Andrei L Gartel

Andrei L Gartel

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Andrei L Gartel

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Honokiol is a FOXM1 antagonist.

Cell Death Dis 2018 01 24;9(2):84. Epub 2018 Jan 24.

Department of Medicine, University of Illinois, Chicago, IL, USA.

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http://dx.doi.org/10.1038/s41419-017-0156-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833612PMC
January 2018

FOXM1 in Cancer: Interactions and Vulnerabilities.

Authors:
Andrei L Gartel

Cancer Res 2017 06 5;77(12):3135-3139. Epub 2017 Jun 5.

Department of Medicine, University of Illinois at Chicago, Chicago, Illinois.

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http://dx.doi.org/10.1158/0008-5472.CAN-16-3566DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5519300PMC
June 2017

A Novel Function of Molecular Chaperone HSP70: SUPPRESSION OF ONCOGENIC FOXM1 AFTER PROTEOTOXIC STRESS.

J Biol Chem 2016 Jan 11;291(1):142-8. Epub 2015 Nov 11.

From the Departments of Medicine and Biochemistry and Molecular Genetics, University of Illinois at Chicago, Chicago, Illinois 60612

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http://www.jbc.org/content/291/1/142.full.pdf
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http://www.jbc.org/lookup/doi/10.1074/jbc.M115.678227
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http://dx.doi.org/10.1074/jbc.M115.678227DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4697151PMC
January 2016

Targeting FOXM1 auto-regulation in cancer.

Authors:
Andrei L Gartel

Cancer Biol Ther 2015 ;16(2):185-6

a Department of Medicine ; University of Illinois at Chicago ; Chicago , IL USA.

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http://dx.doi.org/10.4161/15384047.2014.987566DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4622879PMC
November 2015

Proteasome inhibitors suppress the protein expression of mutant p53.

Cell Cycle 2014 ;13(20):3202-6

a Department of Medicine ; University of Illinois at Chicago ; Chicago , IL USA.

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http://www.tandfonline.com/doi/full/10.4161/15384101.2014.95
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http://dx.doi.org/10.4161/15384101.2014.950132DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4613555PMC
September 2015

Mutual Regulation of FOXM1, NPM and ARF Proteins.

J Cancer 2015 28;6(6):538-41. Epub 2015 Apr 28.

Department of Medicine, University of Illinois at Chicago, Chicago, IL, 60612, USA.

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http://www.jcancer.org/v06p0538.pdf
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http://www.jcancer.org/v06p0538.htm
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http://dx.doi.org/10.7150/jca.11766DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4439939PMC
May 2015

Suppression of the Oncogenic Transcription Factor FOXM1 by Proteasome Inhibitors.

Authors:
Andrei L Gartel

Scientifica (Cairo) 2014 24;2014:596528. Epub 2014 Jun 24.

Department of Medicine, University of Illinois at Chicago, Chicago, IL 606012, USA.

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http://dx.doi.org/10.1155/2014/596528DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4095980PMC
August 2014

Found in transcription: FOXO1 upregulates miRNAs on chromosome X.

Authors:
Andrei L Gartel

Cell Cycle 2013 Aug 29;12(16):2523. Epub 2013 Jul 29.

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http://dx.doi.org/10.4161/cc.25829DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3865033PMC
August 2013

Thiazole Antibiotics Siomycin a and Thiostrepton Inhibit the Transcriptional Activity of FOXM1.

Authors:
Andrei L Gartel

Front Oncol 2013 6;3:150. Epub 2013 Jun 6.

Department of Medicine, University of Illinois at Chicago Chicago, IL, USA.

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http://dx.doi.org/10.3389/fonc.2013.00150DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3674410PMC
June 2013

Targeting FOXM1 in cancer.

Biochem Pharmacol 2013 Mar 24;85(5):644-652. Epub 2012 Oct 24.

