Add article(s) associated with Transthyretin family

Screening for N-glycosylated proteins by liquid chromatography mass spectrometry.
Bunkenborg J., Pilch B.J., Podtelejnikov A.V. et al
2004, Proteomics (4) 454-465
Oculoleptomeningeal amyloidosis in a large kindred with a new transthyretin variant Tyr69His.
Blevins G., Macaulay R., Harder S. et al
2003, Neurology (60) 1625-1630
Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs.
Okazaki Y., Furuno M., Kasukawa T. et al
2002, Nature (420) 563-573
Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.
Strausberg R.L., Feingold E.A., Grouse L.H. et al
2002, Proc. Natl. Acad. Sci. U.S.A. (99) 16899-16903
Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs.
The, FANTOM Consortium, the et al
2002, Nature (420) 563-573
Interspecies subtractive hybridization of cDNA from human and chimpanzee brains.
Nadezhdin E.V., Vinogradova T.V., Sverdlov E.D. et al
2001, Dokl. Biochem. Biophys. (381) 415-418
Functional annotation of a full-length mouse cDNA collection.
RIKEN, FANTOM Consortium
2001, Nature (409) 685-690
Normalization and subtraction of cap-trapper-selected cDNAs to prepare full-length cDNA libraries for rapid discovery of new genes.
Carninci P., Shibata Y., Hayatsu N. et al
2000, Genome Res. (10) 1617-1630
Rational design of potent human transthyretin amyloid disease inhibitors.
Klabunde T., Petrassi H.M., Oza V.B. et al
2000, Nat. Struct. Biol. (7) 312-321
A novel variant of transthyretin (Glu89Lys) associated with familial amyloidotic polyneuropathy.
Nakamura M., Hamidi, Asl K. et al
2000, Amyloid (7) 46-50
The evolution of the thyroid hormone distributor protein transthyretin in the order insectivora, class mammalia.
Prapunpoj P., Richardson S.J., Fumagalli L. et al
2000, Mol. Biol. Evol. (17) 1199-1209
RIKEN integrated sequence analysis (RISA) system-384-format sequencing pipeline with 384 multicapillary sequencer.
Shibata K., Itoh M., Aizawa K. et al
2000, Genome Res. (10) 1757-1771
New transthyretin mutation V28M in a Portuguese kindred with amyloid polyneuropathy.
de, Carvalho M., Moreira P. et al
2000, Muscle Nerve (23) 1016-1021
High-efficiency full-length cDNA cloning.
Carninci P., Hayashizaki Y.
1999, Meth. Enzymol. (303) 19-44
Cloning of putative piscine (Sparus aurata) transthyretin: developmental expression and tissue distribution.
Funkenstein B., Perrot V., Brown C.L. et al
1999, Mol. Cell. Endocrinol. (157) 67-73
The structure of human retinol-binding protein (RBP) with its carrier protein transthyretin reveals an interaction with the carboxy terminus of RBP.
Naylor H.M., Newcomer M.E.
1999, Biochemistry (38) 2647-2653
Transthyretin Ile73Val is associated with familial amyloidotic polyneuropathy in a Bangladeshi family.
Booth D.R., Gillmore J.D., Persey M.R. et al
1998, Hum. Mutat. (12) 135-135
Transthyretin Ile73Val is associated with familial amyloidotic polyneuropathy in a Bangladeshi family.
Booth D.R., Gillmore J.D., Persey M.R. et al
1998, Hum. Mutat. (12) 135-135
A new nonamyloid transthyretin variant, G101S, detected by electrospray ionization/mass spectrometry.
Kishikawa M., Nakanishi T., Miyazaki A. et al
1998, Hum. Mutat. (12) 363-363
New transthyretin variants Ser 91 and Ser 116 associated with familial amyloidotic polyneuropathy.
Misrahi A.M., Plante V., Lalu T. et al
1998, Hum. Mutat. (12) 71-71
New transthyretin variants Ser 91 and Ser 116 associated with familial amyloidotic polyneuropathy.
Misrahi A.M., Plante V., Lalu T. et al
1998, Hum. Mutat. (12) 71-71
Inhibiting transthyretin conformational changes that lead to amyloid fibril formation.
Peterson S.A., Klabunde T., Lashuel H.A. et al
1998, Proc. Natl. Acad. Sci. U.S.A. (95) 12956-12960
Tertiary structures of amyloidogenic and non-amyloidogenic transthyretin variants: new model for amyloid fibril formation.
Schormann N., Murrell J.R., Benson M.D. et al
1998, Amyloid (5) 175-187
Structural characteristics of bullfrog (Rana catesbeiana) transthyretin and its cDNA. Comparison of its pattern of expression during metamorphosis with that of lipocalin.
