275 research outputs found
The Making of a Queen: TOR Pathway Is a Key Player in Diphenic Caste Development
- Author
- ALTO Aase
- AS Cristino
- Avani Patel
- Christine Emore
- CM Nelson
- D Berrigan
- D Berrigan
- DA Guertin
- DE Wheeler
- E Hafen
- ERD Michelette
- Greg Hunt
- Gro V. Amdam
- GV Amdam
- GV Amdam
- GV Amdam
- GV Amdam
- H Rembold
- H Rembold
- H Rembold
- IA Hansen
- J Colombani
- J Woyke
- JD Vandenberg
- K Aronstein
- K Jia
- Katy Frederick
- KR Guidugli
- M Maeterlinck
- M Tatar
- M. Kim Fondrk
- MJ Reiss
- MJ West-Eberhard
- ML Winston
- Osman Kaftanoglu
- P Wirtz
- Pawel Michalak
- RE Page
- S Dedej
- S Oldham
- T Powers
- W Engels
- XM Long
- Publication venue
- Public Library of Science
- Publication date
- 01/06/2007
- Field of study
Honey bees (Apis mellifera) provide a principal example of diphenic development. Excess feeding of female larvae results in queens (large reproductives). Moderate diet yields workers (small helpers). The signaling pathway that links provisioning to female developmental fate is not understood, yet we reasoned that it could include TOR (target of rapamycin), a nutrient- and energy-sensing kinase that controls organismal growth.Here, the role of Apis mellifera TOR (amTOR) in caste determination is examined by rapamycin/FK506 pharmacology and RNA interference (RNAi) gene knockdown. We show that in queen-destined larvae, the TOR inhibitor rapamycin induces the development of worker characters that are blocked by the antagonist FK506. Further, queen fate is associated with elevated activity of the Apis mellifera TOR encoding gene, amTOR, and amTOR gene knockdown blocks queen fate and results in individuals with worker morphology.A much-studied insect dimorphism, thereby, can be governed by the TOR pathway. Our results present the first evidence for a role of TOR in diphenic development, and suggest that adoption of this ancestral nutrient-sensing cascade is one evolutionary pathway for morphological caste differentiation in social insects
Therapy for metastatic melanoma: the past, present, and future
- Author
- A Boni
- A Hauschild
- A Jemal
- A Ribas
- A Srivastava
- AB Turke
- C Beadling
- C Montagut
- C Robert
- CM Johannessen
- DF McDermott
- DG Perez
- DJ Riese
- DJ Schwartzentruber
- DM Rose
- DS Hong
- EM Hersh
- F Leo
- F Su
- FS Hodi
- FS Hodi
- G Hill
- G Phan
- GW J Jackson
- H Chen
- H Davies
- H Kitayama
- HM Kluger
- I Melero
- J Curtin
- J Graells
- J Guo
- J Lord
- J Villanueva
- JA Curtin
- JA Engelman
- JA Jakob
- JA Sosman
- JL Riley
- JP Fruehauf
- JR Brahmer
- JR R Dummer
- KB Kim
- KB Kim
- KH Paraiso
- KR GV Long
- KT Flaherty
- L Si
- LA Kottschade
- Laura Finn
- LM Ellis
- LV AM Menzies
- M Atkins
- M Guix
- M Sabatino
- ME Dudley
- ME Dudley
- ME Gorre
- ME Keir
- MR Frey
- N Wagle
- P Herman
- PB Chapman
- PJ Allen
- R Kefford
- R Nazarian
- RA Morgan
- RD Carvajal
- Richard W Joseph
- RW Joseph
- RW Joseph
- RW Joseph
- S Hirota
- S Hirota
- S Wakita
- SA Rosenberg
- SA Rosenberg
- SA Rosenberg
- SA Rosenberg
- SE Woodman
- SM Wilhelm
- SP Patel
- Svetomir N Markovic
- T Eisen
- T Fu
- T Meyer
- T Okazaki
- TD Prickett
- Publication venue
- BioMed Central
- Publication date
- 01/01/2012
- Field of study