Department of Medicine, University of Illinois at Chicago, Chicago, IL, United States of America. Electronic address:

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http://dx.doi.org/10.1016/j.bcp.2012.10.013DOI Listing
March 2013

FOX(M1) news--it is cancer.

Mol Cancer Ther 2013 Mar 26;12(3):245-54. Epub 2013 Feb 26.

University of Illinois at Chicago, Department of Medicine, Chicago, IL 60612, USA.

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http://dx.doi.org/10.1158/1535-7163.MCT-12-0712DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3596487PMC
March 2013

Paradoxical inhibition of cellular protein expression by proteasome inhibitors.

Authors:
Andrei L Gartel

Biomol Concepts 2012 Dec;3(6):593-5

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http://dx.doi.org/10.1515/bmc-2012-0029DOI Listing
December 2012

The oncogenic transcription factor FOXM1 and anticancer therapy.

Authors:
Andrei L Gartel

Cell Cycle 2012 Sep 23;11(18):3341-2. Epub 2012 Aug 23.

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http://dx.doi.org/10.4161/cc.21841DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3466533PMC
September 2012

Suppression of FOXM1 sensitizes human cancer cells to cell death induced by DNA-damage.

PLoS One 2012 29;7(2):e31761. Epub 2012 Feb 29.

Department of Medicine, University of Illinois, Chicago, Illinois, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0031761PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3290538PMC
July 2012

Mechanisms of apoptosis induced by anticancer compounds in melanoma cells.

Authors:
Andrei L Gartel

Curr Top Med Chem 2012 ;12(1):50-2

University of Illinois at Chicago, Department of Medicine, 840, S. Wood St., Room 1041, Chicago, IL 60612, USA.

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http://dx.doi.org/10.2174/156802612798919196DOI Listing
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 Efthimios Sivridis Vojtech Skop Vladimir P Skulachev Ruth S Slack Soraya S Smaili Duncan R Smith Maria S Soengas Thierry Soldati Xueqin Song Anil K Sood Tuck Wah Soong Federica Sotgia Stephen A Spector Claudia D Spies Wolfdieter Springer Srinivasa M Srinivasula Leonidas Stefanis Joan S Steffan Ruediger Stendel Harald Stenmark Anastasis Stephanou Stephan T Stern Cinthya Sternberg Björn Stork Peter Strålfors Carlos S Subauste Xinbing Sui David Sulzer Jiaren Sun Shi-Yong Sun Zhi-Jun Sun Joseph J Y Sung Kuninori Suzuki Toshihiko Suzuki Michele S Swanson Charles Swanton Sean T Sweeney Lai-King Sy Gyorgy Szabadkai Ira Tabas Heinrich Taegtmeyer Marco Tafani Krisztina Takács-Vellai Yoshitaka Takano Kaoru Takegawa Genzou Takemura Fumihiko Takeshita Nicholas J Talbot Kevin S W Tan Keiji Tanaka Kozo Tanaka Daolin Tang Dingzhong Tang Isei Tanida Bakhos A Tannous Nektarios Tavernarakis Graham S Taylor Gregory A Taylor J Paul Taylor Lance S Terada Alexei Terman Gianluca Tettamanti Karin Thevissen 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 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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

Combination with bortezomib enhances the antitumor effects of nanoparticle-encapsulated thiostrepton.

Cancer Biol Ther 2012 Feb;13(3):184-9

Department of Medicine; University of Illinois at Chicago; Chicago, IL USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3336074PMC
February 2012

Micelle-encapsulated thiostrepton as an effective nanomedicine for inhibiting tumor growth and for suppressing FOXM1 in human xenografts.

Mol Cancer Ther 2011 Dec 8;10(12):2287-97. Epub 2011 Sep 8.

Department of Medicine, University of Illinois at Chicago, 840, S. Wood St., Chicago, IL 60612, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3237785PMC
December 2011

Nucleophosmin interacts with FOXM1 and modulates the level and localization of FOXM1 in human cancer cells.

