468 research outputs found
A mutate-and-map protocol for inferring base pairs in structured RNA
- Author
- CS Chow
- D Moazed
- DH Mathews
- EE Regulski
- JB Lucks
- JG Underwood
- JP Staley
- KA Wilkinson
- M Kertesz
- M Mandal
- N Kulshina
- NB Leontis
- P Cordero
- P Cordero
- P Rocca-Serra
- P Tijerina
- PJ Lukavsky
- R Rydzanicz
- RC Spitale
- RF Gesteland
- S Mitra
- S Washietl
- S Yoon
- SA Mortimer
- SE Wells
- SM Vasa
- SW Brostoff
- VD Sood
- W Kladwang
- W Kladwang
- W Kladwang
- W Kladwang
- Y Rhee
- Publication venue
- Publication date
- 31/01/2013
- Field of study
Chemical mapping is a widespread technique for structural analysis of nucleic
acids in which a molecule's reactivity to different probes is quantified at
single-nucleotide resolution and used to constrain structural modeling. This
experimental framework has been extensively revisited in the past decade with
new strategies for high-throughput read-outs, chemical modification, and rapid
data analysis. Recently, we have coupled the technique to high-throughput
mutagenesis. Point mutations of a base-paired nucleotide can lead to exposure
of not only that nucleotide but also its interaction partner. Carrying out the
mutation and mapping for the entire system gives an experimental approximation
of the molecules contact map. Here, we give our in-house protocol for this
mutate-and-map strategy, based on 96-well capillary electrophoresis, and we
provide practical tips on interpreting the data to infer nucleic acid
structure.Comment: 22 pages, 5 figure
Rapid detection of SMARCB1 sequence variation using high resolution melting
- Author
- Publication venue
- BioMed Central
- Publication date
- 01/01/2009
- Field of study
Background : Rhabdoid tumors are rare cancers of early childhood arising in the kidney, central nervous system and other organs. The majority are caused by somatic inactivating mutations or deletions affecting the tumor suppressor locus SMARCB1 [OMIM 601607]. Germ-line SMARCB1 inactivation has been reported in association with rhabdoid tumor, epitheloid sarcoma and familial schwannomatosis, underscoring the importance of accurate mutation screening to ascertain recurrence and transmission risks. We describe a rapid and sensitive diagnostic screening method, using high resolution melting (HRM), for detecting sequence variations in SMARCB1. Methods : Amplicons, encompassing the nine coding exons of SMARCB1, flanking splice site sequences and the 5\u27 and 3\u27 UTR, were screened by both HRM and direct DNA sequencing to establish the reliability of HRM as a primary mutation screening tool. Reaction conditions were optimized with commercially available HRM mixes. Results : The false negative rate for detecting sequence variants by HRM in our sample series was zero. Nine amplicons out of a total of 140 (6.4%) showed variant melt profiles that were subsequently shown to be false positive. Overall nine distinct pathogenic SMARCB1 mutations were identified in a total of 19 possible rhabdoid tumors. Two tumors had two distinct mutations and two harbored SMARCB1 deletion. Other mutations were nonsense or frame-shifts. The detection sensitivity of the HRM screening method was influenced by both sequence context and specific nucleotide change and varied from 1: 4 to 1:1000 (variant to wild-type DNA). A novel method involving digital HRM, followed by re-sequencing, was used to confirm mutations in tumor specimens containing associated normal tissue. Conclusions : This is the first report describing SMARCB1 mutation screening using HRM. HRM is a rapid, sensitive and inexpensive screening technology that is likely to be widely adopted in diagnostic laboratories to facilitate whole gene mutation screening
Risk of bleeding in surgical patients treated with topical bovine thrombin sealants: a review of the literature
- Author
- A Yellin
- AR La Spada
- AT Cohen
- BL Cmolik
- BM Alving
- D DeEugenio
- G Renda
- I Koukoutsis
