAL JOURNAL C 2010 DEC; 70(3):555-572
A measurement of the underlying activity in scattering processes with p (T) scale in the GeV region is performed in proton-proton collisions at root s = 0.9 TeV, using data collected by the CMS experiment at the LHC. Charged particle production is studied with reference to the direction of a leading object, either a charged particle or a set of charged particles forming a jet. Predictions of several QCD-inspired models as implemented in PYTHIA are compared, after full detector simulation, to the data. The models generally predict too little production of charged particles with pseudorapidity |eta|< 2, p (T) > 0.5 GeV/c, and azimuthal direction transverse to that of the leading object.
Shi H, Blobel G
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UNC-45/CRO1/She4p (UCS) protein forms elongated dimer and joins two myosin heads near their actin binding region
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 2010 DEC 14; 107(50):21382-21387
UNC-45/CRO1/She4p (UCS) proteins have variously been proposed to affect the folding, stability, and ATPase activity of myosins. They are the only proteins known to interact directly with the motor domain. To gain more insight into UCS function, we determined the atomic structure of the yeast UCS protein, She4p, at 2.9 angstrom resolution. We found that 16 helical repeats are organized into an L-shaped superhelix with an amphipathic N-terminal helix dangling off the short arm of the L-shaped molecule. In the crystal, She4p forms a 193-angstrom-long, zigzag-shaped dimer through three distinct and evolutionary conserved interfaces. We have identified She4p's C-terminal region as a ligand for a 27-residue-long epitope on the myosin motor domain. Remarkably, this region consists of two adjacent, but distinct, binding epitopes localized at the nucleotide-responsive cleft between the nucleotide- and actin-filament-binding sites. One epitope is situated inside the cleft, the other outside the cleft. After ATP hydrolysis and Pi ejection, the cleft narrows at its base from 20 to 12 angstrom thereby occluding the inside the cleft epitope, while leaving the adjacent, outside the cleft binding epitope accessible to UCS binding. Hence, one cycle of higher and lower binding affinity would accompany one ATP hydrolysis cycle and a single step in the walk on an actin filament rope. We propose that a UCS dimer links two myosins at their motor domains and thereby functions as one of the determinants for step size of myosin on actin filaments.
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Malik S, Snow GR, Baur U, Godshalk A, Iashvili I, Kharchilava A, Kumar A, Smith K, Zennamo J, Alverson G, Barberis E, Baumgartel D, Boeriu O, Chasco M, Kaadze K, Reucroft S, Swain J, Wood D, Zhang J, Anastassov A, Kubik A, Odell N, Ofierzynski RA, Pollack B, Pozdnyakov A, Schmitt M, Stoynev S, Velasco M, Won S, Antonelli L, Berry D, Hildreth M, Jessop C, Karmgard DJ, Kolb J, Kolberg T, Lannon K, Luo W, Lynch S, Marinelli N, Morse DM, Pearson T, Ruchti R, Slaunwhite J, Valls N, Warchol J, Wayne M, Ziegler J, Bylsma B, Durkin LS, Gu J, Hill C, Killewald P, Ling TY, Rodenburg M, Williams G, Adam N, Berry E, Elmer P, Gerbaudo D, Halyo V, Hebda P, Hunt A, Jones J, Laird E, Pegna DL, Marlow D, Medvedeva T, Mooney M, Olsen J, Piroue P, Saka H, Stickland D, Tully C, Werner JS, Zuranski A, Acosta JG, Huang XT, Lopez A, Mendez H, Oliveros S, Vargas JER, Zatserklyaniy A, Alagoz E, Barnes VE, Bolla G, Borrello L, Bortoletto D, Everett A, Garfinkel AF, Gecse Z, Gutay L, Jones M, Koybasi O, Laasanen AT, Leonardo N, Liu C, Maroussov V, Meier M, Merkel P, Miller DH, Neumeister N, Potamianos K, Shipsey I, Silvers D, Svyatkovskiy A, Yoo HD, Zablocki J, Zheng Y, Jindal P, Parashar N, Boulahouache C, Cuplov V, Ecklund KM, Geurts FJM, Liu JH, Morales J, Padley BP, Redjimi R, Roberts J, Zabel J, Betchart B, Bodek A, Chung YS, de Barbaro P, Demina R, Eshaq Y, Flacher H, Garcia-Bellido A, Goldenzweig P, Gotra Y, Han J, Harel A, Miner DC, Orbaker D, Petrillo G, Vishnevskiy D, Zielinski M, Bhatti A, Demortier L, Goulianos K, Lungu G, Mesropian C, Yan M, Atramentov O, Barker A, Duggan D, Gershtein Y, Gray R, Halkiadakis E, Hidas D, Hits D, Lath