99 research outputs found

    Potentiation of Suntanning Through Ingestion of 8-Methoxypsoralen1

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    Transplantation of Human Melanocytes

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    Recent advances in the culturing of pigment cells from human beings have made it possible to begin the transplantation of autologous melanocytes into areas of skin that are hypopigmented. In a patient with piebaldism we were able to take pigment cells from a shave biopsy of the normally pigmented skin of the back, expand the cells in culture, and return them to an area devoid of pigment cells and get a perfect take. To grow the cells in culture we used 12-O-tetradecanoyl-phorbol-13-acetate (TPA) as well as cholera toxin and isobutylmethyl xanthine. At this time, one can substitute basic fibroblast growth factor for TPA. The procedure of using autologous pigment cell cultures opens the door for further advances in the treatment of patients who do not have melanocytes in certain areas of the skin, as seen in patients with vitiligo or piebaldism, or as a consequence of severe mechanical or thermal trauma

    A Rapid Histochemical Test for Mammalian Tyrosinase

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    A simple, rapid separation of epidermis from dermis was achieved following incubation of human of guinea-pig skin in one molar sodium bromide at 37°C for 30 min. The resulting epidermal sheets incubated at 37°C in 0.1 M phosphate buffer (pH 6.8) for 15 to 120 minutes with 5 × 10-3 M dopa or for 120 to 240 minutes with a mixture of 5 × 10-3 M tyrosine and 5 × 10-3 M ascorbic acid gave good dopa-tyrosinase and tyrosine-tyrosinase reactions. Melanocytes were readily visualized because new melanin formed within the cytoplasm

    Measurement of W± and Z-boson production cross sections in pp collisions at √s=13 TeV with the ATLAS detector

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    See paper for full list of authors - 17 pages plus author list + cover pages (34 pages total), 5 figures, 3 tables, submitted to Phys. Lett. B, All figures including auxiliary figures are available at https://atlas.web.cern.ch/Atlas/GROUPS/PHYSICS/PAPERS/STDM-2015-03/International audienceMeasurements of the W±±νW^{\pm} \rightarrow \ell^{\pm} \nu and Z+Z \rightarrow \ell^+ \ell^- production cross sections (where ±=e±,μ±\ell^{\pm}=e^{\pm},\mu^{\pm}) in proton-proton collisions at s=13\sqrt{s}=13 TeV are presented using data recorded by the ATLAS experiment at the Large Hadron Collider, corresponding to a total integrated luminosity of 81 pb1^{-1}. The total inclusive W±W^{\pm}-boson production cross sections times the single-lepton-flavour branching ratios are σW+tot=11.78±0.02(stat)±0.32(sys)±0.59(lumi)\sigma_{W^+}^{tot}= 11.78 \pm 0.02 (stat) \pm 0.32 (sys) \pm 0.59 (lumi) nb and σWtot=8.75±0.02(stat)±0.24(sys)±0.44(lumi)\sigma_{W^-}^{tot} = 8.75 \pm 0.02 (stat) \pm 0.24 (sys) \pm 0.44 (lumi) nb for W+W^+ and WW^-, respectively. The total inclusive ZZ-boson production cross section times leptonic branching ratio, within the invariant mass window 66<m<11666 < m_{\ell\ell} < 116 GeV, is σZtot=1.97±0.01(stat)±0.04(sys)±0.10(lumi)\sigma_{Z}^{tot} = 1.97 \pm 0.01 (stat) \pm 0.04 (sys) \pm 0.10 (lumi) nb. The W+W^+, WW^-, and ZZ-boson production cross sections and cross-section ratios within a fiducial region defined by the detector acceptance are also measured. The cross-section ratios benefit from significant cancellation of experimental uncertainties, resulting in σW+fid/σWfid=1.295±0.003(stat)±0.010(sys)\sigma_{W^+}^{fid}/\sigma_{W^-}^{fid} = 1.295 \pm 0.003 (stat) \pm 0.010 (sys) and σW±fid/σZfid=10.31±0.04(stat)±0.20(sys)\sigma_{W^{\pm}}^{fid}/\sigma_{Z}^{fid} = 10.31 \pm 0.04 (stat) \pm 0.20 (sys). Theoretical predictions, based on calculations accurate to next-to-next-to-leading order for quantum chromodynamics and next-to-leading order for electroweak processes and which employ different parton distribution function sets, are compared to these measurements

    The genetic architecture of the human cerebral cortex

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    The cerebral cortex underlies our complex cognitive capabilities, yet little is known about the specific genetic loci that influence human cortical structure. To identify genetic variants that affect cortical structure, we conducted a genome-wide association meta-analysis of brain magnetic resonance imaging data from 51,665 individuals. We analyzed the surface area and average thickness of the whole cortex and 34 regions with known functional specializations. We identified 199 significant loci and found significant enrichment for loci influencing total surface area within regulatory elements that are active during prenatal cortical development, supporting the radial unit hypothesis. Loci that affect regional surface area cluster near genes in Wnt signaling pathways, which influence progenitor expansion and areal identity. Variation in cortical structure is genetically correlated with cognitive function, Parkinson's disease, insomnia, depression, neuroticism, and attention deficit hyperactivity disorder

    Multiplatform Analysis of 12 Cancer Types Reveals Molecular Classification within and across Tissues of Origin

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    Recent genomic analyses of pathologically-defined tumor types identify “within-a-tissue” disease subtypes. However, the extent to which genomic signatures are shared across tissues is still unclear. We performed an integrative analysis using five genome-wide platforms and one proteomic platform on 3,527 specimens from 12 cancer types, revealing a unified classification into 11 major subtypes. Five subtypes were nearly identical to their tissue-of-origin counterparts, but several distinct cancer types were found to converge into common subtypes. Lung squamous, head & neck, and a subset of bladder cancers coalesced into one subtype typified by TP53 alterations, TP63 amplifications, and high expression of immune and proliferation pathway genes. Of note, bladder cancers split into three pan-cancer subtypes. The multi-platform classification, while correlated with tissue-of-origin, provides independent information for predicting clinical outcomes. All datasets are available for data-mining from a unified resource to support further biological discoveries and insights into novel therapeutic strategies
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