103 research outputs found
Association of dental enamel lead levels with risk factors for environmental exposure
- Author
- Berglund M
- Browder AA
- Brudevold F
- Brudevold F
- Chiodo LM
- Cleymaet R
- de Freitas CU
- Dietrich KN
- Etelvino José Henriques Bechara
- Gomes VE
- Grosse SD
- Hollingshead AB
- Juliana Naozuka
- Kelly Polido Kaneshiro Olympio
- Landrigan PJ
- Levin R
- Machado PAL
- Maria Regina Alves Cardoso
- Needleman HL
- Olympio KPK
- Olympio KPK
- Pedro Vitoriano Oliveira
- Rhoads GG
- Saper RB
- Wanda Maria Risso Günther
- Weiss B
- Wright JP
- Publication venue
- 'FapUNIFESP (SciELO)'
- Publication date
- Field of study
Prodrug converting enzyme gene delivery by L. monocytogenes
- Author
- Aladar A Szalay
- B Huang
- BE Huber
- BJ Park
- BW Hughes
- C Grillot-Courvalin
- C Kocks
- CU Riedel
- D Niculescu-Duvaz
- DI Löffler
- EJ Sorscher
- EL White
- F McCormick
- F Schoensiegel
- G Dietrich
- I Peter
- J Stritzker
- J Stritzker
- JA Vazquez-Boland
- Jochen Stritzker
- K Miki
- M Hense
- M Rauch
- NG Rainov
- P Erbs
- P Glaser
- R Martiniello-Wilks
- R Singh
- RG Vile
- RG Vile
- RJ Critchley
- S Pilgrim
- Sabine Pilgrim
- SH Landis
- UK Laemmli
- VK Gadi
- WB Parker
- WB Parker
- Werner Goebel
- WM Siders
- YA Yu
- Publication venue
- BioMed Central
- Publication date
- 01/01/2008
- Field of study
<p>Abstract</p> <p>Background</p> <p><it>Listeria monocytogenes </it>is a highly versatile bacterial carrier system for introducing protein, DNA and RNA into mammalian cells. The delivery of tumor antigens with the help of this carrier into tumor-bearing animals has been successfully carried out previously and it was recently reported that <it>L. monocytogenes </it>is able to colonize and replicate within solid tumors after local or even systemic injection.</p> <p>Methods</p> <p>Here we report on the delivery of two prodrug converting enzymes, purine-deoxynucleoside phosphorylase (PNP) and a fusion protein consisting of yeast cytosine deaminase and uracil phosphoribosyl transferase (FCU1) into cancer cells in culture by <it>L. monocytogenes</it>. Transfer of the prodrug converting enzymes was achieved by bacterium mediated transfer of eukaryotic expression plasmids or by secretion of the proteins directly into the host cell cytosol by the infecting bacteria.</p> <p>Results</p> <p>The results indicate that conversion of appropriate prodrugs to toxic drugs in the cancer cells occured after both procedures although <it>L. monocytogenes</it>-mediated bactofection proved to be more efficient than enzyme secretion 4T1, B16 and COS-1 tumor cells. Exchanging the constitutively P<sub>CMV</sub>-promoter with the melanoma specific P<sub>4xTETP</sub>-promoter resulted in melanoma cell-specific expression of the prodrug converting enzymes but reduced the efficiencies.</p> <p>Conclusion</p> <p>These experiments open the way for bacterium mediated tumor specific activation of prodrugs in live animals with tumors.</p
Jet energy measurement with the ATLAS detector in proton-proton collisions at root s=7 TeV
- Author
- Aad G
- Abbott B
- Abdallah J
- Abdelalim AA
- Abdesselam A
- Abdinov O
- Abi B
- Abolins M
- Abramowicz H
- Abreu H
- Acerbi E
- Acharya BS
- Adams DL
- Addy TN
- Adelman J
- Aderholz M
- Adomeit S
- Adragna P
- Adye T
- Aefsky S
- Aguilar-Saavedra JA
- Aharrouche M
- Ahlen SP
- Ahles F
- Ahmad A
- Ahsan M
- Aielli G
- Akdogana T
- Akesson TPA
- Akimoto G
- Akimov AV
- Akiyama A
- Aktas A
- Alam MA
- Alam MS
- Albert J
- Albrand S
- Aleksa M
- Aleksandrov IN
- Alessandria F
- Alexa C
- Alexander G
- Alexandre G
- Alexopoulos T
- Alhroob M
- Aliev M
- Alimonti G
- Alison J
- Aliyev M
- Allport PP
- Allwood-Spiers SE
- Almenar CC
- Almond J
- Aloisio A
- Alon R
- Alonso A
- Alviggi MG
- Amako K
- Amaral P
- Amelung C
- Ammosov VV
- Amorim A
- Amoros G
- Amram N
- Anastopoulos C
- Ancu LS
- Andari N
- Andeen T
- Anders CF
- Anders G
- Anderson KJ
- Andreazza A
- Andrei V
- Andrieux M-L
- Anduaga XS
- Angerami A
- Anghinolfi F
- Anh TV
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- Antonaki A
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- Antonov A
- Antos J
- Anulli F
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- Apolle R
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- Aracena I
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- Aranda CP
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- Archambault JP
- Arfaoui S
- Arguin J-F
- Arik E
- Arik M
- Armbruster AJ
- Arnaez O
- Arnault C
- Artamonov A
- Artoni G
- Arutinov D
- Asai S
