343 research outputs found
Azimuthal anisotropy of charged particles at high transverse momenta in PbPb collisions at sqrt(s[NN]) = 2.76 TeV
- Author
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdullin S
- Abdulsalam A
- Acosta D
- Acosta JG
- Acosta MV
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- Adam N
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- Winer BL
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- Winstrom L
- Wissing C
- Wittich P
- Wittmer B
- Woehri HK
- Wolf M
- Wolf R
- Womersley WJ
- Won S
- Wood D
- Wood J
- Wood JS
- Worm SD
- Wright D
- Wrochna G
- Wu W
- Wuerthwein F
- Wulz C-E
- Wyslouch B
- Xiao H
- Xie S
- Xu M
- Yagil A
- Yalvac M
- Yang F
- Yang M
- Yang Y
- Yang ZC
- Yazgan E
- Yelton J
- Yetkin T
- Yi K
- Yildirim E
- Yilmaz Y
- Yohay R
- Yoo HD
- Yoo J
- Yoon AS
- York A
- Yu I
- Yu SS
- Yumiceva F
- Yun JC
- Zabel J
- Zabi A
- Zablocki J
- Zaganidis N
- Zakaria M
- Zalewski P
- Zanetti M
- Zang J
- Zarubin A
- Zatserklyaniy A
- Zeinali M
- Zeise M
- Zeuner WD
- Zeyrek M
- Zhang J
- Zhang Z
- Zheng Y
- Zhokin A
- Zhu B
- Zhu RY
- Zhukov V
- Zhukova V
- Ziebarth EB
- Ziegler J
- Zielinski M
- Zito G
- Zotto P
- Zou W
- Zumerle G
- Zuranski A
- Publication venue
- 'American Physical Society (APS)'
- Publication date
- 01/01/2012
- Field of study
The azimuthal anisotropy of charged particles in PbPb collisions at
nucleon-nucleon center-of-mass energy of 2.76 TeV is measured with the CMS
detector at the LHC over an extended transverse momentum (pt) range up to
approximately 60 GeV. The data cover both the low-pt region associated with
hydrodynamic flow phenomena and the high-pt region where the anisotropies may
reflect the path-length dependence of parton energy loss in the created medium.
The anisotropy parameter (v2) of the particles is extracted by correlating
charged tracks with respect to the event-plane reconstructed by using the
energy deposited in forward-angle calorimeters. For the six bins of collision
centrality studied, spanning the range of 0-60% most-central events, the
observed v2 values are found to first increase with pt, reaching a maximum
around pt = 3 GeV, and then to gradually decrease to almost zero, with the
decline persisting up to at least pt = 40 GeV over the full centrality range
measured.Comment: Replaced with published version. Added journal reference and DO
X-ray emission from the Sombrero galaxy: discrete sources
- Author
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdullin S
- Acosta D
- Acosta JG
- Acosta MV
- Adam N
- Adam W
- Adams MR
- Adams T
- Adiguzel A
- Adler V
- Adzic P
- Agostino L
- Agram JL
- Aguilar-Benitez M
- Aguilo E
- Ahmad M
- Ahmad WH
- Ahmed I
- Ahuja S
- Akchurin N
- Akgun B
- Akgun U
- Akin IV
- Alagoz E
- Albajar C
- Albayrak EA
- Albergo S
- Albrow M
- Alexander J
- Aliev T
- Allfrey P
- Almeida N
- Alver B
- Alverson G
- Alves GA
- Amapane N
- Amsler C
- Anagnostou G
- Anastassov A
- Anderson J
- Anderson M
- Andrea J
- Andreev V
- Andreev V
- Andreev Y
- Andrews W
- Anghel IM
- Antonelli L
- Antunes JR
- Antunovic Z
- Apanasevich L
- Apollinari G
- Appelt E
- Aranyi A
- Arce P
- Arcidiacono R
- Arenton MW
- Arfaei H
- Argiro S
- Arisaka K
- Arneodo M
- Asaadi J
- Asghar MI
- Askew A
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- Atac M
- Atramentov O
- Attikis A
- Auffray E
- Autermann C
- Auzinger G
- Avery P
- Avetisyan A
- Awad A
- Azarkin M
- Azhgirey I
- Aziz T
- Azzi P
- Azzolini V
- Azzurri P
- Baarmand MM
- Babb J
- Bacchetta N
- Bachtis M
- Baden A
- Baesso P
- Baffioni S
- Bagliesi G
- Bai Y
- Baillon P
- Bainbridge R
- Bakhshiansohi H
- Bakirci MN
- Bakken JA
- Balazs M
- Ball AH
- Ball G
- Ballin J
- Ban Y
- Bandurin D
- Banerjee S
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- Banzuzi K
- Barbagli G
- Barberis E
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- Barnett BA
- Barney D
- Barone L
- Barrett M
- Bartalini P
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- Basegmez S
- Basso L
- Battilana C
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- Bauer J
- Bauerdick LAT
- Baumgartel D
- Baur U
- Bazterra VE
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- Beauceron S
- Beaudette F
- Beaupere N
- Bedjidian M
- Bedoya CF
- Behrenhoff W
- Behrens U
- Belforte S
- Beliy N
- Bell AJ
- Bell KW
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- Bellan P
- Bellan R
- Bellinger JN
- Belotelov I
- Belyaev A
- Benaglia A
- Bencze G
- Bendavid J
- Bender W
- Benedetti D
- Benelli G
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- Benucci L
- Benussi L
- Benvenuti AC
- Beretvas A
- Bergauer T
- Bergholz M
- Beri SB
- Bernardini J
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- Berryhill J
- Bertl W
- Berzano U
- Besancon M
- Besson A
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- Betts RR
- Beuselinck R
- Bhat PC
- Bhatnagar V
- Bhattacharya S
- Bhattacharya S
- Bhatti A
- Bialas W
- Bian JG
- Bianchini L
- Bianco S
- Biasini M
- Biino C
- Bilei GM
- Bilinskas MJ
- Bilki B
- Bilmis S
- Biselli A
- Bisello D
- Bitioukov S
- Blekman F
- Bloch D
- Bloch I
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- Bloom K
- Bluj M
- Blumenfeld B
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- Zumerle G
- Zuranski A
- Publication venue
- 'IOP Publishing'
- Publication date
- 01/01/2010
- Field of study
We present a study of discrete X-ray sources in and around the
bulge-dominated, massive Sa galaxy, Sombrero (M104), based on new and archival
Chandra observations with a total exposure of ~200 ks. With a detection limit
of L_X = 1E37 erg/s and a field of view covering a galactocentric radius of ~30
kpc (11.5 arcminute), 383 sources are detected. Cross-correlation with Spitler
et al.'s catalogue of Sombrero globular clusters (GCs) identified from HST/ACS
observations reveals 41 X-rays sources in GCs, presumably low-mass X-ray
binaries (LMXBs). We quantify the differential luminosity functions (LFs) for
both the detected GC and field LMXBs, whose power-low indices (~1.1 for the
GC-LF and ~1.6 for field-LF) are consistent with previous studies for
elliptical galaxies. With precise sky positions of the GCs without a detected
X-ray source, we further quantify, through a fluctuation analysis, the GC LF at
fainter luminosities down to 1E35 erg/s. The derived index rules out a
faint-end slope flatter than 1.1 at a 2 sigma significance, contrary to recent
findings in several elliptical galaxies and the bulge of M31. On the other
hand, the 2-6 keV unresolved emission places a tight constraint on the field
LF, implying a flattened index of ~1.0 below 1E37 erg/s. We also detect 101
sources in the halo of Sombrero. The presence of these sources cannot be
interpreted as galactic LMXBs whose spatial distribution empirically follows
the starlight. Their number is also higher than the expected number of cosmic
AGNs (52+/-11 [1 sigma]) whose surface density is constrained by deep X-ray
surveys. We suggest that either the cosmic X-ray background is unusually high
in the direction of Sombrero, or a distinct population of X-ray sources is
present in the halo of Sombrero.Comment: 11 figures, 5 tables, ApJ in pres
Performance of CMS muon reconstruction in pp collision events at sqrt(s) = 7 TeV
- Author
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdullin S
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- Acosta MV
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- Ciesielski R
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- Cipriano PMR
- Cirino G
- Cittolin S
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- Civinini C
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- Clement E
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- CMS Collaboration
- Cockerill DJA
- Codispoti G
- Colafranceschi S
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- Zumerle G
- Zuranski A
- Publication venue
- 'IOP Publishing'
- Publication date
- 01/01/2012
- Field of study
The performance of muon reconstruction, identification, and triggering in CMS
has been studied using 40 inverse picobarns of data collected in pp collisions
at sqrt(s) = 7 TeV at the LHC in 2010. A few benchmark sets of selection
criteria covering a wide range of physics analysis needs have been examined.
