620 research outputs found
Upregulation of the Wnt Co-Receptor LRP6 Promotes Hepatocarcinogenesis and Enhances Cell Invasion
- Author
- A Bengochea
- A Teufel
- B Beagle
- Betty Yin-Chi Wong
- BH Hoang
- BT MacDonald
- CC Liu
- CM Wong
- CM Wong
- DW Chan
- Edmund Kwok-Kwan Tung
- H Clevers
- H Huang
- H Kirikoshi
- HC Hsu
- Irene Oi-Lin Ng
- J Ferlay
- J Zhang
- JM Llovet
- JY Park
- K Brennan
- K Mi
- K Tamai
- KI Pinson
- L Hu
- L Zender
- M Kim
- M Wehrli
- N Janssens
- P Bjorklund
- P Bjorklund
- P Merle
- P Merle
- RT Moon
- S Satoh
- S Tommasi
- Surinder K. Batra
- Tai-On Yau
- TR Devereux
- Y Guo
- Y Ishizaki
- Y Li
- Y Li
- Y Takigawa
- YD Kim
- Z Zhang
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2012
- Field of study
Background: Activation of the Wnt/b-catenin signaling pathway plays a crucial role in hepatocellular carcinoma (HCC). Lowdensity lipoprotein (LDL) receptor-related protein-6 (LRP6) is one of the co-receptors of the Wnt/b-catenin pathway and forms a signaling complex with Wnt ligand and Frizzled receptor to activate downstream signaling. However, the role of LRP6 in hepatocarcinogenesis is unclear. In this study, we examined its expression and roles in human HCC. Methodology/Principal Findings: Using real-time quantitative RT-PCR, we found that LRP6 was frequently (45%) overexpressed in human HCCs (P = 0.003). In vitro studies showed that ectopic expression of LRP6 increased the protein level of b-catenin. Moreover, overexpression of the full-length and constitutively active LRP6, respectively, activated the WNT/b-catenin signaling pathway, as shown by the TCF/b-catenin reporter assay. With regard to the effects of LRP6 overexpression in HCC cells, stable overexpression of the constitutively active LRP6 in BEL-7402 HCC cells enhanced cell proliferation, cell migration, and invasion in vitro as well as tumorigenicity in nude mice. Conclusions/Significance: Our findings indicate that overexpression of LRP6 contributes to the hyperactivation of the Wnt
Genetic Associations of Type 2 Diabetes with Islet Amyloid Polypeptide Processing and Degrading Pathways in Asian Populations
- Author
- A Ragvin
- AE Kel
- Alice Pik Shan Kong
- Andrew P. Morris
- AV Matveyenko
- BF Voight
- C Lange
- Cheng Hu
- CJ Groves
- CJ Huang
- Claudia Ha Ting Tam
- D Qi
- Daniel Peng-Keat Ng
- DF Steiner
- E Zeggini
- E. Shyong Tai
- ET Jaikaran
- Gang Xu
- H Chen
- H Zhao
- Heung Man Lee
- Hiroto Furuta
- HL Zhao
- Hong Kyu Lee
- I Prokopenko
- J Paulsson
- JC Barrett
- JC Chan
- Jean Woo
- Jianjun Liu
- JK Li
- JK Wolford
- JP Noonan
- Juliana Chung Ngor Chan
- JZ Bai
- K Piwernetz
- KD Jeffrey
- KH Liu
- Kishio Nanjo
- KJ Gaulton
- Kyong Soo Park
- LJ Martin
- M He
- M Stumvoll
- Maggie Chor Yin Ng
- MB Pepys
- MC Ng
- MC Ng
- MI McCarthy
- MK Kim
- ML Stitzel
- MS German
- N Rudovich
- N Utsunomiya
- Nelson Leung Sang Tang
- P Westermark
- Ping Chung Leung
- Q Yang
- R Bhandare
- R DerSimonian
- RG Bennett
- Risa Ozaki
- Ronald Ching Wan Ma
- S Nordman
- SB Harrap
- SH Kwak
- Shiro Maeda
- Tien-Yin Wong
- TS Leak
- V Steinthorsdottir
- Vincent Kwok Lim Lam
- Wei Ping Jia
- Wing-Yee So
- WP Jia
- X Sim
- XL Li
- Xueling Sim
- Y Cai
- Y Furukawa
- Y Wang
- Ying Wang
- YS Cho
- Publication venue
- 'Public Library of Science (PLoS)'
- Publication date
- 01/01/2013
- Field of study
10.1371/journal.pone.0062378PLoS ONE86
Altered E-cadherin expression and p120 catenin localization in esophageal squamous cell carcinoma
- Author
- A Gamboa-Dominguez
- A Keirsebilck
- A Mialhe
- A Valizadeh
- AK Lam
- Alfred K. Y. Lam
- AO Chan
- AU Jawhari
- BM Ghadimi
- BP Wijnhoven
- CM Franz
- D Fujimoto
- D Sarrio
- DI Bellovin
- F Sato
- FX Bosch
- G Berx
- G Karatzas
- HJ van
- HX Si
- I Grosheva
- John M. Luk
- John Wong
- K Tomita
