Abstract: The present invention relates to polypeptides of Pseudomonas aeruginosa which may be used to prevent, diagnose and/or treat Pseudomonas aeruginosa infection.

Abstract: The present invention relates to polypeptides of Moraxella (Branhamella) catarrhalis which may be useful for prophylaxis, diagnostic and/or therapy purposes.

Abstract: The present invention relates to polypeptides, more particularly polypeptides of Moraxella (Branhamella) catarrhalis which may be used to prevent, diagnose and/or treat Moraxella (Branhamella) catarrhalis infection.

Abstract: The present invention relates to polypeptides of Moraxella (Branhamela) catarrhalis wich may be used for prophy-laxis, diagnostic and/or therapy purposes.

Abstract: The present invention relates to antigens, more particularly antigens of Group B Streptococcus (GBS) (S. agalactiae) which may be useful to prevent, diagnose and/or treat streptococcal infections.

Abstract: The present invention relates to polypeptides of Moraxella(Branhamella) calarrhalis which may be useful for prophylaxis, diagnosis and/or therapy purposes.

Abstract: The present invention relates to polypeptides of Haemophilus influenzae which may be used for prophylaxis, diagnostic and/or therapy purposes.

Abstract: The present invention relates to antigens, more particularly antigens of Group B Streptococcus (GBS) (S. agalactiae) which may be useful to prevent, diagnose and/or treat streptococcal infections.

Abstract: Pharmaceutical compositions comprising a liposome associated to N. meningitidis polypeptides fragments or analogs thereof or corresponding DNA fragments, can be used to prevent, diagnose and/or treat neisserial infections.

Abstract: A multi-channel integrated circuit comprises a plurality of channels (CH1 to CH20). A DAC (3) is provided in each channel (CH1 to CH20) for converting digital data inputted to the circuit (1) through an I/O port (14). Digital data to be converted by the DACs (3) is selectively applied to input registers (10) of each channel (CH1 to CH20) on a digital data bus (16) under the control of an interface and control logic circuit (15). The digital words written to the input registers (10) are in turn written to DAC registers (9) through corresponding digital switches (12) for conversion by the DACs (3). A clear code register (22) stores a clear code for writing to the DAC registers (9) in response to a clear signal applied to a clear terminal (24) of the circuit (1) so that analogue outputs appearing on output terminals (5) of the channels (CH1 to CH20) are of a predetermined value, typically, zero volts, when the circuit (1) is set in a clear condition.

Abstract: The present invention relates to antigens, more particularly antigens of Streptococcus pyogenes (also called group A Streptococcus (GAS)) bacterial pathogen which are useful as vaccine component for therapy and/or prophylaxis.

Abstract: Group B streptococcus polypeptides and polynucleotides encoding them are disclosed. Said polypeptides may be useful for the prophylaxis, diagnostic and/or therapy of streptococcal infection in mammals. Also disclosed are recombinant methods of producing the polypeptide antigens as well as diagnostic assays for detecting streptococcal infections, particularly GBS.

Abstract: The present invention relates to polypeptides of Streptococcus pneumoniae which may be used for prophylaxis, diagnostic and/or therapy purposes.

Abstract: Group B streptococcus (GBS) proteins and polynucleotides encoding them are disclosed. Said proteins are antigenic and therefore useful vaccine components for the prophylaxis or therapy of streptococcus infection in animals. Also disclosed are recombinant methods of producing the protein antigens as well as diagnostic assays for detecting streptococcus bacterial infection.

Abstract: A compound of the formula 1

Abstract: The present invention relates to antigens, more particularly an antigen of Streptococcus pygenes (also called group A Streptococcus (GAS)) bacterial pathogen which is useful as vaccine component for therapy and/or prophylaxis.

Abstract: According to the present invention, during scan conversion, non-scan memory cells of a circuit design are replaced with scan cells to form a scan chain. The scan chain is transformed by the test synthesis tool of the present invention into dynamic scan chains with the addition of reconfiguration circuitry. The reconfiguration circuitry partitions the scan chain into multiple segments and enables each segment to be selectively “bypassed” (or deactivated) during test application. Shorter test patterns that are only pertinent to one or more segments are necessary, resulting in a reduction in overall test data volume and test application time. The present invention also provides a modified ATPG technique for generating test patterns for the dynamic scan chains.

Abstract: Streptococcus polypeptides and polynucleotides encoding them are disclosed. Said polypeptides may be useful vaccine components for the prophylaxis or therapy of streptococcus infection in animals. Also disclosed are recombinant methods of producing the protein antigens as well as diagnostic assays for detecting streptococcus bacterial infection.

Abstract: Chlamydia pneumoniae polypeptides and polynucleotides encoding them are disclosed. Said polypeptides are antigenic and therefore useful components for the prophylaxis, diagnosis or therapy of Chlamydial infection in animals. Also disclosed are recombinant methods of producing the protein antigens as well as diagnostic assays for detecting Chlamydia bacterial infection, particularly C. pneumoniae.

Abstract: A computer implemented process and system for electronic design automation (EDA) using groups of multiple cells having loop-back connections for modeling port electrical characteristics. Multi-bit cells have multiple gates of the same function implemented within a same cell. Multi-bit components have multiple multi-bit cells implemented within a same component. Scannable multi-bit cells and components are similar to multi-bit cells and components but contain scannable sequential elements with scan chains installed. Multi-bit cells may or may not have each sequential cells' input and each sequential cells' output available externally. The scannable sequential elements of a multi-bit component are ordered into a predefined scan chain which is defined by the library containing the multi-bit component or multi-bit cell. During scan replacement processes of the EDA compile process, multi-bit cells and components of the netlist are replaced with scannable multi-bit cells and components.