264 research outputs found
Early cancer detection among rural and urban californians
- Author
- AC Society
- AR Brackeen
- Commission. CRHP
- Courtney Summers
- CP Kaplan
- DJ Van Durme
- Georgia R Sadler
- H Bryant
- Institute NCcAf
- JA McElroy
- JM Liff
- LM Santora
- M Schootman
- MB Horton
- P Case
- P Reynolds
- Rebecca Bristol
- RG Roetzheim
- RJ Campbell
- S Vinnakota
- Sarah L Blair
- Sidney L Saltzstein
- SS Coughlin
- TD Hill
- VK Koka
- WP Carr
- Zanera Tahir
- Publication venue
- BioMed Central
- Publication date
- 01/07/2006
- Field of study
BACKGROUND: Since the stage of cancer detection generally predicts future mortality rates, a key cancer control strategy is to increase the proportion of cancers found in the early stage. This study compared stage of detection for members of rural and urban communities to determine whether disparities were present. METHODS: The California Cancer Registry (CCR), a total population based cancer registry, was used to examine the proportion of early stage presentation for patients with breast, melanoma, and colon cancer from 1988 to 2003. Cancer stage at time of detection for these cancers was compared for rural and urban areas. RESULTS: In patients with breast cancer, there were significantly more patients presenting at early stage in 2003 compared to 1988, but no difference in the percentage of patients presenting with early stage disease between rural and urban dwellers. There were no differences in incidence in early stage cancer incidence between these groups for melanoma patients, as well. In colorectal cancer in 1988, significantly more patients presented with early stage disease in the urban areas (42% vs 34%, p < 0.02). However, over time the rural patients were diagnosed with early stage disease with the same frequency in 2003 as 1988. CONCLUSION: This analysis demonstrates that people in rural and urban areas have their breast, melanoma or colorectal cancers diagnosed at similar stages. Health care administrators may take this information into account in future strategic planning
Mapping of hormones and cortisol responses in patients after Lyme neuroborreliosis
- Author
- A Armario
- AJ Zautra
- DL Musselman
- DL Vesely
- E Hagg
- E Sjogren
- G Mastorakos
- G Stanek
- GA Plotnikoff
- GW Ickenstein
- HW Pfister
- I Steiner
- Ingvar Eliasson
- Ivar Tjernberg
- J Berglund
- J Berglund
- J Treib
- Jan Ernerudh
- JD Amsterdam
- JD Amsterdam
- JH Thakore
- K Jew
- K Shimoda
- M Kupari
- M Vrethem
- M Zarkovic
- Martin Carlsson
- MH Brooks
- MJ Lichtenstein
- Pia Forsberg
- RH Haslam
- RS Jaeckle
- RT Rubin
- RT Rubin
- S Schaefer
- VK Summers
- Publication venue
- BioMed Central
- Publication date
- 01/01/2010
- Field of study
