Showing results (101-110 of 331) with videos related to

Sort By:
Pageof 34
Nature Genetics|March 1, 1993
Hereditary renal amyloidosis associated with a mutant fibrinogen alpha-chainM D Benson, J Liepnieks, T Uemichi, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|June 8, 2000
Expression of SAA and amyloidogenesis in congenic mice of CE/J and C57BL/6 strainsL Wang, J J Liepnieks, M D Benson, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|April 18, 1998
Transthyretin mutation (serine 84) associated with familial amyloid polyneuropathy in a Hungarian familyZ Zólyomi, M D Benson, K Halász, et al.
Scandinavian Journal of Immunology|January 1, 1995
Cathepsin B generates the most common form of amyloid A (76 residues) as a degradation product from serum amyloid AT Yamada, J J Liepnieks, B Kluve-Beckerman, et al.
Genomics|October 1, 1989
Direct sequencing of the gene for Maryland/German familial amyloidotic polyneuropathy type II and genotyping by allele-specific enzymatic amplificationW C Nichols, J J Liepnieks, V A McKusick, et al.
The Journal of Laboratory and Clinical Medicine|March 1, 1991
Senile cardiac amyloidosis associated with homozygosity for a transthyretin variant (ILE-122)W C Nichols, J J Liepnieks, E L Snyder, et al.
American Journal of Medical Genetics|October 1, 1986
Molecular detection of carriers of hereditary amyloidosis in a Swedish-American familyM R Wallace, P M Conneally, G L Long, et al.
Lancet (London, England)|January 4, 1975
Neuropathy, M components, and amyloidM D Benson, A S Cohen, K D Brandt, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|May 1, 1985
Isolation and characterization of amyloid protein AA in the Abyssinian catS P DiBartola, M D Benson, F E Dwulet, et al.
Genomics|October 1, 1990
A mutation in apolipoprotein A-I in the Iowa type of familial amyloidotic polyneuropathyW C Nichols, R E Gregg, H B Brewer, et al.
Pageof 34