A mutation in the SAA1 promoter causes hereditary amyloid A amyloidosis
- 20 September 2021
- journal article
- research article
- Published by Elsevier BV in Kidney International
- Vol. 101 (2), 349-359
- https://doi.org/10.1016/j.kint.2021.09.007
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Clinical Proteome Informatics Workbench Detects Pathogenic Mutations in Hereditary AmyloidosesJournal of Proteome Research, 2014
- Systemic AL amyloidosis with unusual cutaneous presentation unmasked by carotenodermaAmyloid, 2013
- Anti-Cytokine Therapy for AA AmyloidosisPublished by IntechOpen ,2013
- Glucocerebrosidase gene has an alternative upstream promoter, which has features and expression characteristic of housekeeping genesBlood Cells, Molecules, and Diseases, 2011
- Characterization of the Cheetah Serum Amyloid A1 Gene: Critical Role and Functional Polymorphism of a Cis-Acting ElementJournal of Heredity, 2008
- LC MALDI-TOF MS/MS and LC ESI FTMS analyses of HLA-B27 associated peptides isolated from peripheral blood cellsImmunology Letters, 2008
- TRANSFAC(R) and its module TRANSCompel(R): transcriptional gene regulation in eukaryotesNucleic Acids Research, 2006
- Relative transcriptional activities ofSAA1promoters polymorphic at position −13(T/C): Potential association between increased transcription and amyloidosisAmyloid, 2005
- Acute-Phase Proteins and Other Systemic Responses to InflammationThe New England Journal of Medicine, 1999
- A novel allelic variant of serum amyloic A, SAA1γ: genomic evidence, evolution, frequency, and implication as a risk factor for reactive systemic AA– amyloidosisHuman Molecular Genetics, 1995