Tso-Pang Yao

Tso-Pang Yao

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Tso-Pang Yao

Tso-Pang Yao

Publications by authors named "Tso-Pang Yao"

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Targeting HDAC6 Reprograms T 17 Pathogenicity and Facilitates Immunotherapies for Hepatocellular Carcinoma.

Hepatology 2019 Sep 20. Epub 2019 Sep 20.

Key Laboratory of Infection and Immunity of CAS, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Beijing, 100101, China.

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http://dx.doi.org/10.1002/hep.30960DOI Listing
September 2019

PTHrP targets HDAC4 and HDAC5 to repress chondrocyte hypertrophy.

JCI Insight 2019 Mar 7;4(5). Epub 2019 Mar 7.

Endocrine Unit, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, USA.

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http://dx.doi.org/10.1172/jci.insight.97903DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6483522PMC
March 2019

CoA synthase regulates mitotic fidelity via CBP-mediated acetylation.

Nat Commun 2018 03 12;9(1):1039. Epub 2018 Mar 12.

Department of Molecular Genetics and Microbiology, Center for Genomic and Computational Biology, Duke University School of Medicine, Durham, NC, 27710, USA.

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http://dx.doi.org/10.1038/s41467-018-03422-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5847545PMC
March 2018

Discovery of a fluorescent probe with HDAC6 selective inhibition.

Eur J Med Chem 2017 Dec 10;141:596-602. Epub 2017 Oct 10.

Department of Pharmacology and Cancer Biology, Duke University, Durham, NC, 27710, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ejmech.2017.10.022DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5694690PMC
December 2017

A Mec17-Myosin II Effector Axis Coordinates Microtubule Acetylation and Actin Dynamics to Control Primary Cilium Biogenesis.

PLoS One 2014 10;9(12):e114087. Epub 2014 Dec 10.

Department of Pharmacology and Cancer Biology, Duke University, Durham, North Carolina, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0114087PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4262394PMC
October 2017

Dopaminergic abnormalities in Hdac6-deficient mice.

Neuropharmacology 2016 11 17;110(Pt A):470-479. Epub 2016 Aug 17.

Department of Embryology, Institute for Developmental Research, Aichi Human Service Center, Kasugai, Aichi, Japan. Electronic address:

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http://dx.doi.org/10.1016/j.neuropharm.2016.08.018DOI Listing
November 2016

Uncoupling of Protein Aggregation and Neurodegeneration in a Mouse Amyotrophic Lateral Sclerosis Model.

Neurodegener Dis 2015 12;15(6):339-49. Epub 2015 Sep 12.

Graduate School of Analytical Science and Technology (GRAST), Chungnam National University, Daejeon, Republic of Korea.

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https://www.karger.com/Article/FullText/437208
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http://dx.doi.org/10.1159/000437208DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4807135PMC
September 2016

Loss of α-Tubulin Acetylation Is Associated with TGF-β-induced Epithelial-Mesenchymal Transition.

J Biol Chem 2016 Mar 13;291(10):5396-405. Epub 2016 Jan 13.

From the Life Sciences Institute, and Innovation Center for Cell Signaling Network, Zhejiang University, Hangzhou, Zhejiang 310058, China, Michael E. DeBakey Department of Surgery, and Department of Molecular & Cellular Biology, Baylor College of Medicine, Houston, Texas 77030

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http://dx.doi.org/10.1074/jbc.M115.713123DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4777869PMC
March 2016

Parkin Regulation and Neurodegenerative Disorders.

Front Aging Neurosci 2015 12;7:248. Epub 2016 Jan 12.

Neurodegeneration Research Laboratory, National Neuroscience InstituteSingapore, Singapore; Institute of Advanced Materials, Nanjing Tech UniversityNanjing, People's Republic of China; Department of Physiology, National University of SingaporeSingapore, Singapore; Duke-NUS Graduate Medical School, National University of SingaporeSingapore, Singapore.

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http://dx.doi.org/10.3389/fnagi.2015.00248DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4709595PMC
January 2016

HDAC6 maintains mitochondrial connectivity under hypoxic stress by suppressing MARCH5/MITOL dependent MFN2 degradation.

Biochem Biophys Res Commun 2015 Sep 23;464(4):1235-1240. Epub 2015 Jul 23.

Graduate School of Analytical Science and Technology, Chungnam National University, Daejeon, 305-764, Republic of Korea. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S0006291X153034
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http://dx.doi.org/10.1016/j.bbrc.2015.07.111DOI Listing
September 2015

Chaperone-mediated 26S proteasome remodeling facilitates free K63 ubiquitin chain production and aggresome clearance.

J Biol Chem 2015 Apr 24;290(15):9455-64. Epub 2015 Feb 24.

From the Department of Pharmacology and Cancer Biology, Duke University, Durham, North Carolina 27710

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http://dx.doi.org/10.1074/jbc.M114.627950DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4392251PMC
April 2015

HDAC4 regulates muscle fiber type-specific gene expression programs.

Mol Cells 2015 Apr 25;38(4):343-8. Epub 2015 Feb 25.

Department of Pharmacology and Cancer Biology, Duke University, Durham, NC 27710, USA.

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http://dx.doi.org/10.14348/molcells.2015.2278DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4400309PMC
April 2015

Proteomic identification and functional characterization of MYH9, Hsc70, and DNAJA1 as novel substrates of HDAC6 deacetylase activity.

Protein Cell 2015 Jan 15;6(1):42-54. Epub 2014 Oct 15.

State Key Laboratory of Medicinal Chemical Biology, College of Life Sciences, Nankai University, Tianjin, 300071, China.

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http://dx.doi.org/10.1007/s13238-014-0102-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4286133PMC
January 2015

HDAC4 promotes Pax7-dependent satellite cell activation and muscle regeneration.

