RET rearrangements in familial papillary thyroid carcinomas

scientific article published on 01 September 2001

RET rearrangements in familial papillary thyroid carcinomas is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1016/S0304-3835(01)00596-1
P698PubMed publication ID11463498

P50authorFabienne LesueurQ50636993
P2093author name stringG Romeo
A Murat
M Zini
M Martinez-Alfaro
R Corvi
M Decaussin
P2860cites workIs familial non-medullary thyroid carcinoma more aggressive than sporadic thyroid cancer? A multicenter seriesQ46196359
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 familyQ57610575
Systematic Population-Based Assessment of Cancer Risk in First-Degree Relatives of Cancer ProbandsQ59548851
Familial occurrence of papillary thyroid carcinomaQ70721831
Familial papillary carcinoma of the thyroidQ73422872
RET rearrangements in papillary thyroid carcinomas and adenomas detected by interphase FISHQ73694322
Over-representation of a germline RET sequence variant in patients with sporadic medullary thyroid carcinoma and somatic RET codon 918 mutationQ74450246
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 locusQ24563809
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 AQ24611227
RET/PCM-1: a novel fusion gene in papillary thyroid carcinomaQ28138236
The transcription coactivator HTIF1 and a related protein are fused to the RET receptor tyrosine kinase in childhood papillary thyroid carcinomasQ28141552
Enzymatic synthesis of biotin-labeled polynucleotides: novel nucleic acid affinity probesQ30450044
Fusion of a novel gene, ELKS, to RET due to translocation t(10;12)(q11;p13) in a papillary thyroid carcinomaQ33862909
Familial papillary thyroid carcinoma: genetics, criteria for diagnosis, clinical features, and surgical treatmentQ34064449
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 carcinomasQ34372878
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 expressionQ35430801
MYCN is retained in single copy at chromosome 2 band p23-24 during amplification in human neuroblastoma cellsQ35480153
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 carcinomaQ39523655
Familial nonmedullary thyroid cancer. An emerging entity that warrants aggressive treatment.Q40458573
RET mutations in human diseaseQ41196162
A t(10;17) translocation creates the RET/PTC2 chimeric transforming sequence in papillary thyroid carcinomaQ42800418
P433issue2
P407language of work or nameEnglishQ1860
P304page(s)191-198
P577publication date2001-09-01
P1433published inCancer LettersQ326372
P1476titleRET rearrangements in familial papillary thyroid carcinomas
P478volume170

Reverse relations

cites work (P2860)
Q34387003Familial nonmedullary thyroid neoplasia
Q77347322Frequent RET rearrangements in thyroid papillary microcarcinoma detected by interphase fluorescence in situ hybridization
Q28214459RET/PTC rearrangement in thyroid tumors
Q35439328Specific haplotypes of the RET proto-oncogene are over-represented in patients with sporadic papillary thyroid carcinoma.

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