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Silencing of murine transthyretin and retinol binding protein genes has distinct and shared behavioral and neuropathologic effects

Neuroscience, 2014-09, Vol.275, p.352-364

2014

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Variant-Sequence Transthyretin (Isoleucine 122) in Late-Onset Cardiac Amyloidosis in Black Americans

The New England journal of medicine, 1997-02, Vol.336 (7), p.466-473

1997

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The Genetics of the Amyloidoses

Annual review of medicine, 2000-01, Vol.51 (1), p.543-569

2000

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Tissue Damage in the Amyloidoses: Transthyretin Monomers and Nonnative Oligomers Are the Major Cytotoxic Species in Tissue Culture

Proceedings of the National Academy of Sciences - PNAS, 2004-03, Vol.101 (9), p.2817-2822

2004

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Revised transthyretin ile 122 allele frequency in African-Americans

Human genetics, 1996-08, Vol.98 (2), p.236-238

1996

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The V122I Cardiomyopathy Variant of Transthyretin Increases the Velocity of Rate-Limiting Tetramer Dissociation, Resulting in Accelerated Amyloidosis

Proceedings of the National Academy of Sciences - PNAS, 2001-12, Vol.98 (26), p.14943-14948

2001

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Abnormal immunoglobulin synthesis in monoclonal immunoglobulin light chain and light and heavy chain deposition disease

Amyloid, 2001, Vol.8 (2), p.84-93

Buxbaum, Joel N.

2001

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Transthyretin Pro55, a variant associated with early-onset, aggressive, diffuse amyloidosis with cardiac and neurologic involvement

Human genetics, 1992-05, Vol.89 (3), p.353-356

1992

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Amyloid fibril protein nomenclature: 2012 recommendations from the Nomenclature Committee of the International Society of Amyloidosis

Amyloid, 2012-12, Vol.19 (4), p.167-170

2012

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Animal models of human amyloidoses: Are transgenic mice worth the time and trouble?

FEBS letters, 2009-08, Vol.583 (16), p.2663-2673

Buxbaum, Joel N.

2009

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Transthyretin and BRICHOS: The Paradox of Amyloidogenic Proteins with Anti-Amyloidogenic Activity for Aβ in the Central Nervous System

Frontiers in neuroscience, 2017-03, Vol.11, p.119-119

2017

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A homozygous transthyretin variant associated with senile systemic amyloidosis : evidence for a late-onset disease of genetic etiology

American journal of human genetics, 1990-07, Vol.47 (1), p.127-136

1990

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Chaperones mainly suppress primary nucleation during formation of functional amyloid required for bacterial biofilm formation

Chemical science (Cambridge), 2022-01, Vol.13 (2), p.536-553

2022

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Transthyretin Ser 6 gene frequency in individuals without amyloidosis

Human genetics, 1995-03, Vol.95 (3), p.308-312

1995

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Genetic aspects of amyloidosis

Advances in human genetics, 1991, Vol.20, p.69

1991

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Familial amyloidosis in one Chinese family: clinical, immunological, and molecular genetic analysis

Journal of internal medicine, 1997-04, Vol.241 (4), p.327-331

1997

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Transthyretin Ile 122 and cardiac amyloidosis in African-Americans : 2 case reports

Texas Heart Institute journal, 1997, Vol.24 (1), p.45-52

1997

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Monoclonal immunoglobulin deposition disease: light chain and light and heavy chain deposition diseases and their relation to light chain amyloidosis. Clinical features, immunopathology, and molecular analysis

Annals of internal medicine, 1990-03, Vol.112 (6), p.455

1990

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Drop-in, drop-out allele-specific PCR: A highly sensitive, single- tube method

Molecular biotechnology, 2004-11, Vol.28 (3), p.171-174

2004

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Amyloid: Toward terminology clarification Report from the Nomenclature Committee of the International Society of Amyloidosis

Amyloid, 2005-03, Vol.12 (1), p.1-4

2005

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Diseases of protein conformation: what do in vitro experiments tell us about in vivo diseases?