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- Aubert B
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- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/03/2013
- Field of study
The jet energy scale and its systematic uncertainty are determined for jets measured with the ATLAS detector at the LHC in proton-proton collision data at a centre-of-mass energy of √s = 7TeV corresponding to an integrated luminosity of 38 pb-1. Jets are reconstructed with the anti-kt algorithm with distance parameters R=0. 4 or R=0. 6. Jet energy and angle corrections are determined from Monte Carlo simulations to calibrate jets with transverse momenta pT≥20 GeV and pseudorapidities {pipe}η{pipe}<4. 5. The jet energy systematic uncertainty is estimated using the single isolated hadron response measured in situ and in test-beams, exploiting the transverse momentum balance between central and forward jets in events with dijet topologies and studying systematic variations in Monte Carlo simulations. The jet energy uncertainty is less than 2. 5 % in the central calorimeter region ({pipe}η{pipe}<0. 8) for jets with 60≤pT<800 GeV, and is maximally 14 % for pT<30 GeV in the most forward region 3. 2≤{pipe}η{pipe}<4. 5. The jet energy is validated for jet transverse momenta up to 1 TeV to the level of a few percent using several in situ techniques by comparing a well-known reference such as the recoiling photon pT, the sum of the transverse momenta of tracks associated to the jet, or a system of low-pT jets recoiling against a high-pT jet. More sophisticated jet calibration schemes are presented based on calorimeter cell energy density weighting or hadronic properties of jets, aiming for an improved jet energy resolution and a reduced flavour dependence of the jet response. The systematic uncertainty of the jet energy determined from a combination of in situ techniques is consistent with the one derived from single hadron response measurements over a wide kinematic range. The nominal corrections and uncertainties are derived for isolated jets in an inclusive sample of high-pT jets. Special cases such as event topologies with close-by jets, or selections of samples with an enhanced content of jets originating from light quarks, heavy quarks or gluons are also discussed and the corresponding uncertainties are determined. © 2013 CERN for the benefit of the ATLAS collaboration
Measurement of the inclusive and dijet cross-sections of b-jets in pp collisions at sqrt(s) = 7 TeV with the ATLAS detector
- Author
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- zur Nedden M
- Zutshi V
- Zwalinski L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 31/12/2010
- Field of study
The inclusive and dijet production cross-sections have been measured for jets
containing b-hadrons (b-jets) in proton-proton collisions at a centre-of-mass
energy of sqrt(s) = 7 TeV, using the ATLAS detector at the LHC. The
measurements use data corresponding to an integrated luminosity of 34 pb^-1.
The b-jets are identified using either a lifetime-based method, where secondary
decay vertices of b-hadrons in jets are reconstructed using information from
the tracking detectors, or a muon-based method where the presence of a muon is
used to identify semileptonic decays of b-hadrons inside jets. The inclusive
b-jet cross-section is measured as a function of transverse momentum in the
range 20 < pT < 400 GeV and rapidity in the range |y| < 2.1. The bbbar-dijet
cross-section is measured as a function of the dijet invariant mass in the
range 110 < m_jj < 760 GeV, the azimuthal angle difference between the two jets
and the angular variable chi in two dijet mass regions. The results are
compared with next-to-leading-order QCD predictions. Good agreement is observed
between the measured cross-sections and the predictions obtained using POWHEG +
Pythia. MC@NLO + Herwig shows good agreement with the measured bbbar-dijet
cross-section. However, it does not reproduce the measured inclusive
cross-section well, particularly for central b-jets with large transverse
momenta.Comment: 10 pages plus author list (21 pages total), 8 figures, 1 table, final
version published in European Physical Journal
Environmental lead poisoning among children in Porto Alegre state, Southern Brazil
- Author
- Publication venue
- 'FapUNIFESP (SciELO)'
- Publication date
- Field of study
Measurement of the cross-section for b-jets produced in association with a Z boson at root s=7 TeV with the ATLAS detector ATLAS Collaboration
- Author
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- Abdallah J
