scholarly article | Q13442814 |
P819 | ADS bibcode | 1992PNAS...89.1616P |
P356 | DOI | 10.1073/PNAS.89.5.1616 |
P932 | PMC publication ID | 48503 |
P698 | PubMed publication ID | 1542652 |
P5875 | ResearchGate publication ID | 21612378 |
P2093 | author name string | Fusco A | |
Santoro M | |||
Bongarzone I | |||
Grieco M | |||
Pierotti MA | |||
Jenkins RB | |||
Herrmann MA | |||
Sozzi G | |||
Miozzo M | |||
Monzini N | |||
P2860 | cites work | Developmentally regulated expression of a human "finger"-containing gene encoded by the 5' half of the ret transforming gene | Q24298289 |
Activation of the ret-II oncogene without a sequence encoding a transmembrane domain and transforming activity of two ret-II oncogene products differing in carboxy-termini due to alternative splicing | Q24339506 | ||
cDNA cloning and characterization of ret activated in a human papillary thyroid carcinoma cell line | Q28117244 | ||
A human oncogene formed by the fusion of truncated tropomyosin and protein tyrosine kinase sequences | Q28282360 | ||
Bcl-2 is an inner mitochondrial membrane protein that blocks programmed cell death | Q29620000 | ||
Analysis by pulsed field gel electrophoresis reveals complex rearrangements in two MET alleles in a chemically-treated human cell line, MNNG-HOS. | Q34234846 | ||
PTC is a novel rearranged form of the ret proto-oncogene and is frequently detected in vivo in human thyroid papillary carcinomas | Q34372878 | ||
Cloning and structural analysis of cDNAs for bcl-2 and a hybrid bcl-2/immunoglobulin transcript resulting from the t(14;18) translocation | Q34559025 | ||
Differential expression of the normal and of the translocated human c-myc oncogenes in B cells | Q37344941 | ||
Suppressors of the malignant phenotype | Q37833593 | ||
A new oncogene in human thyroid papillary carcinomas and their lymph-nodal metastases | Q42807477 | ||
Molecular cloning of a new transforming gene from a chemically transformed human cell line. | Q45345810 | ||
Megabase inversions in the human genome as physiological events | Q48254994 | ||
The oncogene associated with human papillary thyroid carcinoma (PTC) is assigned to chromosome 10 q11-q12 in the same region as multiple endocrine neoplasia type 2A (MEN2A). | Q52246921 | ||
Fused transcript of abl and bcr genes in chronic myelogenous leukaemia | Q59064021 | ||
Oncogenicity of the ret transforming gene in MMTV/ret transgenic mice | Q67656982 | ||
Frequent occurrence of cytogenetic abnormalities in sporadic nonmedullary thyroid carcinoma | Q68920794 | ||
High frequency of activation of tyrosine kinase oncogenes in human papillary thyroid carcinoma | Q69398273 | ||
Human ret proto-oncogene mapped to chromosome 10q11.2. | Q69558463 | ||
Refined localization to contiguous regions on chromosome 10q of the two genes (H4 and RET) that form the oncogenic sequence PTC | Q70111753 | ||
P433 | issue | 5 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 1616-1620 | |
P577 | publication date | 1992-03-01 | |
P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
P1476 | title | Characterization of an inversion on the long arm of chromosome 10 juxtaposing D10S170 and RET and creating the oncogenic sequence RET/PTC. | |
P478 | volume | 89 |
Q35746558 | 'Chromosomal Rainbows' Detect Oncogenic Rearrangements of Signaling Molecules in Thyroid Tumors |
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Q34013654 | A neoplastic gene fusion mimics trans-splicing of RNAs in normal human cells |
Q37686882 | A novel read-through transcript JMJD7-PLA2G4B regulates head and neck squamous cell carcinoma cell proliferation and survival |
Q42800418 | A t(10;17) translocation creates the RET/PTC2 chimeric transforming sequence in papillary thyroid carcinoma |
Q40849447 | Accumulation of allelic losses on chromosome 10 in human gliomas at recurrence |
Q72684603 | Activated RET oncogene in thyroid cancers of children from areas contaminated by Chernobyl accident |
Q33813441 | Advances in cancer cytogenetics |
Q45829274 | Array CGH demonstrates characteristic aberration signatures in human papillary thyroid carcinomas governed by RET/PTC. |
Q47833329 | Assessment of molecular testing in fine-needle aspiration biopsy samples: an experience in a Chinese population |
Q34550400 | BAC-FISH assays delineate complex chromosomal rearrangements in a case of post-Chernobyl childhood thyroid cancer |
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Q39700806 | CCDC6 represses CREB1 activity by recruiting histone deacetylase 1 and protein phosphatase 1. |
Q47634740 | CCDC6: the identity of a protein known to be partner in fusion. |
Q42497065 | Case report: a p.C618S RET proto-oncogene germline mutation in a large Chinese pedigree with familial medullary thyroid carcinoma |
