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The Journal of Biological Chemistry|August 15, 1992
Production and functional analysis of normal and variant recombinant human transthyretin proteinsJ R Murrell, R G Schoner, J J Liepnieks, et al.Genomics|June 13, 2001
A new human hereditary amyloidosis: the result of a stop-codon mutation in the apolipoprotein AII geneM D Benson, J J Liepnieks, M Yazaki, et al.The Journal of Biological Chemistry|September 25, 1989
Localization of the ankyrin-binding site on erythrocyte membrane protein, band 3B M Willardson, B J Thevenin, M L Harrison, et al.The Journal of Biological Chemistry|February 5, 1993
The x-ray crystal structure refinements of normal human transthyretin and the amyloidogenic Val-30-->Met variant to 1.7-A resolutionJ A Hamilton, L K Steinrauf, B C Braden, et al.Biochemical and Biophysical Research Communications|June 28, 1985
Localization of the human prealbumin gene to chromosome 18M R Wallace, S L Naylor, B Kluve-Beckerman, et al.Journal of Lipid Research|May 11, 1992
In vivo metabolism of a mutant apolipoprotein, apoA-IIowa, associated with hypoalphalipoproteinemia and hereditary systemic amyloidosisD J Rader, R E Gregg, M S Meng, et al.Neurology|May 29, 2003
Oculoleptomeningeal amyloidosis in a large kindred with a new transthyretin variant Tyr69HisG Blevins, R Macaulay, S Harder, et al.The American Journal of Pathology|January 6, 2001
Biochemical characterization of a neuroserpin variant associated with hereditary dementiaM Yazaki, J J Liepnieks, J R Murrell, et al.The American Journal of Pathology|January 23, 1999
Hereditary amyloid cardiomyopathy caused by a variant apolipoprotein A1L Hamidi Asl, J J Liepnieks, K Hamidi Asl, et al.Human Genetics|September 1, 1995
Haplotype analysis of common transthyretin mutationsM R Almeida, N Aoyama-Oishi, Y Sakaki, et al.Pageof 21