Surgical implications of the anatomic situation of the mandibular canal for mandibular osteotomies: a cone beam computed tomographic study.

Purpose: In bilateral sagittal split osteotomy (BSSO), the risk of lesion of the inferior alveolar nerve (IAN) is important. The aim of this study was to investigate the situation of the IAN in the area of the BSSO in preoperative 158 CBCT.

Methods: The situation of the mandibular canal (MC) has been studied in six coronal sections (one section each 4 mm) from the proximal root of the second mandibular molar.

Prevalence of Dentinogenesis Imperfecta in a French Population.

Background: Dentinogenesis imperfecta is a genetic disorder of the dentin occurring during the tooth development. It leads to many structural changes that can be identified clinically (brownish colored teeth, cracked enamel) and radiologically (globular crown, cervical constriction, short roots, and obliterated pulp chamber and/or root canals). The aim of this study was to determine by panoramic radiographs assessment the incidence of dentinogenesis imperfecta in a group of patients attending a specialized maxillofacial imaging center in Paris, France.

Discovery of 1-(4-(5-(5-amino-6-(5-tert-butyl-1,3,4-oxadiazol-2-yl)pyrazin-2-yl)-1-ethyl-1,2,4-triazol-3-yl)piperidin-1-yl)-3-hydroxypropan-1-one (AZD8835): A potent and selective inhibitor of PI3Kα and PI3Kδ for the treatment of cancers.

Starting from potent inhibitors of PI3Kα having poor general kinase selectivity (e.g., 1 and 2), optimisation of this series led to the identification of 25, a potent inhibitor of PI3Kα (wild type, E545K and H1047R mutations) and PI3Kδ, selective versus PI3Kβ and PI3Kγ, with excellent general kinase selectivity.

[Cone Beam computerized tomography and implants].

The authors, both working as radiologist in private practice, have initiated the Cone Beam technique as soon as 1999 and report their own experience. Cone Beam Computerized Tomography (CBCT) is dedicated to hard tissues imaging thus specifically adapted to oral implantology and maxillofacial surgery. It has the advantage to deliver low dose radiation, compared to other techniques.

Discovery of new quinoline ether inhibitors with high affinity and selectivity for PDGFR tyrosine kinases.

A new series of quinoline ether inhibitors, which potently and selectively inhibit PDGFR tyrosine kinases, is described in this Letter. Compounds 23 and 33 are selective, low nanomolar inhibitors of PDGFRα and β, display good pharmacokinetics in rat and dog and are active in vivo at low doses when given orally twice daily. Further evaluation of these compounds is warranted.

Discovery of AZD2932, a new Quinazoline Ether Inhibitor with high affinity for VEGFR-2 and PDGFR tyrosine kinases.

A new series of Quinazoline Ether Inhibitor which potently inhibits VEGFR-2 and PDGFR tyrosine kinases is described here. In vitro, pharmacokinetics and in vivo evaluations led to the selection of AZD2932.

[Diagnostic means using oral and maxillofacial cone beam computed tomography: results].

Every imaging test is justified by clinical facts and optimized to reduce the X-rays dose delivered to patients. If results from orthopantomogram are inadequate, a cross-sectional tomographic technique is indicated. Today, cone beam computed tomography yields images comparable to CT scan or even better.

[Imagery and orthodontics: trends, present and future].

From the first dental image in 1895 and the first image of the head in 1896 by Otto Walkhoff to 3D modern cephalic assessment there has been a continuous evolution in imaging techniques. Digital cephalic volume data processing allows 2D and 3D reformations in accordance with morphologic, topographic and biodimensional anatomic needs. In France, Jacques Treil demonstrated its application in cephalometry through his CT scan research.

Synthesis and SAR of 1-acetanilide-4-aminopyrazole-substituted quinazolines: selective inhibitors of Aurora B kinase with potent anti-tumor activity.

A new class of 1-acetanilide-4-aminopyrazole-substituted quinazoline Aurora kinase inhibitors has been discovered possessing highly potent cellular activity. Continuous infusion into athymic mice bearing SW620 tumors of the soluble phosphate derivative 2 led to dose-proportional exposure of the des-phosphate compound 8 with a high-unbound fraction. The combination of potent cell activity and high free-drug exposure led to pharmacodynamic changes in the tumor at low doses, indicative of Aurora B-kinase inhibition and a reduction in tumor volume.

Investigation of NMR limits of detection for implantable microcoils.

Although NMR has the ability to investigate biological systems non-destructively, its low sensitivity primarily has hampered their investigation compared to other analytical techniques. Therefore, optimi zing radio frequency (RF) coils to improve sensitivity do offer benefits in MR spectroscopy (MRS). Sensitivity may be improved for mass- and volume-limited samples if the size of the detection RF coils matches the sample size.

PCB/polymer based micro-fluidic system for NMR spectroscopy for nanoliters sample volume.

In this work, we report on the realization of an innovating micro system for NMR spectroscopy on small sample volume (30-100 nL). We propose a micro system based on Printed Circuit Board (PCB) technology for the NMR probe associated to a micro fluidic system made with polymer (COC). The comparison of several samples during the same NMR experiments could provide more precise information.

NMR planar micro coils for micro spectroscopy: design and characterisation.

The goal of this study is to determine the concentration sensitivity and the limit of detection of a SNMR receiver planar micro coil with ellipsoidal geometry 1000x500 microm, fabricated using an electroplating technique and used as SNMR receiver coil at 200 MHz. The maximum signal intensity on the NMR images and simulation of RF field distribution allows defining an active volume of 0.8 microL.

Discovery, synthesis, and in vivo activity of a new class of pyrazoloquinazolines as selective inhibitors of aurora B kinase.

The Aurora kinases have been the subject of considerable interest as targets for the development of new anticancer agents. While evidence suggests inhibition of Aurora B kinase gives rise to the more pronounced antiproliferative phenotype, the most clinically advanced agents reported to date typically inhibit both Aurora A and B. We have discovered a series of pyrazoloquinazolines, some of which show greater than 1000-fold selectivity for Aurora B over Aurora A kinase activity, in recombinant enzyme assays.

Discovery of novel and potent thiazoloquinazolines as selective Aurora A and B kinase inhibitors.

The synthesis of a novel series of quinazolines substituted at C4 by five-membered ring aminoheterocycles is reported. Their in vitro structure-activity relationships versus Aurora A and B serine-threonine kinases is discussed. Our results demonstrate that quinazolines with a substituted aminothiazole at C4 possess potent Aurora A and B inhibitory activity and excellent selectivity against a panel of various serine-threonine and tyrosine kinases, as exemplified by compound 46.