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- Wiedenmann W
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- Winkelmann S
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- Yilmaz M
- Yoosoofmiya R
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- Zaets VG
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- Zajacova Z
- Zalite YK
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- Zarzhitsky P
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- Zerwas D
- Zhan Z
- Zhang D
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- Zhang J
- Zhang X
- Zhang Z
- Zhao L
- Zhao T
- Zhao Z
- Zhemchugov A
- Zheng S
- Zhong J
- Zhou B
- Zhou N
- Zhou Y
- Zhu CG
- Zhu H
- Zhu J
- Zhu Y
- Zhuang X
- Zhuravlov V
- Zieminska D
- Zimmermann R
- Zimmermann S
- Zimmermann S
- Ziolkowski M
- Zitoun R
- Zivkovic L
- Zmouchko VV
- Zobernig G
- Zoccoli A
- Zolnierowski Y
- Zsenei A
- zur Nedden M
- Zutshi V
- Zwalinski L
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2011
- Field of study
A measurement is presented of the inclusive cross-section for b-jet production in association with a Z boson in pp collisions at a centre-of-mass energy of root s = 7 TeV. The analysis uses the data sample collected by the ATLAS experiment in 2010, corresponding to an integrated luminosity of approximately 36 pb(-1). The event selection requires a Z boson decaying into high P-T electrons or muons, and at least one b-jet, identified by its displaced vertex, with transverse momentum p(T) > 25 GeV and rapidity vertical bar y vertical bar < 2.1. After subtraction of background processes, the yield is extracted from the vertex mass distribution of the candidate b-jets. The ratio of this cross-section to the inclusive Z cross-section (the average number of b-jets per Z event) is also measured. Both results are found to be in good agreement with perturbative QCD predictions at next-to-leading order
Do Myoepithelial Cells Hold the Key for Breast Tumor Progression?
- Author
- A Chi
- A Orimo
- AC Bell
- AG Naccarato
- AP Feinberg
- B Elenbaas
- BS Wiseman
- C Jones
- CI Li
- CU Dietrich
- D Medina
- D Radisky
- D Santini
- D Trichopoulos
- DA Porter
- F Jolicoeur
- F Miller
- F Moinfar
- FM Waldman
- FR Miller
- G Deng
- G Dontu
- G Dontu
- GD Leonard
- GP Boland
- H Rajagopalan
- H Yaziji
- HJ Burstein
- I Baik
- J Russo
- JJ DeCosse
- JJ DeCosse
- JK Tobacman
- JK Tobacman
- JL Jones
- JM Stephenson
- JR Nevins
- K Fukino
- K Kurose
- K Kurose
- Kornelia Polyak
- KW Hunter
- L Ronnov-Jessen
- L Tait
- LA James
- LM Coussens
- M Allinen
- M Aubele
- M Barbareschi
- M Brittan
- M Clemons
- M Hu
- M Iqbal
- M Nguyen
- MA Deugnier
- MD Sternlicht
- MD Sternlicht
- Min Hu
- MJ Bissell
- MJ Bissell
- MJ Page
- MP Shekhar
- MV Maffini
- N Cheng
- N Hoogerbrugge
- NA Bhowmick
- NC Direkze
- NG Hildreth
- PA Kenny
- PP Osin
- PS Larson
- PT Simpson
- R Anbazhagan
- RM Rohan
- RR Zhang
- S Damiani
- S Peyrol
- SH Barsky
- SH Barsky
- SR Lakhani
- SR Lakhani
- SR Lakhani
- T Gudjonsson
- T Ushijima
- TD Tlsty
- TD Tlsty
- VE Steele
- YG Man
- ZM Shao
- ZM Shao
- ZM Shao
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Direct comparison of the FibroScan XL and M probes for assessment of liver fibrosis in obese and nonobese patients
- Author
- Publication venue
- Dove Medical Press
- Publication date
- 01/07/2013
- Field of study
Esteban Durango,1,* Christian Dietrich,1,* Helmut Karl Seitz,1 Cornelia Ursula Kunz,2 Gilles T Pomier-Layrargues,3 Andres Duarte-Rojo,4 Melanie Beaton,5 Magdy Elkhashab,6 Robert P Myers,7 Sebastian Mueller1,3 1Department of Medicine and Center for Alcohol Research, Liver Disease and Nutrition, Salem Medical Center, 2Institute of Medical Biometry and Informatics, University of Heidelberg, Heidelberg, Germany; 3Liver Unit, Centre Hospitalier de l'Université de Montréal, Hôpital Saint-Luc, Montréal, Quebec, 4Toronto Western Hospital Liver Centre, Toronto, Ontario; 5Multi-Organ Transplant Unit, University of Western Ontario, London, Ontario; 6The Toronto Liver Centre, Toronto, Ontario; 7Liver Unit, Division of Gastroenterology and Hepatology, Department of Medicine, University of Calgary, Calgary, Alberta, Canada *These authors contributed equally to this researchBackground: A novel Fibroscan XL probe has recently been introduced and validated for obese patients, and has a diagnostic accuracy comparable with that of the standard M probe. The aim of this study was to analyze and understand the differences between these two probes in nonobese patients, to identify underlying causes for