69 research outputs found
Histone H1 variant-specific lysine methylation by G9a/KMT1C and Glp1/KMT1D
- Author
- Publication venue
- BioMed Central
- Publication date
- 01/01/2010
- Field of study
BACKGROUND: The linker histone H1 has a key role in establishing and maintaining higher order chromatin structure and in regulating gene expression. Mammals express up to 11 different H1 variants, with H1.2 and H1.4 being the predominant ones in most somatic cells. Like core histones, H1 has high levels of covalent modifications; however, the full set of modifications and their biological role are largely unknown. RESULTS: In this study, we used a candidate screen to identify enzymes that methylate H1 and to map their corresponding methylation sites. We found that the histone lysine methyltransferases G9a/KMT1C and Glp1/KMT1D methylate H1.2 in vitro and in vivo, and we mapped this novel site to lysine 187 (H1.2K187) in the C-terminus of H1. This H1.2K187 methylation is variant-specific. The main target for methylation by G9a in H1.2, H1.3, H1.5 and H1.0 is in the C-terminus, whereas H1.4 is preferentially methylated at K26 (H1.4K26me) in the N-terminus. We found that the readout of these marks is different; H1.4K26me can recruit HP1, but H1.2K187me cannot. Likewise, JMJD2D/KDM4 only reverses H1.4K26 methylation, clearly distinguishing these two methylation sites. Further, in contrast to C-terminal H1 phosphorylation, H1.2K187 methylation level is steady throughout the cell cycle. CONCLUSIONS: We have characterised a novel methylation site in the C-terminus of H1 that is the target of G9a/Glp1 both in vitro and in vivo. To our knowledge, this is the first demonstration of variant-specific histone methylation by the same methyltransferases, but with differing downstream readers, thereby supporting the hypothesis of H1 variants having specific functions
Mouse screen reveals multiple new genes underlying mouse and human hearing loss.
- Author
- Publication venue
- PLoS Biol
- Publication date
- 01/04/2019
- Field of study
Adult-onset hearing loss is very common, but we know little about the underlying molecular pathogenesis impeding the development of therapies. We took a genetic approach to identify new molecules involved in hearing loss by screening a large cohort of newly generated mouse mutants using a sensitive electrophysiological test, the auditory brainstem response (ABR). We review here the findings from this screen. Thirty-eight unexpected genes associated with raised thresholds were detected from our unbiased sample of 1,211 genes tested, suggesting extreme genetic heterogeneity. A wide range of auditory pathophysiologies was found, and some mutant lines showed normal development followed by deterioration of responses, revealing new molecular pathways involved in progressive hearing loss. Several of the genes were associated with the range of hearing thresholds in the human population and one, SPNS2, was involved in childhood deafness. The new pathways required for maintenance of hearing discovered by this screen present new therapeutic opportunities
Horizontal advection, diffusion, and plankton spectra at the sea surface
- Author
- Abraham
- Annalisa Bracco
- Armi
- Bracco
- Bracco
- Bracco
- Bracco
- Capet
- Claudia Pasquero
- Denman
- Elhmaïdi
- Falkowski
- Fasham
- Folt
- Gower
- Horwood
- Klein
- Koszalka
- Ledwell
- Levin
- Levy
- Lévy
- Lévy
- Mackas
- Mahadevan
- Mahadevan
- Mahadevan
- Martin
- Martin
- Martin
- Martin
- McGillicuddy
- McGillicuddy
- McGillicuddy
- McGillicuddy
- Okubo
- Oschlies
- Oschlies
- Park
- Pasquero
- Pasquero
- Pasquero
- Piontkovski
- Platt
- Plumb
- Polzin
- Polzin
- Powell
- Provenzale
- Richards
- Salmon
- Schorghofer
- Siegel
- Smith
- Sophie Clayton
- Spall
- Srokosz
- Steele
- Sundermeyer
- Tsuda
- Weber
- Weiss
- Publication venue
- 'American Geophysical Union (AGU)'
- Publication date
- 04/02/2009
- Field of study
