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Select item 112744031.

Radiation-Induced Endothelial Ferroptosis Accelerates Atherosclerosis via the DDHD2-Mediated Nrf2/GPX4 Pathway

Xi Su, Feng Liang, Ya Zeng, Zhang-Ru Yang, Yue-Zhen Deng, Yun-Hua Xu, Xu-Wei Cai

Biomolecules. 2024 Jul; 14(7): 879. Published online 2024 Jul 22. doi: 10.3390/biom14070879

PMCID:: PMC11274403

Abstract Article PDF–8.7M

Select item 105026692.

Biallelic DDHD2 mutations in patients with adult‐onset complex hereditary spastic paraplegia

Ying‐Tsen Chou, Shao‐Lun Hsu, Yu‐Shuen Tsai, Yi‐Jiun Lu, Kai‐Wei Yu, Hsiu‐Mei Wu, Yi‐Chu Liao, Yi‐Chung Lee

Ann Clin Transl Neurol. 2023 Sep; 10(9): 1603–1612. Published online 2023 Jul 7. doi: 10.1002/acn3.51850

PMCID:: PMC10502669

Abstract Article PDF–1.6M

Select item 102374223.

TRIM67 drives tumorigenesis in oligodendrogliomas through Rho GTPase-dependent membrane blebbing

Engin Demirdizen, Ruslan Al-Ali, Ashwin Narayanan, Xueyuan Sun, Julianna Patricia Varga, Bianca Steffl, Manuela Brom, Damir Krunic, Claudia Schmidt, Gabriele Schmidt, Felix Bestvater, Julian Taranda, Şevin Turcan

Neuro Oncol. 2023 Jun; 25(6): 1031–1043. Published online 2022 Nov 22. doi: 10.1093/neuonc/noac233

PMCID:: PMC10237422

Abstract Article PDF–23M

Select item 99901204.

Interactomes of Glycogen Synthase Kinase-3 Isoforms

Kevin W. Cormier, Brett Larsen, Anne-Claude Gingras, James R. Woodgett

J Proteome Res. 2023 Mar 3; 22(3): 977–989. Published online 2023 Feb 13. doi: 10.1021/acs.jproteome.2c00825

PMCID:: PMC9990120

Abstract Article PDF–3.7M

Select item 81650305.

Dual Proteome-scale Networks Reveal Cell-specific Remodeling of the Human Interactome

Edward L. Huttlin, Raphael J. Bruckner, Jose Navarrete-Perea, Joe R. Cannon, Kurt Baltier, Fana Gebreab, Melanie P. Gygi, Alexandra Thornock, Gabriela Zarraga, Stanley Tam, John Szpyt, Brandon M. Gassaway, Alexandra Panov, Hannah Parzen, Sipei Fu, Arvene Golbazi, Eila Maenpaa, Keegan Stricker, Sanjukta Guha Thakurta, Tian Zhang, Ramin Rad, Joshua Pan, David P. Nusinow, Joao A. Paulo, Devin K. Schweppe, Laura Pontano Vaites, J. Wade Harper, Steven P. Gygi

Cell. Author manuscript; available in PMC 2022 May 27.

Published in final edited form as: Cell. 2021 May 27; 184(11): 3022–3040.e28. Published online 2021 May 6. doi: 10.1016/j.cell.2021.04.011

PMCID:: PMC8165030

Abstract Article PDF–2.2M

Select item 78860166.

Genome-wide landscape of RNA-binding protein target site dysregulation reveals a major impact on psychiatric disorder risk

Christopher Y. Park, Jian Zhou, Aaron K. Wong, Kathleen M. Chen, Chandra L. Theesfeld, Robert B. Darnell, Olga G. Troyanskaya

Nat Genet. Author manuscript; available in PMC 2021 Jul 18.

Published in final edited form as: Nat Genet. 2021 Feb; 53(2): 166–173. Published online 2021 Jan 18. doi: 10.1038/s41588-020-00761-3

PMCID:: PMC7886016

Abstract Article PDF–2.5M

Select item 78199937.

Circular RNA circRUNX1 promotes papillary thyroid cancer progression and metastasis by sponging MiR-296-3p and regulating DDHD2 expression

Junjie Chu, Li Tao, Teng Yao, Zizheng Chen, Xiaoxiao Lu, Li Gao, Liang Fang, Jian Chen, Gaofei He, Shuying Shen, Deguang Zhang

Cell Death Dis. 2021 Jan; 12(1): 112. Published online 2021 Jan 21. doi: 10.1038/s41419-020-03350-8

PMCID:: PMC7819993

Abstract Article PDF–3.6M

Select item 74006718.

