193 research outputs found
In silico prioritisation of candidate genes for prokaryotic gene function discovery: an application of phylogenetic profiles
- Author
- C MĂ©digue
- C Perez-Iratxeta
- CM Fraser
- DM Raskin
- EA Adie
- EA Adie
- EC Lin
- EM Marcotte
- Enrico Coiera
- Frank PY Lin
- FS Turner
- G Michal
- IH Witten
- J Freudenberg
- J Wu
- JP Gogarten
- JP Vert
- KJ Gaulton
- M Kanehisa
- M Pellegrini
- MY Galperin
- N LĂłpez-Bigas
- N Tiffin
- PD Karp
- R Jothi
- Ruiting Lan
- S Aerts
- Vitali Sintchenko
- WJ Kent
- Y Yamanishi
- Y Zheng
- Publication venue
- BioMed Central
- Publication date
- 01/01/2009
- Field of study
Background: In silico candidate gene prioritisation (CGP) aids the discovery of gene functions by ranking genes according to an objective relevance score. While several CGP methods have been described for identifying human disease genes, corresponding methods for prokaryotic gene function discovery are lacking. Here we present two prokaryotic CGP methods, based on phylogenetic profiles, to assist with this task. Results: Using gene occurrence patterns in sample genomes, we developed two CGP methods (statistical and inductive CGP) to assist with the discovery of bacterial gene functions. Statistical CGP exploits the differences in gene frequency against phenotypic groups, while inductive CGP applies supervised machine learning to identify gene occurrence pattern across genomes. Three rediscovery experiments were designed to evaluate the CGP frameworks. The first experiment attempted to rediscover peptidoglycan genes with 417 published genome sequences. Both CGP methods achieved best areas under receiver operating characteristic curve (AUC) of 0.911 in Escherichia coli K-12 (EC-K12) and 0.978 Streptococcus agalactiae 2603 (SA-2603) genomes, with an average improvement in precision of >3.2-fold and a maximum of >27-fold using statistical CGP. A median AUC of >0.95 could still be achieved with as few as 10 genome examples in each group of genome examples in the rediscovery of the peptidoglycan metabolism genes. In the second experiment, a maximum of 109-fold improvement in precision was achieved in the rediscovery of anaerobic fermentation genes in EC-K12. The last experiment attempted to rediscover genes from 31 metabolic pathways in SA-2603, where 14 pathways achieved AUC >0.9 and 28 pathways achieved AUC >0.8 with the best inductive CGP algorithms. Conclusion: Our results demonstrate that the two CGP methods can assist with the study of functionally uncategorised genomic regions and discovery of bacterial gene-function relationships. Our rediscovery experiments also provide a set of standard tasks against which future methods may be compared.12 page(s
BICEPP: an example-based statistical text mining method for predicting the binary characteristics of drugs
- Author
- A Korhonen
- A Koussounadis
- C Perez-Iratxeta
- C Perez-Iratxeta
- CB Giles
- D Fourches
- DR Swanson
- EA Adie
- EA Adie
- EC Fieller
- F Hammann
- Frank PY Lin
- FS Turner
- GR Grimes
- Guy Tsafnat
- H Gurulingappa
- J Freudenberg
- JA Hanley
- KJ Gaulton
- L MĂ rquez
- M Hall
- M Krallinger
- Matthew P Doogue
- MF Porter
- N LĂłpez-Bigas
- N Tiffin
- P Srinivasan
- RJ Epstein
- S Aerts
- S Raychaudhuri
- S Raychaudhuri
- S Rossi
- S Tatar
- S Yu
- Stephen Anthony
- Thomas M Polasek
- TM Polasek
- V Sintchenko
- Y Garten
- Publication venue
- BioMed Central
- Publication date
- 01/01/2011
- Field of study
