389 research outputs found
Effective Rheology of Bubbles Moving in a Capillary Tube
- Author
- Abelev B
- Adam J
- Adamova D
- Adare AM
- Aggarwal MM
- Agocs AG
- Agostinelli A
- Ahammed Z
- Ahmad N
- Ahn SU
- Akindinov A
- Alaniz EC
- Aleksandrov D
- Alessandro B
- Alici A
- Alkin A
- Alme J
- Alt T
- Altini V
- Altinpinar S
- Altsybeev I
- Andrei C
- Andronic A
- Anguelov V
- Anielski J
- Anson C
- Anticic T
- Antinori F
- Antonioli P
- Aphecetche L
- Appelshauser H
- Arbor N
- Arcelli S
- Arend A
- Armesto N
- Arnaldi R
- Aronsson T
- Arsene IC
- Arslandok M
- Asryan A
- Augustinus A
- Averbeck R
- Avina EA
- Awes TC
- Aysto J
- Azmi MD
- Bach M
- Badala A
- Baek YW
- Bailhache R
- Baillie OV
- Bala R
- Balbastre GC
- Baldisseri A
- Baldit A
- Ban J
- Baral RC
- Barbera R
- Bari DD
- Barile F
- Barnafoldi GG
- Barnby LS
- Barret V
- Barros GOVD
- Barroso VC
- Bartke J
- Basile M
- Bastid N
- Bathen B
- Batigne G
- Batyunya B
- Baumann C
- Bearden IG
- Beck H
- Belikov I
- Bellini F
- Bellwied R
- Belmont-Moreno E
- Bencedi G
- Beole S
- Berceanu I
- Bercuci A
- Berdnikov Y
- Berenyi D
- Bergmann C
- Berzano D
- Betev L
- Bhasin A
- Bhati AK
- Bianchi L
- Bianchi N
- Bianchin C
- Bielcik J
- Bielcikova J
- Bjelogrlic S
- Blanco F
- Blanco F
- Blau D
- Blume C
- Boccioli M
- Bock N
- Bogdanov A
- Boggild H
- Bogolyubsky M
- Boldizsar L
- Bombara M
- Book J
- Borel H
- Borissov A
- Bornec YL
- Bose S
- Bossu F
- Botje M
- Bottger S
- Boyer B
- Braidot E
- Braun-Munzinger P
- Bregant M
- Breitner T
- Browning TA
- Broz M
- Brun R
- Bruna E
- Bruno GE
- Budnikov D
- Buesching H
- Bufalino S
- Bugaiev K
- Busch O
- Bustamante RTJ
- Buthelezi Z
- Caffarri D
- Cahuantzi MR
- Cai X
- Caines H
- Camerini P
- Carena F
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- Carminati F
- Caro AD
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- Casula EAR
- Cataldo GD
- Catanescu V
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- Cepila J
- Cerello P
- Cervantes IM
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- Charvet JL
- Chattopadhyay S
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- Chawla I
- Cherney M
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- Chiavassa E
- Chinellato DD
- Chochula P
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- Cicalo C
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- Cleymans J
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- Collaboration ALICE
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- Contreras JG
- Corchero MAD
- Cormier TM
- Corral GH
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- Cosentino MR
- Costa F
- Cotallo ME
- Crescio E
- Crochet P
- Cuautle E
- Cunqueiro L
- Cuveland JD
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- Dalsgaard HH
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- Davalos AM
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- Delagrange H
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- Denes E
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- Dietel T
- Divia R
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- Dominguez I
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- Driga O
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- Emschermann D
- Engel H
- Erasmo GD
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- Espagnon B
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- Evans D
- Eyyubova G
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- Tobon CAM
- Toia A
- Toledo ASD
- Torii H
- Torres EL
- Toscano L
- Tosello F
- Truesdale D
