Auger-spectroscopy in quantum Hall edge channels: a possible resolution to the missing energy problem

Autor: Krähenmann, T., Fischer, S. G., Röösli, M., Ihn, T., Reichl, C., Wegscheider, W., Ensslin, K., Gefen, Y., Meir, Y.

Publikováno v: Nature Communications 10, Article number: 3915 (2019)

Quantum Hall edge channels offer an efficient and controllable platform to study quantum transport in one dimension. Such channels are a prospective tool for the efficient transfer of quantum information at the nanoscale, and play a vital role in exp

Externí odkaz: http://arxiv.org/abs/1902.10065

Auger-spectroscopy in quantum Hall edge channels: a possible resolution to the missing energy problem

Autor: Kr��henmann, T., Fischer, S. G., R����sli, M., Ihn, T., Reichl, C., Wegscheider, W., Ensslin, K., Gefen, Y., Meir, Y.

Quantum Hall edge channels offer an efficient and controllable platform to study quantum transport in one dimension. Such channels are a prospective tool for the efficient transfer of quantum information at the nanoscale, and play a vital role in exp

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d39b7b3c152fe44008b552ff0bbc386
http://arxiv.org/abs/1902.10065

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Mapping, cloning and genetic characterization of the region containing the Wilson disease gene

Autor: Petrukhin, K., Fischer, S. G., Pirastu, M., Tanzi, R. E., Chernov, I., Devoto, Marcella, Brzustowicz, L. M., Cayanis, E., Vitale, E., Russo, J. J., Matseoane, D., Boukhgalter, B., Wasco, W., Figus, A. L., Loudianos, J., Cao, A., Sternlieb, I., Evgrafov, G., Parano, E., Pavone, L., Warburton, D., Ott, J., Penchaszadeh, G. K., Scheinberg, I. H., Gilliam, T. C.

Publikováno v: Nature genetics
5 (1993): 338–343. doi:10.1038/ng1293-338
info:cnr-pdr/source/autori:Petrukhin K.; Fischer S.G.; Pirastu M.; Tanzi R.E.; Chernov I.; Devoto M.; Brzustowicz L.M.; Cayanis E.; Vitale E.; Russo J.J.; Matseoane D.; Boukhgalter B.; Wasco W.; Figus A.L.; Loudianos J.; Cao A.; Sternlieb I.; Evgrafov O.; Parano E./titolo:Mapping, cloning and genetic characterization of the region containing the Wilson disease gene/doi:10.1038%2Fng1293-338/rivista:Nature genetics (Print)/anno:1993/pagina_da:338/pagina_a:343/intervallo_pagine:338–343/volume:5

Wilson disease (WD) is an autosomal recessive disorder of copper transport which maps to chromosome 13q14.3. In pursuit of the WD gene, we developed yeast artificial chromosome and cosmid contigs, and microsatellite markers which span the WD gene reg

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bb9b3e7f527bd0994117a01c1df6b1e
https://doi.org/10.1038/ng1293-338

Cloning of the breakpoints of a de novo inversion of chromosome 8, inv (8)(p11.2q23.1) in a patient with Ambras syndrome.

Autor: Tadin-Strapps, M., Warburton, D., Baumeister, F. A. M., Fischer, S. G., Yonan, J., Gilliam, T. C., Christiano, A. M.

Publikováno v: Cytogenetic & Genome Research; 2004, Vol. 107 Issue 1/2, p68-76, 9p