M. Saraiva

发表

Preimplantation genetic diagnosis for familial amyloidotic polyneuropathy (FAP)

M. Saraiva, M. Sousa, A. Barros, 2001, Prenatal diagnosis.

Transthyretin mutations in hyperthyroxinemia and amyloid diseases

M. Saraiva, 2001, Human mutation.

Immunoassay for Transthyretin Variants associated with Amyloid Neuropathy

A. Teixeira, P. Costa, P. Costa, 1993, Scandinavian journal of immunology.

Human metallothioneins 2 and 3 differentially affect amyloid‐beta binding by transthyretin

T. Quintela, I. Gonçalves, C. Santos, 2010, The FEBS journal.

Family Studies of the Genetic Abnormality in Transthyretin (Prealbumin) in Portuguese Patients with Familial Amyloidotic Poly neuropathy a

M. Saraiva, D. Goodman, S. Birken, 1984, Annals of the New York Academy of Sciences.

Specific Removal of Transthyretin from Plasma of Patients with Familial Amyloidotic Polyneuropathy: Optimization of an Immunoadsorption Procedure

V. Regnault, J. Stoltz, A. Teixeira, 1992, The International journal of artificial organs.

Amyloid nomenclature 2022: update, novel proteins, and recommendations by the International Society of Amyloidosis (ISA) Nomenclature Committee

A. Dispenzieri, M. Fändrich, G. Merlini, 2022, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Vitreous amyloidosis after liver transplantation in patients with familial amyloid polyneuropathy: Ocular synthesis of mutant transthyretin

M. Saraiva, M. Solé, M. Munar-Qués, 2000, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Studies on the synthesis and secretion of transthyretin by the human hepatoma cell line Hep G2

W. Blaner, M. Saraiva, M. Bonifácio, 1991, FEBS letters.

Transthyretin binding to A‐Beta peptide – Impact on A‐Beta fibrillogenesis and toxicity

I. Cardoso, M J Saraiva, I Cardoso, 2008, FEBS letters.

The amyloidogenic potential of transthyretin variants correlates with their tendency to aggregate in solution

R. Brito, A. Quintas, M. Saraiva, 1997, FEBS letters.

Selective recognition of human small transthyretin aggregates by a novel monoclonal antibody

M. Saraiva, A. Teixeira, 2022, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Genetic microheterogeneity of human transthyretin detected by IEF

F. Salvi, M. Skinner, M. Benson, 2007, Electrophoresis.

Transthyretin amyloidosis: a tale of weak interactions

M. Saraiva, 2001, FEBS letters.

Structure and assembly–disassembly properties of wild‐type transthyretin amyloid protofibrils observed with atomic force microscopy

A. Damas, R. H. Pires, M. Saraiva, 2011, Journal of molecular recognition : JMR.

A new transthyretin mutation associated with amyloid cardiomyopathy.

M. Gawinowicz, P. Costa, P. Costa, 1992, American Journal of Human Genetics.

Production of recombinant human transthyretin with biological activities toward the understanding of the molecular basis of familial amyloidotic polyneuropathy (FAP).

Y. Sakaki, M. Saraiva, H. Furuya, 1991, Biochemistry.