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Results: 1 to 20 of 95

1.

A COFRADIC Protocol To Study Protein Ubiquitination.

Stes E, Laga M, Walton A, Samyn N, Timmerman E, De Smet I, Goormachtig S, Gevaert K.

J Proteome Res. 2014 Jun 6;13(6):3107-13. doi: 10.1021/pr4012443. Epub 2014 May 20.

PMID:
24816145
[PubMed - in process]
2.

Identification of New Mechanisms of Cellular Response to Chemotherapy by Tracking Changes in Post-Translational Modifications by Ubiquitin and Ubiquitin-Like Proteins.

Bonacci T, Audebert S, Camoin L, Baudelet E, Bidaut G, Garcia M, Witzel II, Perkins ND, Borg JP, Iovanna JL, Soubeyran P.

J Proteome Res. 2014 Apr 2. [Epub ahead of print]

PMID:
24654937
[PubMed - as supplied by publisher]
3.

Pathway Analysis of ChIP-Seq-Based NRF1 Target Genes Suggests a Logical Hypothesis of their Involvement in the Pathogenesis of Neurodegenerative Diseases.

Satoh J, Kawana N, Yamamoto Y.

Gene Regul Syst Bio. 2013 Nov 4;7:139-52. doi: 10.4137/GRSB.S13204. eCollection 2013.

PMID:
24250222
[PubMed]
Free PMC Article
4.

VPS35 and EIF4G1 mutations are rare in Parkinson's disease among Indians.

Sudhaman S, Behari M, Govindappa ST, Muthane UB, Juyal RC, Thelma BK.

Neurobiol Aging. 2013 Oct;34(10):2442.e1-3. doi: 10.1016/j.neurobiolaging.2013.04.025. Epub 2013 May 28.

PMID:
23726718
[PubMed - indexed for MEDLINE]
5.

The VPS35 gene and Parkinson's disease.

Deng H, Gao K, Jankovic J.

Mov Disord. 2013 May;28(5):569-75. doi: 10.1002/mds.25430. Epub 2013 Mar 27. Review.

PMID:
23536430
[PubMed - indexed for MEDLINE]
6.

The intracellular interactome of tetraspanin-enriched microdomains reveals their function as sorting machineries toward exosomes.

Perez-Hernandez D, Gutiérrez-Vázquez C, Jorge I, López-Martín S, Ursa A, Sánchez-Madrid F, Vázquez J, Yáñez-Mó M.

J Biol Chem. 2013 Apr 26;288(17):11649-61. doi: 10.1074/jbc.M112.445304. Epub 2013 Mar 5.

PMID:
23463506
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Interlaboratory reproducibility of large-scale human protein-complex analysis by standardized AP-MS.

Varjosalo M, Sacco R, Stukalov A, van Drogen A, Planyavsky M, Hauri S, Aebersold R, Bennett KL, Colinge J, Gstaiger M, Superti-Furga G.

Nat Methods. 2013 Apr;10(4):307-14. doi: 10.1038/nmeth.2400. Epub 2013 Mar 3.

PMID:
23455922
[PubMed - indexed for MEDLINE]
8.

Regulation of WASH-dependent actin polymerization and protein trafficking by ubiquitination.

Hao YH, Doyle JM, Ramanathan S, Gomez TS, Jia D, Xu M, Chen ZJ, Billadeau DD, Rosen MK, Potts PR.

Cell. 2013 Feb 28;152(5):1051-64. doi: 10.1016/j.cell.2013.01.051.

PMID:
23452853
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Pathogenic mutation in VPS35 impairs its protection against MPP(+) cytotoxicity.

Bi F, Li F, Huang C, Zhou H.

Int J Biol Sci. 2013;9(2):149-55. doi: 10.7150/ijbs.5617. Epub 2013 Jan 26.

PMID:
23411763
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease.

Nuytemans K, Bademci G, Inchausti V, Dressen A, Kinnamon DD, Mehta A, Wang L, Züchner S, Beecham GW, Martin ER, Scott WK, Vance JM.

Neurology. 2013 Mar 12;80(11):982-9. doi: 10.1212/WNL.0b013e31828727d4. Epub 2013 Feb 13.

PMID:
23408866
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

VPS35 Asp620Asn and EIF4G1 Arg1205His mutations are rare in Parkinson disease from southwest China.

Chen Y, Chen K, Song W, Chen X, Cao B, Huang R, Zhao B, Guo X, Burgunder J, Li J, Shang HF.

Neurobiol Aging. 2013 Jun;34(6):1709.e7-8. doi: 10.1016/j.neurobiolaging.2012.11.003. Epub 2012 Dec 20.

PMID:
23261770
[PubMed - indexed for MEDLINE]
12.

Nucleolar protein trafficking in response to HIV-1 Tat: rewiring the nucleolus.

Jarboui MA, Bidoia C, Woods E, Roe B, Wynne K, Elia G, Hall WW, Gautier VW.