Metastatic melanoma is the most aggressive form of skin cancer with a median overall survival of less than one year. Advancements in our understanding of how melanoma evades the immune system as well as the recognition that melanoma is a molecularly heterogeneous disease have led to major improvements in the treatment of patients with metastatic melanoma. In 2011, the US Food and Drug Administration (FDA) approved two novel therapies for advanced melanoma: a BRAF inhibitor, vemurafenib, and an immune stimulatory agent, ipilimumab. The success of these agents has injected excitement and hope into patients and clinicians and, while these therapies have their limitations, they will likely provide excellent building blocks for the next generation of therapies. In this review we will discuss the advantages and limitations of the two new approved agents, current clinical trials designed to overcome these limitations, and future clinical trials that we feel hold the most promise
Iron Behaving Badly: Inappropriate Iron Chelation as a Major Contributor to the Aetiology of Vascular and Other Progressive Inflammatory and Degenerative Diseases
- Author
- A Abbott
- A Abou-Raya
- A Aljandali
- A Ambesi-Impiombato
- A Aydin
- A Balcerczyk
- A Besarab
- A Brzezinski
- A Campbell
- A Carrillo-Vico
- A Cavalli
- A Chattopadhyay
- A Chattopadhyay
- A Cherubini
- A Dey
- A Doms
- A Donovan
- A Donovan
- A Dávalos
- A Gaeta
- A Garny
- A Gnjec
- A Gomes
- A Gopalakrishnan
- A Hald
- A Henney
- A Hirayama
- A Hoffmann
- A Huber
- A Hugman
- A Iannetti
- A Ide-Ektessabi
- A Jacobs
- A Jeyabalan
- A Kahvejian
- A Karrar
- A Kasztler
- A Kibel
- A Kocyigit
- A Kotha
- A Kumral
- A Lass
- A Lecube
- A Lewén
- A Lotery
- A Maggio
- A Malek
- A Malik
- A Mantovani
- A Matsuzawa
- A Mitra
- A Monge
- A Murakami
- A Murakami
- A Murakami
- A Murakami
- A Mutti
- A Nijnik
- A Nunomura
- A Nunomura
- A Patt
- A Persson
- A Pietrangelo
- A Piga
- A Pirat
- A Post
- A Pradhan
- A Protti
- A Rattner
- A Ravati
- A Rehman
- A Reynolds
- A Richmond
- A Roetto
- A Roetto
- A Rostom
- A Rumbold
- A Russo
- A Rötig
- A Saltelli
- A Saltelli
- A Sandek
- A Sassano
- A Scalbert
- A Scalbert
- A Scalbert
- A Sica
- A Smahi
- A Sola
- A Stintzi
- A Szewczyk
- A Taguchi
- A Tedgui
- A Terman
- A Terman
- A Terman
- A Undas
- A Virdis
- A Wagner
- A Wagner
- A Wagner
- A Wagner
- A Wojas-Pelc
- A Wong
- A Xu
- A Yoritaka
- A Yoshimura
- A-L Barabási
- AA Andreadis
- AA Borisy
- AA Farooqui
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- AA Qutub
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- AB Parsons
- AB Parsons
- AB Thompson
- AB Thomson
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- Ad hoc committee on systemic lupus erythematosus response criteria for fatigue
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- ZZ Chong
- ZZ Chong
- Publication venue
- Publication date
- 09/08/2008
- Field of study
The production of peroxide and superoxide is an inevitable consequence of
aerobic metabolism, and while these particular "reactive oxygen species" (ROSs)
can exhibit a number of biological effects, they are not of themselves
excessively reactive and thus they are not especially damaging at physiological
concentrations. However, their reactions with poorly liganded iron species can
lead to the catalytic production of the very reactive and dangerous hydroxyl
radical, which is exceptionally damaging, and a major cause of chronic
inflammation. We review the considerable and wide-ranging evidence for the
involvement of this combination of (su)peroxide and poorly liganded iron in a
large number of physiological and indeed pathological processes and
inflammatory disorders, especially those involving the progressive degradation
of cellular and organismal performance. These diseases share a great many
similarities and thus might be considered to have a common cause (i.e.
