Abstract: An antenna (100), which is designed for exciting and/or detecting a magnetic resonance in an object (1) under investigation, comprises a conductor loop (10) with an inner conductor (11) and a primary shield conductor (12), which form at least one waveguide, wherein the primary shield conductor (12) is interrupted by a gap (13), and wherein a secondary shield conductor (14) is provided which surrounds the primary shield conductor (12), wherein a dielectric (15) is arranged between the primary shield conductor (12) and the secondary shield conductor (14) and at least the gap is covered by the secondary shield conductor (14). An antenna arrangement which comprises a plurality of such antennas, a magnetic resonance device, and a method for magnetic resonance imaging or magnetic resonance spectroscopy are also described.

Abstract: A solution for synchronizing a network comprising a plurality of interconnected nodes provides a stable synchronized state, especially for large scale networks. Signal transmission speed and the length of each interconnection of the network is configured to cause a delay of the signals received by a node from the other node of the interconnection which is larger than one millionth of the free-running period of the controllable oscillator of the receiving node such that Network-wide synchronization of oscillators is achieved for all nodes of the network in a continuous self-organized process in interaction with the other node of the network.

Abstract: The invention relates to a method for linking at least two target nucleic acid molecules from a single biological compartment, comprising the steps of isolating a fraction from a sample, wherein the fraction comprises the compartment comprising at least two nucleic acid molecules, diluting the fraction and aliquoting the dilution in multiple separate reaction vessels such that each reaction vessel comprises preferably one compartment, or encapsulating the compartment in emulsion droplets such that each droplet comprises preferably one compartment; linking the at least two target nucleic acid molecules, preferably by overlap extension PCR. The method may be employed in the analysis of mutations present in a single cell and in the production of antibodies which are present in a single hybridoma.

Abstract: Described are synthetic promoters capable of mediating gene expression in plants upon pathogen infection. Furthermore, recombinant genes and vectors comprising said chimeric promoters as well as host cells transformed with such chimeric promoters, recombinant genes, or vectors are provided. Additionally, diagnostic compositions and kits comprising such chimeric promoters, recombinant genes, vectors or cells are described. Provided are further methods for the identification of compounds being capable of activating or inhibiting genes that are specifically expressed in plants upon pathogen infection employing the above described means. Furthermore, transgenic plant cells, plant tissue, and plants containing the above-described chimeric promoters, recombinant genes, and vectors as well as the use of the aforementioned chimeric promoters, recombinant genes, vectors and/or compounds identified by the method of the invention in plant cell and tissue culture, plant breeding, and/or agriculture are described.

Abstract: The present invention provides the compounds of formulae (3) and (1) wherein n is 0 or 1, R13 and R14 are the same or different and are selected from the group consisting of NHR310, NR311R312, OR313, SR314 and R315, or R13 and R14 together are selected from the group consisting of (a), (b) and (c), and X is CI, Br of I, and a process for the preparation of compounds of formula (3) comprising the compounds of formula (1) as key intermediates.

Abstract: A method of generating fs laser pulses (1), includes steps of creating a circulating light field in a resonator cavity (10) with multiple resonator mirrors (11-18) by pumping at least one gain medium (21, 22) included in the resonator cavity (10), and passing the circulating light field through a first Kerr medium (31) included in the resonator cavity (10), so that the fs laser pulses (1) are formed by self-amplitude modulation of the circulating light field, wherein the resonator cavity (10) includes at least one supplementary Kerr medium (32-36) enhancing the self-amplitude modulation of the circulating light field, and each of the first Kerr medium (31) and the at least one supplementary Kerr medium (32-36) provide different non-linear Kerr lens contributions to the self-amplitude modulation of the circulating light field. Laser pulse source apparatus (100) for generating fs laser pulses (1) is also described.

