23 research outputs found
Measurement of the Bottom-Strange Meson Mixing Phase in the Full CDF Data Set
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- Alvarez González
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- Tomura
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- Tooze SA
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- Trovato
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- Wicklund
- Wicklund
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- Wilson
- Winer
- Wittich
- Wolbers
- Wolfe
- Wright
- Wu
- Wu
- X.
- Y.
- Y.
- Y.
- Y.
- Y.
- Y.
- Y.
- Y.
- Y.C.
- Y.C.
- Y.D.
- Y.J.
- Y.K.
- Y.S.
- Yamamoto
- Yamato
- Yang
- Yang
- Yang
- Yao
- Yeh
- Yi
- Yoh
- Yorita
- Yoshida
- Yu
- Yu
- Yu
- Yun
- Z.
- Zanetti
- Zeng
- Zhou
- Zucchelli
- Publication venue
- 'American Physical Society (APS)'
- Publication date
- 01/01/2012
- Field of study
We report a measurement of the bottom-strange meson mixing phase \beta_s
using the time evolution of B0_s -> J/\psi (->\mu+\mu-) \phi (-> K+ K-) decays
in which the quark-flavor content of the bottom-strange meson is identified at
production. This measurement uses the full data set of proton-antiproton
collisions at sqrt(s)= 1.96 TeV collected by the Collider Detector experiment
at the Fermilab Tevatron, corresponding to 9.6 fb-1 of integrated luminosity.
We report confidence regions in the two-dimensional space of \beta_s and the
B0_s decay-width difference \Delta\Gamma_s, and measure \beta_s in [-\pi/2,
-1.51] U [-0.06, 0.30] U [1.26, \pi/2] at the 68% confidence level, in
agreement with the standard model expectation. Assuming the standard model
value of \beta_s, we also determine \Delta\Gamma_s = 0.068 +- 0.026 (stat) +-
0.009 (syst) ps-1 and the mean B0_s lifetime, \tau_s = 1.528 +- 0.019 (stat) +-
0.009 (syst) ps, which are consistent and competitive with determinations by
other experiments.Comment: 8 pages, 2 figures, Phys. Rev. Lett 109, 171802 (2012
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)
- Author
- A Ivana Scovassi
- A Murat Kaynar
- A Sue Menko
- Aaron DiAntonio
- Abdel Halim Harrath
- Abdelhaq Rami
- Abhinav Diwan
- Abhishek D Garg
- Abidi A
- Abraham Acevedo Arozena
- Addanki Pratap Kumar
- Adi Kimchi
- Aditya Murthy
- Adolph TE
- Adrian L Harris
- Adrienne M Gorman
- Afshin Samali
- Agnieszka Bagniewska-Zadworna
- Agnieszka Sirko
- Agustin Aranda
- Agustín Hernández
- Ahlberg J
- Ahmed Hamai
- Ai Yamamoto
- Aileen R Ariosa
- Aimee L Edinger
- Akihisa Abe
- Akiko Maeda
- Akio Kihara
- Akira Matsuura
- AL Kovacs
- Al Rawi S
- Alain Bruhat
- Alakananda Basu
- Alan Cheng
- Alastair M Buchan
- Albert Haas
- Albert R La Spada
- Alberto Anel
- Alberto Bartolomé
- Alberto Faggioni
- Alberto Jiménez
- Alberto M Martelli
- Aldrin V Gomes
- Alec C Kimmelman
- Aleksandra J Isakovic
- Alessandra Bolino
- Alessandra Stacchiotti
- Alessandro Fanzani
- Alessandro Fraldi
- Alessia Di Nardo
- Alessio Papini
- Alexander Greenhough