iron-catalysed free radical and especially hydroxyl radical generation). The
studies reviewed include those focused on a series of cardiovascular, metabolic
and neurological diseases, where iron can be found at the sites of plaques and
lesions, as well as studies showing the significance of iron to aging and
longevity. The effective chelation of iron by natural or synthetic ligands is
thus of major physiological (and potentially therapeutic) importance. As
systems properties, we need to recognise that physiological observables have
multiple molecular causes, and studying them in isolation leads to inconsistent
patterns of apparent causality when it is the simultaneous combination of
multiple factors that is responsible. This explains, for instance, the
decidedly mixed effects of antioxidants that have been observed, etc...Comment: 159 pages, including 9 Figs and 2184 reference
Pan-cancer analysis of whole genomes
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- The ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Consortium View Correspondence (jump link)
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- Zhang H. b
- Zhao
- Zheng
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- Ó. A. th
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- Publication venue
- Publication date
- 11/12/2019
- Field of study
Cancer is driven by genetic change, and the advent of massively parallel sequencing has enabled systematic documentation of this variation at the whole-genome scale(1-3). Here we report the integrative analysis of 2,658 whole-cancer genomes and their matching normal tissues across 38 tumour types from the Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium of the International Cancer Genome Consortium (ICGC) and The Cancer Genome Atlas (TCGA). We describe the generation of the PCAWG resource, facilitated by international data sharing using compute clouds. On average, cancer genomes contained 4-5 driver mutations when combining coding and non-coding genomic elements; however, in around 5% of cases no drivers were identified, suggesting that cancer driver discovery is not yet complete. Chromothripsis, in which many clustered structural variants arise in a single catastrophic event, is frequently an early event in tumour evolution; in acral melanoma, for example, these events precede most somatic point mutations and affect several cancer-associated genes simultaneously. Cancers with abnormal telomere maintenance often originate from tissues with low replicative activity and show several mechanisms of preventing telomere attrition to critical levels. Common and rare germline variants affect patterns of somatic mutation, including point mutations, structural variants and somatic retrotransposition. A collection of papers from the PCAWG Consortium describes non-coding mutations that drive cancer beyond those in the TERT promoter(4); identifies new signatures of mutational processes that cause base substitutions, small insertions and deletions and structural variation(5,6); analyses timings and patterns of tumour evolution(7); describes the diverse transcriptional consequences of somatic mutation on splicing, expression levels, fusion genes and promoter activity(8,9); and evaluates a range of more-specialized features of cancer genomes(8,10-18).Peer reviewe
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1.
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- Abdelfatah S
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- Zorzano A
- Zou W
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- Zwerschke W
- Álvarez ÉMC
- Ávalos Y
- Önal G
- Üstün S
- Čolić M
- Đokić J
- Žerovnik E
- Publication venue
- 'Informa UK Limited'
- Publication date
- 01/01/2021
- Field of study
In 2008, we published the first set of guidelines for standardizing research in autophagy. Since then, this topic has received increasing attention, and many scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Thus, it is important to formulate on a regular basis updated guidelines for monitoring autophagy in different organisms. Despite numerous reviews, there continues to be confusion regarding acceptable methods to evaluate autophagy, especially in multicellular eukaryotes. Here, we present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes. These guidelines are not meant to be a dogmatic set of rules, because the appropriateness of any assay largely depends on the question being asked and the system being used. Moreover, no individual assay is perfect for every situation, calling for the use of multiple techniques to properly monitor