Guidelines for the use and interpretation of assays for monitoring autophagy

Klionsky, Daniel J., Abdalla, Fabio C., Abeliovich, Hagai, Abraham, Robert T., Acevedo-Arozena, Abraham, Adeli, Khosrow, Agholme, Lotta, Agnello, Maria, Agostinis, Patrizia, Aguirre-Ghiso, Julio A., Ahn, Hyung Jun, Ait-Mohamed, Ouardia, Ait-Si-Ali, Slimane, Akematsu, Takahiko, Akira, Shizuo, Al-Younes, Hesham M., Al-Zeer, Munir A., Albert, Matthew L., Albin, Roger L., Alegre-Abarrategui, Javier, Aleo, Maria Francesca, Alirezaei, Mehrdad, Almasan, Alexandru, Almonte-Becerril, Maylin, Amano, Atsuo, Amaravadi, Ravi K., Amarnath, Shoba, Amer, Amal O., Andrieu-Abadie, Nathalie, Anantharam, Vellareddy, Ann, David K., Anoopkumar-Dukie, Shailendra, Aoki, Hiroshi, Apostolova, Nadezda, Arancia, Giuseppe, Aris, John P., Asanuma, Katsuhiko, Asare, Nana Y.O., Ashida, Hisashi, Askanas, Valerie, Askew, David S., Auberger, Patrick, Baba, Misuzu, Backues, Steven K., Baehrecke, Eric H., Bahr, Ben A., Bai, Xue-Yuan, Bailly, Yannick, Baiocchi, Robert, Baldini, Giulia, Balduini, Walter, Ballabio, Andrea, Bamber, Bruce A., Bampton, Edward T.W., Juhász, Gábor, Bartholomew, Clinton R., Bassham, Diane C., Bast, Robert C., Batoko, Henri, Bay, Boon-Huat, Beau, Isabelle, Béchet, Daniel M., Begley, Thomas J., Behl, Christian, Behrends, Christian, Bekri, Soumeya, Bellaire, Bryan, Bendall, Linda J., Benetti, Luca, Berliocchi, Laura, Bernardi, Henri, Bernassola, Francesca, Besteiro, Sébastien, Bhatia-Kissova, Ingrid, Bi, Xiaoning, Biard-Piechaczyk, Martine, Blum, Janice S., Boise, Lawrence H., Bonaldo, Paolo, Boone, David L., Bornhauser, Beat C., Bortoluci, Karina R., Bossis, Ioannis, Bost, Frédéric, Bourquin, Jean-Pierre, Boya, Patricia, Boyer-Guittaut, Michaël, Bozhkov, Peter V., Brady, Nathan R, Brancolini, Claudio, Brech, Andreas, Brenman, Jay E., Brennand, Ana, Bresnick, Emery H., Brest, Patrick, Bridges, Dave, Bristol, Molly L., Brookes, Paul S., Brown, Eric J., Brumell, John H., Brunetti-Pierri, Nicola, Brunk, Ulf T., Bulman, Dennis E., Bultman, Scott J., Bultynck, Geert, Burbulla, Lena F., Bursch, Wilfried, Butchar, Jonathan P., Buzgariu, Wanda, Bydlowski, Sergio P., Cadwell, Ken, Cahová, Monika, Cai, Dongsheng, Cai, Jiyang, Cai, Qian, Calabretta, Bruno, Calvo-Garrido, Javier, Camougrand, Nadine, Campanella, Michelangelo, Campos-Salinas, Jenny, Candi, Eleonora, Cao, Lizhi, Caplan, Allan B., Carding, Simon R., Cardoso, Sandra M., Carew, Jennifer S., Carlin, Cathleen R., Carmignac, Virginie, Carneiro, Leticia A.M., Carra, Serena, Caruso, Rosario A., Casari, Giorgio, Casas, Caty, Castino, Roberta, Cebollero, Eduardo, Cecconi, Francesco, Celli, Jean, Chaachouay, Hassan, Chae, Han-Jung, Chai, Chee-Yin, Chan, David C., Chan, Edmond Y., Chang, Raymond Chuen-Chung, Che, Chi-Ming, Chen, 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, Cheng, Alan, Cheng, Christopher H.K., Cheng, Yan, Cheong, Heesun, Cheong, Jae-Ho, Cherry, Sara, Chess-Williams, Russ, Cheung, Zelda H., Chevet, Eric, Chiang, Hui-Ling, Chiarelli, Roberto, Chiba, Tomoki, Chin, Lih-Shen, Chiou, Shih-Hwa, Chisari, Francis V., Cho, Chi Hin, Cho, Dong-Hyung, Choi, Augustine M.K., Choi, DooSeok, Choi, Kyeong Sook, Choi, Mary E., Chouaib, Salem, Choubey, Divaker, Choubey, Vinay, Chu, Charleen T., Chuang, Tsung-Hsien, Chueh, Sheau-Huei, Chun, Taehoon, Chwae, Yong-Joon, Chye, Mee-Len, Ciarcia, Roberto, Ciriolo, Maria R., Clague, Michael J., Clark, Robert S.B., Clarke, Peter G.H., Clarke, Robert, Codogno, Patrice, Coller, Hilary A., Colombo, María I., Comincini, Sergio, Condello, Maria, Condorelli, Fabrizio, Cookson, Mark R., Coombs, Graham H., Coppens, Isabelle, Corbalan, Ramon, Cossart, Pascale, Costelli, Paola, Costes, Safia, Coto-Montes, Ana, Couve, Eduardo, Coxon, Fraser P., Cregg, James M., Crespo, José L., Cronjé, Marianne J., Cuervo, Ana Maria, Cullen, Joseph J., Czaja, Mark J., D'Amelio, Marcello, Darfeuille-Michaud, Arlette, Davids, Lester M., Davies, Faith E., De Felici, Massimo, de