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Items: 1 to 20 of 55

1.

Protein dislocation from the ER.

Bagola K, Mehnert M, Jarosch E, Sommer T.

Biochim Biophys Acta. 2011 Mar;1808(3):925-36. doi: 10.1016/j.bbamem.2010.06.025. Epub 2010 Jul 3. Review.

2.

The AAA-ATPase Cdc48 and cofactor Shp1 promote chromosome bi-orientation by balancing Aurora B activity.

Cheng YL, Chen RH.

J Cell Sci. 2010 Jun 15;123(Pt 12):2025-34. doi: 10.1242/jcs.066043. Epub 2010 May 18.

3.

Mechanism and components of endoplasmic reticulum-associated degradation.

Hoseki J, Ushioda R, Nagata K.

J Biochem. 2010 Jan;147(1):19-25. doi: 10.1093/jb/mvp194. Epub 2009 Nov 18. Review.

PMID:
19923195
4.

Heat shock and oxygen radicals stimulate ubiquitin-dependent degradation mainly of newly synthesized proteins.

Medicherla B, Goldberg AL.

J Cell Biol. 2008 Aug 25;182(4):663-73. doi: 10.1083/jcb.200803022.

5.

The AAA-ATPase p97-Ufd1-Npl4 is required for ERAD but not for spindle disassembly in Xenopus egg extracts.

Heubes S, Stemmann O.

J Cell Sci. 2007 Apr 15;120(Pt 8):1325-9. Epub 2007 Mar 20.

6.

Cdc48 is required for the stability of Cut1/separase in mitotic anaphase.

Ikai N, Yanagida M.

J Struct Biol. 2006 Oct;156(1):50-61. Epub 2006 May 15.

PMID:
16904908
7.
8.
9.

Ufd1 exhibits the AAA-ATPase fold with two distinct ubiquitin interaction sites.

Park S, Isaacson R, Kim HT, Silver PA, Wagner G.

Structure. 2005 Jul;13(7):995-1005.

10.

Distinct machinery is required in Saccharomyces cerevisiae for the endoplasmic reticulum-associated degradation of a multispanning membrane protein and a soluble luminal protein.

Huyer G, Piluek WF, Fansler Z, Kreft SG, Hochstrasser M, Brodsky JL, Michaelis S.

J Biol Chem. 2004 Sep 10;279(37):38369-78. Epub 2004 Jul 12.

11.

CDK activity antagonizes Whi5, an inhibitor of G1/S transcription in yeast.

Costanzo M, Nishikawa JL, Tang X, Millman JS, Schub O, Breitkreuz K, Dewar D, Rupes I, Andrews B, Tyers M.

Cell. 2004 Jun 25;117(7):899-913.

12.

Cln3 activates G1-specific transcription via phosphorylation of the SBF bound repressor Whi5.

de Bruin RA, McDonald WH, Kalashnikova TI, Yates J 3rd, Wittenberg C.

Cell. 2004 Jun 25;117(7):887-98.

13.

The Ubx2 and Ubx3 cofactors direct Cdc48 activity to proteolytic and nonproteolytic ubiquitin-dependent processes.

Hartmann-Petersen R, Wallace M, Hofmann K, Koch G, Johnsen AH, Hendil KB, Gordon C.

Curr Biol. 2004 May 4;14(9):824-8.

14.

The AAA-ATPase Cdc48/p97 regulates spindle disassembly at the end of mitosis.

Cao K, Nakajima R, Meyer HH, Zheng Y.

Cell. 2003 Oct 31;115(3):355-67.

PMID:
14636562
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17.

Regulation of the yeast Rlm1 transcription factor by the Mpk1 cell wall integrity MAP kinase.

Jung US, Sobering AK, Romeo MJ, Levin DE.

Mol Microbiol. 2002 Nov;46(3):781-9.

18.

Distinct AAA-ATPase p97 complexes function in discrete steps of nuclear assembly.

Hetzer M, Meyer HH, Walther TC, Bilbao-Cortes D, Warren G, Mattaj IW.

Nat Cell Biol. 2001 Dec;3(12):1086-91.

PMID:
11781570
19.

The AAA ATPase Cdc48/p97 and its partners transport proteins from the ER into the cytosol.

Ye Y, Meyer HH, Rapoport TA.

Nature. 2001 Dec 6;414(6864):652-6.

PMID:
11740563
20.

HRD4/NPL4 is required for the proteasomal processing of ubiquitinated ER proteins.

Bays NW, Wilhovsky SK, Goradia A, Hodgkiss-Harlow K, Hampton RY.

Mol Biol Cell. 2001 Dec;12(12):4114-28.

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