<p>Abstract</p> <p>Background</p> <p>Persistent symptoms after treatment for neuroborreliosis are common for reasons mainly unknown. These symptoms are often unspecific and could be caused by dysfunctions in endocrine systems, an issue that has not been previously addressed systematically. We therefore mapped hormone levels in patients with previous confirmed Lyme neuroborreliosis of different outcomes and compared them with a healthy control group.</p> <p>Methods</p> <p>Twenty patients of a retrospective cohort of patients treated for definite Lyme neuroborreliosis were recruited 2.3 to 3.7 years (median 2.7) after diagnosis, together with 23 healthy controls. Lyme neuroborreliosis patients were stratified into two groups according to a symptom/sign score. All participants underwent anthropometric and physiological investigation as well as an extensive biochemical endocrine investigation including a short high-dose adrenocorticotropic hormone stimulation (Synacthen<sup>®</sup>) test. In addition to hormonal status, we also examined electrolytes, 25-hydroxy-vitamin D and interleukin-6.</p> <p>Results</p> <p>Eight patients (40%) had pronounced symptoms 2-3 years after treatment. This group had a higher cortisol response to synacthen as compared with both controls and the Lyme neuroborreliosis patients without remaining symptoms (p < 0.001 for both comparisons). No other significant differences in the various baseline biochemical parameters, anthropometric or physiological data could be detected across groups.</p> <p>Conclusions</p> <p>Apart from a positive association between the occurrence of long-lasting complaints after Lyme neuroborreliosis and cortisol response to synacthen, no corticotropic insufficiency or other serious hormonal dysfunction was found to be associated with remaining symptoms after treatment for Lyme neuroborreliosis.</p
Characterization of the commercially-available fluorescent chloroquine-BODIPY conjugate, LynxTag-CQGREEN, as a marker for chloroquine resistance and uptake in a 96-well plate assay
- Author
- A Butler
- A Yayon
- AM Oduola
- B Pradines
- Bruce Russell
- CA Homewood
- Cheryl C. Y. Loh
- CJ Murray
- CP Sanchez
- CP Sanchez
- CP Sanchez
- D De
- D Rathore
- DA Van Schalkwyk
- DE Kyle
- DH Peyton
- DJ Krogstad
- DJ Sullivan Jr
- DK Raj
- E Hempelmann
- F Ariey
- François H. Nosten
- Georges Snounou
- GR Coatney
- J Adovelande
- J Gildenhuys
- J-H Ch'ng
- J-H Ch'ng
- JA Martiney
- JX Kelly
- K Krafts
- K Tram
- Kevin S. W. Tan
- Kit-Ying Choy
- Kitti W. K. Chan
- Larry M. C. Chow
- Laurent Rénia
- LM Alcantara
- M Cabrera
- Martin J. Lear
- MI Veiga
- O Miotto
- RAL Bayoumi
- RE Martin
- RE Martin
- RL Summers
- RL Summers
- RN Price
- Rossarin Suwanarusk
- S Mok
- S Takala-Harrison
- SG Valderramos
- SJ Burgess
- SK Martin
- T Egan
- TE Wellems
- V Lakshmanan
- VK Zishiri
- W Tan
- Yan Quan Lee
- Publication venue
- 'Public Library of Science (PLoS)'
- Publication date
- 01/01/2014
- Field of study
Chloroquine was a cheap, extremely effective drug against Plasmodium falciparum until resistance arose. One approach to reversing resistance is the inhibition of chloroquine efflux from its site of action, the parasite digestive vacuole. Chloroquine accumulation studies have traditionally relied on radiolabelled chloroquine, which poses several challenges. There is a need for development of a safe and biologically relevant substitute. We report here a commercially-available green fluorescent chloroquine-BODIPY conjugate, LynxTag-CQGREEN, as