- I Opitz
- J Caers
- J Wight
- JA Spero
- JF Carroll
- JL Zehnder
- John Clark
- KC Potger
- L Nalysnyk
- M Ihasz
- M Vera-Llonch
- Matthew W Reynolds
- MB Streiff
- MD Tarantino
- MK Cruickshank
- MR Sarfati
- MS Zumberg
- N Winterbottom
- P Balachandran
- R Berguer
- R Vink
- RP Dorion
- S Karthik
- Sheila Crean
- SI Rapaport
- SJ Israels
- SM de Castro
- Srinath Samudrala
- TL Ortel
- TL Ortel
- UO von Oppell
- VD Chow
- W Kang
- W Morawski
- WC Chapman
- Publication venue
- BioMed Central
- Publication date
- 01/01/2008
- Field of study
Observation of associated near-side and away-side long-range correlations in √sNN=5.02 TeV proton-lead collisions with the ATLAS detector
- Author
- Aad G
- Abajyan T
- Abbott B
- Abdallah J
- Abdel Khalek S
- Abdelalim AA
- Abdinov O
- Aben R
- Abi B
- Abolins M
- Abouzeid OS
- Abramowicz H
- Abreu H
- Acharya BS
- Adamczyk L
- Adams DL
- Addy TN
- Adelman J
- Adomeit S
- Adragna P
- Adye T
- Aefsky S
- Aguilar-Saavedra JA
- Agustoni M
- Ahlen SP
- Ahles F
- Ahmad A
- Ahsan M
- Aielli G
- Akesson TP
- Akimoto G
- Akimov AV
- Alam MA
- Albert J
- Albrand S
- Aleksa M
- Aleksandrov IN
- Alessandria F
- Alexa C
- Alexander G
- Alexandre G
- Alexopoulos T
- Alhroob M
- Aliev M
- Alimonti G
- Alison J
- Allbrooke BM
- Allison LJ
- Allport PP
- Allwood-Spiers SE
- Almond J
- Aloisio A
- Alon R
- Alonso A
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- Altheimer A
- Alvarez Gonzalez B
- Alviggi MG
- Amako K
- Amelung C
- Ammosov VV
- Amor Dos Santos SP
- Amorim A
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- Anderson KJ
- Andreazza A
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- Anduaga XS
- Angelidakis S
- Anger P
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- Anghinolfi F
- Anisenkov A
- Anjos N
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- Antonaki A
- Antonelli M
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- Antos J
- Anulli F
- Aoki M
- Aperio Bella L
- Apolle R
- Arabidze G
- Aracena I
- Arai Y
- Arce AT
- Arfaoui S
- Arguin JF
- Argyropoulos S
- Arik E
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- Arnaez O
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- Artamonov A
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- Arutinov D
- Asai S
- Ask S
- Asman B
- Asquith L
- Assamagan K
- Astalos R
- Astbury A
- Atkinson M
- ATLAS Collaboration The
- Auerbach B
- Auge E
- Augsten K
- Aurousseau M
- Avolio G
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- Publication venue
- American Physical Society
- Publication date
- 01/01/2012
- Field of study
Two-particle correlations in relative azimuthal angle (Δϕ) and pseudorapidity (Δη) are measured in √sNN=5.02 TeV p+Pb collisions using the ATLAS detector at the LHC. The measurements are performed using approximately 1 μb-1 of data as a function of transverse momentum (pT) and the transverse energy (ΣETPb) summed over 3.1<η<4.9 in the direction of the Pb beam. The correlation function, constructed from charged particles, exhibits a long-range (2<|Δη|<5) “near-side” (Δϕ∼0) correlation that grows rapidly with increasing ΣETPb. A long-range “away-side” (Δϕ∼π) correlation, obtained by subtracting the expected contributions from recoiling dijets and other sources estimated using events with small ΣETPb, is found to match the near-side correlation in magnitude, shape (in Δη and Δϕ) and ΣETPb dependence. The resultant Δϕ correlation is approximately symmetric about π/2, and is consistent with a dominant cos2Δϕ modulation for all ΣETPb ranges and particle pT
Measurement of the cross-section of high transverse momentum vector bosons reconstructed as single jets and studies of jet substructure in pp collisions at √s = 7 TeV with the ATLAS detector
- Author
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- Zhang J
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- Zhemchugov A
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- Zibell A
