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. S., Menon, Manoj B., Menzies, Fiona M., Mercer, Carol A., Merighi, Adalberto, Merry, Diane E., Meschini, Stefania, Meyer, Christian G., Meyer, Thomas F., Miao, Chao-Yu, Miao, Jun-Ying, Michels, Paul A.M., Michiels, Carine, Mijaljica, Dalibor, Milojkovic, Ana, Minucci, Saverio, Miracco, Clelia, Miranti, Cindy K., Mitroulis, Ioannis, Miyazawa, Keisuke, Mizushima, Noboru, Mograbi, Baharia, Mohseni, Simin, Molero, Xavier, Mollereau, Bertrand, Mollinedo, Faustino, Momoi, Takashi, Monastyrska, Iryna, Monick, Martha M., Monteiro, Mervyn J., Moore, Michael N., Mora, Rodrigo, Moreau, Kevin, Moreira, Paula I., Moriyasu, Yuji, Moscat, Jorge, Mostowy, Serge, Mottram, Jeremy C., Motyl, Tomasz, Moussa, Charbel E.-H., Müller, Sylke, Muller, Sylviane, Münger, Karl, Münz, Christian, Murphy, Leon O., Murphy, Maureen E., Musarò, Antonio, Mysorekar, Indira, Nagata, Eiichiro, Nagata, Kazuhiro, Nahimana, Aimable, Nair, Usha, Nakagawa, Toshiyuki, Nakahira, Kiichi, Nakano, Hiroyasu, Nakatogawa, Hitoshi, Nanjundan, Meera, Naqvi, Naweed I., Narendra, Derek P., Narita, Masashi, Navarro, Miguel, Nawrocki, Steffan T., Nazarko, Taras Y., Nemchenko, Andriy, Netea, Mihai G., Neufeld, Thomas P., Ney, Paul A., Nezis, Ioannis P., Nguyen, Huu Phuc, Nie, Daotai, Nishino, Ichizo, Nislow, Corey, Nixon, Ralph A., Noda, Takeshi, Noegel, Angelika A., Nogalska, Anna, Noguchi, Satoru, Notterpek, Lucia, Novak, Ivana, Nozaki, Tomoyoshi, Nukina, Nobuyuki, Nürnberger, Thorsten, Nyfeler, Beat, Obara, Keisuke, Oberley, Terry D., Oddo, Salvatore, Ogawa, Michinaga, Ohashi, Toya, Okamoto, Koji, Oleinick, Nancy L., Oliver, F. 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. Ashutosh, Rathmell, Jeffrey C., Ravikumar, Brinda, Ray, Swapan K., Reed, Bruce H., Reed, John C., Reggiori, Fulvio, Régnier-Vigouroux, Anne, Reichert, Andreas S., Reiners, Jr., John J., Reiter, Russel J., Ren, Jun, Revuelta, José L., Rhodes, Christopher J., Ritis, Konstantinos, Rizzo, Elizete, Robbins, Jeffrey, Roberge, Michel, Roca, Hernan, Roccheri, Maria C., Rocchi, Stephane, Rodemann, H. Peter, Rodríguez de Córdoba, Santiago, Rohrer, Bärbel, Roninson, Igor B., Rosen, Kirill, Rost-Roszkowska, Magdalena M., Rouis, Mustapha, Rouschop, Kasper M.A., Rovetta, Francesca, Rubin, Brian P., Rubinsztein, David C., Ruckdeschel, Klaus, Rucker, Edmund B., Rudich, Assaf, Rudolf, Emil, Ruiz-Opazo, Nelson, Russo, Rossella, Rusten, Tor Erik, Ryan, Kevin M., Ryter, Stefan W., Sabatini, David M., Sadoshima, Junichi, Saha, Tapas, Saitoh, Tatsuya, Sakagami, Hiroshi, Sakai, Yasuyoshi, Salekdeh, Ghasem Hoseini, Salomoni, Paolo, Salvaterra, Paul M., Salvesen, Guy, Salvioli, Rosa, Sanchez, Anthony M.J., Sánchez-Alcázar, José A., Sánchez-Prieto, Ricardo, Sandri, Marco, Sankar, Uma, Sansanwal, Poonam, Santambrogio, Laura, Saran, Shweta, Sarkar, Sovan, Sarwal, Minnie, Sasakawa, Chihiro, Sasnauskiene, Ausra, Sass, Miklós, Sato, Ken, Sato, Miyuki, Schapira, Anthony H.V., Scharl, Michael, Schätzl, Hermann M., Scheper, Wiep, Schiaffino, Stefano, Schneider, Claudio, Schneider, Marion E., Schneider-Stock, Regine, Schoenlein, Patricia V., Schorderet, Daniel F., Schüller, Christoph, Schwartz, Gary K., Scorrano, Luca, Sealy, Linda, Seglen, Per O., Segura-Aguilar, Juan, Seiliez, Iban, Seleverstov, Oleksandr, Sell, Christian, Seo, Jong Bok, Separovic, Duska, Setaluri, Vijayasaradhi, Setoguchi, Takao, Settembre, Carmine, Shacka, John J., Shanmugam, Mala, Shapiro, Irving M., Shaulian, Eitan, Shaw, Reuben J., Shelhamer, James H., Shen, Han-Ming, Shen, Wei-Chiang, Sheng, Zu-Hang, Shi, Yang, Shibuya, Kenichi, Shidoji, Yoshihiro, Shieh, Jeng-Jer, Shih, Chwen-Ming, Shimada, Yohta, Shimizu, Shigeomi, Shintani, Takahiro, Shirihai, Orian S., Shore, Gordon C., Sibirny, Andriy A., Sidhu, Stan B., Sikorska, Beata, Silva-Zacarin, Elaine C.M., Simmons, Alison, Simon, Anna Katharina, Simon, Hans-Uwe, Simone, Cristiano, Simonsen, Anne, Sinclair, David A., Singh, Rajat, Sinha, Debasish, Sinicrope, Frank A., Sirko, Agnieszka, Siu, Parco