<p>Abstract</p> <p>Background</p> <p>The identification of drug characteristics is a clinically important task, but it requires much expert knowledge and consumes substantial resources. We have developed a statistical text-mining approach (BInary Characteristics Extractor and biomedical Properties Predictor: BICEPP) to help experts screen drugs that may have important clinical characteristics of interest.</p> <p>Results</p> <p>BICEPP first retrieves MEDLINE abstracts containing drug names, then selects tokens that best predict the list of drugs which represents the characteristic of interest. Machine learning is then used to classify drugs using a document frequency-based measure. Evaluation experiments were performed to validate BICEPP's performance on 484 characteristics of 857 drugs, identified from the Australian Medicines Handbook (AMH) and the PharmacoKinetic Interaction Screening (PKIS) database. Stratified cross-validations revealed that BICEPP was able to classify drugs into all 20 major therapeutic classes (100%) and 157 (of 197) minor drug classes (80%) with areas under the receiver operating characteristic curve (AUC) > 0.80. Similarly, AUC > 0.80 could be obtained in the classification of 173 (of 238) adverse events (73%), up to 12 (of 15) groups of clinically significant cytochrome P450 enzyme (CYP) inducers or inhibitors (80%), and up to 11 (of 14) groups of narrow therapeutic index drugs (79%). Interestingly, it was observed that the keywords used to describe a drug characteristic were not necessarily the most predictive ones for the classification task.</p> <p>Conclusions</p> <p>BICEPP has sufficient classification power to automatically distinguish a wide range of clinical properties of drugs. This may be used in pharmacovigilance applications to assist with rapid screening of large drug databases to identify important characteristics for further evaluation.</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
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- 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
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- Allwood-Spiers SE
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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 âs = 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 pTâ„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 60â€pT<800 GeV, and is maximally 14 % for pT<30 GeV in the most forward region 3. 2â€{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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- Abdesselam A
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- 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
Observation of associated near-side and away-side long-range correlations in âsNN=5.02ââTeV proton-lead collisions with the ATLAS detector
- Author
- Aad G
- Abajyan T
- Abbott B
- Abdallah J
- Abdel Khalek S
- Abdelalim AA
- Abdinov O
- Aben R
- Abi B
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- Alam MA
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- Aleksa M
- Aleksandrov IN
- Alessandria F
- Alexa C
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- Alexandre G
- Alexopoulos T
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- Alimonti G
- Alison J
- Allbrooke BM
- Allison LJ
- Allport PP
- Allwood-Spiers SE
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- Yilmaz M
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- Yorita K
- Yoshida R
- Yoshihara K
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- Young CJ
- Youssef S
- Yu D
- Yu DR
- Yu J
- Yu J
- Yuan L
- Yurkewicz A
- Zabinski B
- Zaidan R
- Zaitsev AM
- Zambito S
- Zanello L
- Zanzi D
- Zaytsev A
- Zeitnitz C
- Zeman M
- Zemla A
- Zenin O
- ZeniĆĄ T
- Zerwas D
- Zevi Della Porta G
- Zhang D
- Zhang H
- Zhang J
- Zhang L
- Zhang X
- Zhang Z
- Zhao L
- Zhao Z
- Zhemchugov A
- Zhong J
- Zhou B
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- Zhu CG
- Zhu H
- Zhu J
- Zhu Y
- Zhuang X
- Zhuravlov V
- Zibell A
- Zieminska D
- Zimin NI
- Zimmermann R
- Zimmermann S
- Zimmermann S
- Zinonos Z
- Ziolkowski M
- Zitoun R
- ZivkoviÄ L
- Zmouchko VV
- Zobernig G
- Zoccoli A
- Zur Nedden M
- Zutshi V
- Zwalinski L
- Publication venue
- American Physical Society
- Publication date
- 01/01/2012
- Field of study