- KS Nair
- Kwok-Wah Chan
- KY Lam
- L Nakopoulou
- M Feith
- M Takeichi
- M Yanagisawa
- MA Davis
- MA Thoreson
- MT Nieman
- NK Noren
- O Montonen
- Ping-Yin Lee
- PZ Anastasiadis
- Q Lu
- RB Hazan
- RC Ireton
- RM Bremnes
- S Aho
- S Inada
- Simon Law
- XJ Zhao
- Y Fukudome
- Y Ishizaki
- Y Uchikado
- YC Lin
- Yvonne Chung
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2007
- Field of study
Background: E-cadherin is a well-known tumor suppressor and its dysregulated expression correlates with tumor differentiation, metastasis and survival in esophageal squamous cell carcinoma (ESCC). p120 catenin is an Armadillo protein normally bound to E-cadherin in the cadherin-catenin complex at the adherens junction. Dysregulated expression and mislocalization of p120ctn affect the protective function of the complex. The objective of the present study was to evaluate the clinical significance of E-cadherin and p120ctn expression in ESCC. Methods: Immunohistochemistry was performed to investigate the expression of E-cadherin and p120ctn proteins in 71 patients with ESCC. The relationships between protein expression and clinicopathological characteristics were analyzed. Results: Reduced E-cadherin and p120ctn expressions were observed in 42.3% and 8.5% of ESCC cases, respectively. Reduction of membranous p120ctn was observed in 33.8% of cases. Membranous E-cadherin was preserved when p120ctn co-localized on the membrane of tumor cells (72.3%, P = 0.001). High level E-cadherin expression and membranous p120ctn preservation positively correlated with tumor differentiation (P = 0.001 and P = 0.008, respectively). p120ctn expression was also significantly related to lymph node metastasis (P = 0.003). Heterogeneous expression of both E-cadherin and p120ctn was observed in dysplasia. Conclusions: Altered E-cadherin expression and p120ctn localization were related to tumor differentiation, indicating their important roles in the pathogenesis of ESCC. © 2007 The Society of Surgical Oncology, Inc.postprin
Uncoupling Protein-4 (UCP4) Increases ATP Supply by Interacting with Mitochondrial Complex II in Neuroblastoma Cells
- Author
- A Barrientos
- A Herrero-Mendez
- A Navarro
- A Negre-Salvayre
- A Sanchez-Blanco
- A Smorodchenko
- AC Chu
- AH Schapira
- AH Schapira
- D Arsenijevic
- D Liu
- D Ricquier
- Danny Hon-Fai So
- David Boyer Ramsden
- David Chi-Wai Yiu
- DF Rolfe
- E Gnaiger
- F Distelmaier
- F Mouaffak
- Ho-Man Tse
- Hui-Fang Liu
- Jessica Wing-Man Ho
- JM Duan
- JN Guzman
- JS Kim-Han
- JW Ho
- K Yasuno
- KH Kwok
- Koon-Ho Chan
- KS Echtay
- M Jaburek
- M Klingenberg
- M Zhang
- MA Birch-Machin
- MD Brand
- MD Brand
- MD Brand
- MD Brand
- Michelle Hiu-Wai Kung
- MT Lin
- P Mitchell
- PC Hinkle
- Philip Wing-Lok Ho
- PI Moreira
- PS Brookes
- PS Brookes
- PW Ho
- PW Ho
- PW Ho
- R Horsefield
- R Xu
- S Krauss
- SA Mookerjee
- SH Adams
- Shu-Leong Ho
- SL Chan
- Sookja Chung
- SS Korshunov
- TC Esteves
- V Adam-Vizi
- V Rhein
- W Mao
- WD Parker Jr
- XX Yu
- Y Hatefi
- Y Yin
- YA Lim
- Z Szolnoki
- Z Szolnoki
- Z Wei
- ZB Andrews
- ZB Andrews
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2012
- Field of study
Mitochondrial uncoupling protein-4 (UCP4) protects against Complex I deficiency as induced by 1-methyl-4-phenylpyridinium (MPP+), but how UCP4 affects mitochondrial function is unclear. Here we investigated how UCP4 affects mitochondrial bioenergetics in SH-SY5Y cells. Cells stably overexpressing UCP4 exhibited higher oxygen consumption (10.1%, p<0.01), with 20% greater proton leak than vector controls (p<0.01). Increased ATP supply was observed in UCP4-overexpressing cells compared to controls (p<0.05). Although state 4 and state 3 respiration rates of UCP4-overexpressing and control cells were similar, Complex II