- Zieminska D
- Zimine NI
- Zimmermann C
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- Zinonos Z
- Ziolkowski M
- Zitoun R
- Zobernig G
- Zoccoli A
- Zurzolo G
- Zutshi V
- Zwalinski L
- Publication venue
- 'IOP Publishing'
- Publication date
- 01/01/2014
- Field of study
This paper presents a measurement of the cross-section for high transverse momentum W and Z bosons produced in pp collisions and decaying to all-hadronic final states. The data used in the analysis were recorded by the ATLAS detector at the CERN Large Hadron Collider at a centre-of-mass energy of √s = 7 TeV;{\rm Te}{\rm V}andcorrespondtoanintegratedluminosityof4.6\;{\rm f}{{{\rm b}}^{-1}}.ThemeasurementisperformedbyreconstructingtheboostedWorZbosonsinsinglejets.ThereconstructedjetmassisusedtoidentifytheWandZbosons,andajetsubstructuremethodbasedonenergyclusterinformationinthejetcentre−of−massframeisusedtosuppressthelargemulti−jetbackground.Thecross−sectionforeventswithahadronicallydecayingWorZboson,withtransversemomentum{{p}_{{\rm T}}}\gt 320\;{\rm Ge}{\rm V}andpseudorapidity|\eta |\lt 1.9,ismeasuredtobe{{\sigma }_{W+Z}}=8.5\pm 1.7$ pb and is compared to next-to-leading-order calculations. The selected events are further used to study jet grooming techniques
Search for direct pair production of the top squark in all-hadronic final states in proton-proton collisions at s√=8 TeV with the ATLAS detector
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- Zurzolo G
- Zutshi V
- Zwalinski L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2014
- Field of study
The results of a search for direct pair production of the scalar partner to the top quark using an integrated luminosity of 20.1fb−1 of proton–proton collision data at √s = 8 TeV recorded with the ATLAS detector at the LHC are reported. The top squark is assumed to decay via t˜→tχ˜01 or t˜→ bχ˜±1 →bW(∗)χ˜01 , where χ˜01 (χ˜±1 ) denotes the lightest neutralino (chargino) in supersymmetric models. The search targets a fully-hadronic final state in events with four or more jets and large missing transverse momentum. No significant excess over the Standard Model background prediction is observed, and exclusion limits are reported in terms of the top squark and neutralino masses and as a function of the branching fraction of t˜ → tχ˜01 . For a branching fraction of 100%, top squark masses in the range 270–645 GeV are excluded for χ˜01 masses below 30 GeV. For a branching fraction of 50% to either t˜ → tχ˜01 or t˜ → bχ˜±1 , and assuming the χ˜±1 mass to be twice the χ˜01 mass, top squark masses in the range 250–550 GeV are excluded for χ˜01 masses below 60 GeV
Search for pair-produced long-lived neutral particles decaying to jets in the ATLAS hadronic calorimeter in ppcollisions at √s=8TeV
- Author
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- Zimmermann S
- Zinonos Z
- Ziolkowski M
- Zobernig G
- Zoccoli A
- zur Nedden M
- Zurzolo G
- Zutshi V
- Zwalinski L
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2014
- Field of study
The ATLAS detector at the Large Hadron Collider at CERN is used to search for the decay of a scalar boson to a pair of long-lived particles, neutral under the Standard Model gauge group, in 20.3fb−1of data collected in proton–proton collisions at √s=8TeV. This search is sensitive to long-lived particles that decay to Standard Model particles producing jets at the outer edge of the ATLAS electromagnetic calorimeter or inside the hadronic calorimeter. No significant excess of events is observed. Limits are reported on the product of the scalar boson production cross section times branching ratio into long-lived neutral particles as a function of the proper lifetime of the particles. Limits are reported for boson masses from 100 GeVto 900 GeV, and a long-lived neutral particle mass from 10 GeVto 150 GeV
Comparison of In vitro Nanoparticles Uptake in Various Cell Lines and In vivo Pulmonary Cellular Transport in Intratracheally Dosed Rat Model