For all considered selections, the efficiency to reconstruct and identify a
muon with a transverse momentum pT larger than a few GeV is above 95% over the
whole region of pseudorapidity covered by the CMS muon system, abs(eta) < 2.4,
while the probability to misidentify a hadron as a muon is well below 1%. The
efficiency to trigger on single muons with pT above a few GeV is higher than
90% over the full eta range, and typically substantially better. The overall
momentum scale is measured to a precision of 0.2% with muons from Z decays. The
transverse momentum resolution varies from 1% to 6% depending on pseudorapidity
for muons with pT below 100 GeV and, using cosmic rays, it is shown to be
better than 10% in the central region up to pT = 1 TeV. Observed distributions
of all quantities are well reproduced by the Monte Carlo simulation.Comment: Replaced with published version. Added journal reference and DO
Performance of CMS muon reconstruction in pp collision events at sqrt(s) = 7 TeV
- Author
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdullin S
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- Acosta MV
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- Christiansen T
- Chuang SH
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- Clerbaux B
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- CMS Collaboration
- Cockerill DJA
- Codispoti G
- Colafranceschi S
- Colaleo A
- Cole JE
- Colino N
- Collard C
- Colling D
- Conetti S
- Contardo D
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- Conway J
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- Cooper SI
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- Cornelis T
- Correa Martins Junior M
- Cortezon EP
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- Costantini S
- Coughlan JA
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- Cuevas J
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- Czellar S
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- Da Costa EM
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- Sakuma T
- Sakumoto W
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- Shah MA
- Sharma A
- Sharma A
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- Sharma V
- Sharp P
- Sheldon P
- Shepherd-Themistocleous CH
- Shi X
- Shipkowski SP
- Shipsey I
- Shiu JG
- Shivpuri RK
- Shmatov S
- Shoaib M
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- Shreyber I
- Shukla P
- Shumeiko N
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- Silva P
- Silvers D
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- Sim KS
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- Singh SP
- Singovsky A
- Sinthuprasith T
- Sirois Y
- Siroli G
- Sirunyan AM
- Skhirtladze N
- Skuja A
- Slaunwhite J
- Smirnov I
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- Smith JG
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- Smith WH
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- Snigirev A
- Snoek H
- Snook B
- Snow GR
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- Soares MS
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- Solano A
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- Stein M
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- Stenson K
- Stephans GSF
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- Strauss J
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- Strobbe N
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- Suarez I
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- Sulak L
- Sulimov V
- Sultanov G
- Summers D
- Sumorok K
- Sumowidagdo S
- Sun W
- Sung K
- Surat UE
- Svintradze I
- Svyatkovskiy A
- Swanson J
- Swartz M
- Symonds P
- Szillasi Z
- Szleper M
- Sznajder A
- Tadel M
- Takahashi M
- Tali B
- Tambe N
- Tan P
- Tao J
- Tapper A
- Taroni S
- Tatarinov A
- Taurok A
- Tauscher L
- Taylor L
- Tcholakov V
- Teischinger F
- Temple J
- Tenchini R
- Teng H
- Teo WD
- Teodorescu L
- Teyssier D
- Thea A
- Theofilatos K
- Thiebaux C
- Thom J
- Thomas L
- Thomas S
- Thompson J
- Thomsen J
- Thyssen F
- Tiko A
- Timciuc V
- Tinti G
- Tiras E
- Titov M
- Tkaczyk S
- To W
- Toback D
- Tomalin IR
- Tomaszewska J
- Tonelli G
- Tonjes MB
- Tonwar SC
- Topakli H
- Topaksu AK
- Torassa E
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- Tourtchanovitch L
- Traczyk P
- Tran NV
- Travaglini R
- Trayanov R
- Treille D
- Triantis FA
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- Trocsanyi ZL
- Troendle D
- Troitsky S
- Tropiano A
- Troshin S
- Tsang KV
- Tschudi Y
- Tsirou A
- Tu Y
- Tucker J
- Tully C
- Tumasyan A
- Tuo S
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- Tuominiemi J
- Tuovinen E
- Tupputi S
- Turkewitz J
- Turner M
- Tuuva T
- Tuve C
- Twedt E
- Tytgat M
- Tyurin N
- Tzeng YM
- Ujvari B
- Ulmer KA
- Ungaro D
- Uplegger L
- Urscheler C
- Uvarov L
- Uzun D
- Uzunian A
- Vaandering EW
- Valdata M
- Valls N
- Valuev V
- Van Doninck W
- Van Haevermaet H
- Van Hove P
- Van Mechelen P
- Van Mulders P
- Van Onsem GP
- Van Remortel N
- Van Spilbeeck A
- Vander Velde C
- Vanelderen L
- Vanini S
- Vanlaer P
- Varela J
- Varelas N
- Vargas JER
- Vartak A
- Vasil'ev S
- Vaughan J
- Vavilov S
- Vazquez Valencia F