autophagy in each experimental setting. Finally, several core components of the autophagy machinery have been implicated in distinct autophagic processes (canonical and noncanonical autophagy), implying that genetic approaches to block autophagy should rely on targeting two or more autophagy-related genes that ideally participate in distinct steps of the pathway. Along similar lines, because multiple proteins involved in autophagy also regulate other cellular pathways including apoptosis, not all of them can be used as a specific marker for bona fide autophagic responses. Here, we critically discuss current methods of assessing autophagy and the information they can, or cannot, provide. Our ultimate goal is to encourage intellectual and technical innovation in the field
Combination of searches for heavy spin-1 resonances using 139 fb−1 of proton-proton collision data at s = 13 TeV with the ATLAS detector
- Author
- Aad G
- Aakvaag E
- Abbott B
- Abeling K
- Abicht NJ
- Abidi SH
- Aboelela M
- Aboulhorma A
- Abramowicz H
- Abreu H
- Abulaiti Y
- Acharya BS
- Ackermann A
- Adam Bourdarios C
- Adamczyk L
- Addepalli SV
- Addison MJ
- Adelman J
- Adiguzel A
- Adye T
- Affolder AA
- Afik Y
- Agaras MN
- Agarwala J
- Aggarwal A
- Agheorghiesei C
- Ahmad A
- Ahmadov F
- Ahmed WS
- Ahuja S
- Ai X
- Aielli G
- Aikot A
- Ait Tamlihat M
- Aitbenchikh B
- Aizenberg I
- Akbiyik M
- Akimov AV
- Akiyama D
- Akolkar NN
- Aktas S
- Al Khoury K
- Alberghi GL
- Albert J
- Albicocco P
- Albouy GL
- Alderweireldt S
- Alegria ZL
- Aleksa M
- Aleksandrov IN
- Alexa C
- Alexopoulos T
- Alfonsi F
- Algren M
- Alhroob M
- Ali B
- Ali HMJ
- Ali S
- Alibocus SW
- Aliev M
- Alimonti G
- Alkakhi W
- Allaire C
- Allbrooke BMM
- Allen JF
- Allendes Flores CA
- Allport PP
- Aloisio A
- Alonso F
- Alpigiani C
- Alvarez Estevez M
- Alvarez Fernandez A
- Alves Cardoso M
- Alviggi MG
- Aly M
- Amaral Coutinho Y
- Ambler A
- Amelung C
- Amerl M
- Ames CG
- Amidei D
- Amirie KJ
- Amor Dos Santos SP
- Amos KR
- An S
- Ananiev V
- Anastopoulos C
- Andeen T
- Anders JK
- Andrean SY
- Andreazza A
- Angelidakis S
- Angerami A
- Anisenkov AV
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- Anthony MT
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- Zhemchugov A
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- Zwalinski L
- Åkesson TPA
- Öncel ÖO
- Ženiš T
- Živković L
- Publication venue
- Springer Nature
- Publication date
- 19/04/2024
- Field of study
A combination of searches for new heavy spin-1 resonances decaying into different pairings of W, Z, or Higgs bosons, as well as directly into leptons or quarks, is presented. The data sample used corresponds to 139 fb−1 of proton-proton collisions at
= 13 TeV collected during 2015–2018 with the ATLAS detector at the CERN Large Hadron Collider. Analyses selecting quark pairs (qq, bb,
, and tb) or third-generation leptons (τν and ττ) are included in this kind of combination for the first time. A simplified model predicting a spin-1 heavy vector-boson triplet is used. Cross-section limits are set at the 95% confidence level and are compared with predictions for the benchmark model. These limits are also expressed in terms of constraints on couplings of the heavy vector-boson triplet to quarks, leptons, and the Higgs boson. The complementarity of the various analyses increases the sensitivity to new physics, and the resulting constraints are stronger than those from any individual analysis considered. The data exclude a heavy vector-boson triplet with mass below 5.8 TeV in a weakly coupled scenario, below 4.4 TeV in a strongly coupled scenario, and up to 1.5 TeV in the case of production via vector-boson fusion
Measurement and interpretation of same-sign W boson pair production in association with two jets in pp collisions at s = 13 TeV with the ATLAS detector
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- Zhemchugov A
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- Åkesson TPA
- Öncel ÖO
- Ženiš T
- Živković L
- Publication venue
- Springer Nature
- Publication date
- 01/04/2024
- Field of study