J Biol Chem 2011 Dec 6;286(48):41425-33. Epub 2011 Oct 6.

Department of Medicine, University of Illinois, Chicago, Illinois 60612, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3308854PMC
December 2011

Thiostrepton, proteasome inhibitors and FOXM1.

Authors:
Andrei L Gartel

Cell Cycle 2011 Dec 15;10(24):4341-2. Epub 2011 Dec 15.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3272263PMC
December 2011

The suppression of FOXM1 and its targets in breast cancer xenograft tumors by siRNA.

Oncotarget 2011 Dec;2(12):1218-26

Department of Medicine, University of Illinois at Chicago, Chicago, IL, 60612, USA.

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http://dx.doi.org/10.18632/oncotarget.359DOI Listing
December 2011

Proteasome inhibitors suppress expression of NPM and ARF proteins.

Cell Cycle 2011 Nov 15;10(22):3827-9. Epub 2011 Nov 15.

Department of Medicine, University of Illinois at Chicago, Chicago, IL, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3266112PMC
November 2011

FoxM1 knockdown sensitizes human cancer cells to proteasome inhibitor-induced apoptosis but not to autophagy.

Cell Cycle 2011 Oct 1;10(19):3269-73. Epub 2011 Oct 1.

Department of Medicine, University of Illinois at Chicago, Chicago, IL, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3233624PMC
October 2011

Thiazole antibiotic thiostrepton synergize with bortezomib to induce apoptosis in cancer cells.

PLoS One 2011 Feb 18;6(2):e17110. Epub 2011 Feb 18.

Department of Medicine, University of Illinois at Chicago, Chicago, Illinois, United States of America.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3041825PMC
February 2011

Proteasome inhibitory activity of thiazole antibiotics.

Cancer Biol Ther 2011 Jan 1;11(1):43-7. Epub 2011 Jan 1.

Department of Medicine, University of Illinois at Chicago Chicago, IL, USA.

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http://dx.doi.org/10.4161/cbt.11.1.13854DOI Listing
January 2011

Proteasome inhibitors induce p53-independent apoptosis in human cancer cells.

Am J Pathol 2011 Jan 23;178(1):355-60. Epub 2010 Dec 23.

Department of Medicine, University of Illinois at Chicago, Chicago, Illinois, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069903PMC
January 2011

New potential anti-cancer agents synergize with bortezomib and ABT-737 against prostate cancer.

Prostate 2010 Jun;70(8):825-33

Department of Medicine, University of Illinois, Chicago, Illinois, USA.

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June 2010

ARC synergizes with ABT-737 to induce apoptosis in human cancer cells.

Mol Cancer Ther 2010 Jun 1;9(6):1688-96. Epub 2010 Jun 1.

Department of Medicine, University of Illinois at Chicago, Chicago, Illinois 60612, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2902270PMC
June 2010

A new target for proteasome inhibitors: FoxM1.

Authors:
Andrei L Gartel

Expert Opin Investig Drugs 2010 Feb;19(2):235-42

University of Illinois at Chicago, Department of Medicine, 840 S. Wood St., Room 1041, Chicago, IL 60612, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3532816PMC
February 2010

p53 negatively regulates expression of FoxM1.

Cell Cycle 2009 Oct 25;8(20):3425-7. Epub 2009 Oct 25.

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October 2009

Wild-type p53 protects normal cells against apoptosis induced by thiostrepton.

Cell Cycle 2009 Sep 2;8(17):2850-1. Epub 2009 Sep 2.

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September 2009

Thiazole antibiotics target FoxM1 and induce apoptosis in human cancer cells.

PLoS One 2009 18;4(5):e5592. Epub 2009 May 18.

Department of Medicine, University of Illinois at Chicago, Chicago, Illinois, United States of America.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2680058PMC
August 2009

FoxM1 is a general target for proteasome inhibitors.

PLoS One 2009 Aug 12;4(8):e6593. Epub 2009 Aug 12.