Two-particle correlations in relative azimuthal angle (ÎÏ) and pseudorapidity (Îη) are measured in âsNN=5.02ââTeV p+Pb collisions using the ATLAS detector at the LHC. The measurements are performed using approximately 1ââÎŒb-1 of data as a function of transverse momentum (pT) and the transverse energy (ÎŁETPb) summed over 3.1<η<4.9 in the direction of the Pb beam. The correlation function, constructed from charged particles, exhibits a long-range (2<|Îη|<5) ânear-sideâ (ÎÏâŒ0) correlation that grows rapidly with increasing ÎŁETPb. A long-range âaway-sideâ (ÎÏâŒÏ) correlation, obtained by subtracting the expected contributions from recoiling dijets and other sources estimated using events with small ÎŁETPb, is found to match the near-side correlation in magnitude, shape (in Îη and ÎÏ) and ÎŁETPb dependence. The resultant ÎÏ correlation is approximately symmetric about Ï/2, and is consistent with a dominant cosâĄ2ÎÏ modulation for all ÎŁETPb ranges and particle pT
Search for the neutral Higgs bosons of the minimal supersymmetric standard model in pp collisions at root s=7 TeV with the ATLAS detector
- Author
- Aad G
- Abajyan T
- Abbott B
- Abdallah J
- Abdelalim AA
- Abdinov O
- Abi B
- Abolins M
- AbouZeid OS
- Abramowicz H
- Abreu H
- Acharya BS
- Adam ER
- Adamczyk L
- Adams DL
- Addy TN
- Adelman J
- Adomeit S
- Adragna P
- Adye T
- Aesky S
- Agar-Savedra JA
- Agustoni M
- Ahlen SP
- Ahles F
- Ahmad A
- Ahsan M
- Aielli G
- Akesson TPA
- Akimoto G
- Akimov AV
- Alam MA
- 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
- Allbrooke BMM
- Allison LJ
- Allport PP
- Allwood-Spiers SE
- Almenar CC
- Almond J
- Aloisio A
- Alon R
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- Altheimer A
- Alviggi MG
- Amako K
- Amelung C
- Ammosov VV
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- Anghinolfi F
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- Annovi A
- Antonaki A
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- Zobernig G
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- zur Nedden M
- Zutshi V
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- Publication venue
- Publication date
- 01/02/2013
- Field of study
A search for neutral Higgs bosons of the Minimal Supersymmetric Standard Model (MSSM) is reported. The analysis is based on a sample of proton-proton collisions at a centre-of-mass energy of 7TeV recorded with the ATLAS detector at the Large Hadron Collider. The data were recorded in 2011 and correspond to an integrated luminosity of 4.7 fb-1 to 4.8 fb-1. Higgs boson decays into oppositely-charged muon or Ï lepton pairs are considered for final states requiring either the presence or absence of b-jets. No statistically significant excess over the expected background is observed and exclusion limits at the 95% confidence level are derived. The exclusion limits are for the production cross-section of a generic neutral Higgs boson, Ï, as a function of the Higgs boson mass and for h/A/H production in the MSSM as a function of the parameters mA and tan ÎČ in the mhmax scenario for mA in the range of 90GeV to 500 GeV. Copyright CERN
Search for R-parity-violating supersymmetry in events with four or more leptons in sqrt(s) =7 TeV pp collisions with the ATLAS detector
- Author
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- Yamamura T
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- Yamazaki T
- Yamazaki Y
- Yan Z
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- Yanush S
- Yao L
- Yao Y
- Yasu Y
- Smit GVY
- Ye J
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- Yilmaz M
- Yoosoofmiya R
- Yorita K
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- Yoshihara K
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- Young CJ
- Youssef S
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- Zabinski B
- Zaidan R
- Zaitsev AM
- Zajacova Z
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- Zanzi D
- Zaytsev A
