TRACING THE EVOLUTION OF TISSUE INHIBITOR OF METALLOPROTEINASES IN METAZOA WITH THE PTERIA PENGUIN GENOME


Alkaptonuria: A case report

Alkaptonuria is a rare inborn error of metabolism with autosomal recessive inheritance 7 Piece Dining Room with a mutation in homogentisate 1,2-dioxygenase.It results in accumulation of homogentisic acid in connective tissues (ochronosis).Most common ocular manifestations are bluish-black discoloration of the conjunctiva, cornea, and sclera.In this

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A primer on metagenomics.

Metagenomics is a discipline that enables the genomic study of uncultured microorganisms.Faster, cheaper sequencing technologies and the ability to sequence uncultured microbes sampled directly from their habitats are expanding and transforming our view of the microbial world.Distilling meaningful information from the millions of new genomic sequen

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