M., Sivridis, Efthimios, Skop, Vojtech, Skulachev, Vladimir P., Slack, Ruth S., Smaili, Soraya S., Smith, Duncan R., Soengas, Maria S., Soldati, Thierry, Song, Xueqin, Sood, Anil K., Soong, Tuck Wah, Sotgia, Federica, Spector, Stephen A., Spies, Claudia D., Springer, Wolfdieter, Srinivasula, Srinivasa M., Stefanis, Leonidas, Steffan, Joan S., Stendel, Ruediger, Stenmark, Harald, Stephanou, Anastasis, Stern, Stephan T., Sternberg, Cinthya, Stork, Björn, Strålfors, Peter, Subauste, Carlos S., Sui, Xinbing, Sulzer, David, Sun, Jiaren, Sun, Shi-Yong, Sun, Zhi-Jun, Sung, Joseph J.Y., Suzuki, Kuninori, Suzuki, Toshihiko, Swanson, Michele S., Swanton, Charles, Sweeney, Sean T., Sy, Lai-King, Szabadkai, György, Tabas, Ira, Taegtmeyer, Heinrich, Tafani, Marco, Takács-Vellai, Krisztina, Takano, Yoshitaka, Takegawa, Kaoru, Takemura, Genzou, Takeshita, Fumihiko, Talbot, Nicholas J., Tan, Kevin S.W., Tanaka, Keiji, Tanaka, Kozo, Tang, Daolin, Tang, Dingzhong, Tanida, Isei, Tannous, Bakhos A., Tavernarakis, Nektarios, Taylor, Graham S., Taylor, Gregory A., Taylor, J. Paul, Terada, Lance S., Terman, Alexei, Tettamanti, Gianluca, Thevissen, Karin, Thompson, Craig B., Thorburn, Andrew, Thumm, Michael, Tian, FengFeng, Tian, Yuan, Tocchini-Valentini, Glauco, Tolkovsky, Aviva M., Tomino, Yasuhiko, Tönges, Lars, Tooze, Sharon A., Tournier, Cathy, Tower, John, Towns, Roberto, Trajkovic, Vladimir, Travassos, Leonardo H., Tsai, Ting-Fen, Tschan, Mario P., Tsubata, Takeshi, Tsung, Allan, Turk, Boris, Turner, Lorianne S., Tyagi, Suresh C., Uchiyama, Yasuo, Ueno, Takashi, Umekawa, Midori, Umemiya-Shirafuji, Rika, Unni, Vivek K., Vaccaro, Maria I., Valente, Enza Maria, Van den Berghe, Greet, van der Klei, Ida J., van Doorn, Wouter G., van Dyk, Linda F., van Egmond, Marjolein, van Grunsven, Leo A., Vandenabeele, Peter, Vandenberghe, Wim P., Vanhorebeek, Ilse, Vaquero, Eva C., Velasco, Guillermo, Vellai, Tibor, Vicencio, José Miguel, Vierstra, Richard D., Vila, Miquel, Vindis, Cécile, Viola, Giampietro, Viscomi, Maria Teresa, Voitsekhovskaja, Olga V., von Haefen, Clarissa, Votruba, Marcela, Wada, Keiji, Wade-Martins, Richard, Walker, Cheryl L., Walsh, Craig M., Walter, Jochen, Wan, Xiang-Bo, Wang, 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, Xiujie J., Wang, Ying-Jan, Wang, Yipeng, Wang, Zhen-Bo, Wang, Zhigang Charles, Wang, Zhinong, Wansink, Derick G., Ward, Diane M., Watada, Hirotaka, Waters, Sarah L., Webster, Paul, Wei, Lixin, Weihl, Conrad C., Weiss, William A., Welford, Scott M., Wen, Long-Ping, Whitehouse, Caroline A., Whitton, J. Lindsay, Whitworth, Alexander J., Wileman, Tom, Wiley, John W., Wilkinson, Simon, Willbold, Dieter, Williams, Roger L., Williamson, Peter R., Wouters, Bradly G., Wu, Chenghan, Wu, Dao-Cheng, Wu, William K.K., Wyttenbach, Andreas, Xavier, Ramnik J., Xi, Zhijun, Xia, Pu, Xiao, Gengfu, Xie, Zhiping, Xie, Zhonglin, Xu, Da-zhi, Xu, Jianzhen, Xu, Liang, Xu, Xiaolei, Yamamoto, Ai, Yamamoto, Akitsugu, Yamashina, Shunhei, Yamashita, Michiaki, Yan, Xianghua, Yanagida, Mitsuhiro, Yang, Dun-Sheng, Yang, Elizabeth, Yang, Jin-Ming, Yang, Shi Yu, Yang, Wannian, Yang, Wei Yuan, Yang, Zhifen, Yao, Meng-Chao, Yao, Tso-Pang, Yeganeh, Behzad, Yen, Wei-Lien, Yin, Jia-Jing, Yin, Xiao-Ming, Yoo, Ook-Joon, Yoon, Gyesoon, Yoon, Seung-Yong, Yorimitsu, Tomohiro, Yoshikawa, Yuko, Yoshimori, Tamotsu, Yoshimoto, Kohki, You, Ho Jin, Youle, Richard J., Younes, Anas, Yu, Li, Yu, Long, Yu, Seong-Woon, Yu, Wai Haung, Yuan, Zhi-Min, Yue, Zhenyu, Yun, Cheol-Heui, Yuzaki, Michisuke, Zabirnyk, Olga, Silva-Zacarin, Elaine, Zacks, David, Zacksenhaus, Eldad, Zaffaroni, Nadia, Zakeri, Zahra, Zeh, III, Herbert J., Zeitlin, Scott O., Zhang, Hong, Zhang, Hui-Ling, Zhang, Jianhua, Zhang, Jing-Pu, Zhang, Lin, Zhang, Long, Zhang, Ming-Yong, Zhang, Xu Dong, Zhao, Mantong, Zhao, Yi-Fang, Zhao, Ying, Zhao, Zhizhuang J., Zheng, Xiaoxiang, Zhivotovsky, Boris, Zhong, Qing, Zhou, Cong-Zhao, Zhu, Changlian, Zhu, Wei-Guo, Zhu, Xiao-Feng, Zhu, Xiongwei, Zhu, Yuangang, Zoladek, Teresa, Zong, Wei-Xing, Zorzano, Antonio, Zschocke, Jürgen, Zuckerbraun, Brian·2012·Autophagy