PLoS One. 2012;7(11):e48702. doi: 10.1371/journal.pone.0048702. Epub 2012 Nov 15.

PMID:
23166591
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants.

Sharma M, Ioannidis JP, Aasly JO, Annesi G, Brice A, Bertram L, Bozi M, Barcikowska M, Crosiers D, Clarke CE, Facheris MF, Farrer M, Garraux G, Gispert S, Auburger G, Vilariño-Güell C, Hadjigeorgiou GM, Hicks AA, Hattori N, Jeon BS, Jamrozik Z, Krygowska-Wajs A, Lesage S, Lill CM, Lin JJ, Lynch T, Lichtner P, Lang AE, Libioulle C, Murata M, Mok V, Jasinska-Myga B, Mellick GD, Morrison KE, Meitnger T, Zimprich A, Opala G, Pramstaller PP, Pichler I, Park SS, Quattrone A, Rogaeva E, Ross OA, Stefanis L, Stockton JD, Satake W, Silburn PA, Strom TM, Theuns J, Tan EK, Toda T, Tomiyama H, Uitti RJ, Van Broeckhoven C, Wirdefeldt K, Wszolek Z, Xiromerisiou G, Yomono HS, Yueh KC, Zhao Y, Gasser T, Maraganore D, Krüger R; GEOPD consortium.

J Med Genet. 2012 Nov;49(11):721-6. doi: 10.1136/jmedgenet-2012-101155. Erratum in: J Med Genet. 2013 Mar;50(3):202.

PMID:
23125461
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

VPS35 mutation in Japanese patients with typical Parkinson's disease.

Ando M, Funayama M, Li Y, Kashihara K, Murakami Y, Ishizu N, Toyoda C, Noguchi K, Hashimoto T, Nakano N, Sasaki R, Kokubo Y, Kuzuhara S, Ogaki K, Yamashita C, Yoshino H, Hatano T, Tomiyama H, Hattori N.

Mov Disord. 2012 Sep 15;27(11):1413-7. doi: 10.1002/mds.25145. Epub 2012 Sep 18.

PMID:
22991136
[PubMed - indexed for MEDLINE]
15.

A census of human soluble protein complexes.

Havugimana PC, Hart GT, Nepusz T, Yang H, Turinsky AL, Li Z, Wang PI, Boutz DR, Fong V, Phanse S, Babu M, Craig SA, Hu P, Wan C, Vlasblom J, Dar VU, Bezginov A, Clark GW, Wu GC, Wodak SJ, Tillier ER, Paccanaro A, Marcotte EM, Emili A.

Cell. 2012 Aug 31;150(5):1068-81. doi: 10.1016/j.cell.2012.08.011.

PMID:
22939629
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

VPS35 mutation in Chinese Han patients with late-onset Parkinson's disease.

Deng H, Xu H, Deng X, Song Z, Zheng W, Gao K, Fan X, Tang J.

Eur J Neurol. 2012 Sep;19(9):e96-7. doi: 10.1111/j.1468-1331.2012.03800.x. No abstract available.

PMID:
22891780
[PubMed - indexed for MEDLINE]
17.

A high-throughput approach for measuring temporal changes in the interactome.

Kristensen AR, Gsponer J, Foster LJ.

Nat Methods. 2012 Sep;9(9):907-9. doi: 10.1038/nmeth.2131. Epub 2012 Aug 5.

PMID:
22863883
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Frequency of the D620N mutation in VPS35 in Parkinson disease.

Kumar KR, Weissbach A, Heldmann M, Kasten M, Tunc S, Sue CM, Svetel M, Kostić VS, Segura-Aguilar J, Ramirez A, Simon DK, Vieregge P, Münte TF, Hagenah J, Klein C, Lohmann K.

Arch Neurol. 2012 Oct;69(10):1360-4.

PMID:
22801713
[PubMed - indexed for MEDLINE]
19.

The proteomic analysis of endogenous FAT10 substrates identifies p62/SQSTM1 as a substrate of FAT10ylation.

Aichem A, Kalveram B, Spinnenhirn V, Kluge K, Catone N, Johansen T, Groettrup M.

J Cell Sci. 2012 Oct 1;125(Pt 19):4576-85. doi: 10.1242/jcs.107789. Epub 2012 Jul 13.

PMID:
22797925
[PubMed - indexed for MEDLINE]
Free Article
20.

Identification of Alzheimer disease-associated variants in genes that regulate retromer function.

Vardarajan BN, Bruesegem SY, Harbour ME, Inzelberg R, Friedland R, St George-Hyslop P, Seaman MN, Farrer LA.

Neurobiol Aging. 2012 Sep;33(9):2231.e15-2231.e30. doi: 10.1016/j.neurobiolaging.2012.04.020. Epub 2012 Jun 5. Erratum in: Neurobiol Aging. 2013 Jul;34(7):1923. Inzelberg, Rivka [added]; Friedland, Robert [added].

PMID:
22673115
[PubMed - indexed for MEDLINE]
Free PMC Article

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