Clive R. Pullinger
Department of Physiology
University of California
San Francisco
California
USA
Name/email consistency: high
- Primary hypercholesterolemia: genetic causes and treatment of five monogenic disorders. Pullinger, C.R., Kane, J.P., Malloy, M.J. Expert. Rev. Cardiovasc. Ther (2003)
- Human cholesterol 7alpha-hydroxylase (CYP7A1) deficiency has a hypercholesterolemic phenotype. Pullinger, C.R., Eng, C., Salen, G., Shefer, S., Batta, A.K., Erickson, S.K., Verhagen, A., Rivera, C.R., Mulvihill, S.J., Malloy, M.J., Kane, J.P. J. Clin. Invest. (2002)
- Analysis of hABC1 gene 5' end: additional peptide sequence, promoter region, and four polymorphisms. Pullinger, C.R., Hakamata, H., Duchateau, P.N., Eng, C., Aouizerat, B.E., Cho, M.H., Fielding, C.J., Kane, J.P. Biochem. Biophys. Res. Commun. (2000)