Polymerase chain reaction and analysis of cancer cell markers
- PMID: 2332893
- DOI: 10.1093/jnci/82.10.806
Polymerase chain reaction and analysis of cancer cell markers
Comment on
-
Involvement of the bcl-2 gene in Hodgkin's disease.J Natl Cancer Inst. 1990 May 16;82(10):855-8. doi: 10.1093/jnci/82.10.855. J Natl Cancer Inst. 1990. PMID: 2185367
-
Sensitive detection of estrogen receptor RNA by polymerase chain reaction assay.J Natl Cancer Inst. 1990 May 16;82(10):858-61. doi: 10.1093/jnci/82.10.858. J Natl Cancer Inst. 1990. PMID: 2332903
Similar articles
-
Sensitive detection of estrogen receptor RNA by polymerase chain reaction assay.J Natl Cancer Inst. 1990 May 16;82(10):858-61. doi: 10.1093/jnci/82.10.858. J Natl Cancer Inst. 1990. PMID: 2332903
-
Use of reverse transcription-polymerase chain reaction methodology to detect estrogen-regulated gene expression in small breast cancer specimens.Clin Cancer Res. 1997 Nov;3(11):2165-72. Clin Cancer Res. 1997. PMID: 9815611
-
Diagnostic detection of AML1/ETO gene fusion by polymerase chain reaction.Leukemia. 2002 Aug;16(8):1576-7; author reply 1577. doi: 10.1038/sj.leu.2402667. Leukemia. 2002. PMID: 12145712 No abstract available.
-
The polymerase chain reaction and cancer diagnosis.Cancer Cells. 1989 Oct;1(2):56-61. Cancer Cells. 1989. PMID: 2561871 Review.
-
Genes in the diagnosis of malignant disease. IFCC Scientific Division Committee on Molecular Biology Techniques.J Int Fed Clin Chem. 1992 Dec;4(5):222-7. J Int Fed Clin Chem. 1992. PMID: 10146702 Review. No abstract available.
Cited by
-
Molecular biology in medicine.Postgrad Med J. 1992 Apr;68(798):251-62. doi: 10.1136/pgmj.68.798.251. Postgrad Med J. 1992. PMID: 1409188 Free PMC article. Review. No abstract available.
-
Characterization of V71M mutation in the aquaporin-2 gene causing nephrogenic diabetes insipidus.J Genet. 2008 Dec;87(3):279-82. doi: 10.1007/s12041-008-0044-0. J Genet. 2008. PMID: 19147915 No abstract available.
-
Segregation of S292F TPO gene mutation in three large Tunisian families with thyroid dyshormonogenesis: evidence of a founder effect.Eur J Pediatr. 2015 Nov;174(11):1491-501. doi: 10.1007/s00431-015-2550-4. Epub 2015 May 13. Eur J Pediatr. 2015. PMID: 25968604
-
Congenital lamellar ichthyosis in Tunisia is caused by a founder nonsense mutation in the TGM1 gene.Mol Biol Rep. 2013 Mar;40(3):2527-32. doi: 10.1007/s11033-012-2333-1. Epub 2012 Nov 29. Mol Biol Rep. 2013. PMID: 23192619 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources