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Items: 1 to 20 of 36

1.
KDELR2 promotes breast cancer proliferation via HDAC3‐mediated cell cycle progression
Haoran Wei, Wenhao Ma, Xiaofei Lu, Haiying Liu, Kashuai Lin, Yinghui Wang, Zijian Ye, Linchong Sun, Zhitong Huang, Tingting Pan, Zilong Zhou, Eric Y. Cheng, Huafeng Zhang, Ping Gao, Xiuying Zhong
Cancer Commun (Lond) 2021 Sep; 41(9): 904–920. Published online 2021 Jun 19. doi: 10.1002/cac2.12180
PMCID:
PMC8441056
ArticlePDF–5.8M
2.
Two novel bi‐allelic KDELR2 missense variants cause osteogenesis imperfecta with neurodevelopmental features
Stephanie Efthymiou, Isabella Herman, Fatima Rahman, Najwa Anwar, Reza Maroofian, Janice Yip, Tadahiro Mitani, Daniel G. Calame, Jill V. Hunter, V. Reid Sutton, Elif Yilmaz Gulec, Ruizhi Duan, Jawid M. Fatih, Dana Marafi, Davut Pehlivan, Shalini N. Jhangiani, Richard A. Gibbs, Jennifer E. Posey, SYNAPS Study Group, Shazia Maqbool, James R. Lupski, Henry Houlden
Am J Med Genet A. 2021 Jul; 185(7): 2241–2249. Published online 2021 May 8. doi: 10.1002/ajmg.a.62221
PMCID:
PMC8436746
ArticlePDF–2.0M
3.
A brefeldin A-like phenotype is induced by the overexpression of a human ERD-2-like protein, ELP-1
Victor W. Hsu, Nicky Shah, Richard D. Klausner
Cell. 1992 May 15; 69(4): 625–635. Published online 2004 Apr 16. doi: 10.1016/0092-8674(92)90226-3
PMCID:
PMC7133352
ArticlePDF–2.7M
4.
KDELR2 Competes with Measles Virus Envelope Proteins for Cellular Chaperones Reducing Their Chaperone-Mediated Cell Surface Transport
Vishakha Tiwarekar, Markus Fehrholz, Jürgen Schneider-Schaulies
Viruses. 2019 Jan; 11(1): 27. Published online 2019 Jan 4. doi: 10.3390/v11010027
PMCID:
PMC6356275
ArticlePDF–2.1M
5.
Endoplasmic reticulum resident proteins of normal human dermal fibroblasts are the major targets for oxidative stress induced by hydrogen peroxide.
Dennis van der Vlies, Eward H W Pap, Jan Andries Post, Julio E Celis, Karel W A Wirtz
Biochem J. 2002 Sep 15; 366(Pt 3): 825–830. doi: 10.1042/BJ20020618
PMCID:
PMC1222834
SummaryPDF–213K
6.
KDEL receptor regulates secretion by lysosome relocation- and autophagy-dependent modulation of lipid-droplet turnover
Diego Tapia, Tomás Jiménez, Constanza Zamora, Javier Espinoza, Riccardo Rizzo, Alexis González-Cárdenas, Danitza Fuentes, Sergio Hernández, Viviana A. Cavieres, Andrea Soza, Fanny Guzmán, Gloria Arriagada, María Isabel Yuseff, Gonzalo A. Mardones, Patricia V. Burgos, Alberto Luini, Alfonso González, Jorge Cancino
Nat Commun. 2019; 10: 735. Published online 2019 Feb 13. doi: 10.1038/s41467-019-08501-w
PMCID:
PMC6374470
ArticlePDF–8.8M
7.
A Golgi-based KDELR-dependent signalling pathway controls extracellular matrix degradation
Carmen Ruggiero, Giorgia Fragassi, Mauro Grossi, Benedetta Picciani, Rosaria Di Martino, Mirco Capitani, Roberto Buccione, Alberto Luini, Michele Sallese
Oncotarget. 2015 Feb; 6(5): 3375–3393. Published online 2014 Dec 18. doi: 10.18632/oncotarget.3270
PMCID:
PMC4413660
ArticlePDF–13M
8.
