Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Owen, C. I."'
Autor:
Howes, L. M., Casey, A. R., Asplund, M., Keller, S. C., Yong, D., Nataf, D. M., Poleski, R., Lind, K., Kobayashi, C., Owen, C. I., Ness, M., Bessell, M. S., Da Costa, G. S., Schmidt, B. P., Tisserand, P., Udalski, A., Szymański, M. K., Soszyński, I., Pietrzyński, G., Ulaczyk, K., Wyrzykowski, Ł., Pietrukowicz, P., Skowron, J., Kozłowski, S., Mróz, P.
The first stars are predicted to have formed within 200 million years after the Big Bang, initiating the cosmic dawn. A true first star has not yet been discovered, although stars with tiny amounts of elements heavier than helium ('metals') have been
Externí odkaz:
http://arxiv.org/abs/1511.03930
Publikováno v:
ApJ 818, 115 (2016)
Most modern astrophysical datasets are multi-dimensional; a characteristic that can nowadays generally be conserved and exploited scientifically during the data reduction/simulation and analysis cascades. Yet, the same multi-dimensional datasets are
Externí odkaz:
http://arxiv.org/abs/1510.02796
Autor:
Howes, L., Asplund, M., Casey, A. R., Keller, S. C., Yong, D., Gilmore, G., Lind, K., Worley, C., Bessell, M. S., Casagrande, L., Marino, A. F., Nataf, D. M., Owen, C. I., Da Costa, G. S., Schmidt, B. P., Tisserand, P., Randich, S., Feltzing, S., Vallenari, A., Prieto, C. Allende, Bensby, T., Flaccomio, E., Korn, A. J., Pancino, E., Recio-Blanco, A., Smiljanic, R., Bergemann, M., Costado, M. T., Damiani, F., Heiter, U., Hill, V., Hourihane, A., Jofré, P., Lardo, C., de Laverny, P., Magrini, L., Maiorca, E., Masseron, T., Morbidelli, L., Sacco, G. G., Minniti, D., Zoccali, M.
We present the first results of the EMBLA survey (Extremely Metal-poor BuLge stars with AAOmega), aimed at finding metal-poor stars in the Milky Way bulge, where the oldest stars should now preferentially reside. EMBLA utilises SkyMapper photometry t
Externí odkaz:
http://arxiv.org/abs/1409.7952
Autor:
Howes, L. M., Asplund, M., Casey, A. R., Keller, S. C., Yong, D., Gilmore, G., Lind, K., Worley, C., Bessell, M. S., Casagrande, L., Marino, A. F., Nataf, D. M., Owen, C. I., Da Costa, G. S., Schmidt, B. P., Tisserand, P., Randich, S., Feltzing, S., Vallenari, A., Allende Prieto, C.
Publikováno v:
Monthly Notices of the Royal Astronomical Society; Dec2014, Vol. 445 Issue 4, p4241-4246, 6p
Autor:
Nan, Haitian1 (AUTHOR), Chu, Min1 (AUTHOR), Zhang, Jing1 (AUTHOR), Jiang, Deming1 (AUTHOR), Wang, Yihao1 (AUTHOR), Wu, Liyong1,2 (AUTHOR) wmywly@hotmail.com
Publikováno v:
Molecular Genetics & Genomic Medicine. Mar2024, Vol. 12 Issue 3, p1-11. 11p.
Publikováno v:
Journal of Neuropathology & Experimental Neurology; Jul1945, Vol. 4 Issue 3, p291-294, 4p
Autor:
Lan, Fangfei1 (AUTHOR), Young, Michael1 (AUTHOR), Anderson, Lauren2 (AUTHOR), Ynnerman, Anders3 (AUTHOR), Bock, Alexander1,3 (AUTHOR), Borkin, Michelle A.4 (AUTHOR), Forbes, Angus G.5 (AUTHOR), Kollmeier, Juna A.2 (AUTHOR), Wang, Bei1 (AUTHOR)
Publikováno v:
Computer Graphics Forum. Jun2021, Vol. 40 Issue 3, p635-663. 29p. 11 Color Photographs, 2 Diagrams, 5 Charts.
Autor:
Blanc A; Service de génétique clinique, CHRU de Nancy, Nancy, France., Bonnet C; Laboratoire de génétique médicale, CHRU Nancy, Nancy, France.; Université de Lorraine, INSERM UMR_S1256, NGERE, Nancy, France., Wandzel M; Laboratoire de génétique médicale, CHRU Nancy, Nancy, France., Roth V; Laboratoire de génétique médicale, CHRU Nancy, Nancy, France., Duffourd Y; Unité Fonctionnelle Innovation en Diagnostic génomique des maladies rares, CHU Dijon Bourgogne, Dijon, France.; Université de Bourgogne, INSERM UMR_1231 GAD, Dijon, France., Safraou H; Unité Fonctionnelle Innovation en Diagnostic génomique des maladies rares, CHU Dijon Bourgogne, Dijon, France.; Université de Bourgogne, INSERM UMR_1231 GAD, Dijon, France., Leheup B; Université de Lorraine, INSERM UMR_S1256, NGERE, Nancy, France., Muller F; Service de Chirurgie orthopédique infantile, CHRU Nancy, Nancy, France., D Colne J; Service d'Ophtalmologie, CHRU Nancy, Nancy, France., Feillet F; Université de Lorraine, INSERM UMR_S1256, NGERE, Nancy, France.; Centre de Référence des maladies métaboliques, CHRU Nancy, Nancy, France., Schmitt E; Service de Radiologie, CHRU Nancy, Nancy, France., Castro M; Mendelics Genomic Analysis, São Paulo, Brazil.; Medical Genetics Unit, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo HCFMUSP, São Paulo, Brazil., Savatt J; Autism & Developmental Medicine Institute, Danville, Pennsylvania, USA., Burcheri A; Département de Biopathologie - Anatomie et Cytologie Pathologiques, CHRU de Nancy, Nancy, France., Nemos C; Laboratoire de fœtopathologie et de placentologie, CHRU Nancy, Nancy, France.; Département d'histologie, embryologie et cytogénétique de la faculté de médecine, Université de Lorraine, Nancy, France.; Département de Génie Biologique Santé de l'IUT Nancy-Brabois, Université de Lorraine, Nancy, France.; Université de Lorraine Biofonctionnalités et Risques Neurotoxiques (Calbinotox), Nancy, France., Philippe C; Unité Fonctionnelle Innovation en Diagnostic génomique des maladies rares, CHU Dijon Bourgogne, Dijon, France.; Université de Bourgogne, INSERM UMR_1231 GAD, Dijon, France., Lambert L; Service de génétique clinique, CHRU de Nancy, Nancy, France.; Université de Lorraine, INSERM UMR_S1256, NGERE, Nancy, France.
Publikováno v:
American journal of medical genetics. Part A [Am J Med Genet A] 2024 Sep; Vol. 194 (9), pp. e63642. Date of Electronic Publication: 2024 May 06.
Autor:
Kurtz-Nelson, Evangeline C.1, Beighley, Jennifer S.1, Hudac, Caitlin M.2, Gerdts, Jennifer1, Wallace, Arianne S.1, Hoekzema, Kendra3, Eichler, Evan E.3,4, Bernier, Raphael A.1 rab2@uw.edu
Publikováno v:
Children's Health Care. Oct-Dec2020, Vol. 49 Issue 4, p361-384. 24p. 1 Chart, 7 Graphs.
Autor:
Rhatigan RM, Hardy NM
Publikováno v:
American journal of clinical pathology [Am J Clin Pathol] 1987 Dec; Vol. 88 (6), pp. 763.