- Alexander J Whitworth
- Alexandra Giatromanolaki
- Alexandre Arcaro
- Alexandru Almasan
- Alfonso Schiavi
- Alfred J Meijer
- Alfredo Criollo
- Alibhoy AA
- Alice Carrier
- Alicia Meléndez
- Alicia Rosello
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- Alireza R Rezaie
- Alkesh Jani
- Allan B Caplan
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- Rodrigo Troncoso
- Rodriguez-Muela N
- Roger J Davis
- Roland Malli
- Rolf J Craven
- Romana T Netea-Maier
- Rong-Rong He
- Rong-Yu Liu
- Ronit Pinkas-Kramarski
- Ronit Sagi-Eisenberg
- Ronit Shiri-Sverdlov
- Rosa Ana González-Polo
- Rosa Puertollano
- Rosa Salvioli
- Rosanna Parlato
- Rossella Menghini
- Rossella Russo
- Roswitha Krick
- Roy Parker
- Ru-Jeng Teng
- Rubem FS Menna-Barreto
- Ruben K Dagda
- Rubén Gómez-Sánchez
- Rudolf A Kley
- Ruediger Rudolf
- Rui Kang
- Rui Li
- Rui Sheng
- Rumpelt HJ
- Rupert Beale
- Russ DW
- Russo R
- Rut Valdor
- Ruth Slack
- Ryan J Schulze
- Ryo Ushioda
- Ryuichiro Atarashi
- Régis Delage-Mourroux
- Réz G
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- Sabah NA Hussain
- Sabine Hilfiker
- Sabrina Di Bartolomeo
- Saeid Ghavami
- Safari-Alighiarloo N
- Safia Costes
- Sagar Lonial
- Sakineh Kazemi Noureini
- Salem Chouaib
- Salik Hussain
- Sally S Atherton
- Salvador N
- Salvador Ventura
- Salvatore Florio
- Salvatore Pepe
- Sam Gandy
- Sam W Lee
- Sami Dridi
- Samisubbu R Naidu
- Sanbing Shen
- Sanchez AM
- Sandra Cottet
- Sandra Morais Cardoso
- Sandra Moreno
- Sandrine Silvente-Poirot
- Sandro Alves
- Sandro Goruppi
- Sandy Giuliano
- Sang Won Suh
- Sangeeta Khare
- Sangita Sinha
- Santiago Ambrosio
- Santiago Rodriguez de Cordoba
- Santosh Chauhan
- Santosh Kesari
- Sara Calatayud
- Sara Cherry
- Sara Marinelli
- Sara W Bird
- Sarkar C
- Sarkar S
- Sarron Randall-Demllo
- Sasanka Ramanadham
- Sascha Martens
- Satoaki Matoba
- Satoru Kobayashi
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- Saverio Minucci
- Savita Bhalla
- Savithrama P Dinesh-Kumar
- Schlumpberger M
- Schneider EM
- Scott A Soleimanpour
- Scott J Bultman
- Scott K Powers
- Scott L Friedman
- Scott Pattison
- Seamus J Martin
- Sean T Sweeney
- Sebastian Schuck
- Sebastiano Sciarretta
- Sebastien G Bouret
- Seglen PO
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- Seglen PO
- Sehamuddin Galadari
- Seiliez I
- Seillier M
- Seok S
- Seong Who Kim
- Sepp D Kohlwein
- Serena Carra
- Serena Montagnaro
- Serge Mostowy
- Serge N Manié
- Sergio Comincini
- Sergio Lavandero
- Seung-Hoon Baek
- Seung-Il Choi
- Seung-Jae Lee
- Seung-Yong Yoon
- Seungmin Hwang
- Shahab S
- Shailendra Anoopkumar-Dukie
- Shalmoli Bhattacharyya
- Shane Deegan
- Shang-Der Chen
- Sharad Kumar
- Sharon A Tooze
- Sharon G Adler
- Sharon M Gorski
- Sharon McKenna
- Sharon Prince
- Shaun Martin
- Shazib Pervaiz
- She-Min Lu
- Sheng Li
- Sheng-Han Kuo
- Shengfang Ge
- Shengkan Jin
- Shengyun Fang
- Shengzhou Wu
- Shi Xiao
- Shi-Mei Zhuang
- Shi-Yong Sun
- Shibu M Poulose
- Shigeki Miyamoto
