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Germ line origin and somatic mutations determine the target tissues in systemic AL-amyloidosis

PloS one, 2007-10, Vol.2 (10), p.e981

2007

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The development of PIPA: an integrated and automated pipeline for genome-wide protein function annotation

BMC bioinformatics, 2008-01, Vol.9 (1), p.52-52, Article 52

2008

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Hypothetical structure of human serum amyloid A protein

Amyloid, 2004-06, Vol.11 (2), p.71-80

Stevens, Fred J

2004

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A father and his son with systemic AL amyloidosis

Haematologica (Roma), 2009-03, Vol.94 (3), p.437-439

2009

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Homology versus analogy: possible evolutionary relationship of immunoglobulins, cupredoxins, and Cu,Zn-superoxide dismutase

Journal of molecular recognition, 2008-01, Vol.21 (1), p.20-29

Stevens, Fred J.

2008

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Possible evolutionary links between immunoglobulin light chains and other proteins involved in amyloidosis

Amyloid, 2008-01, Vol.15 (2), p.96-107

Stevens, Fred J.

2008

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Hsp70 and Antifibrillogenic Peptides Promote Degradation and Inhibit Intracellular Aggregation of Amyloidogenic Light Chains

The Journal of cell biology, 2001-02, Vol.152 (4), p.705-715

2001

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Natural Catalytic Antibodies: Peptide-hydrolyzing Activities of Bence Jones Proteins and VL Fragment (∗)

The Journal of biological chemistry, 1995-06, Vol.270 (25), p.15257-15261

1995

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Primary structure-based function characterization of BRCT domain replicates in BRCA1

Biochemical and biophysical research communications, 2006-06, Vol.345 (1), p.188-196

2006

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Inhibition of Amyloid Fiber Assembly by Both BiP and Its Target Peptide

Immunity (Cambridge, Mass.), 2000-10, Vol.13 (4), p.433-442

2000

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Amyloid formation: an emulation of matrix protein assembly?

Amyloid, 2004-12, Vol.11 (4), p.232-244

Stevens, Fred

2004

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Template-based recognition of protein fold within the midnight and twilight zones of protein sequence similarity

Journal of molecular recognition, 2005-05, Vol.18 (3), p.203-212

2005

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A Molecular Model for Self-Assembly of Amyloid Fibrils: Immunoglobulin Light Chains

Biochemistry (Easton), 1995-08, Vol.34 (34), p.10697-10702

1995

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Kappa light chain-associated Fanconi's syndrome: molecular analysis of monoclonal immunoglobulin light chains from patients with and without intracellular crystals

Protein engineering, 1999-04, Vol.12 (4), p.363-369

1999

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Hepatic amyloidosis resulting from deposition of the apolipoprotein A-I variant Leu75Pro

Amyloid, 2003-12, Vol.10 (4), p.215-223

2003

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Recombinant immunoglobulin variable domains generated from synthetic genes provide a system for in vitro characterization of light‐chain amyloid proteins

Protein science, 1995-03, Vol.4 (3), p.421-432

1995

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Protein Conformation and Disease: Pathological Consequences of Analogous Mutations in Homologous Proteins

Biochemistry (Easton), 2000-12, Vol.39 (50), p.15291-15296

2000

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Diversity and Diversification of Light Chains in Myeloma:The Specter of Amyloidogenesis by Proxy

Contributions to nephrology, 2007, Vol.153, p.156-181

2007

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Thermodynamic instability of human lambda 6 light chains: correlation with fibrillogenicity

Biochemistry (Easton), 1999-10, Vol.38 (42), p.14101-14108

1999

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Bence Jones proteins: a powerful tool for the fundamental study of protein chemistry and pathophysiology

Biochemistry (Easton), 1991-07, Vol.30 (28), p.6803-6805

1991

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Protein folding in the ER

Seminars in cell & developmental biology, 1999-10, Vol.10 (5), p.443-454

1999

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Physicochemical consequences of amino acid variations that contribute to fibril formation by immunoglobulin light chains

Protein science, 1999-03, Vol.8 (3), p.509-517

1999

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Both the environment and somatic mutations govern the aggregation pathway of pathogenic immunoglobulin light chain

Journal of molecular biology, 2001-11, Vol.313 (5), p.1021-1034

2001

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Light chain cardiomyopathy. Structural analysis of the light chain tissue deposits

The American journal of pathology, 1996-05, Vol.148 (5), p.1397-1406

1996

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Stringency of Substrate-Specificity of Escherichia coli Malate-Dehydrogenase

Archives of biochemistry and biophysics, 1995-09, Vol.322 (1), p.43-52

1995

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Germ line origin and somatic mutations determine the target tissues in systemic AL-amyloidosis

The development of PIPA: an integrated and automated pipeline for genome-wide protein function annotation

Hypothetical structure of human serum amyloid A protein

A father and his son with systemic AL amyloidosis

Homology versus analogy: possible evolutionary relationship of immunoglobulins, cupredoxins, and Cu,Zn-superoxide dismutase

Possible evolutionary links between immunoglobulin light chains and other proteins involved in amyloidosis

Hsp70 and Antifibrillogenic Peptides Promote Degradation and Inhibit Intracellular Aggregation of Amyloidogenic Light Chains

Natural Catalytic Antibodies: Peptide-hydrolyzing Activities of Bence Jones Proteins and VL Fragment (∗)

Primary structure-based function characterization of BRCT domain replicates in BRCA1

Inhibition of Amyloid Fiber Assembly by Both BiP and Its Target Peptide

Amyloid formation: an emulation of matrix protein assembly?

Template-based recognition of protein fold within the midnight and twilight zones of protein sequence similarity

A Molecular Model for Self-Assembly of Amyloid Fibrils: Immunoglobulin Light Chains

Kappa light chain-associated Fanconi's syndrome: molecular analysis of monoclonal immunoglobulin light chains from patients with and without intracellular crystals

Hepatic amyloidosis resulting from deposition of the apolipoprotein A-I variant Leu75Pro

Recombinant immunoglobulin variable domains generated from synthetic genes provide a system for in vitro characterization of light‐chain amyloid proteins

Protein Conformation and Disease: Pathological Consequences of Analogous Mutations in Homologous Proteins

Diversity and Diversification of Light Chains in Myeloma:The Specter of Amyloidogenesis by Proxy

Thermodynamic instability of human lambda 6 light chains: correlation with fibrillogenicity

Bence Jones proteins: a powerful tool for the fundamental study of protein chemistry and pathophysiology

Protein folding in the ER

Physicochemical consequences of amino acid variations that contribute to fibril formation by immunoglobulin light chains

Both the environment and somatic mutations govern the aggregation pathway of pathogenic immunoglobulin light chain

Light chain cardiomyopathy. Structural analysis of the light chain tissue deposits

Stringency of Substrate-Specificity of Escherichia coli Malate-Dehydrogenase

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