Groot, John F., de Haan, Cornelis A.M., De Martino, Luisa, De Milito, Angelo, De Tata, Vincenzo, Debnath, Jayanta, Degterev, Alexei, Dehay, Benjamin, Delbridge, Lea M.D., Demarchi, Francesca, Deng, Yi Zhen, Dengjel, Jörn, Dent, Paul, Denton, Donna, Deretic, Vojo, Desai, Shyamal D., Devenish, Rodney J., Di Gioacchino, Mario, Di Paolo, Gilbert, Di Pietro, Chiara, Díaz-Araya, Guillermo, Díaz-Laviada, Inés, Diaz-Meco, Maria T., Diaz-Nido, Javier, Dikic, Ivan, Dinesh-Kumar, Savithramma P., Ding, Wen-Xing, Distelhorst, Clark W., Diwan, Abhinav, Djavaheri-Mergny, Mojgan, Dokudovskaya, Svetlana, Dong, Zheng, Dorsey, Frank C., Dosenko, Victor, Dowling, James J., Doxsey, Stephen, Dreux, Marlène, Drew, Mark E., Duan, Qiuhong, Duchosal, Michel A., Duff, Karen E., Dugail, Isabelle, Durbeej, Madeleine, Duszenko, Michael, Edelstein, Charles L., Edinger, Aimee L., Egea, Gustavo, Eichinger, Ludwig, Eissa, N. Tony, Ekmekcioglu, Suhendan, El-Deiry, Wafik S., Elazar, Zvulun, Elgendy, Mohamed, Ellerby, Lisa M., Eng, Kai Er, Engelbrecht, Anna-Mart, Engelender, Simone, Erenpreisa, Jekaterina, Escalante, Ricardo, Esclatine, Audrey, Eskelinen, Eeva-Liisa, Espert, Lucile, Espina, Virginia, Fan, Huizhou, Fan, Jia, Fan, Qi-Wen, Fan, Zhen, Fang, Shengyun, Fang, Yongqi, Fanto, Manolis, Fanzani, Alessandro, Farkas, Thomas, Farre, Jean-Claude, Faure, Mathias, Fechheimer, Marcus, Feng, Carl G., Feng, Jian, Feng, Qili, Feng, Youji, Fésüs, László, Feuer, Ralph, Figueiredo-Pereira, Maria E., Fimia, Gian Maria, Fingar, Diane C., Finkbeiner, Steven, Finkel, Toren, Finley, Kim D., Fiorito, Filomena, Fisher, Edward A., Fisher, Paul B., Flajolet, Marc, Florez-McClure, Maria L., Florio, Salvatore, Fon, Edward A., Fornai, Francesco, Fortunato, Franco, Fotedar, Rati, Fowler, Daniel H., Fox, Howard S., Franco, Rodrigo, Frankel, Lisa B., Fransen, Marc, Fuentes, José M., Fueyo, Juan, Fujii, Jun, Fujisaki, Kozo, Fujita, Eriko, Fukuda, Mitsunori, Furukawa, Ruth H., Gaestel, Matthias, Gailly, Philippe, Gajewska, Malgorzata, Galliot, Brigitte, Galy, Vincent, Ganesh, Subramaniam, Ganetzky, Barry, Ganley, Ian G., Gao, Fen-Biao, Gao, George F., Gao, Jinming, Garcia, Lorena, Garcia-Manero, Guillermo, Garcia-Marcos, Mikel, Garmyn, Marjan, Gartel, Andrei L., Gatti, Evelina, Gautel, Mathias, Gawriluk, Thomas R., Gegg, Matthew E., Geng, Jiefei, Germain, Marc, Gestwicki, Jason E., Gewirtz, David A., Ghavami, Saeid, Ghosh, Pradipta, Giammarioli, Anna M., Giatromanolaki, Alexandra N., Gibson, Spencer B., Gilkerson, Robert W., Ginger, Michael L., Ginsberg, Henry N., Golab, Jakub, Goligorsky, Michael S., Golstein, Pierre, Gomez-Manzano, Candelaria, Goncu, Ebru, Gongora, Céline, Gonzalez, Claudio D., Gonzalez, Ramon, González-Estévez, Cristina, González-Polo, Rosa Ana, Gonzalez-Rey, Elena, Gorbunov, Nikolai V., Gorski, Sharon, Goruppi, Sandro, Gottlieb, Roberta A., Gozuacik, Devrim, Granato, Giovanna Elvira, Grant, Gary D., Green, Kim N., Gregorc, Ales, Gros, Frédéric, Grose, Charles, Grunt, Thomas W., Gual, Philippe, Guan, Jun-Lin, Guan, Kun-Liang, Guichard, Sylvie M., Gukovskaya, Anna S., Gukovsky, Ilya, Gunst, Jan, Gustafsson, Åsa B., Halayko, Andrew J., Hale, Amber N., Halonen, Sandra K., Hamasaki, Maho, Han, Feng, Han, Ting, Hancock, Michael K., Hansen, Malene, Harada, Hisashi, Harada, Masaru, Hardt, Stefan E., Harper, J. Wade, Harris, Adrian L., Harris, James, Harris, Steven D., Hashimoto, Makoto, Haspel, Jeffrey A., Hayashi, Shin-ichiro, Hazelhurst, Lori A., He, Congcong, He, You-Wen, Hébert, Marie-Josée, Heidenreich, Kim A., Helfrich, Miep H., Helgason, Gudmundur V., Henske, Elizabeth P., Herman, Brian, Herman, Paul K., Hetz, Claudio, Hilfiker, Sabine, Hill, Joseph A., Hocking, Lynne J., Hofman, Paul, Hofmann, Thomas G., Höhfeld, Jörg, Holyoake, Tessa L., Hong, Ming-Huang, Hood, David A., Hotamisligil, Gökhan S., Houwerzijl, Ewout J., Høyer-Hansen, Maria, Hu, Bingren, Hu, Chien-an A., Hu, Hong-Ming, Hua, Ya, Huang, Canhua, Huang, Ju, Huang, Shengbing, Huang, Wei-Pang, Huber, Tobias