44 research outputs found
A High-Resolution Whole-Genome Map of Key Chromatin Modifications in the Adult Drosophila melanogaster
- Author
- A Barski
- A Bird
- A Ebert
- A Ebert
- AE Rougvie
- AJ Bannister
- AM Johansson
- AR Kornblihtt
- BE Bernstein
- BR Graveley
- CD Smith
- CHMJ Wu
- CR Vakoc
- D Enderle
- D Vermaak
- DE Cryderman
- DE Schones
- Debasish Raha
- E de Wit
- E de Wit
- EN Andreyeva
- F De Lucia
- G Schotta
- GW Muse
- H Tilgner
- H Yin
- Haifan Lin
- Hang Yin
- J Zeitlinger
- JA Rosenfeld
- JD Keene
- JK Wiencke
- L Piacentini
- L Piacentini
- L Rastelli
- L Ringrose
- L Ringrose
- LP Liu
- M Lachner
- M Pal-Bhadra
- MC Siomi
- MG Guenther
- Michael Snyder
- N Negre
- ND Heintzman
- P Kolasinska-Zwierz
- PV Kharchenko
- R Andersson
- S Nahkuri
- S Nechaev
- S Pepke
- S Schwartz
- Sarah Sweeney
- SC Elgin
- T Jenuwein
- T Kouzarides
- TN Mavrich
- TY Roh
- VV Kapitonov
- Wolf Reik
- Publication venue
- Public Library of Science
- Publication date
- 01/12/2011
- Field of study
Epigenetic research has been focused on cell-type-specific regulation; less is known about common features of epigenetic programming shared by diverse cell types within an organism. Here, we report a modified method for chromatin immunoprecipitation and deep sequencing (ChIPâSeq) and its use to construct a high-resolution map of the Drosophila melanogaster key histone marks, heterochromatin protein 1a (HP1a) and RNA polymerase II (polII). These factors are mapped at 50-bp resolution genome-wide and at 5-bp resolution for regulatory sequences of genes, which reveals fundamental features of chromatin modification landscape shared by major adult Drosophila cell types: the enrichment of both heterochromatic and euchromatic marks in transposons and repetitive sequences, the accumulation of HP1a at transcription start sites with stalled polII, the signatures of histone code and polII level/position around the transcriptional start sites that predict both the mRNA level and functionality of genes, and the enrichment of elongating polII within exons at splicing junctions. These features, likely conserved among diverse epigenomes, reveal general strategies for chromatin modifications
The effectiveness of a low-intensity problem-solving intervention for common adolescent mental health problems in New Delhi, India: protocol for a school-based, individually randomized controlled trial with an embedded stepped-wedge cluster randomized controlled recruitment trial
- Author
- A Nadkarni
- A.-W. Chan
- Adriaan Hoogendoorn
- Amit Dias
- B Bonevski
- BF Chorpita
- BF Chorpita
- Bharath Srikala
- Bhargav Bhat
- Brandon A. Kohrt
- Bruce F. Chorpita
- C Notley
- Christopher G. Fairburn
- D Michelson
- D Moher
- Daisy R. Singla
- Daniel L. Larsen
- Daniel Michelson
- EA Holmes
- Helen A. Weiss
- J GarcĂa-Escalera
- J Morris
- J.A. Thompson
- Jai K. Das
- James L. Peugh
- Jeroen Ruwaard
- John R. Weisz
- JR Weisz
- Kallol Roy
- Kamlesh Singh
- Kanika Malik
- Kate Muse
- KUNG-YEE LIANG
- L Chiappetta
- LC Santucci
- LK Marchette
- LK Murray
- LK Murray
- Madhuri Krishna
- Michael King
- ML Belfer
- MM Boustani
- P Bolton
- Paulomi Sudhir
- Pim Cuijpers
- Poornima Bhola
- Praveetha Patalay
- PY Collins
- R Parikh
- Rachana Parikh
- RC Kessler
- Rhea Sharma
- Robert Goodman
- Rooplata Sahu
- RS Lazarus
- S Vellakkal
- Sachin Shinde
- Sarah Stewart-Brown
- Sheldon Cohen
- Shoba Srinath
- Sonal Mathur
- Thomas R Sullivan
- V Patel
- Vikram Patel
- VW Madurasinghe
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2019
- Field of study
Background
Conduct, anxiety and depressive disorders account for over 75% of the adolescent mental health burden globally. The current protocol will test a low-intensity problem-solving intervention for school-going adolescents with common mental health problems in India. The protocol also tests the effects of a classroom-based sensitization intervention on the demand for counselling services in an embedded recruitment trial.
