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	161.	A Golgi rhomboid protease Rbd2 recruits Cdc48 to cleave yeast SREBP. [electronic resource] by Hwang, Jiwon Ribbens, Diedre Raychaudhuri, Sumana Cairns, Leah Gu, He Frost, Adam Urban, Siniša Espenshade, Peter J Producer: 20170717 In: The EMBO journal vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	162.	Expanding into new markets--VCP/p97 in endocytosis and autophagy. [electronic resource] by Bug, Monika Meyer, Hemmo Producer: 20121213 In: Journal of structural biology vol. 179 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	163.	The Cdc48 protein and its cofactor Vms1 are involved in Cdc13 protein degradation. [electronic resource] by Baek, Guem Hee Cheng, Haili Kim, Ikjin Rao, Hai Producer: 20121105 In: The Journal of biological chemistry vol. 287 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	164.	P97/CDC-48: proteostasis control in tumor cell biology. [electronic resource] by Fessart, Delphine Marza, Esther Taouji, Saïd Delom, Frédéric Chevet, Eric Producer: 20130916 In: Cancer letters vol. 337 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	165.	Perturbations to the ubiquitin conjugate proteome in yeast δubx mutants identify Ubx2 as a regulator of membrane lipid composition. [electronic resource] by Kolawa, Natalie Sweredoski, Michael J Graham, Robert L J Oania, Robert Hess, Sonja Deshaies, Raymond J Producer: 20140509 In: Molecular & cellular proteomics : MCP vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	166.	Novel valosin-containing protein mutations associated with multisystem proteinopathy. [electronic resource] by Al-Tahan, Sejad Al-Obeidi, Ebaa Yoshioka, Hiroshi Lakatos, Anita Weiss, Lan Grafe, Marjorie Palmio, Johanna Wicklund, Matt Harati, Yadollah Omizo, Molly Udd, Bjarne Kimonis, Virginia Producer: 20191023 In: Neuromuscular disorders : NMD vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	167.	The multifaceted clinical presentation of VCP-proteinopathy in a Greek family. [electronic resource] by Papadimas, George K Paraskevas, George P Zambelis, Thomas Karagiaouris, Chrisostomos Bourbouli, Mara Bougea, Anastasia Walter, Maggie C Schumacher, Nicolas U Krause, Sabine Kapaki, Elisabeth Producer: 20181026 In: Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology vol. 36 Availability: No items available. Save to lists Add to cart (remove)
	168.	p97/VCP at the intersection of the autophagy and the ubiquitin proteasome system. [electronic resource] by Ju, Jeong-Sun Weihl, Conrad C Producer: 20100706 In: Autophagy vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	169.	Yeast Derlin Dfm1 interacts with Cdc48 and functions in ER homeostasis. [electronic resource] by Sato, Brian K Hampton, Randolph Y Producer: 20070112 In: Yeast (Chichester, England) vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	170.	[Protein modifications in neurodegenerative disorders]. [electronic resource] by Kakizuka, Akira Koike, Masaaki Producer: 20070713 In: Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme vol. 52 Availability: No items available. Save to lists Add to cart (remove)
	171.	Differential expression pattern of UBX family genes in Caenorhabditis elegans. [electronic resource] by Yamauchi, Seiji Sasagawa, Yohei Ogura, Teru Yamanaka, Kunitoshi Producer: 20070711 In: Biochemical and biophysical research communications vol. 358 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	172.	A novel mutation in VCP causes Charcot-Marie-Tooth Type 2 disease. [electronic resource] by Gonzalez, Michael A Feely, Shawna M Speziani, Fiorella Strickland, Alleene V Danzi, Matt Bacon, Chelsea Lee, Youjin Chou, Tsui-Fen Blanton, Susan H Weihl, Conrad C Zuchner, Stephan Shy, Michael E Producer: 20150209 In: Brain : a journal of neurology vol. 137 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	173.	Valosin-containing protein immunoreactivity in tauopathies, synucleinopathies, polyglutamine diseases and intranuclear inclusion body disease. [electronic resource] by Mori, Fumiaki Tanji, Kunikazu Toyoshima, Yasuko Sasaki, Hidenao Yoshida, Mari Kakita, Akiyoshi Takahashi, Hitoshi Wakabayashi, Koichi Producer: 20140819 In: Neuropathology : official journal of the Japanese Society of Neuropathology vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	174.	Valosin-containing protein mediates the ERAD of squalene monooxygenase and its cholesterol-responsive degron. [electronic resource] by Chua, Ngee Kiat Scott, Nicola A Brown, Andrew J Producer: 20200318 In: The Biochemical journal vol. 476 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	175.	N-ethylmaleimide-sensitive fusion protein (NSF) and CDC48 confirmed as members of the double-psi beta-barrel aspartate decarboxylase/formate dehydrogenase family. [electronic resource] by Mizuguchi, K Dhanaraj, V Blundell, T L Murzin, A G Producer: 19991215 In: Structure (London, England : 1993) vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	176.	The genetics of frontotemporal dementia. [electronic resource] by Pickering-Brown, Stuart Hutton, Michael Producer: 20101207 In: Handbook of clinical neurology vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	177.	Distinct distal myopathy phenotype caused by VCP gene mutation in a Finnish family. [electronic resource] by Palmio, Johanna Sandell, Satu Suominen, Tiina Penttilä, Sini Raheem, Olayinka Hackman, Peter Huovinen, Sanna Haapasalo, Hannu Udd, Bjarne Producer: 20120119 In: Neuromuscular disorders : NMD vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	178.	Valosin-containing protein (VCP) mutations in sporadic amyotrophic lateral sclerosis. [electronic resource] by Abramzon, Yevgeniya Johnson, Janel O Scholz, Sonja W Taylor, J P Brunetti, Maura Calvo, Andrea Mandrioli, Jessica Benatar, Michael Mora, Gabriele Restagno, Gabriella Chiò, Adriano Traynor, Bryan J Producer: 20121129 In: Neurobiology of aging vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	179.	Membrane fusion and the cell cycle: Cdc48p participates in the fusion of ER membranes. [electronic resource] by Latterich, M Fröhlich, K U Schekman, R Producer: 19951027 In: Cell vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	180.	Dfm1 forms distinct complexes with Cdc48 and the ER ubiquitin ligases and is required for ERAD. [electronic resource] by Stolz, Alexandra Schweizer, Regina S Schäfer, Antje Wolf, Dieter H Producer: 20110228 In: Traffic (Copenhagen, Denmark) vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 959 results.