a proxy for chloroquine accumulation. This compound localized to the digestive vacuole of the parasite as observed under confocal microscopy, and inhibited growth of chloroquine-sensitive strain 3D7 more extensively than in the resistant strains 7G8 and K1. Microplate reader measurements indicated suppression of LynxTag-CQGREEN efflux after pretreatment of parasites with known reversal agents. Microsomes carrying either sensitive or resistant-type PfCRT were assayed for uptake; resistant-type PfCRT exhibited increased accumulation of LynxTag-CQGREEN, which was suppressed by pretreatment with known chemosensitizers. Eight laboratory strains and twelve clinical isolates were sequenced for PfCRT and Pgh1 haplotypes previously reported to contribute to drug resistance, and pfmdr1 copy number and chloroquine IC50s were determined. These data were compared with LynxTag-CQGREEN uptake/fluorescence by multiple linear regression to identify genetic correlates of uptake. Uptake of the compound correlated with the logIC50 of chloroquine and, more weakly, a mutation in Pgh1, F1226Y
Fine motor skills of the hands in Polish and Czech female senior citizens from different backgrounds
- Author
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
The challenging interplay between rheumatoid arthritis, ageing and comorbidities
- Author
- A Berrington de Gonzalez
- A Finckh
- A Maghraoui El
- A Parikh-Patel
- A Zink
- AH Mil Van der Helm-van
- AL Smitten
- AM Boots
- Annelies Boonen
- B Fautrel
- BL Richards
- C Konrat
- C Meune
- C Roubille
- C Roubille
- C Turesson
- CH MacLean
- D Sugiyama
- DH Solomon
- DL Mattey
- DMFM Heijde Van der
- DP Rooy De
- DW McCarey
- E Baecklund
- E Krishnan
- E Loza
- EY Lok
- F Lake
- F Matcham
- FL Bawa
- G Plasqui
- GD Summers
- GR Burmester
- GS Metsios
- GS Metsios
- H He
- H John
- H Källberg
- H Radner
- HM Kremers
- IL Engvall
- J Kekow
- J Lindhardsen
- J Mold
- J Serelis
- J Toms
- JA Avina-Zubieta
- JA Papadakis
- JF Fries
- JJ Goronzy
- JJ Goronzy
- JJ Goronzy
- JK Cooney
- K Barnett
- K Michaud
- K Wallin
- L Fraenkel
- LR Baghdadi
- M Bartolini
- M Cross
- M Dougados
- M Dougados
- M Michaud
- M Muscaritoli
- Marloes van Onna
- MB Arnold
- MC Goes Van der
- MF Leitzmann
- MJ Peters
- MT Nurmohamed
- N Ronda
- NJ Gullick
- NP Weng
- R Abbott
- R Rajbhandary
- R Sakthiswary
- RC Kessler
- RC Kessler
- RH Straub
- RS Pinals
- S Ajeganova
- S Appenzeller
- S Ferrari-Lacraz
- S Gabriel
- S Gavan
- S Ramiro
- S Sacre
- S Verschueren
- SB Cohen
- SC Brown
- SE Gabriel
- SM Marcora
- SY Shin
- SY Shin
- T Bongartz
- T Covic
- T Sokka
- T Sokka
- TD Rachner
- TP Staa Van
- V Groot De
- VK Ranganath
- Y Miedany El
- Z Tutuncu
- É Toussirot
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Large expert-curated database for benchmarking document similarity detection in biomedical literature search
- Author
- Aanei CM
- Abid MB
- Abramowitz MK
- Abu-Zaid A
- Afnan M
- Agarabi C
- Ahmad R
- Aizat WM
- Al-Farha AA
- Al-Lawama M
- Alanio A
- Alaux C
- Albiol J
- Albrecht DR
- Albuquerque LG
- Alimba CG
- Allardyce J
- Almeida GMF
- Alonso-Caneiro D
- Alper OM