B., Huh, Won-Ki, Hung, Tai-Ho, Hupp, Ted R., Hur, Gang Min, Hurley, James B., Hussain, Sabah N.A., Hussey, Patrick J., Hwang, Jung Jin, Hwang, Seungmin, Ichihara, Atsuhiro, Ilkhanizadeh, Shirin, Inoki, Ken, Into, Takeshi, Iovane, Valentina, Iovanna, Juan L., Ip, Nancy Y., Isaka, Yoshitaka, Ishida, Hiroyuki, Isidoro, Ciro, Isobe, Ken-ichi, Iwasaki, Akiko, Izquierdo, Marta, Izumi, Yotaro, Jaakkola, Panu M., Jäättelä, Marja, Jackson, George R., Jackson, William T., Janji, Bassam, Jendrach, Marina, Jeon, Ju-Hong, Jeung, Eui-Bae, Jiang, Hong, Jiang, Hongchi, Jiang, Jean X., Jiang, Ming, Jiang, Qing, Jiang, Xuejun, Jiang, Xuejun, Jiménez, Alberto, Jin, Meiyan, Jin, Shengkan V., Joe, Cheol O., Johansen, Terje, Johnson, Daniel E., Johnson, Gail V.W., Jones, Nicola L., Joseph, Bertrand, Joseph, Suresh K., Joubert, Annie M., Juhász, Gábor, Juillerat-Jeanneret, Lucienne, Jung, Chang Hwa, Jung, Yong-Keun, Kaarniranta, Kai, Kaasik, Allen, Kabuta, Tomohiro, Kadowaki, Motoni, Kågedal, Katarina, Kamada, Yoshiaki, Kaminskyy, Vitaliy O., Kampinga, Harm H., Kanamori, Hiromitsu, Kang, Chanhee, Kang, Khong Bee, Kang, Kwang Il, Kang, Rui, Kang, Yoon-A, Kanki, Tomotake, Kanneganti, Thirumala-Devi, Kanno, Haruo, Kanthasamy, Anumantha G., Kanthasamy, Arthi, Karantza, Vassiliki, Kaushal, Gur P., Kaushik, Susmita, Kawazoe, Yoshinori, Ke, Po-Yuan, Kehrl, John H., Kelekar, Ameeta, Kerkhoff, Claus, Kessel, David H., Khalil, Hany, Kiel, Jan A.K.W., Kiger, Amy A., Kihara, Akio, Kim, 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, Kimchi, Adi, Kimmelman, Alec C., King, Jason S., Kinsella, Timothy J., Kirkin, Vladimir, Kirshenbaum, Lorrie A., Kitamoto, Katsuhiko, Kitazato, Kaio, Klein, Ludger, Klimecki, Walter T., Klucken, Jochen, Knecht, Erwin, Ko, Ben C.B., Koch, Jan C., Koga, Hiroshi, Koh, Jae-Young, Koh, Young Ho, Koike, Masato, Komatsu, Masaaki, Kominami, Eiki, Kong, Hee Jeong, Kong, Wei-Jia, Korolchuk, Viktor I., Kotake, Yaichiro, Koukourakis, Michael I., Flores, Juan B. Kouri, Kovács, Attila L., Kraft, Claudine, Krainc, Dimitri, Krämer, Helmut, Kretz-Remy, Carole, Krichevsky, Anna M., Kroemer, Guido, Krüger, Rejko, Krut, Oleg, Ktistakis, Nicholas T., Kuan, Chia-Yi, Kucharczyk, Roza, Kumar, Ashok, Kumar, Raj, Kumar, Sharad, Kundu, Mondira, Kung, Hsing-Jien, Kurz, Tino, Kwon, Ho Jeong, La Spada, Albert R., Lafont, Frank, Lamark, Trond, Landry, Jacques, Lane, Jon D., Lapaquette, Pierre, Laporte, Jocelyn F., László, Lajos, Lavandero, Sergio, Lavoie, Josée N., Layfield, Robert, Lazo, Pedro A., Le, Weidong, Le Cam, Laurent, Ledbetter, Daniel J., Lee, Alvin J.X., Lee, Byung-Wan, Lee, Gyun Min, Lee, Jongdae, lee, Ju-hyun, Lee, Michael, Lee, Myung-Shik, Lee, Sug Hyung, Leeuwenburgh, Christiaan, Legembre, Patrick, Legouis, Renaud, Lehmann, Michael, Lei, Huan-Yao, Lei, Qun-Ying, Leib, David A., Leiro, José, Lemasters, John J., Lemoine, Antoinette, Lesniak, Maciej S., Lev, Dina, Levenson, Victor V., Levine, Beth, Levy, Efrat, Li, Faqiang, Li, Jun-Lin, Li, Lian, Li, Sheng, Li, Weijie, Li, Xue-Jun, Li, Yan-Bo, Li, Yi-Ping, Liang, Chengyu, Liang, Qiangrong, Liao, Yung-Feng, Liberski, Pawel P., Lieberman, Andrew, Lim, Hyunjung J., Lim, Kah-Leong, Lim, Kyu, Lin, Chiou-Feng, Lin, Fu-Cheng, Lin, Jian, Lin, Jiandie D., Lin, Kui, Lin, Wan-Wan, Lin, Weei-Chin, Lin, Yi-Ling, Linden, Rafael, Lingor, Paul, Lippincott-Schwartz, Jennifer, Lisanti, Michael P., Liton, Paloma B., Liu, Bo, Liu, Chun-Feng, Liu, Kaiyu, Liu, Leyuan, Liu, Qiong A., Liu, Wei, Liu, Young-Chau, Liu, Yule, Lockshin, Richard A., Lok, Chun-Nam, Lonial, Sagar, Loos, Benjamin, Lopez-Berestein, Gabriel, López-Otín, Carlos, Lossi, Laura, Lotze, Michael T., Low, Peter, Lu, Binfeng, Lu, Bingwei, Lu, Bo, Lu, Zhen, Luciano, Fréderic, Lukacs, Nicholas W., Lund, Anders H., Lynch-Day, Melinda A., Ma, Yong, Macian, Fernando, MacKeigan, Jeff P., Macleod, Kay F., Madeo, Frank, Maiuri, Luigi, Maiuri, Maria Chiara, Malagoli, Davide, Malicdan, May