Abstract: The present invention relates to cure accelerators useful for anaerobic curable compositions, such as adhesives and sealants. The cure accelerators may be embraced generally within the structure below where X is CH2, O, S, NR?, CR?R?? or C?O; R is hydrogen or (meth)acryl; R6 is hydrogen, halogen, amino, carboxyl, nitro, alkyl, alkenyl, alkynyl, hydroxyalkyl, hydroxyalkenyl, hydroxyalkynyl, or alkaryl; and A and A1 are each individually selected from hydrogen or taken together create a ring structure of 5 to 12 total ring atoms, wherein the ring structure may be cycloaliphatic, cycloheteroaliphatic or aromatic or combinations thereof with or without substitution by one or more hydroxyl or (meth)acryl groups; and n is 0 or 1, provided that when R is hydrogen, A and A? cannot both be hydrogen or taken together cannot be naphthyl.

Abstract: A system and method for securing a pump are disclosed. The system includes a pump that contains a medicament delivery system, a processor operably coupled to the pump, a user interface in operable communication with the processor, a plurality of sensors in operable communication with the processor, and a housing. The housing includes a frame, a door, and a locking mechanism that can be selectively unlocked to allow the door to partially detach from the frame. The security system includes a swivel door assembly, which includes physical redundancies to selectively prevent access to the internal space of the swivel door assembly and a plurality of alarms. For example, in response to receiving an input from the plurality of sensors, the processor initiates at least one of the plurality of alarms to provide an indication to a user that an event has occurred.

Abstract: A method is provided that non-coding RNA profiles can be exploited as a means of monitoring, assessing, comparing, establishing and/or determining certain cell characteristics and/or profiles. Accordingly, the use of non-coding RNA molecules for characterising and/or profiling cells is provided.

Abstract: The present invention concerns the finding that non-coding RNA profiles can be exploited as a means of monitoring, assessing, comparing, establishing and/or determining certain cell characteristics and/or profiles. Accordingly, the invention provides the use of non-coding RNA molecules for characterising and/or profiling cells.

Abstract: The invention to mismatch and ISI shaping in a data converter. The invention provides a dynamic element matching technique that incorporates both mismatch and inter symbol interference shaping. A digital decoder is provided that controls the number of ‘on’ and ‘off’ transitions so that the resulting signal does not contain noise or distortion. The element selection technique of the invention is suitable for high resolution multi-bit continuous time oversampling data converters.

Abstract: The present invention concerns the finding that non-coding RNA profiles can be exploited as a means of monitoring, assessing, comparing, establishing and/or determining certain cell characteristics and/or profiles. Accordingly, the invention provides the use of non-coding RNA molecules for characterising and/or profiling cells.

Abstract: There is disclosed a method comprising the steps of: carrying out a plurality of expression assays, each expression assay comprising the steps of: carrying out an intervention on a biological system, measuring an expression profile of non-coding RNAs in the biological system resulting from the intervention, and storing an expression data set derived from the measured expression profile, the said expression assays concerning either or both a plurality of different interventions and a plurality of different biological systems; and analysing the resulting expression data sets to determine correlations between the effect on the expression profile of non-coding RNAs of the respective intervention in groups of two or more expression assays concerning either or both different interventions or different biological systems.

Abstract: The invention to mismatch and ISI shaping in a data converter. The invention provides a dynamic element matching technique that incorporates both mismatch and inter symbol interference shaping. A digital decoder is provided that controls the number of ‘on’ and ‘off’ transitions so that the resulting signal does not contain noise or distortion. The element selection technique of the invention is suitable for high resolution multi-bit continuous time oversampling data converters.

Abstract: There is disclosed a method comprising the steps of: carrying out a plurality of expression assays, each expression assay comprising the steps of: carrying out an intervention on a biological system, measuring an expression profile of non-coding RNAs in the biological system resulting from the intervention, and storing an expression data set derived from the measured expression profile, the said expression assays concerning either or both a plurality of different interventions and a plurality of different biological systems; and analysing the resulting expression data sets to determine correlations between the effect on the expression profile of non-coding RNAs of the respective intervention in groups of two or more expression assays concerning either or both different interventions or different biological systems.

Abstract: There is disclosed a method comprising the steps of: carrying out a plurality of expression assays, each expression assay comprising the steps of: carrying out an intervention on a biological system, measuring an expression profile of non-coding RNAs in the biological system resulting from the intervention, and storing an expression data set derived from the measured expression profile, the said expression assays concerning either or both a plurality of different interventions and a plurality of different biological systems; and analysing the resulting expression data sets to determine correlations between the effect on the expression profile of non-coding RNAs of the respective intervention in groups of two or more expression assays concerning either or both different interventions or different biological systems.

Abstract: The present invention concerns the finding that non-coding RNA profiles can be exploited as a means of monitoring, assessing, comparing, establishing and/or determining certain cell characteristics and/or profiles. Accordingly, the invention provides the use of non-coding RNA molecules for characterising and/or profiling cells.

Abstract: A test system (1) comprises a system-on-chip with a memory (7) for storing sample data; and a dynamic test engine (4) to control input of dynamic test waveforms including sinusoidal waveforms to an ADC under test (15) and to determine device under test dynamic parameters by analysing the samples. A linear test engine (5) determines device under test (15) static parameters, and controls input of ramp input waveforms to the ADC. A test controller (2) performs finite sate machine control of testing including applying test waveforms, dumping samples to the memory (7), and retrieving static and dynamic results. A DAC (3) generates controlled waveform generation under instructions from the test engines, and an interface (10) communicates with an external host. The components are linked with a bus (11) and are modular.

Abstract: There is disclosed a method comprising the steps of: carrying out a plurality of expression assays, each expression assay comprising the steps of: carrying out an intervention on a biological system, measuring an expression profile of non-coding RNAs in the biological system resulting from the intervention, and storing an expression data set derived from the measured expression profile, the said expression assays concerning either or both a plurality of different interventions and a plurality of different biological systems; and analysing the resulting expression data sets to determine correlations between the effect on the expression profile of non-coding RNAs of the respective intervention in groups of two or more expression assays concerning either or both different interventions or different biological systems.

Abstract: A test system (1) comprises a system-on-chip with a memory (7) for storing sample data; and a dynamic test engine (4) to control input of dynamic test waveforms including sinusoidal waveforms to an ADC under test (15) and to determine device under test dynamic parameters by analysing the samples. A linear test engine (5) determines device under test (15) static parameters, and controls input of ramp input waveforms to the ADC. A test controller (2) performs finite sate machine control of testing including applying test waveforms, dumping samples to the memory (7), and retrieving static and dynamic results. A DAC (3) generates controlled waveform generation under instructions from the test engines, and an interface (10) communicates with an external host. The components are linked with a bus (11) and are modular.

Abstract: An adjustable guide assembly to guide a cutter bit of a tool device about a cutting surface of a workpiece. The guide assembly includes an elongated first guide rail having a first abutting surface adapted to abut a first side wall of the workpiece, and a second guide rail spaced-apart from the first guide rail, and having a second abutting surface adapted to abut a second side wall of the workpiece. A base member is positioned over the first and second guide rails, and includes a tool support surface and an opposed workpiece support surface. The base member includes a contacting wall defining a bit passage therethrough.