The meeting would discuss scientific and clinical advances of hemoglobinopathies. This would include disease mechanisms, new therapeutic strategies, and targets as well as potential curative therapies including bone-marrow transplantation, gene therapy and genome editing approaches.
The meeting would also enable close interaction between clinicians and scientists working in the area towards creating collaborative translational efforts in India
*TBC: To Be Confirmed
Researchers at CSIR-IGIB are involved in a variety of programmes including genetic epidemiology, genome-editing and chemical biology approaches focused on Sickle Cell Anemia. We are a participant in the CSIR Mission Programme on Sickle Cell Anemia.
Through in vivo drug screens we have identified drugs that can modulate the iron regulatory hormone, hepcidin. The Efficient Fe Control in Thalassemics (EFeCT) aims to repurpose drugs for reducing iron overload in Thalassemia.
more at: https://goo.gl/k4XvnH
The Genomics and other omics technologies for Enabling Medical Decisions (GOMED) offers geentic screening for prevalent Hemoglobinopathies including Thalassemia, Sickle Cell Anemia and other rarer forms of Hemoglobin disorders.
more at http://gomed.igib.in
CSIR Institute of Genomics and Integrative Biology (CSIR-IGIB)
CSIR-Institute of Genomics & Integrative Biology (IGIB) is a premier Institute of Council of Scientific and Industrial Research (CSIR), engaged in research of national importance in the areas of genomics, molecular medicine, bioinformatics, proteomics and environmental biotechnology.
We acknowledge financial support from the Council of Scientific and Industrial Research (CSIR), India through Mission programme on Sickle Cell Anemia (HCP008)