- Trzaska WH
- Tsuji T
- Tumkin A
- Turrisi R
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- Ulery J
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- Ulrich J
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- Urban J
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- Viesti G
- Vikhlyantsev O
- Vilakazi Z
- Villar EC
- Vinogradov A
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- Wessels JP
- Westerhoff U
- Wiechula J
- Wikne J
- Wilde M
- Wilk A
- Wilk G
- Williams MCS
- Windelband B
- Yang H
- Yang S
- Yasnopolskiy S
- Yi J
- Yin Z
- Yokoyama H
- Yoo IK
- Yoon J
- Yu W
- Yuan X
- Yushmanov I
- Zach C
- Zampolli C
- Zaporozhets S
- Zarochentsev A
- Zavada P
- Zaviyalov N
- Zbroszczyk H
- Zelnicek P
- Zetina LM
- Zgura IS
- Zhalov M
- Zhang X
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- Zhou Y
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- Zichichi A
- Zimmermann A
- Zinovjev G
- Zoccarato Y
- Zynovyev M
- Publication venue
- 'American Physical Society (APS)'
- Publication date
- 16/03/2012
- Field of study
We calculate the average volumetric flux versus pressure drop of bubbles
moving in a single capillary tube with varying diameter, finding a square-root
relation from mapping the flow equations onto that of a driven overdamped
pendulum. The calculation is based on a derivation of the equation of motion of
a bubble train from considering the capillary forces and the entropy production
associated with the viscous flow. We also calculate the configurational
probability of the positions of the bubbles.Comment: 4 pages, 1 figur
Defining Multiple Characteristic Raman Bands of α-Amino Acids as Biomarkers for Planetary Missions Using a Statistical Method
- Author
- A Culka
- A Culka
- A Culka
- A Pawlukojć
- AL Jenkins
- AP Johnson
- BM Auer
- CR Webster
- DA Long
- FR Dollish
- G Eglinton
- G Levin
- G Zhu
- HE Newsom
- HGM Edwards
- HGM Edwards
- I. Gilmour
- IL Kate ten
- J Aerts
- J Gelder De
- J Parnell
- JC Stern
- JR Cronin
- JR Ferraro
- JTL Navarrete
- K Kvenvolden
- K. Olsson-Francis
- KA Kvenvolden
- M. R. Patel
- MH Hecht
- MJ Matthews
- MTS Rosado
- P Dhamelincourt
- P Dhamelincourt
- P Ehrenfreund
- P Vandenabeele
- P Vítek
- R Navarro-González
- RP Vidano
- S Kumar
- S Kumar
- S. M. Rolfe
- SE Jorge Villar
- SM Mehrens
- T. J. Ringrose
- Z Suo
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2016
- Field of study
Biomarker molecules, such as amino acids, are key to discovering whether life exists elsewhere in the Solar System. Raman spectroscopy, a technique capable of detecting biomarkers, will be on board future planetary missions including the ExoMars rover. Generally, the position of the strongest band in the spectra of amino acids is reported as the identifying band. However, for an unknown sample, it is desirable to define multiple characteristic bands for molecules to avoid any ambiguous identification. To date, there has been no definition of multiple characteristic bands for amino acids of interest to astrobiology. This study examinedL-alanine, L-aspartic acid, L-cysteine, L-glutamine and glycine and defined several Raman bands per molecule for reference as characteristic identifiers. Per amino acid, 240 spectra were recorded and compared using established statistical tests including ANOVA. The number of characteristic bands defined were 10, 12, 12, 14 and 19 for L-alanine (strongest intensity band: 832 cm-1), L-aspartic acid (938 cm-1), L-cysteine (679 cm-1),L-glutamine (1090 cm−1) and glycine (875 cm-1), respectively. The intensity of bands differed by up to six times when several points on the crystal sample were rotated through 360 °; to reduce this effect when defining characteristic bands for other molecules, we find that spectra should be recorded at a statistically significant number of points per sample to remove the effect of sample rotation. It is crucial that sets of characteristic Raman bands are defined for biomarkers that are targets for future planetary missions to ensure a positive identification can be made