Cited by (3,998)

Items 2,501–2,600 of 3,998

  1. Treponema pallidum promoted microglia apoptosis and prevented itself from clearing by human microglia via blocking autophagic flux
    Yun-Ting Hu, Kaixuan Wu, Xiaotong Wang · 2023 · PLoS Pathogens
  2. Structural and functional alterations of cellular components as revealed by electron microscopy
    Maria Condello, Michele Caraglia, MARIA Castellano, Giuseppe Arancia, Stefania Meschini · 2013 · Microscopy Research and Technique
  3. N3-Substituted Temozolomide Analogs Overcome Methylguanine-DNA Methyltransferase and Mismatch Repair Precipitating Apoptotic and Autophagic Cancer Cell Death
    Jihong Zhang, Marc Hummersone, Charles S. Matthews, Malcolm F. G. Stevens, Tracey Dawn Bradshaw · 2014 · Oncology
  4. Downregulated adaptor protein p66Shc mitigates autophagy process by low nutrient and enhances apoptotic resistance in human lung adenocarcinoma A549 cells
    Zhichao Zheng, Jie Yang, Dan Zhao, Dan Gao, Xiaojie Yan, Zhi Yao, Zhe Liu, Zhenyi Ma · 2013 · FEBS Journal
  5. Amyotrophic Lateral Sclerosis-Linked Mutant VAPB Inclusions Do Not Interfere with Protein Degradation Pathways or Intracellular Transport in a Cultured Cell Model
    Paola Genevini, Giulia Papiani, Annamaria Ruggiano, Lavinia Cantoni, Francesca Navone, Nica Borgese · 2014 · PLoS ONE
  6. Overexpression of p62/SQSTM1 promotes the degradations of abnormally accumulated PrP mutants in cytoplasm and relieves the associated cytotoxicities via autophagy–lysosome-dependent way
    Yin Xu, Jin Zhang, Chan Tian, Ke Ren, Yue Yan, Ke Wang, Hui Wang, Cao Chen, Jing Wang, Qi Shi et al. · 2013 · Medical Microbiology and Immunology
  7. Beclin 1 knockdown retards re-endothelialization and exacerbates neointimal formation via a crosstalk between autophagy and apoptosis
    Lan-xiang Ye, Jian Yu, Yin-xing Liang · 2014 · Atherosclerosis
  8. Ulinastatin Reduces the Resistance of Liver Cancer Cells to Epirubicin by Inhibiting Autophagy
    Bin Song, Qi Bian, Cheng Hao Shao, Gang Li, An An Liu, Wei Jing, Rui Liu, Yijie Zhang, Yingqi Zhou, Xiangui Hu et al. · 2015 · PLoS ONE
  9. Differential effects of atorvastatin on autophagy in ischemic and nonischemic myocardium in Ossabaw swine with metabolic syndrome
    Ashraf A. Sabe, Nassrene Y. Elmadhun, Ahmed Sadek, Louis M. Chu, Cesario F. Bianchi, Frank William Sellke · 2014 · Journal of Thoracic and Cardiovascular Surgery
  10. Epizootic Hemorrhagic Disease Virus Induces and Benefits from Cell Stress, Autophagy, and Apoptosis
    Ben Shai, Eran Schmukler, Roy Yaniv, Naomi Ziv, Galit Horn, Velizar Y. Bumbarov, Hagai Yadin, Nechama I. Smorodinsky, Eran Bacharach, Ronit Pinkas‐Kramarski et al. · 2013 · Journal of Virology
  11. The Role of Autophagy and Apoptosis During Embryo Development
    Maria Agnello, Liana Bosco, Roberto Chiarelli, Chiara Martino, Maria Carmela Roccheri · 2015 · InTech eBooks
  12. Involvement of PARPs in cell death
    Francesca Aredia · 2014 · Frontiers in Bioscience-Elite
  13. Hinokitiol protects primary neuron cells against prion peptide-induced toxicity via autophagy flux regulated by hypoxia inducing factor-1
    Ji-Hong Moon, Ju‐Hee Lee, You-Jin Lee, Sang‐Youel Park · 2016 · Oncotarget
  14. Antitumor effect of sunitinib in human prostate cancer cells functions via autophagy
    Bangqi Wang, Dongyuan Lu, Min Xuan, HU Wei-lie · 2017 · Experimental and Therapeutic Medicine
  15. Basal autophagy prevents autoactivation or enhancement of inflammatory signals by targeting monomeric MyD88
    Takeshi Into, Toshi Horie, Megumi Inomata, Jin Gohda, Jun‐ichiro Inoue, Yukitaka Murakami, Shumpei Niida · 2017 · Scientific Reports
  16. Betulinic acid induces cell death by necrosis in Trypanosoma cruzi
    Paloma Leão Sousa, Racquel Oliveira da Silva Souza, Louise Donadello Tessarolo · 2017 · Acta Tropica
  17. Proteomics/phosphoproteomics of left ventricular biopsies from patients with surgical coronary revascularization and pigs with coronary occlusion/reperfusion: remote ischemic preconditioning