Yamauchi K., Takeuchi H.-A., Overall M. et al
1998, Eur. J. Biochem. (256) 287-296
Evolution of shorter and more hydrophilic transthyretin N-termini by stepwise conversion of exon 2 into intron 1 sequences (shifting the 3' splice site of intron 1).
Aldred A.R., Prapunpoj P., Schreiber G. et al
1997, Eur. J. Biochem. (246) 401-409
Transthyretin ILE20, a new variant associated with late-onset cardiac amyloidosis.
Jacobson D.R., Pan T., Kyle R.A. et al
1997, Hum. Mutat. (9) 83-85
Crystal structure of rat transthyretin at 2.5-A resolution: first report on a unique tetrameric structure.
Wojtczak A.
1997, Acta Biochim. Pol. (44) 505-517
The porcine TTR locus maps to chromosome 6q.
Archibald A.L., Couperwhite S., Jiang Z.H. et al
1996, Anim. Genet. (27) 351-353
The crystal structure of transthyretin from chicken.
Sunde M., Richardson S.J., Chang L. et al
1996, Eur. J. Biochem. (236) 491-499
Meningocerebrovascular amyloidosis associated with a novel transthyretin mis-sense mutation at codon 18 (TTRD 18G).
Vidal R., Garzuly F., Budka H. et al
1996, Am. J. Pathol. (148) 361-366
A novel variant of transthyretin, 59Thr-->Lys, associated with autosomal dominant cardiac amyloidosis in an Italian family.
Booth D.R., Tan S.Y., Hawkins P.N. et al
1995, Circulation (91) 962-967
Evolution of transthyretin in marsupials.
Duan W., Richardson S.J., Babon J.J. et al
1995, Eur. J. Biochem. (227) 396-406
Binding of thyroxine to pig transthyretin, its cDNA structure, and other properties.
Duan W., Richardson S.J., Koehrle J. et al
1995, Eur. J. Biochem. (230) 977-986
Amyloid fibril composition and transthyretin gene structure in senile systemic amyloidosis.
Gustavsson A., Jahr H., Tobiassen R. et al
1995, Lab. Invest. (73) 703-708
Structure of a complex of two plasma proteins: transthyretin and retinol-binding protein.
Monaco H.L., Rizzi M., Coda A. et al
1995, Science (268) 1039-1041
Transthyretin mutations in health and disease.
Saraiva M.J.M.
1995, Hum. Mutat. (5) 191-196
The Ile-84-->Ser amino acid substitution in transthyretin interferes with the interaction with plasma retinol-binding protein.
Berni R., Malpeli G., Folli C. et al
1994, J. Biol. Chem. (269) 23395-23398
Transthyretin VAL107, a new variant associated with familial cardiac and neuropathic amyloidosis.
Jacobson D., Gertz M.A., Buxbaum J.N. et al
1994, Hum. Mutat. (3) 399-401
A double-variant transthyretin allele (Ser 6, Ile 33) in the Israeli patient 'SKO' with familial amyloidotic polyneuropathy.
Jacobson D.R., Buxbaum J.N.
1994, Hum. Mutat. (3) 254-260
Familial carpal tunnel syndrome due to amyloidogenic transthyretin His 114 variant.
Murakami T., Tachibana S., Endo Y. et al
1994, Neurology (44) 315-318
Two transthyretin mutations (Glu42Gly, His90Asn) in an Italian family with amyloidosis.
Skare J.C., Jones L.A., Myles N. et al
1994, Clin. Genet. (45) 281-284
Amyloid polyneuropathy in two German-American families: a new transthyretin variant (Val 107).
Uemichi T., Gertz M.A., Benson M.D. et al
1994, J. Med. Genet. (31) 416-417
Familial amyloid polyneuropathy in Taiwan: identification of transthyretin variant (Leu55-->Pro).
Yamamoto K., Hsu S.P., Yoshida K. et al
1994, Muscle Nerve (17) 637-641
Familial amyloidotic polyneuropathy with late-onset and well- preserved autonomic function: a Japanese kindred with novel mutant transthyretin (Ala97 to Gly).
Yasuda T., Sobue G., Doyu M. et al
1994, J. Neurol. Sci. (121) 97-102
Transthyretin gene expression in choroid plexus first evolved in reptiles.
Achen M.G., Duan W., Pettersson T.M. et al
1993, Am. J. Physiol. (265) 0-0
Transthyretin ALA 71: a new transthyretin variant in a Spanish family with familial amyloidotic polyneuropathy.