EMBO Rep 2014 Nov 9;15(11):1175-83. Epub 2014 Sep 9.

Department of Pharmacology and Cancer Biology, Duke University, Durham, NC, USA

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http://dx.doi.org/10.15252/embr.201439195DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4253491PMC
November 2014

MFN1 deacetylation activates adaptive mitochondrial fusion and protects metabolically challenged mitochondria.

J Cell Sci 2014 Nov 30;127(Pt 22):4954-63. Epub 2014 Sep 30.

Department of Pharmacology and Cancer Biology, Duke University, Durham, NC 27710, USA

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http://dx.doi.org/10.1242/jcs.157321DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4231308PMC
November 2014

Microtubule acetylation amplifies p38 kinase signalling and anti-inflammatory IL-10 production.

Nat Commun 2014 Mar 17;5:3479. Epub 2014 Mar 17.

Department of Pharmacology and Cancer Biology, DUMC, Box 3813, Durham, North Carolina 27710, USA.

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http://dx.doi.org/10.1038/ncomms4479DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4000527PMC
March 2014

Proteasomes activate aggresome disassembly and clearance by producing unanchored ubiquitin chains.

Mol Cell 2013 Sep 12;51(6):819-28. Epub 2013 Sep 12.

Department of Pharmacology and Cancer Biology, Duke University, Durham, NC 27710, USA.

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http://dx.doi.org/10.1016/j.molcel.2013.08.016DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3791850PMC
September 2013

Lysine modifications and autophagy.

Essays Biochem 2012 ;52:65-77

Department of Pharmacology and Cancer Biology, Duke University, Durham, NC 27710, U.S.A.

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http://dx.doi.org/10.1042/bse0520065DOI Listing
October 2012

A direct HDAC4-MAP kinase crosstalk activates muscle atrophy program.

Mol Cell 2012 Jul 31;47(1):122-32. Epub 2012 May 31.

Department of Pharmacology and Cancer Biology, Duke University, Durham, NC 27710, USA.

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http://dx.doi.org/10.1016/j.molcel.2012.04.025DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3398192PMC
July 2012

Mitochondrial dynamics and Parkinson's disease: focus on parkin.

Antioxid Redox Signal 2012 May 22;16(9):935-49. Epub 2011 Jul 22.

Department of Physiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.

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http://dx.doi.org/10.1089/ars.2011.4105DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3292756PMC
May 2012

Guidelines for the use and interpretation of assays for monitoring autophagy.