Interaction between KDELR2 and HSP47 as a Key Determinant in Osteogenesis Imperfecta Caused by Bi-allelic Variants in KDELR2
Fleur S. van Dijk, Oliver Semler, Julia Etich, Anna Köhler, Juan A. Jimenez-Estrada, Nathalie Bravenboer, Lauria Claeys, Elise Riesebos, Sejla Gegic, Sander R. Piersma, Connie R. Jimenez, Quinten Waisfisz, Carmen-Lisset Flores, Julian Nevado, Arjan J. Harsevoort, Guus J.M. Janus, Anton A.M. Franken, Astrid M. van der Sar, Hanne Meijers-Heijboer, Karen E. Heath, Pablo Lapunzina, Peter G.J. Nikkels, Gijs W.E. Santen, Julian Nüchel, Markus Plomann, Raimund Wagener, Mirko Rehberg, Heike Hoyer-Kuhn, Elisabeth M.W. Eekhoff, Gerard Pals, Matthias Mörgelin, Simon Newstead, Brian T. Wilson, Victor L. Ruiz-Perez, Alessandra Maugeri, Christian Netzer, Frank Zaucke, Dimitra Micha
Am J Hum Genet. 2020 Nov 5; 107(5): 989–999. Published online 2020 Oct 13. doi: 10.1016/j.ajhg.2020.09.009
PMCID:
PMC7675035
ArticlePDF–2.7M
9.
Cell-type-specific differences in KDEL receptor clustering in mammalian cells
Achim Bauer, Ludger Santen, Manfred J. Schmitt, M. Reza Shaebani, Björn Becker
PLoS One. 2020; 15(7): e0235864. Published online 2020 Jul 9. doi: 10.1371/journal.pone.0235864
PMCID:
PMC7347126
ArticlePDF–1.8M
10.
A molecular specificity code for the three mammalian KDEL receptors
Irina Raykhel, Heli Alanen, Kirsi Salo, Jaana Jurvansuu, Van Dat Nguyen, Maria Latva-Ranta, Lloyd Ruddock
J Cell Biol. 2007 Dec 17; 179(6): 1193–1204. doi: 10.1083/jcb.200705180
Correction in:
J Cell Biol. 2008 Feb 11; 180(3): 645.
PMCID:
PMC2140024
ArticlePDF–2.1M
11.
Phosphorylation of Elp1 by Hrr25 Is Required for Elongator-Dependent tRNA Modification in Yeast
Wael Abdel-Fattah, Daniel Jablonowski, Rachael Di Santo, Kathrin L. Thüring, Viktor Scheidt, Alexander Hammermeister, Sara ten Have, Mark Helm, Raffael Schaffrath, Michael J. R. Stark
PLoS Genet. 2015 Jan; 11(1): e1004931. Published online 2015 Jan 8. doi: 10.1371/journal.pgen.1004931
PMCID:
PMC4287497
ArticlePDF–3.9M
12.
Viral protein engagement of GBF1 induces host cell vulnerability through synthetic lethality
Arti T. Navare, Fred D. Mast, Jean Paul Olivier, Thierry Bertomeu, Maxwell L. Neal, Lindsay N. Carpp, Alexis Kaushansky, Jasmin Coulombe-Huntington, Mike Tyers, John D. Aitchison
J Cell Biol. 2022 Nov 7; 221(11): e202011050. Published online 2022 Oct 28. doi: 10.1083/jcb.202011050
PMCID:
PMC9623979
ArticlePDF–3.7M
13.
The OncoPPi network of cancer-focused protein–protein interactions to inform biological insights and therapeutic strategies
Zenggang Li, Andrei A. Ivanov, Rina Su, Valentina Gonzalez-Pecchi, Qi Qi, Songlin Liu, Philip Webber, Elizabeth McMillan, Lauren Rusnak, Cau Pham, Xiaoqian Chen, Xiulei Mo, Brian Revennaugh, Wei Zhou, Adam Marcus, Sahar Harati, Xiang Chen, Margaret A. Johns, Michael A. White, Carlos S. Moreno, Lee A. D. Cooper, Yuhong Du, Fadlo R. Khuri, Haian Fu
Nat Commun. 2017; 8: 14356. Published online 2017 Feb 16. doi: 10.1038/ncomms14356
Correction in:
Nat Commun. 2017; 8: 15350.
PMCID:
PMC5316855
ArticlePDF–4.1M
14.
Loss-of-Function Variants in TBC1D32 Underlie Syndromic Hypopituitarism
Johanna Hietamäki, Louise C Gregory, Sandy Ayoub, Anna-Pauliina Iivonen, Kirsi Vaaralahti, Xiaonan Liu, Nina Brandstack, Andrew J Buckton, Tiina Laine, Johanna Känsäkoski, Matti Hero, Päivi J Miettinen, Markku Varjosalo, Emma Wakeling, Mehul T Dattani, Taneli Raivio
J Clin Endocrinol Metab. 2020 Jun; 105(6): 1748–1758. Published online 2020 Feb 15. doi: 10.1210/clinem/dgaa078
PMCID:
PMC7138537
Article
15.