This paper presents the measurement of fducial and diferential cross sections for both the inclusive and electroweak production of a same-sign W-boson pair in association with two jets (W±W±jj) using 139 fb−1 of proton-proton collision data recorded at a centre-of-mass energy of √s = 13 TeV by the ATLAS detector at the Large Hadron Collider. The analysis is performed by selecting two same-charge leptons, electron or muon, and at least two jets with large invariant mass and a large rapidity diference. The measured fducial cross sections for electroweak and inclusive W±W±jj production are 2.92 ± 0.22 (stat.) ± 0.19 (syst.)fb and 3.38±0.22 (stat.)±0.19 (syst.)fb, respectively, in agreement with Standard Model predictions. The measurements are used to constrain anomalous quartic gauge couplings by extracting 95% confdence level intervals on dimension-8 operators. A search for doubly charged Higgs bosons H±± that are produced in vector-boson fusion processes and decay into a same-sign W boson pair is performed. The largest deviation from the Standard Model occurs for an H±± mass near 450 GeV, with a global signifcance of 2.5 standard deviations
Measurements of differential cross-sections in top-quark pair events with a high transverse momentum top quark and limits on beyond the Standard Model contributions to top-quark pair production with the ATLAS detector at √s = 13 TeV
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- Abhayasinghe DK
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- Bussey PJ
- Butler JM
- Buttar CM
- Butterworth JM
- Buttinger W
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- Cabras G
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- Calafiura P
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- Camerlingo MT
- Cameron D
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- Camplani A
- Canale V
- Canesse A
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- Cao Y
- Capocasa F
- Capriles FGD
- Capua M
- Carbone A
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- Cardillo F
- Carducci G
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- Carlson BT
- Carlson EM
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- Casado MP
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- Cherepanova E
- Cheu E
- Cheung K
- Chevalier L
- Chiarella V
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- Chiodini G
- Chisholm AS
- Chitan A
- Chiu YH
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- Chou Y
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- Chowdhury T
- Christopher LD
- Chu MC
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- Chwastowski JJ
- Cieri D
- Ciesla KM
- Cindro V
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- Cirotto F
- Citron ZH
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- Clark A
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- Clawson SE
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- Corpe LD
- Corradi M
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- de Renstrom PAB
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- Zaid E
- Zaitsev AM
- Zakareishvili T
- Zakharchuk N
- Zambito S
- Zanzi D
- Zaplatilek O
- Zeissner SV
- Zeitnitz C
- Zeng JC
- Zenger DT
- Zenin O
- Zenis T
- Zenz S
- Zerradi S
- Zerwas D
- Zhang B
- Zhang DF
- Zhang G
- Zhang J
- Zhang K
- Zhang L
- Zhang M
- Zhang R
- Zhang S
- Zhang X
- Zhang X
- Zhang Z
- Zhao H
- Zhao P
- Zhao T
- Zhao Y
- Zhao Z
- Zhemchugov A
- Zheng Z
- Zhong D
- Zhou B
- Zhou C
- Zhou H
- Zhou N
- Zhou Y
- Zhu C
- Zhu CG
- Zhu H
- Zhu HL
- Zhu J
- Zhu Y
- Zhuang X
- Zhukov K
- Zhulanov V
- Zieminska D
- Zimine NI
- Zimmermann S
- Zinsser J
- Ziolkowski M
- Zoccoli A
- Zoch K
- Zorbas TG
- Zormpa O
- Zou W
- Zwalinski L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2022
- Field of study
Cross-section measurements of top-quark pair production where the hadronically decaying top quark has transverse momentum greater than 355 GeV and the other top quark decays into ℓνb are presented using 139 fb−1 of data collected by the ATLAS experiment during proton-proton collisions at the LHC. The fiducial cross-section at s = 13 TeV is measured to be σ = 1.267 ± 0.005 ± 0.053 pb, where the uncertainties reflect the limited number of data events and the systematic uncertainties, giving a total uncertainty of 4.2%. The cross-section is measured differentially as a function of variables characterising the tt¯ system and additional radiation in the events. The results are compared with various Monte Carlo generators, including comparisons where the generators are reweighted to match a parton-level calculation at next-to-next-to-leading order. The reweighting improves the agreement between data and theory. The measured distribution of the top-quark transverse momentum is used to search for new physics in the context of the effective field theory framework. No significant deviation from the Standard Model is observed and limits are set on the Wilson coefficients of the dimension-six operators OtG and Otq(8), where the limits on the latter are the most stringent to date. [Figure not available: see fulltext.]
