156 research outputs found
The involvement of tau in nucleolar transcription and the stress response
- Author
- A Jamsa
- A Noel
- A Postepska-Igielska
- A Sultan
- AA Cohen
- B Frost
- B McStay
- C Federico
- C Guo
- C Mayer
- D Avitabile
- E Bou Samra
- E GĂłmez de Barreda
- F Oyama
- G Rossi
- H Tsoi
- J Lu
- J Lu
- JD Erickson
- JS Ha
- K Holmberg Olausson
- K Yang
- M Bukar Maina
- M Kodiha
- M Kodiha
- M Nampoothiri
- M Violet
- MD Weingarten
- MK Sjoberg
- PA Loomis
- R Santoro
- RM Brady
- SC Papasozomenos
- T Vanderweyde
- V Soura
- Y Lu
- YK Al-Hilaly
- Z Mansuroglu
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/07/2018
- Field of study
Tau is known for its pathological role in neurodegenerative diseases, including Alzheimerâs disease (AD) and other tauopathies. Tau is found in many subcellular compartments such as the cytosol and the nucleus. Although its normal role in microtubule binding is well established, its nuclear role is still unclear. Here, we reveal that tau localises to the nucleolus in undifferentiated and differentiated neuroblastoma cells (SHSY5Y), where it associates with TIP5, a key player in heterochromatin stability and ribosomal DNA (rDNA) transcriptional repression. Immunogold labelling on human brain sample confirms the physiological relevance of this finding by showing tau within the nucleolus colocalises with TIP5. Depletion of tau results in an increase in rDNA transcription with an associated decrease in heterochromatin and DNA methylation, suggesting that under normal conditions tau is involved in silencing of the rDNA. Cellular stress induced by glutamate causes nucleolar stress associated with the redistribution of nucleolar non-phosphorylated tau, in a similar manner to fibrillarin, and nuclear upsurge of phosphorylated tau (Thr231) which doesnât colocalise with fibrillarin or nucleolar tau. This suggests that stress may impact on different nuclear tau species. In addition to involvement in rDNA transcription, nucleolar non-phosphorylated tau also undergoes stress-induced redistribution similar to many nucleolar protein
Serious mental illness and smoking cessation
- Author
- Anthenelli RM
- Apollonio DE
- Ashton M
- Ashton M
- Aveyard P
- Baker A
- Banham L.
- Campion J
- Campion J
- Ebbert JO
- Ferguson D
- George TP
- Godfrey C
- Hall SM
- Hehir AM
- Hertzberg MA
- Hitsman B
- Hughes JR.
- Ingram I
- Johnson JL.
- Kendler KS
- Koegelenberg CF
- Korhonen T
- Lancaster T
- Lawrence D
- Mathew AR
- McClave AK
- McNally L
- Morris CD
- Nohlert E
- Novak G
- Patkar AA
- Prochaska JJ
- Prochaska JJ.
- Ratschen E
- Rigotti NA
- Roberts E
- Robson D
- Sharma R
- Stead LF
- Stead LF
- Szatkowski L
- Taylor G
- Tsoi DT
- Ware JH
- West R
- Publication venue
- 'Mark Allen Group'
- Publication date
- 01/01/2018
- Field of study
Smoking rates among individuals with severe mental illness are significantly higher than in the general population. Contrary to common perception, individuals with severe mental illness have been shown to be motivated to quit smoking. This paper discusses and synthesises literature on smoking among individuals with severe mental illness and contributes to the debate about the significant role mental health professionals can play in targeting the effective cessation therapies towards smokers with severe mental illness. Severe mental illnesses include schizophrenia, paranoid and other psychotic disorders, psychotic depression, bipolar affective disorder, major depression
Effective and safe proton pump inhibitor therapy in acid-related diseases â A position paper addressing benefits and potential harms of acid suppression
- Author
- A Andriulli
- A Berstad
- A Booker
- A Brown
- A Deshpande
- A Fieker
- A Ford
- A Gupta
- A Hoffmeister
- A Jansen
- A Lanas
- A Lanas
- A Lanas
- A Lanas
- A Leodolter
