Advanced search
Publication Cover
Autophagy Volume 8, 2012 - Issue 9
Submit an article Journal homepage
951
Views
11
CrossRef citations to date
0
Altmetric
Autophagic Punctum

Coiling up with SCOC and WAC

Two new regulators of starvation-induced autophagy

Justin Joachim London Research Institute; Cancer Research UK; London, UK
,
Martina Wirth London Research Institute; Cancer Research UK; London, UK
,
Nicole C. McKnight Department of Neurology; Friedman Brain Institute; Mount Sinai School of Medicine New York, NY USA
&
Sharon A. Tooze London Research Institute; Cancer Research UK; London, UKCorrespondence[email protected]
Pages 1397-1400 | Received 01 Jun 2012, Accepted 06 Jun 2012, Published online: 21 Jun 2012

Citations (11)

Keep up to date with the latest research on this topic with citation updates for this article.

Subscribe to citation updates

Read on this site (1)

Fan Qinlin, Wang Bingqiao, Hu Linlin, Shi Peixia, Xie Lexing, Yang Lijun & Yang Qingwu. (2022) miR-129-5p targets FEZ1/SCOC/ULK1/NBR1 complex to restore neuronal function in mice with post-stroke depression. Bioengineered 13:4, pages 9708-9728.
Read now

Articles from other publishers (10)

Daniela Pasquali, Annalaura Torella, Anna Grandone, Caterina Luongo, Manuela Morleo, Cristina Peduto, Rosa di Fraia, Lucia Digitale Selvaggio, Francesca Allosso, Giacomo Accardo, Maria Teresa Zanobio, Silvia Maitz, Milena Mariani, Angelo Selicorni, Sandro Banfi & Vincenzo Nigro. (2022) Patients with DeSanto–Shinawi syndrome: Further extension of phenotype from Italy. American Journal of Medical Genetics Part A 191:3, pages 823-830.
Crossref
Joana Branco, Marta Amorim & Marta Conde. (2022) A novel variant of DeSanto-Shinawi Syndrome with joint manifestations. European Journal of Medical Genetics 65:7, pages 104534.
Crossref
Jie Pan, Nana Ma, Bo Yu, Wei Zhang & Jun Wan. (2020) Transcriptomic profiling of microglia and astrocytes throughout aging. Journal of Neuroinflammation 17:1.
Crossref
Zahra Alsahlawi, Mohamed Jailani, Husain Alaradi & Abdulaziz AlAbbad. (2020) A Case of DeSanto-Shinawi Syndrome in Bahrain with a Novel Mutation. Case Reports in Pediatrics 2020, pages 1-6.
Crossref
Maroulio Pertesi, Molly Went, Markus Hansson, Kari Hemminki, Richard S. Houlston & Björn Nilsson. (2020) Genetic predisposition for multiple myeloma. Leukemia 34:3, pages 697-708.
Crossref
Tomoko Uehara, Takashi Ishige, Shigeto Hattori, Hiroshi Yoshihashi, Michinori Funato, Yu Yamaguchi, Toshiki Takenouchi & Kenjiro Kosaki. (2018) Three patients with DeSanto-Shinawi syndrome: Further phenotypic delineation. American Journal of Medical Genetics Part A 176:6, pages 1335-1340.
Crossref
Sara Vanegas, Diana Ramirez-Montaño, Estephania Candelo, Marwan Shinawi & Harry Pachajoa. (2018) DeSanto-Shinawi Syndrome: First Case in South America. Molecular Syndromology 9:3, pages 154-158.
Crossref
Xiaorong Wang, Peter Cimermancic, Clinton Yu, Andreas Schweitzer, Nikita Chopra, James L. Engel, Charles Greenberg, Alexander S. Huszagh, Florian Beck, Eri Sakata, Yingying Yang, Eric J. Novitsky, Alexander Leitner, Paolo Nanni, Abdullah Kahraman, Xing Guo, Jack E. Dixon, Scott D. Rychnovsky, Ruedi Aebersold, Wolfgang Baumeister, Andrej Sali & Lan Huang. (2017) Molecular Details Underlying Dynamic Structures and Regulation of the Human 26S Proteasome. Molecular & Cellular Proteomics 16:5, pages 840-854.
Crossref
Jonathan S. Mitchell, Ni Li, Niels Weinhold, Asta Försti, Mina Ali, Mark van Duin, Gudmar Thorleifsson, David C. Johnson, Bowang Chen, Britt-Marie Halvarsson, Daniel F. Gudbjartsson, Rowan Kuiper, Owen W. Stephens, Uta Bertsch, Peter Broderick, Chiara Campo, Hermann Einsele, Walter A. Gregory, Urban Gullberg, Marc Henrion, Jens Hillengass, Per Hoffmann, Graham H. Jackson, Ellinor Johnsson, Magnus Jöud, Sigurður Y. Kristinsson, Stig Lenhoff, Oleg Lenive, Ulf-Henrik Mellqvist, Gabriele Migliorini, Hareth Nahi, Sven Nelander, Jolanta Nickel, Markus M. Nöthen, Thorunn Rafnar, Fiona M. Ross, Miguel Inacio da Silva Filho, Bhairavi Swaminathan, Hauke Thomsen, Ingemar Turesson, Annette Vangsted, Ulla Vogel, Anders Waage, Brian A. Walker, Anna-Karin Wihlborg, Annemiek Broyl, Faith E. Davies, Unnur Thorsteinsdottir, Christian Langer, Markus Hansson, Martin Kaiser, Pieter Sonneveld, Kari Stefansson, Gareth J. Morgan, Hartmut Goldschmidt, Kari Hemminki, Björn Nilsson & Richard S. Houlston. (2016) Genome-wide association study identifies multiple susceptibility loci for multiple myeloma. Nature Communications 7:1.
Crossref
Cori DeSanto, Kristin D'Aco, Gabriel C Araujo, Nora Shannon, DDD Study, Hilary Vernon, April Rahrig, Kristin G Monaghan, Zhiyv Niu, Patrik Vitazka, Jonathan Dodd, Sha Tang, Linda Manwaring, Arelis Martir-Negron, Rhonda E Schnur, Jane Juusola, Audrey Schroeder, Vivian Pan, Katherine L Helbig, Bethany Friedman & Marwan Shinawi. (2015) WAC loss-of-function mutations cause a recognisable syndrome characterised by dysmorphic features, developmental delay and hypotonia and recapitulate 10p11.23 microdeletion syndrome . Journal of Medical Genetics 52:11, pages 754-761.
Crossref

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Order Reprints Request Corporate Permissions

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

Request Academic Permissions

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.

Related research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.