- Author
- A Nemmar
- AH Chow
- AM Calcagno
- AT Florence
- BE Lehnert
- BE Rabinow
- E Merisko-Liversidge
- G Oberdorster
- GJ Russell-Jones
- GJ Russell-Jones
- GL Scheffer
- I Behrens
- IJ Hidalgo
- IJ Hidalgo
- J Jinno
- J Kreuter
- J Taipalensuu
- Jason D. Blom
- JC Leroux
- JD Irvine
- Jon G. Selbo
- JP Ebel
- Kimberly Shevlin
- KO Hamilton
- L Jia
- L Zhang
- Liangbiao George Hu
- M Aprahamian
- M Doyle-McCullough
- M Geiser
- M Huang
- MA Clark
- MP Desai
- MP Desai
- N Hussain
- Na Li
- P Garberg
- P Jani
- P Kocbek
- Po-Chang Chiang
- R Ghirardelli
- S Takenaka
- SM Moghimi
- Timothy G. Brayman
- V Castranova
- VD Makhey
- W Easson
- WS Putnam
- Yiding Hu
- Yurong Lai
- Publication venue
- Springer
- Publication date
- 01/01/2008
- Field of study
In present study, the potential drug delivery of nanoformulations was validated via the comparison of cellular uptake of nanoparticles in various cell lines and in vivo pulmonary cellular uptake in intratracheally (IT) dosed rat model. Nanoparticles were prepared by a bench scale wet milling device and incubated with a series of cell lines, including Caco-2, RAW, MDCK and MDCK transfected MDR1 cells. IT dosed rats were examined for the pulmonary cellular uptake of nanoparticles. The processes of nanoparticle preparation did not alter the crystalline state of the material. The uptake of nanoparticles was observed most extensively in RAW cells and the least in Caco-2 cells. Efflux transporter P-gp did not prevent cell from nanoparticles uptake. The cellular uptake of nanoparticles was also confirmed in bronchoalveolar lavage (BAL) fluid cells and in bronchiolar epithelial cells, type II alveolar epithelial cells in the intratracheally administrated rats. The nanoparticles uptake in MDCK, RAW cells and in vivo lung epithelial cells indicated the potential applications of nanoformulation for poorly soluble compounds. The observed limited direct uptake of nanoparticles in Caco-2 cells suggests that the improvement in oral bioavailability by particle size reduction is via increased dissolution rate rather than direct uptake
Expression Profiling of a Genetic Animal Model of Depression Reveals Novel Molecular Pathways Underlying Depressive-Like Behaviours
- Author
- A Barbon
- A Baskys
- A Roy
- A Sakane
- A Sequeira
- A Zangen
- AA Mathé
- Adam Taylor
- Aleksander Mathé
- Alessandra Mallei
- B Molzer
- BC Bond
- C Andriamampandry
- C Aston
- Chiara Piubelli
- DE Comings
- DH Overstreet
- DH Overstreet
- DH Overstreet
- DH Overstreet
- DH Overstreet
- DH Overstreet
- DS Janowsky
- DS Janowsky
- E Wallis
- EJ Nestler
- Ekaterini Blaveri
- EL Abel
- Enrico Domenici
- F Ng
- F Petty
- Fiona Kelly
- G Sanacora
- Girogio Racagni
- GN Pandey
- H Wehr
- Hiromu Tanimoto
- J Glowinski
- JJ Mann
- JJ Mann
- Juliet Reid
- K Nishi
- K Takahashi
- KA Pearson
- KP Lesch
- Kriss Harris
- L Serova
- L Urigüen
- L Weng
- Laura Musazzi
- Lucia Carboni
- M Orsetti
- M Tochigi
- Maria Razzoli
- Maurizio Popoli
- MK Osterlund
- N Nakatani
- P Gass
- PA Jiménez-Vasquez
- PV Choudary
- R Kohen
- RA Kroes
- RC Kessler
- RD Porsolt
- S Cohen-Cole
- S Lemonde
- S Thakker-Varia
- Stewart Bates
- TA Klempan
- TW Chow
- V Arango
- VD Khait
- WE Cullinan
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2010
- Field of study
The Flinders model is a validated genetic rat model of depression that exhibits a number of behavioural, neurochemical and pharmacological features consistent with those observed in human depression.In this study we have used genome-wide microarray expression profiling of the hippocampus and prefrontal/frontal cortex of Flinders Depression Sensitive (FSL) and control Flinders Depression Resistant (FRL) lines to understand molecular basis for the differences between the two lines. We profiled two independent cohorts of Flinders animals derived from the same colony six months apart, each cohort statistically powered to allow independent as