Methods
We will conduct a two-arm individually randomized controlled trial in six Government-run secondary schools in New Delhi. The targeted sample is 240 adolescents in grades 9-12 with persistent, elevated mental health symptoms and associated impact. Participants will receive either a brief problem-solving intervention delivered over 3 weeks by lay counsellors (intervention), or enhanced usual care comprised of problem-solving booklets (control). Self-reported adolescent mental health symptoms and idiographic problems will be assessed at 6 weeks (co-primary outcomes) and again at 12 weeks post-randomization. In addition, adolescent-reported impact of mental health difficulties, perceived stress, mental wellbeing and clinical remission, as well as parent-reported adolescent mental health symptoms and impact scores, will be assessed at 6 and 12 weeks post-randomization. We will also complete a parallel process evaluation, including estimations of the costs of delivering the interventions.
An embedded recruitment trial will apply a stepped-wedge, cluster (class)-randomized controlled design in 70 classes across the six schools. This will evaluate the added impact of a classroom-based sensitization intervention over school-level recruitment sensitization activities on the primary outcome of referral rate into the host trial (i.e. the proportion of adolescents referred as a function of the total sampling frame in each condition of the embedded recruitment trial). Other outcomes will be the proportion of referrals eligible to participate in the host trial, proportion of self-generated referrals, and severity and pattern of symptoms among referred adolescents in each condition. Power calculations were undertaken separately for each trial. A detailed statistical analysis plan will be developed separately for each trial prior to unblinding.
Discussion
Both trials were initiated on 20 August 2018. A single research protocol for both trials offers a resource-efficient methodology for testing the effectiveness of linked procedures to enhance uptake and outcomes of a school-based psychological intervention for common adolescent mental health problems
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Observation of electroweak production of two jets in association with an isolated photon and missing transverse momentum, and search for a Higgs boson decaying into invisible particles at 13 TeV with the ATLAS detector
- Author
- Aad G
- Abbott B
- Abbott DC
- Abeling K
- Abhayasinghe DK
- Abidi SH
- Aboulhorma A
- Abramowicz H
- Abreu H
- Abud A Abed
- Abulaiti Y
- Acharya BS
- Achkar B
- Adam L
- Adamczyk L
- Adamek L
- Addepalli SV
- Adelman J
- Adiguzel A
- Adorni S
- Adye T
- Affolder AA
- Afik Y
- Agapopoulou C
- Agaras MN
- Agarwala J
- Aggarwal A
- Agheorghiesei C
- Aguilar-Saavedra JA
- Agullo P Martinez
- Ahmad A
- Ahmadov F
- Ahmed WS
- Ai X
- Aielli G
- Aizenberg I
- Akatsuka S
- Akbiyik M
- Akesson TPA
- Akimov AV
- Al Khoury K
- Alberghi GL
- Albert J
- Albicocco P
- Alderweireldt S
- Aleksa M
- Aleksandrov IN
- Alexa C
- Alexopoulos T
- Alfonsi A
- Alfonsi F
- Alhroob M
- Ali B
- Ali S
- Aliev M
- Alimonti G
- Allaire C
- Allbrooke BMM
- Allport PP
- Aloisio A
- Alonso F
- Alpigiani C
- Alves FL Lucio
- Alviggi MG
- Ambler A
- Ambroz L
- Amelung C
- Amidei D
- Amoroso S
- Amrouche CS
- Anastopoulos C
- Andana RY Gonzalez
- Andari N
- Andeen T
- Anders JK
- Andrean SY
- Andreazza A
- Angelidakis S
- Angerami A
- Anisenkov AV
- Annovi A
- Antel C
- Anthony MT
- Antipov E
- Antonelli M
- Antrim DJA
- Anulli F
- Aoki M
- Aparo MA
- Aranda C Padilla
- Aranzabal N
- Araya S Tapia
- Arcangeletti C
- Arce ATH
- Arena E
- Arguin J-F
- Argyropoulos S
- Arling J-H
- Armbruster AJ
- Armstrong A
- Arnaez O
- Arnold H
- Artoni G