Authors:
Daniel J Klionsky Fabio C Abdalla Hagai Abeliovich Robert T Abraham Abraham Acevedo-Arozena Khosrow Adeli Lotta Agholme Maria Agnello Patrizia Agostinis Julio A Aguirre-Ghiso Hyung Jun Ahn Ouardia Ait-Mohamed Slimane Ait-Si-Ali Takahiko Akematsu Shizuo Akira Hesham M Al-Younes Munir A Al-Zeer Matthew L Albert Roger L Albin Javier Alegre-Abarrategui Maria Francesca Aleo Mehrdad Alirezaei Alexandru Almasan Maylin Almonte-Becerril Atsuo Amano Ravi Amaravadi Shoba Amarnath Amal O Amer Nathalie Andrieu-Abadie Vellareddy Anantharam David K Ann Shailendra Anoopkumar-Dukie Hiroshi Aoki Nadezda Apostolova Giuseppe Arancia John P Aris Katsuhiko Asanuma Nana Y O Asare Hisashi Ashida Valerie Askanas David S Askew Patrick Auberger Misuzu Baba Steven K Backues Eric H Baehrecke Ben A Bahr Xue-Yuan Bai Yannick Bailly Robert Baiocchi Giulia Baldini Walter Balduini Andrea Ballabio Bruce A Bamber Edward T W Bampton Gábor Bánhegyi Clinton R Bartholomew Diane C Bassham Robert C Bast Henri Batoko Boon-Huat Bay Isabelle Beau Daniel M Béchet Thomas J Begley Christian Behl Christian Behrends Soumeya Bekri Bryan Bellaire Linda J Bendall Luca Benetti Laura Berliocchi Henri Bernardi Francesca Bernassola Sébastien Besteiro Ingrid Bhatia-Kissova Xiaoning Bi Martine Biard-Piechaczyk Janice S Blum Lawrence H Boise Paolo Bonaldo David L Boone Beat C Bornhauser Karina R Bortoluci Ioannis Bossis Frédéric Bost Jean-Pierre Bourquin Patricia Boya Michaël Boyer-Guittaut Peter V Bozhkov Nathan R Brady Claudio Brancolini Andreas Brech Jay E Brenman Ana Brennand Emery H Bresnick Patrick Brest Dave Bridges Molly L Bristol Paul S Brookes Eric J Brown John H Brumell Nicola Brunetti-Pierri Ulf T Brunk Dennis E Bulman Scott J Bultman Geert Bultynck Lena F Burbulla Wilfried Bursch Jonathan P Butchar Wanda Buzgariu Sergio P Bydlowski Ken Cadwell Monika Cahová Dongsheng Cai Jiyang Cai Qian Cai Bruno Calabretta Javier Calvo-Garrido Nadine Camougrand Michelangelo Campanella Jenny Campos-Salinas Eleonora Candi Lizhi Cao Allan B Caplan Simon R Carding Sandra M Cardoso Jennifer S Carew Cathleen R Carlin Virginie Carmignac Leticia A M Carneiro Serena Carra Rosario A Caruso Giorgio Casari Caty Casas Roberta Castino Eduardo Cebollero Francesco Cecconi Jean Celli Hassan Chaachouay Han-Jung Chae Chee-Yin Chai David C Chan Edmond Y Chan Raymond Chuen-Chung Chang Chi-Ming Che Ching-Chow Chen Guang-Chao Chen Guo-Qiang Chen Min Chen Quan Chen Steve S-L Chen WenLi Chen Xi Chen Xiangmei Chen Xiequn Chen Ye-Guang Chen Yingyu Chen Yongqiang Chen Yu-Jen Chen Zhixiang Chen Alan Cheng Christopher H K Cheng Yan Cheng Heesun Cheong Jae-Ho Cheong Sara Cherry Russ Chess-Williams Zelda H Cheung Eric Chevet Hui-Ling Chiang Roberto Chiarelli Tomoki Chiba Lih-Shen Chin Shih-Hwa Chiou Francis V Chisari Chi Hin Cho Dong-Hyung Cho Augustine M K Choi DooSeok Choi Kyeong Sook Choi Mary E Choi Salem Chouaib Divaker Choubey Vinay Choubey Charleen T Chu Tsung-Hsien Chuang Sheau-Huei Chueh Taehoon Chun Yong-Joon Chwae Mee-Len Chye Roberto Ciarcia Maria R Ciriolo Michael J Clague Robert S B Clark Peter G H Clarke Robert Clarke Patrice Codogno Hilary A Coller María I Colombo Sergio Comincini Maria Condello Fabrizio Condorelli Mark R Cookson Graham H Coombs Isabelle Coppens Ramon Corbalan Pascale Cossart Paola Costelli Safia Costes Ana Coto-Montes Eduardo Couve Fraser P Coxon James M Cregg José L Crespo Marianne J Cronjé Ana Maria Cuervo Joseph J Cullen Mark J Czaja Marcello D'Amelio Arlette Darfeuille-Michaud Lester M Davids Faith E Davies Massimo De Felici John F de Groot Cornelis A M de Haan Luisa De Martino Angelo De Milito Vincenzo De Tata Jayanta Debnath Alexei Degterev Benjamin Dehay Lea M D Delbridge Francesca Demarchi Yi Zhen Deng Jörn Dengjel Paul Dent Donna Denton Vojo Deretic Shyamal D Desai Rodney J Devenish Mario Di Gioacchino Gilbert Di Paolo Chiara Di Pietro Guillermo Díaz-Araya Inés Díaz-Laviada Maria T Diaz-Meco Javier Diaz-Nido Ivan Dikic Savithramma P Dinesh-Kumar Wen-Xing Ding Clark W Distelhorst Abhinav Diwan Mojgan Djavaheri-Mergny Svetlana Dokudovskaya Zheng Dong Frank C Dorsey Victor Dosenko James J Dowling Stephen Doxsey Marlène Dreux Mark E Drew Qiuhong Duan Michel A Duchosal Karen Duff Isabelle Dugail Madeleine Durbeej Michael Duszenko Charles L Edelstein Aimee L Edinger Gustavo Egea Ludwig Eichinger N Tony Eissa Suhendan Ekmekcioglu Wafik S El-Deiry Zvulun Elazar Mohamed Elgendy Lisa M Ellerby Kai Er Eng Anna-Mart Engelbrecht Simone Engelender Jekaterina Erenpreisa Ricardo Escalante Audrey Esclatine Eeva-Liisa Eskelinen Lucile Espert Virginia Espina Huizhou Fan Jia Fan Qi-Wen Fan Zhen Fan Shengyun Fang Yongqi Fang Manolis Fanto Alessandro