Identification of α(1,6)fucosylated proteins differentially expressed in human colorectal cancer
- Author
- A Varki
- Almudena Fernández-Briera
- B Campion
- CS Kaetzel
- D Osumi
- E Miyoshi
- Elisa Cuevas
- Emilio Gil-Martín
- F Geng
- H Nomura
- IL Ang
- IP Tomlinson
- JL Traicoff
- K Kobayashi
- L Muinelo-Romay
- L Muinelo-Romay
- Laura Muinelo-Romay
- M Heike
- MA Comunale
- MA Comunale
- ME Johansson
- N Harada
- N Kochibe
- N Okuyama
- N Uozumi
- N Yamashiki
- S Barrabes
- S Hakomori
- S Hammarstrom
- S Lee
- S Toyoshima
- SH Landis
- Susana Villar-Portela
- T Takahashi
- W Jia
- WL Hutchinson
- X Wang
- X Wang
- X Wang
- X Wang
- Y Chang
- Y Ito
- Y Mechref
- Y Yasui
- Y Zhao
- Z Dai
- Z Li
- Publication venue
- BioMed Central
- Publication date
- 01/01/2011
- Field of study
<p>Summary</p> <p>Background</p> <p>A universal hallmark of cancer cells is the change in their glycosylation phenotype. One of the most frequent alterations in the normal glycosylation pattern observed during carcinogenesis is the enhancement of α(1,6)linked fucose residues of glycoproteins, due to the up-regulation of the α(1,6)fucosyltransferase activity. Our previous results demonstrated the specific alteration of this enzyme activity and expression in colorectal cancer, suggesting its implication in tumour development and progression.</p> <p>Methods</p> <p>In the current work we combined a LCA-affinity chromatography with SDS-PAGE and mass spectrometry in order to identify α(1,6)fucosylated proteins differentially expressed in colorectal cancer. This strategy allowed the identification of a group of α(1,6)fucosylated proteins candidates to be involved in CRC malignancy.</p> <p>Results</p> <p>The majority of the identified proteins take part in cell signaling and interaction processes as well as in modulation of the immunological response. Likewise, we confirmed the increased expression of GRP94 in colorectal cancer tissue and the significant down-regulation of the IgGFcBP expression in tumour cells.</p> <p>Conclusion</p> <p>All these results validate the importance of <it>core-</it>fucosylated proteins profile analysis to understand the mechanisms which promote cancer onset and progression and to discover new tumour markers or therapeutic targets.</p
Why Are Clinicians Not Embracing the Results from Pivotal Clinical Trials in Severe Sepsis? A Bayesian Analysis
- Author
- AB Hill
- Adam J. Ratner
- AF Mackenzie
- AH Hamrahian
- Andre C. Kalil
- B Ellger
- B Goldstein
- BC Ho
- C De Block
- C Natanson
- CE Lucas
- CJ Gill
- CJ Wiedermann
- CJ Wiedermann
- CL Sprung
- CL Sprung
- D Annane
- D Annane
- DA Berry
- DJ Spiegelhalter
- DJ Spiegelhalter
- E Abraham
- E Rivers
- EA Toschlog
- F Abroug
- F Davidoff
- FE Harrell Jr
- FM Brunkhorst
- G de Durante
- G van den Berghe
- G Van den Berghe
- G Van den Berghe
- GA Diamond
- GD Rubenfeld
- GR Bernard
- GR Bernard
- GR Bernard
- GY Gandhi
- HS Warren
- I Alia
- I Mitchell
- IL Bennett
- J Briegel
- J Klastersky
- J Tuchschmidt
- J Villar
- JA Sterne
- JC Lacherade
- JD Ricard
- JL Petersen
- JM Brophy