- Asada H
- Asai K
- Asai S
- Asbah NA
- Asimakopoulou EM
- Asquith L
- Assahsah J
- Assamagan K
- Astalos R
- Astigarraga ME Pozo
- Atkin RJ
- Atkinson M
- Atlay NB
- Atmani H
- Atmasiddha PA
- Augsten K
- Auricchio S
- Austrup VA
- Avner G
- Avolio G
- Ayoub MK
- Azuelos G
- Babal D
- Bachacou H
- Bachas K
- Bachiu A
- Backman F
- Badea A
- Bagnaia P
- Bahilo JJ Lozano
- Bahrasemani H
- Bailey AJ
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- Bakker PJ
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- Baldin EM
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- Zagazeta LF Gutierrez
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- Zhemchugov A
- Zheng Z
- Zhong D
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- Zhulanov V
- Zieminska D
- Zimine NI
- Zimmermann S
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- Ziolkowski M
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- Zorbas TG
- Zormpa O
- Zou W
- Zwalinski L
- Publication venue
- EUROPEAN PHYSICAL JOURNAL C
- Publication date
- 03/02/2022
- Field of study
This paper presents the measurement of the electroweak production of two jets
in association with a ZÎł pair with the Z boson decaying into two
neutrinos. It also presents the search for invisible or partially invisible
decays of a Higgs boson with a mass of 125 GeV produced through vector-boson
fusion with a photon in the final state. These results use data from LHC
proton-proton collisions at sâ = 13 TeV collected with the ATLAS
detector corresponding to an integrated luminosity of 139 fbâ1. The event
signature, shared by all benchmark processes considered for measurements and
searches, is characterized by a significant amount of unbalanced transverse
momentum and a photon in the final state, in addition to a pair of forward
jets. For electroweak production of ZÎł in association with two jets, the
background-only hypothesis is rejected with an observed (expected) significance
of 5.2 (5.1) standard deviations. The measured fiducial cross-section for this
process is 1.31±0.29 fb. Observed (expected) upper limit of 0.37 (0.34) at
95% confidence level is set on the branching ratio of a 125 GeV Higgs boson to
invisible particles, assuming the Standard Model production cross-section. The
signature is also interpreted in the context of decays of a Higgs boson to a
photon and a dark photon. An observed (expected) 95% CL upper limit on the
branching ratio for this decay is set at 0.018 (0.017), assuming the 125 GeV
Standard Model Higgs boson production cross-section
Recommended from our members
The ATLAS inner detector trigger performance in pp collisions at 13 TeV during LHC Run 2
- Author
- Aad G
- Abbott B
- Abbott DC
- Abeling K
- Abhayasinghe DK
- Abidi SH
- AbouZeid OS
- Abraham NL
- Abramowicz H
- Abreu H
- Abud A Abed
- Abulaiti Y
- Acharya BS
- Achkar B
- Adam L
- Adamczyk L
- Adamek L
- Adelman J
- Adiguzel A
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- Adye T
- Affolder AA
- Afik Y
- Agapopoulou C
- Agaras MN
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- Agheorghiesei C
- Aguilar-Saavedra JA
- Agullo P Martinez
- Ahmad A
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- Akesson TPA
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- Alberghi GL
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- Aleksa M
- Aleksandrov IN
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- Zhuang X
- Zhukov K
- Zhulanov V
- Zieminska D
- Zimine NI
- Zimmermann S
- Zinonos Z
- Ziolkowski M
- Zivkovic L
- Zoccoli A
- Zoch K
- Zorbas TG
- Zou R
- Zou W
- Zwalinski L
- Publication venue
- EUROPEAN PHYSICAL JOURNAL C
- Publication date
- 08/03/2022
- Field of study
The design and performance of the inner detector trigger for the high level
