120 research outputs found
Performance of the CMS Cathode Strip Chambers with Cosmic Rays
- Author
- Abadjiev K
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdullin S
- Abelev B
- Acosta D
- Acosta JG
- Acosta MV
- Actis O
- Adam N
- Adam W
- Adams MR
- Adams T
- Adiguzel A
- Adler V
- Adolphi R
- Adzic P
- Afaq MA
- Agostino L
- Agram JL
- Aguilar-Benitez M
- Ahmad M
- Ahmad WH
- Ahmed I
- Ahmed W
- Ahuja S
- Aisa D
- Aisa S
- Akchurin N
- Akgun B
- Akgun U
- Akimenko S
- Akin IV
- Alagoz E
- Alampi G
- Albajar C
- Albayrak EA
- Alberdi J
- Albergo S
- Albert E
- Albrow M
- Alexander J
- Alidra M
- Aliev T
- Allfrey P
- Almeida N
- Altenhofer G
- Altsybeev I
- Alver B
- Alverson G
- Alves GA
- Amaglobeli N
- Amapane N
- Ambroglini F
- Amsler C
- Anagnostou G
- Ananthan B
- Anastassov A
- Andelin D
- Anderson M
- Andrea J
- Andreev V
- Andreev Y
- Anghel IM
- Anguelov T
- Anh T. Vu
- Anisimov A
- Antillon E
- Antipov P
- Antonelli L
- Anttila E
- Antunes JR
- Antunovic Z
- Apanasevich L
- Apollinari G
- Apresyan A
- Arce P
- Arcidiacono R
- Arenton MW
- Arfaei H
- Argiro S
- Arisaka K
- Arneodo M
- Arnold B
- Arora S
- Artamonov A
- Asaadi J
- Asghar MI
- Ashby S
- Askew A
- Atac M
- Atramentov O
- Auffray E
- Aurisano A
- Autermann C
- Avery P
- Avetisyan A
- Avila C
- Awan MIM
- Ayan AS
- Ayhan A
- Azhgirey I
- Aziz T
- Azzi P
- Azzurri P
- Baarmand MM
- Babb J
- Babucci E
- Baccaro S
- Bacchetta N
- Bacchi W
- Bachtis M
- Baden D
- Badgett W
- Baechler J
- Baer H
- Baesso P
- Baffioni S
- Bagby L
- Bagliesi G
- Bahk SY
- Bailleux D
- Baillon P
- Bainbridge R
- Bakhshiansohi H
- Bakirci MN
- Bakken JA
- Balazs M
- Baldin B
- Ball G
- Ball H
- Ballin J
- Bally SL
- Ban Y
- Bandurin D
- Banerjee S
- Banerjee S
- Banicz K
- Bansal S
- Banzuzi K
- Barashko V
- Barbagli G
- Barberis E
- Barbone L
- Barcala JM
- Barcellan L
- Bard R
- Bargassa P
- Baringer P
- Barnes VE
- Barnett BA
- Barney D
- Barone L
- Bartalini P
- Bartoloni A
- Bartz E
- Basegmez S
- Battilana C
- Baty C
- Baud A
- Bauer G
- Bauer J
- Bauerdick LAT
- Baur U
- Bawa HS
- Bazterra VE
- Bean A
- Beauceron S
- Beaudette F
- Beaumont W
- Bechtel F
- Bedjidian M
- Bedoya CF
- Beetz CP
- Behrens U
- Bejar JC
- Belforte S
- Beliy N
- Bell KW
- Bellan P
- Bellan R
- Bellato M
- Bellinger JN
- Belotelov I
- Benaglia A
- Bencze G
- Bendavid J
- Bender W
- Benedetti D
- Benelli G
- Benettoni M
- Beni N
- Benucci L
- Benussi L
- Benvenuti AC
- Berengueres JOL
- Beretvas A
- Bergauer H
- Bergauer T
- Beri SB
- Bernardini J
- Bernet C
- Berntzon L
- Berretta L
- Berry D
- Berry E
- Berryhill J
- Bertani M
- Bertl W
- Bertoldi M
- Berzano U
- Besancon M
- Besson A
- Betchart B
- Betev B
- Betts RR
- Beuselinck R
- Bhat PC
- Bhatnagar V
- Bhattacharya S
- Bhattacharya S
- Bhatti A
- Biallass P
- Bianchini L
- Bianco S
- Biasini M
- Biasotto M
- Biery K
- Biino C
- Bilei GM
- Bilki B
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- Bisello D
- Bitioukov S
- Blaha J
- Blekman F
- Bloch D
- Bloch I
- Bloch P
- Bloom K
- Bluj M
- Blum P
- Blumenfeld B
- Blyweert S
- Boccali T
- Bocci A
- Bockelman B
- Bodek A
- Bodin D
- Boeriu O
- Boldini M
- Boldizsar L
- Bolla G
- Bolognesi S
- Bolton T
- Bona M
- Bonacorsi D
- Bonato A
- Bondar N
- Bontenackels M
- Boos E
- Borcherding F
- Borgia MA
- Bornheim A
- Borras K
- Borrello L
- Borsato E
- Bortoletto D
- Bos J
- Bose M
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- Bosi F
- Bostock F
- Botta C
- Boudoul G
- Bouhali O
- Bourgeois N
- Bourilkov D
- Bourrel T
- Boutemeur M
- Boutle S
- Braibant-Giacomelli S
- Branca A
- Branson JG
- Brauer R
- Braunschweig W
- Breedon R
- Brett AM
- Breuker H
- Brew C
- Bricola S
- Briggs R
- Brigljevic V
- Broccolo G
- Brom JM
- Brooke JJ
- Brown RM
- Brun H
- Bruno G
- Buchmuller O
- Budd H
- Buege V
- Buehler M
- Bunin P
- Bunkowski K
- Bunn J
- Buontempo S
- Burkett K
- Burtovoy V
- Busson P
- Busza W
- Butler JN
- Butler PH
- Butt J
- Butz E
- Bylsma B
- Caballero IG
- Cabrillo IJ
- Cafaro VD
- Cai J
- Caiazza SS
- Cakir A
- Cakir I. Turk
- Calderon A
- Cali IA
- Callner J
- Calloni M
- Calvo E
- Calzolari F
- Camanzi B
- Caminada L
- Campagnari C
- Campbell A
- Campderros JD
- Campi D
- Camporesi T
- Cankocak K
- Cano E
- Capiluppi P
- Caponeri B
- Cardaci M
- Carleton M
- Carlin R
- Carlsmith D
- Carroll R
- Cartiglia N
- Carvalho W
- Case M
- Cassel D
- Castaldi R
- Castellani L
- Castello R
- Castro A
- Castro E
- Castro MA
- Cattai A
- Caudron J
- Cavallari F
- Cavallo FR
- Cavallo N
- Cavanaugh R
- Ceballos GG
- Cebra D
- Cepeda M
- Cerati GB
- Cerci S
- Cerizza G
- Cerminara G
- Ceron C
- Cerrada M
- Chabert EC
- Chan M
- Chandra A
- Chang P
- Chang S
- Chang YH
- Chanon N
- Chao Y
- Charaf O
- Charlot C
- Chatelain JP
- Chatrchyan S
- Chatterjee A
- Chauhan S
- Chauvey M
- Checchia P
- Checcucci B
- Chekhovsky V
- Chen EA
- Chen GM
- Chen HS
- Chen J
- Chen KF
- Chen M