activity in UCP4-overexpressing cells was 30% higher (p<0.05), associated with protein binding between UCP4 and Complex II, but not that of either Complex I or IV. Mitochondrial ADP consumption by succinate-induced respiration was 26% higher in UCP4-overexpressing cells, with 20% higher ADP:O ratio (p<0.05). ADP/ATP exchange rate was not altered by UCP4 overexpression, as shown by unchanged mitochondrial ADP uptake activity. UCP4 overexpression retained normal mitochondrial morphology in situ, with similar mitochondrial membrane potential compared to controls. Our findings elucidate how UCP4 overexpression increases ATP synthesis by specifically interacting with Complex II. This highlights a unique role of UCP4 as a potential regulatory target to modulate mitochondrial Complex II and ATP output in preserving existing neurons against energy crisis
Family structure, parent-child conversation time and substance use among Chinese adolescents
- Author
- A Garmiene
- AE Barrett
- B Piko
- BF Piko
- C Jackson
- C Mary Schooling
- C Roustit
- Census and Statistics Department
- Census and Statistics Department
- Census and Statistics Department
- Census and Statistics Department
- CL Broman
- DM Ackard
- DT Shek
- E Spruijt
- EK Tong
- EM Adlaf
- F Vazquez-Nava
- G Neil Thomas
- H Chan
- J Cochrane
- J Shucksmith
- JE Henningfield
- JP Hoffmann
- JT Lau
- K Fromme
- KW Griffin
- Kwok-Kei Mak
- LH Weiss
- LM Richter
- M Stern
- MK Lai
- National Bureau of Statistic of China
- P McArdle
- P Miller
- PR Amato
- R Jessor
- R Otten
- R Otten
- R Otten
- R West
- RA Turner
- RC Engels
- RH Needle
- RL Flewelling
- RN Waizenhofer
- RR Kafka
- S Frojd
- S Ledoux
- Sai-Yin Ho
- Sarah M McGhee
- T Bjarnason
- T Suh
- TA Wills
- Tai-Hing Lam
- U.S Centers for Disease Control and Prevention
- U.S National Center for Health Statistics
- United Nations
- World Health Organization
- Y Theodorakis
- Y Zhao
- Z Harakeh
- Publication venue
- BioMed Central
- Publication date
- 01/01/2010
- Field of study
<p>Abstract</p> <p>Background</p> <p>The family plays a vital role in shaping adolescent behaviours. The present study investigated the associations between family structure and substance use among Hong Kong Chinese adolescents.</p> <p>Methods</p> <p>A total of 32,961 Form 1 to 5 (grade 7-12 in the US) Hong Kong students participated in the Youth Smoking Survey in 2003-4. An anonymous questionnaire was used to obtain information about family structure, daily duration of parent-child conversation, smoking, alcohol drinking and drug use. Logistic regression was used to calculate the adjusted odds ratios (OR) for each substance use by family structure.</p> <p>Results</p> <p>Adjusting for sex, age, type of housing, parental smoking and school, adolescents from non-intact families were significantly more likely to be current smokers (OR = 1.62), weekly drinkers (OR = 1.72) and ever drug users (OR = 1.72), with significant linear increases in ORs from maternal, paternal to no-parent families compared with intact families. Furthermore, current smoking (OR = 1.41) and weekly drinking (OR = 1.46) were significantly more common among adolescents from paternal than maternal families. After adjusting for parent-child conversation time, the ORs for non-intact families remained significant compared with intact families, but the paternal-maternal differences were no longer significant.</p> <p>Conclusions</p> <p>Non-intact families were associated with substance use among Hong Kong Chinese adolescents. The apparently stronger associations with substance use in paternal than maternal families were probably mediated by the poorer communication with the father.</p
Neurodegeneration of the retina in mouse models of Alzheimer’s disease: what can we learn from the retina?