Corrigendum to "Search for flavour-changing neutral-current couplings between the top quark and the photon with the ATLAS detector at √s=13 TeV" (Physics Letters B, 842 (2023), 137379)
- Author
- Aad G
- Abbott B
- Abbott Dc
- Abed Abud A
- Abeling K
- Abidi Sh
- Aboulhorma A
- Abramowicz H
- Abreu H
- Abulaiti Y
- Abusleme Hoffman Ac
- Acharya Bs
- Achkar B
- Adam Bourdarios C
- Adam L
- Adamczyk L
- Adamek L
- Addepalli Sv
- Adelman J
- Adiguzel A
- Adorni S
- Adye T
- Affolder Aa
- Afik Y
- Agaras Mn
- Agarwala J
- Aggarwal A
- Agheorghiesei C
- Aguilar-Saavedra Ja
- Ahmad A
- Ahmadov F
- Ahmed Ws
- Ai X
- Aielli G
- Aizenberg I
- Akbiyik M
- Akimov Av
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- Alberghi Gl
- Albert J
- Albicocco P
- Alconada Verzini Mj
- Alderweireldt S
- Aleksa M
- Aleksandrov In
- Alexa C
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- Alfonsi A
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- Alhroob M
- Ali B
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- Calvet D
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- Camacho Toro R
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- Camarero Munoz D
- Camarri P
- Camerlingo Mt
- Cameron D
- Camincher C
- Campanelli M
- Camplani A
- Canale V
- Canesse A
- Cano Bret M
- Cantero J
- Cao Y
- Capocasa F
- Capua M
- Carbone A
- Cardarelli R
- Cardenas Jcj
- Cardillo F
- Carli T
- Carlino G
- Carlson Bt
- Carlson Em
- Carminati L
- Carnesale M
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- Carratta G
- Carrá S
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- Carter Tm
- Casado Mp
- Casha Af
- Castiglia Eg
- Castillo Garcia L
- Castillo Gimenez V
- Castillo Fl
- Castro Nf
- Catinaccio A
- Catmore Jr
- Cavaliere V
- Cavalli N
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- Celebi E
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- Cerqueira As
- Cerri A
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- Cervelli A
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- Cherkaoui El Moursli R
- Cheu E
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- Chevalier L
- Chiarella V
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- Chiodini G
- Chisholm As
- Chitan A
- Chiu Yh
- Chizhov Mv
- Choi K
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- Czurylo Mm
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- Zhulanov V
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- Ziolkowski M
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- Zwalinski L
- Ženiš T
- Živković L
- Publication venue
- ELSEVIER
- Publication date
- 01/01/2023
- Field of study
Mesenchymal stem cells in cardiac regeneration: a detailed progress report of the last 6 years (2010–2015)
- Author
- A Arminan
- A Behfar
- A Erices
- A Flynn
- A Lindenmair
- A Matsakas
- A Miskon
- A Mohyeldin
- A Shabbir
- A Shabbir
- A Torsvik
- AA Ramkisoensing
- AI Mahmoud
- AJ Wagers
- AP Beltrami
- AR Williams
- AR Williams
- AS Zot
- AV Schittini
- B Assmus
- B Cai
- B Huang
- B Meder
- B Nadal-Ginard
- B Ramesh
- B Shen
- B Shi
- B Shi
- B Short
- B Tao
- B Trachtenberg
- B Zeng
- B Zheng
- BE Tuch
- BJ Kang
- BN Oskouei
- BR Weil
- BR Weil
- C Campagnoli
- C Cao
- C Hodonsky
- C Jopling
