A gene predisposing to familial thyroid tumors with cell oxyphilia maps to chromosome 19p13.2.
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F. Canzian | D. Bonneau | F. Lesueur | P. Amati | P Levillain | G. Romeo | P. Levillain | H. Harach | F Lesueur | F Canzian | P Amati | H R Harach | J L Kraimps | J Barbier | G Romeo | D Bonneau | J. Kraimps | J. Barbier | Dominique Bonneau | Federico Canzian | Giovanni Romeo | Jacques Barbier | Pierre Levillain
[1] K. Lote,et al. Familial occurrence of papillary thyroid carcinoma , 1980, Cancer.
[2] A. Olsen,et al. Physical and genetic mapping of novel microsatellite polymorphisms on human chromosome 19. , 1996, Genomics.
[3] Q. Duh,et al. Familial Nonmedullary Thyroid Cancer: An Emerging Entity That Warrants Aggressive Treatment , 1995 .
[4] J. Parma,et al. Somatic mutations in the thyrotropin receptor gene cause hyperfunctioning thyroid adenomas , 1993, Nature.
[5] M H Skolnick,et al. Systematic population-based assessment of cancer risk in first-degree relatives of cancer probands. , 1994, Journal of the National Cancer Institute.
[6] D. Gorson. Familial papillary carcinoma of the thyroid. , 1992, Thyroid : official journal of the American Thyroid Association.
[7] B. Pasini,et al. RET mutations in human disease. , 1996, Trends in genetics : TIG.
[8] I. Hughes,et al. An autosomal dominant form of adolescent multinodular goiter. , 1986, American journal of human genetics.
[9] D. Bonneau,et al. Familial papillary carcinoma of the thyroid. , 1997, Surgery.
[10] Tom Slezak,et al. An integrated metric physical map of human chromosome 19 , 1995, Nature Genetics.
[11] M. Pierotti,et al. Overexpression of the c-MET/HGF receptor gene in human thyroid carcinomas. , 1992, Oncogene.
[12] L. Degroot,et al. Congenital goiter and the development of metastatic follicular carcinoma with evidence for a leak of nonhormonal iodide: clinical, pathological, kinetic, and biochemical studies and a review of the literature. , 1981, The Journal of clinical endocrinology and metabolism.
[13] A. Allgeier,et al. Germline mutations in the thyrotropin receptor gene cause non–autoimmune autosomal dominant hyperthyroidism , 1994, Nature Genetics.
[14] M. Stratton,et al. Familial nontoxic multinodular thyroid goiter locus maps to chromosome 14q but does not account for familial nonmedullary thyroid cancer. , 1997, American journal of human genetics.
[15] J. Burgess,et al. Two families with an autosomal dominant inheritance pattern for papillary carcinoma of the thyroid. , 1997, The Journal of clinical endocrinology and metabolism.
[16] Jing Li,et al. Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome , 1997, Nature Genetics.
[17] J. Ott. Computer-simulation methods in human linkage analysis. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[18] G. Williams,et al. Familial adenomatous polyposis associated thyroid carcinoma: a distinct type of follicular cell neoplasm , 1994, Histopathology.
[19] L Kruglyak,et al. Parametric and nonparametric linkage analysis: a unified multipoint approach. , 1996, American journal of human genetics.
[20] L. Weiss,et al. Familial papillary carcinoma of the thyroid. , 1986, American journal of medical genetics.
[21] G. Lathrop,et al. Easy calculations of lod scores and genetic risks on small computers. , 1984, American journal of human genetics.
[22] S. Nagataki,et al. Expression of adhesion molecule ICAM-1 (CD54) in thyroid papillary adenocarcinoma , 1994, Journal of endocrinological investigation.
[23] M. Santoro,et al. High frequency of activation of tyrosine kinase oncogenes in human papillary thyroid carcinoma. , 1989, Oncogene.
[24] E. D. Williams,et al. Solitary, multiple, and familial oxyphil tumours of the thyroid gland , 1998, The Journal of pathology.