these differences, and to develop a practical algorithm to translate results for the XL probe to those for the M probe.Methods and results: Both probes were directly compared first in copolymer phantoms of varying stiffness (4.8, 11, and 40 kPa) and then in 371 obese and nonobese patients (body mass index, range 17.2–72.4) from German (n = 129) and Canadian (n = 242) centers. Liver stiffness values for both probes correlated better in phantoms than in patients (r = 0.98 versus 0.82, P < 0.001). Significantly more patients could be measured successfully using the XL probe than the M probe (98.4% versus 85.2%, respectively, P < 0.001) while the M probe produced a smaller interquartile range (21% versus 32%). Failure of the M probe to measure liver stiffness was not only observed in patients with a high body mass index and long skin-liver capsule distance but also in some nonobese patients (n = 10) due to quenching of the signal from subcutaneous fat tissue. In contrast with the phantoms, the XL probe consistently produced approximately 20% lower liver stiffness values in humans compared with the M probe. A long skin-liver capsule distance and a high degree of steatosis were responsible for this discordance. Adjustment of cutoff values for the XL probe (<5.5, 5.5–7, 7–10, and >10 kPa for F0, F1–2, F3, and F4 fibrosis, respectively) significantly improved agreement between the two probes from r = 0.655 to 0.679.Conclusion: Liver stiffness can be measured in significantly more obese and nonobese patients using the XL probe than the M probe. However, the XL probe is less accurate and adjusted cutoff values are required.Keywords: cirrhosis, liver fibrosis, liver stiffness, obesity, steatosis, transient elastography, M probe, XL prob
An Assessment of Trends in the Extent of Swidden in Southeast Asia
- Author
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2009
- Field of study
Swidden systems consisting of temporarily cultivated land and associated fallows often do not appear on land use maps or in statistical records. This is partly due to the fact that swidden is a diverse and dynamic land use system that is difficult to map and partly because of the practice of grouping land covers associated with swidden systems into land use or land cover categories that are not self-evidently linked to swiddening. Additionally, in many parts of Southeast Asia swidden systems have changed or are in the process of changing into other land use systems. This paper assesses the extent of swidden on the basis of regional and national sources for nine countries, and determines the pattern of changes of swidden on the basis of 151 cases culled from 67 articles. Findings include (1) a majority of the cases document swidden being replaced by other forms of agriculture or by other livelihood systems; (2) in cases where swiddening is still practiced, fallow lengths are usually, but not always, shorter; and (3) shortened fallow length does not necessarily indicate a trend away from swidden since it is observed that short fallow swidden is sometimes maintained along with other more intensive farming practices and not completely abandoned. The paper concludes that there is a surprising lack of conclusive data on the extent of swidden in Southeast Asia. In order to remedy this, methods are reviewed that may lead to more precise future assessments
Cytogenetic Approaches to Breast Cancer
- Author
- A Adeyinka
- A Kallioniemi
- A Kallioniemi
- A Lindblom
- B Dutrillaux
- B Staats
- B Zafrani
- BA Bonsing
- C Petersson
- C Petersson
- C Petersson
- C Rohen
- C Rohen
- CF Stephenson
- CR Wenger
- CU Dietrich
- CU Dietrich
- CU Dietrich
- CU Dietrich
- CU Dietrich
- D Ford
- DG Evans
- E Leuschner
- E Schröck
- EA Healey
- F Belda
- F Courjal
- F Kerangueven
- F Mitelman
- F Mitelman
- F Mitelman
- F Thompson
- FE Gump
- G Calabrese
- GF Schwartz
- H Beerman
- J Limon
- J Szöllösi
- J Trent
- JA Fletcher
- JR Harris
- LA James
- LC Chen
- M Steinarsdôttir
- MR Speicher
- MR Teixeira
- MR Teixeira
- MR Teixeira
- MR Teixeira
- MR Teixeira
- N Pandis
- N Pandis
- N Pandis
- N Pandis
- N Pandis
- N Pandis
- N Pandis
- N Pandis
- N Pandis
- N Pandis
- P Broët
- P Cin
- P Devilee
- P Lichter
- PJ Dawson
- PJ Hainsworth
- R Holland
- R Wooster
- S Heim
- S Heim
- S Manoir
- S Seitz
- S. H. Birdsall
- SC Barranco
- SH Birdsall
- SR Wolman
- SV Hodgson
- T Kuukasjärvi
- T Nishizaki
- T Ried
- TI Andersen
- U Lönn
- WF Symmans
- Y Miki
- YJ Lu
- YJ Lu
- YY Ozisik
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/1999
- Field of study
- …