- Zeitnitz C
- Zeman M
- Zemla A
- Zendler C
- Zenin O
- Zenis T
- Zinonos Z
- Zerwas D
- della Porta GZ
- Zhang D
- Zhang H
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- Zhang X
- Zhang Z
- Zhao L
- Zhao Z
- Zhemchugov A
- Zhong J
- Zhou B
- Zhou N
- Zhou Y
- Zhu CG
- Zhu H
- Zhu J
- Zhu Y
- Zhuang X
- Zhuravlov V
- Zibell A
- Zieminska D
- Zimin NI
- Zimmermann R
- Zimmermann S
- Zimmermann S
- Ziolkowski M
- Zitoun R
- Zivkovic L
- Zmouchko VV
- Zobernig G
- Zoccoli A
- zur Nedden M
- Zutshi V
- Zwalinski L
- Collaboration ATLAS
- Publication venue
- Springer Verlag
- Publication date
- 01/01/2008
- Field of study
A search for new phenomena in final states with four or more leptons (electrons or muons) is presented. The analysis is based on 4.7 fbâ1 of sâ=7TeV proton-proton collisions delivered by the Large Hadron Collider and recorded with the ATLAS detector. Observations are consistent with Standard Model expectations in two signal regions: one that requires moderate values of missing transverse momentum and another that requires large effective mass. The results are interpreted in a simplified model of R-parity-violating supersymmetry in which a 95% CL exclusion region is set for charged wino masses up to 540 GeV. In an R-parity-violating MSUGRA/CMSSM model, values of m 1/2 up to 820 GeV are excluded for 10 < tan ÎČ < 40
How ubiquitination and autophagy participate in the regulation of the cell response to bacterial infection
- Author
- Abbott
- Abrami
- Angot
- Bergsbaken
- Birmingham
- Birmingham
- Birmingham
- Bischofberger
- Bjorkoy
- Bonazzi
- Boyden
- Boyer
- Carneiro
- Chau
- Chiu
- Chosed
- Ciechanover
- Deretic
- Dikic
- Dupont
- Dye
- English
- Enninga
- Franchi
- Frank Lafont
- Fujita
- Fukazawa
- Gay
- Geisler
- Geiss-Friedlander
- Geoffroy
- Goldstein
- Gutierrez
- Hailey
- Hampe
- Hayashi-Nishino
- Hicke
- Hochstrasser
- Hoeller
- Hoppe
- Hotson
- Hugot
- Ichimura
- Ichimura
- Inohara
- Isaacson
- Jin
- Kang
- Kanki
- Kerscher
- Kim
- Kim
- Kirkin
- Kirkin
- Knodler
- Komatsu
- Kopito
- Korolchuk
- Korolchuk
- Kumar
- Kumar
- Lafont
- Lafont
- Lafont
- Lamark
- Lamkanfi
- Lee
- Levine
- Lin
- Martinez
- Master
- Mathew
- Matzinger
- Mestre
- Molfetta
- Moreau
- Moscat
- Moscat
- Munro
- Nassima Temime-Smaali
- Nicolas Dupont
- Noda
- O'Neill
- Ogawa
- Okamoto
- Pankiv
- Patel
- Pedra
- Pelegrin
- Pickart
- PietiÀinen
- Ponpuak
- Pujol
- Pursiheimo
- Py
- Radtke
- Raiborg
- Ravikumar
- Ribet
- Rich
- Rioux
- Roduit
- Roduit
- Rust
- Rytkonen
- Seeler
- Seibenhener
- Shahanazari
- Shroff
- Shvets
- Simons
- Skaug
- Spallek
- Stulemeijer
- Terebiznik
- Terebiznik
- Thurston
- Travassos
- Vance
- Veiga
- Yamasaki
- Yano
- Yersin
- Yoshikawa
- Zaas
- Zhang
- Zheng
- Publication venue
- Portland Press Ltd.
- Publication date
- Field of study
Bacterial infection relies on the micro-organism's ability to orchestrate the host's cell signalling such that the immune response is not activated. Conversely, the host cell has dedicated signalling pathways for coping with intrusions by pathogens. The autophagy of foreign micro-organisms (known as xenophagy) has emerged as one of the most powerful of these pathways, although the triggering mode remains largely unknown. In the present paper, we discuss the role that certain post-translational modifications (primarily ubiquitination) may play in the activation of xenophagy and how some bacteria have evolved mechanisms to subvert or hijack this process. In particular, we address the role played by P62/SQSTM1 (sequestosome 1). Finally, we discuss how autophagy can be subverted to eliminate bacteria-induced danger signals
Photography-based taxonomy is inadequate, unnecessary, and potentially harmful for biological sciences
- Author
- Abdala Cristian SimĂłn
- Adler Kraig
- Adriano Edson A.
- Aescht Erna
- Agarwal Ishan
- Agatha Sabine
- Agosti Donat
- Aguiar Antonio J. C.