Christine V., Malorni, Walter, Man, Na, Mandelkow, Eva-Maria, Manon, Stephen, Manov, Irena, Mao, Kai, Mao, Xiang, Mao, Zixu, Marambaud, Philippe, Marazziti, Daniela, Marcel, Yves L., Marchbank, Katie, Marchetti, Piero, Marciniak, Stefan J., Marcondes, Mateus, Mardi, Mohsen, Marfe, Gabriella, Mariño, Guillermo, Markaki, Maria, Marten, Mark R., Martin, Seamus J., Martinand-Mari, Camille, Martinet, Wim, Martinez-Vicente, Marta, Masini, Matilde, Matarrese, Paola, Matsuo, Saburo, Matteoni, Raffaele, Mayer, Andreas, Mazure, Nathalie M., McConkey, David J., McConnell, Melanie J., McDermott, Catherine, McDonald, Christine, McInerney, Gerald M., McKenna, Sharon L., McLaughlin, BethAnn, McLean, Pamela J., McMaster, Christopher R., McQuibban, G. Angus, Meijer, Alfred J., Meisler, Miriam H., Meléndez, Alicia, Melia, Thomas J., Melino, Gerry, Mena, Maria A., Menendez, Javier A., Menna-Barreto, Rubem F. 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Javier, Olsen, Laura J., Olsson, Stefan, Opota, Onya, Osborne, Timothy F., Ostrander, Gary K., Otsu, Kinya, Ou, Jing-hsiung James, Ouimet, Mireille, Overholtzer, Michael, Ozpolat, Bulent, Paganetti, Paolo, Pagnini, Ugo, Pallet, Nicolas, Palmer, Glen E., Palumbo, Camilla, Pan, Tianhong, Panaretakis, Theocharis, Pandey, Udai Bhan, Papackova, Zuzana, Papassideri, Issidora, Paris, Irmgard, Park, Junsoo, Park, Ohkmae K., Parys, Jan B., Parzych, Katherine R., Patschan, Susann, Patterson, Cam, Pattingre, Sophie, Pawelek, John M., Peng, Jianxin, Perlmutter, David H., Perrotta, Ida, Perry, George, Pervaiz, Shazib, Peter, Matthias, Peters, Godefridus J., Petersen, Morten, Petrovski, Goran, Phang, James M., Piacentini, Mauro, Pierre, Philippe, Pierrefite-Carle, Valérie, Pierron, Gérard, Pinkas-Kramarski, Ronit, Piras, Antonio, Piri, Natik, Platanias, Leonidas C., Pöggeler, Stefanie, Poirot, Marc, Poletti, Angelo, Poüs, Christian, Pozuelo-Rubio, Mercedes, Prætorius-Ibba, Mette, Prasad, Anil, Prescott, Mark, Priault, Muriel, Produit-Zengaffinen, Nathalie, Progulske-Fox, Ann, Proikas-Cezanne, Tassula, Przedborski, Serge, Przyklenk, Karin, Puertollano, Rosa, Puyal, Julien, Qian, Shu-Bing, Qin, Liang, Qin, Zheng-Hong, Quaggin, Susan E., Raben, Nina, Rabinowich, Hannah, Rabkin, Simon W., Rahman, Irfan, Rami, Abdelhaq, Ramm, Georg, Randall, Glenn, Randow, Felix, Rao, V. 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  1. SPHK1/sphingosine kinase 1-mediated autophagy differs between neurons and SH-SY5Y neuroblastoma cells
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  2. Gemcitabine-Induced Autophagy Protects Human Lung Cancer Cells from Apoptotic Death
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  3. Glutamate synthase MoGlt1‐mediated glutamate homeostasis is important for autophagy, virulence and conidiation in the rice blast fungus
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  4. Identification of autophagy related genes LC3 and ATG4 from yellow catfish Pelteobagrus fulvidraco and their transcriptional responses to waterborne and dietborne zinc exposure
    Chuan‐Chuan Wei, Zhi Luo, Yu–Feng Song, Ya‐Xiong Pan, Kun Wu, Wenjing You · 2017 · Chemosphere
  5. UBE2L6/UBCH8 and ISG15 attenuate autophagy in esophageal cancer cells
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  6. Haploinsufficiency networks identify targetable patterns of allelic deficiency in low mutation ovarian cancer
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  7. UVRAG Deficiency Exacerbates Doxorubicin-Induced Cardiotoxicity
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  8. Anti-proliferation of triple-negative breast cancer cells with physagulide P: ROS/JNK signaling pathway induces apoptosis and autophagic cell death
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  9. Antimony trichloride induces a loss of cell viability via reactive oxygen species-dependent autophagy in A549 cells
