Zobrazeno 1 - 10
of 229
pro vyhledávání: '"A E, Shrimpton"'
Autor:
Beata Fonferko-Shadrach, Huw Strafford, Carys Jones, Russell A. Khan, Sharon Brown, Jenny Edwards, Jonathan Hawken, Luke E. Shrimpton, Catharine P. White, Robert Powell, Inder M. S. Sawhney, William O. Pickrell, Arron S. Lacey
Publikováno v:
Journal of Biomedical Semantics, Vol 15, Iss 1, Pp 1-5 (2024)
Abstract Background Natural language processing (NLP) is increasingly being used to extract structured information from unstructured text to assist clinical decision-making and aid healthcare research. The availability of expert-annotated documents f
Externí odkaz:
https://doaj.org/article/92eaf5cec1324a318012a2f857b62a25
Autor:
M. B. de Macedo, M. R. Benso, K. S. Sass, E. M. Mendiondo, G. J. da Silva, P. G. C. da Silva, E. Shrimpton, T. Sarmah, D. Huo, M. Jacobson, A. Konak, N. Balta-Ozkan, A. C. Nardocci
Publikováno v:
Natural Hazards and Earth System Sciences, Vol 24, Pp 2165-2173 (2024)
This paper describes the process of creating a global survey of experts to evaluate drought resilience indicators. The lessons learned include five main points: (1) the heterogeneity in the conceptual background should be minimized before the constru
Externí odkaz:
https://doaj.org/article/6eb94709fec646178181e415dba242d4
Publikováno v:
The Cambridge Law Journal, 1951 Jan 01. 11(1), 147-150.
Externí odkaz:
https://www.jstor.org/stable/4504037
Akademický článek
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Akademický článek
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Autor:
David Craig, Justine Coppinger, Joshua L. Goldstein, Dean Sarco, Robert G. Little, John A. Kessler, Joe J. Hoo, Brad Angle, David J. Mathison, William B. Dobyns, Alexander G. Bassuk, Ajit Chary, Ali Jalali, Sophia Khan, Antony E. Shrimpton, Andrew K. Poznanski, Cynthia V. Stack, Lisa G. Shaffer
Publikováno v:
Journal of Pediatric Neurology. :279-283
Chromosomal microdeletion syndromes are frequently associated with neurological disease including epilepsy and behavioral abnormalities. Yet, for most microdeletions, neurological phenotypes are variable and the exact molecular cause of neurological
HOXD10 Mutations Associated With Congenital Vertical Talus and Pes Cavus Claw-Toe Limb Abnormalities
Publikováno v:
Epstein's Inborn Errors of Development: The Molecular Basis of Clinical Disorders of Morphogenesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d56e232b71820db7de52d026271430c1
https://doi.org/10.1093/med/9780199934522.003.0092
https://doi.org/10.1093/med/9780199934522.003.0092
Autor:
Antony E. Shrimpton, Sandra Hudson, Michael P. Link, Donna Barrett, Devin R. Halleran, Robert E. Hutchison, Charu Thakral, Joseph Laver
Publikováno v:
Pediatric Blood & Cancer. 59:440-447
ALK+ anaplastic large cell lymphoma (ALCL) is usually a disease of young patients. We investigated phosphatidylinositol-3 kinase (PI3K)/Akt pathway-associated factors in pediatric cases and cell lines.Patient materials consisted of tissue slides of A
Autor:
Colin White, Anna Lehman, Anita A C Reed, Paul T. Christie, Manuel Rivero Sanchez, David V. Milford, Antony E. Shrimpton, Stephen J. Knohl, Oliver Wrong, Richard R. Hoopes, Philip J. Lee, Takashi Igarashi, Robert J. Unwin, Rajesh V. Thakker, Steven J. Scheinman, Paul Hueber
Publikováno v:
Nephron Physiology. 112:p27-p36
Background/Aims: Dent disease is an X-linked renal proximal tubulopathy associated with mutations in CLCN5 (Dent 1) or OCRL1 (Dent 2). OCRL1 mutations also cause the oculocerebrorenal syndrome of Lowe. Methods: Dent patients with normal sequence for
Autor:
Swee Shan Hue, Mary A. Ritter, Rachel E. Shrimpton, Matt Butler, Anne-Sophie Morel, Efrem Eren
Publikováno v:
Molecular Immunology
CD205 is an endocytic receptor that is expressed at high levels by cortical thymic epithelial cells and by dendritic cell (DC) subsets, including the splenic CD8+ DC population that is responsible for cross-presentation of apoptotic cell-derived anti