Loss of DDHD2, whose mutation causes spastic paraplegia, promotes reactive oxygen species generation and apoptosis-Reference-Cited by-同舟云学术

Loss of DDHD2, whose mutation causes spastic paraplegia, promotes reactive oxygen species generation and apoptosis

Published:2018-07-23 Issue:8 Volume:9 Page:
ISSN:2041-4889
Container-title:Cell Death & Disease
language:en
Short-container-title:Cell Death Dis

Author:

Maruyama Tomohiro,Baba Takashi,Maemoto Yuki,Hara-Miyauchi Chikako,Hasegawa-Ogawa Minami,Okano Hirotaka James,Enda Yuki,Matsumoto Kei,Arimitsu Nagisa,Nakao Kazuki,Hamamoto Hiroshi,Sekimizu Kazuhisa,Ohto-Nakanishi Takayo,Nakanishi Hiroki,Tokuyama Takeshi,Yanagi Shigeru,Tagaya Mitsuo^ORCID,Tani Katsuko

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Cell Biology,Cellular and Molecular Neuroscience,Immunology

Link

http://www.nature.com/articles/s41419-018-0815-3.pdf

Reference45 articles.

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2. de Souza, P. V. S. et al. Hereditary spastic paraplegia: clinical and genetic hallmarks. Cerebellum 16, 525–551 (2017).

3. Deluca, G. C., Ebers, G. C. & Esiri, M. M. The extent of axonal loss in the long tracts in hereditary spastic paraplegia. Neuropathol. Appl. Neurobiol. 30, 576–584 (2004).

4. Tani, K., Kogure, T. & Inoue, H. The intracellular phospholipase A1 protein family. Biomol. Concepts 3, 471–478 (2012).

5. Higgs, H. N. & Glomset, J. A. Purification and properties of a phosphatidic acid-preferring phospholipase A1 from bovine testis. J. Biol. Chem. 271, 10874–10883 (1996).

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