- Amer SEDR
- Amiya E
- Ammerman BA
- Amorim RM
- An Q
- Andersen SU
- Aplin JD
- Argyropoulos C
- Armitage C
- Ascher DB
- Ashry M
- Asmann YW
- Assaeed AM
- Atack JM
- Atanasov AG
- Atchison DA
- Atkins GJ
- Atlas L
- Avery SV
- Avillach P
- Baade PD
- Backman L
- Badie C
- Bae T
- Baier D
- Baker CI
- Bakkach J
- Baldi A
- Ball E
- Bannon R
- Bansal A
- Bardot O
- Barnett AG
- Barraud P
- Basharat Z
- Basner M
- Batra J
- Baumert P
- Bazanova OM
- Beale A
- Beck CR
- Becker D
- Beddoe T
- Bell ML
- Benezeth Y
- Bengtsson-Palme J
- Berbesque C
- Berezikov E
- Bergsland N
- Berners-Price S
- Bernhardt P
- Berrevoet F
- Berry E
- Berthold M
- Bessa TB
- Beyene TJ
- Biedermann PHW
- Bijleveld E
- Billington C
- Birch J
- Bittner F
- Bitzer M
- Blakely RD
- Blanck O
- Blaskovich MAT
- Bleackley M
- Blombach F
- Blum R
- Boehme KA
- Boelaert M
- Bogdanos D
- Bonvin AMJJ
- Bosch C
- Bosch O
- Boudreau SA
- Bourgoin T
- Bourke E
- Bouvard D
- Boykin LM
- Bradley G
- Bradshaw W
- Bramoweth AD
- Brand T
- Braubach O
- Braun D
- Braun RJ
- Brenneisen P
- Bridges KM
- Brown JAL
- Brown P
- Browngardt C
- Brownlie J
- Bruhl A
- Bukowy-Bieryllo Z
- Bull JA
- Burt A
- Bush SJ
- Butler LM
- Byrareddy SN
- Byrne HJ
- Cabantous S
- Cai Y
- Calatayud S
- Campana LG
- Campbell M
- Candal E
- Cao Z
- Cao Z
- Cardoso P
- Carlson K
- Carter D
- Cascella M
- Casillas S
- Castelvetro V
- Caswell PT
- Catry T
- Cavalli G
- Cernava T
- Cerovsky V
- Chacko G
- Chagoyen M
- Chakraborty S
- Chan SS
- Chandrasekaran AR
- Chatzitheochari S
- Chavez-Fumagalli MA
- Chen B
- Chen C-E
- Chen C-S
- Chen DF
- Chen H
- Chen H
- Chen J-T
- Chen X
- Chen Y
- Cheng C
- Cheng J
- Cheng S
- Cheung JTK
- Chinapaw M
- Chinopoulos C
- Cho WCS
- Chong L
- Chowdhury D
- Chung H-J
- Chwalibog A
- Ciresi A
- Cobine PA
- Cockcroft S
- Coelho LP
- Colella V
- Conesa A
- Conway A
- Cook PA
- Cooper DN
- Cooper J
- Coqueret O
- Corea EM
- Cosacak MI
- Costa BM
- Costa E
- Costa VD
- Coupland C
- Crawford SY
- Cruz AD
- Cui H
- Cui Q
- Cuiv PO
- Culver DC
- Cuypers M
- Cyr N
- D'Angiulli A
- Dahms TES
- Dai Z
- Daigle F
- Dalgleish R
- Dalrymple BP
- Danchin A
- Danielsen HE
- Darras S
- Daulatabad SV
- Davidson SM
- Day DA
- de Keersmaecker K
- de Leeuw F-E
- Dean LT
- Debrabant B
- Degirmenci V
- del Tredici AL
- Delahay RM
- Demaison L
- Denzel MS
- Deschodt M
- Devkota HP
- Devriendt K
- Dhariwal R
- Diao J
- Ding J
- Dings RPM
- Diouf B
- Dixon R
- Dlamini SV
- Dogan Y
- Domingues HS
- Dong XC
- Donner CF
- Dono M
- Doxey AC
- Dressick W
- Drevon CA
- Duan H
- Ducho C
- Ducommun B
- Dudley KJ
- Dufies M
- Duijf PHG
- Dumaz N
- Dwarakanath BS
- Ebell MH
- Echeverria N
- Ecke T
- Eckweiler D
- Eerola T
- Effiong A
- Ehret F
- Eisenhardt S
- Eixarch E
- El-Adawy H
- El-Esawi MA
- Elkum N
- Emmrich JV
- Engel MS
- Engel N
- Epp T
- Erickson TB
- Esfahlani SS
- Eskelinen E-L
- Eskew EA
- Esnakul AK
- Eustace AJ
- Evangelou E
- Fairhead M
- Falk S
- Fallah M
- Falter-Wagner CM
- Fan X
- Farber DB
- Faville MJ
- Feghali KA
- Fejzo MS
- Fernandez-Triana J
- Festa F
- Feteira A
- Feyerabend F
- Fierz W
- Filipp FV
- Fiona .