    Nilgün Gedik, Marcus Krüger, Matthias Thielmann et al. · 2017 · Scientific Reports
  18. Vorinostat and metformin sensitize EGFR-TKI resistant NSCLC cells via BIM-dependent apoptosis induction
    Hengyi Chen, Yubo Wang, Caiyu Lin, Conghua Lu, Rui Han, Lin Jiao, Li Li, Yong He · 2017 · Oncotarget
  19. Amyloid β-Derived Diffusible Ligands (ADDLs) Induce Abnormal Autophagy Associated with Aβ Aggregation Degree
    Jie Wen, Fang Fang, Shuhan Guo, Ying Zhang, Xiang-Lei Peng, Weimin Sun, Xiaoran Wei, Jinsheng He, Tao Hung · 2017 · Journal of Molecular Neuroscience
  20. Nano-sized Al2O3 particle-induced autophagy reduces osteolysis in aseptic loosening of total hip arthroplasty by negative feedback regulation of RANKL expression in fibroblasts
    De Li, Chenglong Wang, Zhuokai Li et al. · 2018 · Cell Death and Disease
  21. Loss of BRUCE reduces cellular energy level and induces autophagy by driving activation of the AMPK-ULK1 autophagic initiating axis
    Lixiao Che, Xingyuan Yang, Chunmin Ge, Salim S. El‐Amouri, Qi-En Wang, Dao Pan, Thomas J. Herzog, Chunying Du · 2019 · PLoS ONE
  22. NPS2390, a selective calcium-sensing receptor antagonist controls the phenotypic modulation of hypoxic human pulmonary arterial smooth muscle cells by regulating autophagy
    Xue Peng, Can Wei, Hongzhu Li, Hongxia Li, Shuzhi Bai, Lina Wang, Yuhui Xi, Yan Jin, Changqing Xu · 2019 · Journal of Translational Internal Medicine
  23. Autophagy Related Gene (ATG3) is a Key Regulator for Cell Growth, Development, and Virulence of Fusarium oxysporum
    A. Rehman Khalid, Xiulan Lv, Muhammad Shahbaz Naeem, Khalid Mehmood, Hamayun Shaheen, Pan Dong, Dan Qiu, Maozhi Ren · 2019 · Genes
  24. NDRG1 suppresses basal and hypoxia-induced autophagy at both the initiation and degradation stages and sensitizes pancreatic cancer cells to lysosomal membrane permeabilization
    Sumit Sahni, Josef Gillson, Kyung Chan Park, Shannon Chiang, Lionel Yi Wen Leck, Patric J. Jansson, Des Raymond Richardson · 2020 · Biochimica et Biophysica Acta (BBA) - General Subjects
  25. Aminopeptidase A contributes to biochemical, anatomical and cognitive defects in Alzheimer’s disease (AD) mouse model and is increased at early stage in sporadic AD brain
    Audrey Valverde, Julie Dunys, Thomas Lorivel, Delphine Debayle, Anne-Sophie Gay, Sandra Lacas‐Gervais, Bernard Pierre Roques, Mounia Chami, Frédéric Checler · 2021 · Acta Neuropathologica
  26. Quantifying autophagosomes and autolysosomes in cells using imaging flow cytometry
    Robin Rajan, Magdalena Karbowniczek, Haley Renee Pugsley, Manoj Kumar Sabnani, Aristotelis Astrinidis, Ninh My La-Beck · 2015 · Cytometry Part A
  27. Autophagy in Muscle of Glucose-Infusion Hyperglycemia Rats and Streptozotocin-Induced Hyperglycemia Rats via Selective Activation of m-TOR or FoxO3
    Pengfei Lv, Jian Yuan Huang, Jian Yang, Yujie Deng, Jun Hui Xu, Xiaoyan Zhang, Wenyi Li, Hongli Zhang, Ying Yang · 2014 · PLoS ONE · Retracted
  28. bZIP transcription factor SmJLB1 regulates autophagy-related genes Smatg8 and Smatg4 and is required for fruiting-body development and vegetative growth in Sordaria macrospora
    Oliver Voigt, Britta Herzog, Antonia Jakobshagen · 2013 · Fungal Genetics and Biology
  29. Novel Quantitative Autophagy Analysis by Organelle Flow Cytometry after Cell Sonication
    Michael Y. Degtyarev, Mike Reichelt, Kui Lin · 2014 · PLoS ONE
  30. eEOC-mediated modulation of endothelial autophagy, senescence, and EnMT in murine diabetic nephropathy
    Daniel Patschan, Katrin Schwarze, Elvira Henze · 2014 · American Journal of Physiology-Renal Physiology
  31. Agent-based modeling of autophagy reveals emergent regulatory behavior of spatio-temporal autophagy dynamics
    Christoph S Börlin, Verena Lang, Anne Hamacher‐Brady, Nathan Ryan Brady · 2014 · Cell Communication and Signaling
  32. The Retinoblastoma Tumor Suppressor Protein (pRb)/E2 Promoter Binding Factor 1 (E2F1) Pathway as a Novel Mediator of TGFβ-induced Autophagy