- Veelken C
- Veeraraghavan V
- Velasco M
- Velicanu D
- Velkovska J
- Ventura S
- Venturi A
- Verdier P
- Verdini PG
- Veres GI
- Vergili LN
- Vergili M
- Verwilligen P
- Verzetti M
- Veszpremi V
- Vesztergombi G
- Veverka J
- Vichoudis P
- Vidal R
- Vila I
- Vilar Cortabitarte R
- Villasenor-Cendejas LM
- Villella I
- Vinogradov A
- Virdee T
- Viret S
- Vischia P
- Vishnevskiy D
- Vitulo P
- Viviani C
- Vizan Garcia JM
- Vlasov E
- Vlimant JR
- Vodopiyanov I
- Vogel H
- Volkov A
- Volobouev I
- Volpe R
- Vorobiev I
- Vorobyev A
- Vorobyev A
- Voutilainen M
- Vuosalo C
- Vutova M
- Wagner P
- Wagner SR
- Wagner-Kuhr J
- Wakefield S
- Wallny R
- Walsh R
- Walsh S
- Waltenberger W
- Walzel G
- Wan Z
- Wang D
- Wang J
- Wang J
- Wang M
- Wang S
- Wang X
- Wang Z
- Wardle N
- Wardrope D
- Wasserbaech S
- Wayne M
- Weber H
- Weber HA
- Weber M
- Weber M
- Wehrli L
- Weiler T
- Weinberg M
- Wendland L
- Weng J
- Weng Y
- Wenger EA
- Werner JS
- West C
- Wetzel J
- Whitbeck A
- Whitmore J
- Whyntie T
- Wickens J
- Wickramage N
- Widl E
- Wigmans R
- Wilken R
- Wilkinson R
- Williams G
- Williams T
- Willmott C
- Wimpenny S
- Winn D
- Winstrom L
- Wissing C
- Wittich P
- Wittmer B
- Woehri HK
- Wolf M
- Wolf R
- Womersley WJ
- Won S
- Wood D
- Wood J
- Wood JS
- Worm SD
- Wright D
- Wrochna G
- Wu W
- Wuerthwein F
- Wulz C-E
- Wyslouch B
- Xiao H
- Xie S
- Xu M
- Yagil A
- Yalvac M
- Yang F
- Yang M
- Yang Y
- Yang ZC
- Yazgan E
- Yelton J
- Yetkin T
- Yi K
- Yildirim E
- Yilmaz Y
- Yohay R
- Yoo HD
- Yoo J
- Yoon AS
- York A
- Yu I
- Yu SS
- Yumiceva F
- Yun JC
- Zabel J
- Zabi A
- Zablocki J
- Zaganidis N
- Zakaria M
- Zalewski P
- Zanetti M
- Zang J
- Zang SL
- Zarubin A
- Zatserklyaniy A
- Zeinali M
- Zeise M
- Zeuner WD
- Zeyrek M
- Zhang J
- Zhang Z
- Zheng Y
- Zhokin A
- Zhu B
- Zhu RY
- Zhukov V
- Zhukova V
- Ziebarth EB
- Ziegler J
- Zielinski M
- Zito G
- Zoeller MH
- Zotto P
- Zou W
- Zumerle G
- Zuranski A
- Publication venue
- 'IOP Publishing'
- Publication date
- 01/01/2012
- Field of study
The performance of muon reconstruction, identification, and triggering in CMS
has been studied using 40 inverse picobarns of data collected in pp collisions
at sqrt(s) = 7 TeV at the LHC in 2010. A few benchmark sets of selection
criteria covering a wide range of physics analysis needs have been examined.
For all considered selections, the efficiency to reconstruct and identify a
muon with a transverse momentum pT larger than a few GeV is above 95% over the
whole region of pseudorapidity covered by the CMS muon system, abs(eta) < 2.4,
while the probability to misidentify a hadron as a muon is well below 1%. The
efficiency to trigger on single muons with pT above a few GeV is higher than
90% over the full eta range, and typically substantially better. The overall
momentum scale is measured to a precision of 0.2% with muons from Z decays. The
transverse momentum resolution varies from 1% to 6% depending on pseudorapidity
for muons with pT below 100 GeV and, using cosmic rays, it is shown to be
better than 10% in the central region up to pT = 1 TeV. Observed distributions
of all quantities are well reproduced by the Monte Carlo simulation.Comment: Replaced with published version. Added journal reference and DO
Statistical analysis and molecular dynamics simulations of ambivalent α -helices
- Author
- A Chakrabartty
- AG Murzin
- B Rost
- BH Zim
- BI Cohen
- CA Kim
- CJ Jeffery
- CK Smith
- CM Carr
- DA Case
- DLJ Minor
- DLJ Minor
- DV Waterhous
- FC Bernstein
- G Wang
- H Kim
- H Tidow
- HJC Berendsen
- IB Kuznetsov
- J Guo
- J Guo
- JP Ryckaert
- JW Kelly
- K Abel
- KA Dill
- KF Han
- KT O'Neil
- L Zhong
- LC James
- LC James
- LC James
- LC Serpell
- M Blaber
- M Mezei
- Nicholus Bhattacharjee
- P Argos
- Parbati Biswas
- PC Lyu
- PY Chou
- PY Chou
- R Cerpa
- RB Best
- S Dalal
- S Padmanabhan
- SD Copley
- SE Blondelle
- SJ Hua
- T Darden
- TP Creamer
- U Hobohm
- V Hornak
- V Munoz
- W Kabsch
- W Kabsch
- WZ Yang
- X Zhou
- Publication venue
- BioMed Central
- Publication date
- 01/01/2010
- Field of study
Structural Annotation of Mycobacterium tuberculosis Proteome
- Author
- AG Murzin
- Anshu Bhardwaj
- AS Konagurthu
- B Huang
- B Huang
- B Wallner
- C Colovos
- C Vogel
- C Vogel
- CC Huang
- CH Tung
- CK Wu
- CT Porter
- CT Porter
- D Cozzetto
- D Cozzetto
- D Eramian
- Denis Dupuy
- DT Jones
- F Mancia
- F Melo
- H Berman
- I Kumagai
- IN Shindyalov
- J Pillardy
- J Qian
- JA Barker
- JC Camus
- JK Murray
- JM Lew
- K Henrick
- K Yeturu
- Kalidas Yeturu
- KG Tina
- L Bordoli
- LA Kelley
- LJ McGuffin
- MY Shen
- N Eswar
- Nagasuma Chandra
- O Olakanmi
- P Mereghetti
- Praveen Anand
- R Apweiler
- R Sanchez
- RA Laskowski
- RA Laskowski
- RA Laskowski
- Raghu Bhagavat
- Roman Laskowski
- Samir K. Brahmachari
- Sandhya Sankaran
- SE Brenner
- SF Altschul
- SF Altschul
- SK Burley
- SR Connell
- ST Cole
- Sumanta Mukherjee
- TA Dailey
- TR Ioerger
- U Pieper
- V Carbone
- W Hinrichs
- Y Chen
- Y Kalidas
- Y Loewenstein
- YI Wolf
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2011
- Field of study