Author Posting. © American Geophysical Union, 2009. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Journal of Geophysical Research 114 (2009): C02001, doi:10.1029/2007JC004671.Plankton patchiness is ubiquitous in the oceans, and various physical and biological processes have been proposed as its generating mechanisms. However, a coherent statement on the problem is missing, because of both a small number of suitable observations and an incomplete understanding of the properties of reactive tracers in turbulent media. It has been suggested that horizontal advection may be the dominant process behind the observed distributions of phytoplankton and zooplankton, acting to mix tracers with longer reaction times (Rt) down to smaller scales. Conversely, the relative distributions of sea surface temperature and phytoplankton has been attributed to small-scale upwelling, where tracers with longer Rt are able to homogenize more than those with shorter reaction times. Neither of the above mechanisms can explain simultaneously the (relative) spectral slopes of temperature, phytoplankton, and zooplankton. Here, with a simple advection model and a large suite of numerical experiments, we concentrate on some of the physical processes influencing the relative distributions of tracers at the ocean surface, and we investigate (1) the impact of the spatial scale of tracer supply, (2) the role played by coherent eddies on the distribution of tracers with different Rt, and (3) the role of diffusion (so far neglected). We show that diffusion determines the distribution of temperature, regardless of the nature of the forcing. We also find that coherent structures together with differential diffusion of tracers with different Rt impact the tracer distributions. This may help in understanding the highly variable nature of observed plankton spectra.This work was initiated
at WHOI during the summer of 2006, while S.C. was a summer student
fellow, partially funded by the NSF. A.B. is funded by NSF–OCE 0751775
and NSF–OCE 0815280, and C.P. is funded by NSF–PHY 0551164
Minimal information for studies of extracellular vesicles 2018 (MISEV2018):a position statement of the International Society for Extracellular Vesicles and update of the MISEV2014 guidelines
- Author
- Afd Pharmaceutics
- Afd Pharmacology
- Aikawa Elena
- Alcaraz Maria Jose
- Anderson Johnathon D
- Andriantsitohaina Ramaroson
- Antoniou Anna
- Arab Tanina
- Archer Fabienne
- Atkin-Smith Georgia K
- Ayre D Craig
- Bach Jean-Marie
- Bachurski Daniel
- Baharvand Hossein
- Balaj Leonora
- Baldacchino Shawn
- Bauer Natalie N
- Baxter Amy A
- Bebawy Mary
- Beckham Carla
- Bedina Zavec Apolonija
- Benmoussa Abderrahim
- Berardi Anna C
- Bergese Paolo
- Bielska Ewa
- Blenkiron Cherie
- Bobis-Wozowicz Sylwia
- Boilard Eric
- Boireau Wilfrid
- Bongiovanni Antonella
- Borràs Francesc E
- Bosch Steffi
- Boulanger Chantal M
- Breakefield Xandra
- Breglio Andrew M
- Brennan Meadhbh Á
- Brigstock David R
- Brisson Alain
- Broekman Marike Ld
- Bromberg Jacqueline F
- Bryl-Górecka Paulina
- Buch Shilpa
- Buck Amy H
- Burger Dylan
- Busatto Sara
- Buschmann Dominik
- Bussolati Benedetta
- Buzás Edit I
- Byrd James Bryan
- Camussi Giovanni
- Carter David Rf
- Caruso Sarah
- Celbiologie
- Chamley Lawrence W
- Chang Yu-Ting
- Chen Chihchen
- Chen Shuai
- Cheng Lesley
- Chin Andrew R
- Clayton Aled
- Clerici Stefano P
- Cocks Alex
- Cocucci Emanuele
- Coffey Robert J
- Cordeiro-da-Silva Anabela
- Couch Yvonne
- Coumans Frank Aw
- Coyle Beth
- Crescitelli Rossella
- Criado Miria Ferreira
- D'Souza-Schorey Crislyn
- Das Saumya
- Datta Chaudhuri Amrita
- dB&C I&I
- de Candia Paola
- De Santana Eliezer F
- De Wever Olivier
- Del Portillo Hernando A
- Demaret Tanguy
- Deville Sarah
- Devitt Andrew
- Dhondt Bert
- Di Vizio Dolores
- Dieterich Lothar C
- Dolo Vincenza
- Dominguez Rubio Ana Paula
- Dominici Massimo
- Dourado Mauricio R
- Driedonks Tom Ap
- Duarte Filipe V
- Duncan Heather M
- Eichenberger Ramon M
- Ekström Karin
- El Andaloussi Samir
- Elie-Caille Celine
- Erdbrügger Uta
- Falcón-Pérez Juan M
- Fatima Farah
- Fish Jason E
- Flores-Bellver Miguel
- Frelet-Barrand Annie
- Fricke Fabia
- Fuhrmann Gregor
- Försönits András
- Gabrielsson Susanne
- Gardiner Chris
- Gaudin Raphael
