Zobrazeno 1 - 10
of 126
pro vyhledávání: '"Mark Head"'
Autor:
Siddharthan Chandran, Mark Head, Alison Green, Richard Knight, Diane Ritchie, Paul A. De Sousa
Publikováno v:
De Sousa, P A, Ritchie, D, Green, A, Chandran, S, Knight, R & Head, M W 2018, ' Renewed assessment of the risk of emergent advanced cell therapies to transmit neuroproteinopathies ', Acta Neuropathologica . https://doi.org/10.1007/s00401-018-1941-9
Acta Neuropathologica
Acta Neuropathologica
The inadvertent transmission of long incubating, untreatable and fatal neurodegenerative prionopathies, notably iatrogenic Creutzfeldt–Jakob disease, following transplantation of cadaver-derived corneas, pituitary growth, hormones and dura mater, c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec42998eb64d15c4d697aee2c6c76640
https://www.pure.ed.ac.uk/ws/files/77432124/Sousa2018_Article_RenewedAssessmentOfTheRiskOfEm.pdf
https://www.pure.ed.ac.uk/ws/files/77432124/Sousa2018_Article_RenewedAssessmentOfTheRiskOfEm.pdf
Publikováno v:
Emerging Infectious Diseases
A. Barria, M, Libori, A, Mitchell, G & Head, M 2018, ' Susceptibility of Human Prion Protein to Conversion by Chronic Wasting Disease Prions ', Emerging Infectious Diseases, pp. 1482-1489 . https://doi.org/10.3201/eid2408.161888
Emerging Infectious Diseases, Vol 24, Iss 8, Pp 1482-1489 (2018)
A. Barria, M, Libori, A, Mitchell, G & Head, M 2018, ' Susceptibility of Human Prion Protein to Conversion by Chronic Wasting Disease Prions ', Emerging Infectious Diseases, pp. 1482-1489 . https://doi.org/10.3201/eid2408.161888
Emerging Infectious Diseases, Vol 24, Iss 8, Pp 1482-1489 (2018)
Chronic wasting disease (CWD) is a contagious and fatal neurodegenerative disease and a serious animal health issue for deer and elk in North America. The identification of the first cases of CWD among free-ranging reindeer and moose in Europe brings
Publikováno v:
Barria, M A, Lee, A J, Green, A J, Knight, R & Head, M W 2018, ' Rapid amplification of prions from variant Creutzfeldt-Jakob disease cerebrospinal fluid : Detection of vCJD prions in human CSF samples ', Journal of Pathology: Clinical Research . https://doi.org/10.1002/cjp2.90
Human prion diseases constitute a group of infectious and invariably fatal neurodegenerative disorders associated with misfolding of the prion protein. Variant Creutzfeldt-Jakob disease (vCJD) is a zoonotic prion disease linked to oral exposure to th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb6c217d9cf1fbd1dc9c8cfd8f6d77dc
https://www.pure.ed.ac.uk/ws/files/53400141/Barria_et_al_2018_The_Journal_of_Pathology_Clinical_Research.pdf
https://www.pure.ed.ac.uk/ws/files/53400141/Barria_et_al_2018_The_Journal_of_Pathology_Clinical_Research.pdf
The human prion diseases comprise Creutzfeldt–Jakob disease, variably protease-sensitive prionopathy, Gerstmann–Straussler–Scheinker disease, fatal familial insomnia, and kuru. Each is a uniformly fatal rare neurodegenerative disease in which c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a4bc02548da14d21d79a9a8bc1198f3
https://doi.org/10.1016/b978-0-12-802395-2.00028-6
https://doi.org/10.1016/b978-0-12-802395-2.00028-6
Autor:
Patrick F. Chinnery, James W. Ironside, Margaret Le Grice, Wei Wei, Suzanne Lowrie, Michael J. Keogh, Helen Yull, Diane Ritchie, Peter Adlard, Rosemary J. Jackson, Kimberley Burns, Alexander Peden, Mark Head
Publikováno v:
Acta Neuropathologica