    Xinyuan Zhao, Fengjun Xing, Yewen Cong, Yin Zhuang, Muxi Han, Zhiqiang Wu, Shali Yu, Haiyan Wei, Xiaoke Wang, Gang Chen · 2017 · The International Journal of Biochemistry & Cell Biology
  10. Resveratrol ameliorates autophagic flux to promote functional recovery in rats after spinal cord injury
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  11. Designed Polymer Micelle for Clearing Amyloid Protein Aggregates via Up-Regulated Autophagy
    Koushik Debnath, Nihar Ranjan Jana, Nikhil Ranjan Jana · 2018 · ACS Biomaterials Science & Engineering
  12. Eicosapentaenoic Acid-Enriched Phosphatidylcholine Mitigated Aβ1-42-Induced Neurotoxicity via Autophagy-Inflammasome Pathway
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  13. Mitophagy contributes to endothelial adaptation to simulated microgravity
    Laura Locatelli, Alessandra Cazzaniga, Clara De Palma, Sara Castiglioni, Jeanette A.M. Maier · 2019 · The FASEB Journal
  14. Multifunctional peptide-assembled micelles for simultaneously reducing amyloid-β and reactive oxygen species
    Lei Li, Zhifeng Zou, Jin Liu, Zhiai Xu, Ying Fu, Yang Tian, Wen Zhang · 2021 · Chemical Science
  15. CDK4, CDK6/cyclin-D1 Complex Inhibition and Radiotherapy for Cancer Control: A Role for Autophagy
    Valerio Nardone, Marcella Barbarino, Antonio Angrisani, Pierpaolo Correale, Pierpaolo Pastina, Salvatore Cappabianca, Alfonso Reginelli, Luciano Mutti, Clelia Miracco, Rocco Giannicola et al. · 2021 · International Journal of Molecular Sciences
  16. ATM regulates cell fate choice upon p53 activation by modulating mitochondrial turnover and ROS levels
    Kelly D. Sullivan, Vignesh V Palaniappan, Joaquin Maximiliano Espinosa · 2014 · Cell Cycle
  17. Deletion of ATG5 Shows a Role of Autophagy in Salivary Homeostatic Control
    Maria E. Morgan-Bathke, Her Helen Lin, Alejandro Martinez Chibly, W. Zhang, Xiao‐Jian Sun, C.-H. Chen, Per Flodby, Zea Borok, Reen Wu, Deborah G. Arnett et al. · 2013 · Journal of Dental Research
  18. A Novel Sulindac Derivative Inhibits Lung Adenocarcinoma Cell Growth through Suppression of Akt/mTOR Signaling and Induction of Autophagy
    Evrim Gurpinar, William E. Grizzle, John J. Shacka, Burton J. Mader, Li Nan, Nicholas A. Piazza, Suzanne M. Russo, Adam B. Keeton, Gary Anthony Piazza · 2013 · Molecular Cancer Therapeutics
  19. Mutation of kri1l causes definitive hematopoiesis failure via PERK-dependent excessive autophagy induction
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  20. Motoneuronal and muscle-selective removal of ALS-related misfolded proteins
    V. Crippa, M. Galbiati, Alessandra Boncoraglio, P. Rusmini, Elisa Onesto, Elisa Giorgetti, Riccardo Cristofani, A. Zito, Angelo Poletti · 2013 · Biochemical Society Transactions
  21. Autophagy supports color vision
    Zhou, Zhenqing, Vinberg, Frans, Schottler, Frank, Doggett, Teresa A, Kefalov, Vladimir J, Ferguson, Thomas A · 2015 · Autophagy
  22. Mitochondria-lysosome-related organelles mediate mitochondrial clearance during cellular dedifferentiation
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  23. Synthesis of Improved Lysomotropic Autophagy Inhibitors
    Tong Wang, Megan L. Goodall, Paul Alan Gonzales, Mario Sepulveda, Katie R. Martin, Stephen Thomas Gately, Jeffrey P. MacKeigan · 2015 · Journal of Medicinal Chemistry
  24. Inhibition of mTOR Prevents ROS Production Initiated by Ethidium Bromide-Induced Mitochondrial DNA Depletion
    Timothy Nacarelli, Ashley Azar, Christian Sell · 2014 · Frontiers in Endocrinology
  25. Involvement of autophagy in the direct ER to vacuole protein trafficking route in plants
    Simon Michaeli, Tamar Avin‐Wittenberg, Gad Galili · 2014 · Frontiers in Plant Science
  26. Impairment of autophagosome-lysosome fusion contributes to chronic ethanol-induced liver injury
    Hong‐Ik Cho, Joo-Wan Choi, Sun‐Mee Lee · 2014 · Alcohol
  27. Context-dependent role of ATG4B as target for autophagy inhibition in prostate cancer therapy