trigger of the ATLAS experiment at the Large Hadron Collider during the 2016-18
data taking period is discussed. In 2016, 2017, and 2018 the ATLAS detector
recorded 35.6 fbâ1, 46.9 fbâ1, and 60.6 fbâ1 respectively of
proton-proton collision data at a centre-of-mass energy of 13 TeV. In order to
deal with the very high interaction multiplicities per bunch crossing expected
with the 13 TeV collisions the inner detector trigger was redesigned during the
long shutdown of the Large Hadron Collider from 2013 until 2015. An overview of
these developments is provided and the performance of the tracking in the
trigger for the muon, electron, tau and b-jet signatures is discussed. The
high performance of the inner detector trigger with these extreme interaction
multiplicities demonstrates how the inner detector tracking continues to lie at
the heart of the trigger performance and is essential in enabling the ATLAS
physics programme
The ATLAS inner detector trigger performance in pp collisions at 13 TeV during LHC Run 2
- Author
- Aad G
- Abbott B
- Abbott DC
- Abeling K
- Abhayasinghe DK
- Abidi SH
- AbouZeid OS
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- Abramowicz H
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- Suarez R Gonzalez
- Sulin VV
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- Sultan DMS
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- Suster CJE
- Sutton MR
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- Swift SP
- Swirski T
- Sydorenko A
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- Tosciri C
- Toth J
- Tovey DR
- Traeet A
- Treado CJ
- Trefzger T
- Tresoldi F
- Tricoli A
- Trigger IM
- Trincaz-Duvoid S
- Trischuk DA
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- Trocme B
- Trofymov A
- Troncon C
- Trovato F
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- Trzebinski M
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- Tsiskaridze V
- Tskhadadze EG
- Tsopoulou M
- Tsukerman II
- Tsulaia V
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- Tu Y
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- Tudorache V
- Tuna AN
- Turchikhin S
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- Turner RJ
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- Tuts PM
- Tzamarias S
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- Urban S Cabrera
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- Vacek V
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- Vaidya A
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- Vale T Dias Do
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- Valentinetti S
- Valero A
- Valery L
- Vallance RA
- Vallier A
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- Vandenbroucke M
- Vandewall ER
- Vannicola D
- Vari R
- Varnes EW
- Varni C
- Varol T
- Varouchas D
- Varvell KE
- Vasile ME
- Vasquez GA
- Vazeille F
- Vazquez CJ Buxo
- Vazquez JG Panduro
- Veatch J
- Vecchio V
- Veen MJ
- Veloce LM
- Veloso F
- Veneziano S
- Ventura A
- Vera AM Rodriguez
- Verbytskyi A
- Verducci M
- Vergara JC Rivera
- Vergis C
- Verkerke W
- Vermeulen AT
- Vermeulen JC
- Vernieri C
- Verschuuren PJ
- Verzini MJ Alconada
- Vesterbacka ML
- Vetterli MC
- Vickey T
- Viehhauser GHA
- Vigani L
- Villa M
- Villhauer EM
- Vilucchi E
- Vincter MG
- Virdee GS
- Vishwakarma A
- Vittori C
- Vivarelli I
- Vogel M
- Vokac P
- Volpe D Della
- Vorobel V
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- Vossebeld JH
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- Vrba V
- Vreeswijk M
- Vu NK
- Vuillermet R
- Vukotic I
- Vulpen I Van
- Wada S
- Wagner C
- Wagner P
- Wagner W
- Wahdan S
- Wahlberg H
- Wakasa R
- Walbrecht VM
- Walder J
- Walker R
- Walker SD
- Walkowiak W
- Wallangen V
- Walls FM Garay
- Wang AM
- Wang AZ
- Wang C
- Wang C
- Wang H