Ritchie, D L, Adlard, P, Peden, A H, Lowrie, S, Le Grice, M, Burns, K, Jackson, R J, Yull, H, Keogh, M J, Wei, W, Chinnery, P F, Head, M W & Ironside, J W 2017, ' Amyloid-β accumulation in the CNS in human growth hormone recipients in the UK ', Acta Neuropathologica, vol. 134, no. 2, pp. 221–240 . https://doi.org/10.1007/s00401-017-1703-0
Ritchie, D L, Adlard, P, Peden, A H, Lowrie, S, Le Grice, M, Burns, K, Jackson, R J, Yull, H, Keogh, M J, Wei, W, Chinnery, P F, Head, M W & Ironside, J W 2017, ' Amyloid-β accumulation in the CNS in human growth hormone recipients in the UK ', Acta Neuropathologica, vol. 134, no. 2, pp. 221–240 . https://doi.org/10.1007/s00401-017-1703-0
Human-to-human transmission of Creutzfeldt–Jakob disease (CJD) has occurred through medical procedures resulting in iatrogenic CJD (iCJD). One of the commonest causes of iCJD was the use of human pituitary-derived growth hormone (hGH) to treat prim
Autor:
Michael Jones, Lorenzo González, Marcelo A. Barria, Zuzana Krejciova, Mark Head, James W. Ironside, Martin Jeffrey
Publikováno v:
Journal of Biological Chemistry. 289:26075-26088
Prion diseases are rare fatal neurological conditions of humans and animals, one of which (variant Creutzfeldt-Jakob disease) is known to be a zoonotic form of the cattle disease bovine spongiform encephalopathy (BSE). What makes one animal prion dis
Autor:
Aileen Boyle, Mark Head, Sandra McCutcheon, James W. Ironside, Robert G. Will, Jean Manson, Richard Knight, Abigail B. Diack
Publikováno v:
Diack, A B, Head, M W, McCutcheon, S, Boyle, A, Knight, R, Ironside, J W, Manson, J C & Will, R G 2014, ' Variant CJD : 18 years of research and surveillance ', Prion, vol. 8, no. 4, pp. 286-295 . https://doi.org/10.4161/pri.29237
It is now 18 years since the first identification of a case of vCJD in the UK. Since that time there has been much speculation over how vCJD might impact on human health. To date there have been 177 cases reports in the UK and a further 51 cases worl
Publikováno v:
Prion. 8:85-91
Following the discovery of a causal link between bovine spongiform encephalopathy (BSE) in cattle and variant Creutzfeldt-Jakob disease (vCJD) in humans, several experimental approaches have been used to try to assess the potential risk of transmissi
Publikováno v:
Krejciova, Z, De Sousa, P, Manson, J, Ironside, J W & Head, M W 2014, ' Human Tonsil-Derived Follicular Dendritic-Like Cells are Refractory to Human Prion Infection in Vitro and Traffic Disease-Associated Prion Protein to Lysosomes ', American Journal of Pathology, vol. 184, no. 1, pp. 64-70 . https://doi.org/10.1016/j.ajpath.2013.09.013
The molecular mechanisms involved in human cellular susceptibility to prion infection remain poorly defined. This is due, in part, to the absence of any well characterized and relevant cultured human cells susceptible to infection with human prions,
Autor:
Deyong Jia, Zhicheng Zhou, Oh-Joon Kwon, Li Zhang, Xing Wei, Yiqun Zhang, Mingyang Yi, Martine P. Roudier, Mary C. Regier, Ruth Dumpit, Peter S. Nelson, Mark Headley, Lawrence True, Daniel W. Lin, Colm Morrissey, Chad J. Creighton, Li Xin
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-18 (2022)
Forkhead transcription factor FoxF2 plays a crucial role in the development of organs derived from primitive gut. Here the authors show that reduction of Foxf2 expression in stromal cells is associated with high grade prostate cancer and that increas
Externí odkaz:
https://doaj.org/article/6ef1b8477dc94cb884e5bb6309eb3423