Isolation of a SIR-like gene, SIR-T8, that is overexpressed in thyroid carcinoma cell lines and tissues
暂无分享,去创建一个
G. Viglietto | F. de Nigris | A. Fusco | D. Califano | L. Chiariotti | J. Cerutti | G. Santelli | C. Morelli
[1] R. Frye. ‘SIRT8’ expressed in thyroid cancer is actually SIRT7 , 2002, British Journal of Cancer.
[2] J. Sambrook,et al. Molecular Cloning: A Laboratory Manual , 2001 .
[3] C. J. Chen,et al. PAX8-PPARgamma1 fusion oncogene in human thyroid carcinoma [corrected]. , 2000, Science.
[4] B. Spiegelman,et al. PAX8-PPARγ1 Fusion in Oncogene Human Thyroid Carcinoma , 2000 .
[5] R. Frye,et al. Phylogenetic classification of prokaryotic and eukaryotic Sir2-like proteins. , 2000, Biochemical and biophysical research communications.
[6] R. Sternglanz,et al. The silencing protein SIR2 and its homologs are NAD-dependent protein deacetylases. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[7] L. Guarente,et al. Transcriptional silencing and longevity protein Sir2 is an NAD-dependent histone deacetylase , 2000, Nature.
[8] D. Moazed,et al. An Enzymatic Activity in the Yeast Sir2 Protein that Is Essential for Gene Silencing , 1999, Cell.
[9] M. McVey,et al. The SIR2/3/4 complex and SIR2 alone promote longevity in Saccharomyces cerevisiae by two different mechanisms. , 1999, Genes & development.
[10] J. M. Sherman,et al. The conserved core of a human SIR2 homologue functions in yeast silencing. , 1999, Molecular biology of the cell.
[11] R. Frye,et al. Characterization of five human cDNAs with homology to the yeast SIR2 gene: Sir2-like proteins (sirtuins) metabolize NAD and may have protein ADP-ribosyltransferase activity. , 1999, Biochemical and biophysical research communications.
[12] J. Murnane,et al. Telomere dynamics in a human cancer cell line. , 1999, Experimental cell research.
[13] F. de Nigris,et al. Overexpression of the HIP gene coding for a heparin/heparan sulfate-binding protein in human thyroid carcinomas. , 1998, Cancer research.
[14] D. Sereno,et al. Leishmania major: Cell type dependent distribution of a 43 kDa antigen related to silent information regulatory‐2 protein family , 1998, Biology of the cell.
[15] G. Viglietto,et al. Thymosin β-10 Gene Overexpression Correlated with the Highly Malignant Neoplastic Phenotype of Transformed Thyroid Cells in Vivo and in Vitro , 1998 .
[16] M. P. Miano,et al. Expression of the neoplastic phenotype by human thyroid carcinoma cell lines requires NFκB p65 protein expression , 1997, Oncogene.
[17] J. Shay,et al. A survey of telomerase activity in human cancer. , 1997, European journal of cancer.
[18] A B Rose,et al. Hyperactivation of the silencing proteins, Sir2p and Sir3p, causes chromosome loss. , 1997, Genetics.
[19] M. Borrello,et al. Cytogenetics and molecular genetics of carcinomas arising from thyroid epithelial follicular cells , 1996, Genes, chromosomes & cancer.
[20] J. M. Sherman,et al. The SIR2 gene family, conserved from bacteria to humans, functions in silencing, cell cycle progression, and chromosome stability. , 1995, Genes & development.
[21] P. Nowell,et al. Detection of myc translocations in lymphoma cells by fluorescence in situ hybridization with yeast artificial chromosomes. , 1995, Blood.
[22] G. Chiappetta,et al. The expression of the high mobility group HMGI (Y) proteins correlates with the malignant phenotype of human thyroid neoplasias. , 1995, Oncogene.
[23] R. Paro,et al. Chromatin multiprotein complexes involved in the maintenance of transcription patterns. , 1995, Current opinion in genetics & development.
[24] C B Harley,et al. Specific association of human telomerase activity with immortal cells and cancer. , 1994, Science.
[25] D. Shore,et al. Evidence that a complex of SIR proteins interacts with the silencer and telomere-binding protein RAP1. , 1994, Genes & development.
[26] H. Coon,et al. Long-term culture and functional characterization of follicular cells from adult normal human thyroids. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[27] C. Harley,et al. Telomerase activity in human ovarian carcinoma. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[28] N. Berger,et al. Increased expression of the negative growth factor, galactoside-binding protein, gene in transformed thyroid cells and in human thyroid carcinomas. , 1992, Oncogene.
[29] J. Steitz,et al. Telomere shortening associated with chromosome instability is arrested in immortal cells which express telomerase activity. , 1992, The EMBO journal.
[30] L. Sobin,et al. The WHO histological classification of thyroid tumors: A commentary on the second edition , 1989, Cancer.
[31] K. Fujimori,et al. Enhanced expression of a glyceraldehyde-3-phosphate dehydrogenase gene in human lung cancers. , 1987, Cancer research.
[32] J. Hicks,et al. Cloning and characterization of four SIR genes of Saccharomyces cerevisiae , 1986, Molecular and cellular biology.
[33] A. Feinberg,et al. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. , 1983, Analytical biochemistry.
[34] A. van der Eb,et al. A new technique for the assay of infectivity of human adenovirus 5 DNA. , 1973, Virology.
[35] G. Viglietto,et al. Isolation of a SIR-like gene, SIR-T8, that is overexpressed in thyroid carcinoma cell lines and tissues , 2002, British Journal of Cancer.
[36] M. White,et al. Absence of cancer–associated changes in human fibroblasts immortalized with telomerase , 1999, Nature Genetics.
[37] M. Santoro,et al. Block of c-myc expression by antisense oligonucleotides inhibits proliferation of human thyroid carcinoma cell lines. , 1996, Clinical cancer research : an official journal of the American Association for Cancer Research.
[38] C. Harley,et al. Telomerase, cell immortality, and cancer. , 1994, Cold Spring Harbor symposia on quantitative biology.
[39] H. Sambrook. Molecular cloning : a laboratory manual. Cold Spring Harbor, NY , 1989 .
[40] R. Huber,et al. Transcriptional silencing and longevity protein Sir 2 is an NAD-dependent histone deacetylase , 2022 .