- Shigeko Yamashiro
- Shigeomi Shimizu
- Shigeru Oshima
- Shile Huang
- Shilpa Buch
- Shiming Liu
- Shingo Kajimura
- Shinji Hadano
- Shino Goto-Yamada
- Shiow-Ju Lee
- Shiqian Huang
- Shirley Luckhart
- Shivendra V Singh
- Shohreh Issazadeh-Navikas
- Shoji Notomi
- Shouqing Luo
- Shrawan K Singh
- Shu X
- Shu-Feng Zhou
- Shuilong Leng
- Shuiping Tu
- Shuji Kishi
- Shunhei Yamashina
- Shuo Wang
- Shusaku Shibutani
- Shuwen Liu
- Shuyan Lu
- Shweta Saran
- Shweta Sharma
- Si Chen
- Silvia Alvarez
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- Simin Mohseni
- Simon Michaeli
- Simon Sedej
- Simon Wilkinson
- Simone Cenci
- Simone Di Paola
- Simone Engelender
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- Simone Nardin Weis
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- Skye C McIver
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- Sofie Claerhout
- Soledad Matus
- Song H
- Songshu Meng
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- Sonia Melino
- Sonia Rocha
- Soo Han Bae
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- Sophie Pattingre
- Soraya S Smaili
- Sovan Sarkar
- Spencer B Gibson
- Spitzer C
- Spruessel A
- Sreejayan Nair
- Srikanta Dash
- Srinivasa Subramaniam
- Srinivasan Dasarathy
- Ssang-Goo Cho
- Stefaan J Soenen
- Stefan Böckler
- Stefan Olsson
- Stefan W Ryter
- Stefania Meschini
- Stefanie Pöggeler
- Stefano Santaguida
- Stefano Toldo
- Steffan T Nawrocki
- Stella Y Lee
- Stephanie E Wohlgemuth
- Stephen A Spector
- Stephen Baghdiguian
- Stephen C Pak
- Stephen E Girardin
- Stephen WG Tait
- Steve Jean
- Steve Lancel
- Steve S-L Chen
- Steven Finkbeiner
- Steven Grant
- Steven S Witkin
- Stig U Andersen
- Strappazzon F
- Stéphane D Lemaire
- Stéphane Duvezin-Caubet
- Stęphan T Stern
- Subbiah Pugazhenthi
- Sucheta Telang
- Sug Hyung Lee
- Sujit K Bhutia
- Sumit Sahni
- Sun Y
- Sung Sik Lee
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- Sung-Joon Lee
- Sunhee Lee
- Supawadee Sukseree
- Suresh Awale
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- Suriapranata I
- Susan E Logue
- Susan L Cotman
- Susana Castro-Obregon
- Susmita Kaushik
- Susu M Zughaier
- Suzana Gispert
- Sven R Carlsson
- Svetlana Dokudovskaya
- Svetlana Saveljeva
- Swamynathan Ganesan
- Swapan K Ray
- Sylvain Lefort
- Sylviane Muller
- Szabolcs Takáts
- Sébastien Besteiro
- Søren R Paludan
- Ta Yuan Chang
- Tadashi Suzuki
- Tae-Cheon Kang
- Taeg Kyu Kwon
- Taehoon Chun
- Taijoon Chung
- Taixing Cui
- Takahiko Akematsu
- Takahiro Shintani
- Takahiro Yamada
- Takanobu Otomo
- Takao Setoguchi
- Takashi Ueno
- Takayuki Ohshima
- Takayuki Tsukuba
- Takehiko Matsushita
- Takeshi Into
- Takeshi Matsuzawa
- Takeshi Noda
- Tamara Kravic-Stevovic
- Tamas Korcsmaros
- Tamotsu Yoshimori
- Tania C Felizardo
- Tania Zaglia
- Tapas K Maiti
- Taras Y Nazarko
- Tassula Proikas-Cezanne
- Tatsuya Maeda
- Tatsuya Saitoh
- Tavassoly I
- Ted M Dawson
- Ted Powers
- Teng Jiang
- Teresa LM Thurston