- Wang J
- Wang P
- Wang R
- Wang R
- Wang R-J
- Wang S
- Wang SM
- Wang T
- Wang WT
- Wang WX
- Wang Y
- Wang Z
- Wanotayaroj C
- Warburton A
- Ward CP
- Ward RJ
- Warrack N
- Watson AT
- Watson MF
- Watts G
- Waugh BM
- Webb AF
- Weber C
- Weber MS
- Weber SA
- Weber SM
- Wei Y
- Weidberg AR
- Weingarten J
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- Weiser C
- Wells PS
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- Wendland B
- Wengler T
- Wenig S
- Wermes N
- Wessels M
- Weston TD
- Whalen K
- Wharton AM
- White A
- White AS
- White MJ
- Whiteson D
- Whitmore BW
- Wiedenmann W
- Wiel C
- Wielers M
- Wieseotte N
- Wiglesworth C
- Wiik-Fuchs LAM
- Wilkens HG
- Wilkins LJ
- Williams DM
- Williams HH
- Williams Sarah
- Willocq S
- Windischhofer PJ
- Wingerter-Seez I
- Winkels E
- Winklmeier F
- Winter BT
- Wittgen M
- Wobisch M
- Wolf A
- Wolker R
- Wollrath J
- Wolter MW
- Wolters H
- Wong VWS
- Wongel AF
- Woods NL
- Worm SD
- Wosiek BK
- Wozniak KW
- Wraight K
- Wu SL
- Wu X
- Wu Y
- Wuerzinger J
- Wyatt TR
- Wynne BM
- Xella S
- Xiang J
- Xiao X
- Xie X
- Xiotidis I
- Xu D
- Xu H
- Xu H
- Xu L
- Xu R
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- Xu Z
- Xu Z
- Yabsley B
- Yacoob S
- Yallup David
- Yamaguchi N
- Yamaguchi Y
- Yamatani M
- Yamauchi H
- Yamazaki T
- Yamazaki Y
- Yan J
- Yan Z
- Yang HJ
- Yang HT
- Yang S
- Yang T
- Yang X
- Yang X
- Yang Y
- Yang Z
- Yao W-M
- Yap YC
- Ye H
- Ye J
- Ye S
- Yeletskikh I
- Yexley MR
- Yildiz H Duran
- Yin P
- Yorita K
- Yoshihara K
- Young C
- Young CJS
- Yuan R
- Yue X
- Zaazoua M
- Zabinski B
- Zacharis G
- Zaffaroni E
- Zagazeta LF Gutierrez
- Zaitsev AM
- Zakareishvili T
- Zakharchuk N
- Zambito S
- Zanzi D
- Zeissner SV
- Zeitnitz C
- Zemaityte G
- Zeng JC
- Zenin O
- Zenis T
- Zenz S
- Zerradi S
- Zerwas D
- Zgubic M
- Zhang B
- Zhang DF
- Zhang G
- Zhang J
- Zhang K
- Zhang L
- Zhang L
- Zhang M
- Zhang R
- Zhang S
- Zhang X
- Zhang X
- Zhang Y
- Zhang Z
- Zhao P
- Zhao Y
- Zhao Z
- Zhemchugov A
- Zheng Z
- Zhong D
- Zhou B
- Zhou C
- Zhou H
- Zhou M
- 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
- Zinonos Z
- Ziolkowski M
- Zivkovic L
- Zoccoli A
- Zoch K
- Zorbas TG
- Zou R
- Zou W
- Zwalinski L
- Publication venue
- EUROPEAN PHYSICAL JOURNAL C
- Publication date
- 01/01/2022
- Field of study
The design and performance of the inner detector trigger for the high level
trigger of the ATLAS experiment at the Large Hadron Collider during the 2016-18
data taking period is discussed. In 2016, 2017, and 2018 the ATLAS detector
recorded 35.6 fbâ1, 46.9 fbâ1, and 60.6 fbâ1 respectively of
proton-proton collision data at a centre-of-mass energy of 13 TeV. In order to
deal with the very high interaction multiplicities per bunch crossing expected
with the 13 TeV collisions the inner detector trigger was redesigned during the
long shutdown of the Large Hadron Collider from 2013 until 2015. An overview of
these developments is provided and the performance of the tracking in the
trigger for the muon, electron, tau and b-jet signatures is discussed. The
high performance of the inner detector trigger with these extreme interaction
multiplicities demonstrates how the inner detector tracking continues to lie at
the heart of the trigger performance and is essential in enabling the ATLAS
physics programme
Recommended from our members
Averting biodiversity collapse in tropical forest protected areas
- Author
- Abernethy Kate
- Alvarez Patricia
- Arias-G Juan Carlos
- Arroyo Luzmila
- Arroyo-Rodriguez Victor
- Ashton Mark
- Ashton Peter
- Auzel Philippe
- Babaasa Dennis
- Babweteera Fred
- Baker Patrick
- Banki Olaf
- Bass Margot
- Beisiegel Beatriz de Mello
- Benitez-Malvido Julieta
- Bila-Isia Inogwabini
- Blake Stephen
- Blom Allard
- Bobo Kadiri S.