Common genetic risk variants identified in the SPARK cohort support DDHD2 as a candidate risk gene for autism

Nana Matoba, Dan Liang, Huaigu Sun, Nil Aygün, Jessica C. McAfee, Jessica E. Davis, Laura M. Raffield, Huijun Qian, Joseph Piven, Yun Li, Sriam Kosuri, Hyejung Won, Jason L. Stein

Transl Psychiatry. 2020; 10: 265. Published online 2020 Aug 3. doi: 10.1038/s41398-020-00953-9

PMCID:: PMC7400671

Abstract Article PDF–2.9M

Select item 64839939.

The nuclear interactome of DYRK1A reveals a functional role in DNA damage repair

Steven E. Guard, Zachary C. Poss, Christopher C. Ebmeier, Maria Pagratis, Helen Simpson, Dylan J. Taatjes, William M. Old

Sci Rep. 2019; 9: 6539. Published online 2019 Apr 25. doi: 10.1038/s41598-019-42990-5

PMCID:: PMC6483993

Abstract Article PDF–2.2M

Select item 607772210.

Estrogen-regulated feedback loop limits the efficacy of estrogen receptor–targeted breast cancer therapy

Tengfei Xiao, Wei Li, Xiaoqing Wang, Han Xu, Jixin Yang, Qiu Wu, Ying Huang, Joseph Geradts, Peng Jiang, Teng Fei, David Chi, Chongzhi Zang, Qi Liao, Jonathan Rennhack, Eran Andrechek, Nanlin Li, Simone Detre, Mitchell Dowsett, Rinath M. Jeselsohn, X. Shirley Liu, Myles Brown

Proc Natl Acad Sci U S A. 2018 Jul 31; 115(31): 7869–7878. Published online 2018 Jul 9. doi: 10.1073/pnas.1722617115

PMCID:: PMC6077722

Abstract Article PDF–2.4M

Select item 605654411.

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

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

Cell Death Dis. 2018 Aug; 9(8): 797. Published online 2018 Jul 23. doi: 10.1038/s41419-018-0815-3

PMCID:: PMC6056544

Abstract Article PDF–2.7M

Select item 600581612.

Proteomic and Biochemical Comparison of the Cellular Interaction Partners of Human VPS33A and VPS33B

Morag R. Hunter, Geoffrey G. Hesketh, Tomasz H. Benedyk, Anne-Claude Gingras, Stephen C. Graham

J Mol Biol. 2018 Jul 6; 430(14): 2153–2163. doi: 10.1016/j.jmb.2018.05.019

PMCID:: PMC6005816

Abstract Article PDF–1.6M

Select item 585415113.

Functional Contribution of the Spastic Paraplegia-Related Triglyceride Hydrolase DDHD2 to the Formation and Content of Lipid Droplets

Jordon M. Inloes, William B. Kiosses, Huajin Wang, Tobias C. Walther, Robert V. Farese, Jr., Benjamin F. Cravatt

Biochemistry. Author manuscript; available in PMC 2019 Feb 6.

Published in final edited form as: Biochemistry. 2018 Feb 6; 57(5): 827–838. Published online 2017 Dec 26. doi: 10.1021/acs.biochem.7b01028

PMCID:: PMC5854151

Abstract Article PDF–988K

Select item 553161114.

Architecture of the human interactome defines protein communities and disease networks

Edward L. Huttlin, Raphael J. Bruckner, Joao A. Paulo, Joe R. Cannon, Lily Ting, Kurt Baltier, Greg Colby, Fana Gebreab, Melanie P. Gygi, Hannah Parzen, John Szpyt, Stanley Tam, Gabriela Zarraga, Laura Pontano-Vaites, Sharan Swarup, Anne E. White, Devin K. Schweppe, Ramin Rad, Brian K. Erickson, Robert A. Obar, K.G. Guruharsha, Kejie Li, Spyros Artavanis-Tsakonas, Steven P. Gygi, J. Wade Harper

Nature. Author manuscript; available in PMC 2017 Nov 17.

Published in final edited form as: Nature. 2017 May 25; 545(7655): 505–509. Published online 2017 May 17. doi: 10.1038/nature22366

PMCID:: PMC5531611

Abstract Article PDF–2.7M

Select item 538408815.

Late-onset spastic ataxia phenotype in a patient with a homozygous DDHD2 mutation

Hiroshi Doi, Masao Ushiyama, Takashi Baba, Katsuko Tani, Masaaki Shiina, Kazuhiro Ogata, Satoko Miyatake, Yoko Fukuda-Yuzawa, Shoji Tsuji, Mitsuko Nakashima, Yoshinori Tsurusaki, Noriko Miyake, Hirotomo Saitsu, Shu-ichi Ikeda, Fumiaki Tanaka, Naomichi Matsumoto, Kunihiro Yoshida

Sci Rep. 2014; 4: 7132. Published online 2014 Nov 24. doi: 10.1038/srep07132

PMCID:: PMC5384088

Abstract Article PDF–733K

Select item 461721116.