- JM Luce
- JO Friedrich
- Junfeng Sun
- KJ Deans
- L Brochard
- L Gattinoni
- M Yu
- M Yu
- MA Hayes
- MB Amato
- MJ Schultz
- MJ Schultz
- MJ Tobin
- O Yildiz
- P Barton
- P Loisa
- PE Bollaert
- PE Marik
- PQ Eichacker
- PQ Eichacker
- PQ Eichacker
- PQ Eichacker
- PR Burton
- RC Bone
- RG Brower
- RG Brower
- RP Dellinger
- S Greenland
- S Nadel
- S Sarkar
- SB Clayton
- SM Lin
- SN Goodman
- SN Goodman
- SP LaRosa
- TE Stewart
- TM Vriesendorp
- V Siraux
- W Schumer
- W Xiao-zhi
- WL Thompson
- WS Browner
- Publication venue
- Public Library of Science
- Publication date
- 28/05/2008
- Field of study
BACKGROUND: Five pivotal clinical trials (Intensive Insulin Therapy; Recombinant Human Activated Protein C [rhAPC]; Low-Tidal Volume; Low-Dose Steroid; Early Goal-Directed Therapy [EGDT]) demonstrated mortality reduction in patients with severe sepsis and expert guidelines have recommended them to clinical practice. Yet, the adoption of these therapies remains low among clinicians. OBJECTIVES: We selected these five trials and asked: Question 1--What is the current probability that the new therapy is not better than the standard of care in my patient with severe sepsis? Question 2--What is the current probability of reducing the relative risk of death (RRR) of my patient with severe sepsis by meaningful clinical thresholds (RRR >15%; >20%; >25%)? METHODS: Bayesian methodologies were applied to this study. Odds ratio (OR) was considered for Question 1, and RRR was used for Question 2. We constructed prior distributions (enthusiastic; mild, moderate, and severe skeptic) based on various effective sample sizes of other relevant clinical trials (unfavorable evidence). Posterior distributions were calculated by combining the prior distributions and the data from pivotal trials (favorable evidence). MAIN FINDINGS: Answer 1--The analysis based on mild skeptic prior shows beneficial results with the Intensive Insulin, rhAPC, and Low-Tidal Volume trials, but not with the Low-Dose Steroid and EGDT trials. All trials' results become unacceptable by the analyses using moderate or severe skeptic priors. Answer 2--If we aim for a RRR>15%, the mild skeptic analysis shows that the current probability of reducing death by this clinical threshold is 88% for the Intensive Insulin, 62-65% for the Low-Tidal Volume, rhAPC, EGDT trials, and 17% for the Low-Dose Steroid trial. The moderate and severe skeptic analyses show no clinically meaningful reduction in the risk of death for all trials. If we aim for a RRR >20% or >25%, all probabilities of benefits become lower independent of the degree of skepticism. CONCLUSIONS: Our clinical threshold analysis offers a new bedside tool to be directly applied to the care of patients with severe sepsis. Our results demonstrate that the strength of evidence (statistical and clinical) is weak for all trials, particularly for the Low-Dose Steroid and EGDT trials. It is essential to replicate the results of each of these five clinical trials in confirmatory studies if we want to provide patient care based on scientifically sound evidence
The evolution of the macrophage-specific enhancer (Fms intronic regulatory element) within the CSF1R locus of vertebrates
- Author
- A Balic
- A Sandelin
- AC Li
- AD Buffry
- AD Friedman
- AW Jubb
- C Pridans
- C Pridans
- CP Martinez-Jimenez
- D Panne
- D Villar
- D Villar
- DA Hume
- ED Jarvis
- ET Dermitzakis
- EZ Kvon
- FG Jorgensen
- G Behre
- GA Follows
- H Tagoh
- IL Ross
- JH Levine
- K Lindblad-Toh
- KA Sauter
- KJ Stacey
- KS Moulton
- L Grayfer
