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Keywords: oligomer
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Biochem J (2020) 477 (3): 645–670.
Published: 11 February 2020
..., such as baicalein, (-)-epigallocatechin-3-gallate (EGCG), resveratrol, curcumin and oleuropein have shown promising results in this regard by influencing α - Syn oligomerization and fibrillation through either inhibition of fibrillation to form non-toxic oligomers [ 20–24 ] or by promoting fibrillation to prevent...
Includes: Supplementary data
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Biochem J (2017) 474 (1): 123–147.
Published: 22 December 2016
.... We found that each BPM induced the HuPrP to form unique oligomeric nanostructures differing in their biophysical properties, cellular toxicities and response to conformation-specific antibodies. While Leu-BPMs were found to stabilize the oligomers, Trp-BPMs effected transient oligomerization...
Includes: Supplementary data
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Biochem J (2015) 471 (3): 323–333.
Published: 16 October 2015
... that the inflammatory properties rely on fibril-specific structural features. amyloid fibril cross-β structure nucleotide oligomerization domain-like receptor pyrin domain containing 3 (NLRP3) inflammasome oligomer structure-inflammatory properties relationship α-synuclein Parkinson's disease (PD...
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Biochem J (2015) 468 (3): 485–493.
Published: 15 June 2015
...-syn oligomers. α-syn peaks were extracted from the Driftscope plots and the region >2900 m / z was enlarged to visualize the lower-abundance higher-order oligomeric series. Oligomers fell into the populations of dimers (2), trimers (3), tetramers (4), pentamers (5) and hexamers (6). ( B...
Includes: Supplementary data
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Biochem J (2011) 433 (2): 323–332.
Published: 22 December 2010
... with the existence of unique Aβ42 oligomers. Met 35 oxidation to sulfoxide or sulfone eliminates the differences in early oligomerization between Aβ40 and Aβ42. Met 35 oxidation to sulfoxide has been reported to decrease Aβ assembly kinetics and neurotoxicity, whereas oxidation to sulfone has rarely been studied...
Includes: Supplementary data
Articles
Biochem J (2010) 432 (1): 65–76.
Published: 25 October 2010
... to regulate gene expression. Although other components of the triacylglycerol synthesis pathway can form oligomeric complexes, it is unknown whether lipin proteins also exist as oligomers. In the present study, using various approaches, we revealed that lipin 1 formed stable homo-oligomers with itself...
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Biochem J (2006) 396 (2): 265–275.
Published: 15 May 2006
... the formation of FPN hetero-oligomers. 1 To whom correspondence should be addressed, at INSERM U773, Centre de Recherche Biomédicale Bichat Beaujon, Université Paris 7 site Bichat, 16 rue Henri Huchard, BP416, 75018 Paris, France (email beaumont@bichat.inserm.fr ). 18 10 2005 26 1 2006 3...
Includes: Supplementary data
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Biochem J (2005) 392 (2): 375–381.
Published: 22 November 2005
... to examine previously hidden processes in protein folding [ 1 – 4 ]. Normal protein oligomers are essential for life, whereas unwanted oligomers are the basis of amyloid and prion diseases. Furthermore, the folding of membrane and oligomeric proteins has important implications for both biotechnology...
Includes: Supplementary data
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Biochem J (2003) 371 (2): 515–523.
Published: 15 April 2003
... should be addressed (e-mail decker@biophysik.biologie.uni-mainz.de ). 5 7 2002 8 11 2002 4 12 2002 4 12 2002 The Biochemical Society, London ©2003 2003 catechol oxidase haemocyanin oligomer phenol oxidase structure Abbreviations used: CPC, cetylpyridinium...
Articles
Biochem J (2002) 367 (3): 801–808.
Published: 01 November 2002
... and facilitates Ia entry into the cytosol. By Western-blot analysis, Ib incubated with Vero cells at 37°C generated a cell-associated, SDS-insoluble oligomer of Ib (molecular mass>220kDa) within 15s, which was still evident 110min after washing cells. Ib oligomerization was temperature, but not pH, dependent...
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