- Flegel WA
- Flood-Page P
- Florio T
- Forano E
- Forsayeth J
- Fox SA
- Franks SJ
- Frentiu FD
- Friebe M
- Frilander MJ
- Fu X
- Fujita S
- Furuta S
- Fuss J
- Gabrielsen M
- Gajda M
- Galea I
- Galluzzi L
- Gani F
- Ganpule AP
- Gao J
- Garcia-Alix A
- Gatchell M
- Gaullier G
- Gedye K
- Gelfer Y
- Ghelardi E
- Gill MR
- Gilliham M
- Giordano M
- Giunta C
- Gladue DP
- Gleeson PA
- Gloyn L
- Gnasso A
- Goarant C
- Gobet A
- Goggs R
- Gong H
- Gonzalezlez-Prendes R
- Goodin A
- Goodyear CS
- Gora D
- Gough MJ
- Govender P
- Govinden U
- Goyal R
- Graham EB
- Graham KE
- Grande-Perez A
- Graves PM
- Greene G
- Greenwald NF
- Greidanus H
- Greiff V
- Grice D
- Grimm DG
- Groen EJN
- Gruber J
- Grunau C
- Grundle DS
- Gruneberg P
- Grybos M
- Guisado JL
- Gumede N
- Gumulya Y
- Guo Y
- Gurevich VV
- Gurney-Champion OJ
- Gusev O
- Gutierrez-Sacristan A
- Habes M
- Hacker E
- Hage SR
- Hagen G
- Hahn S
- Haller DM
- Hammerschmidt S
- Han H
- Han J
- Han Q
- Han R
- Handfield M
- Hanson J
- Haore G
- Hapuarachchi HC
- Harder T
- Hardingham JE
- Harrison P
- Hartmann MD
- Harvey DJ
- Haston S
- Heck M
- Heers M
- Heffler E
- Heinrich M
- Helantera H
- Herbelet S
- Hew KF
- Higginbottom DB
- Higuchi Y
- Hilton R
- Hiroi N
- Hobbs E
- Hodzic E
- Hoenner X
- Hojsgaard D
- Hone A
- Hongoh Y
- Honjo K
- Horbar J
- Hori H
- Hu G
- Hu P
- Huber HP
- Huber M
- Hueso LE
- Huirne J
- Hurt L
- Huttner FJ
- Idborg H
- Ide K
- Ikeo K
- Ikonomopoulou MP
- Ingley E
- Jakeman PM
- Janga SC
- Janzen T
- Jayaraman J
- Jeltsch A
- Jensen A
- Jeurissen P
- Jia H
- Jia H
- Jia S
- Jiang F
- Jiang J
- Jiang X
- Jibb LA
- Jin Y
- Jo D
- Johnson AM
- Johnson DM
- Johnston M
- Jongen S
- Jonscher KR
- Jorens PG
- Jorgensen JOL
- Josse C
- Joubert JW
- Jung S-H
- Junior AM
- Jurman G
- Kabra D
- Kahan T
- Kaiser S
- Kamagata K
- Kamboj SK
- Kamiya H
- Kane NC
- Kang Y-K
- Karamanos Y
- Karmakar C
- Karp NA
- Kasian O
- Kauppila JH
- Kaye LK
- Kelly R
- Kelly S
- Kenna R
- Kennedy J
- Kersten B
- Khalaf RA
- Khalid JM
- Khan MM
- Khatlani T
- Khider T
- Kijanka GS
- Kim Y-M
- King SRB
- Kinyanjui T
- Kish JK
- Klempnauer K-H
- Kleppe A
- Klump H