- Author
- A Gruart
- A Ning
- A Pezzini
- Andrew Wu
- AU Bayer
- AY Seo
- B Allen
- B Gold
- B Liu
- B Ron
- C Casas
- C Cudennec Le
- C Duyckaerts
- CH Hung
- D Moechars
- D Morgan
- D Muyllaert
- D Terwel
- DA Valenti
- DH Anderson
- DH Anderson
- DL King
- DL Price
- DL Price
- DL Price
- DM Walsh
- DT Walsh
- EA Pierce
- EB Rodrigues
- F Berisha
- F Yang
- FM LaFerla
- GW Arendash
- GY Kong
- H Tamura
- H Yin
- HC Chan
- HW Wang
- I Grundke-Iqbal
- Irene Yan-Pui Leung
- J Hardy
- J Mey
- J Wan
- JC Blanks
- JD Ding
- JL Eriksen
- JT Gau
- JZ Ji
- K Chiu
- K Chiu
- K Chiu
- K Chiu
- K Hsiao
- K Stamer
- KC Suen
- Kin Chiu
- KR Zahs
- Kwok-Fai So
- L Baum
- L Gasparini
- L Guo
- L Guo
- LV Johnson
- M Garcia-Alloza
- M Garcia-Alloza
- M Hintersteiner
- M Koronyo-Hamaoui
- M Li
- M Nozaki
- M Patel
- M Rizzo
- M Saotome
- M Shimazawa
- MA Westerman
- MA Zarbin
- MF Garcia
- MF Mendez
- ML Scattoni
- MS Malamas
- MS Yu
- MS Yu
- P Caroni
- P Wostyn
- PJ Morin
- Raymond Chuen-Chung Chang
- RCC Chang
- RCC Chang
- RM Dutescu
- RS Roque
- RX Santos
- S Bakalash
- S Frank
- S Jimenez
- S Oddo
- SE Perez
- SJ McKinnon
- SJ McKinnon
- T Kawarabayashi
- T Nakada
- T O’Connor
- T Yoshida
- TA Bayer
- TH Margrain
- Tin-Fung Chan
- TL Spires
- TR Hedges 3rd
- V Carelli
- V Luibl
- V Nimmrich
- WE Klunk
- WK Ju
- X Liu
- X Wang
- Y Ohyagi
- YS Ho
- YS Ho
- YS Ho
- Z Suo
- Publication venue
- Springer Netherlands
- Publication date
- 01/01/2011
- Field of study
Alzheimer’s disease (AD) is an age-related progressive neurodegenerative disease commonly found among elderly. In addition to cognitive and behavioral deficits, vision abnormalities are prevalent in AD patients. Recent studies investigating retinal changes in AD double-transgenic mice have shown altered processing of amyloid precursor protein and accumulation of β-amyloid peptides in neurons of retinal ganglion cell layer (RGCL) and inner nuclear layer (INL). Apoptotic cells were also detected in the RGCL. Thus, the pathophysiological changes of retinas in AD patients are possibly resembled by AD transgenic models. The retina is a simple model of the brain in the sense that some pathological changes and therapeutic strategies from the retina may be observed or applicable to the brain. Furthermore, it is also possible to advance our understanding of pathological mechanisms in other retinal degenerative diseases. Therefore, studying AD-related retinal degeneration is a promising way for the investigation on (1) AD pathologies and therapies that would eventually benefit the brain and (2) cellular mechanisms in other retinal degenerations such as glaucoma and age-related macular degeneration. This review will highlight the efforts on retinal degenerative research using AD transgenic mouse models
Antimicrobial resistance among migrants in Europe: a systematic review and meta-analysis
- Author
- Aahlin Eirik Kjus
- Aamer Ahmed
- Aaniana Kenneth
- Ababneh Ali
- Abaliksta Tomas
- Abantanga Francis
- Abbas Athar
- Abbasy Jibran
- Abbo Olivier
- Abbott Tom
- Abbouch Meryem
- Abd El-Latif Nadia Khalid
- Abd Elkhalek Esraa
- Abd-Elmawla Manar
- Abdallah Emad
- Abdel-Aty Abdulrahman
- Abdel-Hameed Noran
- Abdel-Kader Sara Mahmoud
- Abdelaal Abdelaziz
- Abdelaty Mohamed
- Abdelazeam Anan Rady
- Abdelazim Galaleldin
- Abdelaziz Mohamed A.
- Abdelbadeai Kholoud
- Abdelfatah Afnan
- Abdelhady Samar
- Abdelhamed Rasha
- Abdelhamid Amina
- Abdelhaq Aram
- Abdelkader Mostafa
- Abdelkader Omar
- Abdelkhalek Mohamed
- Abdelmageed Eman
- Abdelmotaleb Ibrahem
- Abdelraouf Ahmed Mahmoud
- Abdelrouf Doaa Maher
- Abdelshakour Mahmoud
- Abdrabou Abdulshafi Khaled
- Abdul-Latif Saiba
- Abdulaziz Hager
- Abdulaziz Mustafa
- Abdulbagi Omar
- Abdulhakeem Eman Mahmoud
- Abdullah Mohamed Abozed
- Abdullah Nik Azim Nik
- Abdullah Noha
- Abdullahi Lawal
- Abdurrazzaaq Abdussemiu
- Abem Owusu Emmanuel
- Abiola Olajide
- Aboelella Majed
- Aboelmagd Omnia
- Aboelsoud Moustafa R.
- Aboul-Naga Mariam Saad
- Abouzaid Arwa
- Abu Qumbos Amjad
- Abu-toyour Maram
- Abubakr Marwan
- Abuowda Yousef
- Abuqwaider Eman
- Abusalem Lana
- Abushamleh Soha
- Ackom Eric
- Acquah Emmanuel
- Adam Ali
- Adam Nourhan
- Adamu Ahmed
- Adawi Ihdaa
- Adawi Mohammad
- Adebanjo Ademola
- Adebola Oluwaseyi
- Adedeji Adesina
- Adel Badr Eldin
- Adel Israa
- Adella Fidelis Jacklyn
- Adelshone Abdelrahman
- Ademuyiwa Adesoji
- Ademuyiwa Adesoji O.