Fanzani Thomas Farkas Jean-Claude Farré Mathias Faure Marcus Fechheimer Carl G Feng Jian Feng Qili Feng Youji Feng László Fésüs Ralph Feuer Maria E Figueiredo-Pereira Gian Maria Fimia Diane C Fingar Steven Finkbeiner Toren Finkel Kim D Finley Filomena Fiorito Edward A Fisher Paul B Fisher Marc Flajolet Maria L Florez-McClure Salvatore Florio Edward A Fon Francesco Fornai Franco Fortunato Rati Fotedar Daniel H Fowler Howard S Fox Rodrigo Franco Lisa B Frankel Marc Fransen José M Fuentes Juan Fueyo Jun Fujii Kozo Fujisaki Eriko Fujita Mitsunori Fukuda Ruth H Furukawa Matthias Gaestel Philippe Gailly Malgorzata Gajewska Brigitte Galliot Vincent Galy Subramaniam Ganesh Barry Ganetzky Ian G Ganley Fen-Biao Gao George F Gao Jinming Gao Lorena Garcia Guillermo Garcia-Manero Mikel Garcia-Marcos Marjan Garmyn Andrei L Gartel Evelina Gatti Mathias Gautel Thomas R Gawriluk Matthew E Gegg Jiefei Geng Marc Germain Jason E Gestwicki David A Gewirtz Saeid Ghavami Pradipta Ghosh Anna M Giammarioli Alexandra N Giatromanolaki Spencer B Gibson Robert W Gilkerson Michael L Ginger Henry N Ginsberg Jakub Golab Michael S Goligorsky Pierre Golstein Candelaria Gomez-Manzano Ebru Goncu Céline Gongora Claudio D Gonzalez Ramon Gonzalez Cristina González-Estévez Rosa Ana González-Polo Elena Gonzalez-Rey Nikolai V Gorbunov Sharon Gorski Sandro Goruppi Roberta A Gottlieb Devrim Gozuacik Giovanna Elvira Granato Gary D Grant Kim N Green Aleš Gregorc Frédéric Gros Charles Grose Thomas W Grunt Philippe Gual Jun-Lin Guan Kun-Liang Guan Sylvie M Guichard Anna S Gukovskaya Ilya Gukovsky Jan Gunst Asa B Gustafsson Andrew J Halayko Amber N Hale Sandra K Halonen Maho Hamasaki Feng Han Ting Han Michael K Hancock Malene Hansen Hisashi Harada Masaru Harada Stefan E Hardt J Wade Harper Adrian L Harris James Harris Steven D Harris Makoto Hashimoto Jeffrey A Haspel Shin-ichiro Hayashi Lori A Hazelhurst Congcong He You-Wen He Marie-Joseé Hébert Kim A Heidenreich Miep H Helfrich Gudmundur V Helgason Elizabeth P Henske Brian Herman Paul K Herman Claudio Hetz Sabine Hilfiker Joseph A Hill Lynne J Hocking Paul Hofman Thomas G Hofmann Jörg Höhfeld Tessa L Holyoake Ming-Huang Hong David A Hood Gökhan S Hotamisligil Ewout J Houwerzijl Maria Høyer-Hansen Bingren Hu Chien-An A Hu Hong-Ming Hu Ya Hua Canhua Huang Ju Huang Shengbing Huang Wei-Pang Huang Tobias B Huber Won-Ki Huh Tai-Ho Hung Ted R Hupp Gang Min Hur James B Hurley Sabah N A Hussain Patrick J Hussey Jung Jin Hwang Seungmin Hwang Atsuhiro Ichihara Shirin Ilkhanizadeh Ken Inoki Takeshi Into Valentina Iovane Juan L Iovanna Nancy Y Ip Yoshitaka Isaka Hiroyuki Ishida Ciro Isidoro Ken-ichi Isobe Akiko Iwasaki Marta Izquierdo Yotaro Izumi Panu M Jaakkola Marja Jäättelä George R Jackson William T Jackson Bassam Janji Marina Jendrach Ju-Hong Jeon Eui-Bae Jeung Hong Jiang Hongchi Jiang Jean X Jiang Ming Jiang Qing Jiang Xuejun Jiang Xuejun Jiang Alberto Jiménez Meiyan Jin Shengkan Jin Cheol O Joe Terje Johansen Daniel E Johnson Gail V W Johnson Nicola L Jones Bertrand Joseph Suresh K Joseph Annie M Joubert Gábor Juhász Lucienne Juillerat-Jeanneret Chang Hwa Jung Yong-Keun Jung Kai Kaarniranta Allen Kaasik Tomohiro Kabuta Motoni Kadowaki Katarina Kagedal Yoshiaki Kamada Vitaliy O Kaminskyy Harm H Kampinga Hiromitsu Kanamori Chanhee Kang Khong Bee Kang Kwang Il Kang Rui Kang Yoon-A Kang Tomotake Kanki Thirumala-Devi Kanneganti Haruo Kanno Anumantha G Kanthasamy Arthi Kanthasamy Vassiliki Karantza Gur P Kaushal Susmita Kaushik Yoshinori Kawazoe Po-Yuan Ke John H Kehrl Ameeta Kelekar Claus Kerkhoff David H Kessel Hany Khalil Jan A K W Kiel Amy A Kiger Akio Kihara Deok Ryong Kim Do-Hyung Kim Dong-Hou Kim Eun-Kyoung Kim Hyung-Ryong Kim Jae-Sung Kim Jeong Hun Kim Jin Cheon Kim John K Kim Peter K Kim Seong Who Kim Yong-Sun Kim Yonghyun Kim Adi Kimchi Alec C Kimmelman Jason S King Timothy J Kinsella Vladimir Kirkin Lorrie A Kirshenbaum Katsuhiko Kitamoto Kaio Kitazato Ludger Klein Walter T Klimecki Jochen Klucken Erwin Knecht Ben C B Ko Jan C Koch Hiroshi Koga Jae-Young Koh Young Ho Koh Masato Koike Masaaki Komatsu Eiki Kominami Hee Jeong Kong Wei-Jia Kong Viktor I Korolchuk Yaichiro Kotake Michael I Koukourakis Juan B Kouri Flores Attila L Kovács Claudine Kraft Dimitri Krainc Helmut Krämer Carole Kretz-Remy Anna M Krichevsky Guido Kroemer Rejko Krüger Oleg Krut Nicholas T Ktistakis Chia-Yi Kuan Roza Kucharczyk Ashok Kumar Raj Kumar Sharad Kumar Mondira Kundu Hsing-Jien Kung Tino Kurz Ho Jeong Kwon Albert R La Spada Frank Lafont Trond Lamark Jacques Landry Jon D Lane Pierre Lapaquette Jocelyn F Laporte Lajos László Sergio Lavandero Josée N Lavoie Robert Layfield Pedro A Lazo Weidong Le