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Journal articleCleverley JR, Desai SR, Wells AU, et al., 2000,
Evaluation of patients undergoing lung volume reduction surgery: Ancillary information available from computed tomography
, CLINICAL RADIOLOGY, Vol: 55, Pages: 45-50, ISSN: 0009-9260- Cite
- Citations: 21
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Journal articleMohantry AK, Bismarck A, Aranberri I, et al., 2000,
Abstract: Characterization of natural fibers using zeta-potential measurements: Surface properties and the water uptake behavior of modified jute, sisal, and coir fibers
, Abstracts of Papers of the American Chemical Society, Vol: 219 -
Journal articleBismarck A, Pfeifer G, Springer J, 2000,
Study on surface- and mechanical fiber characteristics and their effect on epoxy composite properties tuned by continuous anodic carbon fiber oxidation
, Journal of Adhesion, Vol: 14, Pages: 661-690 -
Journal articleErnst M, Bismarck A, Springer J, et al., 2000,
Zeta-potential and rejection rates of a polyethersulfone nanofiltration membrane in single salt solutions
, Journal of Membrane Science, Vol: 165, Pages: 251-259 -
Journal articleIto K, J Barnes P, M Adcock I, 2000,
Histone acetylation and deacetylation.
, Methods Mol Med, Vol: 44, Pages: 309-319, ISSN: 1543-1894In the resting cell, DNA is tightly compacted to prevent transcription factor accessibility. During activation of the cell, this compact inaccessible DNA is made available to DNA-binding proteins, thus allowing the induction of gene transcription (1 ,2). DNA is packaged into chromatin, a highly organized and dynamic protein-DNA complex. The fundamental subunit of chromatin, the nucleosome, is composed of an octomer of four core histones, an H3/H4 tetramer and two H2A/H2B dimers, surrounded by 146 bp DNA (2,3). The packaging of DNA into nucleosomes acts as a barrier to the initiation of transcription by preventing the access of transcriptional factors, and RNA polymerase II, to their cognate recognition sequences (4). Specific lysine residues in the N-terminal tails of the core histone can be post-translationally modified by acetylation of the ε-amino group. The dynamic equilibrium of core histone acetylation is established and maintained by histone acetyltransferase (HAT) and histone deacetylase (HDAC). Several transcriptional regulators possess intrinsic HAT and HDAC activities, strongly suggesting that histone acetylation and deacetylation play a causal role in regulating transcription (5-8). There is compelling evidence that increased gene transcription is associated with an increase in histone acetylation; hypoacetylation of histone is correlated with reduced transcription or gene silencing (2 ,7,8; Fig 1).
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Journal articleBismarck A, Richter D, Wuertz C, et al., 2000,
Adhesion: Comparison Between Physico-chemical Expected and Measured Adhesion of Oxygen-plasma-treated Carbon Fibers and Polycarbonate
, Journal of Adhesion, Vol: 73, Pages: 19-42 -
Conference paperByrne B, Jormakka M, Abramson J, et al., 2000,
A novel, fusion protein strategy for membrane protein crystallisation.
, Publisher: INT UNION CRYSTALLOGRAPHY, Pages: S58-S58, ISSN: 2053-2733 -
Journal articleBismarck A, Springer J, Mohantry AK, et al., 2000,
Characterization of Several Modified Jute Fibers using Zeta-Potential Measurements
, Colloid and Polymer Science, Vol: 287, Pages: 229-235 -
Journal articleHabel WR, Bismarck A, 2000,
Optimization of the adhesion of fiber optic strain sensors embedded in cement matrices: a study into long-term fiber strength
, Journal of Structural Control, Vol: 7, Pages: 51-76 -
Journal articleByrne B, McGregor A, Taylor PL, et al., 1999,
Isolation and characterisation of the marmoset gonadotrophin releasing hormone receptor:: Ser<SUP>140</SUP> of the DRS motif is substituted by Phe
, JOURNAL OF ENDOCRINOLOGY, Vol: 163, Pages: 447-456, ISSN: 0022-0795- Author Web Link
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- Citations: 22
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