- Chen WT
- Chen Z
- Cheng TL
- Chertok M
- Chetluru V
- Cheung HWK
- Chien CY
- Chierici R
- Chiochia V
- Chiorboli M
- Chipaux R
- Chiumarulo F
- Chlebana F
- Choi M
- Choi S
- Choi Y
- Chou JP
- Choudhary BC
- Choudhury RK
- Christian G
- Christiansen T
- Chtchipounov L
- Chuang SH
- Chung J
- Chung K
- Chung YS
- Churin I
- Chwalek T
- Cihangir S
- Cimmino A
- Cirino G
- Cittolin S
- Ciulli V
- Civinini C
- Claes DR
- Clare R
- Clarida W
- Clemente A
- Clemente F
- Clerbaux B
- Cline D
- Cockerill DJA
- Codispoti G
- Colafranceschi S
- Colaleo A
- Cole JE
- Colino N
- Colling D
- Colonna D
- Conetti S
- Contardo D
- Conte E
- Conti E
- Conway J
- Cooper SI
- Cordonnier AM
- Cortabitarte RV
- Cossutti F
- Costa M
- Costa S
- Coughlan JA
- Cousins R
- Covarelli R
- Cox B
- Cox PT
- Crawford M
- Creanza D
- Cremaldi LM
- Cripps N
- Crotty I
- Cuevas J
- Cuffiani M
- Cumalat JP
- Cuplov V
- Cure B
- Cuscela G
- Cushman P
- Cussans D
- Cutts D
- Cwiok M
- Czellar S
- D'Alessandro R
- D'Alfonso M
- D'Angelo P
- D'Antone I
- D'Enterria D
- D'Hondt J
- Dabrowski R
- Dafinei I
- Dagenhart W
- Dahmes B
- Dal Corso F
- Dallavalle GM
- Dambach S
- Damgov J
- Damiao DD
- Dammann D
- Daniel M
- Danielson T
- Darmenov N
- Das S
- Daskalakis G
- Dasu S
- Dattola D
- Daubie E
- David A
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- Davies G
- de Abril IM
- de Abril MM
- de Barbaro P
- De Benedetti A
- De Boer W
- de Cassagnac RG
- de Fatis TT
- De Filippis N
- De Gruttola M
- De Guio F
- De La Cruz B
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- De Mattia M
- de Monchenault GH
- De Palma M
- De Robertis G
- De Roeck A
- De Souza SF
- de Troconiz JF
- De Visscher S
- De Weirdt S
- De Wolf EA
- Debbins P
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- Deiters K
- Dejardin M
- Del Alamo MB
- del Arbol PMR
- Del Re D
- Delachenal V
- Delaere C
- Deliomeroglu M
- Dell'Orso R
- Della Negra M
- Della Ricca G
- Dellacasa G
- Delmeire E
- Demaria N
- Demarteau M
- Demin P
- Demina R
- Demir D
- Demortier L
- Denegri D
- Denisov A
- Deniz M
- Depasse P
- Dermenev A
- Dero V
- Derylo G
- Descamps J
- Devroede O
- Deyrail D
- Dharmaratna WGD
- Di Calafiori DRDS
- Di Giovanni GP
- Di Marco E
- Di Vincenzo S
- Dias MAF
- Diemoz M
- Dierlamm A
- Dimitrov A
- Dimitrov L
- Dinardo ME
- Dinu N
- Dirkes G
- Dissertori G
- Dittmar M
- Djaoshvili N
- Djordjevic M
- Do Amaral SMS
- Dobrzynski L
- Dobur D
- Dolen J
- Dolgopolov A
- Dominguez A
- Dominik W
- Donckt MV
- Donvito G
- Dorigo T
- Doroba K
- Dos Santos S
- Dosselli U
- Draeger J
- Dragicevic M
- Dragoiu C
- Drell BR
- Dremin I
- Drouhin F
- Drozdetskiy A
- Druzhkin D
- Dubinin M
- Duda M
- Dudero PR
- Dudko L
- Dugad S
- Dughera G
- Dumanoglu I
- Dumitrache F
- Dupasquier T
- Dupont T
- Duric S
- Durkin LS
- Duru F
- Dusinberre E
- Dutta D
- Dutta S
- Dvornikov O
- Dykstra D
- Dyulendarova M
- Dzelalija M
- Eads M
- Eartly DP
- Eckerlin G
- Ecklund KM
- Eckstein D
- Edelhoff M
- Edera LM
- Efron J
- Egeland R
- Eggel C
- Eichberger M
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- Elgammal S
- Elias JE
- Elliott-Peisert A
- Ellison JA
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- Elvira VD
- Emeliantchik I
- Engh D
- Eno SC
- Eppard M
- Epshteyn V
- Erbacher R
- Erdmann M
- Erdmann W
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- Ero J
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- Ershov Y
- Esen S
- Eskut E
- Esser H
- Eugster J
- Eulisse G
- Eusebi R
- Evangelou I
- Evans D
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- Everett A
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- Fabbricatore P
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- Faber G
- Fabozzi F
- Faccioli P
- Fahim A
- Fanfani A
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- Fanzago F
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- Fasanella D
- Fassi F
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- Favart D
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- Fedele F
- Fedorov A
- Fehling D
- Feindt M
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- Feng L
- Ferencek D
- Fereos R
- Ferguson T
- Fernandez M
- Ferrando A
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- Ferrer J. A. Valls
- Ferri F
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- Feyzi F
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- Filozova I
- Finger M
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- Fischler M
- Fisk I
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- Frangenheim J
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- Gennai S
- Genta C
- Gentit FX
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- Gerbaudo D
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- Gershtein Y
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- Landsberg G
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- van Vulpen I.
