Search Results - "Wolf, N."

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    Masses of exotic calcium isotopes pin down nuclear forces by Wienholtz, F., Beck, D., Blaum, K., Borgmann, Ch, Breitenfeldt, M., Cakirli, R. B., George, S., Herfurth, F., Holt, J. D., Kowalska, M., Kreim, S., Lunney, D., Manea, V., Menéndez, J., Neidherr, D., Rosenbusch, M., Schweikhard, L., Schwenk, A., Simonis, J., Stanja, J., Wolf, R. N., Zuber, K.

    Published in Nature (London) (20-06-2013)
    “…The masses of the exotic calcium isotopes 53 Ca and 54 Ca measured by a multi-reflection time-of-flight method confirm predictions of calculations including…”
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    Revisiting default mode network function in major depression: evidence for disrupted subsystem connectivity by Sambataro, F, Wolf, N D, Pennuto, M, Vasic, N, Wolf, R C

    Published in Psychological medicine (01-07-2014)
    “…Major depressive disorder (MDD) is characterized by alterations in brain function that are identifiable also during the brain's 'resting state'. One functional…”
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    Effects of short and prolonged transcutaneous vagus nerve stimulation on heart rate variability in healthy subjects by De Couck, M, Cserjesi, R, Caers, R, Zijlstra, W.P, Widjaja, D, Wolf, N, Luminet, O, Ellrich, J, Gidron, Y

    Published in Autonomic neuroscience (01-03-2017)
    “…Abstract The vagus nerve is strategically located in the body, and has multiple homeostatic and health-promoting effects. Low vagal activity predicts onset and…”
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    Riboflavin transporter deficiency, the search for the undiagnosed: a retrospective data mining study by Jaeger, B, Hoytema van Konijnenburg, E, Groenveld, M. A, Langeveld, M, Wolf, N. I, Bosch, A. M

    Published in Orphanet journal of rare diseases (01-11-2024)
    “…Abstract Background Riboflavin transporter deficiency (RTD) is an inborn error of riboflavin transport causing progressive neurological symptoms if left…”
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    Direct Exoplanet Detection using Convolutional Image Reconstruction (ConStruct): A New Algorithm for Post-processing High-contrast Images by Wolf, Trevor N., Jones, Brandon A., Bowler, Brendan P.

    Published in The Astronomical journal (01-03-2024)
    “…Abstract We present a novel machine-learning approach for detecting faint point sources in high-contrast adaptive optics (AO) imaging data sets. The most…”
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    Helicobacter pylori versus the host: remodeling of the bacterial outer membrane is required for survival in the gastric mucosa by Cullen, Thomas W, Giles, David K, Wolf, Lindsey N, Ecobichon, Chantal, Boneca, Ivo G, Trent, M Stephen

    Published in PLoS pathogens (01-12-2011)
    “…Modification of bacterial surface structures, such as the lipid A portion of lipopolysaccharide (LPS), is used by many pathogenic bacteria to help evade the…”
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    Imaging Patterns Characterizing Mitochondrial Leukodystrophies by Roosendaal, S D, van de Brug, T, Alves, C A P F, Blaser, S, Vanderver, A, Wolf, N I, van der Knaap, M S

    Published in American journal of neuroradiology : AJNR (01-07-2021)
    “…Achieving a specific diagnosis in leukodystrophies is often difficult due to clinical and genetic heterogeneity. Mitochondrial defects cause 5%-10% of…”
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    Efficacy of MitoTracker Green™ and CMXrosamine to measure changes in mitochondrial membrane potentials in living cells and tissues by Pendergrass, W., Wolf, N., Poot, M.

    Published in Cytometry. Part A (01-10-2004)
    “…Background Chloromethyl‐X‐rosamine (CMXRos) and MitoTracker Green (MTG) have proved to be useful dyes with which to measure mitochondrial function. CMXRos is a…”
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    Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement by Harting, I, Karch, S, Moog, U, Seitz, A, Pouwels, P J W, Wolf, N I

    Published in American journal of neuroradiology : AJNR (01-05-2019)
    “…Oculodentodigital dysplasia, a rare genetic disorder caused by mutations in the gene encoding gap junction protein 1, classically presents with typical facial…”
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    Degeneration alters the biomechanical properties and structural composition of lateral human menisci by Warnecke, D., Balko, J., Haas, J., Bieger, R., Leucht, F., Wolf, N., Schild, N.B., Stein, S.E.C., Seitz, A.M., Ignatius, A., Reichel, H., Mizaikoff, B., Dürselen, L.

    Published in Osteoarthritis and cartilage (01-11-2020)
    “…Because the literature relating to the influence of degeneration on the viscoelasticity and tissue composition of human lateral menisci remains contradictory…”
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    Suppression of methylation-mediated transcriptional gene silencing by βC1-SAHH protein interaction during geminivirus-betasatellite infection by Yang, Xiuling, Xie, Yan, Raja, Priya, Li, Sizhun, Wolf, Jamie N, Shen, Qingtang, Bisaro, David M, Zhou, Xueping

    Published in PLoS pathogens (01-10-2011)
    “…DNA methylation is a fundamental epigenetic modification that regulates gene expression and represses endogenous transposons and invading DNA viruses. As a…”
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    Data-driven Dynamic Motion Planning for Practical FES-Controlled Reaching Motions in Spinal Cord Injury by Wolf, Derek N., Van den Bogert, Antonie J., Schearer, Eric M.

    “…Functional electrical stimulation (FES) is a promising technology for restoring reaching motions to individuals with upper-limb paralysis caused by a spinal…”
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    Geminivirus AL2 and L2 Proteins Suppress Transcriptional Gene Silencing and Cause Genome-Wide Reductions in Cytosine Methylation by BUCHMANN, R. Cody, ASAD, Shaheen, WOLF, Jamie N, MOHANNATH, Gireesha, BISARO, David M

    Published in Journal of Virology (15-05-2009)
    “…Article Usage Stats Services JVI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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    Arsenic-Doped CdSeTe Solar Cells Achieve World Record 22.3% Efficiency by Mallick, R., Li, X., Reich, C., Shan, X., Zhang, W., Nagle, T., Bok, L., Bicakci, E., Rosenblatt, N., Modi, D., Farshchi, R., Lee, C., Hack, J., Grover, S., Wolf, N., Metzger, W.K., Lu, D., Xiong, G.

    Published in IEEE journal of photovoltaics (01-07-2023)
    “…For more than three decades, Cu has been critical to dope CdSeTe solar cells, form effective contacts, and maximize efficiency. At the same time, Cu defect…”
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    A novel mutation causing DEND syndrome : A treatable channelopathy of pancreas and brain by SHIMOMURA, K, HORSTER, F, DE WET, H, FLANAGAN, S. E, ELLARD, S, HATTERSLEY, A. T, WOLF, N. I, ASHCROFT, F, EBINGER, F

    Published in Neurology (25-09-2007)
    “…Activating mutations in the human KCNJ11 gene, encoding the pore-forming subunit (Kir6.2) of the ATP-sensitive potassium (K(ATP)) channel, are one cause of…”
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