BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 1483923)

  • 1. Inactivation of the p53 gene is not required for tumorigenesis of medullary thyroid carcinoma or pheochromocytoma.
    Yana I; Nakamura T; Shin E; Karakawa K; Kurahashi H; Kurita Y; Kobayashi T; Mori T; Nishisho I; Takai S
    Jpn J Cancer Res; 1992 Nov; 83(11):1113-6. PubMed ID: 1483923
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Absence of TP53 alterations in pheochromocytomas and medullary thyroid carcinomas.
    Herfarth KK; Wick MR; Marshall HN; Gartner E; Lum S; Moley JF
    Genes Chromosomes Cancer; 1997 Sep; 20(1):24-9. PubMed ID: 9290950
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutations in the cysteine-rich region of the RET proto-oncogene in patients diagnosed as having sporadic medullary thyroid carcinoma.
    Kimura T; Yoshimoto K; Yokogoshi Y; Saito S
    Endocr J; 1995 Aug; 42(4):517-25. PubMed ID: 8556059
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Loss of heterozygosity suggests multiple genetic alterations in pheochromocytomas and medullary thyroid carcinomas.
    Khosla S; Patel VM; Hay ID; Schaid DJ; Grant CS; van Heerden JA; Thibodeau SN
    J Clin Invest; 1991 May; 87(5):1691-9. PubMed ID: 2022740
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Rudolf-Virchow-Preis 1995. The role of RET proto-oncogene mutation analysis in the diagnosis of multiple endocrine neoplasia type 2 (MEN 2) gene carriers and in the discrimination of sporadic and familial medullary thyroid carcinomas and pheochromocytomas.
    Komminoth P
    Verh Dtsch Ges Pathol; 1995; 79():L-LV. PubMed ID: 8600671
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Loss of genes on chromosome 22 in medullary thyroid carcinoma and pheochromocytoma.
    Takai S; Tateishi H; Nishisho I; Miki T; Motomura K; Miyauchi A; Kato M; Ikeuchi T; Yamamoto K; Okazaki M
    Jpn J Cancer Res; 1987 Sep; 78(9):894-8. PubMed ID: 2889715
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutations of the p53 gene in human functional adrenal neoplasms.
    Lin SR; Lee YJ; Tsai JH
    J Clin Endocrinol Metab; 1994 Feb; 78(2):483-91. PubMed ID: 8106638
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Frequent loss of 17p, but no p53 mutations or protein overexpression in benign and malignant pheochromocytomas.
    Petri BJ; Speel EJ; Korpershoek E; Claessen SM; van Nederveen FH; Giesen V; Dannenberg H; van der Harst E; Dinjens WN; de Krijger RR
    Mod Pathol; 2008 Apr; 21(4):407-13. PubMed ID: 18223555
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Low frequency of ras gene mutations in neuroblastomas, pheochromocytomas, and medullary thyroid cancers.
    Moley JF; Brother MB; Wells SA; Spengler BA; Biedler JL; Brodeur GM
    Cancer Res; 1991 Mar; 51(6):1596-9. PubMed ID: 1998949
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic events in tumour initiation and progression in multiple endocrine neoplasia type 2.
    Mulligan LM; Gardner E; Smith BA; Mathew CG; Ponder BA
    Genes Chromosomes Cancer; 1993 Mar; 6(3):166-77. PubMed ID: 7682102
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic aberrance of sporadic MEN 2A component tumours: analysis of RET.
    Cho NH; Lee HW; Lim SY; Kang S; Jung WY; Park CS
    Pathology; 2005 Feb; 37(1):10-3. PubMed ID: 15875728
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Loss of heterozygosity on the long arm of chromosome 22 in pheochromocytoma.
    Tanaka N; Nishisho I; Yamamoto M; Miya A; Shin E; Karakawa K; Fujita S; Kobayashi T; Rouleau GA; Mori T
    Genes Chromosomes Cancer; 1992 Nov; 5(4):399-403. PubMed ID: 1283329
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Differential expression of RET isoforms in normal thyroid tissues, papillary and medullary thyroid carcinomas.
    Ramone T; Romei C; Ciampi R; Tacito A; Piaggi P; Torregrossa L; Ugolini C; Elisei R
    Endocrine; 2019 Sep; 65(3):623-629. PubMed ID: 31278686
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Low incidence of loss of chromosome 10 in sporadic and hereditary human medullary thyroid carcinoma.
    Nelkin BD; Nakamura Y; White RW; de Bustros AC; Herman J; Wells SA; Baylin SB
    Cancer Res; 1989 Aug; 49(15):4114-9. PubMed ID: 2568166
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The RET proto-oncogene and cancer.
    Donis-Keller H
    J Intern Med; 1995 Oct; 238(4):319-25. PubMed ID: 7595167
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A (Sipple's syndrome).
    Oishi S; Sato T; Takiguchi-Shirahama S; Nakamura Y
    Endocr J; 1995 Aug; 42(4):527-36. PubMed ID: 8556060
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Consistent association of 1p loss of heterozygosity with pheochromocytomas from patients with multiple endocrine neoplasia type 2 syndromes.
    Moley JF; Brother MB; Fong CT; White PS; Baylin SB; Nelkin B; Wells SA; Brodeur GM
    Cancer Res; 1992 Feb; 52(4):770-4. PubMed ID: 1346584
    [TBL] [Abstract][Full Text] [Related]  

  • 18. RET proto-oncogene point mutations in sporadic neuroendocrine tumors.
    Komminoth P; Roth J; Muletta-Feurer S; Saremaslani P; Seelentag WK; Heitz PU
    J Clin Endocrinol Metab; 1996 Jun; 81(6):2041-6. PubMed ID: 8964826
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Absence of mutations at codon 768 of the RET proto-oncogene in sporadic and hereditary pheochromocytomas.
    Yoshimoto K; Kimura T; Tanaka C; Moritani M; Iwahana H; Itakura M
    Endocr J; 1996 Feb; 43(1):109-14. PubMed ID: 8732460
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutation analysis of the c-mos proto-oncogene and the endothelin-B receptor gene in medullary thyroid carcinoma and phaeochromocytoma.
    Eng C; Foster KA; Healey CS; Houghton C; Gayther SA; Mulligan LM; Ponder BA
    Br J Cancer; 1996 Aug; 74(3):339-41. PubMed ID: 8695346
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.