Almeida M.R., Lopez-Andreu F., Munar-Ques M. et al
1993, Hum. Mutat. (2) 420-421
A transthyretin variant (alanine 71) associated with familial amyloidotic polyneuropathy in a French family.
Benson M.D., II, Turpin J.C. et al
1993, J. Med. Genet. (30) 120-122
Gly47Ala: a new transthyretin gene mutation in hereditary amyloidosis TTR-related.
Ferlini A., Salvi F., Patrosso C. et al
1993, J. Rheumatol. (20) 187-187
Gly47Ala: a new transthyretin gene mutation in hereditary amyloidosis TTR-related.
Ferlini A., Salvi F., Patrosso C. et al
1993, J. Rheumatol. (20) 187-187
The X-ray crystal structure refinements of normal human transthyretin and the amyloidogenic Val-30-->Met variant to 1.7-A resolution.
Hamilton J.A., Steinrauf L.K., Braden B.C. et al
1993, J. Biol. Chem. (268) 2416-2424
Cardiac amyloidosis: a review and report of a new transthyretin (prealbumin) variant.
Hesse A., Altland K., Linke R.P. et al
1993, Br. Heart J. (70) 111-115
A basic transthyretin variant (Glu61-->Lys) causes familial amyloidotic polyneuropathy: protein and DNA sequencing and PCR-induced mutation restriction analysis.
Shiomi K., Nakazato M., Matsukura S. et al
1993, Biochem. Biophys. Res. Commun. (194) 1090-1096
Structure of Met30 variant of transthyretin and its amyloidogenic implications.
Terry C.J., Damas A.M., Oliveira P. et al
1993, EMBO J. (12) 735-741
Purification and characterization of a 3,5,3'-L-triiodothyronine- specific binding protein from bullfrog tadpole plasma: a homolog of mammalian transthyretin.
Yamauchi K., Kasahara T., Hayashi H. et al
1993, Endocrinology (132) 2254-2261
Two transthyretin variants (TTR Ala-49 and TTR Gln-89) in two Sicilian kindreds with hereditary amyloidosis.
Almeida M.R., Ferlini A., Forabosco A. et al
1992, Hum. Mutat. (1) 211-215
Familial amyloidotic polyneuropathy presenting with carpal tunnel syndrome and a new transthyretin mutation, asparagine 70.
Izumoto S., Younger D., Hays A.P. et al
1992, Neurology (42) 2094-2102
Transthyretin Pro55, a variant associated with early-onset, aggressive, diffuse amyloidosis with cardiac and neurologic involvement.
Jacobson D.R., McFarlin D.E., Kane I. et al
1992, Hum. Genet. (89) 353-356
Familial amyloidotic polyneuropathy: a new transthyretin position 30 mutation (alanine for valine) in a family of German descent.
Jones L.A., Skare J.C., Cohen A.S. et al
1992, Clin. Genet. (41) 70-73
Characterization of a transthyretin-related amyloid fibril protein from cerebral amyloid angiopathy in type I familial amyloid polyneuropathy.
Kametani F., Ikeda S., Yanagisawa N. et al
1992, J. Neurol. Sci. (108) 178-183
A novel transthyretin mutation at position 30 (Leu for Val) associated with familial amyloidotic polyneuropathy.
Murakami T., Atsumi T., Maeda S. et al
1992, Biochem. Biophys. Res. Commun. (187) 397-403
A novel transthyretin mutation associated with familial amyloidotic polyneuropathy.
Murakami T., Maeda S., Yi S. et al
1992, Biochem. Biophys. Res. Commun. (182) 520-526
Novel variant transthyretin gene (Ser50 to Ile) in familial cardiac amyloidosis.
Nishi H., Kimura A., Harada H. et al
1992, Biochem. Biophys. Res. Commun. (187) 460-466
A new transthyretin mutation associated with amyloid cardiomyopathy.
Saraiva M.J.M., Almeida M.R., Sherman W. et al
1992, Am. J. Hum. Genet. (50) 1027-1030
A new mutant transthyretin (Arg 10) associated with familial amyloid polyneuropathy.
Uemichi T., Murrel J.R., Zeldenrust S. et al
1992, J. Med. Genet. (29) 888-891
The transthyretin cDNA sequence is normal in transthyretin-derived senile systemic amyloidosis.
Christmanson L., Betsholtz C., Gustavsson A. et al
1991, FEBS Lett. (281) 177-180
Isolation, characterization, cDNA cloning and gene expression of an avian transthyretin. Implications for the evolution of structure and function of transthyretin in vertebrates.
Duan W., Achen M.G., Richardson S.J. et al
1991, Eur. J. Biochem. (200) 679-687
Transthyretin (prealbumin) gene in human primary hepatic cancer.
