Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Camille Deering"'
Autor:
Stanley B. Prusiner, Jiri G. Safar, Camille Deering, Man-Lik Choi Edward, Bruce L. Miller, Michael D. Geschwind, Kristen Pomeroy, Amy Kuo
Publikováno v:
Laboratory investigation; a journal of technical methods and pathology
Choi, EM; Geschwind, MD; Deering, C; Pomeroy, K; Kuo, A; Miller, BL; et al.(2009). Prion proteins in subpopulations of white blood cells from patients with sporadic Creutzfeldt-Jakob disease. Laboratory Investigation, 89(6), 624-635. doi: 10.1038/labinvest.2009.30. UCSF: Retrieved from: http://www.escholarship.org/uc/item/7dm359gc
Laboratory investigation; a journal of technical methods and pathology, vol 89, iss 6
Choi, EM; Geschwind, MD; Deering, C; Pomeroy, K; Kuo, A; Miller, BL; et al.(2009). Prion proteins in subpopulations of white blood cells from patients with sporadic Creutzfeldt-Jakob disease. Laboratory Investigation, 89(6), 624-635. doi: 10.1038/labinvest.2009.30. UCSF: Retrieved from: http://www.escholarship.org/uc/item/7dm359gc
Laboratory investigation; a journal of technical methods and pathology, vol 89, iss 6
Recent cases of prion transmission in humans following transfusions using blood donated by patients with asymptomatic variant Creutzfeldt-Jakob disease (CJD) implicate the presence of prion infectivity in peripheral blood. In this study, we examined
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6efe8c1cf6223a1ce5b212ac01c1f7dd
http://europepmc.org/articles/PMC2786774
http://europepmc.org/articles/PMC2786774
Autor:
Jiri G. Safar, Yevgeniy Freyman, Gültekin Tamgüney, Frederic Letessier, Stanley B. Prusiner, Camille Deering, Stephen J. DeArmond, Pierre Lessard
In chronic wasting disease (CWD) in cervids and in scrapie in sheep, prions appear to be transmitted horizontally. Oral exposure to prion-tainted blood, urine, saliva, and feces has been suggested as the mode of transmission of CWD and scrapie among
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::032550121315d68f5a3fb20d474af5a9
https://europepmc.org/articles/PMC2803675/
https://europepmc.org/articles/PMC2803675/
Autor:
David J. King, Giuseppe Legname, Stephen J. DeArmond, Michael D. Geschwind, Stanley B. Prusiner, Diane Latawiec, Jiri G. Safar, Camille Deering, Karl H. Weisgraber, Holger Wille, Ana Serban, Bruce L. Miller, Robert W. Mahley
Prions are composed solely of an alternatively folded isoform of the prion protein (PrP), designated PrP Sc . The polyoxometalate phosphotungstic acid has been used to separate PrP Sc from its precursor PrP C by selective precipitation; notably, nati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::feb0392c81c0c304d243328ba78bc08f
https://europepmc.org/articles/PMC1544083/
https://europepmc.org/articles/PMC1544083/
Autor:
Mamta Sattavat, Bruce L. Miller, Henry Sanchez, Stephen J. DeArmond, Jiri G. Safar, Camille Deering, Michael D. Geschwind, Martin Vey, Henry Baron, Stanley B. Prusiner, Ana Serban, Svetlana Didorenko, Kurt Giles
Publikováno v:
Safar, Jiri G; Geschwind, Michael D; Deering, Camille; Didorenko, Svetlana; Sattavat, Mamta; Sanchez, Henry; et al.(2005). Diagnosis of human prion disease. Proceedings of the National Academy of Sciences of the United States of America, 102(9), 3501-3506. UC San Francisco: Retrieved from: http://www.escholarship.org/uc/item/9fh1n8gp
With the discovery of the prion protein (PrP), immunodiagnostic procedures were applied to diagnose Creutzfeldt–Jakob disease (CJD). Before development of the conformation-dependent immunoassay (CDI), all immunoassays for the disease-causing PrP is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34a81343e11022fdd0e78f9efb79e20e
https://pubmed.ncbi.nlm.nih.gov/15741275
https://pubmed.ncbi.nlm.nih.gov/15741275
Autor:
Stephen J. DeArmond, Essia Bouzamondo-Bernstein, Patricia Spilman, Stephanie D. Hopkins, Jiri G. Safar, Jane Uyehara-Lock, Stanley B. Prusiner, Camille Deering, Henry J. Ralston
Publikováno v:
Journal of neuropathology and experimental neurology. 63(8)
Loss of the GABAergic system of neurons has been reported to be the first detectable neuropathological change in prion diseases, which features the accumulation of an aberrant isoform of the prion protein (PrP(Sc)). To determine the timing of GABAerg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d2b0437490ea1df950fe1a0a04fde3a
https://pubmed.ncbi.nlm.nih.gov/15330342
https://pubmed.ncbi.nlm.nih.gov/15330342
Autor:
Darlene Groth, Stanley B. Prusiner, Jiri G. Safar, Camille Deering, Jeff Monaghan, Haydn L. Ball, Michael R. Scott, Svetlana Didorenko, Laura Solforosi, Hana Serban, Dennis R. Burton, Julie Vergara, R. Anthony Williamson, Giuseppe Legname, Estelle Leclerc
There is increasing concern over the extent to which bovine spongiform encephalopathy (BSE) prions have been transmitted to humans, as a result of the rising number of variant Creutzfeldt-Jakob disease (vCJD) cases. Toward preventing new transmission
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d830eaf4df2f6103fad51a3b39eea5d7
http://hdl.handle.net/20.500.11767/16806
http://hdl.handle.net/20.500.11767/16806
Autor:
J. Launspach, Mordechai Bodner, Camille Deering, Jianqiang Shao, Paul B. McCray, Joseph Zabner, Beverly L. Davidson, Guoshun Wang, Doug J. Jolly
Publikováno v:
American journal of respiratory cell and molecular biology. 22(2)
Gene transfer to airway epithelia is the most direct approach for treating the progressive lung disease associated with cystic fibrosis. However, the transduction efficiency is poor when viral vectors are applied to the mucosal surface. We reported p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71cbc6d3e2be2dca6d76398da7702743
https://pubmed.ncbi.nlm.nih.gov/10657931
https://pubmed.ncbi.nlm.nih.gov/10657931