- A Marengoni
- A Murata
- A Pendleton
- A PottegÄrd
- A Rackoff
- A Rostom
- A Rostom
- A Sbrozzi-Vanni
- A Shiotani
- A Sreedharan
- A Turkiewicz
- A Wang
- A Zullo
- A Zullo
- AA Lambert
- AB Chang
- AB Lodrup
- AB Thomson
- AC Ford
- AF Goddard
- AG McNicholl
- AJ Berry
- AJ Lucendo
- AJ Lucendo
- AM Dries
- AM Ladd
- AM Schjerning Olsen
- AN Barkun
- AN Barkun
- AN Lau
- Angelo Zullo
- ASHP Therapeutic Guidelines on Stress Ulcer Prophylaxis
- AT Lassen
- B Chaveli-Lopez
- B Haenisch
- B Lebwohl
- B Liu
- BD Rhijn van
- BE Lacy
- BJ Marshall
- BJ Marshall
- C Andrade
- C Bavishi
- C Blandizzi
- C Blandizzi
- C Blandizzi
- C Blandizzi
- C Blandizzi
- C Blandizzi
- C Donnellan
- C Faisy
- C Gheorghe
- C Hom
- C Roman
- C Scarpignato
- C Scarpignato
- C Scarpignato
- C Scarpignato
- C Scarpignato
- C Scarpignato
- C Scarpignato
- C Scarpignato
- C Scarpignato
- C Scarpignato
- C Scarpignato
- C Sostres
- C Wei
- CA Liacouras
- Carmelo Scarpignato
- CB Steer
- CH Park
- CH Wang
- CH Wilder-Smith
- CH Wilder-Smith
- CM Wilcox
- Corrado Blandizzi
- CS Eom
- CS Lieber
- D Ahrens
- D Armstrong
- D Armstrong
- D Hartmann
- D Ravizza
- D Scott
- D Trenk
- D Yadav
- DA Johnson
- DA Katzka
- DB McGuire
- DC Lin
- DC Metz
- DE Freedberg
- DE Peterson
- DG Moledina
- DJ Cook
- DJ Cook
- DJ Cook
- DJ Robertson
- DL Bhatt
- DW Clark
- E de-Madaria
- E Lahner
- E Savarino
- E Sheen
- E Umegaki
- E Washio
- E Yucel
- EA Lew
- EA Lo
- EH Boath
- EP DiMagno
- EP Mitchell
- ES Dellon
- EW Yu
- F Alshamsi
- F Fiore Di
- F Lodato
- F Pace
- F Parente
- F Piccoli
- F Sierra
- FC Free Martin
- FJ Abajo de
- FK Chan
- FW Green Jr
- G Anand
- G Capurso
- G Cavallini
- G Holtmann
- G Liamis
- G Triadafilopoulos
- GE Boeckxstaens
- GI Leontiadis
- GI Leontiadis
- GI Leontiadis
- GI Leontiadis
- GM Masclee
- H Anthony
- H Blume
- H Guo
- H Malenstein van
- H Sachar
- H Suzuki
- HB Xu
- HF Boardman
- HJ Andreyev
- HL Tang
- HO Conn
- HP Parkman
- HV Worthington
- HW Daniell
- HY Jiang
- I Otremba
- I Sheikh
- IA Issa
- IM Gralnek
- IM Gralnek
- IM Modlin
- IM Tleyjeh
- IM Zacharioudakis
- J Akiyama
- J Andreyev
- J Andreyev
- J Cai
- J Chen
- J Dent
- J Freston
- J Hallas
- J Hallas
- J Kirchheiner
- J Labenz
- J Leonard
- J Martinek
- J Messer
- J Molina-Infante
- J Molina-Infante
- J Molina-Infante
- J Molina-Infante
- J Mossner
- J Sodikoff
- J Tol
- J Tong
- J Toouli
- J Weil
- J Yang
- J Zacny
- JC Luo
- JC Yang
- JE Dominguez-Munoz
- JE Richter
- JF Rehfeld
- JG Lieb 2nd
- JH Yoo
- JI Kim
- JJ Heidelbaugh
- JJ Heidelbaugh
- JJ Heidelbaugh
- JJ Meier
- JJ Sung
- JJ Sung
- JK Aronson
- JL Chan
- JL Goldstein
- JL Wallace
- JM Braganza
- JM Burgstaller
- JM Inadomi
- JM Nieto
- JM Piper
- JM Shin
- JP Galmiche
- JP Galmiche
- JP Galmiche
- JP Galmiche
- JP Gisbert
- JP Gisbert
- JP Quenot
- JQ Huang
- JQ Yuan
- JR Malagelada
- JR Pisegna
- JS Ahn
- JS Bajaj
- JV Ojeaburu
- JY Lau
- K Ahsberg
- K Iwakiri
- K Johnell
- K Rohss
- K Sugano
- K Takeda
- KD Bardhan
- KE McColl
- KE McColl
- KE McColl
- KE Sigterman
- KJ Kelly
- KJ Lin
- KK Tsoi
- KM Fock
- L Buendgens
- L Eslami
- L Filaretova
- L Filaretova
- L Frulloni
- L Gatta
- L Gatta
- L Gatta
- L Ibanez
- L Laine
- L Laine
- L Laine
- L Lugini
- L Lundell
- L Lundell
- L Lundell
- L Pasina
- LA Garcia Rodriguez
- LB Gerson
- LE Targownik
- LE Targownik
- LE Targownik
- LR Lundell
- Luigi Gatta
- M Bardou
- M Bergmann
- M Chen
- M Dall
- M Delhaye
- M Guslandi
- M Khan
- M Krag
- M Meli
- M Nakao
- M Sugimoto
- M Sugimoto
- M Teichert
- M Vaduganathan
- M Vaduganathan
- M Vallve
- M Vergara
- M Wermeling
- MA Bianco
- MA Qadeer
- MC Bradley
- ME Rothenberg
- MI Doria Jr
- MJ Vehreschild
- ML Brandi
- ML Grayson
- ML Schubert
- MM Abdelfatah
- MR Rickels
- MT Hong
- N Badiola
- N Bhala
- N Bortoli de
- N Nagata
- N Vakil
- N Vakil