- Aguiar Jonas José Mendes
- Ahrens Dirk
- Aleixo Alexandre
- Alqarni Abdulaziz S.
- Alves Maria Judite
- Ananjeva Natalia
- Andrade Marcelo C.
- Andreone Franco
- Aquino Pedro P. U.
- Araujo Paula Beatriz
- Arnaud Henrard
- Arroyave Jairo
- Arthofer Wolfgang
- Artois Tom J.
- AstĂșa Diego
- Azevedo Celso
- Bagley Justin C.
- Baldo Diego
- Barber James Helen Margaret
- Bastos Silveira Cristiane
- Bates Michael F.
- Bauer Aaron M.
- Bauer Franziska
- Benine Ricardo C.
- Bennett Daniel J.
- Bentlage Bastian
- Berning Björn
- Bharti Daizy
- Biondo Cibele
- Birindelli José
- Blick Theo
- Boano Giovanni
- Bockmann FlĂĄvio A.
- Bogdanowicz Wieslaw
- Borgo Enrico
- Borkin Leo
- Bornschein Marcos Ricardo
- Bour Roger
- Branch William R.
- Brasileiro Cinthia A.
- Braun Janet K.
- Bravo Gustavo A.
- Brendonck Luc
- Brito Guilherme R. R.
- Britto Marcelo R.
- Buckup Paulo A.
- Burckhardt Daniel
- Burkhardt Ulrich
- Busack Stephen D.
- BĂ€rmann Eva V.
- Böhme Wolfgang
- Campos Luiz A.
- Canard Alain
- Cancello Eliana M.
- Caramaschi Ulisses
- Carpenter James M.
- Carr Martin
- Carrenho Renan
- Cartaxana Alexandra
- Carvajal Mariom A.
- Carvalho GervĂĄsio Silva
- CerĂaco Luis M. P.
- Chaabane Amira
- Chagas Cinthia
- Chakrabarty Prosanta
- Chandra Kailas
- Chatzimanolis Stylianos
- Chordas Stephen W.
- Christoff Alexandre U.
- Cianferoni Fabio
- Claramunt Santiago
- CogĂŁlniceanu Dan
- Collette Bruce B.
- Colli Guarino R.
- Colston Timothy J.
- Conradie Werner
- Constant JĂ©rĂŽme
- Constantino Reginaldo
- Cook Joseph A.
- Cordeiro Danilo
- Correia Alexandra Marçal
- Costa Leonora Pires
- Cotterill Fenton P. D.
- Coyner Brandi
- Cozzuol Mario A.
- Cracraft Joel
- Crottini Angelica
- Cuccodoro Giulio
- Curcio Felipe Franco
- D'ElĂa Guillermo
- D'Haese Cyrille
- D'Udekem D'Acoz CĂ©dric
- Das Indraneil
- Datovo Aléssio
- Datta Roy Aniruddha
- David Patrick
- Day John G.
- Daza Juan D.
- De Andrade Marco Brandalise
- De Bisthoven Luc Janssens
- De Carvalho Marcelo Rodrigues
- De La Riva De La Viña Ignacio Jose
- De Lucena Carlos A. S.
- De Lucena Zilda Margarete S.
- De Muizon Christian
- De Oliveira FavĂzia Freitas
- De Oliveira Marcio Luiz
- De Oliveira Otto MĂŒller PatrĂŁo
- De Pinna Mario
- De Resbecq Thierry Deuve
- De SĂĄ Rafael O.
- De Vivo Mario
- Decher Jan
- Dekoninck Wouter
- Delabie Jacques H. C.
- Delfino Massimo
- Delmastro Giovanni B.
- Delsinne Thibaut
- Denys Christiane
- Denzer Wolfgang
- Desutter Grandcolas Laure
- Deuti Kaushik
- Di Dario Fabio
- Dinets Vladimir
- Do Amaral Fabio Raposo
- Donascimiento Carlos
- Donoso David A.
- Doria Giuliano
- Drewes Robert C.
- Drouet Eric
- Duarte Marcelo
- Dubois Alain
- Durette Desset Marie Claude
- Dusoulier François
- Dutta Sushil Kumar
- Engel Michael S.
