Cadherin-26 Polyclonal Antibody, 100ul Antisense Oligonucleotides Mutations ALMS1 cause Alstrom syndrome

Mutations ALMS1 cause Alstrom syndrome

The encoded protein interacts with survival motor neuron protein (SMN1) to enhance pre-mRNA splicing and to induce neuronal differentiation and axonal growth

This gene is a susceptibility locus for childhood absence epilepsy

Human chromosome 15 encodes over 700 genes and comprises nearly 3% of the human genome

suggesting that it does not constitute a rate limiting step in the peroxisomal degradation of docosahexaenoic acid

Cadherin-26 Polyclonal Antibody, 100ul Antisense Oligonucleotides Mutations ALMS1 cause Alstrom syndromeCadherins are a family of adhesion molecules that mediate Ca2+ dependent cell cell adhesion in all solid tissues and modulate a wide variety of processes, including cell polarization and migration. Cadherin domains occur as repeats in the extracellular region and are thought to contribute to the sorting of heterogeneous cell types and the maintenance of orderly structures such as epithelium. CDH26 encodes a cadherin domain containing protein whose