Mitochondrial DNA ‘common’ deletion in Hürthle cell lesions of the thyroid

1. Yun K, Merrie AEH, Gunn J, Phillips LV, McCall JL. Keratin 20 is a speci®c marker of submicroscopic lymph node metastases in colorectal cancer: validation by K-RAS mutations. J Pathol 2000; 191: 21±26. 2. Moll R, Franke WW, Schiller DL, et al. The catalog of human cytokeratins: patterns of expression in normal epithelia, tumors and cultured cells. Cell 1982; 31: 11±24. 3. Moll R, Lowe A, Laufer J, Franke WW. Cytokeratin 20 in human carcinomas. A new histodiagnostic marker detected by monoclonal antibodies. Am J Pathol 1992; 140: 427±447. 4. Gunn J, McCall JL, Yun K, Wright PA. Detection of micrometastases in colorectal cancer patients by K19 and K20 reversetranscription polymerase chain reaction. Lab Invest 1996; 75: 611±616. 5. Merrie AEH, Yun K, van Rij AM, McCall JL. Detection and signi®cance of minimal residual disease in colorectal cancer. Histol Histopathol 1999; 14: 561±569. 6. Merrie AEH, Yun K, Gunn J, McCall JL. Analysis of potential markers for detection of submicroscopic lymph node metastases in breast cancer. Br J Cancer 1999; 80: 2019±2024. 7. Harnden P, Eardley I, Joyce AD, Southgate J. Cytokeratin 20 as an objective marker of urothelial dysplasia. Br J Urol 1996; 78: 870±875. 8. Harnden P, Mahmood N, Southgate J. Expression of cytokeratin 20 rede®nes urothelial papillomas of the bladder. Lancet 1999; 353: 974±977. 9. Ghossein RA, Rosai J. Polymerase chain reaction in the detection of micrometastases and circulating tumor cells. Cancer 1996; 78: 10±16.

[1]  M. Sobrinho-Simões,et al.  Hürthle cell tumours of the thyroid. A review with emphasis on mitochondrial abnormalities with clinical relevance , 2000, Virchows Archiv.

[2]  D. Skibinski,et al.  Detection of damage to the mitochondrial genome in the oncocytic cells of Warthin's tumour , 2000, The Journal of pathology.

[3]  R. Seruca,et al.  Comments on: mutations in mitochondrial control region DNA in gastric tumours of Japanese patients, Tamura, et al. Eur J Cancer 1999, 35, 316-319. , 1999, European journal of cancer.

[4]  M. Sobrinho-Simões,et al.  The common deletion of mitochondrial DNA is found in goiters and thyroid tumors with and without oxyphil cell change. , 1998, Ultrastructural pathology.

[5]  P. Seibel,et al.  Hashimoto thyroiditis is associated with defects of cytochrome-c oxidase in oxyphil Askanazy cells and with the common deletion (4,977) of mitochondrial DNA. , 1998, Ultrastructural pathology.

[6]  S. Loening,et al.  Polymerase chain reaction in the detection of micrometastases and circulating tumor cells , 1996, Cancer.

[7]  M. Ladanyi,et al.  Analysis of nuclear and mitochondrial DNA alterations in thyroid and renal oncocytic tumors. , 1994, Cytogenetics and cell genetics.

[8]  J. Müller-Höckey.  Random Cytochrome-C-Oxidase Deficiency of Oxyphil Cell Nodules in the Parathyroid Gland: A Mitochondrial Cytopathy Related to Cell Ageing? , 1992 .

[9]  S. Harawi,et al.  Oncocytes, oncocytosis, and oncocytic tumors. , 1992, Pathology annual.

[10]  J. Müller‐Höcker.  Random cytochrome-C-oxidase deficiency of oxyphil cell nodules in the parathyroid gland. A mitochondrial cytopathy related to cell ageing? , 1992, Pathology, research and practice.