Encode chains of type I

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Mutations in type I Collagen genes resulting in osteogenesis imperfecta in Northern Vietnamese patients

Osteogenesis imperfecta (OI), commonly known as “brittle bone disease”, is an autosomal dominant disorder characterized by bone fragility and abnormalities in connective tissue. Biochemical and molecular genetic studies have shown that the vast majority of affected individuals have mutations in either the COL1A1 or COL1A2 genes that encode chains of type I procollagen.

7p quenchua1 04-11-2019 15 0 Download

Sequence, linkage mapping and early developmental expression of the intestinal-type fatty acid-binding protein gene (fabp2) from zebrafish (Danio rerio)

The intestinal fatty acid-binding protein (I-FABP) shows binding specificity for long-chain fatty acids and is proposed to be involved in uptake of dietary fatty acids and their intracellular transport. We have determined the sequence of the gene encoding I-FABP in zebrafish. The zebrafish I-FABP gene contains four exons interrupted by three introns. Radiation hybrid mapping assigned the I-FABP gene to linkage group 1. A 924 bp sequence 5Vupstream of the initiation codon in the I-FABP gene contained several putative cis-acting regulatory elements.

8p vankim10a11 08-06-2015 41 3 Download