Of the ∼4000 ORFs identified through the genome sequence of Mycobacterium tuberculosis (TB) H37Rv, experimentally determined structures are available for 312. Since knowledge of protein structures is essential to obtain a high-resolution understanding of the underlying biology, we seek to obtain a structural annotation for the genome, using computational methods. Structural models were obtained and validated for ∼2877 ORFs, covering ∼70% of the genome. Functional annotation of each protein was based on fold-based functional assignments and a novel binding site based ligand association. New algorithms for binding site detection and genome scale binding site comparison at the structural level, recently reported from the laboratory, were utilized. Besides these, the annotation covers detection of various sequence and sub-structural motifs and quaternary structure predictions based on the corresponding templates. The study provides an opportunity to obtain a global perspective of the fold distribution in the genome. The annotation indicates that cellular metabolism can be achieved with only 219 folds. New insights about the folds that predominate in the genome, as well as the fold-combinations that make up multi-domain proteins are also obtained. 1728 binding pockets have been associated with ligands through binding site identification and sub-structure similarity analyses. The resource (http://proline.physics.iisc.ernet.in/Tbstructuralannotation), being one of the first to be based on structure-derived functional annotations at a genome scale, is expected to be useful for better understanding of TB and for application in drug discovery. The reported annotation pipeline is fairly generic and can be applied to other genomes as well
Comprehensive Structural and Substrate Specificity Classification of the Saccharomyces cerevisiae Methyltransferome
- Author
- A Bernsel
- A Hoglund
- A Kudlicki
- A Marchler-Bauer
- A Niewmierzycka
- A Pierleoni
- AG Murzin
- Andrzej Dziembowski
- Andrzej Kudlicki
- B Seraphin
- BP Tu
- C Martin
- C Saveanu
- CH Wade
- Christos A. Ouzounis
- CK Yang
- CS Chow
- CT Walsh
- CW Carreras
- D Piekna-Przybylska
- DJ Anderson
- DT Jones
- E de Castro
- E Gasteiger
- EC Thompson
- EM Gustilo
- HL Schubert
- HL Schubert
- HM Berman
- J Franke
- J Hansen
- J Mouaikel
- Jan Kutner
- JE Katz
- JM Cherry
- Joanna Towpik
- K Ginalski
- K Ginalski
- K Ginalski
- K Subbaramaiah
- K Tarassov
- KJ Webb
- KJ Webb
- Krzysztof Ginalski
- L Kall
- Leszek Rychlewski
- Lukasz Knizewski
- M Arai
- M Delorenzi
- MA Brown
- Maga Rowicka
- MD Rose
- MJ Clancy
- MM Dixon
- MT McCammon
- O Emanuelsson
- P Horton
- PK Chiang
- RD Finn
- RL Tatusov
- RM Anderson
- RS Lipson
- S Dunin-Horkawicz
- S Shuman
- SC Dillon
- SF Altschul
- T Jenuwein
- T Kiss
- T Kodaki
- T Petrossian
- TC Petrossian
- Tomasz Wlodarski
- V Anantharaman
- WK Paik
- X Cheng
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2011
- Field of study
Methylation is one of the most common chemical modifications of biologically active molecules and it occurs in all life forms. Its functional role is very diverse and involves many essential cellular processes, such as signal transduction, transcriptional control, biosynthesis, and metabolism. Here, we provide further insight into the enzymatic methylation in S. cerevisiae by conducting a comprehensive structural and functional survey of all the methyltransferases encoded in its genome. Using distant homology detection and fold recognition, we found that the S. cerevisiae methyltransferome comprises 86 MTases (53 well-known and 33 putative with unknown substrate specificity). Structural classification of their catalytic domains shows that these enzymes may adopt nine different folds, the most common being the Rossmann-like. We also analyzed the domain architecture of these proteins and identified several new domain contexts. Interestingly, we found that the majority of MTase genes are periodically expressed during yeast metabolic cycle. This finding, together with calculated isoelectric point, fold assignment and cellular localization, was used to develop a novel approach for predicting substrate specificity. Using this approach, we predicted the general substrates for 24 of 33 putative MTases and confirmed these predictions experimentally in both cases tested. Finally, we show that, in S. cerevisiae, methylation is carried out by 34 RNA MTases, 32 protein MTases, eight small molecule MTases, three lipid MTases, and nine MTases with still unknown substrate specificity
Prodepth: Predict Residue Depth by Support Vector Regression Approach from Protein Sequences Only
- Author
- A Pintar
- A Pintar
- A Pintar
- A Schlessinger
- A Schlessinger
- A Schlessinger
- A Schlessinger
- A Shrake
- AG Murzin
- AR Kinjo
- AR Kinjo
- Ashley M. Buckle
- B Lee
- B Rost
- B Rost
- B Rost
- C Chothia
- CK Smith
- D Baker
- D Varrazzo
- D Xie
- DT Jones
- DT Jones
- E Schmitt
- EM Marcotte
- F Ferre
- G Pollastri
- Geoffrey I. Webb
- GP Raghava
- H Chen
- H Zhang
- H Zhou
- Hao Tan
- HM Berman
- J Cheng
- J Cheng
- J Qiu
- J Song
- J Song
- J Song
- J Song
- J Wan
- James C. Whisstock
- JC Whisstock
- Jiangning Song
- JJ Ward
- JM Chandonia
- JU Bowie
- K Bajaj
- K Chen
- K Vlahovicek
- Khalid Mahmood
- L Kurgan
- LA Kurgan