- Gho Yong Song
- Giebel Bernd
- Gilbert Caroline
- Gimona Mario
- Giusti Ilaria
- Goberdhan Deborah Ci
- Gorski Sharon M
- Greening David W
- Gross Julia Christina
- Gualerzi Alice
- Gupta Gopal N
- Gustafson Dakota
- Gámez-Valero Ana
- Gärtner Kathrin
- Görgens André
- Handberg Aase
- Haraszti Reka A
- Harrison Paul
- Hegyesi Hargita
- Hendrix An
- Hill Andrew F
- Hochberg Fred H
- Hoffmann Karl F
- Holder Beth
- Holthofer Harry
- Hosseinkhani Baharak
- Hu Guoku
- Huang Yiyao
- Huber Veronica
- Hunt Stuart
- Ibrahim Ahmed Gamal-Eldin
- Ikezu Tsuneya
- Inal Jameel M
- Isin Mustafa
- Ivanova Alena
- Jackson Hannah K
- Jacobsen Soren
- Jay Steven M
- Jayachandran Muthuvel
- Jenster Guido
- Jiang Lanzhou
- Johnson Suzanne M
- Jones Jennifer C
- Jong Ambrose
- Jovanovic-Talisman Tijana
- Jung Stephanie
- Kalluri Raghu
- Kano Shin-Ichi
- Kaur Sukhbir
- Kawamura Yumi
- Keller Evan T
- Khamari Delaram
- Khomyakova Elena
- Khvorova Anastasia
- Kierulf Peter
- Kim Kwang Pyo
- Kislinger Thomas
- Klingeborn Mikael
- Klinke David J
- Kornek Miroslaw
- Kosanović Maja M
- Kovács Árpád Ferenc
- Krasemann Susanne
- Krause Mirja
- Krämer-Albers Eva-Maria
- Kurochkin Igor V
- Kusuma Gina D
- Kuypers Sören
- Laitinen Saara
- Langevin Scott M
- Languino Lucia R
- Lannigan Joanne
- Laurent Louise C
- Lavieu Gregory
- Le Lay Soazig
- Lee Myung-Shin
- Lee Yi Xin Fiona
- Lemos Debora S
- Lenassi Metka
- Leszczynska Aleksandra
- Li Isaac Ts
- Liao Ke
- Libregts Sten F
- Ligeti Erzsebet
- Lim Rebecca
- Lim Sai Kiang
- Linnemannstöns Karen
- Linē Aija
- Llorente Alicia
- Lombard Catherine A
- Lorenowicz Magdalena J
- Lovett Jason
- Lowry Michelle C
- Loyer Xavier
- LS Celbiologie-Algemeen
- Lu Quan
- Lukomska Barbara
- Lunavat Taral R
- Lázaro-Ibáñez Elisa
- Lässer Cecilia
- Lörincz Ákos M
- Lötvall Jan
- Maas Sybren Ln
- Malhi Harmeet
- Marcilla Antonio
- Mariani Jacopo
- Mariscal Javier
- Martens-Uzunova Elena S
- Martin-Jaular Lorena
- Martinez M Carmen
- Martins Vilma Regina
- Mathieu Mathilde
- Mathivanan Suresh
- Maugeri Marco
- McGinnis Lynda K
- McVey Mark J
- Meckes David G
- Meehan Katie L
- Mertens Inge
- Minciacchi Valentina R
- Morales-Kastresana Aizea
- Morhayim Jess
- Mullier François
- Muraca Maurizio
- Musante Luca
- Mussack Veronika
- Muth Dillon C
- Myburgh Kathryn H
- Möller Andreas
- Møller Jørgensen Malene
- Najrana Tanbir
- Nawaz Muhammad
- Nazarenko Irina
- Nejsum Peter
- Neri Christian
- Neri Tommaso
- Nieuwland Rienk
- Nimrichter Leonardo
- Nolan John P
- Nolte-'t Hoen Esther NM
- Noren Hooten Nicole
- O'Driscoll Lorraine
- O'Grady Tina
- O'Loghlen Ana
- Ochiya Takahiro
- Olivier Martin
- Ortiz Alberto
- Ortiz Luis A
- Osteikoetxea Xabier
- Ostrowski Matias
- Park Jaesung
- Pegtel D Michiel
- Peinado Hector
- Perut Francesca
- Pfaffl Michael W
- Phinney Donald G
- Pieters Bartijn Ch
- Pink Ryan C
- Pisetsky David S
- Pogge von Strandmann Elke
- Polakovicova Iva
- Poon Ivan Kh
- Powell Bonita H
- Prada Ilaria
- Pulliam Lynn
- Quesenberry Peter
- Radeghieri Annalisa
- Raffai Robert L
- Raimondo Stefania
- Rak Janusz
- Ramirez Marcel I
- Raposo Graça
- Rayyan Morsi S
- Regev-Rudzki Neta
- Ricklefs Franz L
- Robbins Paul D
- Roberts David D
- Rodrigues Silvia C
- Rohde Eva
- Rome Sophie
- Rouschop Kasper Ma
- Rughetti Aurelia
- Russell Ashley E
- Sahoo Susmita
- Salas-Huenuleo Edison
- Saugstad Julie A
- Saul Meike J
- Saá Paula
- Schiffelers Raymond M
- Schneider Raphael
- Schøyen Tine Hiorth
- Scott Aaron
- Shahaj Eriomina
- Sharma Shivani
- Shatnyeva Olga
- Shekari Faezeh
- Shelke Ganesh Vilas
- Shetty Ashok K
- Shiba Kiyotaka
- Siljander Pia R-M
- Silva Andreia M
- Skowronek Agata
- Snyder Orman L
- Soares Rodrigo Pedro
- Soekmadji Carolina
- Sotillo Javier
- Stahl Philip D
- Stoorvogel Willem
- Stott Shannon L
- Strasser Erwin F
- Sub Biomol.Mass Spect. and Proteomics
- Sub General Pharmaceutics
- Swift Simon
- Sánchez Catherine
- Sódar Barbara W
- Tahara Hidetoshi
- Tewari Muneesh
- Théry Clotilde
- Timms Kate
- Tiwari Swasti
- Tixeira Rochelle
- Tkach Mercedes
- Toh Wei Seong
- Tomasini Richard
- Torrecilhas Ana Claudia