- LF Fowles
- P Herbomel
- Q Chen
- R Rademakers
- R Rojo
- RP DeKoter
- RT Sasmono
- S Gallus
- S Heinz
- S Song
- SR Himes
- T Wang
- TH Pham
- V Chitu
- V Garceau
- X Yue
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/12/2017
- Field of study
The Csf1r locus encodes the receptor for macrophage colony-stimulating factor, which controls the proliferation, differentiation and survival of macrophages. The 300 bp Fms intronic regulatory element (FIRE), within the second intron of Csf1r, is necessary and sufficient to direct macrophage-specific transcription. We have analysed the conservation and divergence of the FIRE DNA sequence in vertebrates. FIRE is present in the same location in the Csf1r locus in reptile, avian and mammalian genomes. Nearest neighbor analysis based upon this element alone largely recapitulates phylogenies inferred from much larger genomic sequence datasets. One core element, containing binding sites for AP1 family and the macrophage-specific transcription factor, PU.1, is conserved from lizards to humans. Around this element, the FIRE sequence is conserved within clades with the most conserved elements containing motifs for known myeloid-expressed transcription factors. Conversely, there is little alignment between clades outside the AP1/PU.1 element. The analysis favours a hybrid between "enhanceosome" and "smorgasbord" models of enhancer function, in which elements cooperate to bind components of the available transcription factor milieu
Detection of occult hepatitis B in serum and oral fluid samples
- Author
- Bréchot C
- Carlos Eduardo Brandão-Mello
- Chen HY
- Coppola N
- Cristiane Alves Villela-Nogueira
- Elisabeth Lampe
- Geane Lopes Flores
- Heiberg IL
- José Henrique Pilotto
- Kidd-Ljunggren K
- Larrubia JR
- Leticia Cancella Nabuco
- Lia Laura Lewis-Ximenez
- Livia Melo Villar
- Maldonado-Rodríguez A
- Mallory MA
- Morsica G
- Moyra Machado Portilho
- Noppornpanth S
- Piroth L
- Portilho MM
- Raimondo G
- Squadrito G
- Tamura K
- Van der Ejik AA
- Zhang YL
- Publication venue
- 'FapUNIFESP (SciELO)'
- Publication date
- Field of study
K0S and Λ production in Pb-Pb collisions at sNN−−−−√=2.76 TeV
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- Abelev B
- Adam J.
- Adamovã¡ D.
- Adare A. M.
- Aggarwal M. M.
- Aglieri Rinella G.
- Agnello M.
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- Agostinelli A.
- Ahammed Z.
- Ahmad Masoodi A.
- Ahmad N.
- Ahmed I.
- Ahn S. A.
- Ahn S. U.
- Aimo I.
- Aiola S.
- Ajaz M.
- Akindinov A.
- Aleksandrov D.
- Alessandro B.
- Alexandre D.
- Alici A.
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- Alme J.
- Alt T.
- Altini V.
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- Altsybeev I.
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- Wang Y.
- Wang Y.
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- Watanabe K.
- Weber M.
- Wessels J. P.
- Westerhoff U.
- Wiechula J.
- Wikne J.
- Wilde M.
- Wilk G.
- Wilkinson J.
- Williams M. C. S.
- Windelband B.
- Winn M.
- Xiang C.
- Yaldo C. G.
- Yamaguchi Y.
- Yang H.
- Yang P.
- Yang S.
- Yano S.
- Yasnopolskiy S.
- Yi J.
- Yin Z.
- Yoo I. K.
- Yushmanov I.
- Zaccolo V.
- Zach C.
- Zampolli C.
- Zaporozhets S.
- Zarochentsev A.
- Zaviyalov N.
- Zbroszczyk H.
- Zelnicek P.
- Zgura I. S.
- Zhalov M.
- Zhang F.
- Zhang H.
- Zhang X.
- Zhang Y.
- Zhou D.
- Zhou F.
- Zhou Y.
- Zhu H.
- Zhu J.
- Zhu J.
- Zhu X.
- Zichichi A.
- Zimmermann A.
- Zimmermann M. B.
- Zinovjev G.
- Zoccarato Y.
- Zynovyev M.
- Zyzak M.
- Zã¡vada P.
- Å. afaåãk K.
- Å. umbera M.
- Å. ã¡ndor L.