    Juliana Korah, Lucie Canaff, J J Lebrun · 2015 · Journal of Biological Chemistry
  33. Using multispectral imaging flow cytometry to assess an in vitro intracellular Burkholderia thailandensis infection model
    Dominic C. Jenner, Catherine B. Ducker, Graeme C. Clark · 2016 · Cytometry Part A
  34. Autophagy is required for sea urchin oogenesis and early development
    Maria Agnello, Roberto Chiarelli, Chiara Martino, Liana Bosco, Maria Carmela Roccheri · 2016 · Zygote
  35. 3-Decylcatechol induces autophagy-mediated cell death through the IRE1α/JNK/p62 in hepatocellular carcinoma cells
    Da-Hye Go, Yu Geon Lee, Da-Hye Lee, Jin‐A Kim, In-Hwa Jo, Yeon Soo Han, Yong Hun Jo, Kwang-Youn Kim, Young‐Kyo Seo, Jae‐Hak Moon et al. · 2017 · Oncotarget
  36. Primary fibroblasts from CSPα mutation carriers recapitulate hallmarks of the adult onset neuronal ceroid lipofuscinosis
    Bruno A. Benítez, Mark S. Sands · 2017 · Scientific Reports
  37. Neuroprotective effects of hydrogen sulfide on sodium azide-induced autophagic cell death in PC12 cells
    Haiyan Shan, Yang Chu, Pan Chang, Lijun Yang, Yi Wang, Shaohua Zhu, Mingyang Zhang, Luyang Tao · 2017 · Molecular Medicine Reports
  38. Loss of the ubiquitin conjugating enzyme UBE2E3 induces cellular senescence
    Kendra S. Plafker, Katarzyna Zyla, William L. Berry, Scott M. Plafker · 2018 · Redox Biology
  39. Quantitative Proteomics Links the LRRC59 Interactome to mRNA Translation on the ER Membrane
    Molly M. Hannigan, Alyson M. Hoffman, J. Will Thompson, Tianli Zheng, Christopher V. Nicchitta · 2020 · Molecular & Cellular Proteomics
  40. Rosiglitazone Prevents Autophagy by Regulating Nrf2-Antioxidant Response Element in a Rat Model of Lithium-pilocarpine-induced Status Epilepticus
    Ying Peng, Li Chen, Youyang Qu, Di Wang, Yanmei Zhu, Yulan Zhu · 2020 · Neuroscience
  41. Targeting Mitophagy in Alzheimer’s Disease
    Dona Pamoda W. Jayatunga, Eugene Hone, Prashant Bharadwaj, Manohar L. Garg, Giuseppe Verdile, Gilles J. Guillemin, Ralph Nigel Martins · 2020 · Journal of Alzheimer s Disease
  42. Heat Treatment Improves Hepatic Mitochondrial Respiratory Efficiency via Mitochondrial Remodeling
    Alex T. Von Schulze, Fengyan Deng, Kelly N. Z. Fuller, Edziu Franczak, Josh Miller, Julie Allen, Colin S. McCoin, Kartik Shankar, Wen‐Xing Ding, John P. Thyfault et al. · 2021 · Function
  43. Novel and conventional inhibitors of canonical autophagy differently affect LC3‐associated phagocytosis
    Femmy C. Stempels, M.H. Janssens, Martin ter Beest, Rob Mesman, Natalia H. Revelo, Melina Ioannidis, Geert van den Bogaart · 2022 · FEBS Letters
  44. Dl-3-n-butylphthalide attenuates myocardial ischemia reperfusion injury by suppressing oxidative stress and regulating cardiac mitophagy via the PINK1/Parkin pathway in rats
    Dongqin Zhang, Nan Zheng, Xiaoli Fu, Jian Shi, Jun Zhang · 2022 · Journal of Thoracic Disease
  45. Trim25 restricts rabies virus replication by destabilizing phosphoprotein
    Yueming Yuan, An Fang, Zongmei Wang et al. · 2022 · Cell Insight
  46. Myosin light-chain 4 gene-transfer attenuates atrial fibrosis while correcting autophagic flux dysregulation
    Yuan Zhong, Kai Tang, Stanley Nattel, Ming Zhai, Shiyu Gong, Qing Yu, Yanxi Zeng, E Guangxi, Nuerbiyemu Maimaitiaili, Jun Wang et al. · 2023 · Redox Biology
  47. Autophagy is induced by swine acute diarrhea syndrome coronavirus through the cellular IRE1-JNK-Beclin 1 signaling pathway after an interaction of viral membrane-associated papain-like protease and GRP78
    Da Shi, Ling Zhou, Hongyan Shi, Jiyu Zhang, Jialin Zhang, Liaoyuan Zhang, Dakai Liu, Tingshuai Feng, Miaomiao Zeng, Jianfei Chen et al. · 2023 · PLoS Pathogens
  48. Role of autophagy in the pathogenesis and regulation of pain
    Guangda Zheng, Juanxia Ren, Lu Shang, Yanju Bao · 2023 · European Journal of Pharmacology
  49. The Role of Autophagy in Salivary Gland Homeostasis and Stress Responses
    Maria E. Morgan-Bathke, Her Helen Lin, David Kong Ann, Kirsten H. Limesand · 2015 · Journal of Dental Research
