Zobrazeno 1 - 10
of 255
pro vyhledávání: '"GM Taylor"'
Publikováno v:
Journal of Archaeological Science. 33:1569-1579
Using ancient DNA methods, we have examined in detail two archaeological cases of leprosy from Mediaeval England. The first was a child skeleton with rhino-maxillary changes typical of lepromatous leprosy (LL). The second case was the skeleton of a m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::05d61ddd87ce8d12107aedaed1080eeb
https://doi.org/10.1016/j.jas.2006.02.008
https://doi.org/10.1016/j.jas.2006.02.008
Autor:
Douglas B. Young, M. Cooke, S. Palmer, J. Kirkup, S. Ladva, S. Chaplin, GM Taylor, Graham R. Stewart
Publikováno v:
Microbiology. 149:3213-3220
Using molecular methods the authors have studied mycobacterial DNA taken from a 19th century victim of tuberculosis. This was the case from which Robert Koch first isolated and cultured the organism responsible for tuberculosis. The mycobacteria were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d3ddb04cc5e21eca7935b639b4a0b4b
https://doi.org/10.1099/mic.0.26654-0
https://doi.org/10.1099/mic.0.26654-0
Autor:
GM Taylor, Simon Mays
Publikováno v:
Journal of Archaeological Science. 29:1267-1276
Two skeletons from Mediaeval Wharram Percy, England, show osteological lesions consistent with hypertrophic osteoarthropathy. The primary cause of hypertrophic osteoarthropathy is generally chronic pulmonary disease, usually either cancer or infectio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9cdf0e8607fb3e0911c51e9c4472f813
https://doi.org/10.1006/jasc.2001.0769
https://doi.org/10.1006/jasc.2001.0769
Publikováno v:
American Journal of Physical Anthropology. 119:27-36
Seven human skeletons from a large assemblage from a rural English Medieval burial site show lesions, predominantly proliferative in nature, on the visceral surfaces of the ribs. In order to investigate whether these rib lesions were regularly associ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79ae66e26d1f127de143d19e9a3b32d1
https://doi.org/10.1002/ajpa.10099
https://doi.org/10.1002/ajpa.10099
Publikováno v:
American Journal of Physical Anthropology. 114:298-311
Nine human skeletons of medieval date from a rural English burial site show signs of skeletal tuberculosis. They were subject to polymerase chain reaction (PCR) assays aimed at detecting traces of DNA from infecting mycobacteria, with the purpose bot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1187772b1f8c18c5e732e22e91fbbf0
https://doi.org/10.1002/ajpa.1042
https://doi.org/10.1002/ajpa.1042
Publikováno v:
Scopus-Elsevier
Summary: Three medieval bone samples with osteological evidence of tuberculosis infection were analysed for the presence of DNA sequences from Mycobacterium tuberculosis using a series of PCRs. In each case amplification of IS6110 and part of the β-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44634ae6f3957e8706cc34c5941829ca
https://doi.org/10.1099/13500872-145-4-899
https://doi.org/10.1099/13500872-145-4-899
Publikováno v:
Pediatric Nephrology. 11:404-410
Experimental studies have pointed to charge selectivity as an important determinant of glomerular permeability to macromolecules. Loss of glomerular basement membrane (GBM) polyanion has been proposed as a cause of the selective proteinuria in minima
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0dea214041f3cdf363e166f7e0ea4ace
https://doi.org/10.1007/s004670050305
https://doi.org/10.1007/s004670050305
Publikováno v:
Europe PubMed Central
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::734b8ce3d484bb7ab46ca75f4c8fa0ca
https://pubmed.ncbi.nlm.nih.gov/7670416
https://pubmed.ncbi.nlm.nih.gov/7670416
Autor:
Da, Gokhale, Gareth Evans, Crowther D, Woll P, Cj, Watson, Sp, Dearden, Wd, Fergusson, Rf, Stevens, Gm, Taylor
Publikováno v:
Europe PubMed Central
We describe a family in which two sisters with the autosomal dominant skeletal dysplasia, Leri-Weill dyschondrosteosis (LWD), developed Hodgkin's disease (HD) in late adolescence. In a preliminary attempt to identify HD susceptibility gene(s), HLA-ty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::74d598b5f90fcb987e1ff71fafbea9b6
https://pubmed.ncbi.nlm.nih.gov/7769845
https://pubmed.ncbi.nlm.nih.gov/7769845
Publikováno v:
Clinical Science. 104:29P-30P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bdf04c3e6258c3d0112f204462d463f1
https://doi.org/10.1042/cs104029pc
https://doi.org/10.1042/cs104029pc