- Publication venue
- 'American Physical Society (APS)'
- Publication date
- 01/01/2013
- Field of study
The ALICE measurement of K0S and Λ production at midrapidity in Pb-Pb collisions at sNN−−−√=2.76 TeV is presented. The transverse momentum (pT) spectra are shown for several collision centrality intervals and in the pT range from 0.4 GeV/c (0.6 GeV/c for Λ) to 12 GeV/c. The pT dependence of the Λ/K0S ratios exhibits maxima in the vicinity of 3 GeV/c, and the positions of the maxima shift towards higher pT with increasing collision centrality. The magnitude of these maxima increases by almost a factor of three between most peripheral and most central Pb-Pb collisions. This baryon excess at intermediate pT is not observed in pp interactions at s√=0.9 TeV and at s√=7 TeV. Qualitatively, the baryon enhancement in heavy-ion collisions is expected from radial flow. However, the measured pT spectra above 2 GeV/c progressively decouple from hydrodynamical-model calculations. For higher values of pT, models that incorporate the influence of the medium on the fragmentation and hadronization processes describe qualitatively the pT dependence of the Λ/K0S ratio
Charged-particle distributions at low transverse momentum in √s=13 13 TeV pp interactions measured with the ATLAS detector at the LHC
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- Zhemchugov A
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- Zieminska D
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- Zwalinski L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2016
- Field of study
Measurements of distributions of charged particles produced in proton–proton collisions with a centre-of-mass energy of 13 TeV are presented. The data were recorded by the ATLAS detector at the LHC and correspond to an integrated luminosity of 151 μb −1 μb−1 . The particles are required to have a transverse momentum greater than 100 MeV and an absolute pseudorapidity less than 2.5. The charged-particle multiplicity, its dependence on transverse momentum and pseudorapidity and the dependence of the mean transverse momentum on multiplicity are measured in events containing at least two charged particles satisfying the above kinematic criteria. The results are corrected for detector effects and compared to the predictions from several Monte Carlo event generators
Measurement of W+W− production in association with one jet in proton–proton collisions at sqrt(s) = 8TeV with the ATLAS detector
- Author
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- Youssef S
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- Zalieckas J
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- Zeitnitz C
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- Zhao Z
- Zhemchugov A
- Zhong J
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- Zhu CG
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- Zhuang X
- Zhukov K
- Zibell A
- Zieminska D
- Zimine NI
- Zimmermann C
- Zimmermann S
- Zinonos Z
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- Zoccoli A
- Zu Theenhausen HM
- zur Nedden M
- Zwalinski L
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2016
- Field of study