- M Connolly
- M Kumar
- M Lee
- M Stout
- ME Lacombe-Harvey
- MK Kalita
- MN Nguyen
- O Schueler-Furman
- P Radivojac
- RG Coleman
- Ruby H. P. Law
- S Ahmad
- S Chakravarty
- S Liu
- S Miller
- Sean David Mooney
- SF Altschul
- T Hamelryck
- T Ishida
- T Joachims
- T Noguchi
- Tatsuya Akutsu
- TL Blundell
- V Vapnik
- V Vapnik
- W Kabsch
- W Liu
- W Zhang
- WL DeLano
- X Wang
- Y Bromberg
- Y Kalidas
- Y Ofran
- Y Ofran
- Z Yuan
- Z Yuan
- ZX Wang
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2009
- Field of study
Residue depth (RD) is a solvent exposure measure that complements the information provided by conventional accessible surface area (ASA) and describes to what extent a residue is buried in the protein structure space. Previous studies have established that RD is correlated with several protein properties, such as protein stability, residue conservation and amino acid types. Accurate prediction of RD has many potentially important applications in the field of structural bioinformatics, for example, facilitating the identification of functionally important residues, or residues in the folding nucleus, or enzyme active sites from sequence information. In this work, we introduce an efficient approach that uses support vector regression to quantify the relationship between RD and protein sequence. We systematically investigated eight different sequence encoding schemes including both local and global sequence characteristics and examined their respective prediction performances. For the objective evaluation of our approach, we used 5-fold cross-validation to assess the prediction accuracies and showed that the overall best performance could be achieved with a correlation coefficient (CC) of 0.71 between the observed and predicted RD values and a root mean square error (RMSE) of 1.74, after incorporating the relevant multiple sequence features. The results suggest that residue depth could be reliably predicted solely from protein primary sequences: local sequence environments are the major determinants, while global sequence features could influence the prediction performance marginally. We highlight two examples as a comparison in order to illustrate the applicability of this approach. We also discuss the potential implications of this new structural parameter in the field of protein structure prediction and homology modeling. This method might prove to be a powerful tool for sequence analysis
Clustering of disulfide-rich peptides provides scaffolds for hit discovery by phage display: application to interleukin-23
- Author
- A Gupta
- AD de Araujo
- AE Nixon
- AG Murzin
- AG Poth
- AG Poth
- AJ Lembo
- Andrej Sali
- AP Silverman
- Ashok Bhandari
- B Pan
- CA Orengo
- Charles S. Craik
- CJ White
- CK Wang
- CTT Wong
- D Fass
- David T. Barkan
- DJ Craik
- DS King
- EAB Undheim
- ES Lovelace
- F Zoller
- G Batoni
- GRS Hartig
- Herodion Celino
- J Li
- JJ Smith
- JL Dutton
- JM Berg
- JM Mas
- JP Tam
- K Fosgerau
- L Niederreiter
- LT Nguyen
- M Rubinstein
- MA Starovasnik
- Mark L. Smythe
- MJP de Vega
- MT Dohm
- NJ Skelton
- P D’haeseleer
- PA Hollander
- PK Pallaghy
- PY Muller
- R Rauck
- R Tonikian
- R Yu
- RJ Clark
- RR Thangudu
- S Cheek
- S Henikoff
- S Luckett
- S Ranganath
- S-G Chang
- Schrodinger
- The UniProt Consortium
- Tran T. Tran
- TT Tran
- V Alva
- WDF Meutermans
- Xiao-li Cheng
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Recommended from our members
Search for neutral MSSM Higgs bosons decaying to a pair of tau leptons in pp collisions
- Author
- Abbaneo D. Cv
- Abbiendi G. Bc
- Abbrescia M. Bb
- Abdullin S. Dz
- Abdulsalam A. Ax
- Acosta D. Ea
- Acosta J. G. En
- Adair A. Ey
- Adam W. B
- Adams M. R. Ee
- Adams T. Ec
- Adiguzel A. Dc
- Adler V. G
- Adzic P. Cq
- Afanasiev S. Ci
- Agapitos A. Ao
- Agram J. L. ad
- Ahmad A. Cf
- Ahmad M. Cf
- Ahuja S. Av
- Akchurin N. Fe
- Akgun B. Ey
- Akin I. V. Dd
- Albajar C. Cs
- Albayrak E. A. Ef
- Albergo S. Bd
- Albrow M. Dz
- Alcaraz Maestre J. Cr
- Aldaya Martin M. Al
- Alderweireldt S. D
- Aleksandrov A. M
- Alexander J. Dx
- Alimena J. Do
- Alverson G. Eq
- Alves G. A. J
- Amapane N. Bo
- Amsler C. Cy
- Anagnostou G. An
- Anastassov A. Er
- Anderson J. Dz
- Andrea J. Ad
- Andreev V. Cn
- Andreev Y. Cl
- Andrews W. Ds
- Androsov K. Bm
- Antonelli L. Et
- Antunovic Z. S
- Apanasevich L. Ee
- Apollinari G. Dz
- Appelt E. Ff
- Apresyan A. Du
- Apyan A. El
- Arcidiacono R. Bo
- Arenton M. W. Fg
- Argiro S. Bo
- Arneodo M. Bo
- Arora S. Fb
- Asavapibhop B. Db
- Asawatangtrakuldee C. P
- Asin I. Ak
- Askew A. Ec
- Aslanoglou X. Ap
- Assran Y. W
- Ata M. Ai
- Attikis A. U
- Aubin A. Ad
- Auffray E. Cv
- Autermann C. Ah
- Auzinger G. Cv
- Avdeeva E. Eo
- Avery P. Ea
- Avetisyan A. Dn
- Avila C. Q
- Azarkin M. Cn
- Azhgirey I. Cp
- Aziz T. Ay
- Azzi P. Bj
- Azzolini V. Dv
- Azzurri P. Bm
- Baarmand M. M. Ed
- Babb J. Dr
- Baber M. Dj
- Bacchetta N. Bj
- Bachmair F. Cx
- Bachtis M. Cv
- Baden A. Ek
- Baffioni S. Ac
- Bagliesi G. Bm
- Baillon P. Cv
- Bainbridge R. Dj
- Bakhshiansohi H. Az
- Bakirci M. N. Dc
- Ball A. H. Cv
- Ban Y. P
- Banerjee S. Aw
- Banerjee S. Ay
- Bansal M. D
- Bansal S. D
- Barbagli G. Be
- Barberis E. Eq
