196 related articles for article (PubMed ID: 8382610)
1. Structure of Met30 variant of transthyretin and its amyloidogenic implications.
Terry CJ; Damas AM; Oliveira P; Saraiva MJ; Alves IL; Costa PP; Matias PM; Sakaki Y; Blake CC
EMBO J; 1993 Feb; 12(2):735-41. PubMed ID: 8382610
[TBL] [Abstract][Full Text] [Related]
2. Presence of a plasma transthyretin (prealbumin) variant in familial amyloidotic polyneuropathy in a kindred of Greek origin.
Saraiva MJ; Sherman W; Goodman DS
J Lab Clin Med; 1986 Jul; 108(1):17-22. PubMed ID: 3011930
[TBL] [Abstract][Full Text] [Related]
3. Comparison of lethal and nonlethal transthyretin variants and their relationship to amyloid disease.
McCutchen SL; Lai Z; Miroy GJ; Kelly JW; Colón W
Biochemistry; 1995 Oct; 34(41):13527-36. PubMed ID: 7577941
[TBL] [Abstract][Full Text] [Related]
4. Biochemical marker in familial amyloidotic polyneuropathy, Portuguese type. Family studies on the transthyretin (prealbumin)-methionine-30 variant.
Saraiva MJ; Costa PP; Goodman DS
J Clin Invest; 1985 Dec; 76(6):2171-7. PubMed ID: 3908483
[TBL] [Abstract][Full Text] [Related]
5. Family studies of the genetic abnormality in transthyretin (prealbumin) in Portuguese patients with familial amyloidotic polyneuropathy.
Saraiva MJ; Birken S; Costa PP; Goodman DS
Ann N Y Acad Sci; 1984; 435():86-100. PubMed ID: 6099706
[TBL] [Abstract][Full Text] [Related]
6. Homozygosity for the transthyretin-met30-gene in two Swedish sibs with familial amyloidotic polyneuropathy.
Holmgren G; Haettner E; Nordenson I; Sandgren O; Steen L; Lundgren E
Clin Genet; 1988 Nov; 34(5):333-8. PubMed ID: 3229002
[TBL] [Abstract][Full Text] [Related]
7. Familial amyloidotic polyneuropathy: transthyretin (prealbumin) variants in kindreds of Italian origin.
Saraiva MJ; Costa PP; Almeida Mdo R; Banzhoff A; Altland K; Ferlini A; Rubboli G; Plasmati R; Tassinari CA; Romeo G
Hum Genet; 1988 Dec; 80(4):341-3. PubMed ID: 2848756
[TBL] [Abstract][Full Text] [Related]
8. Cysteine 10 is a key residue in amyloidogenesis of human transthyretin Val30Met.
Takaoka Y; Ohta M; Miyakawa K; Nakamura O; Suzuki M; Takahashi K; Yamamura K; Sakaki Y
Am J Pathol; 2004 Jan; 164(1):337-45. PubMed ID: 14695346
[TBL] [Abstract][Full Text] [Related]
9. Production of recombinant human transthyretin with biological activities toward the understanding of the molecular basis of familial amyloidotic polyneuropathy (FAP).
Furuya H; Saraiva MJ; Gawinowicz MA; Alves IL; Costa PP; Sasaki H; Goto I; Sakaki Y
Biochemistry; 1991 Mar; 30(9):2415-21. PubMed ID: 1848097
[TBL] [Abstract][Full Text] [Related]
10. Simplified method for screening populations at risk for transthyretin Met30-associated familial amyloidotic polyneuropathy.
Saraiva MJ; Alves IL; Costa PP
Clin Chem; 1989 Jun; 35(6):1033-5. PubMed ID: 2543515
[TBL] [Abstract][Full Text] [Related]
11. Analysis of x-ray diffraction patterns from amyloid of biopsied vitreous humor and kidney of transthyretin (TTR) Met30 familial amyloidotic polyneuropathy (FAP) patients: axially arrayed TTR monomers constitute the protofilament.
Inouye H; Domingues FS; Damas AM; Saraiva MJ; Lundgren E; Sandgren O; Kirschner DA
Amyloid; 1998 Sep; 5(3):163-74. PubMed ID: 9818053
[TBL] [Abstract][Full Text] [Related]
12. Formation of cytotoxic transthyretin is not dependent on inter-molecular disulphide bridges commonly found within the amyloid form.
Lindhagen-Persson M; Vestling M; Reixach N; Olofsson A
Amyloid; 2008 Dec; 15(4):240-5. PubMed ID: 19065295
[TBL] [Abstract][Full Text] [Related]
13. Studies on plasma transthyretin (prealbumin) in familial amyloidotic polyneuropathy, Portuguese type.
Saraiva MJ; Costa PP; Goodman DS
J Lab Clin Med; 1983 Oct; 102(4):590-603. PubMed ID: 6311926
[TBL] [Abstract][Full Text] [Related]
14. Genetic expression of a transthyretin mutation in typical and late-onset Portuguese families with familial amyloidotic polyneuropathy.
Saraiva MJ; Costa PP; Goodman DS
Neurology; 1986 Nov; 36(11):1413-7. PubMed ID: 3762958
[TBL] [Abstract][Full Text] [Related]
15. Transthyretin amyloidosis: a tale of weak interactions.
Saraiva MJ
FEBS Lett; 2001 Jun; 498(2-3):201-3. PubMed ID: 11412857
[TBL] [Abstract][Full Text] [Related]
16. Modifications of transthyretin in amyloid fibrils: analysis of amyloid from homozygous and heterozygous individuals with the Met30 mutation.
Thylén C; Wahlqvist J; Haettner E; Sandgren O; Holmgren G; Lundgren E
EMBO J; 1993 Feb; 12(2):743-8. PubMed ID: 8095018
[TBL] [Abstract][Full Text] [Related]
17. Amyloid fibril protein in familial amyloidotic polyneuropathy, Portuguese type. Definition of molecular abnormality in transthyretin (prealbumin).
Saraiva MJ; Birken S; Costa PP; Goodman DS
J Clin Invest; 1984 Jul; 74(1):104-19. PubMed ID: 6736244
[TBL] [Abstract][Full Text] [Related]
18. The binding of 2,4-dinitrophenol to wild-type and amyloidogenic transthyretin.
Morais-de-Sá E; Neto-Silva RM; Pereira PJ; Saraiva MJ; Damas AM
Acta Crystallogr D Biol Crystallogr; 2006 May; 62(Pt 5):512-9. PubMed ID: 16627944
[TBL] [Abstract][Full Text] [Related]
19. Comparative calorimetric study of non-amyloidogenic and amyloidogenic variants of the homotetrameric protein transthyretin.
Shnyrov VL; Villar E; Zhadan GG; Sanchez-Ruiz JM; Quintas A; Saraiva MJ; Brito RM
Biophys Chem; 2000 Dec; 88(1-3):61-7. PubMed ID: 11152276
[TBL] [Abstract][Full Text] [Related]
20. A low amyloidogenic E61K transthyretin mutation may cause familial amyloid polyneuropathy.
Murakami T; Yokoyama T; Mizuguchi M; Toné S; Takaku S; Sango K; Nishimura H; Watabe K; Sunada Y
J Neurochem; 2021 Mar; 156(6):957-966. PubMed ID: 32852783
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