Abstract: Boron-comprising perylene monoimides and a process for producing the boron-comprising perylene monoimides are provided. The boron-comprising perylene monoimides are useful as building blocks for producing perylene monoimide derivatives and monoimide derivatives. The boron-comprising perylene monoimides are also useful for preparing dye-sensitized solar cells.

Abstract: A method of spatially splitting a primary radiation beam (1) with a first radiation component (2) including an optical wavelength and a second radiation component (3) having a wavelength shorter than the first radiation component wavelength, said second radiation component (3) having a second or higher harmonic wavelength relative to the optical wavelength, comprises directing the primary radiation beam (1) onto a deflection mirror (10) having a reflective mirror surface (12) and carrying a refractive plate element (20), reflecting the first radiation component (2) at the reflective mirror surface (12) and reflecting the second radiation component (3) at an exposed plate surface (22) of the refractive plate element (20), wherein the reflected radiation components (4, 5) travel along different beam paths.

Abstract: The present invention concerns ortho-Terphenyls of general formula (I); wherein R1, R2, R3 and R4 are independently selected from the group consisting of H; CN; NO2; and saturated, unsaturated or aromatic C1-C40 hydrocarbon residues, which can be substituted 1- to 5-fold with F, CI, OH, NH2, CN and/or NO2, and wherein one or more —CH2-groups can be replaced by —O—, —NH—, —S—, —C(?O)O—, —OC(?O)— and/or —C(?O)—; and X and Y are the same or different, and selected from the group consisting of F, CI, Br, I, and OTf (trifluoromethanesulfonate); and their use for the preparation of graphene nanoribbons as well as a process for the preparation of graphene nanoribbons from said ortho-Terphenyls.

Abstract: The present invention relates to sequence and structural features of single-stranded (ss)RNA molecules required to mediate target-specific nucleic acid modifications by RNA-interference (RNAi), such as target mRNA degradation and/or DNA methylation.

Abstract: An enhancement resonator (20) being configured for generating intra-resonator laser light (1) by coherent superposition of input laser light, comprises at least three resonator mirrors (21, 22, 23, 24) spanning a ring resonator path in one common resonator plane, said resonator path being free of a laser light amplifying medium, wherein the at least three resonator mirrors (21, 22, 23, 24) include at least two toroidal mirrors and/or at least one cylindrical mirror. Furthermore, a laser device (100) comprising the enhancement resonator (20) and a method of generating intra-resonator laser light (1) are described.

Abstract: The present invention relates to a process for preparing graphene, comprising (i) providing in a chemical deposition chamber a substrate which has a surface S1, (ii) subjecting the substrate to a thermal pre-treatment while feeding at least one gaseous or supercritical oxidant into the chemical deposition chamber so as to bring the surface S1 into contact with the at least one gaseous or supercritical oxidant and obtain a pre-treated surface S2, (iii) preparing graphene on the pre-treated surface S2 by chemical deposition.

Abstract: Double-stranded RNA (dsRNA) induces sequence-specific post-transcriptional gene silencing in many organisms by a process known as RNA interference (RNAi). Using a Drosophila in vitro system, we demonstrate that 19-23 nt short RNA fragments are the sequence-specific mediators of RNAi. The short interfering RNAs (siRNAs) are generated by an RNase III-like processing reaction from long dsRNA. Chemically synthesized siRNA duplexes with overhanging 3? ends mediate efficient target RNA cleavage in the lysate, and the cleavage site is located near the center of the region spanned by the guiding siRNA. Furthermore, we provide evidence that the direction of dsRNA processing determines whether sense or antisense target RNA can be cleaved by the produced siRNP complex.