  50. Regulation of innate immunity by the molecular machinery of macroautophagy
    Christian Münz · 2014 · Cellular Microbiology
  51. Interactions between Autophagy and Bacterial Toxins: Targets for Therapy?
    Jacques Mathieu · 2015 · Toxins
  52. Early Delivery of Misfolded PrP from ER to Lysosomes by Autophagy
    Constanza J. Cortés, Kefeng Qin, Eric M. Norstrom, William N. Green, Vytautas P. Bindokas, James A. Mastrianni · 2013 · International Journal of Cell Biology
  53. Critical Significance of the Region between Helix 1 and 2 for Efficient Dominant-Negative Inhibition by Conversion-Incompetent Prion Protein
    Yuzuru Taguchi, Arla Mistica, Tetsuyuki Kitamoto · 2013 · PLoS Pathogens
  54. Identification and pharmacological induction of autophagy in the larval stages of Echinococcus granulosus: an active catabolic process in calcareous corpuscles
    Julia A. Loos, Pedro A. Caparros, María Celeste Nicolao, Guillermo M. Denegri, Andrea C. Cumino · 2014 · International Journal for Parasitology
  55. The p53 tumor suppressor protein protects against chemotherapeutic stress and apoptosis in human medulloblastoma cells
    Sarah E. Waye, Aisha Naeem, Muhammad Umer Choudhry et al. · 2015 · Aging
  56. Developing a set of guidelines for your research field: a practical approach
    Daniel J. Klionsky · 2016 · Molecular Biology of the Cell
  57. Coxsackievirus B3 infection induces autophagic flux, and autophagosomes are critical for efficient viral replication
    Xiaodan Shi, Zijian Chen, Shengjie Tang, Fei Wu, Sidong Xiong, Chunsheng Dong · 2016 · Archives of Virology
  58. Autophagy protects against oxidized low density lipoprotein-mediated inflammation associated with preeclampsia
    Yan Zhang, Xiaoyu Hu, Guoqiang Gao, Yufang Wang, Pingping Chen, Yuanhua Ye · 2016 · Placenta
  59. Autophagic targeting and avoidance in intracellular bacterial infections
    Lara J. Kohler, Craig R. Roy · 2016 · Current Opinion in Microbiology
  60. Autophagy deactivation is associated with severe prostatic inflammation in patients with lower urinary tract symptoms and benign prostatic hyperplasia
    Cosimo De Nunzio, Simona Giglio, Antonella Stoppacciaro · 2017 · Oncotarget
  61. Synergism and mechanism of Astragaloside IV combined with Ginsenoside Rg1 against autophagic injury of PC12 cells induced by oxygen glucose deprivation/reoxygenation
    Huang Xiao-ping, Huang Ding, Xiaoqian Yang, Jingxian Li, Biao Tang, Xiao-Dan Liu, Yinghong Tang, Chang-Qing Deng · 2017 · Biomedicine & Pharmacotherapy
  62. Staphylococcal lipoteichoic acid promotes osteogenic differentiation of mouse mesenchymal stem cells by increasing autophagic activity
    Xin Liu, Yuan Wang, Zhen Cao, Ce Dou, Yun Bai, Chuan Liu, Shiwu Dong, Jun Fei · 2017 · Biochemical and Biophysical Research Communications
  63. Autophagy induced by bovine viral diarrhea virus infection counteracts apoptosis and innate immune activation
    Yulong Zhou, Yachao Ren, Yanlong Cong, Mu Yu, Renfu Yin, Zhuang Ding · 2017 · Archives of Virology
  64. ATG5 overexpression is neuroprotective and attenuates cytoskeletal and vesicle-trafficking alterations in axotomized motoneurons
    Tatiana Leiva-Rodríguez, David Romeo-Guitart, Sara Marmolejo-Martínez-Artesero, Mireia Herrando‐Grabulosa, Assumpció Bosch, Joaquím Forés, Caty Casas · 2018 · Cell Death and Disease
  65. Compensatory increases of select proteostasis networks after Hsp70 inhibition in cancer cells
    Sara Sannino, Christopher J. Guerriero, Amit J. Sabnis, Donna Beer Stolz, Callen T. Wallace, Peter Wipf, Simon C. Watkins, Trever Grant Bivona, Jeffrey L. Brodsky · 2018 · Journal of Cell Science
  66. Leptin stimulates autophagy/lysosome-related degradation of long-lived proteins in adipocytes
    Nir Goldstein, Yulia Haim, Pamela Mattar, Sapir Bechor, Nitzan Maixner, Peter Louis Kovacs, Matthias Blüher, Assaf Rudich · 2019 · Adipocyte
  67. ATG10 (autophagy-related 10) regulates the formation of autophagosome in the anti-virus immune response of pacific oyster (Crassostrea gigas)
    Zirong Han, Weilin Wang, Xiaojing Lv, Yanan Zong, Shujing Liu, Zhaoqun Liu, Lingling Wang, Linsheng Song · 2019 · Fish & Shellfish Immunology
  68. Autophagy is required for performance adaptive response to resistance training and exercise‐induced adult neurogenesis
