scholarly article | Q13442814 |
P356 | DOI | 10.1016/S0304-3835(01)00596-1 |
P698 | PubMed publication ID | 11463498 |
P50 | author | Fabienne Lesueur | Q50636993 |
P2093 | author name string | G Romeo | |
A Murat | |||
M Zini | |||
M Martinez-Alfaro | |||
R Corvi | |||
M Decaussin | |||
P2860 | cites work | Is familial non-medullary thyroid carcinoma more aggressive than sporadic thyroid cancer? A multicenter series | Q46196359 |
Genetic heterogeneity in familial nonmedullary thyroid carcinoma: exclusion of linkage to RET, MNG1, and TCO in 56 families. NMTC Consortium. | Q53345252 | ||
At least three genes account for familial papillary thyroid carcinoma: TCO and MNG1 excluded as susceptibility loci from a large Tasmanian family | Q57610575 | ||
Systematic Population-Based Assessment of Cancer Risk in First-Degree Relatives of Cancer Probands | Q59548851 | ||
Familial occurrence of papillary thyroid carcinoma | Q70721831 | ||
Familial papillary carcinoma of the thyroid | Q73422872 | ||
RET rearrangements in papillary thyroid carcinomas and adenomas detected by interphase FISH | Q73694322 | ||
Over-representation of a germline RET sequence variant in patients with sporadic medullary thyroid carcinoma and somatic RET codon 918 mutation | Q74450246 | ||
A 1.5-megabase yeast artificial chromosome contig from human chromosome 10q11.2 connecting three genetic loci (RET, D10S94, and D10S102) closely linked to the MEN2A locus | Q24563809 | ||
Molecular characterization of a thyroid tumor-specific transforming sequence formed by the fusion of ret tyrosine kinase and the regulatory subunit RI alpha of cyclic AMP-dependent protein kinase A | Q24611227 | ||
RET/PCM-1: a novel fusion gene in papillary thyroid carcinoma | Q28138236 | ||
The transcription coactivator HTIF1 and a related protein are fused to the RET receptor tyrosine kinase in childhood papillary thyroid carcinomas | Q28141552 | ||
Enzymatic synthesis of biotin-labeled polynucleotides: novel nucleic acid affinity probes | Q30450044 | ||
Fusion of a novel gene, ELKS, to RET due to translocation t(10;12)(q11;p13) in a papillary thyroid carcinoma | Q33862909 | ||
Familial papillary thyroid carcinoma: genetics, criteria for diagnosis, clinical features, and surgical treatment | Q34064449 | ||
The two genes generating RET/PTC3 are localized in chromosomal band 10q11.2. | Q34293074 | ||
PTC is a novel rearranged form of the ret proto-oncogene and is frequently detected in vivo in human thyroid papillary carcinomas | Q34372878 | ||
A gene predisposing to familial thyroid tumors with cell oxyphilia maps to chromosome 19p13.2. | Q34388217 | ||
Specific polymorphisms in the RET proto-oncogene are over-represented in patients with Hirschsprung disease and may represent loci modifying phenotypic expression | Q35430801 | ||
MYCN is retained in single copy at chromosome 2 band p23-24 during amplification in human neuroblastoma cells | Q35480153 | ||
Characterization of an inversion on the long arm of chromosome 10 juxtaposing D10S170 and RET and creating the oncogenic sequence RET/PTC. | Q36850030 | ||
Familial occurrence of differentiated, nonmedullary thyroid carcinoma | Q39523655 | ||
Familial nonmedullary thyroid cancer. An emerging entity that warrants aggressive treatment. | Q40458573 | ||
RET mutations in human disease | Q41196162 | ||
A t(10;17) translocation creates the RET/PTC2 chimeric transforming sequence in papillary thyroid carcinoma | Q42800418 | ||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 191-198 | |
P577 | publication date | 2001-09-01 | |
P1433 | published in | Cancer Letters | Q326372 |
P1476 | title | RET rearrangements in familial papillary thyroid carcinomas | |
P478 | volume | 170 |
Q34387003 | Familial nonmedullary thyroid neoplasia |
Q77347322 | Frequent RET rearrangements in thyroid papillary microcarcinoma detected by interphase fluorescence in situ hybridization |
Q28214459 | RET/PTC rearrangement in thyroid tumors |
Q35439328 | Specific haplotypes of the RET proto-oncogene are over-represented in patients with sporadic papillary thyroid carcinoma. |
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