- NH Shah
- NJ Shaheen
- NJ Talley
- NM Blijlevens
- NT Gunaratnam
- OC Coba de la
- P Bytzer
- P Chang
- P Haastrup
- P Jepsen
- P Malfertheiner
- P Miner
- P Miner Jr
- P Moayyedi
- P Moayyedi
- P Moayyedi
- P Moayyedi
- P Poitras
- P Sen
- PA Banks
- PC Lin
- PE Marik
- PG Gibson
- PJ Kahrilas
- PJ Kahrilas
- PJ Kahrilas
- PJ Kahrilas
- PJ Zed
- PO Erah
- PO Katz
- PW Weijenborg
- PW Weijenborg
- Q Aziz
- R Anglin
- R Carlsson
- R Casado Arroyo
- R Fiocca
- R Flower
- R Gupta
- R Hunt
- R Pezzilli
- R Pezzilli
- R Steinbrook
- R Terg
- RA Moore
- RC Fitzgerald
- RD Madanick
- RE Redfern
- RF Harvey
- RH Hunt
- RH Hunt
- RH Hunt
- RH Hunt
- RJ Daley
- RM Zagari
- RM Zagari
- RN Cardoso
- RP Dellinger
- RR Grube
- RR Kedika
- RS Wedemeyer
- RT Jensen
- RT Jensen
- RT Jensen
- RT Kavitt
- RV Lalla
- RV McCaleb
- RV Thakker
- RW McCallum
- S Agewall
- S Boussios
- S Bruley des Varannes
- S Cammarota
- S Contini
- S Contini
- S Dorward
- S Fais
- S Fujimori
- S Haag
- S Hernandez-Diaz
- S Kambhampati
- S Majumder
- S Mercadante
- S Miehlke
- S Montagnani
- S Morini
- S Narum
- S Ngamruengphong
- S Padol
- S Papagerakis
- S Pongprasobchai
- S Ranjitkar
- S Sartori
- S Sartori
- S Sartori
- S Shi
- S Shin
- S Singh
- S Taylor
- S Trelle
- SB Jung
- SB Menees
- SE Attwood
- SE Patchett
- SF Moss
- SG Worrell
- SH Woolf
- SJ Edwards
- SJ Edwards
- SJ Pandol
- SJ Spechler
- SM Eid
- SM Harding
- SM Weisman
- SW Lai
- T Abu-Hejleh
- T Furuta
- T Furuta
- T Hackert
- T Ishizaki
- T Ito
- T Ito
- T Ito
- T Lind
- T Ogata
- T Uwagawa
- T Yu
- TA Attumi
- TB Gardner
- TB Nealis
- TJ Lee
- TJ Schnitzer
- TP Dorlo
- TU Wheeldon
- US Preventive Services Task Force
- V Savarino
- V Savarino
- V Savarino
- V Stanghellini
- W Alhazzani
- W Cheungpasitporn
- W Gomm
- W Marlicz
- W Thompson
- WD Chey
- WK Lo
- WO Rohof
- Working Party of the British Society of Gastroenterology
- WP Geus
- WP Geus
- WY Chey
- Y Loriot
- Y Oka
- Y Ro
- Y Touchefeu
- Y Wang
- Y Yuan
- Y Yuan
- Y Yuan
- YK Loke
- YL Xie
- YS Zhang
- YT Ghebremariam
- YW Noh
- YX Yang
- Z Desta
- Z Jian
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Principles and management of neuropsychiatric symptoms in Alzheimerâs dementia
- Author
- AA Sepehry
- AC Khandai
- AH Nagahara
- AJ Thomas
- Alzheimerâs Association
- AP Porsteinsson
- Aâs Association
- B Marcos
- CG Lyketsos
- CG Lyketsos
- Constantine G Lyketsos
- CR Jack Jr
- D Weinshenker
- Department of Economic and Social Affairs
- DI Kaufer
- DL Sultzer
- DL Sultzer
- DL Sultzer
- DL Sultzer
- DY Lee
- E Moniz-Cook
- F Assal
- FE Taragano
- G Livingston
- G McKhann
- G Spalletta
- G TrifirĂČ
- G Waldemar
- GA Marshall
- GM McKhann
- H Forstl
- H Tatsumi
- HS Kang
- IS Shin
- J Garre-Olmo
- J OlazarĂĄn
- J Vilalta-Franch
- J Vilalta-Franch
- JJ Rodriguez
- JL Cummings
- JL Cummings
- JM Allman
- K Banno
- K Hirao
- K Medeiros de
- K Mizukami
- KL Lanctot
- KL Lanctot
- L Bidzan
- L Marner
- L Serra
- LB Zahodne
- LL Frakey
- LL Tan
- LS Schneider
- LS Schneider
- LT Drye
- LT Drye
- M Canevelli
- M Catani
- M Garcia-Alloza
- M Garcia-Alloza
- M Prince
- M Steinberg
- M Steinberg
- MA Nowrangi
- ME Vugt de
- MF Kraus
- Milap A Nowrangi
- MK Lai
- ML Balthazar
- MM Mielke
- MS Mega
- MS Rafii
- MW Hopkins
- N Herrmann
- N Mokhber
- O Devinsky
- OL Lopez
- P Aalten
- P Aalten
- P Hollingworth
- Paul B Rosenberg
- PB Rosenberg
- PD Bruen
- PN Tariot
- PR Padala
- PS Murray
- PT Francis
- PT Trzepacz
- PT Trzepacz
- R David
- RJ Melrose
- RM Zweig
- RM Zweig
- RN Kalaria
- S Erkulwater
- S Konovalov
- S Reeves
- S Wood
- S Wuwongse
- SA Lyness
- SE Starkstein
- SL Minger
- ST Cheng
- T Imamura
- T Insel
- T Mori
- T Tsoi
- V Menon
- Y Ouchi
- YE Geda
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2015
- Field of study