- Vandelli W.
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- Vankov I
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- Vanlaer P
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- Vavilov S
- Vazeille F.
- Vedaee A
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- Velde CV
- Velichko G
- Velikzhanin Y
- Vellidis C.
- Veloso F.
- Velthuis J
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- Ventura D.
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- Verdier P
- Verdini PG
- Verducci M.
- Veres GI
- Vergili LN
- Vergili M
- Verkerke W.
- Vermeulen J. C.
- Verrecchia P
- Verwilligen P
- Veszpremi V
- Vesztergombi G
- Vetterli M. C.
- Veverka J
- Vichou I.
- Vicini A
- Vickey T.
- Vidal R
- Viegas F. J. Tique Aires
- Viehhauser G. H. A.
- Vila I
- Villa M.
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- Vilucchi E.
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- Vinek E.
- Vinogradov A
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- Virdee T
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- Virto AL
- Virzi J.
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- Vishnevskiy A
- Vishnevskiy D
- Vitale A.
- Vitells O.
- Vitulo P
- Vivarelli I.
- Viviani C
- Vlachos S.
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- Vlimant JR
- Vodopiyanov I
- Vogel A.
- Vogel H
- Vokac P.
- Volkov A
- Volkov S
- Volobouev I
- Volodko A
- Volpe R
- Volpi M.
- Volyanskyy D
- von der Schmitt H.
- von Dratzig AS
- von Loeben J.
- von Radziewski H.
- von Toerne E.
- Vorobel V.
- Vorobiev I
- Vorobyev A
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- Vukotic I.
- Wagner P
- Wagner P.
- Wagner SR
- Wagner W
- Wagner-Kuhr J
- Wakefield S
- Walbersloh J.
- Walder J.
- Walker R.
- Walkowiak W.
- Wall R.
- Wallny R
- Waltenberger W
- Walton R
- Walzel G
- Wan Z
- Wang C.
- Wang CC
- Wang D
- Wang H.
- Wang J
- Wang J.
- Wang M
- Wang S. M.
- Wang Z
- Warburton A.
- Warchol J
- Ward C. P.
- Wardrope D
- Warsinsky M.
- Washington E
- Wastie R.
- Watkins P. M.
- Watson A. T.
- Watson M. F.
- Watts G.
- Watts S.
- Watts TL
- Waugh A. T.
- Waugh B. M.
- Wayne M
- Weber M
- Weber M
- Weber M.
- Weber M. D.
- Weber M. S.
- Weber P.
- Wehrli L
- Weidberg A. R.
- Weinberg M
- Weinberger M
- Weingarten J.
- Weiser C.
- Wellenstein H.
- Wells P. S.
- Wen M.
- Wenaus T.
- Wendland L
- Wendler S.
- Weng J
- Weng Y
- Wenger EA
- Wengler T.
- Wenig S.
- Wenman D
- Wensveen M
- Wermes N.
- Werner JS
- Werner M.
- Werner P.
- Wertelaers P
- Werth M.
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- Wessels M.
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- Whalen K.
- White A White AE. A.
- White A.
- White M. J.
- White S.
- Whitehead S. R.
- Whiteson D.
- Whitmore J
- Whittington D.
- Whyntie T
- Wicek F.
- Wicke D.
- Wickens F. J.
- Wickens J
- Wicklund E
- Widl E
- Wiedenmann W.
- Wielers M.
- Wienemann P.
- Wiglesworth C.
- Wigmans R
- Wiik L. A. M.
- Wildauer A.
- Wildish T
- Wildt M. A.
- Wilke L
- Wilken R
- Wilkens H. G.
- Wilkinson R
- Williams E.
- Williams G
- Williams H. H.
- Williams JC
- Williams JH
- Willmott C
- Willocq S.
- Wilson A.
- Wilson J. A.
- Wilson M. G.
- Wimpenny S
- Wingerter-Seez I.
- Wingham M
- Winklmeier F.
- Winn D
- Wissing C
- Witherell M
- Wittgen M.
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- Wittmer B
- Wlochal M
- Wohri HK
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- Wolter M. W.
- Wolters H.
- Womersley WJ
- Won S
- Wood JS
- Worm SD
- Wosiek B. K.
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- Wraight K.
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- Wright D
- Wright D.
- Wrochna G
- Wrona B.
- Wu S
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- Wu W
- Wu X.
- Wulf E.
- Wulz CE
- Wurthwein F
- Wynne B. M.
- Wyslouch B
- Xaplanteris L.
- Xella S.
- Xie S
- Xie S.
- Xie Z
- Xu D.
- Xu N.
- Xue Z
- Yagil A
- Yamada M.