- Kluz T
- Knox P
- Kobayashi T
- Kobold S
- Koch K-W
- Kohanbash G
- Kohls G
- Kohonen-Corish MRJ
- Koleva-Kolarova RG
- Kong X
- Konkle-Parker D
- Korpela KM
- Kostrikis LG
- Kraiczy P
- Kratz H
- Krause G
- Krebsbach PH
- Kristensen SR
- Kristiansson E
- Kueberuwa G
- Kugler J-M
- Kulkarni A
- Kumar G
- Kumar N
- Kumar N
- Kumari P
- Kunimatsu A
- Kurdak H
- Kurgan L
- Kurniawan NA
- Kwon YD
- Lachat C
- Lacy-Colson J
- Lagisz M
- Lai HM
- Laky B
- Lalaouna D
- Lammerding J
- Lange M
- Larrosa M
- Laslett AL
- Latif A
- Lau CL
- Lauschke VM
- LeClair EE
- Lee K-W
- Lee M-S
- Lee M-Y
- Lee S
- Li B
- Li G
- Li J
- Li J
- Li J
- Li Z
- Liang D
- Liang S
- Lidbury BA
- Lieb K
- Liehr T
- Liew AWC
- Lim CJ
- Lim YY
- Lin MZ
- Lindsey ML
- Line P-D
- Liu D
- Liu E
- Liu F
- Liu F
- Liu H
- Liu H
- Liu S
- Liu X
- Liu Y-P
- Lloyd VK
- Lo T-W
- Locci E
- Loft ND
- Loidl J
- Lopez-Escamez JA
- Lopez-Ruiz FJ
- Lorenzen J
- Lorkowski S
- Lovell NH
- Lu H
- Lu J-J
- Lu Q
- Lu W
- Lu Z
- Luengo GS
- Lund BA
- Lundh L-G
- Lussier AA
- Luu AM
- Lynch I
- Lysy PA
- Ma C
- Ma L
- Ma L
- Ma L
- Ma R
- Ma W
- Mabb A
- Mack HG
- Mackey DA
- Mahavadi P
- Mahdavi SR
- Maher P
- Maher T
- Maibach EW
- Maity SN
- Malgrange B
- Mamoulakis C
- Mangoni AA
- Manke T
- Manstead ASR
- Mantalaris A
- Marchbank KJ
- Marinello F
- Marsal J
- Marschalek R
- Marschall H-U
- Martin CS
- Martin FL
- Martinez-Raga J
- Martinez-Salas E
- Martis E
- Marzocchi U
- Mather DE
- Mathieu D
- Matsui Y
- Maza E
- McCrum C
- McCutcheon JE
- McGarrigle CA
- Mckay GJ
- McMillan B
- McMillan N
- Meads C
- Medina L
- Merrick BA
- Meseko C
- Metzger DW
- Meule A
- Meunier FA
- Michaelis M
- Micheau O
- Miele AE
- Mier P
- Mihara H
- Min R
- Mintz EM
- Miotla P
- Mitchell KM
- Mizukami T
- Moal I
- Moalic Y
- Mohapatra DP
- Molari M
- Molleman L
- Mondal SR
- Montagutelli X
- Monteiro A
- Montes M
- Moore MD
- Moran JV
- Morcillo E
- Morozov SY
- Mort M
- Moss WN
- Moultos OA
- Moyer R
- Mukherjee M
- Murai N
- Murphy DJ
- Murphy SK
- Murray SA
- Muth T
- Naganawa S
- Nagler K
- Nakayama K
- Nammi S
- Nandakumar KS
- Narayan E
- Nasios G
- Natoli RM
- Navaratnarajah .