A, Panwalkar S, Patel R, Richards A, Rose K, Schnetzer S, Somalwar S, Stone R, Thomas S, Cerizza G, Hollingsworth M, Spanier S, Yang ZC, York A, Asaadi J, Eusebi R, Gilmore J, Gurrola A, Kamon T, Khotilovich V, Montalvo R, Nguyen CN, Pivarski J, Safonov A, Sengupta S, Tatarinov A, Toback D, Weinberger M, Akchurin N, Bardak C, Damgov J, Jeong C, Kovitanggoon K, Lee SW, Mane P, Roh Y, Sill A, Volobouev I, Wigmans R, Yazgan E, Appelt E, Brownson E, Engh D, Florez C, Gabella W, Johns W, Kurt P, Maguire C, Melo A, Sheldon P, Velkovska J, Arenton MW, Balazs M, Boutle S, Buehler M, Conetti S, Cox B, Francis B, Hirosky R, Ledovskoy A, Lin C, Neu C, Patel T, Yohay R, Gollapinni S, Harr R, Karchin PE, Mattson M, Milstene C, Sakharov A, Anderson M, Bachtis M, Bellinger JN, Carlsmith D, Dasu S, Efron J, Gray L, Grogg KS, Grothe M, Hall-Wilton R, Herndon M, Klabbers P, Klukas J, Lanaro A, Lazaridis C, Leonard J, Liu J, Lomidze D, Loveless R, Mohapatra A, Parker W, Reeder D, Ross I, Savin A, Smith WH, Swanson J, Weinberg M
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Search for Quark Compositeness with the Dijet Centrality Ratio in pp Collisions at root s=7 TeV
PHYSICAL REVIEW LETTERS 2010 DEC 20; 105(26):? Article 262001
A search for quark compositeness in the form of quark contact interactions, based on hadronic jet pairs (dijets) produced in proton-proton collisions at root s = 7 eV, is described. The data sample of the study corresponds to an integrated luminosity of 2.9 pb(-1) collected with the CMS detector at the LHC. The dijet centrality ratio, which quantifies the angular distribution of the dijets, is measured as a function of the invariant mass of the dijet system and is found to agree with the predictions of the standard model. A statistical analysis of the data provides a lower limit on the energy scale of quark contact interactions. The sensitivity of the analysis is such that the expected limit is 2.9 TeV; because the observed value of the centrality ratio at high invariant mass is below the expectation, the observed limit is 4.0 TeV at the 95% confidence level.
Schober J, Cooney T, Pfaff D, Mayoglou L, Martin-Alguacil N
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Innervation of the Labia Minora of Prepubertal Girls
JOURNAL OF PEDIATRIC AND ADOLESCENT GYNECOLOGY 2010 DEC; 23(6):352-357
Introduction: Surgical and histologic sources of information give little reference to innervation, vascular, and epithelial details of the labia minora. Little is known about areas of nerve density, epithelial qualities, and vascular compartments of the labial minora that contribute to sexual arousal and orgasm. Surgical procedure development and counsel about surgical risks related to labioplasty and surgical flaps created from labial tissue may be based on inadequate information. Methods: Labial samples from 10 normal girls (aged 2-9 years) who underwent surgery for labial fusion utilized waste tissue strips for immunohistochemical identification of S-100 and neuronal nitric oxide synthase (nNOS) in the labia minora. Results: Vascular and lymphatic plexus lie within the reticular dermis, which contains a dense mesh of nerve fibers with a higher concentration of nerve fiber at the level of the subepithelial plexus. Dense innervations are located at the epidermis, extending along the basal and spinous layers of the epithelium of labia minora. Nerve bundles in the papillary dermis are associated with sebaceous and eccrine glands and nerve terminals located throughout the epithelium. The introital epithelium of the labia minora is highly innervated with widespread and intense staining, detected in the introital border of the labia minora versus the external one. The dermis appeared to display S-100 and nNOS immunolabelling. S-100 was also immunopositive in the epidermis. Conclusion: Labia minora is highly innervated along its entire edge. Related vascular compartment tissue involved in engorgement during sexual arousal makes this tissue important for sexual response. Labioplasty risks removal of tissue with an important contribution to sensory sexual arousal. Movement of labial tissue during genitoplasty may have different sensory outcomes dependent on which labial surface is used.
