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This is the histopathological image of BRAIN tissue sample obtained in Medical University Gdańsk and deposited in ZMDL-GUMED. The sample image was taken using: Pannoramic 250 3DHistech slide scanner (20x magnification) and saved to DICOM format. The detailed information about the patient, sample, and diagnosis are as follows: Patient:Age: 45Clinical description: Brain tumor.Gender: MaleDiagnosis:Classification: ICD-O_3.2Classification code: NEUROEPITHELIOMATOUS NEOPLASMSDiagnosis: Ganglioglioma, NOSResult of the histopathological examination: Fragments of cerebellar cortex and fragments of Ganglioglioma (WHO I), the astrocytic component of the tumor is pilocytic astrocytoma. IHC: GFAP+, synaptophysin+ in some cells, Ki67 low (about 1%). NFP(-), EMA (-), NeuN in part of cells +, CD34 (-), BRAF600V(-).Sample:Material: FFPECollecting method: Surgical specimenTopography: EYE, BRAIN AND OTHER PARTS OF CENTRAL NERVOUS SYSTEMOrgan: BRAINTissue: Temporal lobeType of staining: positive/HEStaining: Not applicableAntibody: Not applicableTechnology:Equipment: Pannoramic 250 3DHistechLens: 20xOrganization:Source: Medical University Gdańsk

This is the histopathological image of BRAIN tissue sample obtained in Medical University Gdańsk and deposited in ZMDL-GUMED. The sample image was taken using: Pannoramic 250 3DHistech slide scanner (20x magnification) and saved to DICOM format. The detailed information about the patient, sample, and diagnosis are as follows: Patient:Age: 50Clinical description: CMV pneumonia. Shock. Encephalitis.Gender: MaleDiagnosis:Classification: ICD-10_10-20Classification code: Chapter I - Certain infectious and parasitic diseasesDiagnosis: Cytomegaloviral disease, unspecifiedResult of the histopathological examination: The brain specimens show markers of encephalitis with glial-microglial nodules, rod-shaped glaze, neuronophagia and segmental dentation of the cerebral cortex. In the basal ganglia, there are small foci of incomplete necrosis, corresponding to healed inflammatory foci. Corpora amylacea periventricular deposits. Atrophy of the brain and cerebellum cortex.Sample:Material: FFPECollecting method: Autopsy specimenTopography: EYE, BRAIN AND OTHER PARTS OF CENTRAL NERVOUS SYSTEMOrgan: BRAINTissue: Brain, NOSType of staining: positive/HEStaining: Not applicableAntibody: Not applicableTechnology:Equipment: Pannoramic 250 3DHistechLens: 20xOrganization:Source: Medical University Gdańsk

F2 OBTAINED IN ASSUMPTION OF SIGL/SIGT= 0. No description provided.

MUON MOMENTUM SPREAD IS OF ORDER OF DELTAP/P=5 PCT. FINAL RESULTS ON PROTON STRUCTURE FUNCTIONS FROM THE EUROPEAN MUON COLLABORATION (EMC). STRUCTURE FUNCTIONS ARE GIVEN IN THE RANGE 0.2 & lt; X & lt; 0.8 AND 3 & lt; Q**2 & lt; 190. GEV**2 , ASSUMING R=SIG(L)/SIG(T)=0. THE RESULTS OF MEASURING R ARE ALSO TABULATED. THE PAPER ALSO CONTAINS TABLES OF THE DIFFERENTIAL CROSS-SECTIONS D2(SIG)/D(X)/D(Q**2) (SEE PARTS=1,2 OF THE RECORD). THE VALUE OF R DETERMINED GLOBALLY OVER THE WHOLE KINEMATIC REGION IS -0.010 +- 0.037 (STAT) +- 0.102 (SYST). Final data on F2 obtained by combining data at all energies and presented in the Table 10, were not encoded. No description provided.

This is the histopathological image of BRAIN tissue sample obtained in Medical University Gdańsk and deposited in ZMDL-GUMED. The sample image was taken using: Pannoramic 250 3DHistech slide scanner (20x magnification) and saved to DICOM format. The detailed information about the patient, sample, and diagnosis are as follows: Patient:Age: 68Clinical description: Suspicion of glioblastoma G4 of the brainGender: MaleDiagnosis:Classification: ICD-O_3.2Classification code: NEOPLASMS, NOSDiagnosis: Neoplasm, malignantResult of the histopathological examination: Glioblastoma multiforme WHO G4Sample:Material: FFPECollecting method: Surgical specimenTopography: EYE, BRAIN AND OTHER PARTS OF CENTRAL NERVOUS SYSTEMOrgan: BRAINTissue: CerebrumType of staining: positive/HEStaining: Hematoxylin & eosinAntibody: Not applicableTechnology:Equipment: Pannoramic 250 3DHistechLens: 20xOrganization:Source: Medical University Gdańsk