- Barbieri R. El
- Barbone L. Bb
- Barfuss A. F. Ei
- Bargassa P. Ci
- Barge D. Dt
- Baringer P. Eh
- Barker A. Fb
- Barnes V. E. Ew
- Barnett B. A. Eg
- Barney D. Cv
- Barone L. Bn
- Barth C. Am
- Bartosik N. Ak
- Basegmez S. H
- Battilana C. Cr
- Bauer G. El
- Bauerdick L. A. T. Dz
- Baumgartel D. Eq
- Baus C. Am
- Bayshev I. Cp
- Bazterra V. E. Ee
- Bean A. Eh
- Beauceron S. Af
- Beaudette F. Ac
- Beaupere N. Af
- Beernaert K. G
- Behnamian H. Az
- Behr J. Ak
- Behrenhoff W. Ak
- Behrens U. Ak
- Beirão Da Cruz E. Silva C. Ci
- Belforte S. Bp
- Beliy N. I
- Belknap D. A. Fi
- Bell A. J. Ak
- Bell K. W. Di
- Bellan R. Bo
- Bellato M. Bj
- Belloni A. Ek
- Beluffi C. H
- Belyaev A. Co
- Belyaev A. Di
- Benaglia A. Cv
- Bencze G. Aq
- Bendavid J. Cv
- Benedetti D. Ew
- Benelli G. Eh
- Benhabib L. Cv
- Beni N. Ar
- Benitez J. F. Cv
- Benucci L. G
- Benussi L. Bf
- Benvenuti A. C. Bc
- Beranek S. Ah
- Beretvas A. Dz
- Bergauer T. B
- Berger J. Am
- Bergholz M. Ak
- Beri S. B. Au
- Bernardes C. A. L
- Bernardini J. Bm
- Bernet C. Cv
- Berry D. Ee
- Berry E. Do
- Berryhill J. Dz
- Bertl W. Cw
- Besancon M. Ab
- Betchart B. Ez
- Bethani A. Ak
- Betts R. R. Ee
- Bhardwaj A. Av
- Bhat P. C. Dz
- Bhatnagar V. Au
- Bhattacharya S. Aw
- Bhattacharya S. Do
- Bhawandeep U. Au
- Bhowmik S. Ay
- Bialkowska H. Cg
- Bian J. G. O
- Bianchi G. Cv
- Bianchini L. Cx
- Bianco S. Bf
- Biasini M. Bl
- Biasotto M. Bj
- Biino C. Bo
- Bilei G. M. Bl
- Bilin B. Dd
- Bilki B. Ef
- Bilmis S. Dd
- Bitioukov S. Cp
- Blekman F. E
- Blobel V. Al
- Bloch D. Ad
- Bloch P. Cv
- Bloom K. Eo
- Bluj M. Cg
- Blumenfeld B. Eg
- Blyweert S. E
- Boccali T. Bm
- Bocci A. Cv
- Bochenek J. Ec
- Bodek A. Ez
- Bodlak M. V
- Boimska B. Cg
- Bolla G. Ew
- Bolognesi S. Eg
- Bonacorsi D. Bc
- Bonato A. Cv
- Bondu O. Cv
- Bontenackels M. Ah
- Boos E. Co
- Bornheim A. Du
- Borras K. Ak
- Bortignon P. Cx
- Bortoletto D. Ew
- Bose S. Eo
- Bose T. Dn
- Botta C. Cv
- Boudoul G. Af
- Bouhali O. Fd
- Bourilkov D. Ea
- Boutle S. Fg
- Bouvier E. Af
- Bradmiller Feld J. Dt
- Braibant Giacomelli S. Bc
- Branca A. Bj
- Branson J. G. Ds
- Breedon R. Dp
- Breto G. Dp
- Breuker H. Cv
- Brew C. Di
- Brigliadori L. Bc
- Brigljevic V. T
- Brinkerhoff A. Es
- Brinson J. Et
- Brito L. J
- Broccolo G. Bm
- Brochero Cifuentes J. A. Cu
- Brochet S. Af
- Brodski M. Ai
- Brom J. M. ad
- Brona G. Ch
- Brooke J. J. Dh
- Brown R. M. Di
- Brownson E. Ev
- Brun H. Ct
- Bruner C. Eh
- Bruno G. H
- Buchmann M. A. Cx
- Buchmuller O. Dj
- Bucinskaite I. Ee
- Bunin P. Cj
- Bunkowski K. Ch
- Bunn J. Du
- Buontempo S. Bi
- Burgmeier A. Ak
- Burkett K. Dz
- Burt K. Dr
- Burton D. Dj
- Busson P. Ac
- Busza W. El
- Butler J. N. Dz
- Butler P. H. Ce
- Butz E. Am
- Bylsma B. Et
- Bäni L. Cx
- Böser C. Am
- Cabrillo I. J. Cu
- Caebergs T. I
- Caillol C. F
- Caiulo D. Bm
- Cakir A. Ak
- Calabria C. Bb
- Calamba A. Dv
- Calderon De La Barca Sanchez M. Dp
- Calderon A. Cu
- Cali I. A. El
- Calligaris L. Ak
- Calvert B. Ek
- Calvo E. Cr
- Campagnari C. Dt
- Campanini R. Bc
- Campbell A. Ak
- Camporesi T. Cv
- Candelise V. Bp
- Canelli M. F. Cy
- Cankocak K. Df
- Capiluppi P. Bc
- Cappello G. Bd
- Cardaci M. Cz
- Carlsmith D. Fi
- Carlson B. Dv
- Carrillo Montoya C. A. Af
- Carrillo Moreno S. Ca
- Cartiglia N. Bo
- Carvalho W. K
- Carver M. Ea
- Casal B. Cx
- Casarsa M. Bp
- Casasso S. Bo
- Casimiro Linares E. Cc
- Castaldi R. Bm
- Castello R. H
- Castilla Valdez H. Bz
- Castro A. Bc
- Caudron A. H
- Cavallari F. Bn
- Cavallo F. R. Bc
- Cavallo N. Bi
- Cavanaugh R. Ee
- Ceard L. H
- Centis Vignali M. Al
- Cepeda M. Fi
- Cerati G. B. Ds
- Cerci S. Dc
- Cerminara G. Cv
- Cerrada M. Cr
- Chabert E. C. Ad
- Chakaberia I. Ei
- Chamizo Llatas M. Cr
- Chan K. M. Es
- Chan M. El
- Chang P. Da
- Chang S. Bq
- Chang Y. H. Da
- Chang Y. W. Da
- Chanon N. Cx
- Chao Y. Da
- Chaparro Sierra L. F. Q
- Charaf O. Dm
- Charlot C. Ac
- Chasco M. Eq
- Chasserat J. Af
- Chatterjee A. Dx
- Chatterjee K. Aw
- Chatterjee R. M. Ay
- Chauhan S. Dp
- Chen G. M. O
- Chen H. S. O
- Chen K. F. Da
- Chen K. H. Cz
- Chen M. O
- Chen P. H. Da
- Chen Y. Du
- Cheng T. Ea
- Cherepanov V. Aj
- Chertok M. Dp
- Cheung H. W. K. Dz
- Chhibra S. S. Bb
- Chierici R. Af
- Chinellato J. K
- Chiochia V. Cy
- Chiorboli M. Bd
- Chlebana F. Dz
- Choi M. Bv
- Choi S. Bu
- Choi Y. Bw
- Choi Y. K. Bw
- Chou J. P. Fb
- Choudhary B. C. Av
- Choudhury S. Ak
- Christopher G. Do
- Chu J. Dx
- Chwalek T. Am
- Ciangottini D. Bl
- Ciesielski R. Fa
- Cihangir S. Dz
- Cimmino A. G
- Ciocci M. A. Bm
- Cittolin S. Ds
- Ciulli V. Be
- Civinini C. Be
- Claes D. R. Eo
- Clare R. Dr
- Clarida W. Ef
- Clarke C. Fg
- Clement E. Dh
- Clerbaux B. F
- Cockerill D. J. A. Di
- Codispoti G. Bc
- Colafranceschi S. Cv
- Colaleo A. Bb
- Cole J. E. Dk
- Colino N. Cr
- Collard C. Ad
- Colling D. Dj
- Contardo D. Af
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- Contreras Campana C. Fb
- Contreras Campana E. Fb
- Conway J. Dp
- Conway R. Dp
- Cooper S. I. Dm
- Cornelis T. D
- Correa Martins Junior M. J
- Cossutti F. Bp
- Costa M. Bo
- Costa S. Bd
- Costantini S. G
- Costanza F. Ak
- Couderc F. Ab
- Coughlan J. A. Di
- Cousins R. Dq
- Covarelli R. Ez
- Cowden C. Fe
- Cox B. Fg
- Cox P. T. Dp