- Tosar Juan Pablo
- Toxavidis Vasilis
- Urbanelli Lorena
- Vader Pieter
- van Balkom Bas Wm
- van der Grein Susanne G
- Van Deun Jan
- van Herwijnen Martijn Jc
- Van Keuren-Jensen Kendall
- van Niel Guillaume
- van Royen Martin E
- van Wijnen Andre J
- Vasconcelos M Helena
- Vechetti Ivan J
- Veit Tiago D
- Vella Laura J
- Velot Émilie
- Verweij Frederik J
- Vestad Beate
- Visnovitz Tamás
- Viñas Jose L
- Vukman Krisztina V
- Wahlgren Jessica
- Watson Dionysios C
- Wauben Marca Hm
- Weaver Alissa
- Webber Jason P
- Weber Viktoria
- Wehman Ann M
- Weiss Daniel J
- Welsh Joshua A
- Wendt Sebastian
- Wheelock Asa M
- Wiener Zoltán
- Witte Leonie
- Witwer Kenneth W
- Wolfram Joy
- Xagorari Angeliki
- Xander Patricia
- Xu Jing
- Yan Xiaomei
- Yin Hang
- Yuana Yuana
- Yáñez-Mó María
- Zappulli Valentina
- Zarubova Jana
- Zhang Jian-Ye
- Zhao Zezhou
- Zheng Lei
- Zheutlin Alexander R
- Zickler Antje M
- Zimmermann Pascale
- Zivkovic Angela M
- Zocco Davide
- Zuba-Surma Ewa K
- Østergaard Ole
- Žėkas Vytautas
- Publication venue
- Publication date
- 01/01/2018
- Field of study
The last decade has seen a sharp increase in the number of scientific publications describing physiological and pathological functions of extracellular vesicles (EVs), a collective term covering various subtypes of cell-released, membranous structures, called exosomes, microvesicles, microparticles, ectosomes, oncosomes, apoptotic bodies, and many other names. However, specific issues arise when working with these entities, whose size and amount often make them difficult to obtain as relatively pure preparations, and to characterize properly. The International Society for Extracellular Vesicles (ISEV) proposed Minimal Information for Studies of Extracellular Vesicles (“MISEV”) guidelines for the field in 2014. We now update these “MISEV2014” guidelines based on evolution of the collective knowledge in the last four years. An important point to consider is that ascribing a specific function to EVs in general, or to subtypes of EVs, requires reporting of specific information beyond mere description of function in a crude, potentially contaminated, and heterogeneous preparation. For example, claims that exosomes are endowed with exquisite and specific activities remain difficult to support experimentally, given our still limited knowledge of their specific molecular machineries of biogenesis and release, as compared with other biophysically similar EVs. The MISEV2018 guidelines include tables and outlines of suggested protocols and steps to follow to document specific EV-associated functional activities. Finally, a checklist is provided with summaries of key points
Observation of gravitational waves from the coalescence of a 2.5−4.5 M⊙ compact object and a neutron star
- Author
- Abac Adrian
- Abbott R.
- Abouelfettouh I.
- Acernese F.
- Ackley Kendall
- Adhicary S.
- Adhikari Naresh
- Adhikari Rana X.
- Adkins V. K.
- Afif Ismail M.
- Agarwal Deepali
- Agathos Michalis
- Aghaei Abchouyeh Maryam
- Aguiar Odylio D.
- Aguilar I.
- Aiello Lorenzo
- Ain Anirban
- Ajith Parameswaran
- Akcay Sarp
- Akseli Hannuksela Otto
- Akutsu Tomotada
- Al-Jodah Ammar
- Al-Shammari S.
- Albanesi Simone
- Alex iandolo Guido
- Alfaidi Reem Atallah E
- Allocca Annalisa
- Alléné C.
- Altin Paul
- Alvarez-Lopez Sofia
- Amato Alex
- Amez-Droz L.
- Amorosi A.
- Amra C.
- Ananyeva A.
- Anderson Stuart
- Anderson Warren G.
- Andia Manuel
- Ando M.
- Andrade T.
- Andrea Prodi Giovanni
- Andres Nicolas
- Andric Tomislav
- Andrés Vallejo Peña Sergio
- Andrés-Carcasona Marc
- Anglin J.
- Anne Bizouard Marie
- Ansoldi Stefano
- Antelis Javier M.
- Antier Sarah
- Antoni Ramis Vidal Felip
- Antonietta Palaia Maria
- Antonio Font Roda Jose
- Aoumi M.
- Appavuravther E. Z.
- Appert S.
- Apple S. K.
- Arai Koji
- Araya Akito
- Araya Melody
- Areeda Joseph
- Argianas L.
- Arif Shaikh Md
- Aritomi N.
- Armato Federico
- Arnaud Nicolas
- Arogeti Megan
- Aronson Scott
- Arun K. G.
- Ashton Gregory
- Aso Yoichi
- Assiduo M.
- Aston S. M.
- Astone Pia
- Attadio Francesca
- Aubin Florian
- AVALLONE Guerino
- Azrad D.