- Ademuyiwa Adesoji O.
- Adenekan Babajide
- Adeniran James
- Adeniyi Adewale
- Adesanya Opeoluwa
- Adesina Alaba
- Adeyeye Ademola
- Adeyeye Ademola
- Adhitama Novia
- Adil Muhammad
- Adisa Adewale O.
- Adiyaman Can
- Adu-Aryee Niiarmah
- Afana Samah
- Agalianos Christos
- Agarwal Arnav
- Agarwal Arnav
- Agbedinu Kwabena
- Aglan Amro
- Aguado Suarez Nuria
- Aguilera Maria Lorena
- Aguilera Maria Lorena
- Aguilera-Arevalo Maria-Lorena
- Ahlonsou Germain
- Ahlqvist Sandra
- Ahlqvist Sandra
- Ahmed Asdaq
- Ahmed Ataa
- Ahmed Hayam
- Ahmed Hussien
- Ahmed Lopna Ahmed Mohamed
- Ahmed Sara
- Ahmed Saraibrahim
- Ahounou Ernest Yemalin Stephane
- Ajah Jonathan
- Ajai Olalekan
- Ajao Akinlabi
- Ajiboye Anthony
- Akoto Elliot
- Akpenyi Onyinye
- Al Amin Shadid
- Al Attar Samaa Mahmoud
- Al Barraw Fayez Elian
- Al Bastawis Fatema
- Al Meligy Amgad
- Al Rafati Ahmad Abdel Razaq
- Al Raouf Eman Abd
- Al Saied Ghiath
- Al Subaie Norah
- Al-Bahrani Ahmed
- Al-Buhaisi Alaa
- Al-Dakka Emad
- Al-faqawi Maha
- Al-farram Hadeel
- Al-khatib Ahmed
- Al-Marakby Dina
- Al-saqqa Sara
- Al-Saqqa Sara W.
- Al-Slaibi Ibrahim
- Al-taher Taher
- AlaaelDein Shahinaz
- Alada Muslimat
- Alakaloko Felix
- Alaloul Enas
- Alamin Shadid
- Alamoudi Mohammed
- Albiety Adel
- Alcca Ticona Willy
- Alejos Bermudez Ysabel Esthefany
- Alexander Philip
- Alexander Philip
- Alexandre Challine
- Alghamdi Ahmed
- Alghamdi Mohammed Saleh A.
- Alhady Khaled
- Alhammali Tariq
- Alhassan Basmah
- Alhazmi Wedyan
- Alherz Mohammad
- Ali Ahmed
- Ali Citra Dewi Mohd
- Ali Elsayed
- Ali Safia
- Ali Syed Abdul Wahhab Eusoffee Wan
- Ali Tebian Hassanein Ahmed
- Ali Wadah
- Alihonou Thierry
- Alis Halil
- Aliyu Halima
- Aliyu Mohammad
- Aliyu Shamsudeen
- Aljboor Khaled
- Aljiffry Murad
- Alkaaki Aroub
- Alkelani Muhammad
- Allam Meran
- Allam Yomna
- Alnaby Mohamed Hassab
- Alnusairat Aseel
- Alqahtani Saleh
- Alsaggaf Mohammed Ubaid
- Alser Osaid H.
- Alshareef Reham
- Altaf Abdulmalik
- Altamimi Abdullah
- Altamimi Afnan
- Altamini Afnan
- Altarayra Marwa
- Altibi Ahmed
- Altinel Yuksel
- Altinel Yuksel
- Altwijri Abdulaziz
- Alvi Abdul Rehman
- Aly Mohammed Yahia Mohamed
- Alyacoubi Said
- Alyahya Reem
- Alzahrani Ahmed
- Aman Nowrin F.