Genetic and Epigenetic Fine-Mapping of Causal Autoimmune Disease Variants
- Author
- A Franke
- A Hinks
- A Jolma
- A Kanhere
- A Marson
- Alexander A. Shishkin
- Alexander Marson
- B Langmead
- BE Bernstein
- Bradley E. Bernstein
- C. John Luckey
- CA Anderson
- CA Gifford
- Charles B. Epstein
- CM Rivera
- D Altshuler
- D Ellinghaus
- D Hnisz
- D Welter
- David A. Hafler
- Dita Mayer
- F Birzele
- FA Wright
- FJ Quintana
- G Caron
- G Trynka
- G Trynka
- G Vahedi
- H Li
- Holly Whitton
- J Ernst
- J Zhu
- JC Barrett
- JD Cooper
- JH Buckner
- Jiang Zhu
- JL Browning
- JM Engreitz
- JZ Liu
- JZ Liu
- Kyle Kai-How Farh
- L Zhou
- LA Hindorff
- LC Tsoi
- LC West
- M Beyer
- M Bulger
- M Ciofani
- M Parkes
- Mark J. Daly
- Markus Kleinewietfeld
- Marlene J. Carrasco-Alfonso
- MB Gerstein
- Meital Hatan
- MO Li
- MT Lam
- MT Maurano
- Nikolaos A. Patsopoulos
- Noam Shoresh
- P Armitage
- Philip L. De Jager
- R Gordan
- R Ostuni
- RD Hawkins
- RH Duerr
- RM Samstein
- Russell J. H. Ryan
- S Eyre
- S Heinz
- S Heinz
- S Pidasheva
- Samantha Beik
- SC Parker
- TJ Vyse
- V Brucklacher-Waldert
- Vijay K. Kuchroo
- W BĂ©guelin
- William J. Housley
- X Xie
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/02/2015
- Field of study
Summary Genome-wide association studies have identified loci underlying human diseases, but the causal nucleotide changes and mechanisms remain largely unknown. Here we developed a fine-mapping algorithm to identify candidate causal variants for 21 autoimmune diseases from genotyping data. We integrated these predictions with transcription and cis-regulatory element annotations, derived by mapping RNA and chromatin in primary immune cells, including resting and stimulated CD4+ T-cell subsets, regulatory T-cells, CD8+ T-cells, B-cells, and monocytes. We find that ~90% of causal variants are noncoding, with ~60% mapping to immune-cell enhancers, many of which gain histone acetylation and transcribe enhancer-associated RNA upon immune stimulation. Causal variants tend to occur near binding sites for master regulators of immune differentiation and stimulus-dependent gene activation, but only 10â20% directly alter recognizable transcription factor binding motifs. Rather, most noncoding risk variants, including those that alter gene expression, affect non-canonical sequence determinants not well-explained by current gene regulatory models
P3HT-Based Solar Cells: Structural Properties and Photovoltaic Performance
- Author
- A Kumar
- A Pivrikas
- A Zen
- A Zen
- AC Arias
- AJ Ferguson
- AJ Moulé
- AJ Moulé
- AJ Moulé
- AJ Moulé
- AJ Moulé
- AJ Moulé
- AJ Moulé
- AJ Pearson
- AL Ayzner
- AM Ballantyne
- AM Goodman
- B Schmidt-Hansberg
- B Watts
- BA Collins
- BA Collins
- BA Collins
- C Deibel
- C Deibel
- C Deibel
- C Girotto
- C Groves
- C MĂŒller
- C Scharsich
- CG Shuttle
- CG Shuttle
- CG Shuttle
- CG Shuttle
- CG Shuttle
- CL Braun
- CN Hoth
- CN Hoth
- CR McNeill
- CW Tang
- D Caruso
- D Chen
- D Chirvase
- D Credgington
- D Rauh
- D Vak
- D Veldman
- DM DeLongchamp
- DM Huang
- DP McMahon
- ET Niles
- F Padinger
- FC Jamieson
- FC Krebs
- FC Krebs
- FC Krebs
- FC Krebs
- FC Krebs
- FC Krebs
- FC Krebs
- FC Spano
- FC Spano
- FJ Wentz
- FL Zhang
- G Garcia-Belmonte
- G Li
- G Li
- G Li
- G Li
- G Li
- G Wetzelaer
- G Yu
- H Hoppe
- H Hoppe
- H Jin
- H Tamura
- H Xin
- HJ Kim
- HP Yan
- HP Yan
- IA Howard
- J Clark
- J Clark
- J Gierschner
- J Jo
- J Kniepert
- J Kniepert
- J Lee
- J Nelson
- J Peet
- J Rivnay
- J Zhao
- J-J Yun
- JA Bartelt
- JD Roehling
- JD Roehling
- JE Parmer
- JJM Halls
- JK Lee
- JM Guo
- JM Guo
- JM Mativetsky
- JM Warman
- JW Chen
- JY Kim
- K Emanuel
- K Vandewal
- K Vandewal
- KJ Ihn
- KW Chou
- KX Steirer
- L Chang
- LAA Pettersson
- LH Nguyen
- LJA Koster
- LJA Koster
- LM Chen
- LSC Pingree
- LW Barbour
- M Al-Ibrahim
- M Brinkmann
- M Brinkmann
