论文信息 - AL 366 - a glycosylated protein of kappa 1b origin in a patient with systemic amyloidosis of predominantly non-parenchymatous distribution - 字舞流文

AL 366 - a glycosylated protein of kappa 1b origin in a patient with systemic amyloidosis of predominantly non-parenchymatous distribution

AL 366 - a glycosylated protein of kappa 1b origin in a patient with systemic amyloidosis of predominantly non-parenchymatous distribution.

K. Olsen | K. Sletten | I. Samdal | P. Westermark

[1] F. Stevens,et al. Structural Bases of Light Chain-Related Pathology , 1999 .

[2] K. Olsen,et al. Constant Region of a κ III Immunoglobulin Light Chain as a Major AL‐Amyloid Protein , 1998, Scandinavian journal of immunology.

[3] K. Sletten,et al. The Primary Structure of Serum Amyloid A Protein in the Sheep: Comparison with Serum Amyloid A in Other Species , 1994, Scandinavian journal of immunology.

[4] E. Osserman,et al. Patterns of amyloidosis and their association with plasma-cell dyscrasia, monoclonal immunoglobulins and Bence-Jones proteins. , 1974, The New England journal of medicine.

[5] U. K. Laemmli,et al. Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 , 1970, Nature.

[6] K. Sletten,et al. The carbohydrate structure of the amyloid immunoglobulin light chain protein EPS , 1995 .

[7] K. Sletten,et al. The amino acid sequence and carbohydrate composition of an immunoglobulin kappa light chain amyloid fibril protein (AL) of variable subgroup I , 1995 .