Trends in biochemical sciences (Amsterdam. Regular ed.), 2003-11, Vol.28 (11), p.585-592

Buxbaum, Joel N

2003

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Transthyretin Pro 36 associated with familial amyloidotic polyneuropathy in an Ashkenazic Jewish kindred

Human genetics, 1992-09, Vol.90 (1-2), p.158-160

1992

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γ Heavy Chain Disease in Man: cDNA Sequence Supports Partial Gene Deletion Model

Proceedings of the National Academy of Sciences - PNAS, 1982-05, Vol.79 (10), p.3260-3264

1982

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Infiltrative Nonamyloidotic Monoclonal Immunoglobulin Light Chain Cardiomyopathy: An Underappreciated Manifestation of Plasma Cell Dyscrasias

Cardiology, 2000-01, Vol.93 (4), p.220-228

2000

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Restriction fragment analysis confirms the position 33 mutation in transthyretin from an Israeli patient (SKO) with familial amyloidotic polyneuropathy

Biochemical and biophysical research communications, 1988-05, Vol.153 (1), p.198-202

1988

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Silencing of murine transthyretin and retinol binding protein genes has distinct and shared behavioral and neuropathologic effects

Variant-Sequence Transthyretin (Isoleucine 122) in Late-Onset Cardiac Amyloidosis in Black Americans

The Genetics of the Amyloidoses

Tissue Damage in the Amyloidoses: Transthyretin Monomers and Nonnative Oligomers Are the Major Cytotoxic Species in Tissue Culture

Revised transthyretin ile 122 allele frequency in African-Americans

The V122I Cardiomyopathy Variant of Transthyretin Increases the Velocity of Rate-Limiting Tetramer Dissociation, Resulting in Accelerated Amyloidosis

Abnormal immunoglobulin synthesis in monoclonal immunoglobulin light chain and light and heavy chain deposition disease

Transthyretin Pro55, a variant associated with early-onset, aggressive, diffuse amyloidosis with cardiac and neurologic involvement

Amyloid fibril protein nomenclature: 2012 recommendations from the Nomenclature Committee of the International Society of Amyloidosis

Animal models of human amyloidoses: Are transgenic mice worth the time and trouble?

Transthyretin and BRICHOS: The Paradox of Amyloidogenic Proteins with Anti-Amyloidogenic Activity for Aβ in the Central Nervous System

A homozygous transthyretin variant associated with senile systemic amyloidosis : evidence for a late-onset disease of genetic etiology

Chaperones mainly suppress primary nucleation during formation of functional amyloid required for bacterial biofilm formation

Transthyretin Ser 6 gene frequency in individuals without amyloidosis

Genetic aspects of amyloidosis

Familial amyloidosis in one Chinese family: clinical, immunological, and molecular genetic analysis

Transthyretin Ile 122 and cardiac amyloidosis in African-Americans : 2 case reports

Monoclonal immunoglobulin deposition disease: light chain and light and heavy chain deposition diseases and their relation to light chain amyloidosis. Clinical features, immunopathology, and molecular analysis

Drop-in, drop-out allele-specific PCR: A highly sensitive, single- tube method

Amyloid: Toward terminology clarification Report from the Nomenclature Committee of the International Society of Amyloidosis

Diseases of protein conformation: what do in vitro experiments tell us about in vivo diseases?

Transthyretin Pro 36 associated with familial amyloidotic polyneuropathy in an Ashkenazic Jewish kindred

γ Heavy Chain Disease in Man: cDNA Sequence Supports Partial Gene Deletion Model

Infiltrative Nonamyloidotic Monoclonal Immunoglobulin Light Chain Cardiomyopathy: An Underappreciated Manifestation of Plasma Cell Dyscrasias

Restriction fragment analysis confirms the position 33 mutation in transthyretin from an Israeli patient (SKO) with familial amyloidotic polyneuropathy

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