- Amandito Radhian
- Amandito Radhian
- Ambrona-Zafra David
- Amin Hager Abdul Aziz
- Amjad Mohammadasim
- Amoah Michael
- Amoako Joachim
- Amoako Philip Taah
- Amoako-Boateng Mabel
- Amole Isaac
- Amreia Mahmoud
- Anderson Frank
- Andika Ferry Fitriya Ayu
- Andreotti Dario
- Andress Cedar
- Andriola Valeria
- Ang Yun Lin
- Angelieri Daniele
- Anis Echaieb
- Ansaloni Luca
- Ansaloni Luca
- Ansaloni Luca
- Antezana Diego
- Anthoulakis Christos
- Antoniozzi Angelo
- Anwar Nourhan
- Anyanwu Lofty-John
- Aonzo Paolo
- Appeadu-Mensah William
- Appiah Eric Kofi
- Aquilino Fabrizio
- Arafa Omar
- Arafa Sara
- Arango Maria Clara Mendoza
- Arcudi Claudio
- Armellini Andrea
- Arnaud Alexis
- Arnaud Alexis Pierre
- Arshad Mohammad Mohsin
- Arslan Ekin
- Arsyad Hasbi Maulana
- Arthur Tom
- Aruldas Neerav
- Asar Yomna Hosny
- Asare-Bediako Kwasi
- Ashour Ahmad
- Ashour Ahmad
- Ashour Khlood
- Ashtari Morvarid
- Asi Fatema
- Asilah Siti Mohd Desa
- Assal Abdelrahman
- Asturias Sabrina
- Asumah Hamza
- Ata Ahmed
- Ata Aya Yehia
- Atiyeh Anwar
- Atkins Ebenezer Takyi
- Attia Attia
- Augestad Knut Magne
- Aviles Susan
- Avoka Anthony
- Awad Israa
- Awad Sawsan Adel
- Awadallah Salwa
- Ayandipo Omobolaji
- Aydin Mehmet Can
- Aziz Dayang Nita Abdul
- Aziz Mohamed Rezal Abdul
- Aziz Nora Abdul
- Azizeldine Mohammed G.
- Azzie Georges
- Azzis Olivier
- Baba Suleiman
- Bachri Houda
- Badawy Mahmoud
- Badenjki Mohamed Adel
- Badicel Maria
- Badr Mohamed Fawzy Mahrous
- Badwi Nermin Mohamed
- Bahar Suraya
- Baillie Katie
- Baki Bahadir Emre
- Bakr Ahmad
- Bakry Hesham Mohammed
- Bala Miklosh
- Balalis Dimitrios
- Balducci Genoveffa
- Ballouhey Quentin
- Balmaceda Ruben
- Balmaceda Ruben
- Balogun Fatai
- Baltrunas Robertas
- Baluch Fatima
- Bamford Rebecca
- Bamicha Athanasia
- Banaitis Vincas Jonas
- Bandi Ashwath
- Bandoh Dickson
- Bani-Sadar Ahmad
- Banipal Gurpreet Singh
- Baquero Suarez Alibeth Andres
- Baraka Heba
- Barendegere Venerand
- Barkolias Christos
- Barmayehvar Behrad
- Barnabas Gandau Naa
- Barrios Emmanuel
- Basilico Silvia
- Basir Elissa Rifhan Mohd
- Bassem Monica
- Bassit Khalil Abdul
- Basso Stefano M. M.
- Bayram Sefa
- Beamon Mieshia
- Bedada Alemayehu Ginbo
- BediakoBowan Antoinette
- Bekhet Amira Hassan
- Bekhet Nada Mohamed
- Beleno Alvaro Enrique Mendoza
- Belkouchi Abdelkader
- Belli Andrea
- Bello Bashir
- Benammi Sarah
- Benevento Angelo
- Bennai Redouane Mammar
- Bentounsi Zineb
- Benyaiche Chaymae
- Berti Stefano
- Bertuello Isaac
- Beuran Mircea
- Bhangu Aneel
- Bhangu Aneel
- Bhangu Anna
- Bhatnagar Ankur
- Bhopal Kamran Faisal
- Bianco Federica
- Bigaran Annamaria
- Billy Matthew
- Bin Adnan Ahmad
- Bin Hasnan Muhammad
- Bin Ismail Mohamad Jeffrey
- Birindelli Arianna
- Bisset Carly
- Bjorklund Ida
- Blacker Sarah
- Blackwell James
- Blanco Ruth
- Blanco-Colino Ruth
- Blencowe Natalie
- Bliksoen Marte
- Bluelle Rafael
- Bocchetti Tommaso
- Bode Chris
- Bodur Selim
- Boggon Adam
- Bonavia Karl
- Bonavina Luigi
- Bond-Smith Giles
- Bondin John
- Bondurri Andrea
- Boni Silvia
- Bonney William
- Borda-Luque Giuliano
- Borg Elaine
- Borg Elaine
- Bortolasi Luca
- Bottini Corrado
- Bougard Heather
- Boukhal Khaoula
- Bowabsak Alaa
- Bowling Kirk
- Bradulskis Saulius
- Bratu Matei
- Bratu Matei Razvan
- Breaud Jean
- Breistrand Michaela
- Breslin Ryan
- Brincat Svetlana Doris
- Broch Aline
- Brunoni Beatrice
- Bsisu Isam
- Bucci Luigi
- Buisson Philippe
- Bunting David
- Burger Sule
- Burmistrovas Andrius
- Bustangi Nasir
- Bustangi Nasir
- Butt Muhammad Talha
- Cakaloglu Haluk Cem
- Caliman Celeste
- Callan Rory
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- Upadhyaya Vijaid
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- Vilcinskas Mantas
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- Waterman Ade
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- Whitaker John
- White Rebecca
- Whitehurst Katharine
- Wiborg Joachim
- Widiastini T. Ariani
- Widmer Lukas Werner
- Wijayarathna L. S.
