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European Journal of Cancer
Volume 37, Issue 18
, Pages 2470-2474
, December 2001
Screening of selected genomic areas potentially involved in thyroid neoplasms
References
- . Clonal composition of benign and malignant human thyroid tumors. J. Clin. Invest. 1990;86:120–125
- . Clonal origin of toxic thyroid nodules with constitutively activating thyrotropin receptor mutations. J. Clin. Endocrinol. Metab. 1998;83:130–134
-
.
Point mutations of ras oncogenes are an early event in thyroid tumorigenesis.
Mol. Endocrinol. 1990;15:1162–1168
- . Ras mutations are uncommon in sporadic thyroid cancer in children and young adults. J. Endocrinol. Invest. 1999;22:781–789
- . Gsp mutations in human thyroid tumours. Oncogene. 1991;6:677–679
- Somatic mutations in the thyrotropin receptor gene cause hyperfunctioning thyroid adenomas. Nature. 1993;365:649–651
- PTC is a novel rearranged form of the ret protooncogene and is frequently detected in vivo in human papillary carcinomas. Cell. 1990;60:557–563
- . Oncogenic rearrangements of the ret proto-oncogene in thyroid tumors induced after exposure to ionizing radiation. Biochimie. 1997;79:619–623
-
Prevalences of Gs alpha, ras, p53 mutations and ret/PTC rearrangement in differentiated thyroid tumours in a Korean population.
Clin. Endocrinol. 1998;49:317–323
- Unique association of P53 mutations with undifferentiated but not with differentiated carcinomas of the thyroid gland. Cancer Res. 1992;52:1369–1371
- . High prevalence of mutations of the P53 gene in poorly differentiated human thyroid carcinoma. J. Clin. Invest. 1993;91:179–184
- Frequent loss of heterozygosity on chromosomes 3p and 17p without VHL or p53 mutations suggests involvement of unidentified tumor suppressor genes in follicular thyroid carcinoma. J. Clin. Endocrinol. Metab. 1997;82:3684–3691
- Chromosome 3p24-26 and 3p22-12 loss in human prostatic adenocarcinoma. Int. J. Cancer. 1997;71:20–25
- PAX8-PPARγ1 fusion in oncogene human thyroid carcinoma. Science. 2000;289:1357–1360
- Differential loss of heterozygosity at 7q31.2 in follicular and papillary thyroid tumors. Oncogene. 1998;17:789–793
- Loss of heterozygosity of the long arm of chromosome 7 in follicular and anaplastic thyroid cancer, but not in papillary thyroid cancer. J. Clin. Endocrinol. Metab. 1999;84:3235–3240
- . Deletion mapping on chromosome 10q25–q26 in human endometrial cancer. Br. J. Cancer. 1996;74:1979–1983
- Allelotyping of follicular thyroid tumors. Hum. Genet. 1995;96:27–32
- Deletions of the long arm of chromosome 10 in progression of follicular thyroid tumors. Hum. Genet. 1996;97:299–303
- Somatic deletions and mutations in the Cowden disease gene, PTEN, in sporadic thyroid tumors. Cancer Res. 1997;57:4710–4713
- An allelotype of papillary thyroid cancer. Int. J. Cancer. 1996;69:442–444
- . Molecular defects in thyroid gland neoplasia. J. Clin. Endocrinol. Metab. 1992;75:1398–1400
- . Molecular basis of thyroid cancer. Endocr. Rev. 1994;15:202–232
- . Origin and progression of thyroid epithelial tumours (cellular and molecular mechanisms). Horm. Res. 1997;47:145–157
- . Loss of heterozygosity on chromosome 11q13 in lobular lesions of the breast using tissue microdissection and polymerase chain reaction. Hum. Pathol. 1997;28:277–282
- Molecular cloning and characterization of LOH11CR2A, a new gene within a refined minimal region of LOH at 11q23. Genomics. 1997;46:217–222
- . Deletion mapping on chromosome 17p in medulloblastoma. Br. J. Cancer. 1997;76:1284–1287
- . Methylation of the HIC-1 candidate tumor supressor gene in human breast cancer. Oncogene. 1998;16:2159–2164
PII: S0959-8049(01)00302-1
doi: 10.1016/S0959-8049(01)00302-1
© 2001 Elsevier Science Ltd. All rights reserved.
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European Journal of Cancer
Volume 37, Issue 18
, Pages 2470-2474
, December 2001