    Elisa Tran, Annabelle Chow, Takeshi Goda, Amy Wong, Kim M. Blakely, Michelle Rocha, Samira Taeb, Van C. Hoang, Stanley K. Liu, Urban Emmenegger · 2013 · Biochemical and Biophysical Research Communications
  28. How to Take Autophagy and Endocytosis Up a Notch
    Julia M. I. Barth, Katja Köhler · 2014 · BioMed Research International
  29. Autophagic flux and autophagosome morphogenesis require the participation of sphingolipids
    Chiara Tommasino, Matteo Marconi, Laura Ciarlo, Paola Matarrese, Walter Malorni · 2015 · APOPTOSIS
  30. Inhibition of Mitochondrial Clearance and Cu/Zn-SOD Activity Enhance 6-Hydroxydopamine-Induced Neuronal Apoptosis
    Sua In, Chang-Won Hong, Boyoung Choi, Bong-Geum Jang, Min-Ju Kim · 2015 · Molecular Neurobiology
  31. Radiosensitizing effect of carboplatin and paclitaxel to carbon-ion beam irradiation in the non-small-cell lung cancer cell line H460
    Nobuteru Kubo, Shin‐ei Noda, Akihisa Takahashi, Yukari Yoshida, Takahiro Oike, Kazutoshi Murata, Atsushi Musha, Yoshiyuki Suzuki, Tatsuya Ohno, Takeo Takahashi et al. · 2015 · Journal of Radiation Research
  32. Inhibition of autophagy augments the anticancer activity of α-mangostin in chronic myeloid leukemia cells
    Jia-Jie Chen, Zi‐Jie Long, Dong-Fan Xu · 2013 · Leukemia & lymphoma/Leukemia and lymphoma
  33. Impaired autophagy affects acid α‐glucosidase processing and enzyme replacement therapy efficacy in late‐onset glycogen storage disease type II
    Anna Chiara Nascimbeni, Marina Fanin, Elisabetta Tasca, Corrado Italo Angelini, Marco Sandri · 2015 · Neuropathology and Applied Neurobiology
  34. Elastase induces lung epithelial cell autophagy through placental growth factor
    Hsin‐Han Hou, Shih-Lung Cheng, Kuei‐Pin Chung, Mark Yen‐Ping Kuo, Cheng‐Chang Yeh, Bei‐En Chang, Hsuan‐Hsuan Lu, Hao‐Chien Wang, Chong‐Jen Yu · 2014 · Autophagy
  35. Ethanol-mediated activation of the NLRP3 inflammasome in iPS cells and iPS cells-derived neural progenitor cells
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  36. βIII-Tubulin alters glucose metabolism and stress response signaling to promote cell survival and proliferation in glucose-starved non-small cell lung cancer cells
    Amelia L. Parker, Nigel A. Turner, Joshua A. McCarroll, Maria Kavallaris · 2016 · Carcinogenesis
  37. MEK Inhibition Sensitizes Precursor B-Cell Acute Lymphoblastic Leukemia (B-ALL) Cells to Dexamethasone through Modulation of mTOR Activity and Stimulation of Autophagy
    Anna Polak, Przemysław Kiliszek, Tomasz Sewastianik, Maciej Szydłowski, Ewa Jabłońska, Emilia Białopiotrowicz, Patryk Górniak, Sergiusz Markowicz, Eliza Nowak, Monika Anna Grygorowicz et al. · 2016 · PLoS ONE
  38. Effect of natural uranium on the UMR-106 osteoblastic cell line: impairment of the autophagic process as an underlying mechanism of uranium toxicity
    Valérie Pierrefite‐Carle, Sabine Santucci‐Darmanin, Véronique Breuil, Tatiana Gritsaenko, Claude Vidaud, Gaëlle Creff, Pier Lorenzo Solari, Sophie Pagnotta, Rasha Al-Sahlanee, Christophe Den Auwer et al. · 2016 · Archives of Toxicology
  39. Autophagy inhibition impairs the epithelial-mesenchymal transition and enhances cisplatin sensitivity in nasopharyngeal carcinoma
    Zhongwu Su, Guo Li, Chao Liu, Shuling Ren, Tengbo Deng, Shuiting Zhang, Yongquan Tian, Yong Liu, Yuanzheng Qiu · 2017 · Oncology Letters
  40. Degradation of protein translation machinery by amino acid starvation-induced macroautophagy
    Christine Gretzmeier, Sven Eiselein, Gregory R. Johnson, Rudolf Engelke, Heike Nowag, Mostafa Zarei, Victoria Küttner, Andrea C. Becker, Kristoffer T. G. Rigbolt, Maria Helena Høyer-Hansen et al. · 2017 · Autophagy
  41. Liraglutide activates autophagyviaGLP-1R to improve functional recovery after spinal cord injury
    Jian Chen, Zhouguang Wang, Yuqin Mao, Zengming Zheng, Yu Chen, Sinan Khor, Kesi Shi, Zili He, Jiawei Li, Fanghua Gong et al. · 2017 · Oncotarget
  42. Downregulated apoptosis and autophagy after anti‐Aβ immunotherapy in Alzheimer's disease