- Teresa S Hawley
- Teresa Zoladek
- Terje Johansen
- Terrence M Donohue
- Terry H Landowski
- Terry Kwok
- Tetsuo Shioi
- Tewin Tencomnao
- Theo Rein
- Theocharis Panaretakis
- Thierry Arnould
- Thirumala-Devi Kanneganti
- Thomas A Ferguson
- Thomas Farkas
- Thomas IS Hwang
- Thomas J Begley
- Thomas J Evans
- Thomas Kawula
- Thomas L Schwarz
- Thomas M Durcan
- Thomas Neill
- Thomas S Jacques
- Thomas Simmet
- Thomas Thum
- Thomas Vaccari
- Thomas Weide
- Thomas Wollert
- Thorsten Hoppe
- Thorsten Nürnberger
- Tiago F Outeiro
- Tian Xia
- Tianwei Lin
- Tibor Kovács
- Tibor Vellai
- Tilman Grune
- Tim Lahm
- Timothy E Weaver
- Timothy Lyons
- Timothy P Devarenne
- Ting-Fang Wang
- Tino Kurz
- Tiziana Bachetti
- Tiziana Cocco
- Tiziana Crepaldi
- Tobias B Huber
- Tobias Eisenberg
- Tobias M Rasse
- Tom Wileman
- Tomasz M Stepkowski
- Tomohiro Kabuta
- Tomonori Kimura
- Tomotake Kanki
- Tony George Jacob
- Tor Erik Rusten
- Toren Finkel
- Toshiro Okazaki
- Tracey O'Donovan
- Trevor G Shepherd
- Trocoli A
- Trond Lamark
- Troy T Rohn
- Truong Lam
- Tsui-Fen Chou
- Tsunenori Saito
- Tsung-Hsien Chuang
- Tuck Wah Soong
- Tuttle DL
- Ubaldo Martinez-Outschoorn
- Uddin MN
- Udelnow A
- Udo Hasler
- Ugo Pagnini
- Ulrich E Schaible
- Ulrich Koenig
- Umamaheswar Duvvuri
- Umesh Kumar Jinwal
- Urban Emmenegger
- Usha P Andley
- Uta Dahmen
- Ute-Christiane Meier
- Utpal Sen
- V Ashutosh Rao
- Valentina Cianfanelli
- Valentina Iovane
- Valentina Izzo
- Valentina Sica
- Valentín Ceña
- Valeria Crippa
- Valerie Askanas
- Valerie B O'Donnell
- Valina L Dawson
- Valérie Pierrefite-Carle
- Valérie Vouret-Craviari
- Vanessa Ginet
- Vania Gelmetti
- Vania MM Braga
- Vasilis J Promponas
- Vassiliki E Mpakou
- Vassiliki Karantza
- Vassilis Stratoulias
- Venerando R
- Veronika Stoka
- Verónica I Dumit
- Verónica Pérez-de la Cruz
- Victor Dosenko
- Victor H Villar
- Victor M Darley-Usmar
- Victoria El-Khoury
- Victoria Ryabovol
- Vijittra Leardkamolkarn
- Vikash Kumar Dubey
- Viktor Billes
- Viktor I Korolchuk
- Vinay Choubey
- Vinay Eapen
- Vincent CO Njar
- Vincent Galy
- Vincent Kam Wai Wong
- Vincent Zecchini
- Vincenzo De Tata
- Vinod Sundaramoorthy
- Vinoth KM Khandelwal
- Virawudh Soontornniyomkij
- Vitaliy O Kaminskyy
- Vito Turk
- Vitor A Lira
- Vladimir Bumbasirevic
- Vladimir I Titorenko
- Vladimir Kirkin
- Vladimir N Uversky
- Vladimir Trajkovic
- Vladimir V Rogov
- Vojo Deretic
- Volker Doetsch
- Volodymyr Y Nazarko
- Vrajesh V Parekh
- W Douglas Fairlie
- W Haung Yu
- Wafik S El-Deiry
- Waleska Kerllen Martins
- Walter Balduini
- Walter Malorni
- Walter T Klimecki
- Wan-Wan Lin
- Wanderley de Souza
- Wang KC
- Wannian Yang
- Wei Chen
- Wei Li
- Wei Li
- Wei Liu
- Wei Pan
- Wei Song
- Wei Y
- Wei Yuan Yang
- Wei-Guo Zhu
- Wei-Jung Chen
- Wei-Li Zhao
- Wei-Pang Huang
- Wei-Xing Zong
- Weibel ER
- Weibel ER
- Weidong Han
- Weili Shen
- Weiliang Xia
- Wen Qiang Chen
- Wen-bin Qian
- Wen-Xing Ding
- Wenhua Zhu
- Wenjie Dai
- Wenjie Guo
- Wenli Chen