An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures. Related Article: J.Leclaire, R.Dagiral, S.Fery-Forgues, Y.Coppel, B.Donnadieu, A.-M.Caminade, J.-P.Majoral|2005|J.Am.Chem.Soc.|127|15762|doi:10.1021/ja054797b

Higher cognition may require the globally coordinated integration of specialized brain regions into functional networks. A collection of structural cortical hubs—referred to as the rich club—has been hypothesized to support task-specific functional integration. In the present paper, we use a whole-cortex model to estimate directed interactions between 68 cortical regions from functional magnetic resonance imaging activity for four different tasks (reflecting different cognitive domains) and resting state. We analyze the state-dependent input and output effective connectivity (EC) of the structural rich club and relate these to whole-cortex dynamics and network reconfigurations. We find that the cortical rich club exhibits an increase in outgoing EC during task performance as compared with rest while incoming connectivity remains constant. Increased outgoing connectivity targets a sparse set of peripheral regions with specific regions strongly overlapping between tasks. At the same time, community detection analyses reveal massive reorganizations of interactions among peripheral regions, including those serving as target of increased rich club output. This suggests that while peripheral regions may play a role in several tasks, their concrete interplay might nonetheless be task-specific. Furthermore, we observe that whole-cortex dynamics are faster during task as compared with rest. The decoupling effects usually accompanying faster dynamics appear to be counteracted by the increased rich club outgoing EC. Together our findings speak to a gating mechanism of the rich club that supports fast-paced information exchange among relevant peripheral regions in a task-specific and goal-directed fashion, while constantly listening to the whole network. DATA_TASK_3DMOV_HP_CSF_WDBriefly, data comes from five functional runs consisting of a resting-state measurement (eyes closed), four individual task measurements including a visual n-back (n=2) task (Kirchner, 1958), the Eriksen flanker task (Eriksen & Eriksen, 1974), a mental rotation task (Shepard & Metzler, 1971), and a verbal odd-man-out task (Flowers & Robertson, 1985). All runs comprise 192 data points with tasks being continuously performed during this period. For the n-back and flanker task, stimuli were presented at a rate of 0.5 Hz; for the mental rotation and odd-man out tasks they were presented at a rate of 0.25 Hz. Task sequence was counterbalanced across participants with the exception that the resting state functional run was always acquired first to prevent carry-over effects (Grigg & Grady, 2010). The data were acquired using a 3 Tesla Siemens Prisma Fit (upgraded Tim Trio) scanner and a 64-channel head coil. Initial preprocessing was performed using BrainVoyager QX (v2.6; Brain Innovation, Maastricht, the Netherlands). This includes slice scan time correction, 3D-motion correction, high-pass filtering with a frequency cutoff of .01 Hz, and registration of functional and anatomical images. Subsequently, using MATLAB (2013a, The MathWorks,Natick, MA), signals were cleaned by performing wavelet despiking (Patel & Bullmore, 2015) and regressing out a global noise signal given by the first principal component of signals observed within the cerebrospinal fluid of the ventricles. Next, voxels were uniquely assigned to one of the 68 cortical ROIs specified by the DK atlas and an average BOLD time-series was computed for each region as the mean time-series over all voxels of that region.

Strong coupling constant ALPHA_S(M_Z) determined from fits of different event variables. The systematic errors represents theoretical uncertaintie The last row is a fit to the combined T_c, T_z and Jet Mass variables with possible correlations between them NOT taken into account. DESY-HERA. Study of Event Shape Variables in Deep Inelastic ep scattering in the Breit frame in the Q range from 7 to 100 GeV and Y range from 0.05 to 0.8.Data come from the 1994 low Q (7-10 GeV) e+ sample (2.9 pb-1) and the 1994-1996 high Q (14-100 GeV) e+- sample (11.7 pb-1).

CERN-HOLLAND-UK ISR COLLABORATION FOR PI+/- AND K+/- PRODUCTION IN THE REGION 0.41<X<0.95 AND 0.35<PT<1.45. THE TOTAL SYSTEMATIC ERROR,INCLUDING CONTRIBUTIONS FROM ERRORS IN THE LUMINOSITY (3 PCT),THE DECAY AND ABSORPTION CORRECTION (3 PCT) AND THE MONTE -CARLO CALCULATIONS (3 PCT) WAS ESTIMATED TO BE LESS THAN 6 PCT. SQRT(S)=45.0 M**2 DISTBNS AT FIXED T IN THIS RECORD. No description provided.

DESY-HERA. Measurement of the structure function F2(NAME=D3) in the deep inelastic scattering process e p --& gt; e X Y where X and Y are final hadronic statesseparated by the largest rapidity gap interval. The system Y is that which has rapidity closest to that of the incident proton and is selected to have mass & lt; 1.6 GeV. It is coded here as P. The variable X(NAME=POMERON) is defined as q.(P-PY)/q.P where q, P and PY are the 4-momenta respectively of the exchanged virtual boson, the incident proton and the subsystem Y. BETA is defined as X/X(NAME=POMERON). The data come from the 1994 running period corresponding to 1.96 pb-1 integrated luminosity. No description provided.