Borroto-Escuela DO, Romero-Fernandez W, Tarakanov AO, Gomez-Soler M, Corrales F, Marcellino D, Narvaez M, Frankowska M, Flajolet M, Heintz N, Agnati LF, Ciruela F, Fuxe K
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Characterization of the A(2A)R-D2R interface Focus on the role of the C-terminal tail and the transmembrane helices
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 2010 NOV 26; 402(4):801-807
A single serine point mutation (S374A) in the adenosine A(2A) receptor (A(2A)R) C-terminal tall reduces A(2A)R-D2R heteromerization and prevents its allosteric modulation of the dopamine D-2 receptor (D2R) By means of site directed mutagenesis of the A(2A)R and synthetic transmembrane (TM) alpha-helix peptides of the D2R we further explored the role of electrostatic interactions and TM helix interactions of the A(2A)R-D2R heteromer interface We found evidence that the TM domains IV and V of the D2R play a major role in the A(2A)R-D2R heteromer interface since the incubation with peptides corresponding to these domains significantly reduced the ability of A(2A)R and D2R to heteromenze In addition the incubation with TM-IV or TM-V blocked the allosteric modulation normally found in A(2A)R-D2R heteromers The mutation of two negatively charged aspartates in the A(2A)R C-terminal tail (D401A/D402A) in combination with the S374A mutation drastically reduced the physical A(2A)R-D2R interaction and lost the ability of antagonistic allosteric modulation over the A(2A)R-D2R Interface suggesting further evidence for the existence of an electrostatic interaction between the C-terminal tail of A(2A)R and the intracellular loop 3 (IL3) of D2R. On the other hand molecular dynamic model and bioinformatic analysis propose that specific AAR AQE and VLS protriplets as an important motive in the A(2A)R-D2LR heteromer interface together with D2LR TM segments IV/V interacting with A(2A)R TM-IV/V or TM-I/VII (C)2010 Elsevier Inc All rights reserved
Butterwick JA, MacKinnon R
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Solution Structure and Phospholipid Interactions of the Isolated Voltage-Sensor Domain from KvAP
JOURNAL OF MOLECULAR BIOLOGY 2010 NOV 5; 403(4):591-606
Voltage-sensor domains (VSDs) are specialized transmembrane segments that confer voltage sensitivity to many proteins such as ion channels and enzymes. The activities of these domains are highly dependent on both the chemical properties and the physical properties of the surrounding membrane environment. To learn about VSD-lipid interactions, we used nuclear magnetic resonance spectroscopy to determine the structure and phospholipid interface of the VSD from the voltage-dependent K(+) channel KvAP (prokaryotic Kv from Aeropyrum pernix). The solution structure of the KvAP VSD solubilized within phospholipid micelles is similar to a previously determined crystal structure solubilized by a nonionic detergent and complexed with an antibody fragment. The differences observed include a previously unidentified short amphipathic alpha-helix that precedes the first transmembrane helix and a subtle rigid-body repositioning of the S3-S4 voltage-sensor paddle. Using (15)N relaxation experiments, we show that much of the VSD, including the pronounced kink in S3 and the S3-S4 paddle, is relatively rigid on the picosecond-to-nanosecond timescale. In contrast, the kink in S3 is mobile on the microsecond-to-millisecond timescale and may act as a hinge in the movement of the paddle during channel gating. We characterized the VSD-phospholipid micelle interactions using nuclear Overhauser effect spectroscopy and showed that the micelle uniformly coats the KvAP VSD and approximates the chemical environment of a phospholipid bilayer. Using paramagnetically labeled phospholipids, we show that bilayer-forming lipids interact with the S3 and S4 helices more strongly than with Si and S2. (C) 2010 Elsevier Ltd. All rights reserved.
Ronzhin A, Albrow MG, Demarteau M, Los S, Malik S, Pronko A, Ramberg E, Zatserklyaniy A
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Development of a 10 ps level time of flight system in the Fermilab Test Beam Facility
NUCLEAR INSTRUMENTS & METHODS IN PHYSICS RESEARCH SECTION A-ACCELERATORS SPECTROMETERS DETECTORS AND ASSOCIATED EQUIPMENT 2010 NOV 21; 623(3):931-941
We describe here the development of a time of flight (TOF) system with 10-20 ps resolution for particle identification in a beam line. The detector resolution also was measured with the start and stop counters close together in the 120 GeV proton beam of the Fermilab Test Beam Facility. We tested both microchannel plate photomultipliers (MCP PMT) and silicon photomultipliers (SiPMs), in both cases using Cherenkov light produced in fused silica (quartz) radiators. Published by Elsevier B.V.