- Epstein Mark
- Escalona Moisés
- Esselstyn Jacob A.
- Eto Koshiro
- Faivovich JuliĂĄn
- Falaschi Rafaela Lopes
- Falin Zachary H.
- Faundez Eduardo I.
- FeijĂł Anderson
- Feitosa Rodrigo M.
- Fernandes Daniel Silva
- FikĂĄÄek Martin
- Fisher Brian L.
- Fitzpatrick Moira J.
- Forero Dimitri
- Franz Ismael
- Freitag Hendrik
- Fritz Uwe
- Frétey Thierry
- Gallut Cyril
- Gao Shan
- Garbino Guilherme S. T.
- Garcete Barrett BolĂvar R.
- Garcia Paulo C. A.
- GarcĂa Prieto Luis
- GarcĂa Franger J.
- Gardner Alfred L.
- Gardner Scott Lyell
- Garrouste Romain
- Geiger Matthias F.
- Giarla Thomas C.
- Giri Varad
- Glaubrecht Matthias
- Glotzhober Robert C.
- Godoi Fabio S. P.
- Gofas Serge
- Gong Jun
- Gonzalez Victor H.
- Gonzålez Orej José Antonio
- GonzĂĄlez SantillĂĄn Edmundo
- GonzĂĄlez Soriano Enrique
- Gonçalves Pablo R.
- Goodman Steven M.
- Grandcolas Philippe
- Grande Lance
- Greenbaum Eli
- Gregorin Renato
- Grillitsch Heinz
- Grismer Larry Lee
- Grootaert Patrick
- Grosjean Stéphane
- GUARINO FABIO MARIA
- Guayasamin Juan M.
- Guevara LĂĄzaro
- Guidoti Marcus
- Gupta Devanshu
- Gutiérrez Eliécer E.
- Guénard Benoit
- GvoĆŸdĂk VĂĄclav
- Haddad CĂ©lio F. B.
- Hallermann Jakob
- Hassanin Alexandre
- Hausmann Axel
- Heaney Lawrence R.
- Heinicke Matthew P.
- Helgen Kristofer M.
- Henle Klaus
- Hirschmann Alice
- Holmes Michael W.
- Hormiga Gustavo
- HoĆyĆska Maria
- HoĆyĆski Roman
- Huber Bernhard A.
- Hugot Jean Pierre
- Hutterer Rainer
- Iskandar Djoko
- Iverson John B.
- Janssen Ronald
- Jerep Fernando
- Jocqué Rudy
- Jungfer Karl Heinz
- Justine Jean Lou
- JĂ€ger Peter
- Kamei Rachunliu G.
- KamiĆski Marcin Jan
- Karner Michael
- Kearney Teresa
- Khot Rahul
- Kieckbusch Max
- Koepfli Klaus Peter
- Kondorosy Elöd
- Krogmann Lars
- Krolow Tiago KĂŒtter
- KrĂŒger Martin
- Kucharzewski Christoph
- Kullander Sven O.
- Kumar Santosh
- Kupfer Alexander
- Kuramoto Mitsuru
- Kurina Olavi
- Kury Adriano
- Kvist Sebastian
- Köhler Jörn
- La Marca Enrique
- La Terza Antonietta
- Lacher Thomas E.
- Lamas Carlos J. E.
- Lambert Max R.
- Landry Bernard
- Langeani Francisco
- Langone José A.
- Lattke John E.
- Laval Richard
- Lavilla Esteban O.
- Leenders Twan
- Lees David C.
- Lehmann Thomas
- Leite Yuri L. R.
- Lhano Marcos Gonçalves
- Lim Burton K.
- Lin Xiaofeng
- Lucinda Paulo
- Lujan Nathan K.
- Luporini Pierangelo
- Luz David R.
- Lynch John D.
- Löbl Ivan
- Machado Leonardo Ferreira
- Mahony Stephen
- Malabarba Luiz R.
- Manuel Santos Marivene
- Marinho Filho Jader
- Marini Miguel Ă.
- Marques Antonio Carlos
- Marques Mariana P.