- Bradshaw Corey J. A.
- Brockelman Warren
- Brokaw Nicholas
- Bruehl Carsten A.
- Bunyavejchewin Sarayudh
- Campbell Mason
- Cannon Charles H.
- Cao Min
- Carroll Richard
- Chao Jung-Tai
- Chapman Colin
- Chave Jerome
- Chellam Ravi
- Clark Connie J.
- Clavijo Jose
- Coates Rosamond
- Congdon Robert
- Cords Marina
- Corlett Richard
- da Silva Rosa de Nazarepaes
- Danielsen Finn
- Dattaraja H. S.
- Dave Chittaranjan
- Davies Glyn
- de Almeida Samuel Soares
- de Castilho Carolina Volkmer
- De Dijn Bart
- Di Fiore Anthony
- Diesmos Arvin
- Dinerstein Eric
- Dirzo Rodolfo
- Donnelly Maureen A.
- Doran-Sheehy Diane
- Eaton Mitchell
- Edwards David
- Edwards Felicity
- Emmons Louise
- Estrada Alejandro
- Ewango Corneille
- Farwig Nina
- Fashing Peter
- Fedigan Linda
- Feer Francois
- Forget Pierre-Michel
- Foster Mercedes
- Fruth Barbara
- Gale George
- Goodale Uromi
- Goodman Steven
- Guix Juan C.
- Guthiga Paul
- Haber William
- Hamer Keith
- Harris David
- Harrison Rhett
- Hart John
- Herbinger Ilka
- Hill Jane
- Huang Zhongliang
- Ickes Kalan
- Itoh Akira
- Ivanauskas Natalia
- Jackes Betsy
- Janovec John
- Janzen Daniel
- Jiangming Mo
- Jin Chen
- Jones Trevor
- Justiniano Hermes
- Kalka Margareta
- Kalko Elisabeth
- Karpanty Sarah
- Kasangaki Aventino
- Killeen Timothy
- King Hen-biau
- Klop Erik
- Knott Cheryl
- Kone Inza
- Kress W. John
- Krishnaswamy Jagdish
- Kudavidanage Enoka
- Lattke John
- Laurance Susan G.
- Laurance William F.
- Laval Richard
- Lawton Robert
- Leal Miguel
- Leighton Mark
- Lentino Miguel
- Leonel Cristiane
- Lindsell Jeremy
- Ling-Ling Lee
- Linsenmair K. Eduard
- Logsdon Willis
- Losos Elizabeth
- Lovett Jon
- Lugo Ariel
- Lwanga Jeremiah
- Mack Andrew L.
- Magnusson William
- Maisels Fiona
- Marshall Andrew R.
- Martins Marlucia
- McClearn Deedra
- McGraw W. Scott
- McNab Roan
- Montag Luciano
- Mudappa Divya
- Nabe-Nielsen Jacob
- Nakagawa Michiko
- Nepal Sanjay
- Nielsen Martin R.
