Research Topics
Genomes and GenesSpecies | C GicquelSummaryCountry: France Publications
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Publications
Hormonal regulation of fetal growthC Gicquel
Laboratoire d Explorations Fonctionnelles Endocriniennes, Hopital Armand Trousseau, Paris, France
Horm Res 65:28-33. 2006....
Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndromeChristine Gicquel
Laboratoire d Explorations Fonctionnelles Endocriniennes, Inserm U515 et UPMC Paris 6, Hopital Armand Trousseau, AP HP, 26 Avenue Arnold Netter, 75012 Paris, France
Nat Genet 37:1003-7. 2005..These findings provide new insight into the pathogenesis of SRS and strongly suggest that the 11p15 imprinted region, in addition to those of 7p11.2-p13 and 7q31-qter, is involved in SRS...
Alterations of the 11p15 imprinted region and the IGFs system in a case of recurrent non-islet-cell tumour hypoglycaemia (NICTH)J Bertherat
Clinique des Maladies Endocriniennes et Métaboliques CNRS UPR 1524, Hopital Cochin, Universite Rene Descartes, Laboratoire d Explorations Fonctionnelles Endocriniennes, Hopital Armand Trousseau, Paris, France
Clin Endocrinol (Oxf) 53:213-20. 2000..We report an extensive study of IGF-II and IGFBPs as well as chromosome 11p15 gene expression regulation in a case of a pleural fibrosarcoma in a 63-year-old patient presenting with NICTH...
Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith-Wiedemann syndromeV Gaston
Laboratoire d Explorations Fonctionnelles Endocriniennes, Hopital Trousseau, AP HP, Paris, France
Eur J Hum Genet 9:409-18. 2001..We also evaluated clinical and molecular features as prognostic factors for tumour and showed that mosaicism for 11p15 UPD and hypermethylation of the H19 gene in blood cells were associated with an increased risk of tumour...
Molecular markers and long-term recurrences in a large cohort of patients with sporadic adrenocortical tumorsC Gicquel
Laboratoire d Explorations Fonctionnelles Endocriniennes, Hopital Trousseau, AP HP, 75012 Paris, France
Cancer Res 61:6762-7. 2001..In patients who have undergone curative surgery, routine assessment of these tumor markers is a useful complement to histological scoring for predicting recurrence and guiding decisions for subsequent follow-up and management...
Epigenetics, genomic imprinting and assisted reproductive technologyY Le Bouc
Explorations Fonctionnelles Endocriniennes, Hopital d Enfants Armand Trousseau, AP HP, 75571 Paris, France
Ann Endocrinol (Paris) 71:237-8. 2010..3]). This suggests that unfaithful maintenance of DNA methylation marks following fertilization involves the dysregulation of a trans-acting regulatory factor that could be altered by ART...
Fibroblast growth factor-2 inhibits the maturation of pro-insulin-like growth factor-II (Pro-IGF-II) and the expression of insulin-like growth factor binding protein-2 (IGFBP-2) in the human adrenocortical tumor cell line NCI-H295RN Boulle
Laboratoire d Explorations Fonctionnelles Endocriniennes, Hopital Trousseau, Paris, France
Endocrinology 141:3127-36. 2000..Moreover, this study shows a novel effect of FGF-2, by which this growth factor modulates the processing of pro-IGF-II...
Evaluation of plasma insulin-like growth factor binding protein-2 as a marker for adrenocortical tumorsN Boulle
Laboratoire d Explorations Fonctionnelles Endocriniennes, Hopital Trousseau, 26 Avenue Arnold Netter, AP HP and Unité INSERM U515, Hôpital Saint Antoine 75012 Paris, France
Eur J Endocrinol 144:29-36. 2001..Circulating markers specific for adrenocortical carcinoma are needed and the aim of this study was to evaluate plasma IGFBP-2 as a marker for these malignant tumors...
Monoclonality of corticotroph macroadenomas in Cushing's diseaseC Gicquel
Laboratoire d Explorations Fonctionnelles Endocriniennes, Hopital Trousseau, Paris, France
J Clin Endocrinol Metab 75:472-5. 1992..Ours results show that a somatic modification plays an important role in the pathogenesis of corticotroph macroadenomas allowing monoclonal expansion of a genetically aberrant cell...
The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 regionS Rossignol
Laboratoire d'Explorations Fonctionnelles Endocriniennes, , , Paris, France
J Med Genet 43:902-7. 2006..Moreover, the mosaic distribution of epimutations suggests that imprinting is lost after fertilisation owing to a failure to maintain methylation marks during pre-implantation development...
Insights into the molecular biology of adrenocortical tumorsL Groussin
, Endocrinology Department, , Paris, France
Exp Clin Endocrinol Diabetes 115:175-8. 2007
Epigenetic abnormalities of the mannose-6-phosphate/IGF2 receptor gene are uncommon in human overgrowth syndromesC Gicquel
J Med Genet 41:e4. 2004
Sonographic findings in Beckwith-Wiedemann syndrome related to H19 hypermethylationC Le Caignec
Service de Genetique Medicale, Centre Hospitalo Universitaire, Nantes, France
Prenat Diagn 24:165-8. 2004..The rest of the fetal anatomy and the amniotic fluid volume appeared normal. After termination of the pregnancy, molecular analysis confirmed the diagnosis of BWS by showing an isolated hypermethylation of the H19 gene...
Mutation and methylation analysis of TP53 in adrenal carcinogenesisS Sidhu
Cancer Genetics, Kolling Institute of Medical Research, Royal North Shore Hospital, St Leonards, NSW 2065, Australia
Eur J Surg Oncol 31:549-54. 2005..To investigate the role of coding region mutation and promoter hypermethylation of TP53 in adrenocortical cancer formation...
[Involvement of the IGF system in the pathogenesis of adrenocortical tumors]C Gicquel
Laboratoire d'Explorations Fonctionnelles Endocriniennes, , 75012 Paris
Ann Endocrinol (Paris) 62:189-92. 2001..These markers of the malignant phenotype might markedly improve our diagnosis and prognosis abilities...