    Claire Paquet, James A. R. Nicoll, Seth Love, François Mouton‐Liger, Clive Holmes, Jacques Hugon, Delphine Boche · 2017 · Brain Pathology
  43. Helicobacter pyloricholesterol glucosylation modulates autophagy for increasing intracellular survival in macrophages
    Chih‐Ho Lai, Ju-Chun Huang, Hsin‐Hung Cheng et al. · 2018 · Cellular Microbiology
  44. Autophagy: A necessary process during the Trypanosoma cruzi life-cycle
    Betiana Nebaí Salassa, Patricia Silvia Romano · 2018 · Virulence
  45. Molecular Determinants of Cancer Therapy Resistance to HDAC Inhibitor-Induced Autophagy
    Maria Mrakovcic, Leopold F. Fröhlich · 2019 · Cancers
  46. Hippocampal ornithine decarboxylase/spermidine pathway mediates H2S-alleviated cognitive impairment in diabetic rats: Involving enhancment of hippocampal autophagic flux
    Xuan Kang, Li Cheng, Yan Shi Xie · 2020 · Journal of Advanced Research
  47. Identification of autophagy‐related long non‐coding RNA prognostic signature for breast cancer
    Qianxue Wu, Qing Li, Wenming Zhu, Xiang Zhang, Hongyuan Li · 2021 · Journal of Cellular and Molecular Medicine
  48. Neuroprotective Effect of Alpha-asarone on the Rats Model of Cerebral Ischemia–Reperfusion Stroke via Ameliorating Glial Activation and Autophagy
    Kun Zhang, Qi Liu, Lijun Luo · 2021 · Neuroscience
  49. Secretion of pro‐angiogenic extracellular vesicles during hypoxia is dependent on the autophagy‐related protein GABARAPL1
    Tom G. Keulers, Sten F.W.M. Libregts, Joël E.J. Beaumont, Kim G.M. Savelkouls, Johan Bussink, Hans Duimel, Ludwig Jerome Dubois, Marijke I. Zonneveld, Carmen López‐Iglesias, Karel Bezstarosti et al. · 2021 · Journal of Extracellular Vesicles
  50. Autophagy in light-induced retinal damage
    Yu Chen, Lindsay Perusek, Akiko Maeda · 2015 · Experimental Eye Research
  51. Autophagy plays a protective role as an anti‐oxidant system in human T cells and represents a novel strategy for induction of T ‐cell apoptosis
    Ryu Watanabe, Hiroshi Fujii, Tsuyoshi Shirai, Shinichiro Saito, Tomonori Ishii, Hideo Harigae · 2014 · European Journal of Immunology
  52. Herp depletion protects from protein aggregation by up-regulating autophagy
    Clara Quiroga, Damián Gatica, Felipe Paredes, Roberto Bravo, Rodrigo Troncoso, Zully Pedrozo, Andrea E. Rodriguez, Barbra Toro, Mario Chiong, Jose Miguel Vicencio et al. · 2013 · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research
  53. Essential Role of the Redox-Sensitive Kinase p66 shc in Determining Energetic and Oxidative Status and Cell Fate in Neuronal Preconditioning
    Jacquelynn E. Brown, Stephanie L.H. Zeiger, Jane C. Hettinger, Joshua D. Brooks, Benjamin Holt, Jason D. Morrow, Erik S. Musiek, Ginger L. Milne, BethAnn McLaughlin · 2010 · Journal of Neuroscience
  54. Mask loss-of-function rescues mitochondrial impairment and muscle degeneration of Drosophila pink1 and parkin mutants
    Mingwei Zhu, Xia Li, Xiaolin Tian, Chunlai Wu · 2015 · Human Molecular Genetics
  55. Involvement of PRRSV NSP3 and NSP5 in the autophagy process
    Wei Zhang, Keren Chen, Yang Guo · 2019 · Virology Journal
  56. Loss of long‐chain acyl‐CoA synthetase isoform 1 impairs cardiac autophagy and mitochondrial structure through mechanistic target of rapamycin complex 1 activation
    Trisha Jean Grevengoed, Daniel E. Cooper, Pamela A. Young, Jessica Mary Ellis, Rosalind Coleman · 2015 · The FASEB Journal
  57. Role of autophagy in cancer prevention, development and therapy
    G. Vignir Helgason, Tessa L. Holyoake, Kevin M. Ryan · 2013 · Essays in Biochemistry
  58. Glucocorticoids induce autophagy in rat bone marrow mesenchymal stem cells
    Long Wang, Jing Fan, Yanshui Lin, Yunshan Guo, Bo Gao, QI-YUE SHI, Bo-Yuan Wei, Li Chen, Liu Yang, Jian Liu et al. · 2014 · Molecular Medicine Reports
  59. Recent progress in research on molecular mechanisms of autophagy in the heart