- M Campoy-Quiles
- M Drees
- M Gluecker
- M Koppe
- M Lenes
- M Limpinsel
- M Mingebach
- M Pientka
- M Reyes-Reyes
- M Shin
- M Trznadel
- M Wojcik
- MA Ruderer
- MC Scharber
- MM Bouman
- MO Reese
- MT Dang
- ND Treat
- NS Sariciftci
- O Wodo
- OF Pascui
- P Peumans
- P Schilinsky
- PJ Webster
- PWM Blom
- R Cugola
- R Green
- R Hamilton
- R Mauer
- R Mauer
- RA Marsh
- RA Street
- RC Hiorns
- RC Hiorns
- RD Pensack
- RD Pensack
- RJ Kline
- RJ Kline
- RM Beal
- RP Allan
- S Bavel van
- S Berson
- S Cho
- S Shoaee
- S-S Kim
- SA Mauger
- SE Shaheen
- SE Shaheen
- SK Hau
- SR Cowan
- SS Bavel van
- ST Turner
- T Agostinelli
- T Erb
- T Kietzke
- T Kirchartz
- T Wang
- TGJ Hofstad van der
- TM Clarke
- TM Clarke
- TP Martin
- U Zhokhavets
- V Shrotriya
- VD Mihailetchi
- VD Mihailetchi
- VD Mihailetchi
- VD Mihailetchi
- W Chen
- W Ma
- W Ma
- W Shockley
- W Tress
- W Yin
- WC Tsoi
- WC Tsoi
- WD Oosterbaan
- WL Leong
- X He
- XN Yang
- Y Kim
- Y Kim
- Y Kim
- Y Liang
- Y Yao
- Y Zhang
- YF Lim
- ZL Guan
- ZY Wu
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2014
- Field of study
Each year we are bombarded with B.Sc. and Ph.D. applications from students that want to improve the world. They have learned that their future depends on changing the type of fuel we use and that solar energy is our future. The hope and energy of these young people will transform future energy technologies, but it will not happen quickly. Organic photovoltaic devices are easy to sketch, but the materials, processing steps, and ways of measuring the properties of the materials are very complicated. It is not trivial to make a systematic measurement that will change the way other research groups think or practice. In approaching this chapter, we thought about what a new researcher would need to know about organic photovoltaic devices and materials in order to have a good start in the subject. Then, we simplified that to focus on what a new researcher would need to know about poly-3-hexylthiophene:phenyl-C61-butyric acid methyl ester blends (P3HT: PCBM) to make research progress with these materials. This chapter is by no means authoritative or a compendium of all things on P3HT:PCBM. We have selected to explain how the sample fabrication techniques lead to control of morphology and structural features and how these morphological features have specific optical and electronic consequences for organic photovoltaic device applications
Global, regional, and national incidence, prevalence, and years lived with disability for 354 diseases and injuries for 195 countries and territories, 1990-2017: a systematic analysis for the Global Burden of Disease Study 2017
- Author
- Abate D
- Abate KH
- Abay SM
- Abbafati C
- Abbasi N
- Abbastabar H
- Abd El Razek MM
- Abd El Razelk HM
- Abd-Allah F
- Abdela J
- Abdelalim A
- Abdollahpour I
- Abdulkader RS
- Abebe Z
- Abera SF
- Abil OZ
- Abraha HN
- Abu-Raddad LJ
- Abu-Rmeileh NME
- Accrombessi MMK
- Acharya D
- Acharya P
- Ackerman IN
- Adamu AA
- Adebayo OM
- Adekanmbi V
- Adetokunboh OO
- Adib MG
- Adsuar JC
- Afanvi KA
- Afarideh M
- Afshin A
- Agarwal G
- Agesa KM
- Aggarwal R
- Aghayan SA
- Agrawal S
- Ahmadi A
- Ahmadi M
- Ahmadieh H
- Ahmed MB
- Aichour AN
- Aichour I
- Aichour MTE
- Akinyemiju T
- Akseer N
- Al-Aly Z
- Al-Eyadhy A
- Al-Mekhlafi HM
- Al-Raddadi RM
- Alahdab F
- Alam K
- Alam T
- Alashi A
- Alavian SM
- Alene KA
- Alijanzadeh M
- Alizadeh-Navaei R
- Aljunid SM
- Alkerwi A
- Alla F
- Allebeck P
- Alouani MML
- Altirkawi K
- Alvis-Guzman N
- Amare AT
- Aminde LN
- Ammar W
- Amoako YA
- Anber NH
- Andrei CL
- Androudi S
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- Yu C
- Zadnik V
- Zaidi Z
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- Zeleke AJ
- Zenebe ZM
- Zhang K
- Zhao Z
- Zhou M
- Zodpey S
- Zucker I