- Babak Stanislav
- Badaracco Francesca
- Badger C.
- Bae Sangwook
- Bagnasco Stefano
- Bagui E.
- Baier Jeremy
- Baiotti Luca
- Bajpai Rishabh
- Baka T.
- Ball M.
- Ballardin G.
- Ballmer S. W.
- Banagiri Sharan
- Banerjee Biswajit
- Bankar Deepak
- Baral Pratyusava
- Barayoga J. C.
- Barish B. C.
- Barker D.
- Barneo Pablo
- Barone Fabrizio
- Barr Bryan
- Barsotti Lisa
- Barsuglia Matteo
- Barta Dániel
- Bartoletti A. M.
- Barton Mark Andrew
- Bartos I.
- Basak Soummyadip
- Basalaev Artem
- Bassiri Riccardo
- Basti Andrea
- Bates D. E.
- Bawaj Mateusz
- Baxi P.
- Bayley Joseph
- Baylor Amanda
- Baynard II. P. A.
- Bazzan M.
- Bedakihale V. M.
- Beirnaert Freija
- Bejger Michał
- Belardinelli Daniele
- Bell Angus
- Benedetto V.
- Benoit William
- Bentley Joe
- Bera Sayantani
- Berbel Marina
- Bergamin Fabio
- Berger Beverly
- Bernuzzi Sebastiano
- Beroiz Martin
- Berry Christopher P. L.
- Bersanetti Diego
- Bertolini A.
- Betzwieser Joseph
- Beveridge Damon
- Bevins Nathaniel
- Bhandare R.
- Bhardwaj Uddipta
- Bhatt R.
- Bhattacharjee Dripta
- Bhaumik Shubhagata
- Bhowmick S.
- Bianchi A.
- Bilenko I. A.
- Billingsley GariLynn
- Binetti Alberto
- Bini Sophie
- Birnholtz Ofek
- Bisht A.
- Bitossi Massimiliano
- Blackburn Kent
- Blagg L. A.
- Blair C. D.
- Blair D. G.
- Bobba F.
- Bode Nina
- Boileau Guillaume
- Boldrini Mattia
- Bolingbroke Georgia
- Bolliand A.
- Bondarescu Ruxandra
- Bondu François
- Bonilla Carrasquel Edgard
- Bonino A.
- Bonnand Romain
- Booker P.
- Borchers A.
- Boschi Valerio
- Bose S.
- Bossilkov V.
- Boudart Vincent
- Boudon A.
- Bozzi A.
- Bradaschia C.
- Brady Patrick R.
- Braglia Matteo
- Branch A.
- BRANCHESI Marica
- Brandt J.
- Braun I.
- Breschi Matteo
- Briant Tristan
- Brillet A.
- Brinkmann M.
- Brockill P.
- Brockmüller Eike
- Brooks Aidan
- Brown B. C.
- Brown D. D.
- Brunett S.
- Bruno G.
- Bruntz Robert
- Bryant J.
- Bucci F.
- Buchanan J.
- Bulashenko Oleg
- Bulik T.
- Bulten H. J.
- Buonanno Alessandra
- Burtnyk K.
- Buscicchio Riccardo
- Buskulic D.
- Bustillo J. Calderón
- Buy Christelle
- Byer R. L.
- Cabourn Davies Gareth
- Cabras Giuseppe
- Cabrita Ricardo
- Cadonati Laura
- Cagnoli Gianpietro
- Cahillane Craig
- Callister T. A.
- Calloni E.
- Camp J. B.
- Canepa M.
- Caneva Santoro Giada
- Cannon Kipp C.
- Cao H.
- Capistran L. A.
- Capocasa Eleonora
- Capote Elenna
- Carapella G.
- Carbognani F.
- Carlassara M.
- Carlin Julian
- Carolina Silva Oliveira Ana
- Carpinelli Massimo
- Carrillo G.
- Carter Jonathan
- Carullo Gregorio
- Casentini Claudio
- Castro-Lucas S. Y.
- Caudill S.
- Cavaglia Marco
- Cavalieri Roberto
- Cella Giancarlo
- Cerdá-Durán Pablo
- Cesarini Elisabetta
- Chaibi W.
- Chakraborty Pratik
- Chalathadka Subrahmanya Shreevathsa
- Chan M.
- Chandra K.
- Chang R. -J.
- Chao Shiuh
- Char Prasanta
- Charlton E. L.
- Charlton Philip
- Chassande-Mottin Eric
- Chatterjee Chayan
- Chatterjee Debarati
- Chatterjee Deep
- Chattopadhyay Debatri
- Chaturvedi M.
- Chaty Sylvain
- Chatziioannou Katerina
- Chen A.
- Chen A. H. -Y.
- Chen Dan
- Chen H.
- Chen Hsin-Yu
- Chen Junxin
- Chen K. H.
- Chen Y.
- Chen Yanbei
- Chen Yitian
- Cheng H. P.
- Chessa Piero
- Cheung H. T.
- Cheung S. Y.