Abstract: A phosphate based compound basically comprising —A: exchangeable cations used in charging and discharging, e.g. Li, Na, K, Ag, —B: non-exchangeable cations from the transition metals, group 3-12 of the periodic table of elements, e.g. Fe, Mn, Co, Cr, Ti, V, Cu, Sc, —C: 60 Mol-%-90 Mol-%, preferably 75 Mol-% of the compound being phosphate (PO4)3? anions, where oxygen is or may be partially substituted by a halide (e.g. F, Cl) and/or OH? to a maximum concentration of 10 Mol-% of the oxygen of the anions and wherein said (PO4)3? coordination polyhedra may be partially substituted by one or more of: SiO44 silicate, BO33? borate, CO32? carbonate, H2O water up to a maximum amount of <31 Mol-% of the anions, said compound being in crystalline form and having open elongate channels extending through the unit cell of the structure and with the compound being present either in single crystal form or as an anisotropic microcrystalline or nanocrystalline material.

Abstract: The present invention relates to a method of generating an induced pluripotent stem (iPS) cell comprising the step of introducing into a target cell one or two coding sequences each giving rise upon transcription to a factor that contributes to the reprogramming of said target cell into an induced pluripotent stem cell and selected from Oct3/4 or a factor belonging to the Myc, Klf and Sox families of factors, wherein the target cell endogenously expresses at least the factors that are not encoded by the coding sequences to be introduced and selected from Oct3/4 or factors belonging to the Myc, Klf and Sox families of factors, and wherein the cell resulting from the introduction of the one or two coding sequences expresses the combination of factor Oct3/4 and at least one factor of each family of factors selected from the group of Myc, Klf and Sox.

Abstract: In Caenorhabditis elegans, lin-4 and let-7 enclode 22- and 21-nucleotide RNAs, respectively, that function as key regulators of developmental timing. Because the appearance of these short RNAs is regulated during development, they are also referred to as “small temporal RNAs” (stRNAs). We show that many more 21- and 22-nt expressed RNAs, termed microRNAs, (miRNAs), exist in invertebrates and vertebrates, and that some of these novel RNAs, similar to let-7 stRAN, are also highly conserved. This suggests that sequence-specific post-transcriptional regulatory mechanisms mediated by small RNAs are more general than previously appreciated.

Abstract: In a STED fluorescence light microscope pulses of excitation light (3) are applied to a sample, which excite fluorescent entities contained in the sample for fluorescence, and which are focused on at least one focal area. Further, de-excitation light (12) is applied to the sample, which de-excites the excited fluorescent entities and which comprises an intensity zero point in the at least one focal area, as a continuous wave. Fluorescence light emitted by the excited fluorescent entities in the sample is registered after each pulse of the excitation light (3) and overlapping with applying the de-excitation light (13) with high temporal resolution between consecutive pulses of the excitation light (3).

Abstract: An oligophenylene monomer of general formula (I) wherein R1 and R2 are independently of each other H, halogene, —OH, —NH2, —CN, —NO2 or a linear or branched, saturated or unsaturated C1-C40 hydrocarbon residue, which can be substituted 1-to 5-fold with halogene (F, Cl, Br, I), —OH, —NH2, —CN and/or —NO2, and wherein one or more CH2-groups can be replaced by —O— or —S—, or an optionally substituted aryl, alkylaryl or alkoxyaryl residue; and m represents 0, 1 or 2.

Abstract: A modifiable server is utilized to reliably seal and unseal data according to a measurement of the server, by structuring the server to have a modifiable sandbox component for sealing, unsealing the data, and a non-modifiable checker component for enabling or disabling said sandbox component. The checker component determines whether the sandbox component complies with pre-determined standards. If the sandbox component is compliant, the checker component enables the sandbox component to seal and unseal the data using a measurement of the checker component. Otherwise, the checker component disables the sandbox component.

Abstract: A method for encoding high dynamic range (HDR) images involves providing a lower dynamic range (LDR) image, generating a prediction function for estimating the values for pixels in the HDR image based on the values of corresponding pixels in the LDR image, and obtaining a residual frame based on differences between the pixel values of the HDR image and estimated pixel values. The LDR image, prediction function and residual frame can all be encoded in data from which either the LDR image of HDR image can be recreated.