- Neumann P-A
- Ng G
- Nguyen F
- Nicol C
- Nicoletti R
- Nie J
- Nie Y
- Niehof M
- Niemeyer F
- Nilsen EB
- Nilsson H
- Nixon B
- Nobile CJ
- Norris AD
- Nwaiwu O
- O'Mahony M
- O'Toole R
- Ogami K
- Ohgami RS
- Ohlsson S
- Ohtomo T
- Olatunbosun O
- Oldenmenger WH
- Olofsson P
- Olumayede E
- Orme MW
- Ortiz A
- Oster H
- Ostrikov K
- Otto S
- Ou J
- Outeiro TF
- Ouyang S
- Paganoni S
- Page A
- Pallebage-Gamarallage M
- Palm C
- Palma J-A
- Pan Z
- Panthee S
- Paradies Y
- Parchi P
- Parsons JR
- Parsons MH
- Parsons N
- Pascal P
- Paterson R
- Paul E
- Pearce SP
- Pearson JA
- Peckham M
- Pedemonte N
- Peifer M
- Pelkonen T
- Pelleri MC
- Pellizzon MA
- Peng Y
- Perco P
- Pereira JL
- Peres MA
- Petrelli M
- Pheko M
- Pichugin A
- Pinto CJC
- Pinto IM
- Pinto KA
- Piotrowski M
- Piovesan A
- Plevris JN
- Pluess M
- Podolsky IM
- Pollesello P
- Polz M
- Ponti G
- Popoola SI
- Porcelli P
- Portilla M
- Portillo MC
- Pourret O
- Prajapati AS
- Pranata R
- Prescott J
- Prieto D
- Prince M
- Pritchard AL
- Pusch S
- Qi D
- Qi X
- Quinn GP
- Quinn TJ
- Raghava GPS
- Rahimi F
- Rahman MS
- Raikou VD
- Ramula S
- Ranft A
- Rappsilber J
- Reddan T
- Rehfeldt F
- Reiling JH
- Remacle C
- Reschke CR
- Rezaei M
- Rhodes J
- Riddick EW
- Ritter U
- Riva G
- Roach NW
- Roberts DD
- Roberts NJ
- Robles G
- Rodrigues T
- Rodriguez C
- Roislien J
- Roobol MJ
- Ross K
- Ross SA
- Rotge J-Y
- Rowe AD
- Rowe JA
- Ruepp A
- Rust P
- Saad S
- Sabnis SC
- Sack GH
- Saggar M
- Saito Y
- Salama MF
- Sallmon H
- Santos M
- Saudemont A
- Sava G
- Schrading S
- Schramm A
- Schreiber M
- Schuele B
- Schuler S
- Schulte LN
- Schuon RA
- Schymkowitz J
- Sczyrba A
- Seib KL
- Senghore T
- Seow E
- Sergeant K
- Shabalin IG
- Shahid S
- Shalchyan V
- Shen J
- Shi H-P
- Shimada T
- Shin J-S
- Shortt C
- Siebers R
- Sillanpaa E
- Silveyra P
- Skinner D
- Small I
- Smeets PAM
- Smith SS
- So P-W
- Solano F
- Sonenshine DE
- Song H
- Song J
- Sorzano CO
- Southall T
- Speakman JR
- Srinivasan MV
- St Hilaire C
- Stabile LP
- Staege MS
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- Ziegler A
- Zinke K
- Zuberbier T
- Publication venue
- OXFORD UNIV PRESS
- Publication date
- 29/10/2019
- Field of study
Document recommendation systems for locating relevant literature have mostly relied on methods developed a decade ago. This is largely due to the lack of a large offline gold-standard benchmark of relevant documents that cover a variety of research fields such that newly developed literature search techniques can be compared, improved and translated into practice. To overcome this bottleneck, we have established the RElevant LIterature SearcH consortium consisting of more than 1500 scientists from 84 countries, who have collectively annotated the relevance of over 180 000 PubMed-listed articles with regard to their respective seed (input) article/s. The majority of annotations were contributed by highly experienced, original authors of the seed articles. The collected data cover 76% of all unique PubMed Medical Subject Headings descriptors. No systematic biases were observed across different experience levels, research fields or time spent on annotations. More importantly, annotations of the same document pairs contributed by different scientists were highly concordant. We further show that the three representative baseline methods used to generate recommended articles for evaluation (Okapi Best Matching 25, Term Frequency–Inverse Document Frequency and PubMed Related Articles) had similar overall performances. Additionally, we found that these methods each tend to produce distinct collections of recommended articles, suggesting that a hybrid method may be required to completely capture all relevant articles. The established database server located at https://relishdb.ict.griffith.edu.au is freely available for the downloading of annotation data and the blind testing of new methods. We expect that this benchmark will be useful for stimulating the development of new powerful techniques for title and title/abstract-based search engines for relevant articles in biomedical research
Search for strongly interacting massive particles generating trackless jets in proton-proton collisions at s = 13 TeV
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- Simone FM
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- Österberg K
- Özçelik Ö
- Široký J
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2022
