Delayed or absent pi(h(11/2))(2) alignment in Xe-111

Autor: Capponi, L, Smith, JF, Ruotsalainen, P, Scholey, C, Rahkila, P, Bianco, L, Boston, AJ, Boston, HC, Cullen, DM, Derkx, X, Drummond, MC, Grahn, T, Greenlees, PT, Grocutt, L, Hadinia, B, Jakobsson, U, Joss, DT, Julin, R, Juutinen, S, Labiche, M, Leino, M, Leach, KG, McPeake, C, Mulholland, KF, Nieminen, P, O'Donnell, D, Pa, ES ul, Peura, P, Sandzelius, M, Saren, J, Saygi, B, Sorri, J, Stolze, S, Thornthwaite, A, Taylor, MJ, Uusitalo, J

Publikováno v: PHYSICAL REVIEW C

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::d041ed73988bfef55db224e40e24c1c3
http://livrepository.liverpool.ac.uk/3074117/1/Capponi_Xe111_PRC_Accepted.pdf

α decay of the very neutron-deficient isotopes 197–199Fr

Autor: Kalaninova, Z, Andreyev, AN, Antalic, S, Heßberger, FP, Ackermann, D, Andel, B, Drummond, MC, Hofmann, S, Huyse, Mark, Kindler, B, Lane, JFW, Liberati, V, Lommel, B, Page, RD, Rapisarda, Elisa, Sandhu, K, Saro, S, Thornthwaite, A, Van Duppen, Piet

Decay properties of the very neutron-deficient isotopes 197–199Fr were studied at the velocity filter Separator for Heavy Ion reaction Products (SHIP) at GSI in Darmstadt. The isotopes were produced in the 2n–4n evaporation channels of the fusion

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______1131::fba334084484e1696dac3e931404f796
https://lirias.kuleuven.be/handle/123456789/399837

Characterizing the atomic mass surface beyond the proton drip line via alpha-decay measurements of the pi s(1/2) ground state of Re-165 and the pi h(11/2) isomer in Ta-161

Autor: Ertuğral Yamaç, Filiz

The alpha-decay chains originating from the pi s(1/2) and pi h(11/2) states in Au-173 have been investigated following fusion-evaporation reactions. Four generations of alpha radioactivities have been correlated with Au-173(m) leading to a measuremen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______9534::aadbf387f3953a1aa539f9d4969632b0
https://hdl.handle.net/20.500.12619/32072

Population-scale analysis of common and rare genetic variation associated with hearing loss in adults.

Autor: Praveen K; Regeneron Genetics Center, Tarrytown, NY, 10591, USA. kavita.praveen@regeneron.com., Dobbyn L; Regeneron Genetics Center, Tarrytown, NY, 10591, USA., Gurski L; Regeneron Genetics Center, Tarrytown, NY, 10591, USA., Ayer AH; Regeneron Genetics Center, Tarrytown, NY, 10591, USA., Staples J; Regeneron Genetics Center, Tarrytown, NY, 10591, USA., Mishra S; Regeneron Pharmaceuticals, Inc., Tarrytown, NY, 10591, USA., Bai Y; Regeneron Pharmaceuticals, Inc., Tarrytown, NY, 10591, USA., Kaufman A; Regeneron Pharmaceuticals, Inc., Tarrytown, NY, 10591, USA., Moscati A; Regeneron Genetics Center, Tarrytown, NY, 10591, USA., Benner C; Regeneron Genetics Center, Tarrytown, NY, 10591, USA., Chen E; Regeneron Genetics Center, Tarrytown, NY, 10591, USA., Chen S; Regeneron Genetics Center, Tarrytown, NY, 10591, USA., Popov A; Regeneron Genetics Center, Tarrytown, NY, 10591, USA., Smith J; Regeneron Pharmaceuticals, Inc., Tarrytown, NY, 10591, USA., Melander O; Lund University, Department of Clinical Sciences Malmö, Malmö, Sweden.; Skåne University Hospital, Department of Emergency and Internal Medicine, Malmö, Sweden., Jones MB; Regeneron Genetics Center, Tarrytown, NY, 10591, USA., Marchini J; Regeneron Genetics Center, Tarrytown, NY, 10591, USA., Balasubramanian S; Regeneron Genetics Center, Tarrytown, NY, 10591, USA., Zambrowicz B; Regeneron Pharmaceuticals, Inc., Tarrytown, NY, 10591, USA., Drummond MC; Regeneron Pharmaceuticals, Inc., Tarrytown, NY, 10591, USA., Baras A; Regeneron Genetics Center, Tarrytown, NY, 10591, USA., Abecasis GR; Regeneron Genetics Center, Tarrytown, NY, 10591, USA., Ferreira MA; Regeneron Genetics Center, Tarrytown, NY, 10591, USA., Stahl EA; Regeneron Genetics Center, Tarrytown, NY, 10591, USA., Coppola G; Regeneron Genetics Center, Tarrytown, NY, 10591, USA. giovanni.coppola@regeneron.com.

Publikováno v: Communications biology [Commun Biol] 2022 Jun 03; Vol. 5 (1), pp. 540. Date of Electronic Publication: 2022 Jun 03.

Gene Therapy Restores Balance and Auditory Functions in a Mouse Model of Usher Syndrome.

Autor: Isgrig K; Neurotology Program, National Institute on Deafness and Other Communication Disorders (NIDCD), NIH, Bethesda, MD 20892, USA., Shteamer JW; Neurotology Program, National Institute on Deafness and Other Communication Disorders (NIDCD), NIH, Bethesda, MD 20892, USA., Belyantseva IA; Laboratory of Molecular Genetics, NIDCD, NIH, Bethesda, MD 20892, USA., Drummond MC; Laboratory of Molecular Genetics, NIDCD, NIH, Bethesda, MD 20892, USA., Fitzgerald TS; Mouse Auditory Testing Core Facility, NIDCD, NIH, Bethesda, MD 20892, USA., Vijayakumar S; Department of Special Education and Communication Disorders, University of Nebraska, Lincoln, NE 68583, USA., Jones SM; Department of Special Education and Communication Disorders, University of Nebraska, Lincoln, NE 68583, USA., Griffith AJ; Molecular Biology and Genetics Section, NIDCD, NIH, Bethesda, MD 20892, USA., Friedman TB; Laboratory of Molecular Genetics, NIDCD, NIH, Bethesda, MD 20892, USA., Cunningham LL; Section on Sensory Cell Biology, NIDCD, NIH, Bethesda, MD 20892, USA., Chien WW; Neurotology Program, National Institute on Deafness and Other Communication Disorders (NIDCD), NIH, Bethesda, MD 20892, USA; Department of Otolaryngology-Head and Neck Surgery, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA. Electronic address: wade.chien@nih.gov.

Publikováno v: Molecular therapy : the journal of the American Society of Gene Therapy [Mol Ther] 2017 Mar 01; Vol. 25 (3), pp. 780-791. Date of Electronic Publication: 2017 Feb 21.