Gu J.R., Jiang H.Q., He L.P. et al
1991, Sci. China, Ser. B, Chem. Life Sci. Earth Sci. (34) 1312-1318
A second transthyretin mutation at position 33 (Leu/Phe) associated with familial amyloidotic polyneuropathy.
Harding J., Skare J., Skinner M. et al
1991, Biochim. Biophys. Acta (1097) 183-186
Biochemical and clinical characterization of prealbuminCHICAGO: an apparently benign variant of serum prealbumin (transthyretin) discovered with high-resolution two-dimensional electrophoresis.
Harrison H.H., Gordon E.D., Nichols W.C. et al
1991, Am. J. Med. Genet. (39) 442-452
Two-tiered DNA-based diagnosis of transthyretin amyloidosis reveals two novel point mutations.
Li S., Minnerath S., Li K. et al
1991, Neurology (41) 893-898
New mutant gene (transthyretin Arg 58) in cases with hereditary polyneuropathy detected by non-isotope method of single-strand conformation polymorphism analysis.
Saeki Y., Ueno S., Yorifuji S. et al
1991, Biochem. Biophys. Res. Commun. (180) 380-385
A new transthyretin variant from a patient with familial amyloidotic polyneuropathy has asparagine substituted for histidine at position 90.
Skare J.C., Milunsky J.M., Milunsky A. et al
1991, Clin. Genet. (39) 6-12
A point mutation in transthyretin increases affinity for thyroxine and produces euthyroid hyperthyroxinemia.
Moses A.C., Rosen H.N., Moller D.E. et al
1990, J. Clin. Invest. (86) 2025-2033
Two novel variants of transthyretin identified in Japanese cases with familial amyloidotic polyneuropathy: transthyretin (Glu42 to Gly) and transthyretin (Ser50 to Arg).
Ueno S., Uemichi T., Takahashi N. et al
1990, Biochem. Biophys. Res. Commun. (169) 1117-1121
A novel variant of transthyretin (Tyr114 to Cys) deduced from the nucleotide sequences of gene fragments from familial amyloidotic polyneuropathy in Japanese sibling cases.
Ueno S., Uemichi T., Yorifuji S. et al
1990, Biochem. Biophys. Res. Commun. (169) 143-147
Cloning and nucleotide sequencing of transthyretin (prealbumin) cDNA from rat choroid plexus and liver.
Duan W., Cole T., Schreiber G. et al
1989, Nucleic Acids Res. (17) 3979-3979
The nucleotide sequence of transthyretin cDNA isolated from a sheep choroid plexus cDNA library.
Tu G., Cole T., Duan W. et al
1989, Nucleic Acids Res. (17) 6384-6384
Evidence that the amyloid fibril protein in senile systemic amyloidosis is derived from normal prealbumin.
Cornwell G.G., III, Sletten K. et al
1988, Biochem. Biophys. Res. Commun. (154) 648-653
Structure and expression of the rat transthyretin (prealbumin) gene.
Fung W.P., Thomas T., Dickson P.W. et al
1988, J. Biol. Chem. (263) 480-488
Identification of a new hereditary amyloidosis prealbumin variant, Tyr-77, and detection of the gene by DNA analysis.
Wallace M.R., Dwulet F.E., Williams E.C. et al
1988, J. Clin. Invest. (81) 189-193
Identification and characterization of a human transthyretin variant.
Strahler J.R., Rosenblum B.B., Hanash S.M. et al
1987, Biochem. Biophys. Res. Commun. (148) 471-477
Structure and expression of the mutant prealbumin gene associated with familial amyloidotic polyneuropathy.
Maeda S., Mita S., Araki S. et al
1986, Mol. Biol. Med. (3) 329-338
Analyses of prealbumin mRNAs in individuals with familial amyloidotic polyneuropathy.
Mita S., Maeda S., Shimada K. et al
1986, J. Biochem. (100) 1215-1222
Structure and expression of the mouse prealbumin gene.
Wakasugi S., Maeda S., Shimada K. et al
1986, J. Biochem. (100) 49-58
Biochemical and molecular genetic characterization of a new variant prealbumin associated with hereditary amyloidosis.
Wallace M.R., Dwulet F.E., Conneally P.M. et al
1986, J. Clin. Invest. (78) 6-12
Rat transthyretin (prealbumin). Molecular cloning, nucleotide sequence, and gene expression in liver and brain.
Dickson P.W., Howlett G.J., Schreiber G. et al
1985, J. Biol. Chem. (260) 8214-8219
Structure of the chromosomal gene for human serum prealbumin.