- Werner J Kovacs
- Wiep Scheper
- Wilhelm Krek
- Wilian A Silveira
- William A Dunn
- William C Cho
- William D Hill
- William KK Wu
- William T Jackson
- Williams MA
- Williams RA
- Wim Martinet
- Wim Vandenberghe
- Wolfdieter Springer
- Won-Ki Huh
- Wouter G van Doorn
- Wu D
- Wuhan Xiao
- X Charlie Dong
- Xi-Long Zheng
- Xian Wang
- Xian-De Liu
- Xian-Hui He
- Xiangbo Wan
- Xiangguo Liu
- Xianghua Yan
- Xiangmei Chen
- Xiangnan Zhang
- Xianyong Sheng
- Xiao-Fang Yu
- Xiao-Feng Zhu
- Xiao-Hong Liu
- Xiao-jia Wang
- Xiao-Ming Yin
- Xiao-Wei Wang
- Xiaofeng Yao
- Xiaohong Zhuang
- Xiaolei Xu
- Xiaonan Dong
- Xiaonan Zhao
- Xiaotao Li
- Xiaoxiang Zheng
- Xiaoyan Jiang
- Xin Qi
- Xin Wang
- Xin Wen
- Xinbing Sui
- Xinfeng Liu
- Xingcong Ren
- Xiu-Fen Ming
- Xu C
- Xu Dong Zhang
- Xu Liu
- Xu-Guang Guo
- Xu-jie Zhou
- Xue-Yuan Bai
- Xuejun Jiang
- Xuejun Jiang
- Xuejun Wang
- Xueqin Liu
- Xuesong Yang
- Ya Hua
- Yacine Graba
- Yan Burelle
- Yan G Zhao
- Yan Wang
- Yan Zhang
- Yang KC
- Yang Liu
- Yang Sun
- Yang Zhang
- Yangqing Xu
- Yanjin Zhang
- Yanjun Kou
- Yanming Wang
- Yannick Bailly
- Yaohua Wu
- Yasuhito Sakuraba
- Yasuko Rikihisa
- Yasuo Kitajima
- Yasuo Uchiyama
- Yasuo Yanagi
- Yasushi Kitaoka
- Yau-Hung Chen
- Ye Xu
- Ye Y
- Ye-Guang Chen
- Yee-Joo Tan
- Yee-Shin Lin
- Yeong-Min Yoo
- Yi Ma
- Yi Sun
- Yi Yang
- Yi-Hsin Tseng
- Yi-Ran Huang
- Yibin Feng
- Yide Mei
- Yin Chen
- Ying Jiang
- Ying Wang
- Ying Yang
- Ying Zhao
- Ying-Jan Wang
- Ying-Ray Lee
- Yingjie Sun
- Yingmei Zhang
- Yingying Lu
- Yingyu Chen
- Yipeng Wang
- Yizhen Deng
- Yohta Shimada
- Yokota S
- Yong Huang
- Yong J Lee
- Yong Lin
- Yong Ma
- Yong Tae Kwon
- Yong Xia
- Yong-Joon Chwae
- Yong-Keun Jung
- Yong-Sun Kim
- Yong-Yeon Cho
- Yongchao Zhao
- Yonggeun Hong
- Yonghyun Kim
- Yongjun Jiang
- Yongsheng Che
- Yongshun Chen
- Yoshiaki Kamada
- Yoshihiro Shidoji
- Yoshihisa Watanabe
- Yoshimori T
- Yoshinori Takahashi
- Yoshio Fujitani
- Yoshitaka Isaka
- Yoshitaka Nagai
- Yotaro Izumi
- You-Wen He
- Young H Lee
- Young Ho Koh
- Young Hyun Yoo
- Young J Oh
- Young-Seok Cho
- Yu Qiu
- Yu Tian Wang
- Yu Wang
- Yu Xue
- Yu-Chen Hu
- Yu-Jen Chen
- Yu-xia Zhao
- Yu-Xiong Su
- Yu-Ying He
- Yuchen Feng
- Yue-Qin Chen
- Yuen-Li Chung
- Yuguang Shi
- Yuhua Zhu
- Yuichiro J Suzuki
- Yuji Moriyasu
- Yuji Ogura
- Yujie Chen
- Yukitoshi Nagahara
- Yule Liu
- Yulin Liao
- Yumin Li
- Yun Chau Long
- Yun Dai
- Yunfei Huang
- Yunfei Wen
- Yunjiao Zhang
- Yuqing Wang
- Yuuki Fujiwara
- Yuyan Xiong
- Yuzuru Imai
- Zahra Zakeri
- Zdena Palková
- Zexian Liu
- Zhang H
- Zhang J
- Zhao X
- Zhaoliang Su
- Zhe Liu
- Zhen Chen
- Zhen Yan
- Zhendong Zhao
- Zheng Dong
- Zheng-Hong Qin
- Zhengping Yu
- Zhenlong Wu
- Zhenyi An
- Zhenyi Ma
- Zhenyu Yao
- Zhenyu Yue
- Zhi-Min Yuan
- Zhi-Nong Wang
- Zhi-Xiang Xu
- Zhifen Yang
- Zhihong Yang
- Zhiping Xie
- Zhiyuan Yao
- Zhizhuang J Zhao
- Zhong Chen
- Zhonglin Xie
- Zhuo-Wei Hu
- Ziheng Xu
- Ziwei Qu
- Zixu Mao
- Zong-Wan Mao
