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Huib N. Caron

Researcher at University of Amsterdam

Publications -  74
Citations -  10178

Huib N. Caron is an academic researcher from University of Amsterdam. The author has contributed to research in topics: Neuroblastoma & Gene. The author has an hindex of 41, co-authored 72 publications receiving 9388 citations. Previous affiliations of Huib N. Caron include Boston Children's Hospital.

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N-myc enhances the expression of a large set of genes functioning in ribosome biogenesis and protein synthesis.

TL;DR: In this paper, the authors applied serial analysis of gene expression (SAGE) to identify targets of N-myc in neuroblastoma cells and found that the large majority of the ribosomal proteins were induced, as well as genes controlling rRNA maturation.
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Relapsed neuroblastomas show frequent RAS-MAPK pathway mutations

TL;DR: It is shown that RAS-MAPK pathway mutations may function as a biomarker for new therapeutic approaches to refractory disease and provide a rationale for genetic characterization of relapse neuroblastomas.
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Clinical heart failure in a cohort of children treated with anthracyclines: a long-term follow-up study.

TL;DR: One in every 10 children treated with a cumulative anthracycline dose of 300 mg/m2 or more will eventually develop A-CHF, a extremely high risk and it reinforces the need of re-evaluating the cumulative AnthracyCline dose used in different treatment protocols.
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NF1 Is a Tumor Suppressor in Neuroblastoma that Determines Retinoic Acid Response and Disease Outcome

TL;DR: Using a large-scale RNAi genetic screen, crosstalk between the tumor suppressor NF1 and retinoic acid-induced differentiation in neuroblastoma is identified and inhibition of MEK signaling downstream of NF1 restores responsiveness to RA, suggesting a therapeutic strategy to overcome RA resistance in NF1-deficient neuroblastomas.
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Allelic loss of chromosome 1 and additional chromosome 17 material are both unfavourable prognostic markers in neuroblastoma

TL;DR: LOH 1p was shown to be the most significant predictor of a poor outcome (P < 0.00001), independent of age and stage, and is also of prognostic value in those cases without N-myc amplification, indicating a stronger prognosticvalue for LOH 1 p.