The stems dûm and damám in Hebrew ...

Published also in Journal of Biblical literature, v.32, p.219-243.

Logica Martini Smiglecii Societatis Iesu, S. Theologi Doctoris : selectis disputationibus & qustionibus illustrata, et in duos tomos distributa: in qua quicquid in Aristotelico organo vel cognitu necessarium, vel obscuritate perplexum, tam claráe & perspicuáe, quam solidáe ac nervosáe pertractur. Cum indice rerum copioso. Ad perillustrem ac magnificum dominum, Dm Thomam Zamoyscium, &c.

Mode of access: Internet.

Die Dm̃onen : Roman in zwei Bñden /

Mode of access: Internet.

DM&S ADP plan, fiscal years 1984-1989.

"February 1984."

Unit and intermediate maintenance repair parts and special tools list for heater, duct type portable, trailer mounted, 400,000 BTU/hr, Fiesta model FC-400-1, NSN 4520-01-071-7191.

"27 March 1987."

Operator's, organizational, direct support and general support maintenance manual : heater, duct type, portable, trailer mounted, 400,000 Btu/hr, Fiesta model FC-400-1 (4520-01-071-7191).

"11 July 1980."

Operator's and organizational maintenance : survey electronic distance measuring equipment, infrared, model DM-60 (M-1), NSN 6675-01-010-5948.

Includes index.

Direct support and general support maintenance manual : survey electronic distance measuring equipment, infrared, model DM-60 (M-1), NSN 6675-01-010-5948.

"20 November 1980."

Eph/Ephrin memhrane proteins: A mammalian expression vector pTIg-BOS-Fc allowing rapid protein purification

There is an urgent need for high purity, single chain, fully functional Eph/ephrin membrane proteins. This report outlines the pTIg-BOS-Fc vector and purification approach resulting in rapid increased production of fully functional single chain extracellular proteins that were isolated with high purity and used in structure-function analysis and pre-clinical studies.

Real-Time Gene-Expression Extraction with Fast Classification (FC) Networks

Fast Classification (FC) networks were inspired by a biologically plausible mechanism for short term memory where learning occurs instantaneously. Both weights and the topology for an FC network are mapped directly from the training samples by using a prescriptive training scheme. Only two presentations of the training data are required to train an FC network. Compared with iterative learning algorithms such as Back-propagation (which may require many hundreds of presentations of the training data), the training of FC networks is extremely fast and learning convergence is always guaranteed. Thus FC networks may be suitable for applications where real-time classification is needed. In this paper, the FC networks are applied for the real-time extraction of gene expressions for Chlamydia microarray data. Both the classification performance and learning time of the FC networks are compared with the Multi-Layer Proceptron (MLP) networks and support-vector-machines (SVM) in the same classification task. The FC networks are shown to have extremely fast learning time and comparable classification accuracy.

Identification of the HLA-DM/HLA-DR interface

Human leukocyte antigen (HLA)-DM is a critical participant in antigen presentation that catalyzes the dissociation of the Class II-associated Invariant chain-derived Peptide (CLIP) from the major histocompatibility complex (MHC) Class II molecules. There is competition amongst peptides for access to an MHC Class II groove and it has been hypothesised that DM functions as a 'peptide editor' that catalyzes the replacement of one peptide for another within the groove. It is established that the DM catalyst interacts directly with the MHC Class II but the precise location of the interface is unknown. Here, we combine previously described mutational data with molecular docking and energy minimisation simulations to identify a putative interaction site of >4000A2 which agrees with known point mutational data for both the DR and DM molecule. The docked structure is validated by comparison with experimental data and previously determined properties of protein-protein interfaces. A possible dissociation mechanism is suggested by the presence of an acidic cluster near the N terminus of the bound peptide.