- Norconk Marilyn
- Novotny Vojtech
- O'Donnell Sean
- Opiang Muse
- Ouboter Paul
- Parker Kenneth
- Parthasarathy N.
- Pearson Richard
- Pisciotta Katia
- Pitman Nigel
- Plumptre Andrew
- Poulsen John
- Prawiradilaga Dewi
- Pringle Catherine
- Quesada Mauricio
- Rainey Hugo
- Rajathurai Subaraj
- Reichard Ulrich
- Reinartz Gay
- Rendeiro Julio
- Renton Katherine
- Reynolds Glen
- Reynolds Vernon
- Ribeiro Jose Lahoz da Silva
- Riley Erin
- Rivera Jorge Vega
- Robinson Douglas
- Roedel Mark-Oliver
- Roetgers Christiane
- Rothman Jessica
- Round Philip
- Rovero Francesco
- Sakai Shoko
- Sanaiotti Tania
- Savini Tommaso
- Scatena Frederick
- Schaab Gertrud
- Schulze Christian
- Seidensticker John
- Sheil Douglas
- Siaka Alhaji
- Silman Miles R.
- Sloan Sean P.
- Smith Thomas B.
- Sodhi Navjot
- Stanford Craig
- Stewart Kristine
- Stokes Emma
- Stoner Kathryn E.
- Struhsaker Thomas
- Sukumar Raman
- Sun I. Fang
- Surbeck Martin
- Terborgh John
- Thomas Duncan
- Thompson Jo Myers
- Timm Robert
- Tobler Mathias
- Tscharntke Teja
- Turkalo Andrea
- Umapathy Govindaswamy
- Urbina-Cardona J. Nicolas
- Useche D. Carolina
- van der Ploeg Jan
- van Weerd Merlijn
- Vasudevan Karthikeyan
- Venkataraman Meena
- Venn Linda
- Verea Carlos
- Waltert Matthias
- Wang Benjamin
- Watts David
- Weber William
- West Paige
- Whitacre David
- Whitney Ken
- Wilkie David
- Williams Stephen
- Willis Jacalyn Giacalone
- Wright Debra D.
- Wright Patricia
- Wright S. Joseph
- Xiankai Lu
- Yonzon Pralad
- Zamzani Franky
- Publication venue
- Macmillan Publishers Limited
- Publication date
- Field of study
The rapid disruption of tropical forests probably imperils global biodiversity more than any other contemporary phenomenonÂčâ»Âł. With deforestation advancing quickly, protected areas are increasingly becoming final refuges for threatened species and natural ecosystem processes. However, many protected areas in the tropics are themselves vulnerable to human encroachment and other environmental stressesâŽâ»âč. As pressures mount, it is vital to know whether existing reserves can sustain their biodiversity. A critical constraint in addressing this question has been that data describing a broad array of biodiversity groups have been unavailable for a sufficiently large and representative sample of reserves. Here we present a uniquely comprehensive data set on changes over the past 20 to 30 years in 31 functional groups of species and 21 potential drivers of environmental change, for 60 protected areas stratified across the worldâs major tropical regions. Our analysis reveals great variation in reserve âhealthâ: about half of all reserves have been effective or performed passably, but the rest are experiencing an erosion of biodiversity that is often alarmingly widespread taxonomically and functionally. Habitat disruption, hunting and forest-product exploitation were the strongest predictors of declining reserve health. Crucially, environmental changes immediately outside reserves seemed nearly as important as those inside in determining their ecological fate, with changes inside reserves strongly mirroring those occurring around them. These findings suggest that tropical protected areas are often intimately linked ecologically to their surrounding habitats, and that a failure to stem broad-scale loss and degradation of such habitats could sharply increase the likelihood of serious biodiversity declines.Keywords: Ecology, Environmental scienc
Caspase-1-Independent Interleukin-1ÎČ Is Required for Clearance of <i>Bordetella pertussis</i> Infections and Whole-Cell Vaccine-Mediated Immunity
- Author
- Publication venue
- Publication date
- 08/09/2014
- Field of study
