Recueil. Documents concernant l'histoire de France jusqu'en 1293 (chronique du ménestrel d'Alphonse, comte de Poitiers), prière, commentaire du psaume L, moralité.

Contient : 1 « Ci commence la generacion de tous les rois qui ont esté en France ». Liste enluminée des rois de France jusqu'à Louis IX ; 2 « Ci commence le prologues dou livre des croniques des roys qui ont esté en France ». Premiers mots : « A son tres chier seigneur... conte de Poitiers et de Thoulouse, cil qui est ses serjanz, ses clers et ses obeissanz, qui a ceste oevre translatée en françois... Sire, ce sachiés vous et trestuit cil qui cest escript verront... » ; 3 « Ci commence la generacion des rois de France. Il issirent du lignage Francio qui fu fiex Hector,... » ; 4 Prière ; 5 Commentaire du psaume L ; 6 Moralités ou discours sur les vertus et les vices

Dose optimization approach to fast X-ray microtomography of the lung alveoli.

A basic prerequisite for in vivo X-ray imaging of the lung is the exact determination of radiation dose. Achieving resolutions of the order of micrometres may become particularly challenging owing to increased dose, which in the worst case can be lethal for the imaged animal model. A framework for linking image quality to radiation dose in order to optimize experimental parameters with respect to dose reduction is presented. The approach may find application for current and future in vivo studies to facilitate proper experiment planning and radiation risk assessment on the one hand and exploit imaging capabilities on the other.

X-chromosome tiling path array detection of copy number variants in patients with chromosome X-linked mental retardation

Background: Aproximately 5–10% of cases of mental retardation in males are due to copy number variations (CNV) on the X chromosome. Novel technologies, such as array comparative genomic hybridization (aCGH), may help to uncover cryptic rearrangements in X-linked mental retardation (XLMR) patients. We have constructed an X-chromosome tiling path array using bacterial artificial chromosomes (BACs) and validated it using samples with cytogenetically defined copy number changes. We have studied 54 patients with idiopathic mental retardation and 20 controls subjects. Results: Known genomic aberrations were reliably detected on the array and eight novel submicroscopic imbalances, likely causative for the mental retardation (MR) phenotype, were detected. Putatively pathogenic rearrangements included three deletions and five duplications (ranging between 82 kb to one Mb), all but two affecting genes previously known to be responsible for XLMR. Additionally, we describe different CNV regions with significant different frequencies in XLMR and control subjects (44% vs. 20%). Conclusion:This tiling path array of the human X chromosome has proven successful for the detection and characterization of known rearrangements and novel CNVs in XLMR patients.