Laurent Le Cam Daniel J Ledbetter Alvin J X Lee Byung-Wan Lee Gyun Min Lee Jongdae Lee Ju-Hyun Lee Michael Lee Myung-Shik Lee Sug Hyung Lee Christiaan Leeuwenburgh Patrick Legembre Renaud Legouis Michael Lehmann Huan-Yao Lei Qun-Ying Lei David A Leib José Leiro John J Lemasters Antoinette Lemoine Maciej S Lesniak Dina Lev Victor V Levenson Beth Levine Efrat Levy Faqiang Li Jun-Lin Li Lian Li Sheng Li Weijie Li Xue-Jun Li Yan-bo Li Yi-Ping Li Chengyu Liang Qiangrong Liang Yung-Feng Liao Pawel P Liberski Andrew Lieberman Hyunjung J Lim Kah-Leong Lim Kyu Lim Chiou-Feng Lin Fu-Cheng Lin Jian Lin Jiandie D Lin Kui Lin Wan-Wan Lin Weei-Chin Lin Yi-Ling Lin Rafael Linden Paul Lingor Jennifer Lippincott-Schwartz Michael P Lisanti Paloma B Liton Bo Liu Chun-Feng Liu Kaiyu Liu Leyuan Liu Qiong A Liu Wei Liu Young-Chau Liu Yule Liu Richard A Lockshin Chun-Nam Lok Sagar Lonial Benjamin Loos Gabriel Lopez-Berestein Carlos López-Otín Laura Lossi Michael T Lotze Peter Lőw Binfeng Lu Bingwei Lu Bo Lu Zhen Lu Frédéric Luciano Nicholas W Lukacs Anders H Lund Melinda A Lynch-Day Yong Ma Fernando Macian Jeff P MacKeigan Kay F Macleod Frank Madeo Luigi Maiuri Maria Chiara Maiuri Davide Malagoli May Christine V Malicdan Walter Malorni Na Man Eva-Maria Mandelkow Stéphen Manon Irena Manov Kai Mao Xiang Mao Zixu Mao Philippe Marambaud Daniela Marazziti Yves L Marcel Katie Marchbank Piero Marchetti Stefan J Marciniak Mateus Marcondes Mohsen Mardi Gabriella Marfe Guillermo Mariño Maria Markaki Mark R Marten Seamus J Martin Camille Martinand-Mari Wim Martinet Marta Martinez-Vicente Matilde Masini Paola Matarrese Saburo Matsuo Raffaele Matteoni Andreas Mayer Nathalie M Mazure David J McConkey Melanie J McConnell Catherine McDermott Christine McDonald Gerald M McInerney Sharon L McKenna BethAnn McLaughlin Pamela J McLean Christopher R McMaster G Angus McQuibban Alfred J Meijer Miriam H Meisler Alicia Meléndez Thomas J Melia Gerry Melino Maria A Mena Javier A Menendez Rubem F S Menna-Barreto Manoj B Menon Fiona M Menzies Carol A Mercer Adalberto Merighi Diane E Merry Stefania Meschini Christian G Meyer Thomas F Meyer Chao-Yu Miao Jun-Ying Miao Paul A M Michels Carine Michiels Dalibor Mijaljica Ana Milojkovic Saverio Minucci Clelia Miracco Cindy K Miranti Ioannis Mitroulis Keisuke Miyazawa Noboru Mizushima Baharia Mograbi Simin Mohseni Xavier Molero Bertrand Mollereau Faustino Mollinedo Takashi Momoi Iryna Monastyrska Martha M Monick Mervyn J Monteiro Michael N Moore Rodrigo Mora Kevin Moreau Paula I Moreira Yuji Moriyasu Jorge Moscat Serge Mostowy Jeremy C Mottram Tomasz Motyl Charbel E-H Moussa Sylke Müller Sylviane Muller Karl Münger Christian Münz Leon O Murphy Maureen E Murphy Antonio Musarò Indira Mysorekar Eiichiro Nagata Kazuhiro Nagata Aimable Nahimana Usha Nair Toshiyuki Nakagawa Kiichi Nakahira Hiroyasu Nakano Hitoshi Nakatogawa Meera Nanjundan Naweed I Naqvi Derek P Narendra Masashi Narita Miguel Navarro Steffan T Nawrocki Taras Y Nazarko Andriy Nemchenko Mihai G Netea Thomas P Neufeld Paul A Ney Ioannis P Nezis Huu Phuc Nguyen Daotai Nie Ichizo Nishino Corey Nislow Ralph A Nixon Takeshi Noda Angelika A Noegel Anna Nogalska Satoru Noguchi Lucia Notterpek Ivana Novak Tomoyoshi Nozaki Nobuyuki Nukina Thorsten Nürnberger Beat Nyfeler Keisuke Obara Terry D Oberley Salvatore Oddo Michinaga Ogawa Toya Ohashi Koji Okamoto Nancy L Oleinick F Javier Oliver Laura J Olsen Stefan Olsson Onya Opota Timothy F Osborne Gary K Ostrander Kinya Otsu Jing-hsiung James Ou Mireille Ouimet Michael Overholtzer Bulent Ozpolat Paolo Paganetti Ugo Pagnini Nicolas Pallet Glen E Palmer Camilla Palumbo Tianhong Pan Theocharis Panaretakis Udai Bhan Pandey Zuzana Papackova Issidora Papassideri Irmgard Paris Junsoo Park Ohkmae K Park Jan B Parys Katherine R Parzych Susann Patschan Cam Patterson Sophie Pattingre John M Pawelek Jianxin Peng David H Perlmutter Ida Perrotta George Perry Shazib Pervaiz Matthias Peter Godefridus J Peters Morten Petersen Goran Petrovski James M Phang Mauro Piacentini Philippe Pierre Valérie Pierrefite-Carle Gérard Pierron Ronit Pinkas-Kramarski Antonio Piras Natik Piri Leonidas C Platanias Stefanie Pöggeler Marc Poirot Angelo Poletti Christian Poüs Mercedes Pozuelo-Rubio Mette Prætorius-Ibba Anil Prasad Mark Prescott Muriel Priault Nathalie Produit-Zengaffinen Ann Progulske-Fox Tassula Proikas-Cezanne Serge Przedborski Karin Przyklenk Rosa Puertollano Julien Puyal Shu-Bing Qian Liang Qin Zheng-Hong Qin Susan E Quaggin Nina Raben Hannah Rabinowich Simon W Rabkin Irfan Rahman Abdelhaq Rami Georg Ramm Glenn Randall Felix Randow V Ashutosh Rao Jeffrey C Rathmell Brinda Ravikumar Swapan K Ray Bruce H Reed John C Reed