Search Results - "Stolpe, L"

Mapping a 50-spin-qubit network through correlated sensing by van de Stolpe, G. L., Kwiatkowski, D. P., Bradley, C. E., Randall, J., Abobeih, M. H., Breitweiser, S. A., Bassett, L. C., Markham, M., Twitchen, D. J., Taminiau, T. H.

“…Spins associated to optically accessible solid-state defects have emerged as a versatile platform for exploring quantum simulation, quantum sensing and quantum…”
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Hyperpolarization of nuclear spins: Polarization blockade by Whaites, O. T., Ioannou, C. I., Pingault, B. J., van de Stolpe, G. L., Taminiau, T. H., Monteiro, T. S.

“…Efficient hyperpolarization of nuclear spins via optically active defect centers, such as the nitrogen vacancy (NV) center in diamond, has great potential for…”
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Frequency of four cystic fibrosis mutations in a Swedish population by Dahl, N, Grandell, U, Martinsson, T, Allen, M, Johansson, L, Stolpe, L, Gyllensten, U, Hjelte, L, Kollberg, H, Strandvik, B

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Mapping a 50-spin-qubit network through correlated sensing by van de Stolpe, G. L, Kwiatkowski, D. P, Bradley, C. E, Randall, J, Abobeih, M. H, Breitweiser, S. A, Bassett, L. C, Markham, M, Twitchen, D. J, Taminiau, T. H

“…Nat Commun 15, 2006 (2024) Spins associated to optically accessible solid-state defects have emerged as a versatile platform for exploring quantum simulation,…”
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The Trophoblastic Epithelial Barrier Is Not Infected in Full-Term Placentae of Human Immunodeficiency Virus-Seropositive Mothers Undergoing Antiretroviral Therapy by Tscherning-Casper, C, Papadogiannakis, N, Anvret, M, Stolpe, L, Lindgren, S, Bohlin, A B, Albert, J, Fenyö, E M

“…Article Usage Stats Services JVI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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Check-probe spectroscopy of lifetime-limited emitters in bulk-grown silicon carbide by van de Stolpe, G. L, Feije, L. J, Loenen, S. J. H, Das, A, Timmer, G. M, de Jong, T. W, Taminiau, T. H

“…Solid-state single-photon emitters provide a versatile platform for exploring quantum technologies such as optically connected quantum networks. A key…”
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Hyperpolarisation of nuclear spins: polarisation blockade by Whaites, O. T, Ioannou, C. I, Pingault, B. J, van de Stolpe, G. L, Taminiau, T. H, Monteiro, T. S

“…Efficient hyperpolarisation of nuclear spins via optically active defect centers, such as the nitrogen vacancy (NV) center in diamond, has great potential for…”
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Improved Electron-Nuclear Quantum Gates for Spin Sensing and Control by van Ommen, H. B, van de Stolpe, G. L, Demetriou, N, Beukers, H. K. C, Yun, J, Fortuin, T. R. J, Iuliano, M, Montblanch, A. R. -P, Hanson, R, Taminiau, T. H

“…The ability to sense and control nuclear spins near solid-state defects might enable a range of quantum technologies. Dynamically Decoupled Radio-Frequency…”
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394delTT : a Nordic cystic fibrosis mutation by SCHWARTZ, M, ANVRET, M, CLAUSTRES, M, EIKEN, H. G, EIKLID, K, SCHAEDEL, C, STOLPE, L, TRANEBJÆRG, L

“…In a systematic screening for mutations in the gene encoding the cystic fibrosis transmembrane regulator among Danish cystic fibrosis (CF) patients, we…”
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Moisture streaks and their relation to baggy paper webs by Land, Cecilia, Wahlström, Torbjörn, Stolpe, Lennart

“…Significant and controlled wet streaks were imparted to laboratory-made kraft paper sheets having an initial moisture content of 50 %. The sheets were then…”
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Molecular analysis of 4p deletion associated with Wolf-Hirschhorn syndrome moving the critical segment towards the telomere by ANVRET, M, NORDENSKJÖLD, M, STOLPE, L, JOHANSSON, L, BRÖNDUM-NIELSEN, K

“…We report molecular studies in 2 patients with Wolf-Hirschhorn syndrome, probing genomic DNA from the patients and their parents with markers that have been…”
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A normal male with an inherited deletion of one exon within the DMD gene by NORDENSKJÖLD, M, NICHOLSON, L, EDSTRÖM, L, ANVRET, M, EISERMAN, M, SLATER, C, STOLPE, L

“…We describe two brothers with identical inherited deletions of one single exon within the middle of the DMD gene; one brother has Becker muscular dystrophy…”
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Characterization of the frequency of delta F508 mutation and CF haplotypes in Swedish families by Anvret, M, Stolpe, L, Dahl, N, Eiserman, M, Nordenskjöld, M, Starborg, M, Johansson, L

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