- Yamamoto A
- Yan M
- Yang X
- Yang Y
- Yang ZC
- Yarba J
- Yaselli I
- Yazgan E
- Yelton J
- Yetkin T
- Yi K
- Yilmaz Y
- Yohay R
- Yoo HD
- Yoon AS
- York A
- Yumiceva F
- Yun JC
- Yuste C
- Zabi A
- Zabolotny W
- Zachariadou A
- Zalewski P
- Zampieri A
- Zanetti M
- Zang SL
- Zarubin A
- Zatzerklyany A
- Zeidler C
- Zeinali M
- Zeise M
- Zelepoukine S
- Zeuner WD
- Zeyrek M
- Zhang J
- Zhang L
- Zhang Y
- Zhang Z
- Zheng Y
- Zhiltsov V
- Zhokin A
- Zhu B
- Zhu K
- Zhu RY
- Zhukov V
- Zhukova V
- Ziebarth EB
- Zielinski M
- Zilizi G
- Zinonos Z
- Zito G
- Zoeller MH
- Zotto P
- Zub S
- Zumerle G
- Zuranski A
- Zuyeuski R
- Zych P
- Publication venue
- 'IOP Publishing'
- Publication date
- 01/01/2009
- Field of study
The Cathode Strip Chambers (CSCs) constitute the primary muon tracking device
in the CMS endcaps. Their performance has been evaluated using data taken
during a cosmic ray run in fall 2008. Measured noise levels are low, with the
number of noisy channels well below 1%. Coordinate resolution was measured for
all types of chambers, and fall in the range 47 microns to 243 microns. The
efficiencies for local charged track triggers, for hit and for segments
reconstruction were measured, and are above 99%. The timing resolution per
layer is approximately 5 ns
Unsaturated Fatty Acids Revert Diet-Induced Hypothalamic Inflammation in Obesity
- Author
- AA Rivellese
- AK Johnson
- Alicia J. Kowaltowski
- AN van den Pol
- AP Arruda
- BE Wisse
- C Bjorbak
- Claudio T. de Souza
- CM Reynolds
- CT De Souza
- CT De Souza
- Dennys E. Cintra
- DF Bertelli
- DP Figlewicz
- DY Oh
- E Bonora
- Eduardo R. Ropelle
- EF Martins
- EP Araujo
- G Paxinos
- JC Moraes
- JK Howard
- JM Zabolotny
- Joseane Morari
- JosĂŠ B. Carvalheira
- JosĂŠ R. Pauli
- JR Weinstein
- Juliana C. Moraes
- K Morgan
- KA Anderson
- KA Posey
- L Plum
- L Yang
- LA Velloso
- Licio A. Velloso
- M Bjornholm
- M Milanski
- Marcela Stahl
- Mario J. Saad
- MG Myers Jr
- MM Bradford
- MS Kim
- MW Schwartz
- Renato Grimaldi
- S Endres
- S Obici
- T Romanatto
- TH Lee
- TK Lam
- VE Cotero
- X Zhang
- Publication venue
- Public Library of Science
- Publication date
- 18/01/2012
- Field of study
Background: In experimental models, hypothalamic inflammation is an early and determining factor in the installation and progression of obesity. Pharmacological and gene-based approaches have proven efficient in restraining inflammation and correcting the obese phenotypes. However, the role of nutrients in the modulation of hypothalamic inflammation is unknown. Methodology/Principal Findings: Here we show that, in a mouse model of diet-induced obesity, partial substitution of the fatty acid component of the diet by flax seed oil (rich in C18:3) or olive oil (rich in C18:1) corrects hypothalamic inflammation, hypothalamic and whole body insulin resistance, and body adiposity. In addition, upon icv injection in obese rats, both v3 and v9 pure fatty acids reduce spontaneous food intake and body mass gain. These effects are accompanied by the reversal of functional and molecular hypothalamic resistance to leptin/insulin and increased POMC and CART expressions. In addition, both, v3 and v9 fatty acids inhibit the AMPK/ACC pathway and increase CPT1 and SCD1 expression in the hypothalamus. Finally, acute hypothalamic injection of v3 and v9 fatty acids activate signal transduction through the recently identified GPR120 unsaturated fatty acid receptor. Conclusions/Significance: Unsaturated fatty acids can act either as nutrients or directly in the hypothalamus, reverting dietinduced inflammation and reducing body adiposity. These data show that, in addition to pharmacological and geneti
Regulation of Brown Fat Adipogenesis by Protein Tyrosine Phosphatase 1B
- Author
- A Cederberg
- Ahmed Bettaieb
- AJ Entingh
- AJ Flint
- AM Cypess
- AM Valverde
- B Cannon
- B Xue
- B Xue
- BJ Goldstein
- BJ Goldstein
- BT Nave
- CL Venable
- CN Bennett
- DG Hardie
- ED Rosen
- ED Rosen
- EU Frevert
- Fawaz G. Haj
- FG Haj
- FG Haj
- FM Gregoire
- G Xu
- G Xu
- H Koutnikova
- H Sun
- Heike Keilhack
- HS Camp
- HS Sul
- Izumi Matsuo
- J Klein
- J Kopecky
- JM Zabolotny
- JS Moyers
- JV Frangioni
- K Tsukiyama-Kohara
- KA Virtanen
- KK Bence
- Kosuke Matsuo
- LD Klaman
- M Delibegovic
- M Delibegovic
- M Elchebly
- M Fasshauer
- M Fasshauer
- M Moldes
- M Saito
- MR Calera
- Naoto Nagata
- NK Tonks
- NK Tonks
- R Vila-Bedmar
- RJ Shaw
- S Dadke
- S Kajimura
- S Miranda
- SA Hawley
- Sandra Orsulic
- SE Ross
- SF Clark
- SM Rangwala
- SR Farmer
- SR Farmer
- TA Woodford-Thomas
- WD van Marken Lichtenbelt
- WW Winder
- YH Tseng
- YH Tseng
- YH Tseng
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2011
- Field of study
