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Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|June 21, 2001
Biophysical analysis of normal transthyretin: implications for fibril formation in senile systemic amyloidosisC M Chung, L H Connors, M D Benson, et al.
The Journal of Biological Chemistry|November 26, 1998
Role of the alpha2-integrin in osteoblast-specific gene expression and activation of the Osf2 transcription factorG Xiao, D Wang, M D Benson, et al.
Arthritis and Rheumatism|February 1, 1987
Hereditary amyloidosis: description of a new American kindred with late onset cardiomyopathy. Appalachian amyloidM D Benson, M R Wallace, E Tejada, et al.
The Journal of Clinical Investigation|July 1, 1986
Biochemical and molecular genetic characterization of a new variant prealbumin associated with hereditary amyloidosisM R Wallace, F E Dwulet, P M Conneally, et al.
Clinical Rheumatology|December 1, 1988
Amyloidosis secondary to gout. Identification with a monoclonal antibody to amyloid protein AS Jacobelli, S Vial, H Rosenberg, et al.
Annals of the Rheumatic Diseases|August 1, 1980
Methylprednisolone pulse therapy for nonrenal lupus erythematosusS Eyanson, M H Passo, M A Aldo-Benson, et al.
Comparative Biochemistry and Physiology. B, Comparative Biochemistry|January 1, 1989
Primary structures of dog and cat amyloid A proteins: comparison to human AAB Kluve-Beckerman, F E Dwulet, S P DiBartola, et al.
American Journal of Medical Genetics|June 15, 1991
Biochemical and clinical characterization of prealbuminCHICAGO: an apparently benign variant of serum prealbumin (transthyretin) discovered with high-resolution two-dimensional electrophoresisH H Harrison, E D Gordon, W C Nichols, et al.
Der Nervenarzt|November 11, 1999
[Indications for simultaneous origin of a German and American family with type II hereditary amyloid neuropathy]S Seddigh, N Dahmen, H H Goebel, et al.
Biochemical and Biophysical Research Communications|December 15, 1993
Characterization of amyloid fibril beta-peptide in familial Alzheimer's disease with APP717 mutationsJ J Liepnieks, B Ghetti, M Farlow, et al.
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