- Creanza D. Bb
- Cremaldi L. M. En
- Cripps N. Dj
- Crucy S. G
- Cuevas J. Ct
- Cuffiani M. Bc
- Cumalat J. P. Dw
- Curry D. Ea
- Cussans D. Dh
- Custódio A. K
- Cutajar M. Dj
- Cutts D. Do
- Cwiok M. Ch
- Czellar S. Ar
- Da Costa E. M. K
- Da Silveira G. G. H
- Dabrowski A. Cv
- Daci N. E
- Dahmes B. Em
- Dahms T. Ac
- Dalchenko M. Ac
- Dallavalle G. M. Bc
- Dall’Osso M. Bj
- Damgov J. Fe
- Danielson T. Dt
- Das S. Ea
- Daskalakis G. An
- Dasu S. Fi
- Daubie E. I
- Dauncey P. Dj
- David A. Cv
- Davies G. Dj
- de Barbaro P. Ez
- De Benedetti A. Em
- De Boer W. Am
- De Cosa A. Cy
- De Filippis N. Bb
- De Gruttola M. Ea
- De Guio F. Cv
- De Jesus Damiao D. K
- De La Cruz Burelo E. Bz
- De La Cruz B. Cr
- De Lentdecker G. F
- De Mattia M. Ew
- De Oliveira Martins C. K
- De Palma M. Bb
- De Roeck A. Cv
- de Trocóniz J. F. Cs
- De Visscher S. Cv
- De Wolf E. A. D
- Degano A. Bo
- Deisher A. Cx
- Deiters K. Cw
- Dejardin M. Ab
- Del Re D. Bn
- Delaere C. H
- Delannoy A. G. Ff
- Delgado Peris A. Cr
- Della Negra M. Dj
- Della Ricca G. Bp
- Dell’Orso R. Bm
- Demaria N. Bo
- Demina R. Ez
- Demiragli Z. Do
- Demortier L. Fa
- Denegri D. Ab
- Depasse P. Af
- Dermenev A. Cl
- Descroix A. Am
- Dewanjee R. K. Ay
- Dhingra N. Do
- Di Giovanni G. P. Ea
- Di Guida S. Bi
- Di Marco E. Du
- Di Matteo L. El
- Diamond B. Ec
- Diemoz M. Bn
- Dierlamm A. Am
- Dietz Laursonn E. Ai
- Dietz C. Da
- Diez Pardos C. Ak
- Dildick S. G
- Dilsiz K. Ef
- Dimitrov A. N
- Dinardo M. E. Bh
- Dishaw A. Dt
- Dissertori G. Cx
- Dittmann J. Dl
- Dittmar M. Cx
- Dittmer S. Dx
- Dobrzynski L. Ac
- Dobson M. Cv
- Dobur D. F
- Dodd L. Fi
- Dogra S. L
- Dolen J. Ep
- Dominguez A. Eo
- Dominik W. Ch
- Domínguez Vázquez D. Cr
- Donato S. Bm
- Donegà M. Cx
- Dooling S. Ak
- Dordevic M. Cv
- Dorigo T. Bj
- Dorland T. Ak
- Doroba K. Ch
- Dosselli U. Bj
- Dozen C. Dc
- Draeger A. R. Al
- Dragicevic M. B
- Dragoiu C. Fe
- Dremin I. Cn
- Driga O. Eu
- Drozdetskiy A. Es
- du Pree T. H
- Du R. O
- Duarte Campderros J. Cu
- Duarte J. Du
- Duchardt D. Ai
- Dudero P. R. Fe
- Dugad S. Ay
- Duggan D. Fb
- Dumanoglu I. Dc
- Dunne P. Dj
- Dupont Sagorin N. Cv
- Duric S. Fi
- Durkin L. S. Et
- Duru F. Ef
- Dutta D. Ax
- Dutta S. Aw
- Dutta V. El
- Dünser M. Cx
- D’Agnolo R. T. Ds
- D’Alessandro R. Be
- D’Alfonso M. Cv
- D’Enterria D. Cv
- D’Hondt J. E
- D’Imperio G. Bn
- Eckerlin G. Ak
- Ecklund K. M. Ey
- Eckstein D. Ak
- Edelhoff M. Ah
- Eerola P. Y
- Eggert N. Dx
- Eichhorn T. Ak
- Ekmedzic M. Cq
- El Mamouni H. Af
- Eller P. Cx
- Elliott Peisert A. Cv
- Ellison J. Dr
- Elmer P. Eu
- Elvira V. D. Dz
- Eno S. C. Ek
- Epshteyn V. Cm
- Erbacher R. Dp
- Erdmann M. Ai
- Erdmann W. Cw
- Erdogan Y. Aj
- Erfle J. Al
- Ershov A. Co
- Erö J. B
- Escalante Del Valle A. Cr
- Eshaq Y. Ez
- Eskut E. Dc
- Etesami S. M. Az
- Eugster J. Cv
- Eusebi R. Fd
- Evangelou I. Ap
- Evans D. Ds
- Evdokimov O. Ee
- Everaerts P. Dq
- Fabbri F. Bc
- Fabbri F. Bf
- Fabbro B. Ab
- Fabjan C. B
- Fabozzi F. Bi
- Faccioli P. Ci
- Fagot A. G
- Fahim A. Az
- Fan J. Af
- Fanfani A. Bc
- Fantasia C. Dn
- Fanò L. Bl
- Farrell C. Dq
- Fasanella D. Bc
- Faulkner J. Fe
- Faure J. L. Ab
- Favaro C. Ab
- Favart D. H
- Favart L. F
- Fay J. Af
- Fedi G. Y
- Fehling D. Eg
- Feindt M. Am
- Felcini M. Ba
- Feld L. Ah
- Ferapontov A. Do
- Ferbel T. Ez
- Ferencek D. Fb
- Ferguson T. Dv
- Ferguson W. Dj
- Fernandez Bedoya C. Cr
- Fernandez Menendez J. Ct
- Fernandez Perez Tomei T. R. L
- Fernandez M. Cu
- Fernández Ramos J. P. Cr
- Ferreira Parracho P. G. Ci
- Ferri F. Ab
- Ferro C. Cz
- Ferro F. Bg
- Field R. D. Ea
- Filipovic N. Ac
- Finco L. Bo
- Finger M.
- Finger M. V
- Fiore L. Bb
- Fiorendi S. Bh
- Fiori F. Bm
- Fischer R. Ai
- Fisher M. Ea
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- Flix J. Cr
- Florent A. Ac
- Florez C. Q
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- Focardi E. Be
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- Fonseca De Souza S. K
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- Forthomme L. H
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- Franzoni G. Cv
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- Friis E. Fi
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- Frühwirth R. B
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- Gabusi M. Bk
- Gadrat S. Ae
- Galanti M. Bj
- Gallinaro M. Ci
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- Gamsizkan H. Dd
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- Ganjour S. Ab
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- Garabedian A. Do
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- Garcia G. G
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- Gaz A. Dw
- Geenen H. Aj
- Geffert P. Dt
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- Geisler M. Aj
- Gelé D. Ad
- Genchev V. M
- Gennai S. Bh
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- Giakoumopoulou V. A. An
- Giammanco A. H
- Giassi A. Bm
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- Giubilato P. Bj
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- Godinovic N. R
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- Granier de Cassagnac R. Ac