Protein-tyrosine phosphatase 1B (PTP1B) is a physiological regulator of insulin signaling and energy balance, but its role in brown fat adipogenesis requires additional investigation.To precisely determine the role of PTP1B in adipogenesis, we established preadipocyte cell lines from wild type and PTP1B knockout (KO) mice. In addition, we reconstituted KO cells with wild type, substrate-trapping (D/A) and sumoylation-resistant (K/R) PTP1B mutants, then characterized differentiation and signaling in these cells. KO, D/A- and WT-reconstituted cells fully differentiated into mature adipocytes with KO and D/A cells exhibiting a trend for enhanced differentiation. In contrast, K/R cells exhibited marked attenuation in differentiation and lipid accumulation compared with WT cells. Expression of adipogenic markers PPARγ, C/EBPι, C/EBPδ, and PGC1ι mirrored the differentiation pattern. In addition, the differentiation deficit in K/R cells could be reversed completely by the PPARγ activator troglitazone. PTP1B deficiency enhanced insulin receptor (IR) and insulin receptor substrate 1 (IRS1) tyrosyl phosphorylation, while K/R cells exhibited attenuated insulin-induced IR and IRS1 phosphorylation and glucose uptake compared with WT cells. In addition, substrate-trapping studies revealed that IRS1 is a substrate for PTP1B in brown adipocytes. Moreover, KO, D/A and K/R cells exhibited elevated AMPK and ACC phosphorylation compared with WT cells.These data indicate that PTP1B is a modulator of brown fat adipogenesis and suggest that adipocyte differentiation requires regulated expression of PTP1B
Novel Regulatory Mechanisms for Generation of the Soluble Leptin Receptor: Implications for Leptin Action
- Author
- A Batra
- A Chalaris
- A Chalaris
- A Lammert
- A Ludwig
- A Suzuki
- AS Reed
- C Hundhausen
- C Lizama
- CA Belmokhtar
- D Duksin
- DF Seals
- DW White
- FM van Dielen
- G Yang
- H Ge
- H Mori
- H Tu
- Henriette Kausch
- IK Lund
- J Bacart
- J Hakulinen
- J Kratzsch
- J Kratzsch
- J Kratzsch
- J Wauman
- J Zhang
- JL Chan
- JM Zabolotny
- Joachim Thiery
- Juergen Klammt
- Juergen Kratzsch
- Juergen Scheller
- KK Bence
- L Huo
- L Ozcan
- LA Tartaglia
- LL Atkinson
- LL Listenberger
- LL Listenberger
- M Maamra
- M Tanaka
- Marcin Nowicki
- Massimo Federici
- MG Myers
- Michael Schaab
- MY Wang
- NI Shapiro
- O Zastrow
- P Gutwein
- PH Lou
- Q Sun
- QL Lam
- Rolf Gebhardt
- S Uotani
- SH Bates
- SM Hileman
- Stefan Rose-John
- T Amit
- T Fujikawa
- T Hosoi
- T Reinehr
- Ulf Anderegg
- V Budagian
- X Yu
- X Zhang
- Y Akasaka
- Y Minokoshi
- Y Wang
- Y Zhang
- YT Zhou
- YT Zhou
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2012
- Field of study
The adipokine leptin realizes signal transduction via four different membrane-anchored leptin receptor (Ob-R) isoforms in humans. However, the amount of functionally active Ob-R is affected by constitutive shedding of the extracellular domain via a so far unknown mechanism. The product of the cleavage process the so-called soluble leptin receptor (sOb-R) is the main binding protein for leptin in human blood and modulates its bioavailability. sOb-R levels are differentially regulated in metabolic disorders like type 1 diabetes mellitus or obesity and can, therefore, enhance or reduce leptin sensitivity.To describe mechanisms of Ob-R cleavage and to investigate the functional significance of differential sOb-R levels we established a model of HEK293 cells transiently transfected with different human Ob-R isoforms. Using siRNA knockdown experiments we identified ADAM10 (A Disintegrin And Metalloproteinase 10) as a major protease for constitutive and activated Ob-R cleavage. Additionally, the induction of lipotoxicity and apoptosis led to enhanced shedding shown by increased levels of the soluble leptin receptor (sOb-R) in cell supernatants. Conversely, high leptin concentrations and ER stress reduced sOb-R levels. Decreased amounts of sOb-R due to ER stress were accompanied by impaired leptin signaling and reduced leptin binding.Lipotoxicity and apoptosis increased Ob-R cleavage via ADAM10-dependent mechanisms. In contrast high leptin levels and ER stress led to reduced sOb-R levels. While increased sOb-R concentrations seem to directly block leptin action, reduced amounts of sOb-R may reflect decreased membrane expression of Ob-R. These findings could explain changes of leptin sensitivity which are associated with variations of serum sOb-R levels in metabolic diseases
Regulation of Signaling at Regions of Cell-Cell Contact by Endoplasmic Reticulum-Bound Protein-Tyrosine Phosphatase 1B
- Author
- A Apolloni
- A Cheng
- AJ Flint
- Ali Kinkhabwala
- Benjamin G. Neel
- BL Sprague
- BL Sprague
- C Bouchet-Marquis
- C Ramachandran