- Chiadini Francesco
- Chiarini G.
- Chierici R.
- Chincarini Andrea
- Chiofalo Maria Luisa
- Chiummo Antonino
- Chou C.
- Choudhary Sunil
- Christensen Nelson
- Chua Sheon S. Y.
- Chugh P.
- Chun Lung Chan Juno
- Ciani Giacomo
- Ciecieląg Paweł
- Cieślar Marek
- Cifaldi Maria
- Ciolfi Riccardo
- Clara F.
- Clark James
- Clarke J.
- Clarke Teagan
- Clasey Essick Reed
- Claudio Diaz Mario
- Clearwater P.
- Clesse S.
- Coccia E.
- Codazzo Elena
- Cohadon Pierre-François
- Colace Stefano
- Colleoni Marta
- Collette C. G.
- Collins J.
- Colloms S.
- Colombo Alberto
- Colpi Monica
- Compton C. M.
- Concetta Tringali Maria
- Connolly G.
- Conti Livia
- Corbitt Thomas
- Cordero-Carrión Isabel
- Corezzi S.
- Cornish Neil
- Corsi Alessandra
- Cortese Stefano
- Costa C. A.
- Cottingham R.
- Coughlin Michael
- Couineaux A.
- Coulon J. -P.
- Countryman Stefan
- Coupechoux J. -F.
- Couvares Peter
- Coward D. M.
- Cowart M. J.
- Coyne Dennis
- Coyne Robert
- Craig K.
- Creed R.
- Creighton Jolien
- Creighton T. D.
- Cremonese Paolo
- Criswell Alexander
- Crockett-Gray J. C. G.
- Crook S.
- Crouch R.
- Csizmazia J.
- Cudell Jean-René
- Cullen Torrey
- Cumming Alan
- Cuoco E.
- Cusinato Marco
- Cáceres-Barbosa V.
- César Martins Julio
- D'Angelo Beatrice
- D'Antonio Sabrina
- d'Emilio V.
- D'Onofrio Luca
- D'Urso D.
- Dabadie P.
- Dal Canton Tito
- Dal Pra Stefano
- DALL'OSSO Simone
- Danilishin Stefan
- Danzmann K.
- Darroch K. E.
- Dartez L. P.
- Dasgupta A.
- Datta Sayantani
- Dattilo V.
- Daumas A.
- Davari N.
- Dave I.
- Davenport A.
- Davier M.
- Davies T. F.
- Davis Derek
- Davis L.
- Davis Michael C.
- Davis Philip J.
- Dax Maximilian
- De Bolle Jorden
- De Laurentis Martina
- De Lillo Federico
- de Lluc Planas Maria
- De Marco F.
- De Matteis Fabio
- De Pietri Roberto
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- Árpád Gergely László
- 劉 國欽
- 都丸 隆行
- Publication venue
- Publication date
- 23/04/2024
- Field of study
Search for gravitational-lensing signatures in the full third observing run of the LIGO-Virgo network
- Author
- Abbott R.
- Abe H.
- Acernese F.
- Ackley Kendall
- Adhicary S.
- Adhikari Naresh
- Adhikari Rana X.
- Adkins V. K.
- Adya V. B.
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- Agathos Michalis
- Aguiar Odylio D.
- Aiello Lorenzo
- Ain A.
- Ajith Parameswaran
- Akutsu Tomotada
- Albanesi S.
- Alfaidi R. A.
- Allocca Annalisa
- Alléné C.
- Altin Paul
- Amato Alex
- Anand S.
- Ananyeva A.
- Anderson Stuart
- Anderson Warren G.
- Ando M.
- Andrade T.
- Andrea Prodi Giovanni
- Andres Nicolas
- Andric Tomislav
- Andrés-Carcasona Marc
- Anne Bizouard Marie
- Ansoldi S.
- Antelis Javier M.
- Antier Sarah
- Antonio Font Roda Jose
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- Zanolin M.
- Zeidler Simon
- Zelenova T.
- Zendri J. -P.
- Zevin Michael
- Zhan M.
- Zhang H.
- Zhang Jue
- Zhang L.
- Zhang Rui
- Zhang T.
- Zhang Y.
- Zhao C.
- Zhao G.
- Zhao Yue
- Zhao Yuhang
- Zheng Yanyan
- Zhou R.
- Zhu Xingjiang
- Zhu Zong-Hong
- Zimmerman Aaron
- Zucker M. E.
- Árpád Gergely László
- 劉 國欽
- 曹周键
- 王谨
- 都丸 隆行
- Publication venue
- Publication date
- 01/04/2023
- Field of study
Gravitational lensing by massive objects along the line of sight to the source causes distortions of gravitational wave-signals; such distortions may reveal information about fundamental physics, cosmology and astrophysics. In this work, we have extended the search for lensing signatures to all binary black hole events from the third observing run of the LIGO--Virgo network. We search for repeated signals from strong lensing by 1) performing targeted searches for subthreshold signals, 2) calculating the degree of overlap amongst the intrinsic parameters and sky location of pairs of signals, 3) comparing the similarities of the spectrograms amongst pairs of signals, and 4) performing dual-signal Bayesian analysis that takes into account selection effects and astrophysical knowledge. We also search for distortions to the gravitational waveform caused by 1) frequency-independent phase shifts in strongly lensed images, and 2) frequency-dependent modulation of the amplitude and phase due to point masses. None of these searches yields significant evidence for lensing. Finally, we use the non-detection of gravitational-wave lensing to constrain the lensing rate based on the latest merger-rate estimates and the fraction of dark matter composed of compact objects
Search for eccentric black hole coalescences during the third observing run of LIGO and Virgo
- Author
- Abac A. G.
