1. |
- Backlund, Ulf, et al.
(author)
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Semi-Bloch functions in several complex variables
- 2013
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Reports (other academic/artistic)abstract
- Let $M$ be an $n$-dimensional complex manifold. A holomorphic function $f:M\to \mathbb C$ is said to be semi-Bloch if for every $\lambda\in \mathbb C$ the function $g_\lambda=\exp(\lambda f(z))$ is normal on $M$. We characterise Semi-Bloch functions on infinitesimally Kobayashi non-degenerate $M$ in geometric as well as analytic terms. Moreover, we show that on such manifolds, semi-Bloch functions are normal.
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2. |
- Brännström, Åke, 1975-, et al.
(author)
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On the convergence of the Escalator Boxcar Train
- 2013
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In: SIAM Journal on Numerical Analysis. - : Society for Industrial & Applied Mathematics (SIAM). - 0036-1429 .- 1095-7170. ; 51:6, s. 3213-3231
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Journal article (peer-reviewed)abstract
- The Escalator Boxcar Train (EBT) is a numerical method that is widely used in theoretical biology to investigate the dynamics of physiologically structured population models, i.e., models in which individuals differ by size or other physiological characteristics. The method was developed more than two decades ago, but has so far resisted attempts to give a formal proof of convergence. Using a modern framework of measure-valued solutions, we investigate the EBT method and show that the sequence of approximating solution measures generated by the EBT method converges weakly to the true solution measure under weak conditions on the growth rate, birth rate, and mortality rate. In rigorously establishing the convergence of the EBT method, our results pave the way for wider acceptance of the EBT method beyond theoretical biology and constitutes an important step towards integration with established numerical schemes.Read More: http://epubs.siam.org/doi/abs/10.1137/120893215
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3. |
- Carlsson, Linus, 1972-
(author)
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An equivalence to the Gleason problem
- 2010
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In: Journal of Mathematical Analysis and Applications. - : Elsevier BV. - 0022-247X .- 1096-0813. ; 370:2, s. 373-378
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Journal article (peer-reviewed)abstract
- In this article we study the Gleason problem locally. A new method for solving the Gleason A problem is presented. This is done by showing an equivalent statement to the Gleason A problem. In order to prove this statement, necessary and a sufficient conditions for a bounded domain to have the Gleason A property are found. Also an example of a bounded but not smoothly-bounded domain in C(n) is given, which satisfies the sufficient condition at the origin, and hence has the Gleason A property there.
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4. |
- Carlsson, Linus, 1972-
(author)
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Nebenhülle and the Gleason problem
- 2010
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In: Proceedings of the American Mathematical Society. - : American Mathematical Society (AMS). - 0002-9939 .- 1088-6826. ; 138:1, s. 267-273
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Journal article (peer-reviewed)
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5. |
- Hellgren, Mikko, 1972-, et al.
(author)
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Enrichment of ligands with molecular dockings and subsequent characterization for human alcohol dehydrogenase 3
- 2010
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In: CELLULAR AND MOLECULAR LIFE SCIENCES. - : Springer Science Business Media. - 1420-682X .- 1420-9071. ; 67:17, s. 3005-3015
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Journal article (peer-reviewed)abstract
- Alcohol dehydrogenase 3 (ADH3) has been assigned a role in nitric oxide homeostasis due to its function as an S-nitrosoglutathione reductase. As altered S-nitrosoglutathione levels are often associated with disease, compounds that modulate ADH3 activity might be of therapeutic interest. We performed a virtual screening with molecular dockings of more than 40,000 compounds into the active site of human ADH3. A novel knowledge-based scoring method was used to rank compounds, and several compounds that were not known to interact with ADH3 were tested in vitro. Two of these showed substrate activity (9-decen-1-ol and dodecyltetraglycol), where calculated binding scoring energies correlated well with the logarithm of the k (cat)/K (m) values for the substrates. Two compounds showed inhibition capacity (deoxycholic acid and doxorubicin), and with these data three different lines for specific inhibitors for ADH3 are suggested: fatty acids, glutathione analogs, and cholic acids.
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