Q34085418 | Case-Control Genome-Wide Association Study of Attention-Deficit/Hyperactivity Disorder |
Q34711521 | Chromosomal rearrangements in post-Chernobyl papillary thyroid carcinomas: evaluation by spectral karyotyping and automated interphase FISH |
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Q72046520 | Cytogenetic findings in 31 papillary thyroid carcinomas |
Q37212268 | DNA probe pooling for rapid delineation of chromosomal breakpoints |
Q42281387 | Detection of RET oncogene activation in human papillary thyroid carcinomas by in situ hybridisation |
Q35833808 | Detection of RET proto-oncogene point mutations in paraffin-embedded pheochromocytoma specimens by nonradioactive single-strand conformation polymorphism analysis and direct sequencing |
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Q34617571 | Involvement of H4(D10S170) protein in ATM-dependent response to DNA damage. |
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Q67482944 | Keeping track of the translocations |
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Q42828135 | Loss of function effect of RET mutations causing Hirschsprung disease. |
Q54781483 | Loss of heterozygosity mutations of tumor suppressor genes in cytologically atypical areas in chronic lymphocytic thyroiditis. |
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Q38466453 | Molecular cytogenetic characterization of chromosome 9-derived material in a human thyroid cancer cell line |
Q37924088 | Molecular genetics and diagnosis of thyroid cancer |
Q35208510 | Molecular pathogenesis of thyroid cancer |
Q42798821 | New breakpoints in both the H4 and RET genes create a variant of PTC-1 in a post-Chernobyl papillary thyroid carcinoma |
Q36361115 | New treatment in advanced thyroid cancer |
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Q27824825 | Oncogenic AKAP9-BRAF fusion is a novel mechanism of MAPK pathway activation in thyroid cancer |
Q36135918 | RET activation in adult and childhood papillary thyroid carcinoma using a reverse transcriptase-n-polymerase chain reaction approach on archival-nested material |
Q74235643 | RET rearrangements in familial papillary thyroid carcinomas |
Q54250039 | RET/PTC activation in human thyroid carcinomas |
Q33599429 | RET/PTC and CK19 expression in papillary thyroid carcinoma and its clinicopathologic correlation |
Q28214459 | RET/PTC rearrangement in thyroid tumors |
Q70588382 | Regional assignment of the gene coding for a human Graves' disease autoantigen to 10q21.3-q22.1. |
Q41019851 | Ret oncogene activation in human thyroid neoplasms is restricted to the papillary cancer subtype. |
Q41878891 | Rethinking the role of oncogenes in papillary thyroid cancer initiation |
Q24533621 | Shc and Enigma are both required for mitogenic signaling by Ret/ptc2. |
Q28776010 | Single missense mutation in the tyrosine kinase catalytic domain of the RET protooncogene is associated with multiple endocrine neoplasia type 2B |
Q55023816 | Somatic mutations in RET exons 12 and 15 in sporadic medullary thyroid carcinomas: different spectrum of mutations in sporadic type from hereditary type. |
Q45130742 | TIMP1 and SERPIN-A overexpression and TFF3 and CRABP1 underexpression as biomarkers for papillary thyroid carcinoma. |
Q79894991 | TPM3/PDGFRB fusion transcript and its reciprocal in chronic eosinophilic leukemia |
Q24311495 | The DNA rearrangement that generates the TRK-T3 oncogene involves a novel gene on chromosome 3 whose product has a potential coiled-coil domain |
Q34735847 | The Pathology of Medullary Carcinoma of the Thyroid: Review of the Literature and Personal Experience on 62 Cases |
Q41350370 | The RET proto-oncogene: a challenge to our understanding of disease pathogenesis |
Q38496502 | The emerging complexity of gene fusions in cancer |
Q36760027 | The impact of translocations and gene fusions on cancer causation |
Q58453418 | The management of thyroid nodules and cancer in the molecular era |
Q47920723 | The molecular genetics of endocrine tumours |
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Q36455074 | The role of immunohistochemical markers in the diagnosis of follicular-patterned lesions of the thyroid |
Q40931125 | The role of the immune system in anti-tumour responses. Potential for drug therapy |
Q34293074 | The two genes generating RET/PTC3 are localized in chromosomal band 10q11.2. |
Q38135137 | Translational research in endocrine surgery |
Q37363960 | Translocations in epithelial cancers |
Q38020834 | Vandetanib for the treatment of metastatic medullary thyroid cancer |
Q46211426 | XB130, a tissue-specific adaptor protein that couples the RET/PTC oncogenic kinase to PI 3-kinase pathway. |
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