Fulvio Reggiori Anne Régnier-Vigouroux Andreas S Reichert John J Reiners Russel J Reiter Jun Ren José L Revuelta Christopher J Rhodes Konstantinos Ritis Elizete Rizzo Jeffrey Robbins Michel Roberge Hernan Roca Maria C Roccheri Stephane Rocchi H Peter Rodemann Santiago Rodríguez de Córdoba Bärbel Rohrer Igor B Roninson Kirill Rosen Magdalena M Rost-Roszkowska Mustapha Rouis Kasper M A Rouschop Francesca Rovetta Brian P Rubin David C Rubinsztein Klaus Ruckdeschel Edmund B Rucker Assaf Rudich Emil Rudolf Nelson Ruiz-Opazo Rossella Russo Tor Erik Rusten Kevin M Ryan Stefan W Ryter David M Sabatini Junichi Sadoshima Tapas Saha Tatsuya Saitoh Hiroshi Sakagami Yasuyoshi Sakai Ghasem Hoseini Salekdeh Paolo Salomoni Paul M Salvaterra Guy Salvesen Rosa Salvioli Anthony M J Sanchez José A Sánchez-Alcázar Ricardo Sánchez-Prieto Marco Sandri Uma Sankar Poonam Sansanwal Laura Santambrogio Shweta Saran Sovan Sarkar Minnie Sarwal Chihiro Sasakawa Ausra Sasnauskiene Miklós Sass Ken Sato Miyuki Sato Anthony H V Schapira Michael Scharl Hermann M Schätzl Wiep Scheper Stefano Schiaffino Claudio Schneider Marion E Schneider Regine Schneider-Stock Patricia V Schoenlein Daniel F Schorderet Christoph Schüller Gary K Schwartz Luca Scorrano Linda Sealy Per O Seglen Juan Segura-Aguilar Iban Seiliez Oleksandr Seleverstov Christian Sell Jong Bok Seo Duska Separovic Vijayasaradhi Setaluri Takao Setoguchi Carmine Settembre John J Shacka Mala Shanmugam Irving M Shapiro Eitan Shaulian Reuben J Shaw James H Shelhamer Han-Ming Shen Wei-Chiang Shen Zu-Hang Sheng Yang Shi Kenichi Shibuya Yoshihiro Shidoji Jeng-Jer Shieh Chwen-Ming Shih Yohta Shimada Shigeomi Shimizu Takahiro Shintani Orian S Shirihai Gordon C Shore Andriy A Sibirny Stan B Sidhu Beata Sikorska Elaine C M Silva-Zacarin Alison Simmons Anna Katharina Simon Hans-Uwe Simon Cristiano Simone Anne Simonsen David A Sinclair Rajat Singh Debasish Sinha Frank A Sinicrope Agnieszka Sirko Parco M Siu 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Craig B Thompson Andrew Thorburn Michael Thumm FengFeng Tian Yuan Tian Glauco Tocchini-Valentini Aviva M Tolkovsky Yasuhiko Tomino Lars Tönges Sharon A Tooze Cathy Tournier John Tower Roberto Towns Vladimir Trajkovic Leonardo H Travassos Ting-Fen Tsai Mario P Tschan Takeshi Tsubata Allan Tsung Boris Turk Lorianne S Turner Suresh C Tyagi Yasuo Uchiyama Takashi Ueno Midori Umekawa Rika Umemiya-Shirafuji Vivek K Unni Maria I Vaccaro Enza Maria Valente Greet Van den Berghe Ida J van der Klei Wouter van Doorn Linda F van Dyk Marjolein van Egmond Leo A van Grunsven Peter Vandenabeele Wim P Vandenberghe Ilse Vanhorebeek Eva C Vaquero Guillermo Velasco Tibor Vellai Jose Miguel Vicencio Richard D Vierstra Miquel Vila Cécile Vindis Giampietro Viola Maria Teresa Viscomi Olga V Voitsekhovskaja Clarissa von Haefen Marcela Votruba Keiji Wada Richard Wade-Martins Cheryl L Walker Craig M Walsh Jochen Walter Xiang-Bo Wan Aimin Wang Chenguang Wang Dawei Wang Fan Wang Fen Wang Guanghui Wang Haichao Wang Hong-Gang Wang Horng-Dar Wang Jin Wang Ke Wang Mei Wang Richard C Wang Xinglong Wang Xuejun Wang Ying-Jan Wang Yipeng Wang Zhen Wang Zhigang Charles Wang Zhinong Wang Derick G Wansink Diane M Ward Hirotaka Watada Sarah L Waters Paul Webster Lixin Wei Conrad C Weihl William A Weiss Scott M Welford Long-Ping Wen Caroline A Whitehouse J Lindsay Whitton Alexander J Whitworth Tom Wileman John W Wiley Simon Wilkinson Dieter Willbold Roger L Williams Peter R Williamson Bradly G Wouters Chenghan Wu Dao-Cheng Wu William K K Wu Andreas Wyttenbach Ramnik J Xavier Zhijun Xi Pu Xia Gengfu Xiao Zhiping Xie Zhonglin Xie Da-zhi Xu Jianzhen Xu Liang Xu Xiaolei Xu Ai Yamamoto Akitsugu Yamamoto Shunhei Yamashina Michiaki Yamashita Xianghua Yan Mitsuhiro Yanagida Dun-Sheng Yang Elizabeth Yang Jin-Ming Yang Shi Yu Yang Wannian Yang Wei Yuan Yang Zhifen Yang Meng-Chao Yao Tso-Pang Yao Behzad Yeganeh Wei-Lien Yen Jia-jing Yin Xiao-Ming Yin Ook-Joon Yoo Gyesoon Yoon Seung-Yong Yoon Tomohiro Yorimitsu Yuko Yoshikawa Tamotsu Yoshimori Kohki Yoshimoto Ho Jin You Richard J Youle Anas Younes Li Yu Long Yu Seong-Woon Yu Wai Haung Yu Zhi-Min Yuan Zhenyu Yue Cheol-Heui Yun Michisuke Yuzaki Olga Zabirnyk Elaine Silva-Zacarin David Zacks Eldad Zacksenhaus Nadia Zaffaroni Zahra Zakeri Herbert J Zeh Scott O Zeitlin Hong Zhang Hui-Ling Zhang Jianhua Zhang Jing-Pu Zhang Lin Zhang Long Zhang Ming-Yong Zhang Xu Dong Zhang Mantong Zhao Yi-Fang Zhao Ying Zhao Zhizhuang J Zhao Xiaoxiang Zheng Boris Zhivotovsky Qing Zhong Cong-Zhao Zhou Changlian Zhu Wei-Guo Zhu Xiao-Feng Zhu Xiongwei Zhu Yuangang Zhu Teresa Zoladek Wei-Xing Zong Antonio Zorzano Jürgen Zschocke Brian Zuckerbraun

