Zobrazeno 1 - 10 of 136 pro vyhledávání: '"David A. Kasper"'
1
Akademický článek
Monitoring AGNs with Hβ Asymmetry. IV. First Reverberation Mapping Results of 14 Active Galactic Nuclei
Autor: T. E. Zastrocky, Michael S. Brotherton, Pu Du, Jacob N. McLane, Kianna A. Olson, D. A. Dale, H. A. Kobulnicky, Jaya Maithil, My L. Nguyen, William T. Chick, David H. Kasper, Derek Hand, C. Adelman, Z. Carter, G. Murphree, M. Oeur, T. Roth, S. Schonsberg, M. J. Caradonna, J. Favro, A. J. Ferguson, I. M. Gonzalez, L. M. Hadding, H. D. Hagler, C. J. Rogers, T. R. Stack, Franklin Chapman, Dong-Wei Bao, Feng-Na Fang, Shuo Zhai, Sen Yang, Yong-Jie Chen, Hua-Rui Bai, Yi-Xin Fu, Jun-Rong Liu, Zhu-Heng Yao, Yue-Chang Peng, Yu-Yang Songsheng, Yan-Rong Li, Jin-Ming Bai, Chen Hu, Ming Xiao, Luis C. Ho, Jian-Min Wang
Publikováno v: The Astrophysical Journal Supplement Series, Vol 272, Iss 2, p 29 (2024)
We report first-time reverberation-mapping results for 14 active galactic nuclei (AGNs) from the ongoing Monitoring AGNs with H β Asymmetry campaign (MAHA). These results utilize optical spectra obtained with the Long Slit Spectrograph on the Wyomin
Externí odkaz: https://doaj.org/article/083e7e8b79bc4fef990c806f4d6e2c08
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2
Akademický článek
A Six Year, Low-resolution, Multibroadband Transit Photometry Study of HD 189733b
Autor: Cristilyn N. Gardner-Watkins, Henry A. Kobulnicky, Hannah Jang-Condell, David H. Kasper, Brock A. Parker, Ted Bucci, Evan M. Cook, Kaitlin A. Doublestein, Cade Freels, Dax G. T. Galloway, Sabrina Helck, Corinne Komlodi, Michael J. Lindman, McKell Lyon, Ashley N. Piccone, Samantha Wilkerson
Publikováno v: The Astronomical Journal, Vol 165, Iss 1, p 5 (2022)
Transmission spectroscopy offers an invaluable opportunity to characterize the atmospheres of exoplanets. We present new ground-based optical transmission spectra of the hot Jupiter HD 189733b, derived from nine transits observed over a six year time
Externí odkaz: https://doaj.org/article/f7277f4e760442e28bffbe23b1b74709
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4
Akademický článek
Negative screening of Fabry disease in patients with conduction disorders requiring a pacemaker
Autor: Ángela López-Sainz, Vicente Climent, Tomas Ripoll-Vera, Maria Angeles Espinosa, Roberto Barriales-Villa, Marina Navarro, Javier Limeres, Diana Domingo, David C. Kasper, Pablo Garcia-Pavia
Publikováno v: Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-3 (2019)
Abstract Identification of Fabry disease (FD) in cardiac patients has been restricted so far to patients with left ventricular hypertrophy. Conduction problems are frequent in FD and could precede other manifestations, offering a possible earlier dia
Externí odkaz: https://doaj.org/article/d8ecfe0ef8a84cb9ac424890cc7c4b67
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5
Akademický článek
Targeted Metabolomic Profiling of Peritoneal Dialysis Effluents Shows Anti-oxidative Capacity of Alanyl-Glutamine
Autor: Florian M. Wiesenhofer, Rebecca Herzog, Michael Boehm, Anja Wagner, Markus Unterwurzacher, David C. Kasper, Seth L. Alper, Andreas Vychytil, Christoph Aufricht, Klaus Kratochwill
Publikováno v: Frontiers in Physiology, Vol 9 (2019)
Readily available peritoneal dialysis (PD) effluents from PD patients in the course of renal replacement therapy are a potentially rich source for molecular markers for predicting clinical outcome, monitoring the therapy, and therapeutic intervention
Externí odkaz: https://doaj.org/article/a483c1d98e744a5b851d16c109e73257
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6
Akademický článek
At-Risk Testing for Pompe Disease Using Dried Blood Spots: Lessons Learned for Newborn Screening
Autor: Zoltan Lukacs, Petra Oliva, Paulina Nieves Cobos, Jacob Scott, Thomas P. Mechtler, David C. Kasper
Publikováno v: International Journal of Neonatal Screening, Vol 6, Iss 4, p 96 (2020)
Pompe disease (GSD II) is an autosomal recessive disorder caused by deficiency of the lysosomal enzyme acid-α-glucosidase (GAA, EC 3.2.1.20), leading to generalized accumulation of lysosomal glycogen especially in the heart, skeletal, and smooth mus
Externí odkaz: https://doaj.org/article/7a9076a7fdcf474eb8c3ff88343c2e95
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7
Molecular basis of mucopolysaccharidosis IVA (Morquio A syndrome): A review and classification of GALNS gene variants and reporting of 68 novel variants
Autor: Moeenaldeen Al-Sayed, Yin-Hsiu Chien, Francesca D’Avanzo, Rodolfo Tonin, Hsiang-Yu Lin, Akashdeep Singh, Emanuela Izzo, Ana Carolina Brusius-Facchin, Alessandra Zanetti, Laura Pollard, David C Kasper, Roberto Giugliani, Shuan-Pei Lin, Rosella Tomanin, Tim Wood, Amelia Morrone
Publikováno v: Human Mutation. 42:1384-1398
Mucopolysaccharidosis IVA (MPS IVA, Morquio A syndrome) is a rare autosomal recessive lysosomal storage disorder caused by mutations in the N-acetylgalactosamine-6-sulfatase (GALNS) gene. We collected, analyzed, and uniformly summarized all published
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb41b8131b26c8b3f9f3a3fa629b7906
https://doi.org/10.1002/humu.24270
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8
Akademický článek
Congenital toxoplasmosis in Austria: Prenatal screening for prevention is cost-saving.
Autor: Andrea-Romana Prusa, David C Kasper, Larry Sawers, Evelyn Walter, Michael Hayde, Eileen Stillwaggon
Publikováno v: PLoS Neglected Tropical Diseases, Vol 11, Iss 7, p e0005648 (2017)
Primary infection of Toxoplasma gondii during pregnancy can be transmitted to the unborn child and may have serious consequences, including retinochoroiditis, hydrocephaly, cerebral calcifications, encephalitis, splenomegaly, hearing loss, blindness,
Externí odkaz: https://doaj.org/article/1d009628a01e470ca710c7b704c2b0c5
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