PAFAH1B1 wt Allele

Human PAFAH1B1 wild-type allele is located in the vicinity of 17p13.3 and is approximately 92 kb in length. This allele, which encodes platelet-activating factor acetylhydrolase, isoform Ib, alpha subunit protein, plays a role in the regulation of neuronal migration. Mutations in the gene are associated with lissencephaly type 1, subcortical band heterotopia, and Miller-Dieker lissencephaly syndrome. (NCI Thesaurus)

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PAFAH1B1 Gene

This gene is involved in the modulation of neuronal migration.

Paenibacillaceae

A taxonomic family of Gram positive bacterium in the phylum Firmicutes that includes the genera Brevibacillus and Paenibacillus, among others.

PADRE-CMV Fusion Peptide Vaccine

A peptide-based vaccine containing a pan HLA DR-binding epitope (PADRE) fused to a cytomegalovirus (CMV) peptide epitope, with potential anti-viral and immunomodulating…

PADRE 965.10

Pan-DR epitope (PADRE) 965.10 is a helper peptide. PADRE peptides have been shown the capacity to deliver help for antibody responses…

PADI4 wt Allele

Human PADI4 wild-type allele is located in the vicinity of 1p36.13 and is approximately 56 kb in length. This allele, which encodes…

PADI4 Gene

This gene is involved in arginine modification.