Department of Medicine, University of Illinois at Chicago, Chicago, IL, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2721658PMC
August 2009

A novel mode of FoxM1 regulation: positive auto-regulatory loop.

Cell Cycle 2009 Jun 9;8(12):1966-7. Epub 2009 Jun 9.

Department of Medicine, University of Illinois at Chicago, Chicago, IL 60612, USA.

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June 2009

p21(WAF1/CIP1) and cancer: a shifting paradigm?

Authors:
Andrei L Gartel

Biofactors 2009 Mar-Apr;35(2):161-4

Department of Medicine, University of Illinois at Chicago, Chicago, IL, USA.

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June 2009

Transcriptional inhibitors, p53 and apoptoss.

Authors:
Andrei L Gartel

Biochim Biophys Acta 2008 Dec 8;1786(2):83-6. Epub 2008 May 8.

Department of Medicine, University of Illinois at Chicago, Chicago, IL 60612, USA.

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December 2008

[Novel anticancer compounds induce apoptosis in human tumor cells].

Authors:
Andrei L Gartel

Ai Zheng 2008 Jul;27(7):675-6

Department of Medicine, University of Illinois at Chicago, Chicago, IL 60612, USA.

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July 2008

FoxM1 inhibitors as potential anticancer drugs.

Authors:
Andrei L Gartel

Expert Opin Ther Targets 2008 Jun;12(6):663-5

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June 2008

Novel anticancer compounds induce apoptosis in melanoma cells.

Cell Cycle 2008 Jun 30;7(12):1851-5. Epub 2008 Jun 30.

Department of Medicine, University of Illinois at Chicago, Chicago, Illinois 60612, USA.

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June 2008

miRNAs: Little known mediators of oncogenesis.

Semin Cancer Biol 2008 Apr 16;18(2):103-10. Epub 2008 Jan 16.

Department of Medicine, University of Illinois at Chicago, 840, South Wood Street, Room 1041, Chicago, IL 60612, United States.

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April 2008

Differential sensitivity of human colon cancer cell lines to the nucleoside analogs ARC and DRB.

Int J Cancer 2008 Mar;122(6):1426-9

Department of Medicine, University of Illinois at Chicago, Chicago, IL 60612, USA.

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http://dx.doi.org/10.1002/ijc.23239DOI Listing
March 2008

FOXM1: the Achilles' heel of cancer?

Nat Rev Cancer 2008 Mar;8(3):c1; author reply c2

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http://dx.doi.org/10.1038/nrc2223-c1DOI Listing
March 2008

P21(WAF1/CIP1) may be a tumor suppressor after all.

Authors:
Andrei L Gartel

Cancer Biol Ther 2007 Aug 9;6(8):1171-2. Epub 2007 Jul 9.

Department of Medicine, University of Illinois at Chicago, Chicago, Illinois 60612 USA,

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http://dx.doi.org/10.4161/cbt.6.8.4712DOI Listing
August 2007

Inducer and inhibitor: "antagonistic duality" of p21 in differentiation.

Authors:
Andrei L Gartel

Leuk Res 2006 Oct 5;30(10):1215-6. Epub 2006 Apr 5.

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October 2006

Identification of a chemical inhibitor of the oncogenic transcription factor forkhead box M1.

Cancer Res 2006 Oct;66(19):9731-5

Department of Medicine, University of Illinois at Chicago, Chicago, IL 60612, USA.

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http://dx.doi.org/10.1158/0008-5472.CAN-06-1576DOI Listing
October 2006

Is p21 an oncogene?

Authors:
Andrei L Gartel

Mol Cancer Ther 2006 Jun;5(6):1385-6

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http://dx.doi.org/10.1158/1535-7163.MCT-06-0163DOI Listing
June 2006

RNA interference in cancer.

Biomol Eng 2006 Mar 8;23(1):17-34. Epub 2006 Feb 8.

Department of Medicine, University of Illinois at Chicago, 60612, USA.