- C Wiesmann
- CI Maeder
- Claude Antony
- CY Park
- DM Soumpasis
- E Nievergall
- ER Eden
- F Liu
- F. Gisou van der Goot
- Fawaz G. Haj
- FG Haj
- FG Haj
- G Huyer
- G Lavieu
- G Xu
- GH Patterson
- GK Voeltz
- H Takeshima
- Hong-Mei Han
- HT McMahon
- I Anderie
- IA Yudushkin
- J Balsamo
- J Kirchner
- J Liou
- J Lippincott-Schwartz
- J Lippincott-Schwartz
- JM Zabolotny
- JV Frangioni
- JV Frangioni
- L Lu
- L Orci
- LD Klaman
- M Elchebly
- M Stuible
- M Terasaki
- M Terasaki
- Markus Grabenbauer
- Martin Bierbaum
- MJ Kleijmeer
- MV Hernandez
- N Boute
- NB Cole
- NK Tonks
- NL Thompson
- Ola Sabet
- P Mertins
- P Pathre
- PB Stathopulos
- Philippe I. Bastiaens
- RG Parton
- S Dadke
- S Nehls
- Sabine Wimmer-Kleikamp
- SJ Plowman
- TA Woodford-Thomas
- TK Meyvis
- TO Johnson
- Vassilis Roukos
- W Liou
- WA Cromlish
- Y Nakamura
- Y Romsicki
- Y Shibata
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2012
- Field of study
Protein-tyrosine phosphatase 1B (PTP1B) is a ubiquitously expressed PTP that is anchored to the endoplasmic reticulum (ER). PTP1B dephosphorylates activated receptor tyrosine kinases after endocytosis, as they transit past the ER. However, PTP1B also can access some plasma membrane (PM)-bound substrates at points of cell-cell contact. To explore how PTP1B interacts with such substrates, we utilized quantitative cellular imaging approaches and mathematical modeling of protein mobility. We find that the ER network comes in close proximity to the PM at apparently specialized regions of cell-cell contact, enabling PTP1B to engage substrate(s) at these sites. Studies using PTP1B mutants show that the ER anchor plays an important role in restricting its interactions with PM substrates mainly to regions of cell-cell contact. In addition, treatment with PTP1B inhibitor leads to increased tyrosine phosphorylation of EphA2, a PTP1B substrate, specifically at regions of cell-cell contact. Collectively, our results identify PM-proximal sub-regions of the ER as important sites of cellular signaling regulation by PTP1B
A Genome-Wide Association Study Identifies Susceptibility Variants for Type 2 Diabetes in Han Chinese
- Author
- AF Moore
- AJ Paige
- AK Bednarek
- AL Gloyn
- C Chouabe
- C Hu
- C Wang
- Cathy S. J. Fann
- CD Langefeld
- Chi-Fan Yang
- Chieh-Hsiang Lu
- Chien-Hsiun Chen
- Chih-Chun Chang
- Ching-Chu Chen
- Chiung-Fang Shiu
- Chwen-Tzuei Chang
- D Agnello
- D Altshuler
- D Iliopoulos
- D Meyre
- D Zhou
- DW Bowden
- E Zeggini
- E Zeggini
- EM Nielsen
- F Takeuchi
- Fuu-Jen Tsai
- G Bertrand
- H Unoki
- H Wolosker
- H Wolosker
- H Wolosker
- H Zouali
- HM Ledermann
- I Prokopenko
- J Barhanin
- J Batt
- J De Miranda
- J Gudmundsson
- J Imaki
- JA Maassen
- JC Florez
- Jer-Yuarn Wu
- JI Kim
- JM Ren
- JM Zabolotny
- JP Mothet
- K Imai
- K Kataoka
- K Ried
- K Xiang
- K Yasuda
- KM Boini
- L Ji
- Lee-Ming Chuang
- LJ Scott
- M Sakai
- M Sato
- M Stumvoll
- M Tsuchiya
- MC Casimiro
- MC Sanguinetti
- MJ Chagnon
- MJ Chagnon
- MP Lee
- MS Sandhu
- MS Serria
- N Bouatia-Naji
- N Inagaki
- N Neyroud
- N Uetani
- N Vionnet
- P An
- P Zimmet
- Pei Chen
- Peter M. Visscher
- Q Wang
- R Pulido
- R Saxena
- R Sladek
- RL Hanson
- Rong-Hsing Chen
- S Demolombe
- S Ghosh
- S Omori
- S Purcell
- S Ullrich
- S Wiltshire
- S Wright
- S Yendamuri
- SC Elbein
- SF Grant
- SS Fajans
- T Gonoi
- T Klupa
- T Kuroki
- T Kuroki
- T Ronn
- Tzu-Yuan Wang
- V Lyssenko
- V Steinthorsdottir
- W Winckler
- WC Hsueh
- WH Pan
- Y Gosmain
- Y Wu
- YC Chang
- YH Chen
- Yi-Min Liu
- Yuan-Tsong Chen
- Publication venue
- Public Library of Science
- Publication date
- 01/02/2010
- Field of study
To investigate the underlying mechanisms of T2D pathogenesis, we looked for diabetes susceptibility genes that increase the risk of type 2 diabetes (T2D) in a Han Chinese population. A two-stage genome-wide association (GWA) study was conducted, in which 995 patients and 894 controls were genotyped using the Illumina HumanHap550-Duo BeadChip for the first genome scan stage. This was further replicated in 1,803 patients and 1,473 controls in stage 2. We found two loci not previously associated with diabetes susceptibility in and around the genes protein tyrosine phosphatase receptor type D (PTPRD) (Pâ=â8.54Ă10â10; odds ratio [OR]â=â1.57; 95% confidence interval [CI]â=â1.36â1.82), and serine racemase (SRR) (Pâ=â3.06Ă10â9; ORâ=â1.28; 95% CIâ=â1.18â1.39). We also confirmed that variants in KCNQ1 were associated with T2D risk, with the strongest signal at rs2237895 (Pâ=â9.65Ă10â10; ORâ=â1.29, 95% CIâ=â1.19â1.40). By identifying two novel genetic susceptibility loci in a Han Chinese population and confirming the involvement of KCNQ1, which was previously reported to be associated with T2D in Japanese and European descent populations, our results may lead to a better understanding of differences in the molecular pathogenesis of T2D among various populations