Sasaki H., Yoshioka N., Takagi Y. et al
1985, Gene (37) 191-197
Demonstration of transthyretin mRNA in the brain and other extrahepatic tissues in the rat.
Soprano D.R., Herbert J., Soprano K.J. et al
1985, J. Biol. Chem. (260) 11793-11798
The primary structure of rabbit and rat prealbumin and a comparison with the tertiary structure of human prealbumin.
Sundelin J., Melhus H., Das S. et al
1985, J. Biol. Chem. (260) 6481-6487
Structure of the human prealbumin gene.
Tsuzuki T., Mita S., Maeda S. et al
1985, J. Biol. Chem. (260) 12224-12227
Structural comparisons between mouse and human prealbumin.
Wakasugi S., Maeda S., Shimada K. et al
1985, J. Biochem. (98) 1707-1714
Localization of the human prealbumin gene to chromosome 18.
Wallace M.R., Naylor S.L., Kluve-Beckerman B. et al
1985, Biochem. Biophys. Res. Commun. (129) 753-758
Primary structure of an amyloid prealbumin and its plasma precursor in a heredofamilial polyneuropathy of Swedish origin.
Dwulet F.E., Benson M.D.
1984, Proc. Natl. Acad. Sci. U.S.A. (81) 694-698
Cloning and sequence analysis of cDNA for human prealbumin.
Mita S., Maeda S., Shimada K. et al
1984, Biochem. Biophys. Res. Commun. (124) 558-564
Revised analysis of amino acid replacement in a prealbumin variant (SKO-III) associated with familial amyloidotic polyneuropathy of Jewish origin.
Nakazato M., Kangawa K., Minamino N. et al
1984, Biochem. Biophys. Res. Commun. (123) 921-928
Primary structure of an amyloid prealbumin variant in familial polyneuropathy of Jewish origin.
Pras M., Prelli F., Franklin E.C. et al
1983, Proc. Natl. Acad. Sci. U.S.A. (80) 539-542
Identification of amyloid prealbumin variant in familial amyloidotic polyneuropathy (Japanese type).
Tawara S., Nakazato M., Kangawa K. et al
1983, Biochem. Biophys. Res. Commun. (116) 880-888
Structure of prealbumin: secondary, tertiary and quaternary interactions determined by Fourier refinement at 1.8 A.
Blake C.C.F., Geisow M.J., Oatley S.J. et al
1978, J. Mol. Biol. (121) 339-356
Protein-DNA and protein-hormone interactions in prealbumin: a model of the thyroid hormone nuclear receptor?
Blake C.C.F., Oatley S.J.
1977, Nature (268) 115-120
Rat plasma prealbumin. Isolation and partial characterization.
Navab M., Mallia A.K., Kanda Y. et al
1977, J. Biol. Chem. (252) 5100-5106
Structure of human plasma prealbumin at 2.5-A resolution. A preliminary report on the polypeptide chain conformation, quaternary structure and thyroxine binding.
Blake C.C.F., Geisow M.J., Swan I.D.A. et al
1974, J. Mol. Biol. (88) 1-12
The amino acid sequence of human plasma prealbumin.
Kanda Y., Goodman D.S., Canfield R.E. et al
1974, J. Biol. Chem. (249) 6796-6805
DNA sequences of macaque genes expressed in brain or testis and its evolutionary implications.
Submitted JUN-2005 to the EMBL GenBank DDBJ databases
Characterization of carp transthyretin.
Apreda M., Morgado I., Power D. et al
Submitted SEP-2005 to the EMBL GenBank DDBJ databases
Wallaby transthyretin.
Brack C.M., Duan W., Hulbert A.J. et al
Comp Biochem Physiol 110B:523-529 1995
Cloning of bovine homolog of transthyretin.
Irikura D., Kanaoka Y., Urade Y. et al
Submitted DEC-1997 to the EMBL GenBank DDBJ databases
Cloning of human full-length CDSs in BD Creator(TM) system donor vector.
Kalnine N., Chen X., Rolfs A. et al
Submitted MAY-2003 to the EMBL GenBank DDBJ databases
Isolation and characterization of cDNA for macaque neurological disease genes.
Kusuda J., Osada N., Hida M. et al
Submitted APR-2002 to the EMBL GenBank DDBJ databases
Isolation and characterization of cDNA for macaque neurological disease genes.
Kusuda J., Osada N., Hida M. et al
Submitted APR-2002 to the EMBL GenBank DDBJ databases
Transthyretin expression evolved more recently in liver than in brain.
Schreiber G., Pettersson T.M., Southwell B.R. et al
Comp Biochem Physiol 105B:317-325 1993