DMD wt Allele

Human DMD wild-type allele is located in the vicinity of Xp21.2 and is approximately 2225 kb in length. This allele, which encodes dystrophin protein, plays a role in muscle cell development. Mutation of the gene is associated with cardiomyopathy dilated X-linked type 3B and with both the Duchenne and Becker types of muscular dystrophy. (NCI Thesaurus)

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DMD Gene

This gene is involved in muscle development.

DMBT1 wt Allele

Human DMBT1wild-type allele is located within 10q25.3-q26.1and is approximately 85 kb in length. This allele, which encodes deleted in malignant brain tumors…

DMBT1 Gene

This gene may play a role in tumor cells and immune system interactions; however this function has not been substantiated.

DM4-Conjugated Anti-Cripto Monoclonal Antibody BIIB015

A humanized IgG1 monoclonal antibody directed against the cell surface-associated protein Cripto and conjugated to the maytansinoid DM4 with potential antineoplastic…

DM-CHOC-PEN

A cholesterol carbonate derivative of 4-demethylpenclomedine (DM-PEN) with potential antineoplastic alkylating activity. Upon intravenous administration of 4-demethylcholesteryloxycarbonylpenclomedine, the carbonium moiety binds to…

DLL4 wt Allele

Human DLL4 wild-type allele is located in the vicinity of 15q14 and is approximately 10 kb in length. This allele, which encodes…