- Publication venue
- ELSEVIER SCIENCE INC
- Publication date
- 01/01/2018
- Field of study
Background:
The Global Burden of Diseases, Injuries, and Risk Factors Study 2017 (GBD 2017) includes a comprehensive assessment of incidence, prevalence, and years lived with disability (YLDs) for 354 causes in 195 countries and territories from 1990 to 2017. Previous GBD studies have shown how the decline of mortality rates from 1990 to 2016 has led to an increase in life expectancy, an ageing global population, and an expansion of the non-fatal burden of disease and injury. These studies have also shown how a substantial portion of the world's population experiences non-fatal health loss with considerable heterogeneity among different causes, locations, ages, and sexes. Ongoing objectives of the GBD study include increasing the level of estimation detail, improving analytical strategies, and increasing the amount of high-quality data.
Methods:
We estimated incidence and prevalence for 354 diseases and injuries and 3484 sequelae. We used an updated and extensive body of literature studies, survey data, surveillance data, inpatient admission records, outpatient visit records, and health insurance claims, and additionally used results from cause of death models to inform estimates using a total of 68â781 data sources. Newly available clinical data from India, Iran, Japan, Jordan, Nepal, China, Brazil, Norway, and Italy were incorporated, as well as updated claims data from the USA and new claims data from Taiwan (province of China) and Singapore. We used DisMod-MR 2.1, a Bayesian meta-regression tool, as the main method of estimation, ensuring consistency between rates of incidence, prevalence, remission, and cause of death for each condition. YLDs were estimated as the product of a prevalence estimate and a disability weight for health states of each mutually exclusive sequela, adjusted for comorbidity. We updated the Socio-demographic Index (SDI), a summary development indicator of income per capita, years of schooling, and total fertility rate. Additionally, we calculated differences between male and female YLDs to identify divergent trends across sexes. GBD 2017 complies with the Guidelines for Accurate and Transparent Health Estimates Reporting.
Findings:
Globally, for females, the causes with the greatest age-standardised prevalence were oral disorders, headache disorders, and haemoglobinopathies and haemolytic anaemias in both 1990 and 2017. For males, the causes with the greatest age-standardised prevalence were oral disorders, headache disorders, and tuberculosis including latent tuberculosis infection in both 1990 and 2017. In terms of YLDs, low back pain, headache disorders, and dietary iron deficiency were the leading Level 3 causes of YLD counts in 1990, whereas low back pain, headache disorders, and depressive disorders were the leading causes in 2017 for both sexes combined. All-cause age-standardised YLD rates decreased by 3·9% (95% uncertainty interval [UI] 3·1â4·6) from 1990 to 2017; however, the all-age YLD rate increased by 7·2% (6·0â8·4) while the total sum of global YLDs increased from 562 million (421â723) to 853 million (642â1100). The increases for males and females were similar, with increases in all-age YLD rates of 7·9% (6·6â9·2) for males and 6·5% (5·4â7·7) for females. We found significant differences between males and females in terms of age-standardised prevalence estimates for multiple causes. The causes with the greatest relative differences between sexes in 2017 included substance use disorders (3018 cases [95% UI 2782â3252] per 100â000 in males vs s1400 [1279â1524] per 100â000 in females), transport injuries (3322 [3082â3583] vs 2336 [2154â2535]), and self-harm and interpersonal violence (3265 [2943â3630] vs 5643 [5057â6302]).