- Williams Omolara
- Wilson Ling
- Wilson Michael
- Wilson Michael
- Wimalge P. M. S. N.
- Wogensen Fredrik
- Wolf Bernhard
- Wondoh Paul
- Wondoh Paul
- Wong Chui Yee
- Wong Francisca
- Wong Hong Yee
- Wood Greta
- Worku Mengistu
- Worku Tewodros
- Wright Naomi
- Yahaya Muhammad Taqiyuddin
- Yakubu Musah
- Yam Sir Young
- Yang James
- Yap Suhhuey
- Yau Jih Dar
- Ye Joselyn
- Yeang Li Jing
- Yeung Man Hon Andrew
- Yifieyeh Abiboye
- Yildirim Reyyan
- Yip Chingwan
- Ymeri Shpetim
- Yoganathan Pigeneswaren
- Yolcu Sinem
- Yong Guo Liang
- Younis Abobaker
- Youssef Mohamed
- Yuksek Mahmut Arif
- Yusufali Taha
- Zaa'treh Rula
- Zadoroznas Antanas
- Zahran Diaaaldin
- Zakaria Esraay
- Zakaria Mahmoud
- Zakaria Yehia
- Zaki Ahmed
- Zammit Stefan
- Zampitis Nikolaos
- Zani Augusto
- Zani Augusto
- Zanini Nicola
- Zapata Felipe
- Zarb Ciskje
- Zeta Solis Ludwing Alexander
- Zielinski Martin
- Zilinskas Justas
- Zilinskas Justas
- Zilinskas Justas
- Zilinskiene Reda
- Ziubryte Greta
- Zohair Ahmed
- Zuber Markus
- Zuk Grzegorz
- Zulkifli Athirah
- Zumbuhl Lucius
- Publication venue
- Elsevier
- Publication date
- 01/06/2003
- Field of study
BACKGROUND: Rates of antimicrobial resistance (AMR) are rising globally and there is concern that increased migration is contributing to the burden of antibiotic resistance in Europe. However, the effect of migration on the burden of AMR in Europe has not yet been comprehensively examined. Therefore, we did a systematic review and meta-analysis to identify and synthesise data for AMR carriage or infection in migrants to Europe to examine differences in patterns of AMR across migrant groups and in different settings. METHODS: For this systematic review and meta-analysis, we searched MEDLINE, Embase, PubMed, and Scopus with no language restrictions from Jan 1, 2000, to Jan 18, 2017, for primary data from observational studies reporting antibacterial resistance in common bacterial pathogens among migrants to 21 European Union-15 and European Economic Area countries. To be eligible for inclusion, studies had to report data on carriage or infection with laboratory-confirmed antibiotic-resistant organisms in migrant populations. We extracted data from eligible studies and assessed quality using piloted, standardised forms. We did not examine drug resistance in tuberculosis and excluded articles solely reporting on this parameter. We also excluded articles in which migrant status was determined by ethnicity, country of birth of participants' parents, or was not defined, and articles in which data were not disaggregated by migrant status. Outcomes were carriage of or infection with antibiotic-resistant organisms. We used random-effects models to calculate the pooled prevalence of each outcome. The study protocol is registered with PROSPERO, number CRD42016043681. FINDINGS: We identified 2274 articles, of which 23 observational studies reporting on antibiotic resistance in 2319 migrants were included. The pooled prevalence of any AMR carriage or AMR infection in migrants was 25·4% (95% CI 19·1-31·8; I2 =98%), including meticillin-resistant Staphylococcus aureus (7·8%, 4·8-10·7; I2 =92%) and antibiotic-resistant Gram-negative bacteria (27·2%, 17·6-36·8; I2 =94%). The pooled prevalence of any AMR carriage or infection was higher in refugees and asylum seekers (33·0%, 18·3-47·6; I2 =98%) than in other migrant groups (6·6%, 1·8-11·3; I2 =92%). The pooled prevalence of antibiotic-resistant organisms was slightly higher in high-migrant community settings (33·1%, 11·1-55·1; I2 =96%) than in migrants in hospitals (24·3%, 16·1-32·6; I2 =98%). We did not find evidence of high rates of transmission of AMR from migrant to host populations. INTERPRETATION: Migrants are exposed to conditions favouring the emergence of drug resistance during transit and in host countries in Europe. Increased antibiotic resistance among refugees and asylum seekers and in high-migrant community settings (such as refugee camps and detention facilities) highlights the need for improved living conditions, access to health care, and initiatives to facilitate detection of and appropriate high-quality treatment for antibiotic-resistant infections during transit and in host countries. Protocols for the prevention and control of infection and for antibiotic surveillance need to be integrated in all aspects of health care, which should be accessible for all migrant groups, and should target determinants of AMR before, during, and after migration. FUNDING: UK National Institute for Health Research Imperial Biomedical Research Centre, Imperial College Healthcare Charity, the Wellcome Trust, and UK National Institute for Health Research Health Protection Research Unit in Healthcare-associated Infections and Antimictobial Resistance at Imperial College London
Global patient outcomes after elective surgery: prospective cohort study in 27 low-, middle- and high-income countries.
