scholarly journals Genotype-phenotype analysis in inherited prion disease with eight octapeptide repeat insertional mutation

Prion ◽  
2013 ◽  
Vol 7 (6) ◽  
pp. 501-510 ◽  
Author(s):  
Martin Paucar ◽  
Fengqing Xiang ◽  
Richard Moore ◽  
Ruth H Walker ◽  
Elisabeth Winnberg ◽  
...  
Keyword(s):  
Prion Disease ◽  
Insertional Mutation ◽  
Phenotype Analysis

Distinct neuropsychological profiles correspond to distribution of cortical thinning in inherited prion disease caused by insertional mutation

2011 ◽  
Vol 83 (1) ◽  
pp. 109-114 ◽  
Author(s):  
K Alner ◽  
H Hyare ◽  
S Mead ◽  
P Rudge ◽  
S Wroe ◽  
...  
Keyword(s):  
Prion Disease ◽  
Insertional Mutation ◽  
Cortical Thinning

A prion disease with a novel 96-base pair insertional mutation in the prion protein gene

Neurology ◽  
1996 ◽  
Vol 46 (3) ◽  
pp. 761-766 ◽  
Author(s):  
T. A. Campbell ◽  
M. S. Palmer ◽  
R. G. Will ◽  
W.R.G. Gibb ◽  
P. J. Luthert ◽  
...  
Keyword(s):  
Prion Protein ◽  
Prion Disease ◽  
Base Pair ◽  
Protein Gene ◽  
Prion Protein Gene ◽  
Insertional Mutation

POD03 Distinct neuropsychological profiles correspond to distribution of cortical thinning in inherited prion disease caused by insertional mutation

2010 ◽  
Vol 81 (11) ◽  
pp. e42-e43
Author(s):  
P. Rudge ◽  
N. C. Fox ◽  
L. Cipolotti ◽  
S. Mead ◽  
H. Hyare ◽  
...  
Keyword(s):  
Prion Disease ◽  
Insertional Mutation ◽  
Cortical Thinning

scholarly journals Prominent psychiatric features and early onset in an inherited prion disease with a new insertional mutation in the prion protein gene

Brain ◽  
1999 ◽  
Vol 122 (12) ◽  
pp. 2375-2386 ◽  
Author(s):  
Jean-Louis Laplanche ◽  
Khalid Hamid El Hachimi ◽  
Isabelle Durieux ◽  
Pascaline Thuillet ◽  
Luc Defebvre ◽  
...  
Keyword(s):  
Prion Protein ◽  
Prion Disease ◽  
Early Onset ◽  
Protein Gene ◽  
Prion Protein Gene ◽  
Insertional Mutation

Prion disease

AccessScience ◽  
2015 ◽  
Keyword(s):  
Prion Disease

Human Prion Disease Surveillance

2005 ◽  
Author(s):  
Lon Kightlinger
Keyword(s):  
Prion Disease ◽  
Disease Surveillance ◽  
Human Prion Disease

Diagnosis of human prion disease

2007 ◽  
Vol 2007 ◽  
pp. 175
Author(s):  
J.R. Berger
Keyword(s):  
Prion Disease ◽  
Human Prion Disease

Molecular profiling and antimicrobial susceptibility of Escherichia coli O157:H7 isolated in Bulgaria

2020 ◽  
Vol 23 (3) ◽  
pp. 310-318
Author(s):  
K. Koev ◽  
T. Stoyanchev ◽  
G. Zhelev ◽  
P. Marutsov ◽  
K. Gospodinova ◽  
...  
Keyword(s):  
Escherichia Coli ◽  
Escherichia Coli O157 ◽  
Acid Sensitivity ◽  
Lower Extent ◽  
Phenotype Analysis ◽  
Anal Swab ◽  
Amoxicillin Clavulanic Acid ◽  
Primary Identification ◽  
Stx1 Gene ◽  
Cattle Farms

The purpose of this study was to detect the presence of shiga-toxin producing Escherichia coli (STEC) in faeces of healthy dairy cattle and to determine the sensitivity of isolates to several anti­microbial drugs. A total of 1,104 anal swab samples originating from 28 cattle farms were examined. After the primary identification, 30 strains were found to belong to serogroup О157. By means of conventional multiplex PCR, isolates were screened for presence of resistance genes stx1, stx2 and eaeА. Twenty-nine strains possesses amplicons with a size corresponding to genes stx2 and eaeA, one had amplicons also for the stx1 gene and one lacked amplicons of all three genes. Twenty-eight strains demonstrated amplicons equivalent to gene H7. The results from phenotype analysis of resistance showed preserved sensitivity to ceftriaxone, ceftazidime, cefotaxime, cephalothin, streptomycin, gentamicin, tetracycline, enrofloxacin and combinations sulfamethoxazole/trimethoprim and amoxicillin/clavulanic acid. Sensitivity to ampicillin was relatively preserved, although at a lower extent.

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