- Mateus OctĂĄvio
- Matsui Masafumi
- Mazuch TomĂĄĆĄ
- Mccranie James
- Mckellar Ryan C.
- Mcmahan Caleb D.
- Mecke Sven
- MeiĂner Karin
- Mendoza Becerril MarĂa A.
- Mendoza Palmero Carlos A.
- Merker Stefan
- MEZZASALMA MARCELLO
- Midgley John Mark
- Miller Jeremy
- Miller Matthew J.
- Mincarone Michael Maia
- Minet Joël
- Miralles Aurélien
- Miranda ThaĂs P.
- Missoup Alain Didier
- ModrĂœ David
- Molinari JesĂșs
- Monadjem Ara
- Montreuil Olivier
- Moratelli Ricardo
- Moreira Cristiano Rangel
- Moreira Felipe F. F.
- Mourer Chauviré Cécile
- Mulieri Pablo Ricardo
- Munroe Thomas A.
- Naomi Shun Ichiro
- Nascimento Fabio
- Neifar Lassad
- Netto Ferreira Andre L.
- Niamir Aidin
- Nielsen Stuart V.
- Nihei Silvio S.
- Nistri Annamaria
- NĂ€ssig Wolfgang A.
- Oceguera Figueroa Alejandro
- ODIERNA GAETANO
- Ohler Annemarie
- Ojanguren Affilastro Andres A.
- Oliveira Sarah Siqueira
- Olson Link E.
- Ong'Ondo Geoffrey O.
- Orlov Nikolai
- Ornelas GarcĂa Claudia Patricia
- Ortega Andrade Mauricio
- Ortega Hernan
- Ota Hidetoshi
- Pariselle Antoine
- Passos Paulo
- Pastana Murilo N. L.
- Patitucci Luciano D.
- Patterson Bruce D.
- Patton James L.
- Pavan Ana C.
- Pavan Silvia E.
- Pavia Marco
- Peloso Pedro L. V.
- Pelzer Alexander
- Pereyra MartĂn O.
- Perez Gonzalez Abel
- Peterhans Julian Kerbis
- Peterson A. Townsend
- Philips Thomas Keith
- Piacentini VĂtor De Q.
- PICARIELLO ORFEO LUCIO ANTONIO
- Pie Marcio R.
- Pikart Tiago G.
- Pine Ronald H.
- Pinheiro Ulisses
- Pinho Luiz Carlos
- Pinto Ăngelo P.
- Poggi Roberto
- Pombal José P.
- Prabhu Mrugank
- Prendini Elizabeth
- Prendini Lorenzo
- Purushothaman Jasmine
- Py Daniel Lucia H. Rapp
- Pyron Robert Alexander
- PĂ©rez Luz Blanca
- PĂ©rez Cristian Hernan Fulvio
- PĂ©tillon Julien
- Quetzalli HernĂĄndez DĂaz Yoalli
- Quintela Alonso Pablo
- Quinteros Andres Sebastian
- Quiroga Carmona Marcial
- Rabitsch Wolfgang
- Raffaëlli Jean
- Rage Jean Claude
- Rajaei Hossein
- RamĂrez MartĂn J.
- Raposo Marcos A.
- Rasplus Jean Yves
- Ratcliffe Brett C.
- Reddy Sushma
- Reis Roberto E.
- Remsen James V.
- Richards Leigh R.
- Richling Ira
- Robillard Tony
- Rocha Marcelo Salles
- Rocha Rosana Moreira
- Rodrigues Fernando P.
- Rodrigues Miguel Trefaut
- Rodriguez Estefania
- Rogers Duke S.
- Rojas Runjaic Fernando J. M.
- Rosenberger Alfred L.
- Rowley Jodi
- Roza André Silva
- Ruedi Manuel
- Rödder Dennis
- Rödel Mark Oliver
- Röll Beate
- Salazar Bravo Jorge
- Salcedo Norma J.
- Samyn Yves
- Santana Sharlene E.
- Santoferrara Luciana
- Santos Bernardo F.
- Santos Charles Morphy D.
- Santos Jean Carlos
- Santos Marcos PĂ©rsio Dantas
- Sargis Eric J.