Interpretation:
Global all-cause age-standardised YLD rates have improved only slightly over a period spanning nearly three decades. However, the magnitude of the non-fatal disease burden has expanded globally, with increasing numbers of people who have a wide spectrum of conditions. A subset of conditions has remained globally pervasive since 1990, whereas other conditions have displayed more dynamic trends, with different ages, sexes, and geographies across the globe experiencing varying burdens and trends of health loss. This study emphasises how global improvements in premature mortality for select conditions have led to older populations with complex and potentially expensive diseases, yet also highlights global achievements in certain domains of disease and injury
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- Author
- Aarrestad TK
- Aarup Petersen H
- Abbaneo D
- Abbiendi G
- Abbott S
- Abbrescia M
- Abdullin S
- Abreu A
- Abu Zeid S
- Acharya H
- Acharya S
- Acosta D
- Adam W
- Adamidis K
- Adams E
- Adams MR
- Adams T
- Addesa FM
- Adloff C
- Adzic P
- Aebi D
- Afanasiev S
- Agapitos A
- Agarwal G
- Agram J-L
- Aguilar-Benitez M
- Agyel D
- Ahmad A
- Ahmad M
- Ahmed A
- AimĂš C
- Ajmal S
- Akchurin N
- Akgun B
- Akpinar A
- Al Kadhim A
- Albert A
- Albrecht A
- Albrecht S
- Albrow M
- Alcaraz Maestre J
- Alcerro Alcerro LF
- Aldaya Martin M
- AldĂĄ JĂșnior WL
- Aleksandrov A
- Alexander J
- Alhusseini M
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- Alison J
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- Alvarez Gonzalez B
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- Yockey H
- Yohay R
- Yoo HD
- Yoo J
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- Yoon I
- You Z
- Yu D
- Yu I
- Yu SS
- Yuan L
- Yuan S
- Yuldashev BS
- Yusuff I
- Zabi A
- Zabolotny W
- Zacharopoulou A
- Zaleski S
- Zalewski P
- Zanetti M
- Zarubin A
- Zarucki M
- Zaza A
- Zecchinelli AG
- Zehetner P
- Zeinali M
- Zejdl P
- Zeuner WD
- Zghiche A
- Zhang F
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- Zhizhin I
- Zhokin A
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- Zhu RY
- Ziemons T
- Zilizi G
- Zimermmane Castro Santos A
- Zipper N
- Zisopoulos I
- Zoi I
- Zolkapli Z
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- Zorbilmez C
- Zotto P
- Zotz A
- Zou R
- Zucchetta A
- Zuo X
- Zuolo D
- Zygala L
- Publication venue
- Elsevier BV
- Publication date
- 21/06/2024
- Field of study
Data availability - https://www.sciencedirect.com/science/article/pii/S0370269324003733?via%3Dihub#dav0001 [Release and preservation of data used by the CMS Collaboration as the basis for publications is guided by the CMS data preservation, re-use and open access policy (https://cms-docdb.cern.ch/cgi-bin/PublicDocDB/RetrieveFile?docid=6032&filename=CMSDataPolicyV1.2.pdf&version=2)]The first evidence for the standard model production of a top quark in association with a W boson and a Z boson is reported. The measurement is performed in multilepton final states, where the Z boson is reconstructed via its decays to electron or muon pairs. At least one W boson, associated or from top quark decay, decays leptonically, too. The analysed data were recorded by the CMS experiment at the CERN LHC in 2016â2018 in proton-proton collisions at âs=13 TeV, and correspond to an integrated luminosity of 138 fbâ1. The measured cross section is 354±54(stat)±95(syst) fb, and corresponds to a statistical significance of 3.4 standard deviations.SCOAP
Recommended from our members
Search for new heavy resonances decaying to WW, WZ, ZZ, WH, or ZH boson pairs in the all-jets final state in proton-proton collisions at sâ = 13 TeV
- Author
- Aarrestad TK
- Aarup Petersen H
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdelalim AA
- Abdullin S
- Abercrombie D
- Abreu A
- Abu Zeid S
- Acharya H
- Acosta D
- Adam W
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- Adams E
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- Addesa FM
- Adloff C
- Adzic P
- Afanasiev S
- Agapitos A
- Agarwal G
- Aggleton R
- Agram J-L
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- Agyel D
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- Akchurin N
- Akgun B
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- Alcaraz Maestre J
- Alcerro Alcerro LF
- Aldaya Martin M
- AldĂĄ JĂșnior WL
- Aleksandrov A
- Alexander J
- Alhusseini M
- Alimena J
- Alison J
- Allmond B
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- Alpana A
