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Profil bibliographique

G. Danglot

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

20Publications signalées
823Citations signalées
0Affiliations récentes

Les domaines associés

Genomic variations and chromosomal abnormalitiesNeuroblastoma Research and TreatmentsNeurofibromatosis and Schwannoma CasesAnimal Genetics and ReproductionGlioma Diagnosis and Treatment

Les publications récentes

2009 article OpenAlex

Two populations of double minute chromosomes harbor distinct amplicons, the MYC locus at 8q24.2 and a 0.43-Mb region at 14q24.1, in the SW613-S human carcinoma cell line

Marine Guillaud-Bataille, Olivier Brison, G. Danglot, Christian Lavialle et autres

High-level amplifications observed in tumor cells are usually indicative of genes involved in oncogenesis. We report here a high resolution characterization of a new amplified region in the SW613-S carcinoma cell line. This cell line contains tumorigenic cells displaying high-level MYC amplification …

fr (code pays fourni par la source)

10 citations Cytogenetic and Genome Research
Accès ouvert 2009 supplementary-materials OpenAlex

Supplementary Material for: Two populations of double minute chromosomes harbor distinct amplicons, the MYC locus at 8q24.2 and a 0.43-Mb region at 14q24.1, in the SW613-S human carcinoma cell line

Marine Guillaud-Bataille, Olivier Brison, G. Danglot, Christian Lavialle et autres

High-level amplifications observed in tumor cells are usually indicative of genes involved in oncogenesis. We report here a high resolution characterization of a new amplified region in the SW613-S carcinoma cell line. This cell line contains tumorigenic cells displaying high-level MYC amplification …

0 citations Figshare
2008 article OpenAlex

MDM2 amplification in a primary alveolar rhabdomyosarcoma displaying a t(2;13)(q35;q14)

Mounira Meddeb, A. Valent, G. Danglot, V.C. Nguyen et autres

This report describes a case of rhabdomyosarcoma associated with a 2;13 translocation and multiple double minute chromosomes. The origin of the amplified DNA was identified using comparative genomic hybridization, which pinpointed a unique spot at 12q13-->q14. Band 12q13 has been shown to …

fr (code pays fourni par la source)

30 citations Cytogenetics and Cell Genetics
2006 article OpenAlex

High promoter hypermethylation frequency of p14/ARF in supratentorial PNET but not in medulloblastoma

M M Inda, J Muñoz, P. Coullin, Didier Fauvet et autres

AIMS: Medulloblastoma (MB) is the most common primitive neuroectodermal tumour (PNET) of the central nervous system. Although supratentorial PNET (sPNET) and MB are histologically similar, their clinical behaviour differs, sPNET being more aggressive than MB. The aim of this study was to …

fr, es (code pays fourni par la source)

28 citations Histopathology
2005 article OpenAlex

Genetic heterogeneity in supratentorial and infratentorial primitive neuroectodermal tumours of the central nervous system

M M Inda, Christine Pérot, Marine Guillaud-Bataille, G. Danglot et autres

AIMS: Medulloblastoma (MB), a kind of infratentorial primitive neuroectodermal tumour (PNET), is the most frequent malignant brain tumour in childhood. In contrast, supratentorial PNET (sPNET) are very infrequent tumours, but they are histologically similar to MB, although they present a worse clinical …

fr, us, es (code pays fourni par la source)

39 citations Histopathology
1999 article OpenAlex

Gain of Chromosome Arm 17q and Adverse Outcome in Patients with Neuroblastoma

Nick Bown, Simon Cotterill, Maria Łastowska, Seamus O’Neill et autres

BACKGROUND: Gain of genetic material from chromosome arm 17q (gain of segment 17q21-qter) is the most frequent cytogenetic abnormality of neuroblastoma cells. This gain has been associated with advanced disease, patients who are > or =1 year old, deletion of chromosome arm …

gb (code pays fourni par la source)

549 citations New England Journal of Medicine
Accès ouvert 1997 article OpenAlex

Recurrent chromosomal abnormalities in hepatocellular carcinoma detected by comparative genomic hybridization

Agnès Marchio, Mounira Meddeb, Pascal Pineau, G. Danglot et autres

Chromosomal aberrations associated with hepatocellular carcinoma (HCC) were previously characterized by focusing on changes in particular known genes at the assigned loci, but not those in unidentified genes affected at other loci in whole metaphase chromosomes. In the present study, we examined …

fr (code pays fourni par la source)

0 citations Hepatology Research

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