    Helena Codina‐Martínez, Benjamín Fernández‐Garcia, Carlos Díez‐Planelles, Álvaro F. Fernández, Sara G. Higarza, Manuel Fernández‐Sanjurjo, Sergio Díez‐Robles, Eduardo Iglesias‐Gutiérrez, Cristina Tomás‐Zapico · 2019 · Scandinavian Journal of Medicine and Science in Sports
  69. The dual role of c‐src in cell‐to‐cell transmission of α‐synuclein
    Yu Ree Choi, Jae‐Bong Kim, Seo‐Jun Kang, Hye Rin Noh, Ilo Jou, Eun-hye Joe, Sang Myun Park · 2020 · EMBO Reports
  70. Reduction of Cardiac Cell Death after Helium Postconditioning in Rats: Transcriptional Analysis of Cell Death and Survival Pathways
    Gezina T.M.L. Oei, Michal Heger, Rowan F. van Golen, Lindy K. Alles, Moritz Flick, Allard C. van der Wal, Thomas M. van Gulik, Markus Werner Hollmann, Benedikt Preckel, Nina Claudia Weber · 2014 · Molecular Medicine
  71. Lapatinib induces autophagic cell death and differentiation in acute myeloblastic leukemia
    Huey-Lan Huang, Li-Wen Fang, Wen‐Chi Su, Wen-Yi Hsu, Kai‐Chien Yang, Yu-Jen Chen · 2016 · OncoTargets and Therapy
  72. New derivatives of the antimalarial drug Pyrimethamine in the control of melanoma tumor growth: an in vitro and in vivo study
    Chiara Tommasino, Lucrezia Gambardella, Maria Buoncervello, Roger J. Griffin, Bernard T. Golding, Manuela Alberton, Daniele Macchia, Massimo Spada, Bruna Cerbelli, Giulia d’Amati et al. · 2016 · Journal of Experimental & Clinical Cancer Research
  73. Mammalian nucleophagy: process and function
    Fujian Ji, Enyong Dai, Rui Kang, Daniel J. Klionsky, Tong Liu, Yu Hu, Daolin Tang, Kun Zhu · 2025 · Autophagy
  74. Ischemic postconditioning regulates cardiomyocyte autophagic activity following ischemia/reperfusion injury
    Liang Guo, Junmei Xu, Xiaoye Mo · 2012 · Molecular Medicine Reports
  75. mTOR kinase inhibitor pp242 causes mitophagy terminated by apoptotic cell death in E1A-Ras transformed cells
    Serguei A. Gordeev, Tatiana V. Bykova, Svetlana G. Zubova, Olga A. Bystrova, Marina G. Martynova, Valery A. Pospelov, Tatiana V. Pospelova · 2015 · Oncotarget
  76. RETRACTED: Cytotoxic Properties of a DEPTOR-mTOR Inhibitor in Multiple Myeloma Cells
    Yijiang Shi, Tracy R. Daniels‐Wells, Patrick Frost, Jihye Lee, Richard S. Finn, Carolyne Bardeleben, Manuel L. Penichet, Michael E. Jung, Joseph Gera, Alan K. Lichtenstein · 2016 · Cancer Research · Retracted
  77. Effects Of Oral Glutamine on Inflammatory and Autophagy Responses in Cancer Patients Treated With Abdominal Radiotherapy: A Pilot Randomized Trial
    Juan José Ortiz de Urbina, Beatriz San‐Miguel, Alfonso Vidal‐Casariego · 2017 · International Journal of Medical Sciences
  78. Mechanisms of Cell Death Induced by Optical Hyperthermia
    Marta Pérez-Hernández · 2019 · Elsevier eBooks
  79. HBx‑associated long non‑coding RNA activated by TGF‑β promotes cell invasion and migration by inducing autophagy in primary liver cancer
    Yuheng Zhang, Jun Li, Shuai Wang · 2019 · International Journal of Oncology
  80. Functional Analysis of MaWRKY24 in Transcriptional Activation of Autophagy-Related Gene 8f/g and Plant Disease Susceptibility to Soil-Borne Fusarium oxysporum f. sp. cubense
    Guoyin Liu, Hongqiu Zeng, Xiang Li · 2019 · Pathogens
  81. Autophagy Promotes Porcine Parvovirus Replication and Induces Non-Apoptotic Cell Death in Porcine Placental Trophoblasts
    Xiujuan Zhang, Yingli Xiong, Jie Zhang, Ting Shao, Songbiao Chen, Bichen Miao, Zhenyu Wang, Qian Du, Yong Huang, Dewen Tong · 2019 · Viruses
  82. RETRACTED: LOXL2 Upregulation in Gliomas Drives Tumorigenicity by Activating Autophagy to Promote TMZ Resistance and Trigger EMT
    Qing Zhang, Lian‐He Yang, Gefei Guan, Peng Cheng, Wen Cheng, Anhua Wu · 2020 · Frontiers in Oncology · Retracted
  83. Starvation and pH stress conditions induced mitochondrial dysfunction, ROS production and autophagy in Trypanosoma cruzi epimastigotes
    Yasmin Pedra-Rezende, Michelle C. Fernandes, Camila Mesquita‐Rodrigues, Renata Stiebler, Ana Cristina S. Bombaça, Nathalia Pinho, Patrícia Cuervo, Solange Lisboa de Castro, Rubem F. S. Menna‐Barreto · 2020 · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
  84. The role of FOS-mediated autophagy activation in the indocyanine green-based photodynamic therapy for treating melanoma