- Zsuzsanna Szatmari
- Zu-Hang Sheng
- Zufeng Ding
- Zully Pedrozo
- Zun-Ji Ke
- Zuzana Papackova
- Zuzana Storchova
- Zvenyslava Husak
- Zvonimir Marelja
- Zvulun Elazar
- Álvaro F Fernández
- Åsa B Gustafsson
- Publication venue
- Publication date
- 22/09/2015
- Field of study
In 2008 we published the first set of guidelines for standardizing research in autophagy. Since then, research on this topic has continued to accelerate, and many new scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Accordingly, it is important to update these guidelines for monitoring autophagy in different organisms. Various reviews have described the range of assays that have been used for this purpose. Nevertheless, there continues to be confusion regarding acceptable methods to measure autophagy, especially in multicellular eukaryotes. For example, a key point that needs to be emphasized is that there is a difference between measurements that monitor the numbers or volume of autophagic elements (e.g., autophagosomes or autolysosomes) at any stage of the autophagic process versus those that measure fl ux through the autophagy pathway (i.e., the complete process including the amount and rate of cargo sequestered and degraded). In particular, a block in macroautophagy that results in autophagosome accumulation must be differentiated from stimuli that increase autophagic activity, defi ned as increased autophagy induction coupled with increased delivery to, and degradation within, lysosomes (inmost higher eukaryotes and some protists such as Dictyostelium ) or the vacuole (in plants and fungi). In other words, it is especially important that investigators new to the fi eld understand that the appearance of more autophagosomes does not necessarily equate with more autophagy. In fact, in many cases, autophagosomes accumulate because of a block in trafficking to lysosomes without a concomitant change in autophagosome biogenesis, whereas an increase in autolysosomes may reflect a reduction in degradative activity. It is worth emphasizing here that lysosomal digestion is a stage of autophagy and evaluating its competence is a crucial part of the evaluation of autophagic flux, or complete autophagy. Here, we present a set of guidelines for the selection and interpretation of methods for use by investigators who aim to examine macroautophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes. These guidelines are not meant to be a formulaic set of rules, because the appropriate assays depend in part on the question being asked and the system being used. In addition, we emphasize that no individual assay is guaranteed to be the most appropriate one in every situation, and we strongly recommend the use of multiple assays to monitor autophagy. Along these lines, because of the potential for pleiotropic effects due to blocking autophagy through genetic manipulation it is imperative to delete or knock down more than one autophagy-related gene. In