- Field of study
A search for dark matter in the form of strongly interacting massive particles (SIMPs) using the CMS detector at the LHC is presented. The SIMPs would be produced in pairs that manifest themselves as pairs of jets without tracks. The energy fraction of jets carried by charged particles is used as a key discriminator to suppress efficiently the large multijet background, and the remaining background is estimated directly from data. The search is performed using proton-proton collision data corresponding to an integrated luminosity of 16.1 fb - 1 , collected with the CMS detector in 2016. No significant excess of events is observed above the expected background. For the simplified dark matter model under consideration, SIMPs with masses up to 100 GeV are excluded and further sensitivity is explored towards higher masses
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- Abdelfatah S
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- Ávalos Y
- Önal G
- Üstün S
- Čolić M
- Đokić J
- Žerovnik E
- Publication venue
- 'Informa UK Limited'
- Publication date
- 01/01/2021
- Field of study
In 2008, we published the first set of guidelines for standardizing research in autophagy. Since then, this topic has received increasing attention, and many scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Thus, it is important to formulate on a regular basis updated guidelines for monitoring autophagy in different organisms. Despite numerous reviews, there continues to be confusion regarding acceptable methods to evaluate autophagy, especially in multicellular eukaryotes. Here, we present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes. These guidelines are not meant to be a dogmatic set of rules, because the appropriateness of any assay largely depends on the question being asked and the system being used. Moreover, no individual assay is perfect for every situation, calling for the use of multiple techniques to properly monitor autophagy in each experimental setting. Finally, several core components of the autophagy machinery have been implicated in distinct autophagic processes (canonical and noncanonical autophagy), implying that genetic approaches to block autophagy should rely on targeting two or more autophagy-related genes that ideally participate in distinct steps of the pathway. Along similar lines, because multiple proteins involved in autophagy also regulate other cellular pathways including apoptosis, not all of them can be used as a specific marker for bona fide autophagic responses. Here, we critically discuss current methods of assessing autophagy and the information they can, or cannot, provide. Our ultimate goal is to encourage intellectual and technical innovation in the field
Evidence for Top Quark Production in Nucleus-Nucleus Collisions
- Author
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- Aarup Petersen H
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- Abbiendi G
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- Álvarez Fernández A
- Özçelik Ö
- Publication venue
- Publication date
- 01/01/2019
- Field of study
Peer reviewe
Observation of the B-s(0) -> X(3872)phi Decay
- Author
- Aarrestad TK
- Aarup Petersen H
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdullin S
- Abercrombie D
- Acharya H
- Acosta D
- Acosta JG
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- Publication venue
- Publication date
- 01/01/2020
- Field of study
Using a data sample of proton-proton collisions at root s = 13 TeV, corresponding to an integrated luminosity of 140 fb(-1) collected by the CMS experiment in 2016-2018, the B-s(0) -> X(3872)phi decay is observed. Decays into J/psi pi(+)pi(-) and K+K- are used to reconstruct, respectively, the X(3872) and phi. The ratio of the product of branching fractions B[B-s(0) -> X(3872)phi]B[X(3872) -> J/psi pi(+)pi(-)] to the product B[B-s(0) ->psi(2S)phi]B[psi(2S) -> J/psi pi(+)pi(-)] is measured to be [2.21 +/- 0.29(stat) +/- 0.17(syst)]%. The ratio B[B-s(0) -> X(3872)phi]/B[B-0 -> X(3872)K-0] is found to be consistent with one, while the ratio B[B-s(0) -> X(3872)phi]/B[B+-> X(3872)K+] is two times smaller. This suggests a difference in the production dynamics of the X(3872) in B-0 and B(0)s meson decays compared to B+. The reported observation may shed new light on the nature of the X(3872) particle.Peer reviewe
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