The BioPlex Network: A Systematic Exploration of the Human Interactome

Edward L. Huttlin, Lily Ting, Raphael J. Bruckner, Fana Gebreab, Melanie P. Gygi, John Szpyt, Stanley Tam, Gabriela Zarraga, Greg Colby, Kurt Baltier, Rui Dong, Virginia Guarani, Laura Pontano Vaites, Alban Ordureau, Ramin Rad, Brian K. Erickson, Martin Wühr, Joel Chick, Bo Zhai, Deepak Kolippakkam, Julian Mintseris, Robert A. Obar, Tim Harris, Spyros Artavanis-Tsakonas, Mathew E. Sowa, Pietro DeCamilli, Joao A. Paulo, J. Wade Harper, Steven P. Gygi

Cell. Author manuscript; available in PMC 2016 Jul 16.

Published in final edited form as: Cell. 2015 Jul 16; 162(2): 425–440. doi: 10.1016/j.cell.2015.06.043

PMCID:: PMC4617211

Abstract Article PDF–2.2M

Select item 448229617.

Truncating mutation in intracellular phospholipase A₁ gene (DDHD2) in hereditary spastic paraplegia with intellectual disability (SPG54)

Nuha Alrayes, Hussein Sheikh Ali Mohamoud, Musharraf Jelani, Saleem Ahmad, Nirmal Vadgama, Khadijah Bakur, Michael Simpson, Jumana Yousuf Al-Aama, Jamal Nasir

BMC Res Notes. 2015; 8: 271. Published online 2015 Jun 27. doi: 10.1186/s13104-015-1227-4

PMCID:: PMC4482296

Abstract Article PDF–1.2M

Select item 432648118.

miR-503 represses human cell proliferation and directly targets the oncogene DDHD2 by non-canonical target pairing

Damon Polioudakis, Nathan S Abell, Vishwanath R Iyer

BMC Genomics. 2015; 16(1): 40. Published online 2015 Feb 5. doi: 10.1186/s12864-015-1279-9

PMCID:: PMC4326481

Abstract Article PDF–1.2M

Select item 379883719.

Mutations in phospholipase DDHD2 cause autosomal recessive hereditary spastic paraplegia (SPG54)

Michael Gonzalez, Sheela Nampoothiri, Cornelia Kornblum, Andrés Caballero Oteyza, Jochen Walter, Ioanna Konidari, William Hulme, Fiorella Speziani, Ludger Schöls, Stephan Züchner, Rebecca Schüle

Eur J Hum Genet. 2013 Nov; 21(11): 1214–1218. Published online 2013 Mar 13. doi: 10.1038/ejhg.2013.29

PMCID:: PMC3798837

Abstract Article PDF–912K

Select item 351659520.

Mutations in DDHD2, Encoding an Intracellular Phospholipase A₁, Cause a Recessive Form of Complex Hereditary Spastic Paraplegia

Janneke H.M. Schuurs-Hoeijmakers, Michael T. Geraghty, Erik-Jan Kamsteeg, Salma Ben-Salem, Susanne T. de Bot, Bonnie Nijhof, Ilse I.G.M. van de Vondervoort, Marinette van der Graaf, Anna Castells Nobau, Irene Otte-Höller, Sascha Vermeer, Amanda C. Smith, Peter Humphreys, Jeremy Schwartzentruber, FORGE Canada Consortium, Bassam R. Ali, Saeed A. Al-Yahyaee, Said Tariq, Thachillath Pramathan, Riad Bayoumi, Hubertus P.H. Kremer, Bart P. van de Warrenburg, Willem M.R. van den Akker, Christian Gilissen, Joris A. Veltman, Irene M. Janssen, Anneke T. Vulto-van Silfhout, Saskia van der Velde-Visser, Dirk J. Lefeber, Adinda Diekstra, Corrie E. Erasmus, Michèl A. Willemsen, Lisenka E.L.M. Vissers, Martin Lammens, Hans van Bokhoven, Han G. Brunner, Ron A. Wevers, Annette Schenck, Lihadh Al-Gazali, Bert B.A. de Vries, Arjan P.M. de Brouwer

Am J Hum Genet. 2012 Dec 7; 91(6): 1073–1081. doi: 10.1016/j.ajhg.2012.10.017

PMCID:: PMC3516595

Abstract Article PDF–764K

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