Autophagy 2012 Apr;8(4):445-544

Life Sciences Institute, University of Michigan, Ann Arbor, MI, USA.

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http://dx.doi.org/10.4161/auto.19496DOI Listing
April 2012

HDACs in skeletal muscle remodeling and neuromuscular disease.

Handb Exp Pharmacol 2011 ;206:79-101

Department of Pharmacology and Cancer Biology, Duke University, C325 LSRC, DUMC, 3813, Durham, NC 27710, USA.

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November 2011

The discovery of histone deacetylase.

Handb Exp Pharmacol 2011 ;206

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November 2011

The role of ubiquitin in autophagy-dependent protein aggregate processing.

Authors:
Tso-Pang Yao

Genes Cancer 2010 Jul;1(7):779-786

Department of Pharmacology and Cancer Biology, Duke University, Durham, NC 27710, USA.

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July 2010

Quality control autophagy: a joint effort of ubiquitin, protein deacetylase and actin cytoskeleton.

Autophagy 2010 May 16;6(4):555-7. Epub 2010 May 16.

Department of Pharmacology and Cancer Biology, Duke University, Durham, NC, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3752377PMC
May 2010

Disease-causing mutations in parkin impair mitochondrial ubiquitination, aggregation, and HDAC6-dependent mitophagy.

J Cell Biol 2010 May 10;189(4):671-9. Epub 2010 May 10.

Department of Pharmacology and Cancer Biology, Duke University, Durham, NC 27710, USA.

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May 2010

The microtubule-associated histone deacetylase 6 (HDAC6) regulates epidermal growth factor receptor (EGFR) endocytic trafficking and degradation.

J Biol Chem 2010 Apr 4;285(15):11219-26. Epub 2010 Feb 4.

Department of Pharmacology and Cancer Biology, Duke University, Durham, North Carolina 27710, USA.

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April 2010

Parathyroid hormone-related peptide represses chondrocyte hypertrophy through a protein phosphatase 2A/histone deacetylase 4/MEF2 pathway.

Mol Cell Biol 2009 Nov 24;29(21):5751-62. Epub 2009 Aug 24.

Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, 240 Longwood Ave., Boston, MA 02115, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2772746PMC
November 2009

Acetylation goes global: the emergence of acetylation biology.

Sci Signal 2009 Nov 17;2(97):pe76. Epub 2009 Nov 17.

Department of Pharmacology and Cancer Biology, Duke University, Durham, NC 27710, USA.

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http://dx.doi.org/10.1126/scisignal.297pe76DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2812806PMC
November 2009

The deacetylase HDAC4 controls myocyte enhancing factor-2-dependent structural gene expression in response to neural activity.

FASEB J 2009 Jan 9;23(1):99-106. Epub 2008 Sep 9.

Department of Pharmacology and Cancer Biology, Box 3813, Duke University Medical Center, Durham, NC 27710, USA.

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January 2009

Effects of downregulated HDAC6 expression on the proliferation of lung cancer cells.

Biochem Biophys Res Commun 2008 Sep 3;374(1):84-9. Epub 2008 Jul 3.

Chemical Genetics Laboratory, RIKEN Advanced Science Institute, Wako, Saitama 351-0198, Japan.

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September 2008

Requirement of HDAC6 for transforming growth factor-beta1-induced epithelial-mesenchymal transition.

J Biol Chem 2008 Jul 21;283(30):21065-73. Epub 2008 May 21.

Department of Medicine and Tulane Cancer Center, Tulane University Health Sciences Center, 1430 Tulane Avenue, New Orleans, LA 70112, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2475688PMC
July 2008

HDAC6 is required for epidermal growth factor-induced beta-catenin nuclear localization.

J Biol Chem 2008 May 20;283(19):12686-90. Epub 2008 Mar 20.

Cell Signaling Technology, Danvers, Massachusetts 01923, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3762558PMC
May 2008

Histone deacetylase 6 regulates growth factor-induced actin remodeling and endocytosis.

Mol Cell Biol 2007 Dec 15;27(24):8637-47. Epub 2007 Oct 15.

Duke University, Department of Pharmacology and Cancer Biology, Durham, NC 27710, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2169396PMC
December 2007

The histone deacetylase HDAC4 connects neural activity to muscle transcriptional reprogramming.

J Biol Chem 2007 Nov 16;282(46):33752-9. Epub 2007 Sep 16.

Department of Pharmacology and Cancer Biology and Department of Neurobiology, Duke University, Durham, North Carolina 27710, USA.

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November 2007

The neurodegenerative disease protein ataxin-1 antagonizes the neuronal survival function of myocyte enhancer factor-2.

J Biol Chem 2007 Oct 23;282(40):29186-92. Epub 2007 Jul 23.

Department of Pharmacology and Cancer Biology, Duke University, Durham, North Carolina 27710, USA.