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- Ab Majid MA
- Ab Rahman AS
- Ab Rahman R
- Abayasinghe C
- Abbott T
- Abdullah NH
- Abdur-Rahman L
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- Publication venue
- 'Oxford University Press (OUP)'
- Publication date
- 01/01/2016
- Field of study
BACKGROUND: As global initiatives increase patient access to surgical treatments, there remains a need to understand the adverse effects of surgery and define appropriate levels of perioperative care. METHODS: We designed a prospective international 7-day cohort study of outcomes following elective adult inpatient surgery in 27 countries. The primary outcome was in-hospital complications. Secondary outcomes were death following a complication (failure to rescue) and death in hospital. Process measures were admission to critical care immediately after surgery or to treat a complication and duration of hospital stay. A single definition of critical care was used for all countries. RESULTS: A total of 474 hospitals in 19 high-, 7 middle- and 1 low-income country were included in the primary analysis. Data included 44 814 patients with a median hospital stay of 4 (range 2-7) days. A total of 7508 patients (16.8%) developed one or more postoperative complication and 207 died (0.5%). The overall mortality among patients who developed complications was 2.8%. Mortality following complications ranged from 2.4% for pulmonary embolism to 43.9% for cardiac arrest. A total of 4360 (9.7%) patients were admitted to a critical care unit as routine immediately after surgery, of whom 2198 (50.4%) developed a complication, with 105 (2.4%) deaths. A total of 1233 patients (16.4%) were admitted to a critical care unit to treat complications, with 119 (9.7%) deaths. Despite lower baseline risk, outcomes were similar in low- and middle-income compared with high-income countries. CONCLUSIONS: Poor patient outcomes are common after inpatient surgery. Global initiatives to increase access to surgical treatments should also address the need for safe perioperative care. STUDY REGISTRATION: ISRCTN5181700
Measurement of the total cross section and ρ -parameter from elastic scattering in pp collisions at √s=13 TeV with the ATLAS detector
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- Zwalinski L.
- Publication venue
- Publication date
- 01/01/2023
- Field of study
Measurement of exclusive pion pair production in proton–proton collisions at √s=7 TeV with the ATLAS detector
- Author
- Aad G.
- Abbott B.
- Abbott D. C.
- Abeling K.
- Abidi S. H.
- Aboulhorma A.
- Abramowicz H.
- Abreu H.
- Abulaiti Y.
- Acharya B. S.
- Achkar B.
- Adamczyk L.
- Adamek L.
- Addepalli S. V.
- Adelman J.
- Adiguzel A.
- Adorni S.
- Adye T.
- Affolder A. A.
- Afik Y.
- Agaras M. N.
- Agarwala J.
- Aggarwal A.
- Agheorghiesei C.
- Aguilar-Saavedra J. A.
- Agullo P. M.
- Ahmad A.
- Ahmadov F.
- Ahmed W. S.
- Ahnen J. V.
- Ahuja S.
- Ai X.
- Aielli G.
- Aizenberg I.
- Akbiyik M.
- Akesson T. P. A.
- Akimov A. V.
- Alberghi G. L.
- Albert J.
- Albicocco P.
- Alderweireldt S.
- Aleksa M.
- Aleksandrov I. N.
- Alexa C.
- Alexopoulos T.
- Alfonsi A.
- Alfonsi F.
- Alhroob M.
- Ali B.
- Ali S.
- Aliev M.
- Alimonti G.
- Alkakhi W.
- Allaire C.
- Allbrooke B. M. M.
- Allport P. P.
- Aloisio A.
- Alonso F.
- Alpigiani C.
- Alves F. L. L.
- Alviggi M. G.
- Aly M.
- Ambler A.
- Amelung C.
- Amerl M.
- Ames C. G.
- Amidei D.
- Amoroso S.
- Amos K. R.
- Ananiev V.
- Anastopoulos C.
- Andana R. Y. G.
- Andeen T.
- Anders J. K.
- Andrean S. Y.
- Andreazza A.
- Angelidakis S.
- Angerami A.
- Anisenkov A. V.
- Annovi A.
- Antel C.
- Anthony M. T.
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- Bergmann B.
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- Berlingen J. M.
- Bernardi G.
- Bernius C.
- Bernlochner F. U.
- Berry T.
- Berta P.
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- Bertram I. A.
- Bethke S.
- Betti A.
- Bevan A. J.
- Bhamjee M.
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- Bhattarai P.
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- Bird G. A.
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- Biswas D.
- Bitadze A.
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- Bloch I.
- Blocker C.
- Blue A.
- Blumenschein U.
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- Publication venue
- Publication date
- 01/01/2023
- Field of study
- …