WRN polymorphisms affect expression levels of plasminogen activator inhibitor type 1 in cultured fibroblasts

Author:

Castro Elena,Oviedo-Rodríguez Vladimir,Angel-Chávez Luis I

Publisher

Springer Science and Business Media LLC

Subject

Cardiology and Cardiovascular Medicine

Reference38 articles.

1. Yu CE, Oshima J, Goddard KA, Miki T, Nakura J, Ogihara T, Poot M, Hoehn H, Fraccaro M, Piussan C, Fu YM, Mulligan J, Ouis S, Martin GM: Linkage disequilibrium and haplotype studies of chromosome 8p11.1-21.1 markers and Werner syndrome. Am J Hum Genet. 1994, 55: 356-364.

2. Fukuchi K, Martin GM, Monnat RJ: Mutator phenotype Werner syndrome is characterized by extensive deletion. Proc Natl Acad Sci USA. 1989, 86: 5893-5897. 10.1073/pnas.86.15.5893.

3. Harrigan JA, Wilson DM, Prasad R, Opresko PL, Beck G, May A, Wilson SH, Bohr VA: The Werner syndrome protein operates in base excision repair and cooperates with DNA polymerase beta. Nucleic Acids Res. 2006, 34: 745-754. 10.1093/nar/gkj475.

4. Martin GM: Genetic syndromes in man with potential relevance to the pathology of aging. Birth Defects Orig Artic Ser. 1978, 14: 5-39.

5. Goto M, Miller RW, Ishikawa Y, Sugano H: Excess of rare cancers in Werner syndrome (Adult progeria). Cancer Epidem Biomarkers Prev. 1996, 5: 239-246.

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