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http://dx.doi.org/10.1016/j.bioeng.2006.01.002DOI Listing
March 2006

A novel transcriptional inhibitor induces apoptosis in tumor cells and exhibits antiangiogenic activity.

Cancer Res 2006 Mar;66(6):3264-70

Department of Medicine, University of Illinois at Chicago, Illinois 60612, USA.

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http://dx.doi.org/10.1158/0008-5472.CAN-05-3940DOI Listing
March 2006

CDK9 phosphorylates p53 on serine residues 33, 315 and 392.

Cell Cycle 2006 Mar 1;5(5):519-21. Epub 2006 Mar 1.

Department of Medicine, University of Illinois at Chicago, Chicago, Illinois 60612, USA.

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March 2006

The conflicting roles of the cdk inhibitor p21(CIP1/WAF1) in apoptosis.

Authors:
Andrei L Gartel

Leuk Res 2005 Nov;29(11):1237-8

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November 2005

Lost in transcription: p21 repression, mechanisms, and consequences.

Cancer Res 2005 May;65(10):3980-5

Department of Medicine, University of Illinois at Chicago, Chicago, Illinois 60612, USA.

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May 2005

The PPAR-gamma agonist pioglitazone post-transcriptionally induces p21 in PC3 prostate cancer but not in other cell lines.

Cell Cycle 2005 Apr 2;4(4):582-4. Epub 2005 Apr 2.

Department of Medicine, University of Illinois at Chicago, Chicago, Ilinois 60612, USA.

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April 2005

A novel p21WAF1/CIP1 transcript is highly dependent on p53 for its basal expression in mouse tissues.

Oncogene 2004 Oct;23(49):8154-7

Department of Medicine, 840 S Wood St, University of Illinois at Chicago, Chicago, IL 60612, USA.

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http://www.nature.com/articles/1207820
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October 2004

Myc-ARF (alternate reading frame) interaction inhibits the functions of Myc.

J Biol Chem 2004 Aug 15;279(35):36698-707. Epub 2004 Jun 15.

Department of Biochemistry and Molecular Genetics, University of Illinois at Chicago, 900 S. Ashland Avenue, Chicago, IL 60607, USA.

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http://dx.doi.org/10.1074/jbc.M312305200DOI Listing
August 2004

RNA interference as a new strategy against viral hepatitis.

Virology 2004 Jun;323(2):173-81

Department of Medicine, University of Illinois at Chicago, Chicago, IL 60612, USA.

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http://dx.doi.org/10.1016/j.virol.2004.02.021DOI Listing
June 2004

A new method for determining the status of p53 in tumor cell lines of different origin.

Oncol Res 2003 ;13(6-10):405-8

Department of Molecular Genetics, University of Illinois at Chicago, 900 S. Ashland Ave. Chicago, IL 60607, USA.

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http://dx.doi.org/10.3727/096504003108748429DOI Listing
July 2003

Mechanisms of c-myc-mediated transcriptional repression of growth arrest genes.

Exp Cell Res 2003 Feb;283(1):17-21

Department of Molecular Genetics, M/C 669, 900 S Ashland Avenue, University of Illinois at Chicago, Chicago, IL 60607, USA.

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http://dx.doi.org/10.1016/s0014-4827(02)00020-4DOI Listing
February 2003

The role of the cyclin-dependent kinase inhibitor p21 in apoptosis.

Mol Cancer Ther 2002 Jun;1(8):639-49

Department of Molecular Genetics, University of Illinois College of Medicine, Chicago, Illinois 60607, USA.

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June 2002

A Novel P53-Related Activity in a Colon Adenocarcinoma Cell Line With Mutant P53.

ScientificWorldJournal 2001 23;1:36. Epub 2001 Oct 23.

Department of Molecular Genetics, University of Illinois at Chicago, 900 S. Ashland Ave., Chicago, IL 60607, USA.

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http://dx.doi.org/10.1100/tsw.2001.162DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6084099PMC
October 2001