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1 - 10 of 17 results found for SAA1. Did you mean: saad

  1. SAA1 alleles as risk factors in reactive systemic AA amyloidosis.

    SAA1 is the predominant isoform of acute phase human SAA deposited as AA amyloid fibrils in reactive systemic amyloidosis. It has recently been reported that in the Japanese population, in whom the SAA1 gamma allele occurs with a frequency of 37%,

    http://iris.ucl.ac.uk/iris/publication/164447/2

  2. Assyrian empire builders - Bibliography

    Download PDF version of SAA 1 introduction (808 KB) [/downloads/saa1_intro.pdf] (requires free Adobe Acrobat reader [http://www.adobe.com/uk/products/acrobat/readstep2.html]).

    https://www.ucl.ac.uk/sargon/bibliography/

  3. Molecular Genetic Testing | Centre for Amyloidosis and Acute Phase...

    APOC3. 11q23.3. Serum amyloid A1. SAA1. 11p15.1. Serum amyloid A2. SAA2.

    https://www.ucl.ac.uk/amyloidosis/national-amyloidosis-centre/molecular-genetic-testing

  4. Transcriptional regulation of serum amyloid A1 gene expression in human aortic smooth...

    Regulation of acute-phase serum amyloid A (A-SAA) synthesis by proinflammatory cytokines and steroid hormones in human aortic smooth muscle cells (HASMCs) is distinct from that in HepG2 cells. To study the cis- and trans-activating promoter element

    http://iris.ucl.ac.uk/iris/publication/25546/1

  5. Use of somatic cell hybrids and fluorescence in situ hybridization to localize the...

    The serum amyloid A (SAA) superfamily consists of two acute phase genes, SAA1 and SAA2; a pseudogene, SAA3; and a constitutively expressed gene, SAA4. The SAA proteins, which are found associated with high-density lipoprotein, are believed to have

    http://iris.ucl.ac.uk/iris/publication/248397/1

  6. British kindred with dominant FMF associated with high incidence of AA amyloidosis caused...

    OBJECTIVES: Hereditary systemic autoinflammatory diseases are rare genetic disorders, which if untreated, can be complicated by AA amyloidosis leading to renal failure and premature death. Our objective was to find a genetic cause in a British

    http://iris.ucl.ac.uk/iris/publication/1681324/1

  7. Expression of recombinant human serum amyloid A in mammalian cells and demonstration of...

    Site-directed mutagenesis of the acute-phase human serum amyloid A (SAA1 alpha) protein was used to evaluate the importance of the N-terminal amino acid residues, namely RSFFSFLGEAF The full-length cDNA clone of SAA1 alpha (pA1.mod.) was used to

    http://iris.ucl.ac.uk/iris/publication/97598/1

  8. The human serum amyloid A protein (SAA) superfamily gene cluster: mapping to chromosome...

    The human serum amyloid A protein (SAA) family comprises a number of small, hepatically produced, differentially expressed apolipoproteins encoded by genes localized on the short arm of chromosome 11.SAA1 and SAA2 are highly related genes that

    http://iris.ucl.ac.uk/iris/publication/1000303/2

  9. Structure of a human serum amyloid A gene and modulation of its expression in transfected...

    The structure of a human serum amyloid A (SAA) genomic clone (SAAg9) has been analyzed and the nucleotide sequence of the coding regions is compared with that of the cDNA for apoSAA1. The leader and coding sequences of exons 2 and 3 are identical to

    http://iris.ucl.ac.uk/iris/publication/248426/1

  10. The human acute-phase serum amyloid A gene family: structure, evolution and expression in...

    Serum amyloid A (SAA) proteins are a group of phylogenetically conserved acute-phase reactants. Evidence is presented here for the existence of four genetic loci for the human serum amyloid A (SAA) genes. The first locus was defined by three

    http://iris.ucl.ac.uk/iris/publication/248316/1

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