CMS Data Processing Workflows during an Extended Cosmic Ray Run
- Author
- Abadjiev K
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdullin S
- Abelev B
- Acosta D
- Acosta JG
- Acosta MV
- Actis O
- Adam N
- Adam W
- Adams MR
- Adams T
- Adiguzel A
- Adler V
- Adolphi R
- Adzic P
- Afaq MA
- Agostino L
- Agram JL
- Aguilar-Benitez M
- Ahmad M
- Ahmad WH
- Ahmed I
- Ahmed W
- Ahuja S
- Aisa D
- Aisa S
- Akchurin N
- Akgun B
- Akgun U
- Akimenko S
- Akin IV
- Alagoz E
- Alampi G
- Albajar C
- Albayrak EA
- Alberdi J
- Albergo S
- Albert E
- Albrow M
- Alexander J
- Alidra M
- Aliev T
- Allfrey P
- Almeida N
- Altenhofer G
- Altsybeev I
- Alver B
- Alverson G
- Alves GA
- Amaglobeli N
- Amapane N
- Ambroglini F
- Amsler C
- Anagnostou G
- Ananthan B
- Anastassov A
- Andelin D
- Anderson M
- Andrea J
- Andreev V
- Andreev Y
- Anghel IM
- Anguelov T
- Anisimov A
- Antillon E
- Antipov P
- Antonelli L
- Anttila E
- Antunes JR
- Antunovic Z
- Apanasevich L
- Apollinari G
- Apresyan A
- Arce P
- Arcidiacono R
- Arenton MW
- Arfaei H
- Argiro S
- Arisaka K
- Arneodo M
- Arnold B
- Arora S
- Artamonov A
- Asaadi J
- Asghar MI
- Ashby S
- Askew A
- Atac M
- Atramentov O
- Auffray E
- Aurisano A
- Autermann C
- Avery P
- Avetisyan A
- Avila C
- Awan MIM
- Ayan AS
- Ayhan A
- Azhgirey I
- Aziz T
- Azzi P
- Azzurri P
- Baarmand MM
- Babb J
- Babucci E
- Baccaro S
- Bacchetta N
- Bacchi W
- Bachtis M
- Baden D
- Badgett W
- Baechler J
- Baer H
- Baesso P
- Baffioni S
- Bagby L
- Bagliesi G
- Bahk SY
- Bailleux D
- Baillon P
- Bainbridge R
- Bakhshiansohi H
- Bakirci MN
- Bakken JA
- Balazs M
- Baldin B
- Ball AH
- Ball G
- Ballin J
- Bally SL
- Ban Y
- Bandurin D
- Banerjee S
- Banerjee S
- Banicz K
- Bansal S
- Banzuzi K
- Barashko V
- Barbagli G
- Barberis E
- Barbone L
- Barcala JM
- Barcellan L
- Bard R
- Bargassa P
- Baringer P
- Barnes VE
- Barnett BA
- Barney D
- Barone L
- Bartalini P
- Bartoloni A
- Bartz E
- Basegmez S
- Battilana C
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- Yohay R
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- Zachariadou A
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- Zeidler C
- Zeinali M
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- Zelepoukine S
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- Publication venue
- INSTITUTE OF PHYSICS PUBLISHING
- Publication date
- 01/01/2009
- Field of study
Peer reviewe
Aligning the CMS Muon Chambers with the Muon Alignment System during an Extended Cosmic Ray Run
- Author
- Abadjiev K
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdullin S
- Abelev B
- Acosta D
- Acosta JG
- Acosta MV
- Actis O
- Adam N
- Adam W
- Adams MR
- Adams T
- Adiguzel A
- Adler V
- Adolphi R
- Adzic P
- Afaq MA
- Agostino L
- Agram JL
- Aguilar Benitez M
- Ahmad M
- Ahmad WH
- Ahmed I
- Ahmed W
- Ahuja S
- Aisa D
- Aisa S
- Akchurin N
- Akgun B
- Akgun U
- Akimenko S
- Akin IV
- Alagoz E
- Alampi G
- Albajar C
- Albayrak EA
- Alberdi J
- Albergo S
- Albert E
- Albrow M
- Alexander J
- Alidra M
- Aliev T
- Allfrey P
- Almeida N
- Altenhofer G
- Altsybeev I
- Alver B
- Alverson G
- Alves GA
- Amaglobeli N
- Amapane N
- Ambroglini F
- Amsler C
- Anagnostou G
- Ananthan B
- Anastassov A
- Andelin D
- Anderson M
- Andrea J
- Andreev V
- Andreev Y
- Anghel IM
- Anguelov T
- Anh T. Vu
- Anisimov A
- Antillon E
- Antipov P
- Antonelli L
- Anttila E
- Antunes JR
- Antunovic Z
- Apanasevich L
- Apollinari G
- Apresyan A
- Arce P
- Arcidiacono R
- Arenton MW
- Arfaei H
- Argiro S
- Arisaka K
- Arneodo M
- Arnold B
- Arora S
- Artamonov A
- Asaadi J
- Asghar MI
- Ashby S
- Askew A
- Atac M
- Atramentov O
- Auffray E
- Aurisano A
- Autermann C
- Avery P
- Avetisyan A
- Avila C
- Awan MIM
- Ayan AS
- Ayhan A
- Azhgirey I
- Aziz T
- Azzi P
- Azzurri P
- Baarmand MM
- Babb J
- Babucci E
- Baccaro S
- Bacchetta N
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- Badgett W
- Baechler J
- Baer H
- Baesso P
- Baffioni S
- Bagby L
- Bagliesi G
- Bahk SY
- Bailleux D
- Baillon P
- Bainbridge R
- Bakhshiansohi H
- Bakirci MN
- Bakken JA
- Balazs M
- Baldin B
- Ball AH
- Ball G
- Ballin J
- Bally SL
- Ban Y
- Bandurin D
- Banerjee S
- Banerjee S
- Banicz K
- Bansal S
- Banzuzi K
- Barashko V
- Barbagli G
- Barberis E
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- Belforte S
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- Bellan R
- Bellato M
- Bellinger JN
- Belotelov I
- Benaglia A
- Bencze G
- Bendavid J
- Bender W
- Benedetti D
- Benelli G
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- Beni N