well as combined analysis. Using this approach, we were able to validate using real-time-PCR a core set of gene expression differences that showed statistical significance in each of the temporally distinct cohorts, representing consistently maintained features of the model. Small but statistically significant increases were confirmed for cholinergic (chrm2, chrna7) and serotonergic receptors (Htr1a, Htr2a) in FSL rats consistent with known neurochemical changes in the model. Much larger gene changes were validated in a number of novel genes as exemplified by TMEM176A, which showed 35-fold enrichment in the cortex and 30-fold enrichment in hippocampus of FRL animals relative to FSL.These data provide significant insights into the molecular differences underlying the Flinders model, and have potential relevance to broader depression research
The genome of the sea urchin Strongylocentrotus purpuratus
- Author
- ADAMS N
- AGCA C
- ALLGOOD EL
- AMORE G
- ANDERSON MK
- ANGERER LM
- ANGERER RC
- ARBOLEDA E
- ARNONE MI
- BELLE R
- BERGERON KF
- BERNEY K
- BOSDET I
- BOTTJER DJ
- BRANDHORST BP
- BRANNO M
- BROCKTON V
- BROWN ER
- BUCKLEY KM
- BURGESS DR
- BURKE RD
- CALESTANI C
- CAMERON RA
- CARBONNEAU S
- CAVALIERI Vincenzo
- CHEN N
- CHEUNG R
- CHOW E
- CHURCHER AM
- COFFMAN JA
- COHEN AH
- COLE B
- COOL J
- CORMIER P
- COSSON B
- CROCE J
- DAVIDSON EH
- DEAN M
- DUBOC V
- DULOQUIN L
- DURBIN KJ
- ELHAIK E
- ELPHICK MR
- ELSIK CG
- EPEL D
- ERMOLAEVA O
- ETTENSOHN CA
- FEDRIGO O
- FERNANDEZ GUERRA A
- FLYTZANIS C
- FOLTZ KR
- FUGMANN SD
- GAASTERLAND T
- GACHE C
- GALINDO BE
- GARFIELD D
- GENEVIERE AM
- GIBBONS IR
- GIBBS RA
- GOEL M
- GOLD B
- GOLDSTONE JV
- GONZALEZ GARAY ML
- GRAUR D
- GUNARATNE HJ
- HAHN ME
- HALLBOOK F
- HAMDOUN A
- HAYGOOD R
- HEESUN S
- HIBINO T
- HLAVINA W
- HOFFMAN MP
- HOFMANN G
- HOWARD ASHBY M
- HUMPHREY GW
- HYNES RO
- IDRIS MM
- ISTRAIL S
- JACKSON AR
- JUDKINS KM
- JULIANO C
- KELKAR H
- KILLIAN CE
- KINUKAWA M
- KITTS P
- KIYAMA T
- KLEIN WH
- LANDRUM MJ
- LAPRAZ F
- LEONE A
- LEPAGE T
- LIANG S
- LIVINGSTON BT
- LOCASCIO A
- LOZA COLL M
- MACKEY AJ
- MAGLOTT D
- MAJESKE AJ
- MARRA MA
- MART
- MARZLUFF W
- MATERNA SC
- MCCAFFERTY SS
- MCCLAY DR
- MELLOTT D
- MESSIER C
- MILOSAVLJEVIC A
- MORALES J
- MORRIS RL
- MOY GW
- MU X
- MULNER LORILLON O
- MURRAY G
- MUSANTE AM
- MUSHEGIAN A
- NAIR SV
- NEILL AT
- NOMURA M
- OBAR RA
- OLINSKI RP
- PANCER Z
- PANOPOULOU G
- PETERSON K
- POUSTKA AJ
- PRIMUS A
- PRUITT K
- RAIBLE F
- RAISCH M
- RAST JP
- RAWSON AP
- READE A
- REESE JT
- ROBERTSON AJ
- ROSSETTI BJ
- ROUX MM
- ROWE M
- SAMANTA MP
- SAPOJNIKOV V
- SATIJA R
- SCALLY M
- SCHEIN J
- SEA URCHIN GENOME SEQUENCING CONSORTIUM
- SEVERSON T
- SHEN Y
- SMITH LC
- SODERGREN E
- SOLOVYEV V
- SONG JL
- SONG X
- SOUVOROV A
- STEGEMAN JJ
- STOLC V
- SU YH
- TAYLOR JS
- TERWILLIGER DP
- TESSMAR RAIBLE K
- THORNDYKE MC
- TONG M
- TONGPRASIT W
- TOWNLEY IK
- TU Q
- VACQUIER VD
- VORONINA E
- WANG D
- WEI Z
- WEINSTOCK GM
- WESSEL GM
- WHITTAKER CA
- WHITTLE J
- WILSON KH
- WILT FH
- WONG JL
- WORLEY K
- WRAY G
- YAGUCHI S
- YUAN QA
- ZHANG L
- Publication venue
- 'American Association for the Advancement of Science (AAAS)'
- Publication date
- 01/01/2006
- Field of study
We report the sequence and analysis of the 814-megabase genome of the sea urchin Strongylocentrotus
purpuratus, a model for developmental and systems biology. The sequencing strategy combined
whole-genome shotgun and bacterial artificial chromosome (BAC) sequences. This use of BAC clones,
aided by a pooling strategy, overcame difficulties associated with high heterozygosity of the genome.
The genome encodes about 23,300 genes, including many previously thought to be vertebrate
innovations or known only outside the deuterostomes. This echinoderm genome provides an
evolutionary outgroup for the chordates and yields insights into the evolution of deuterostomes
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