    Yasuhiro Maejima, Yun Chen, Mitsuaki Isobe, Åsa B. Gustafsson, Richard N. Kitsis, Junichi Sadoshima · 2014 · American Journal of Physiology-Heart and Circulatory Physiology
  60. Resveratrol regulates autophagy signaling in chronically ischemic myocardium
    Ashraf A. Sabe, Nassrene Y. Elmadhun, Rahul S. Dalal, Michael P. Robich, Frank William Sellke · 2013 · Journal of Thoracic and Cardiovascular Surgery
  61. Modulatory roles of glycolytic enzymes in cell death
    Claudia Cerella, Mario A. Dicato, Marc F. Diederich · 2014 · Biochemical Pharmacology
  62. Melatonin Reverses Fas, E2F-1 and Endoplasmic Reticulum Stress Mediated Apoptosis and Dysregulation of Autophagy Induced by the Herbicide Atrazine in Murine Splenocytes
    Shweta Sharma, Jayanta Sarkar, Chandana Haldar, Sudhir Kumar Sinha · 2014 · PLoS ONE
  63. Interleukin-1 receptor-associated kinase M (IRAK-M) promotes human rhinovirus infection in lung epithelial cells via the autophagic pathway
    Qun Wu, Linda Faye van Dyk, Di Jiang, Azzeddine Dakhama, Liwu Li, Steven R. White, Ashley Gross, Hong Wei Chu · 2013 · Virology
  64. Association of Dioxin and Other Persistent Organic Pollutants (POPs) with Diabetes: Epidemiological Evidence and New Mechanisms of Beta Cell Dysfunction
    Vincenzo De Tata · 2014 · International Journal of Molecular Sciences
  65. Environmental Stress Affects the Activity of Metabolic and Growth Factor Signaling Networks and Induces Autophagy Markers in MCF7 Breast Cancer Cells
    Pedro Casado, Benoît Bilanges, Vinothini Rajeeve, Bart Vanhaesebroeck, Pedro R. Cutillas · 2014 · Molecular & Cellular Proteomics
  66. Renal cancer-selective Englerin A induces multiple mechanisms of cell death and autophagy
    Richard T Williams, Alice Lin-Tsing Yu, Mitchell B. Diccianni, Emmanuel A. Theodorakis, Ayse Batova · 2013 · Journal of Experimental & Clinical Cancer Research
  67. TMEM106B, a frontotemporal lobar dementia (FTLD) modifier, associates with FTD-3-linked CHMP2B, a complex of ESCRT-III
    Mi-Hee Jun, Jeong Ho Han, Yu-Kyung Lee, Deok‐Jin Jang, Bong‐Kiun Kaang, Jin‐A Lee · 2015 · Molecular Brain
  68. Unraveling the complexity of autophagy: Potential therapeutic applications in Pancreatic Ductal Adenocarcinoma
    Valentina E. Gómez‐Mellado, Elisa Giovannetti, Godefridus J. Peters · 2015 · Seminars in Cancer Biology
  69. B5, a thioredoxin reductase inhibitor, induces apoptosis in human cervical cancer cells by suppressing the thioredoxin system, disrupting mitochondrion-dependent pathways and triggering autophagy
    Fangyuan Shao, Zhiyun Du, Dong-Lei Ma, Wenbo Chen, Wu-Yu Fu, Bi-Bo Ruan, Wen Rui, Jiaxuan Zhang, Sheng Wang, Nai-Sum Wong et al. · 2015 · Oncotarget
  70. Looking at the metabolic consequences of the colchicine-based in vivo autophagic flux assay
    Iban Seiliez, Ikram Belghit, Yujie Gao, Sandrine Cassy, Karine Dias, Marianne Cluzeaud, Didier Rémond, Nordine Hafnaoui, Bénédicte Salin, Nadine M. Camougrand et al. · 2016 · Autophagy
  71. MicroRNA-27a Promotes Inefficient Lysosomal Clearance in the Hippocampi of Rats Following Chronic Brain Hypoperfusion
    Hui Che, Yan Yan, Xiaohui Kang, Fei Guo, Meiling Yan, Huailei Liu, Xu Hou, Tong Liu, De‐Kang Zong, Linlin Sun et al. · 2016 · Molecular Neurobiology
  72. G protein γ subunit 7 induces autophagy and inhibits cell division
    Juanjuan Liu, Xinmiao Ji, Zhiyuan Li, Xingxing Yang, Wenchao Wang, Xin Zhang · 2016 · Oncotarget
  73. The reverse-mode NCX1 activity inhibitor KB-R7943 promotes prostate cancer cell death by activating the JNK pathway and blocking autophagic flux
    Zhou Long, BaiJun Chen, Qian Liu et al. · 2016 · Oncotarget
  74. Dysregulation of Autophagy Contributes to Anal Carcinogenesis
    Evie H. Carchman, Kristina A. Matkowskyj, Louise M. Meske, Paul F. Lambert · 2016 · PLoS ONE
  75. Phospholipase D1-regulated autophagy supplies free fatty acids to counter nutrient stress in cancer cells
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