- Benucci L
- Benussi L
- Benvenuti AC
- Berengueres JOL
- Beretvas A
- Bergauer H
- Bergauer T
- Beri SB
- Bernardini J
- Bernet C
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- Zoeller MH
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- Zumerle G
- Zuranski A
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- Publication venue
- Publication date
- 01/01/2009
- Field of study
Peer reviewe
Commissioning of the CMS high-level trigger with cosmic rays
- Author
- Abadjiev K
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdullin S
- Abelev B
- Acosta D
- Acosta JG
- Acosta MV
- Actis O
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- Waltenberger W
- Walton R
- Walzel G
- Wan Z
- Wang CC
- Wang D
- Wang J
- Wang M
- Wang Z
- Warchol J
- Wardrope D
- Washington E
- Watts TL
- Wayne M
- Weber M
- Weber M
- Wehrli L
- Weinberg M
- Weinberger M
- Wendland L
- Weng J
- Weng Y
- Wenger EA
- Wenman D
- Wensveen M
- Werner JS
- Wertelaers P
- Wetzel J
- White A
- Whitmore J
- Whyntie T
- Wickens J
- Wicklund E
- Widl E
- Wigmans R
- Wildish T
- Wilke L
- Wilken R
- Wilkinson R
- Williams G
- Williams JC
- Williams JH
- Willmott C
- Wimpenny S
- Wingham M
- Winn D
- Wissing C
- Witherell M
- Wittich P
- Wittmer B
- Wlochal M
- Wohri HK
- Wolf R
- Womersley WJ
- Won S
- Wood JS
- Worm SD
- Wright D
- Wrochna G
- Wu S
- Wu W
- Wulz CE
- Wurthwein F
- Wyslouch B
- Xie S
- Xie Z
- Xue Z
- Yagil A
- Yan M
- Yang X
- Yang Y
- Yang ZC
- Yarba J
- Yaselli I
- Yazgan E
- Yelton J
- Yetkin T
- Yi K
- Yilmaz Y
- Yohay R
- Yoo HD
- Yoon AS
- York A
- Yumiceva F
- Yun JC
- Yuste C
- Zabi A
- Zabolotny W
- Zachariadou A
- Zalewski P
- Zampieri A
- Zanetti M
- Zang SL
- Zarubin A
- Zatzerklyany A
- Zeidler C
- Zeinali M
- Zeise M
- Zelepoukine S
- Zeuner WD
- Zeyrek M
- Zhang J
- Zhang L
- Zhang Y
- Zhang Z
- Zheng Y
- Zhiltsov V
- Zhokin A
- Zhu B
- Zhu K
- Zhu RY
- Zhukov V
- Zhukova V
- Ziebarth EB
- Zielinski M
- Zilizi G
- Zinonos Z
- Zito G
- Zoeller MH
- Zotto P
- Zub S
- Zumerle G
- Zuranski A
- Zuyeuski R
- Zych P
- Publication venue
- 'IOP Publishing'
- Publication date
- 26/11/2009
- Field of study
This is the Pre-print version of the Article. The official published version of the paper can be accessed from the link below - Copyright @ 2010 IOPThe CMS High-Level Trigger (HLT) is responsible for ensuring that data samples with potentially interesting events are recorded with high efficiency and good quality. This paper gives an overview of the HLT and focuses on its commissioning using cosmic rays. The selection of triggers that were deployed is presented and the online grouping of triggered events into streams and primary datasets is discussed. Tools for online and offline data quality monitoring for the HLT are described, and the operational performance of the muon HLT algorithms is reviewed. The average time taken for the HLT selection and its dependence on detector and operating conditions are presented. The HLT performed reliably and helped provide a large dataset. This dataset has proven to be invaluable for understanding the performance of the trigger and the CMS experiment as a whole.This work is supported by FMSR (Austria); FNRS and FWO (Belgium); CNPq, CAPES, FAPERJ,
and FAPESP (Brazil); MES (Bulgaria); CERN; CAS, MoST, and NSFC (China); COLCIENCIAS
(Colombia); MSES (Croatia); RPF (Cyprus); Academy of Sciences and NICPB (Estonia);
Academy of Finland, ME, and HIP (Finland); CEA and CNRS/IN2P3 (France); BMBF, DFG, and HGF (Germany); GSRT (Greece); OTKA and NKTH (Hungary); DAE and DST (India); IPM (Iran); SFI (Ireland); INFN (Italy); NRF (Korea); LAS (Lithuania); CINVESTAV, CONACYT, SEP, and UASLP-FAI (Mexico); PAEC (Pakistan); SCSR (Poland); FCT (Portugal); JINR
(Armenia, Belarus, Georgia, Ukraine, Uzbekistan); MST and MAE (Russia); MSTDS (Serbia); MICINN and CPAN (Spain); Swiss Funding Agencies (Switzerland); NSC (Taipei); TUBITAK and TAEK (Turkey); STFC (United Kingdom); DOE and NSF (USA)
Transcriptional response of porcine skeletal muscle to feeding a linseed-enriched diet to growing pigs
- Author
- A Albers
- A Berger
- AA Gingras
- AI Saeed
- AN Gerber
- BJ Goldstein
- BN Finck
- C Li
- CJ Watson
- CP Velloso
- CT Lee
- CY Logan
- DB Jump
- DB Jump
- E Schothorst van
- EA Bryhni
- F Gu
- FR Huang
- G Dennis
- G Wu
- HF Luo
- J Lin
- JD Storey
- JE Reseland
- JM Zabolotny
- JT Leek
- K Bergeron
- KJ Livak
- KS Rhee
- LG Puskas
- M Enser
- M Gormley
- MJ Potthoff
- NH Le
- O Takase
- PP Tak
- RS Chapkin
- RV Sousa
- S Heikkinen
- S Tsai
- S Zheng
- SC Bodine
- T Matsuzaka
- TA Davis
- Y Wang
- Y Zhao
- ZP Zhan
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
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