Literature DB >> 6093805

Cloning and sequence analysis of cDNA for human prealbumin.

S Mita, S Maeda, K Shimada, S Araki.   

Abstract

A cDNA coding for human prealbumin has been cloned from a cDNA library prepared from human liver. The DNA sequence codes for a polypeptide which consists of 147 amino acids including a whole human prealbumin sequence and a putative signal sequence. The elucidation of this prealbumin cDNA sequence is expected to facilitate a prenatal diagnosis of familial amyloidotic polyneuropathy.

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Year:  1984        PMID： 6093805     DOI： 10.1016/0006-291x(84)91590-0

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN： 0006-291X            Impact factor:   3.575


  18 in total

1.  Assignment of the prealbumin (PALB) gene (familial amyloidotic polyneuropathy) to human chromosome region 18q11.2-q12.1.

Authors:  R S Sparkes; H Sasaki; T Mohandas; K Yoshioka; I Klisak; Y Sakaki; C Heinzmann; M I Simon
Journal:  Hum Genet       Date:  1987-02       Impact factor: 4.132

2.  Fibril in senile systemic amyloidosis is derived from normal transthyretin.

Authors:  P Westermark; K Sletten; B Johansson; G G Cornwell
Journal:  Proc Natl Acad Sci U S A       Date:  1990-04       Impact factor: 11.205

3.  The nucleotide sequence of transthyretin cDNA isolated from a sheep choroid plexus cDNA library.

Authors:  G F Tu; T Cole; W Duan; G Schreiber
Journal:  Nucleic Acids Res       Date:  1989-08-11       Impact factor: 16.971

4.  Transcriptional control of the mouse prealbumin (transthyretin) gene: both promoter sequences and a distinct enhancer are cell specific.

Authors:  R H Costa; E Lai; J E Darnell
Journal:  Mol Cell Biol       Date:  1986-12       Impact factor: 4.272

5.  Gene structure and evolution of transthyretin in the order Chiroptera.

Authors:  Jiraporn Khwanmunee; Ladda Leelawatwattana; Porntip Prapunpoj
Journal:  Genetica       Date:  2015-12-17       Impact factor: 1.082

6.  Molecular diagnosis of the transthyretin (TTR) Met111 mutation in familial amyloid cardiomyopathy of Danish origin.

Authors:  B Y Nordvåg; G Husby; I Ranløv; M R el-Gewely
Journal:  Hum Genet       Date:  1992-06       Impact factor: 4.132

7.  Characterization of a transthyretin (prealbumin) variant associated with familial amyloidotic polyneuropathy type II (Indiana/Swiss).

Authors:  F E Dwulet; M D Benson
Journal:  J Clin Invest       Date:  1986-10       Impact factor: 14.808

Review 8.  Systemic amyloidosis in transgenic mice carrying the human mutant transthyretin (Met 30) gene. Pathological and immunohistochemical similarity to human familial amyloidotic polyneuropathy, type I.

Authors:  S Araki; S Yi; T Murakami; S Watanabe; S Ikegawa; K Takahashi; K Yamarnura
Journal:  Mol Neurobiol       Date:  1994-02       Impact factor: 5.590

9.  Ligation-mediated amplification of RNA from murine erythroid cells reveals a novel class of beta globin mRNA with an extended 5'-untranslated region.

Authors:  V Volloch; B Schweitzer; S Rits
Journal:  Nucleic Acids Res       Date:  1994-07-11       Impact factor: 16.971

10.  Meningocerebrovascular amyloidosis associated with a novel transthyretin mis-sense mutation at codon 18 (TTRD 18G)

Authors:  R Vidal; F Garzuly; H Budka; M Lalowski; R P Linke; F Brittig; B Frangione; T Wisniewski
Journal:  Am J Pathol       Date:  1996-02       Impact factor: 4.307
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