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- Heredia de La Cruz I. Bz
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- Horvath D. Aq
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- Justus C. Dt
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- Kalogeropoulos A. Ak
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- Khan W. A. Cf
- Kharchilava A. Ep
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- Suarez I. Fd
- Sudano E. Ds
- Sudhakar K. Ay
- Sudic L. T
- Sulak L. Dn
- Sulimov V. Ck
- Sultanov G. M
- Summers D. En
- Sumorok K. El
- Sumowidagdo S. Dr
- Sun W. Dx
- Sunar Cerci D. Dc
- Sung K. Er
- Surat U. E. Dd
- Suwonjandee N. Db
- Svintradze I. Ei
- Svyatkovskiy A. Ew
- Swain S. K. At
- Swanson J. Do
- Swartz M. Eg
- Symonds P. Dk
- Szillasi Z. Ar
- Szleper M. Cg
- Sznajder A. K
- Tabarelli de Fatis T. Bh
- Tadel M. Ds
- Takahashi M. Cx
- Takahashi Y. Cv
- Takasugi E. Dq
- Tali B. Dc
- Talvitie J. Aa
- Tambe N. Em
- Tamponi U. Bo
- Tan P. Ef
- Tao J. O
- Tapper A. Dj
- Taroni S. Cy
- Tatarinov A. Fd
- Taurok A. B
- Tavernier S. E
- Taylor L. Dz
- Tcholakov V. M
- Tenchini R. Bm
- Teo W. D. Dx
- Teodorescu L. Dk
- Teyssier D. Ai
- Thea A. Di
- Theofilatos K. Cx
- Thom J. Dx
- Thomas L. F
- Thomas S. Fb
- Thomassen P. Fb
- Thompson J. Dx
- Thyssen F. G
- Thüer S. Ai
- Tiko A. X
- Timciuc V. Du
- Tiras E. Ef
- Titov M. Ab
- Tkaczyk S. Dz
- Tlisov D. Cl
- To W. Dt
- Tomalin I. R. Di
- Tonelli Manganote E. J. K
- Tonelli G. Bm
- Tonjes M. B. Ek
- Tonwar S. C. Ek
- Topakli H. Dc
- Topkar A. Ax
- Topsis Giotis I. An
- Torassa E. Bj
- Toropin A. Cl
- Tosi M. Bj
- Tosi N. Bc
- Tosi S. Bg
- Tourtchanovitch L. Cp
- Traczyk P. Bn
- Tran N. V. Dz
- Travaglini R. Bc
- Treberer Treberspurg W. B
- Treille D. Cv
- Tricomi A. Bd
- Trioss A. Bj
- Tripathi M. Dp
- Trocino D. Eq
- Trocsanyi Z. L. As
- Troendle D. Al
- Tropiano A. Be
- Troshin S. Cp
- Tsamalaidze Z. Ag
- Tsirou A. Cv
- Tu Y. Ds
- Tucker J. Dx
- Tully C. Eu
- Tumasyan A. A
- Tuo S. Ff
- Tuominen E. Z
- Tuominiemi J. Z
- Tuovinen E. Z
- Turkewitz J. Em
- Turner M. Dk
- Turner P. Ee
- Tuuva T. Aa
- Tuve C. Bd
- Tytgat M. G
- Tyurin N. Cp
- Tzeng Y. M. Da
- Ujvari B. As
- Ulmer K. A. Dw
- Ulrich R. Am
- Umer T. Bp
- Uplegger L. Dz
- Usai E. Al
- Uvarov L. Ck
- Uzunian A. Cp
- Vaandering E. W. Dz
- Valls N. Es
- Valuev V. Dq
- Van De Klundert M. D
- Van Doninck W. E
- Van Haevermaet H. D
- Van Hove P. Ad
- Van Mechelen P. D
- Van Mulders P. E
- Van Onsem G. P. E
- Van Remortel N. D
- Van Spilbeeck A. D
- Vander Donckt M. Af
- Vander Velde C. F
- Vanelderen L. Al
- Vanini S. Bj
- Vanlaer P. F
- Vardarlı F. I. Df
- Varela J. Ci
- Varelas N. Ee
- Vargas Trevino A. D. R. Ak
- Vartak A. Ds
- Vavilov S. Ck
- Vazquez Acosta M. Dj
- Vazquez Valencia F. Ca
- Veelken C. Ac
- Veeraraghavan V. Ec
- Velasco M. Er
- Velicanu D. El
- Velkovska J. Ff
- Venditti R. Bb
- Ventura S. Bj
- Venturi A. Bm
- Verdier P. Af
- Verdini P. G. Bm
- Veres G. I. Cv
- Vergili M. Dc
- Vernieri C. Bm
- Verwilligen P. Bb
- Verzetti M. Cy
- Veszpremi V. Aq
- Vesztergombi G. Aq
- Veverka J. El
- Vidal Marono M. H
- Vidal R. Dz
- Vila I. Cu
- Vilar Cortabitarte R. Cu
- Vilela Pereira A. K
- Villella I. E
- Vinogradov A. Cn
- Virdee T. Dj
- Viret S. Af
- Vischia P. Ci
- Vishnevskiy D. Ez
- Vitulo P. Bk
- Vizan Garcia J. M. H
- Vlasov E. Cm
- Vlimant J. R. Cv
- Vogel H. Dv
- Volkov A. Cp
- Volobouev I. Fe
- Volpe R. Cz
- Vorobiev I. Dv
- Vorobyev A. Ck
- Vorobyev A. Ck
- Voutilainen M. Y
- Vuosalo C. Fi
- Vutova M. M
- Wagner Kuhr J. Am
- Wagner S. R. Dw
- Walker M. Fb
- Wallny R. Cx
- Walsh R. Ak
- Waltenberger W. B
- Wang D. P
- Wang F. Ew
- Wang J. F
- Wang Q. Eh
- Wang R. J. eq
- Wang X. O
- Wang Z. O
- Wardle N. Cv
- Wayand S. Am
- Wayne M. Es
- Weber H. A. Cx
- Weber H. Ah
- Weber M. Ai
- Weber M. Dq
- Weiler T. Am
- Weinberg M. Ec
- Welke C. Ds
- Wendland L. Z
- Weng Y. Dx
- Werner J. S. Eu
- West C. Dt
- Wetzel J. Ef
- Whitbeck A. Dz
- Whitmore J. Dz
- Wickramage N. Ay
- Wilbur S. Dp
- Wilken R. Da
- Wilkinson R. Du
- Williams T. Dh
- Wimpenny S. Dr
- Winer B. L. Et
- Winn D. Dy
- Winstrom L. Dx
- Wissing C. Ak
- Wittich P. Dx
- Wittmer B. Ah
- Wolf M. Es
- Wolf R. Am
- Wolfe H. Et
- Wollny H. Cv
- Wolszczak W. Ch
- Womersley W. J. Di
- Won S. Er
- Wood D. Eq
- Wood J. Fg
- Wood J. S. Eh
- Woodard A. Es
- Woods N. Fi
- Worm S. D. Di
- Wright D. Ej
- Wulsin H. W. Et
- Wulz C. E. b
- Wyslouch B. El
- Wöhri H. K. Cv
- Würthwein F. Ds
- Xiao H. Af
- Xie S. Du
- Xie W. Ew
- Xu L. Ew
- Yagil A. Ds
- Yalvac M. Dd
- Yang F. Dz
- Yang M. El
- Yang Y. Cy
- Yazgan E. G
- Yelton J. Ea
- Yetkin T. Ef
- Yi K. Ef
- Yilmaz Y. Ac
- Yohay R. Dp
- Yoo H. D. Ew
- Yoo J. Ds
- Yoon A. S. El
- York A. Fc
- Yu I. Bw
- Yu S. S. Cz
- Yumiceva F. Ed
- Zabel J. Ey
- Zabi A. Ac
- Zablocki J. Ew
- Zaganidis N. G
- Zakaria M. Ea
- Zalewski P. Cg
- Zanetti A. Bp
- Zanetti M. El
- Zarubin A. Cj
- Zeinali M. Az
- Zenz S. C. Dj
- Zeuner W. D. Cv
- Zeyrek M. Dd
- Zhang J. Eq
- Zhang L. P
- Zheng Y. Ew
- Zhokin A. Cm
- Zhu R. Y. Du
- Zhukov V. Ah
- Zhukova V. El
- Zito G. Bb
- Zotto P. Bj
- Zou W. P
- Zsigmond A. J. Aq
- Zucchetta A. Bj
- Zuranski A. Eu
- Publication venue
- Publication date
- 01/01/2014
- Field of study
Peer reviewe
- …