addition, some individual Atg proteins, or groups of proteins, are involved in other cellular pathways so not all Atg proteins can be used as a specific marker for an autophagic process. In these guidelines, we consider these various methods of assessing autophagy and what information can, or cannot, be obtained from them. Finally, by discussing the merits and limits of particular autophagy assays, we hope to encourage technical innovation in the field
Cell death and renewal during prey capture and digestion in the carnivorous sponge Asbestopluma hypogea (Porifera: Poecilosclerida)
- Publication venue
- 'The Company of Biologists'
- Publication date
- 01/01/2012
- Field of study
International audienceThe sponge Asbestopluma hypogea is unusual among sponges due to its peculiar carnivorous feeding habit. During various stages of its nutrition cycle, the sponge is subjected to spectacular morphological modifications. Starved animals are characterized by many elongated filaments, which are crucial for the capture of prey. After capture, and during the digestion process, these filaments actively regress before being regenerated during a subsequent period of starvation. Here, we demonstrate that these morphological events rely on a highly dynamic cellular turnover, implying a coordinated sequence of programmed cell death (apoptosis and autophagy), cell proliferation and cell migration. A candidate niche for cell renewal by stem cell proliferation and differentiation was identified at the base of the sponge peduncle, characterized by higher levels of BrdU/EdU incorporation. Therefore, BrdU/EdU-positive cells of the peduncle base are candidate motile cells responsible for the regeneration of the prey-capturing main sponge body, i.e. the dynamic filaments. Altogether, our results demonstrate that dynamics of cell renewal in sponge appear to be regulated by cellular mechanisms as multiple and complex as those already identified in bilaterian metazoans
Cellular uptake and intracellular fate of antisense oligonucleotides
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2003
- Field of study
The Non-Proliferative Nature of Ascidian Folliculogenesis as a Model of Highly Ordered Cellular Topology Distinct from Proliferative Epithelia
- Author
- A Salic
- AM Martinez
- Anne-Marie Martinez
- B Maury
- B Monier
- Bernard Maurin
- C Martinand-Mari
- Camille Martinand-Mari
- CS Chen
- DW Thompson
- Emilie Le Goff
- F Prodon
- F Rousset
- François Rousset
- Hector Escriva
- JP Chambon
- Julien Averseng
- K Ragkousi
- Karim Azzag
- M Milán
- Martine Daujat-Chavanieu
- MC Gibson
- MJ Pankratz
- Nelly Godefroy
- Paul Mangeat
- R Farhadifar
- R Hooke
- RA Cloney
- SS Blair
- Stephen Baghdiguian
- T Lecuit
- T Okada
- WT Gibson
- WT Gibson
- Y Chélin
- Y Chélin
- Y Sugino
- Y Toyama
- Yoann Chelin
- Publication venue
- 'Public Library of Science (PLoS)'
- Publication date
- Field of study
Shaping Phases by Phasing Shapes
- Author
- Barrett C. J.
