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Recent related articles ( bystolic tm novel):

Cutting edge: fimh adhesin of type 1 fimbriae is a novel tlr4 ligand.
In this study we report that FimH induces potent innate responses in a MyD88-dependent fashion. The FimH-induced innate activity was restricted to cells expressing TLR4. In addition, FimH was able to bind directly to TLR4. More importantly, cells unresponsive to LPS were responsive to FimH and the presence
Cutting edge: fimh adhesin of type 1 fimbriae is a novel tlr4 ligand....

A novel cd19-directed recombinant bispecific antibody derivative with enhanced immune effector functions for human leukemic cells.
Page: 871DOI: 10.1097/CJI.0b013e318186c8b4Authors: Kellner, Christian *; Bruenke, Joerg *; Stieglmaier, Julia *; Schwemmlein, Michael *; Schwenkert, Michael *; Singer, Heiko *; Mentz, Kristin *; Peipp, Matthias +; Lang, Peter ++; Oduncu, Fuat [S]; Stockmeyer, Bernhard [//]; Fey, Georg H. * (Source: Journal of Immunotherapy) MedWorm Sponsored Message: MD Consult
A novel cd19-directed recombinant bispecific antibody derivative with enhanced immune effector functions for human leukemic cells....

Trius Therapeutics awarded $28 million to develop novel drugs targeting bacterial DNA Gyrase and Topoisomerase IV
Trius Therapeutics, Inc., today announced the award of a $28 million contract from the National Institute of Allergy and Infectious Diseases (NIAID), a component of the National Institutes of Health, for the development of novel antibiotics directed against multiple Gram-negative bacterial pathogens.
Trius Therapeutics awarded $28 million to develop novel drugs targeting bacterial DNA Gyrase and Topoisomerase IV...

Novel truncating mutations in pkp1 and dsp cause similar skin phenotypes in two brazilian families
Inherited mutations in components of desmosomes result in a spectrum of syndromes characterized by variable abnormalities in the skin and its appendages, including blisters and erosions, palmoplantar hyperkeratosis, woolly hair or hypotrichosis and, in some cases, extracutaneous features such as cardiomyopathy. We investigated the molecular basis of two
Novel truncating mutations in pkp1 and dsp cause similar skin phenotypes in two brazilian families...

Phenotypic consequences of a novel sco2 gene mutation
SCO2 is a cytochrome c oxidase (COX) assembly gene. Mutations in the SCO2 gene have been associated with fatal infantile cardioencephalomyopathy. We report on the phenotype of a novel SCO2 mutation in two siblings with fatal infantile cardioencephalomyopathy. The index patient died of heart failure at 25 days
Phenotypic consequences of a novel sco2 gene mutation...

Global expression profiling identifies a novel biosignature for protein aggregation r120gcryab cardiomyopathy in mice
Protein aggregation cardiomyopathy is a life-threatening manifestation of a multisystem disorder caused by the exchange mutation in the gene encoding the human small heat shock protein B-crystallin (hR120GCryAB). Genetic studies in mice have established cardiac hR120GCryAB expression causes increased activity of glucose 6-phosphate dehydrogenase (G6PD) and "reductive stress"
Global expression profiling identifies a novel biosignature for protein aggregation r120gcryab cardiomyopathy in mice...

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