- C Liu
- C Mias
- C Peng
- C Wan
- CA Herberts
- CH Fang
- CH Li
- CK Sun
- CM Kolf
- CM Wang
- CY Fong
- CY Tay
- D Baksh
- D Dakhlallah
- D Konstantinou
- D Pankajakshan
- D Shinmura
- D Szczesna
- D Wang
- D Yang
- DE Michele
- DF Lu
- DP Bartel
- E Bostjancic
- E Fiumana
- E Gunsilius
- EC Perin
- EG Schmuck
- EJ Lee
- EJ Lee
- F Santos dos
- F Wei
- FP Barry
- FR Sharp
- FZ Asumda
- G Chamberlain
- G Neufeld
- G Tan
- G Vunjak-Novakovic
- GF Zhao
- GV Srikanth
- GW Serrao
- GW Zhang
- H Liang
- H Okura
- H Tsuji
- H Xu
- HD Guo
- HI Ammar
- HJ Kang
- HM Hodgkiss-Geere
- HW Lee
- I Cerrada
- I Moscoso
- I Perea-Gil
- IA Ikhapoh
- IA Ikhapoh
- IK Ko
- J Chen
- J Chen
- J Cho
- J Doostzadeh
- J Guan
- J Guo
- J He
- J Hou
- J Jin
- J Liang
- J Mao
- J Otto Beitnes
- J Radhakrishnan
- J Tang
- J Tang
- J Yang
- J Yao
- J Yu
- J Zhang
- J Zhang
- J Zhang
- J Zhang
- J Zhao
- JA Passipieri
- JA Poynter
- JC Kovacic
- JE Morgan
- JF Marti Masso
- JG He
- JJ Minguell
- JJ Zhao
- JK Fraser
- JL Carvalho
- JL Herrmann
- JL Liu
- JM Hare
- JM Hare
- JM Hows
- JM Singelyn
- JM Wiehe
- JO Jeong
- JS Silva Da
- JT Buijs
- JT Shieh
- JW Lee
- JX Wang
- K Alestalo
- K Anastasiadis
- K Kang
- K Mareschi
- K Yang
- K Zeng
- KE Hatzistergos
- KE Sullivan
- KR Brunt
- L Coultas
- L Gao
- L Hao
- L Hegyi
- L Li
- L Song
- L Timmers
- L Ye
- LJ Nesti
- LL Zhang
- LR Gao
- LR Gao
- LR Gao
- LT Weckbach
- M Alvarez-Viejo
- M Autiero
- M Bilal
- M Dominici
- M Gyongyosi
- M Latifpour
- M Mazo
- M Mushtaq
- M Nayan
- M Tachibana
- M Tang
- M Wang
- M Wang
- M Zamani
- MA Laflamme
- MA Ngo
- MC Collins
- ME Bernardo
- ME Jeffords
- MF Pittenger
- MG Frid
- MJ Griffiths
- MJ Hoogduijn
- MK Singh
- ML Steinhauser
- MM Zaruba
- MS Oliveira
- MS Penn
- MY Emmert
- N Amariglio
- N Li
- N Liu
- N Ma
- N Yin
- NA Turner
- NH Chi
- O Ham
- OK Lee
- P Antonitsis
- P Bourin
- P Dixit
- P Hua
- P Li
- P Maureira
- P Musialek
- P Quijada
- P Zhao
- PA Hall
- PH Carvalho
- Q Cao
- Q Li
- Q Mao
- Q Mao
- Q Qian
- Q Sun
- Q Yu
- R Bolli
- R Das
- R Hass
- R Herrmann
- R Huss
- R Jong de
- R Koninckx
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- R Santhakumar
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- RF Wynn
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- S Movafagh
- S Mureli
- S Sharma
- S Tomita
- S Vellasamy
- S Vogel
- S Vogel
- S Willis
- S Wisel
- SA Doppler
- SF Askar
- SF Rodrigo
- SH Kim
- SJ Matkovich
- SK Ling
- SL Zhao
- SW Kim
- SW Kim
- SX Zheng
- T Lawrence
- T Li
- T Mohri
- T Mohri
- T Nagamura-Inoue
- T Tsubokawa
- T Wang
- TB Rogers
- TI Spoel van der
- TJ Standiford
- TT Lau
- V Dayan
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- W Xiao
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- X Yan
- X Yao
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- XP Huang
- XP Long
- Y Chen
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- Y Mu
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- Y Sawa
- Y Tong
- Y Wang
- Y Wang
- Y Wang
- Y Wang
- Y Xing
- Y Xu
- Y Ye
- Y Zhang
- Y Zhao
- YA Romanov
- YL Chen
- YL Liu
- YL Xu
- YS Kim
- YS Kim
- YY Du
- YY Du
- Z Li
- Z Wen
- Z Zhang
- Z Zhong
- ZB Ruan
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
- …