Search Results for "MYL3"

10:39 EDT 6th October 2015 | BioPortfolio

Matching Channels


Matching News

Regulators support C-Path's skeletal muscle biomarkers

FDA and EMA issued Letters of Support for four skeletal muscle biomarkers identified by the Predictive Safety Testing Consortium (PSTC) of the Critical Path Institute (C-Path). Elevated levels of myos...

Critical Path Institute Secures Regulatory Support for Skeletal Muscle Safety Biomarkers

FDA and EMA Letters of Support Suggest Valuable Research Potential The Critical Path Institute (C-Path) announced today that both the U.S. Food and Drug Administration ...

Matching PubMed Articles

Comparative transcriptome analysis of atrial septal defect identify dysregulated genes during heart septum morphogenesis.

Congenital heart disease (CHD) is one of most common birth defect, causing fetal loss and death in newborn all over the world. Atrial and ventricular septal defects were the most common CHD subtypes i...

Coexistence of Digenic Mutations in Both Thin (TPM1) and Thick (MYH7) Filaments of Sarcomeric Genes Leads to Severe Hypertrophic Cardiomyopathy in a South Indian FHCM.

Mutations in sarcomeric genes are the leading cause for cardiomyopathies. However, not many genetic studies have been carried out on Indian cardiomyopathy patients. We performed sequence analyses of a...

Search Whole site using Google


Advertisement Advertisement