- Batista V. M. O.
- Bian K. F.
- Bianchi E.
- Damasceno P. F.
- Gebhardt K. E.
- Grzelczak M.
- Haji-Akbari A.
- Jiao Y.
- Jiao Y.
- Jones M. R.
- Kolafa J.
- Leng J.
- Li Y. B.
- Mann S.
- Martin J. L.
- Martinand-Mari C.
- Maye M. M.
- Nguyen T. D.
- Nie Z. H.
- Oleg Gang
- Quan Z.
- Russo J.
- Rybtchinski B.
- Sacanna S.
- Solomon M. J.
- Starr F. W.
- Stuart M. A. C.
- Sun D.
- Torquato S.
- Xiong H. M.
- Xiong H. M.
- Yoo J. W.
- Yugang Zhang
- Zhang Y. G.
- Zhang Z. L.
- Publication venue
- 'American Chemical Society (ACS)'
- Publication date
- Field of study
Oligonucleotide-Based Antiviral Strategies
- Author
- A. Arzumanov
- A. Banerjea
- A. Fire
- A. Grunweller
- A. Khvorova
- A. Khvorova
- A. Michienzi
- A. Peracchi
- A. Reynolds
- A.A. Levin
- A.J. Bridge
- A.L. Jackson
- A.P. McCaffrey
- A.P. McCaffrey
- A.T. Das
- B. Haley
- B.A. Sullenger
- C. Klein
- C. Martinand-Mari
- C. Zhou
- C.A. Sledz
- C.D. Novina
- C.E. Thomas
- D. Boden
- D. Macejak
- D. Semizarov
- D.S. Schwarz
- E. Clercq De
- F. Arias
- F. Darfeuille
- F. Eckstein
- F.K. Ngok
- G. Meister
- G. Randall
- G. Randall
- G.A. Coburn
- G.J. Hannon
- H. Takahashi
- H.J. Arteaga
- J. Bai
- J. Elmén
- J. Kurreck
- J. Kurreck
- J. Silva
- J. Soutschek
- J. Yuan
- J. Zhang
- J.-M. Jacque
- J.A. Doudna
- J.A. Wilson
- J.G. Doench
- J.O. Ojwang
- J.S. Jepsen
- K.L. McKnight
- K.M. Phipps
- L. Beigelman
- L. Gitlin
- M. Enserink
- M. Sioud
- M. Sohail
- M.-C. Saleh
- N. Jing
- N. Usman
- O. Seksek
- P.C. Scacheri
- P.C. Zamecnik
- P.C.J. Haasnoot
- Q. Ge
- Q. Ge
- R. Goila
- R. Kretschmer-Kazemi Far
- R.C.C. Ryther
- S. Agrawal
- S. Barik
- S. Schubert
- S. Schubert
- S. Schubert
- S. Schubert
- S. Schubert
- S.K. Radhakrishnan
- S.L. Uprichard
- S.M. Elbashir
- S.M. Tompkins
- S.T. Crooke
- S.W. Santoro
- T.R. Brummelkamp
- U. Kühl
- V. Bitko
- V. Bitko
- V. Mittal
- W. Zhang
- W.-H. Pan
- W.-Y. Hu
- X. Zhang
- X.-F. Qin
- Y. Dorsett
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2006
- Field of study
Hepatitis C Virus Translation Inhibitors Targeting the Internal Ribosomal Entry Site
- Author
- Abu Almakarem A. S.
- Ali N.
- Alotte C.
- Altschul S. F.
- Aoki H.
- Baugh C.
- Beales L. P.
- Berry K. E.
- Berry K. E.
- Boehringer D.
- Bradford S.
- Caldarelli S. A.
- Carnevali M.
- Chevalier C.
- Collier A. J.
- Das S.
- Dasgupta A.
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- Publication venue
- 'Informa UK Limited'
- Publication date
- 01/01/2016
- Field of study
No abstract available