<div><p>Whooping cough remains a significant disease worldwide and its re-emergence in highly vaccinated populations has been attributed to a combination of imperfect vaccines and evolution of the pathogen. The focus of this study was to examine the role of IL-1α/ÎČ and the inflammasome in generation of the interleukin-1 (IL-1) response, which is required for the clearance of <i>Bordetella pertussis</i>. We show that IL-1ÎČ but not IL-1α is required for mediating the clearance of <i>B. pertussis</i> from the lungs of mice. We further found that IL-1ÎČ and IL-1R deficient mice, compared to wild-type, have similar but more persistent levels of inflammation, characterized by immune cell infiltration, with significantly increased IFNÎł and a normal IL-17A response during <i>B. pertussis</i> infection. Contrary to expectations, the cleavage of precursor IL-1ÎČ to its mature form did not require caspase-1 during primary infections within the lung despite being required by bone marrow-derived macrophages exposed to live bacteria. We also found that the caspase-1 inflammasome was not required for protective immunity against a <i>B. pertussis</i> challenge following vaccination with heat-killed whole cell <i>B. pertussis,</i> despite IL-1R signaling being required. These findings demonstrate that caspase-1-independent host factors are involved in the processing of protective IL-1ÎČ responses that are critical for bacterial clearance and vaccine-mediated immunity.</p></div
Molecular Autopsy for Sudden Death in the Young: Is Data Aggregation the Key?
- Author
- Publication venue
- 'Frontiers Media SA'
- Publication date
- 01/11/2017
- Field of study
The Scripps molecular autopsy study seeks to incorporate genetic testing into the postmortem examination of cases of sudden death in the young (<45âyears old). Here, we describe the results from the first 2âyears of the study, which consisted of whole exome sequencing (WES) of a cohort of 50 cases predominantly from San Diego County. Apart from the individual description of cases, we analyzed the data at the cohort-level, which brought new perspectives on the genetic causes of sudden death. We investigated the advantages and disadvantages of using WES compared to a gene panel for cardiac disease (usually the first genetic test used by medical examiners). In an attempt to connect complex clinical phenotypes with genotypes, we classified samples by their genetic fingerprint. Finally, we studied the benefits of analyzing the mitochondrial DNA genome. In this regard, we found that half of the cases clinically diagnosed as sudden infant death syndrome had an increased ratio of heteroplasmic variants, and that the variants were also present in the mothers. We believe that community-based data aggregation and sharing will eventually lead to an improved classification of variants. Allele frequencies for the all cases can be accessed via our genomics browser at https://genomics.scripps.edu/browser
Adaptive immune responses are IL-1 dependent but Caspase-1 independent.
- Author
- Publication venue
- Publication date
- Field of study
<p>Groups of four mice were either sham vaccinated with PBS or vaccinated with heat-killed <i>B. pertussis</i> (wP) by administering 200 ”L <i>i.p.</i> at 28 and 14 days prior to challenge inoculation with 5Ă10<sup>5</sup> CFU. Lungs were excised at seven days post-challenge and to determine bacterial CFUs. Bar graphs represent the mean CFU per lung ± standard deviation. Significance was determined by one-way ANOVA and Tukeyâs multiple comparison post-hoc test with *p<0.05, ***p<0.001. Data is representative of two independent experiments.</p
IL-1 signaling limits lung inflammation during <i>B. pertussis</i> infection.
- Author
- Publication venue
- Publication date
- Field of study
<p>Groups of four mice were either (AâD) uninfected or inoculated with <i>B. pertussis</i> and euthanized at (EâH) 7 days or (IâL) 28 days post-inoculation. Automated H&E staining was performed on 5 ”m paraffin-embedded sections. Images were taken and are representative of 10â12 fields per group. Lung homogenate cytokine measurements (MâN) were measured by ELISA from uninfected mice or on days 3, 7, 14, or 28 post-inoculation (nâ=â4â8). ELISA significance was determined by one-way ANOVA with Dunnetâs post-hoc test. *p<0.05 represents a significant difference from WT mice.</p