- Abbott R.
- Abe H.
- Acernese F.
- Ackley Kendall
- Adamcewicz C.
- Adhicary S.
- Adhikari Naresh
- Adhikari Rana X.
- Adkins V. K.
- Adya V. B.
- Affeldt C.
- Afif Ismail M.
- Agarwal D.
- Agathos Michalis
- Aguiar Odylio D.
- Aguilar I.
- Aiello Lorenzo
- Ain Anirban
- Ajith Parameswaran
- Akseli Hannuksela Otto
- Akutsu Tomotada
- Al-Jodah Ammar
- Albanesi S.
- Alberto Trani Alessandro
- Alfaidi Reem Atallah E
- Allocca Annalisa
- Alléné C.
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- Andrea Prodi Giovanni
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- Yeung T. Y.
- Yokoyama Jun'ichi
- Yokozawa T.
- Yoo Jooheon
- Yu Hang
- Yuzurihara Hirotaka
- Zadrożny A.
- Zahoor Jan Aasim
- Zannelli A. J.
- Zanolin M.
- Zeeshan M.
- Zelenova T.
- Zendri J. -P.
- Zevin Michael
- Zhang Jue
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- Zhang Rui
- Zhang T.
- Zhang Ya
- Zhang Yanqi
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- Zhao Yue
- Zhao Yuhang
- Zheng Yanyan
- Zhong Haowen
- Zhou R.
- Zhu Zong-Hong
- Zimmerman Aaron
- Zucker M. E.
- Zweizig John
- Álvarez-López S.
- Árpád Gergely László
- 劉 國欽
- 曹周键
- 都丸 隆行
- Publication venue
- Publication date
- 01/08/2023
- Field of study
Despite the growing number of confident binary black hole coalescences observed through gravitational waves so far, the astrophysical origin of these binaries remains uncertain. Orbital eccentricity is one of the clearest tracers of binary formation channels. Identifying binary eccentricity, however, remains challenging due to the limited availability of gravitational waveforms that include effects of eccentricity. Here, we present observational results for a waveform-independent search sensitive to eccentric black hole coalescences, covering the third observing run (O3) of the LIGO and Virgo detectors. We identified no new high-significance candidates beyond those that were already identified with searches focusing on quasi-circular binaries. We determine the sensitivity of our search to high-mass (total mass M>70 M⊙) binaries covering eccentricities up to 0.3 at 15 Hz orbital frequency, and use this to compare model predictions to search results. Assuming all detections are indeed quasi-circular, for our fiducial population model, we place an upper limit for the merger rate density of high-mass binaries with eccentricities 0<e≤0.3 at 0.33 Gpc−3 yr−1 at 90\% confidence level
Ultralight vector dark matter search using data from the KAGRA O3GK run
- Author
- Abac A. G.
- Abbott R.
- Abe H.
- Abouelfettouh I.
- Acernese F.
- Ackley Kendall
- Adamcewicz Christian
- Adhicary S.
- Adhikari Naresh
- Adhikari Rana X.
- Adkins V. K.
- Adya V. B.
- Affeldt C.
- Afif Ismail M.
- Agarwal Deepali
- Agathos Michalis
- Aguiar Odylio D.
- Aguilar I.
- Aiello Lorenzo
- Ain Anirban
- Ajith Parameswaran
- Akseli Hannuksela Otto
- Akutsu Tomotada
- Al-Jodah Ammar
- Al-Shammari S.
- Albanesi S.
- Alberto Trani Alessandro
- Alfaidi Reem Atallah E
- Allocca Annalisa
- Alléné C.
- Altin Paul
- Alvarez-Lopez Sofia
- Amato Alex
- Amez-Droz L.
- Amorosi A.
- Amra C.
- Anand S.
- Ananyeva A.
- Anderson Stuart
- Anderson Warren G.
- Andia Manuel
- Ando M.
- Andrade T.
- Andrea Prodi Giovanni
- Andres Nicolas
- Andric Tomislav
- Andrés-Carcasona Marc
- Anglin J.
- Anne Bizouard Marie
- Ansoldi S.
- Antelis Javier M.
- Antier Sarah
- Antoni Ramis Vidal Felip
- Antonietta Palaia Maria
- Antonio Font Roda Jose
- Aoumi M.
- Appavuravther E. Z.
- Appert S.
- Apple S. K.
- Arai Koji
- Araya Akito
- Araya Melody
- Areeda Joseph
- Argianas L. Granda
- Arif Shaikh Md
- Aritomi Naoki
- Armato F.
