Literature DB >> 3005035

Identification of a c-myc oncogene lacking the exon 1 in the normal cells of a patient carrying a thyroid carcinoma.

L Del Senno, E Degli Uberti, M Rossi, D Buzzoni, R Barbieri, P Rossi, P Patracchini, F Bernardi, G Marchetti, F Conconi.   

Abstract

In this paper we describe an alteration of the c-myc oncogene present in the white blood cells and normal as well as neoplastic thyroid cells of a subject carrying a thyroid carcinoma. Restriction enzyme mapping and hybridization to human c-myc probes specific for different regions of this gene demonstrate that this subject carries, in addition to the normal one, a c-myc oncogene lacking the first exon and part of the first intron. The levels of the c-myc mRNA in thyroid cells of this subject do not show differences with respect to thyroid cells from other subjects. Taken together, these findings indicate that the deletion of the first exon of the c-myc oncogene, in itself, does not produce overtranscription of this oncogene nor hematopoietic malignancies.

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Year:  1986        PMID: 3005035     DOI: 10.1016/0014-5793(86)80266-6

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  6 in total

1.  Molecular cytogenetic analysis of human breast tumors: methylation pattern of the HLA-DRα gene.

Authors:  R Barbieri; R Piva; C Mischiati; R Gambari
Journal:  Cytotechnology       Date:  1987-10       Impact factor: 2.058

2.  A 5'-truncated c-myc gene variant not associated with a risk of cancer.

Authors:  N S Pellegata; G Bergamaschi; D Amadori; A Aloia; P Ballarini; L Del Senno; L Amaducci; G N Ranzani
Journal:  Hum Genet       Date:  1991-09       Impact factor: 4.132

3.  Differential levels of thyroid peroxidase and thyroglobulin messenger ribonucleic acids in congenital goiter with defective thyroglobulin synthesis.

Authors:  H M Targovnik; V Varela; G J Juvenal; F Propato; H A Chester; L Krawiec; G Frechtel; D H Moran; H A Perinetti; M A Pisarev
Journal:  J Endocrinol Invest       Date:  1990-11       Impact factor: 4.256

4.  Hypomethylation of the human HLA-DR alpha gene in breast carcinomas and autologous metastases.

Authors:  R Barbieri; A P Rimondi; D Buzzoni; L Luppi; C Nastruzzi; P Orlando; R Gambari
Journal:  Clin Exp Metastasis       Date:  1989 Jul-Aug       Impact factor: 5.150

5.  RFLP analysis in families with sporadic hemophilia A. Estimate of the mutation ratio in male and female gametes.

Authors:  F Bernardi; G Marchetti; V Bertagnolo; L Faggioli; S Volinia; P Patracchini; S Bartolai; F Vannini; L Felloni; L Rossi
Journal:  Hum Genet       Date:  1987-07       Impact factor: 4.132

6.  De novo complex autosomal translocation involving chromosomes 8, 13 and 15 in a girl with a sporadic retinoblastoma.

Authors:  E Calzolari; P Palazzi; V Aiello; E Mazzeo; P Perri; A Minelli; L del Senno; P Patracchini; F Bernardi
Journal:  Hum Genet       Date:  1987-09       Impact factor: 4.132

  6 in total

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