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October 2007

HDAC6 controls major cell response pathways to cytotoxic accumulation of protein aggregates.

Genes Dev 2007 Sep;21(17):2172-81

Institut National de la Santé et de la Recherche Médicale (INSERM), U823, Institut Albert Bonniot, Grenoble F-38706, France.

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http://dx.doi.org/10.1101/gad.436407DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1950856PMC
September 2007

HDAC6 deacetylation of tubulin modulates dynamics of cellular adhesions.

J Cell Sci 2007 Apr 27;120(Pt 8):1469-79. Epub 2007 Mar 27.

Department of Biological Sciences, Columbia University, New York, NY 10027, USA.

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http://dx.doi.org/10.1242/jcs.03431DOI Listing
April 2007

Chaperoning steroid hormone signaling via reversible acetylation.

Nucl Recept Signal 2005 21;3:e004. Epub 2005 Oct 21.

Department of Pharmacology and Cancer Biology, Duke University, Durham, North Carolina 27710, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1402214PMC
May 2006

Histone deacetylase 3 binds to and regulates the GCMa transcription factor.

Nucleic Acids Res 2006 9;34(5):1459-69. Epub 2006 Mar 9.

Graduate Institute of Biochemical Sciences, National Taiwan University, Taipei 106, Taiwan.

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April 2006

Charge modification at multiple C-terminal lysine residues regulates p53 oligomerization and its nucleus-cytoplasm trafficking.

J Biol Chem 2006 Jan 15;281(3):1394-400. Epub 2005 Nov 15.

Department of Pharmacology and Cancer Biology, Duke University, Durham, North Carolina 27710, USA.

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January 2006

Regulation of the dynamics of hsp90 action on the glucocorticoid receptor by acetylation/deacetylation of the chaperone.

J Biol Chem 2005 Oct 8;280(40):33792-9. Epub 2005 Aug 8.

Department of Pharmacology, The University of Michigan Medical School, Ann Arbor, Michigan 48109, USA.

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October 2005

Regulation of MEF2 by histone deacetylase 4- and SIRT1 deacetylase-mediated lysine modifications.

Mol Cell Biol 2005 Oct;25(19):8456-64

Department of Pharmacology and Cancer Biology, P.O. Box 3813, Duke University Medical Center, Durham, NC 27710, USA.

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October 2005

Intracellular trafficking of histone deacetylase 4 regulates neuronal cell death.

J Neurosci 2005 Oct;25(41):9544-53

Department of Pharmacology and Cancer Biology, Duke University, Durham, North Carolina 27710, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6725694PMC
October 2005

A mechanism of COOH-terminal binding protein-mediated repression.

Mol Cancer Res 2005 Oct;3(10):575-83

Department of Molecular Genetics and Microbiology, Duke University Medical Center, Box 3054, Durham, North Carolina 27710, USA.

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http://dx.doi.org/10.1158/1541-7786.MCR-05-0088DOI Listing
October 2005

Cyclin D1 inhibits peroxisome proliferator-activated receptor gamma-mediated adipogenesis through histone deacetylase recruitment.

J Biol Chem 2005 Apr 14;280(17):16934-41. Epub 2005 Feb 14.

Lombardi Comprehensive Cancer Center, Department of Oncology, Georgetown University, Washington, D. C. 20057, USA.

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http://dx.doi.org/10.1074/jbc.M500403200DOI Listing
April 2005

FBW2 targets GCMa to the ubiquitin-proteasome degradation system.

J Biol Chem 2005 Mar 8;280(11):10083-90. Epub 2005 Jan 8.

Graduate Institute of Biochemical Sciences, National Taiwan University, Taipei 106, Taiwan.

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March 2005

AcK-knowledge reversible acetylation.

Sci STKE 2004 Aug 3;2004(245):pe42. Epub 2004 Aug 3.

Department of Pharmacology and Cancer Biology, Duke University, Durham, NC 27710, USA.

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August 2004

The HDAC complex and cytoskeleton.

Novartis Found Symp 2004 ;259:170-7; discussion 178-81, 223-5

Department of Pharmacology and Cancer Biology, Duke University, Durham, North Carolina 27710, USA.

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June 2004

Deactylase inhibitors disrupt cellular complexes containing protein phosphatases and deacetylases.

J Biol Chem 2004 Feb 10;279(9):7685-91. Epub 2003 Dec 10.

Department of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, North Carolina 27710, USA.

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February 2004

The deacetylase HDAC6 regulates aggresome formation and cell viability in response to misfolded protein stress.

Cell 2003 Dec;115(6):727-38

Department of Pharmacology and Cancer Biology, Duke University, Durham, NC 27710, USA.

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December 2003

Regulation of E2A activities by histone acetyltransferases in B lymphocyte development.

J Biol Chem 2003 Jan 14;278(4):2370-6. Epub 2002 Nov 14.

Department of Immunology, Duke University Medical Center, Durham, North Carolina 27710, USA.

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January 2003

MDM2-HDAC1-mediated deacetylation of p53 is required for its degradation.

EMBO J 2002 Nov;21(22):6236-45

Department of Pharmacology and Cancer Biology, Duke University, Durham, NC 27710, USA.

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http://dx.doi.org/10.1093/emboj/cdf616DOI Listing
November 2002

HDAC6 is a microtubule-associated deacetylase.

Nature 2002 May;417(6887):455-8

Department of Pharmacology and Cancer Biology, Duke University, Durham, North Carolina 27710, USA.

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May 2002

Molecular cloning and characterization of a novel histone deacetylase HDAC10.

J Biol Chem 2002 Feb 28;277(5):3350-6. Epub 2001 Nov 28.

Department of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, North Carolina 27710, USA.

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February 2002