- Schargel Walter E.
- Scherz Mark D.
- Schlick Steiner Birgit C.
- Schmidt Ray C.
- Schmitt Thomas
- Schodde Richard
- Schoeman Colin S.
- Schweiger Silke
- Schwertner Cristiano F.
- SchÀtti Beat
- Seamark Ernest C. J.
- Semedo Thiago B. F.
- Shin Mann Kyoon
- Siler Cameron D.
- Silveira LuĂs FĂĄbio
- Simison W. Brian
- SimÔes Marcello
- Sites Jack W.
- Smith Brian Tilston
- Smith Krister T.
- Song Weibo
- Soulier Perkins Adeline
- Sousa Leandro M.
- Sparks John S.
- Stampar SĂ©rgio N.
- Steiner Florian M.
- Steyer Jean SĂ©bastien
- Stiassny Melanie L. J.
- Stoeck Thorsten
- Stopiglia Renata
- Streicher Jeffrey W.
- Sturaro Marcelo J.
- Stys Pavel
- Swierk Lindsey
- Taeger Andreas
- Takiya Daniela M.
- Taphorn Donald C.
- Tavares Marcos
- Tavares Valeria Da C.
- Taylor Peter John
- Tello Jose G.
- Teta Pablo
- Tillack Frank
- Timm Robert M.
- Tokaryk Tim
- Tominaga Atsushi
- Tonini JoĂŁo Filipe Riva
- Tornabene Luke
- Torres Carvajal Omar
- Townsend Josiah
- Trape Jean François
- Trusch Robert
- Tschopp Emanuel
- Uhl Dieter
- Upham Nathan S.
- Vacher Jean Pierre
- Valdesalici Stefano
- Valero Katharina C. Wollenberg
- Van Bocxlaer Bert
- Van Cakenberghe Victor
- Van De Kamp Thomas
- Van De Velde Isabella
- Van Den Spiegel Didier
- Vanhove Maarten P. M.
- Vasudevan Karthikeyan
- Veerappan Deepak
- Velazco PaĂșl M.
- Verdade Vanessa K.
- Verheyen Erik
- Victoriano Pedro F.
- Vieira Leandro M.
- Vitt Laurie J.
- Wagner Philipp
- Watkins Colwell Gregory J.
- Weisse Thomas
- Werneck Fernanda P.
- Wheeler Ward C.
- Wilson Don E.
- Wood Perry Lee
- Woodman Neal
- Yoshikawa Natsuhiko
- Zaher Hussam
- Ziegler Thomas
- Zima Jan
- Zink Robert M.
- Zug George
- Publication venue
- Magnolia Press
- Publication date
- 01/01/2015
- Field of study
The question whether taxonomic descriptions naming new animal species without type specimen(s) deposited in collections should be accepted for publication by scientific journals and allowed by the Code has already been discussed in Zootaxa (Dubois & NemĂ©sio 2007; Donegan 2008, 2009; NemĂ©sio 2009aâb; Dubois 2009; Gentile & Snell 2009; Minelli 2009; Cianferoni & Bartolozzi 2016; Amorim et al. 2016). This question was again raised in a letter supported
by 35 signatories published in the journal Nature (Pape et al. 2016) on 15 September 2016. On 25 September 2016, the following rebuttal (strictly limited to 300 words as per the editorial rules of Nature) was submitted to Nature, which on
18 October 2016 refused to publish it. As we think this problem is a very important one for zoological taxonomy, this text is published here exactly as submitted to Nature, followed by the list of the 493 taxonomists and collection-based
researchers who signed it in the short time span from 20 September to 6 October 2016
ICAR: endoscopic skullâbase surgery
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- NORDIC Idiopathic Intracranial Hypertension Study Group Writing Committee
- Nuwer MR
- Nyquist GG
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- Pacca P
- Padhye V
- Padhye V
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- Padhye V
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- Palani A
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- Pasztor E
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- Patel MR
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- Patel SN
- Patel TD
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- Pereira EAC
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- Sanghvi S
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- Publication venue
- Publication date
- 01/07/2019
- Field of study
n/
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