33 research outputs found

    Central-to-peripheral nuclear modification factors in Pb-Pb collisions at sqrt{s_NN} = 17.3 GeV

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    We present central-to-peripheral nuclear modification factors, R_CP, for the p_T distributions of K^0_S, Lambda, Anti-Lambda, and negatively charged particles, measured at central rapidity in Pb-Pb collisions at top SPS energy. The data cover the 55% most central fraction of the inelastic cross section. The K^0_S and Lambda R_CP(p_T) are similar in shape to those measured at sqrt{s_NN} = 200 GeV at RHIC, though they are larger in absolute value. We have compared our K^0_S R_CP data to a theoretical calculation. The prediction overestimates the data at p_T \approx 3-4 GeV/c, unless sizeable parton energy loss is included in the calculation.Comment: 13 pages, 5 figures, submitted to Physics Letters

    Retinal Structure and Function in Achromatopsia : Implications for Gene Therapy

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    Purpose: To characterize retinal structure and function in achromatopsia (ACHM) in preparation for clinical trials of gene therapy. Design: Cross-sectional study. Participants: Forty subjects with ACHM. Methods: All subjects underwent spectral domain optical coherence tomography (SD-OCT), microperimetry, and molecular genetic testing. Foveal structure on SD-OCT was graded into 5 distinct categories: (1) continuous inner segment ellipsoid (ISe), (2) ISe disruption, (3) ISe absence, (4) presence of a hyporeflective zone (HRZ), and (5) outer retinal atrophy including retinal pigment epithelial loss. Foveal and outer nuclear layer (ONL) thickness was measured and presence of hypoplasia determined. Main Outcome Measures: Photoreceptor appearance on SD-OCT imaging, foveal and ONL thickness, presence of foveal hypoplasia, retinal sensitivity and fixation stability, and association of these parameters with age and genotype. Results: Forty subjects with a mean age of 24.9 years (range, 6e52 years) were included. Disease-causing variants were found in CNGA3 (n [ 18), CNGB3 (n ¼ 15), GNAT2 (n ¼ 4), and PDE6C (n ¼ 1). No variants were found in 2 individuals. In all, 22.5% of subjects had a continuous ISe layer at the fovea, 27.5% had ISe disruption, 20% had an absent ISe layer, 22.5% had an HRZ, and 7.5% had outer retinal atrophy. No significant differences in age (P ¼ 0.77), mean retinal sensitivity (P ¼ 0.21), or fixation stability (P ¼ 0.34) across the 5 SD-OCT categories were evident. No correlation was found between age and foveal thickness (P ¼ 0.84) or between age and foveal ONL thickness (P ¼ 0.12). Conclusions: The lack of a clear association of disruption of retinal structure or function in ACHM with age suggests that the window of opportunity for intervention by gene therapy is wider in some individuals than previously indicated. Therefore, the potential benefit for a given subject is likely to be better predicted by specific measurement of photoreceptor structure rather than simply by age. The ability to directly assess cone photoreceptor preservation with SD-OCT and/or adaptive optics imaging is likely to prove invaluable in selecting subjects for future trials and measuring the trials’ impact
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