The production of W boson pairs in association with one jet in pp collisions at View the MathML sources=8 TeV is studied using data corresponding to an integrated luminosity of 20.3 fb−1 collected by the ATLAS detector during 2012 at the CERN Large Hadron Collider. The cross section is measured in a fiducial phase-space region defined by the presence of exactly one electron and one muon, missing transverse momentum and exactly one jet with a transverse momentum above 25 GeV and a pseudorapidity of |η|<4.5|η|<4.5. The leptons are required to have opposite electric charge and to pass transverse momentum and pseudorapidity requirements. The fiducial cross section is found to be View the MathML sourceσWWfid,1-jet=136±6(stat)±14(syst)±3(lumi) fb. In combination with a previous measurement restricted to leptonic final states with no associated jets, the fiducial cross section of WW production with zero or one jet is measured to be View the MathML sourceσWWfid,≤1-jet=511±9(stat)±26(syst)±10(lumi) fb. The ratio of fiducial cross sections in final states with one and zero jets is determined to be 0.36±0.050.36±0.05. Finally, a total cross section extrapolated from the fiducial measurement of WW production with zero or one associated jet is reported. The measurements are compared to theoretical predictions and found in good agreement
Measurement of the W±Z boson pair-production cross section in pp collisions at √s=13TeV with the ATLAS detector
- Author
- Aaboud M
- Aad G
- Abbott B
- Abdallah J
- Abdinov O
- Abeloos B
- Aben R
- AbouZeid OS
- Abraham NL
- Abramowicz H
- Abreu H
- Abreu R
- Abulaiti Y
- Acharya BS
- Adamczyk L
- Adams DL
- Adelman J
- Adomeit S
- Adye T
- Affolder AA
- Agatonovic-Jovin T
- Agricola J
- Aguilar-Saavedra JA
- Ahlen SP
- Ahmadov F
- Aielli G
- Akerstedt H
- Akesson TPA
- Akimov AV
- Alberghi GL
- Albert J
- Albrand S
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- Tapia Araya S
- Tapprogge S
- Tarem S
- Tartarelli GF
- Tas P
- Tasevsky M
- Tashiro T
- Tassi E
- Tavares Delgado A
- Tayalati Y
- Taylor AC
- Taylor GN
- Taylor PTE
- Taylor W
- Tehrani FS
- Teischinger FA
- Teixeira-Dias P
- Temming KK
- Temple D
- Ten Kate H
- Teng PK
- Teoh JJ
- Tepel F
- Terada S
- Terashi K
- Terron J
- Terzo S
- Testa M
- Teuscher J
- Theveneaux-Pelzer T
- Thomas JP
- Thomas-Wilsker J
- Thompson AS
- Thompson EN
- Thompson PD
- Thomsen LA
- Thomson E
- Thomson M
- Tibbetts MJ
- Tikhomirov VO
- Tikhonov YA
- Timoshenko S
- Tipton P
- Tisserant S
- Todome K
- Todorov T
- Todorova-Nova S
- Tojo J
- Tokar S
- Tokushuku K
- Tolley E
- Tomlinson L
- Tomoto M
- Tompkins L
- Toms K
- Tong B
- Toro RC
- Torregrosa EF
- Torrence E
- Torres H
- Torres RET
- Toth J
- Touchard F
- Tovey DR
- Trefzger T
- Tricoli A
- Trigger IM
- Trincaz-Duvoid S
- Tripiana MF
- Trischuk W
- Trocme B
- Trofymov A
- Troncon C
- Trottier-McDonald M
- Trovatelli M
- Truong L
- Trzebinski M
- Trzupek A
- Tseng JC-L
- Tsiareshka PV
- Tsipolitis G
- Tsirintanis N
- Tsiskaridze S
- Tsiskaridze V
- Tskhadadze EG
- Tsui KM
- Tsukerman II
- Tsulaia V
- Tsuno S
- Tsybychev D
- Tudorache A
- Tudorache V
- Tuna AN
- Tupputi SA
- Turchikhin S
- Turecek D
- Turgeman D
- Turra R
- Turvey AJ
- Tuts PM
- Tyndel M
- Ucchielli G
- Ueda I
- Ughetto M
- Ukegawa F
- Unal G
- Undrus A
- Unel G
- Ungaro FC
- Unno Y
- Unverdorben C
- Urban J
- Urquijo P
- Urrejola P
- Usai G
- Usanova A
- Vacavant L
- Vacek V
- Vachon B
- Valderanis C