Insight into hepatocellular carcinogenesis at transcriptome level by comparing gene expression profiles of hepatocellular carcinoma with those of corresponding noncancerous liver
Xiang-Ru Xu, Jian Huang, Zhi-Gang Xu, Bin-Zhi Qian, Zhi-Dong Zhu, Qing Yan, Ting Cai, Xin Zhang, Hua-Sheng Xiao, Jian Qu, Feng Liu, Qiu-Hua Huang, Zhi-Hong Cheng, Neng-Gan Li, Jian-Jun Du, Wei Hu, Kun-Tang Shen, Gang Lu, Gang Fu, Ming Zhong, Shu-Hua Xu, Wen-Yi Gu, Wei Huang, Xin-Tai Zhao, Geng-Xi Hu, Jian-Ren Gu, Zhu Chen, Ze-Guang Han
Proc Natl Acad Sci U S A. 2001 Dec 18; 98(26): 15089–15094. doi: 10.1073/pnas.241522398
PMCID:
PMC64988
ArticlePDF–341K
16.
Proteomic Analysis Reveals a Role for RSK in p120-catenin Phosphorylation and Melanoma Cell-Cell Adhesion
Antoine Méant, Beichen Gao, Geneviève Lavoie, Sami Nourreddine, Flora Jung, Léo Aubert, Joseph Tcherkezian, Anne-Claude Gingras, Philippe P. Roux
Mol Cell Proteomics. 2020 Jan; 19(1): 50–64. Published online 2019 Nov 2. doi: 10.1074/mcp.RA119.001811
PMCID:
PMC6944238
ArticlePDF–5.7M
17.
CRISPR/Cas9-mediated Genomic Editing of Cluap1/IFT38 Reveals a New Role in Actin Arrangement
Tina Beyer, Sylvia Bolz, Katrin Junger, Nicola Horn, Muhammad Moniruzzaman, Yasmin Wissinger, Marius Ueffing, Karsten Boldt
Mol Cell Proteomics. 2018 Jul; 17(7): 1285–1294. Published online 2018 Apr 3. doi: 10.1074/mcp.RA117.000487
PMCID:
PMC6030719
ArticlePDF–2.7M
18.
GREB1: An evolutionarily conserved protein with a glycosyltransferase domain links ERα glycosylation and stability to cancer
Eun Myoung Shin, Vinh Thang Huynh, Sultan Abda Neja, Chia Yi Liu, Anandhkumar Raju, Kelly Tan, Nguan Soon Tan, Jayantha Gunaratne, Xuezhi Bi, Lakshminarayan M. Iyer, L. Aravind, Vinay Tergaonkar
Sci Adv. 2021 Mar; 7(12): eabe2470. Published online 2021 Mar 17. doi: 10.1126/sciadv.abe2470
PMCID:
PMC7968844
ArticlePDF–1.1M
19.
Perturbation of the mutated EGFR interactome identifies vulnerabilities and resistance mechanisms
Jiannong Li, Keiryn Bennett, Alexey Stukalov, Bin Fang, Guolin Zhang, Takeshi Yoshida, Isamu Okamoto, Jae-Young Kim, Lanxi Song, Yun Bai, Xiaoning Qian, Bhupendra Rawal, Michael Schell, Florian Grebien, Georg Winter, Uwe Rix, Steven Eschrich, Jacques Colinge, John Koomen, Giulio Superti-Furga, Eric B Haura
Mol Syst Biol. 2013; 9: 705. Published online 2013 Nov 5. doi: 10.1038/msb.2013.61
PMCID:
PMC4039310
ArticlePDF–3.2M
20.
Quantitative Interaction Proteomics of Neurodegenerative Disease Proteins
Fabian Hosp, Hannes Vossfeldt, Matthias Heinig, Djordje Vasiljevic, Anup Arumughan, Emanuel Wyler, Genetic and Environmental Risk for Alzheimer’s Disease (GERAD1) Consortium, Markus Landthaler, Norbert Hubner, Erich E. Wanker, Lars Lannfelt, Martin Ingelsson, Maciej Lalowski, Aaron Voigt, Matthias Selbach
Cell Rep. Author manuscript; available in PMC 2022 Apr 18.
Published in final edited form as: Cell Rep. 2015 May 19; 11(7): 1134–1146. Published online 2015 May 7. doi: 10.1016/j.celrep.2015.04.030
PMCID:
PMC9014711
ArticlePDF–2.2M

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