- Alvarez Gonzalez B
- Alverson G
- Alves Gallo Pereira M
- Alves GA
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- Andrejkovic JW
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- Ălvarez FernĂĄndez A
- Ăzçelik Ă
- Publication venue
- Elsevier
- Publication date
- 26/02/2023
- Field of study
A preprint version of this article is available at arXiv:2210.00043v2 [hep-ex], https://arxiv.org/abs/2210.00043v2 . Comments: Replaced with the published version. Added the journal reference and the DOI. All the figures and tables, including additional supplementary figures, can be found at https://cms-results.web.cern.ch/cms-results/public-results/publications/B2G-20-009 (CMS Public Pages). Report number: CMS-B2G-20-009, CERN-EP-2022-152.Data availability: see: https://cms-results.web.cern.ch/cms-results/public-results/publications/B2G-20-009 .A search for new heavy resonances decaying to WW, WZ, ZZ, WH, or ZH boson pairs in the all-jets final state is presented. The analysis is based on proton-proton collision data recorded by the CMS detector in 2016-2018 at a centre-of-mass energy of 13 TeV at the CERN LHC, corresponding to an integrated luminosity of 138 fb^{-1}. The search is sensitive to resonances with masses between 1.3 and 6 TeV, decaying to bosons that are highly Lorentz-boosted such that each of the bosons forms a single large-radius jet. Machine learning techniques are employed to identify such jets. No significant excess over the estimated standard model background is observed. A maximum local significance of 3.6 standard deviations, corresponding to a global significance of 2.3 standard deviations, is observed at masses of 2.1 and 2.9 TeV. In a heavy vector triplet model, spin-1 Z' and W' resonances with masses below 4.8 TeV are excluded at the 95% confidence level (CL). These limits are the most stringent to date. In a bulk graviton model, spin-2 gravitons and spin-0 radions with masses below 1.4 and 2.7 TeV, respectively, are excluded at 95% CL. Production of heavy resonances through vector boson fusion is constrained with upper cross section limits at 95% CL as low as 0.1 fb.SCOAP3
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- Author
- Aarrestad TK
- Aarup Petersen H
- Abbaneo D
- Abbiendi G
- Abbott S
- Abbrescia M
- Abdalla H
- Abdullah Al-Mashad M
- Abdullin S
- Abreu A
- Abu Zeid S
- Acharya H
- Acosta D
- Adam W
- Adamidis K
- Adams E
- Adams MR
- Adams T
- Addesa FM
- Adloff C
- Adzic P
- Afanasiev S
- Agapitos A
- Agarwal G
- Agram J-L
- Aguilar-Benitez M
- Agyel D
- Ahmad A
- Ahmad M
- Ahmed A
- AimĂš C
- Ajmal S
- Akchurin N
- Akgun B
- Akpinar A
- Al Kadhim A
- Albert A
- Albrecht A
- Albrecht S
- Albrow M
- Alcaraz Maestre J
- Alcerro Alcerro LF
- Aldaya Martin M
- AldĂĄ JĂșnior WL
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- Publication venue
- Springer Nature on behalf of SISSA
- Publication date
- 30/01/2024
- Field of study
A preprint version of the article is available at arXiv:2308.01253v2 [hep-ex], https://arxiv.org/abs/2308.01253v2 . Comments: Replaced with the published version. Added the journal reference and the DOI. All the figures and tables can be found at https://cms-results.web.cern.ch/cms-results/public-results/publications/HIG-22-009 (CMS Public Pages). Report number: CMS-HIG-22-009, CERN-EP-2023-110.A measurement of the Higgs boson (H) production via vector boson fusion (VBF) and its decay into a bottom quark-antiquark pair (bbÂŻ) is presented using proton-proton collision data recorded by the CMS experiment at sâ = 13 TeV and corresponding to an integrated luminosity of 90.8 fbâ1. Treating the gluon-gluon fusion process as a background and constraining its rate to the value expected in the standard model (SM) within uncertainties, the signal strength of the VBF process, defined as the ratio of the observed signal rate to that predicted by the SM, is measured to be ÎŒqqHHbbÂŻ = 1.01 +0.55â0.46. The VBF signal is observed with a significance of 2.4 standard deviations relative to the background prediction, while the expected significance is 2.7 standard deviations. Considering inclusive Higgs boson production and decay into bottom quarks, the signal strength is measured to be ÎŒincl.HbbÂŻ = 0.99 +0.48â0.41, corresponding to an observed (expected) significance of 2.6 (2.9) standard deviations.SCOAP3, STFC; Marie-Curie program and the European Research Council and Horizon 2020 Gran
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