    Junyi Shao, Fan Jiang, Murong Hu, Enci Mei, Zhaoqi Pan, Cunguo Chen, Lele Lin, Tianyin Zheng, Weiyang Cai, Zhiming Li et al. · 2020 · Journal of Photochemistry and Photobiology B Biology
  85. An Experimentally Induced Mutation in the UBA Domain of p62 Changes the Sensitivity of Cisplatin by Up-Regulating HK2 Localisation on the Mitochondria and Increasing Mitophagy in A2780 Ovarian Cancer Cells
    Sihang Yu, Xiaoyu Yan, Rui Tian, Long Xu, Yuanxin Zhao, Liankun Sun, Jing Su · 2021 · International Journal of Molecular Sciences
  86. In vivo autophagy quantification: Measuring LC3 and P62 puncta in 3D image system from zebrafish larvae
    Abdalla Elbialy · 2021 · Journal of Cellular Biochemistry
  87. Graphene quantum dot antioxidant and proautophagic actions protect SH-SY5Y neuroblastoma cells from oxidative stress-mediated apoptotic death
    Matija Krunić, Biljana Z. Ristic, Mihajlo Bošnjak, Verica Paunović, Gordana Tovilović-Kovačević, Nevena S. Zogovic, Aleksandar Mirčić, Zoran M Marković, Biljana M. Todorović Marković, Svetlana Jovanović et al. · 2021 · Free Radical Biology and Medicine
  88. Vinexin contributes to autophagic decline in brain ageing across species
    So Jung Park, Rebecca A. Frake, Cansu Karabiyik, Sung Min Son, Farah H. Siddiqi, Carla F. Bento, Peter Sterk, Mariella Vicinanza, Mariana Pavel Tanasa, David Chaim Rubinsztein · 2021 · Cell Death and Differentiation
  89. Mechanism of Pterostilbene-Induced Cell Death in HT-29 Colon Cancer Cells
    Joanna Wawszczyk, Katarzyna Jesse, Sławomir Smolik, Małgorzata Kapral · 2022 · Molecules
  90. Rift Valley Fever Virus Nucleoprotein Triggers Autophagy to Dampen Antiviral Innate Immune Responses
    Xiangtao Zhu, Zihan Guan, Yujie Fang, Yulan Zhang, Zhenqiong Guan, Shufen Li, Ke Peng · 2023 · Journal of Virology
  91. Indoxacarb triggers autophagy and apoptosis through ROS accumulation mediated by oxidative phosphorylation in the midgut of Bombyx mori
    Wanwan Wang, Yue Su, Ruinan Qi, Hao Li, Hongrui Jiang, Fanchi Li, Bing Li, Haina Sun · 2024 · Pesticide Biochemistry and Physiology
  92. The mechanism of reactive oxygen species generation, DNA damage and apoptosis in hemocytes of Litopenaeus vannamei under ammonia nitrogen exposure
    Ruixue Tong, Yaobing Li, Xin Yu, Ning Zhang, Qilong Liao, Luqing Pan · 2024 · Aquatic Toxicology
  93. Rapamycin Induces Apoptosis When Autophagy is Inhibited in T-47D Mammary Cells and Both Processes are Regulated by Phlda1
    Ahmed Ismail Hassan Moad, Tengku Sifzizul Tengku Muhammad, Chern Ein Oon, Ming Tan · 2013 · Cell Biochemistry and Biophysics
  94. A cell-penetrating ester of the neural metabolite lanthionine ketimine stimulates autophagy through the mTORC1 pathway: Evidence for a mechanism of action with pharmacological implications for neurodegenerative pathologies
    Marni E. Harris‐White, Kathie G. Ferbas, Ming F. Johnson, Pirooz Eslami, Aleksandra Poteshkina, Kalina M. Venkova, Alexandar Christov, Kenneth Hensley · 2015 · Neurobiology of Disease
  95. Experimental investigation of axially non-uniform catalysis for methanol steam reforming
    Guoqiang Wang, Feng Wang, Longjian Li · 2013 · Journal of Power Sources
  96. Tracking autophagy during proliferation and differentiation of Trypanosoma brucei
    William R. Proto, Nathaniel G. Jones, Graham H. Coombs · 2014 · Microbial Cell
  97. LAPTM4B is associated with poor prognosis in NSCLC and promotes the NRF2-mediated stress response pathway in lung cancer cells
    Yuho Maki, Junya Fujimoto, Wenhua Lang, Xu Li, Carmen Behrens, Ignacio Ivan Wistuba, Humam N. Kadara · 2015 · Scientific Reports
  98. Pexophagy is induced by increasing peroxisomal reactive oxygen species in 1′10-phenanthroline-treated cells
    Doo Sin Jo, Dong‐Jun Bae, So Jung Park, Hae Mi Seo, Han Byeol Kim, Jeong Su Oh, Jong Wook Chang, Sang‐Yeob Kim, Jung-Won Shin, Dong‐Hyung Cho · 2015 · Biochemical and Biophysical Research Communications
  99. The two Dictyostelium autophagy eight proteins, ATG8a and ATG8b, associate with the autophagosome in succession
    Jan Matthias, Susanne Meßling, Ludwig Eichinger · 2015 · European Journal of Cell Biology
  100. Autophagy and 3-Phosphoinositide-Dependent Kinase 1 (PDK1)-Related Kinome in Pagetic Osteoclasts
    Stephen McManus, Martine Bisson, Richard Chamberland, Michèle Roy, Shekeba Nazari, Sophie Roux · 2016 · Journal of Bone and Mineral Research