- Arnaud Nicolas
- Arogeti Megan
- Aronson Scott
- Arun K. G.
- Ashton Gregory
- Aso Yoichi
- Assiduo M.
- Aston S. M.
- Astone Pia
- Aubin Florian
- AVALLONE Guerino
- Babak Stanislav
- Badaracco Francesca
- Badger C.
- Bae Sangwook
- Bagnasco Stefano
- Bagui E.
- Bai Y.
- Baier Jeremy
- Bajpai Rishabh
- Baka T.
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- Ballardin G.
- Ballmer S. W.
- Banagiri Sharan
- Banerjee Biswajit
- Bankar Deepak
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- Barker D.
- Barneo Pablo
- Barone Fabrizio
- Barr Bryan
- Barsotti Lisa
- Barsuglia Matteo
- Barta Dániel
- Barthelmy S. D.
- Barton Mark Andrew
- Bartos I.
- Basak Soummyadip
- Basalaev Artem
- Bassiri Riccardo
- Basti Andrea
- Bawaj Mateusz
- Baxi P.
- Bayley Joseph
- Baylor Amanda
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- Bedakihale V. M.
- Beirnaert Freija
- Bejger Michał
- Belardinelli Daniele
- Bell Angus
- Benedetto V.
- Beniwal D.
- Benoit William
- Bentley Joe
- Bera Sayantani
- Berbel Marina
- Bergamin Fabio
- Berger Beverly
- Bernuzzi Sebastiano
- Beroiz Martin
- Bersanetti Diego
- Bertolini A.
- Betzwieser Joseph
- Beveridge Damon
- Bevins Nathaniel
- Bhandare R.
- Bhardwaj Uddipta
- Bhatt R.
- Bhattacharjee Dripta
- Bhaumik Shubhagata
- Bhowmick S.
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- Bitossi Massimiliano
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- Boldrini Mattia
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- Bondarescu Ruxandra
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- Borchers A.
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- Bossilkov V.
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- CHIOFALO MARIA. LUISA.
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- KARATHANASIS CHRISTOS.
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- MORALES ESTER. RUIZ.
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- Zweizig John
- Árpád Gergely László
- 劉 國欽
- 曹周键
- 都丸 隆行
- Publication venue
- Publication date
- 01/03/2024
- Field of study
Among the various candidates for dark matter (DM), ultralight vector DM can be probed by laser interferometric gravitational wave detectors through the measurement of oscillating length changes in the arm cavities. In this context, KAGRA has a unique feature due to differing compositions of its mirrors, enhancing the signal of vector DM in the length change in the auxiliary channels. Here we present the result of a search for U(1)B−L gauge boson DM using the KAGRA data from auxiliary length channels during the first joint observation run together with GEO600. By applying our search pipeline, which takes into account the stochastic nature of ultralight DM, upper bounds on the coupling strength between the U(1)B−L gauge boson and ordinary matter are obtained for a range of DM masses. While our constraints are less stringent than those derived from previous experiments, this study demonstrates the applicability of our method to the lower-mass vector DM search, which is made difficult in this measurement by the short observation time compared to the auto-correlation time scale of DM
Quality of Life in Obese Subjects Following Biliopancreatic Diversion
- Author
- Publication venue
- 'Informa UK Limited'
- Publication date
- Field of study
Histone H1 variant-specific lysine methylation by G9a/KMT1C and Glp1/KMT1D
- Author
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/03/2010
- Field of study
Abstract Background The linker histone H1 has a key role in establishing and maintaining higher order chromatin structure and in regulating gene expression. Mammals express up to 11 different H1 variants, with H1.2 and H1.4 being the predominant ones in most somatic cells. Like core histones, H1 has high levels of covalent modifications; however, the full set of modifications and their biological role are largely unknown. Results In this study, we used a candidate screen to identify enzymes that methylate H1 and to map their corresponding methylation sites. We found that the histone lysine methyltransferases G9a/KMT1C and Glp1/KMT1D methylate H1.2 in vitro and in vivo, and we mapped this novel site to lysine 187 (H1.2K187) in the C-terminus of H1. This H1.2K187 methylation is variant-specific. The main target for methylation by G9a in H1.2, H1.3, H1.5 and H1.0 is in the C-terminus, whereas H1.4 is preferentially methylated at K26 (H1.4K26me) in the N-terminus. We found that the readout of these marks is different; H1.4K26me can recruit HP1, but H1.2K187me cannot. Likewise, JMJD2D/KDM4 only reverses H1.4K26 methylation, clearly distinguishing these two methylation sites. Further, in contrast to C-terminal H1 phosphorylation, H1.2K187 methylation level is steady throughout the cell cycle. Conclusions We have characterised a novel methylation site in the C-terminus of H1 that is the target of G9a/Glp1 both in vitro and in vivo. To our knowledge, this is the first demonstration of variant-specific histone methylation by the same methyltransferases, but with differing downstream readers, thereby supporting the hypothesis of H1 variants having specific functions.</p
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