- Valencic N
- Valentinetti S
- Valero A
- Valery L
- Valkar S
- Vallecorsa S
- Van den Wollenberg W
- Van der Deijl PC
- van der Geer R
- van der Graaf H
- van Eldik N
- van Gemmeren P
- Van Nieuwkoop J
- van Vulpen I
- van Woerden MC
- Vanadia M
- Vandelli W
- Vanguri R
- Vaniachine A
- Vankov P
- Vardanyan G
- Vari R
- Varnes EW
- Varol T
- Varouchas D
- Vartapetian A
- Varvell KE
- Vasquez JG
- Vazeille F
- Vazquez JGP
- Veatch J
- Veloce LM
- Veloso F
- Veneziano S
- Ventura A
- Venturi M
- Venturi N
- Venturini A
- Vercesi V
- Verducci M
- Verkerke W
- Vermeulen JC
- Vest A
- Vetterli MC
- Viazlo O
- Vichou I
- Vickey T
- Viehhauser GHA
- Viel S
- Vigani L
- Villa M
- Villar DIN
- Vilucchi E
- Vincter MG
- Vinogradov VB
- Vittori C
- Vivarelli I
- Vlachos S
- Vlasak M
- Vogel M
- Vokac P
- Volpi G
- Volpi M
- von der Schmitt H
- von Toerne E
- Vorobel V
- Vorobev K
- Vos M
- Voss R
- Vossebeld JH
- Vranjes N
- Vrba V
- Vreeswijk M
- Vuillermet R
- Vukotic I
- Vykydal Z
- Wagner P
- Wagner W
- Wahlberg H
- Wahrmund S
- Wakabayashi J
- Walder J
- Walker R
- Walkowiak W
- Wallangen V
- Walls FMG
- Wang C
- Wang C
- Wang F
- Wang H
- Wang H
- Wang J
- Wang J
- Wang K
- Wang R
- Wang SM
- Wang T
- Wang T
- Wang W
- Wang X
- Wanotayaroj C
- Warburton A
- Ward CP
- Wardrope DR
- Washbrook A
- Watkins PM
- Watson AT
- Watson MF
- Watts G
- Watts S
- Waugh BM
- Webb S
- Weber MS
- Weber SW
- Webster JS
- Weidberg AR
- Weinert B
- Weingarten J
- Weiser C
- Weits H
- Wells PS
- Wenaus T
- Wengler T
- Wenig S
- Wermes N
- Werner M
- Werner MD
- Werner P
- Wessels M
- Wetter J
- Whalen K
- Whallon NL
- Wharton AM
- White A
- White MJ
- White R
- Whiteson D
- Wickens FJ
- Wiedenmann W
- Wielers M
- Wienemann P
- Wiglesworth C
- Wiik-Fuchs LAM
- Wildauer A
- Wilk F
- Wilkens HG
- Williams HH
- Williams S
- Willis C
- Willocq S
- Wilson JA
- Wingerter-Seez I
- Winklmeier F
- Winston OJ
- Winter BT
- Wittgen M
- Wittkowski J
- Wolf TMH
- Wolter MW
- Wolters H
- Wong KHY
- Worm SD
- Wosiek BK
- Wotschack J
- Woudstra MJ
- Wozniak KW
- Wu M
- Wu M
- Wu SL
- Wu X
- Wu Y
- Wyatt TR
- Wynne BM
- Xella S
- Xu D
- Xu L
- Yabsley B
- Yacoob S
- Yakabe R
- Yamaguchi D
- Yamaguchi Y
- Yamamoto A
- Yamamoto S
- Yamanaka T
- Yamauchi K
- Yamazaki Y
- Yan Z
- Yang H
- Yang H
- Yang Y
- Yang Z
- Yao W-M
- Yap YC
- Yasu Y
- Yatsenko E
- Ye J
- Ye S
- Yeletskikh I
- Yen AL
- Yildirim E
- Yildiz HD
- Yorita K
- Yoshida R
- Yoshihara K
- Young C
- Young CJS
- Youssef S
- Yu DR
- Yu J
- Yu J
- Yu JM
- Yuan L
- Yuen SPY
- Yusuff I
- Zabinski B
- Zaidan R
- Zaitsev AM
- Zakharchuk N
- Zalieckas J
- Zaman A
- Zambito S
- Zanello L
- Zanzi D
- Zeitnitz C
- Zeman M
- Zemla A
- Zeng JC
- Zeng Q
- Zengel K
- Zenin O
- Zenis T
- Zerwas D
- Zhang D
- Zhang F
- Zhang G
- Zhang H
- Zhang J
- Zhang L
- Zhang R
- Zhang R
- Zhang X
- Zhang Z
- Zhao X
- Zhao Y
- Zhao Z
- Zhemchugov A
- Zhong J
- Zhou B
- Zhou C
- Zhou L
- Zhou L
- Zhou M
- Zhou N
- Zhu CG
- Zhu H
- Zhu J
- Zhu Y
- Zhuang X
- Zhukov K
- Zibell A
- Zieminska D
- Zimine NI
- Zimmermann C
- Zimmermann S
- Zinonos Z
- Zinser M
- Ziolkowski M
- Zivkovic L
- Zobernig G
- Zoccoli A
- Zu Theenhausen HM
- zur Nedden M
- Zwalinski L
- Publication venue
- Netherlands
- Publication date
- 01/01/2016
- Field of study
published_or_final_versio
- …