Zobrazeno 1 - 10
of 809
pro vyhledávání: '"J H Smith"'
Autor:
R P Taylor, T P Martin, R D Montgomery, J H Smith, A P Micolich, C Boydston, B C Scannell, M S Fairbanks, B Spehar
Publikováno v:
PLoS ONE, Vol 12, Iss 2, p e0171289 (2017)
Rorschach inkblots have had a striking impact on the worlds of art and science because of the remarkable variety of associations with recognizable and namable objects they induce. Originally adopted as a projective psychological tool to probe mental
Externí odkaz:
https://doaj.org/article/5ed40cf0397a4976b9ea971c0dd6201e
Autor:
Cobey J. H. Donelson, Nicolo Ghiringhelli Borsa, Amanda O. Taylor, Richard J. H. Smith, Yuzhou Zhang
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
The regulatory serine protease, complement factor I (FI), in conjunction with one of its cofactors (FH, C4BP, MCP, or CR1), plays an essential role in controlling complement activity through inactivation of C3b and C4b. The functional impact by misse
Externí odkaz:
https://doaj.org/article/221d1b499b1f4d6697c25441e7dda17e
Publikováno v:
Journal of Lipid Research, Vol 35, Iss 7, Pp 1251-1266 (1994)
Incubation of Chinese hamster ovary cells (CHO-K1) with 14 alpha-ethyl-5 alpha-cholest-7-ene-3 beta,15 alpha-diol (0.1 microM) in lipid-deficient medium led to a major change in cellular sterol composition, which was characterized by a very marked ac
Externí odkaz:
https://doaj.org/article/2d5900ff9cd24c27a010ce35f5422de4
Autor:
Andrew S, Bomback, David, Kavanagh, Marina, Vivarelli, Matthias, Meier, Yaqin, Wang, Nicholas J A, Webb, Angelo J, Trapani, Richard J H, Smith
Publikováno v:
Kidney International Reports. 7:2150-2159
Complement 3 glomerulopathy (C3G) is a rare kidney disease characterized by dysregulation of the alternative pathway (AP) of the complement system. About 50% of patients with C3G progress to kidney failure within 10 years of diagnosis. Currently, the
Autor:
A. D. Kane, R. A. Armstrong, E. Kursumovic, T. M. Cook, F. C. Oglesby, L. Cortes, I. K. Moppett, S. R. Moonesinghe, S. Agarwal, D. C. Bouch, J. Cordingley, M. T. Davies, J. Dorey, S. J. Finney, G. Kunst, D. N. Lucas, G. Nickols, R. Mouton, J. P. Nolan, B. Patel, V. J. Pappachan, F. Plaat, K. Samuel, B. R. Scholefield, J. H. Smith, L. Varney, C. Vindrola‐Padros, S. Martin, E. C. Wain, S. W. Kendall, S. Ward, S. Drake, J. Lourtie, C. Taylor, J. Soar
Publikováno v:
Kane, A D, Armstrong, R A, Kursumovic, E, Cook, T M, Oglesby, F C, Moppett, I K, Moonesinghe, S R, Bouch, D C, Cordingley, J, Dorey, J, Finney, S J, Kunst, G, Nickols, G, Mouton, R, Nolan, J P, Pappachan, V J, Plaat, F, Samuel, K, Scholefield, B R, Varney, L, Vindrola-Padros, C, Wain, E C, Kendall, S W, Lourtie, J & Soar, J 2022, ' Methods of the 7th National Audit Project (NAP7) of the Royal College of Anaesthetists : peri-operative cardiac arrest ', Anaesthesia, vol. 77, no. 12, pp. 1376-1385 . https://doi.org/10.1111/anae.15856
Cardiac arrest in the peri-operative period is rare but associated with significant morbidity and mortality. Current reporting systems do not capture many such events, so there is an incomplete understanding of incidence and outcomes. As peri-operati
Publikováno v:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 190:344-357
C3 glomerulopathy (C3G) describes a pathologic pattern of injury diagnosed by renal biopsy. It is characterized by the dominant deposition of the third component of complement (C3) in the renal glomerulus as resolved by immunofluorescence microscopy.
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
C3 Glomerulopathy (C3G) is a renal disease mediated primarily by dysregulation of the alternative pathway of complement. Complement is the cornerstone of innate immunity. It targets infectious microbes for destruction, clears immune complexes, and ap
Externí odkaz:
https://doaj.org/article/c2ee36351c9c4e24872c8441dbc779ab
Publikováno v:
The Laryngoscope.
Autor:
Ryan K. Thorpe, W. Daniel Walls, Rae Corrigan, Amanda Schaefer, Kai Wang, Patrick Huygen, Thomas L. Casavant, Richard J. H. Smith
Publikováno v:
Hum Genet
Human Genetics, 141, 3-4, pp. 877-887
Human Genetics, 141, 877-887
Human Genetics, 141, 3-4, pp. 877-887
Human Genetics, 141, 877-887
Contains fulltext : 251701.pdf (Publisher’s version ) (Closed access) Autosomal dominant non-syndromic hearing loss (ADNSHL) displays gene-specific progression of hearing loss, which is amenable to sequential audioprofiling. We sought to refine the
Autor:
Mallory R. Tollefson, Rose A. Gogal, A. Monique Weaver, Amanda M. Schaefer, Robert J. Marini, Hela Azaiez, Diana L. Kolbe, Donghong Wang, Amy E. Weaver, Thomas L. Casavant, Terry A. Braun, Richard J. H. Smith, Michael J. Schnieders
Hearing loss is the leading sensory deficit, affecting ~ 5% of the population. It exhibits remarkable heterogeneity across 223 genes with 6328 pathogenic missense variants, making deafness-specific expertise a prerequisite for ascribing phenotypic co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::983e3a56b4361851b456ddfb36b4c059
https://doi.org/10.21203/rs.3.rs-2508462/v1
https://doi.org/10.21203/rs.3.rs-2508462/v1