-
1
-
-
0035902194
-
Shattuck lecture-neurodegenerative diseases and prions
-
SB Prusiner 2001 Shattuck lecture-neurodegenerative diseases and prions N Engl J Med 344 1516 1526
-
(2001)
N Engl J Med
, vol.344
, pp. 1516-1526
-
-
Prusiner, S.B.1
-
3
-
-
0029782193
-
Prion protein genotype and pathological phenotype studies in sporadic Creutzfeldt-Jakob disease
-
ST [tmp] MacDonald K Sutherland JW Ironside 1996 Prion protein genotype and pathological phenotype studies in sporadic Creutzfeldt-Jakob disease Neuropathol Appl Neurobiol 22 285 292
-
(1996)
Neuropathol Appl Neurobiol
, vol.22
, pp. 285-292
-
-
MacDonald, S.T.1
Sutherland, K.2
Ironside, J.W.3
-
4
-
-
0026095028
-
The phenotypic expression of different mutations in transmissible familial Creutzfeldt-Jakob disease
-
P Brown LG Goldfarb CJ Gibbs Jr DC Gajdusek 1991 The phenotypic expression of different mutations in transmissible familial Creutzfeldt-Jakob disease Eur J Epidemiol 7 469 476
-
(1991)
Eur J Epidemiol
, vol.7
, pp. 469-476
-
-
Brown, P.1
Goldfarb, L.G.2
Gibbs Jr., C.J.3
Gajdusek, D.C.4
-
6
-
-
0033562770
-
Codon 129 prion protein genotype and sporadic Creutzfeldt-Jakob disease
-
A Alperovitch I Zerr M Pocchiari 1999 Codon 129 prion protein genotype and sporadic Creutzfeldt-Jakob disease Lancet 353 1673 1674
-
(1999)
Lancet
, vol.353
, pp. 1673-1674
-
-
Alperovitch, A.1
Zerr, I.2
Pocchiari, M.3
-
7
-
-
0038304770
-
Distribution of codon 129 genotype in human growth hormone-treated CJD patients in France and the UK
-
JP Brandel M Preece P Brown 2003 Distribution of codon 129 genotype in human growth hormone-treated CJD patients in France and the UK Lancet 362 128 130
-
(2003)
Lancet
, vol.362
, pp. 128-130
-
-
Brandel, J.P.1
Preece, M.2
Brown, P.3
-
8
-
-
0025859996
-
Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease
-
J Collinge MS Palmer AJ Dryden 1991 Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease Lancet 337 1441 1442
-
(1991)
Lancet
, vol.337
, pp. 1441-1442
-
-
Collinge, J.1
Palmer, M.S.2
Dryden, A.J.3
-
9
-
-
0027972696
-
Similar genetic susceptibility in iatrogenic and sporadic Creutzfeldt-Jakob disease
-
JP Deslys D Marce D Dormont 1994 Similar genetic susceptibility in iatrogenic and sporadic Creutzfeldt-Jakob disease J Gen Virol 75 23 27
-
(1994)
J Gen Virol
, vol.75
, pp. 23-27
-
-
Deslys, J.P.1
Marce, D.2
Dormont, D.3
-
10
-
-
0030775632
-
Transmissions to mice indicate that 'new variant' CJD is caused by the BSE agent
-
ME Bruce RG Will JW Ironside 1997 Transmissions to mice indicate that 'new variant' CJD is caused by the BSE agent Nature 389 498 501
-
(1997)
Nature
, vol.389
, pp. 498-501
-
-
Bruce, M.E.1
Will, R.G.2
Ironside, J.W.3
-
11
-
-
0035978032
-
Geographical distribution of variant Creutzfeldt-Jakob disease in Great Britain, 1994-2000
-
S Cousens PG Smith H Ward 2001 Geographical distribution of variant Creutzfeldt-Jakob disease in Great Britain, 1994-2000 Lancet 357 1002 1007
-
(2001)
Lancet
, vol.357
, pp. 1002-1007
-
-
Cousens, S.1
Smith, P.G.2
Ward, H.3
-
12
-
-
0342951746
-
A new variant of Creutzfeldt-Jakob disease in the UK
-
RG Will JW Ironside M Zeidler 1996 A new variant of Creutzfeldt-Jakob disease in the UK Lancet 347 921 925
-
(1996)
Lancet
, vol.347
, pp. 921-925
-
-
Will, R.G.1
Ironside, J.W.2
Zeidler, M.3
-
14
-
-
0042422345
-
Diagnosis of new variant Creutzfeldt-Jakob disease
-
RG Will M Zeidler GE Stewart 2000 Diagnosis of new variant Creutzfeldt-Jakob disease Ann Neurol 47 575 582
-
(2000)
Ann Neurol
, vol.47
, pp. 575-582
-
-
Will, R.G.1
Zeidler, M.2
Stewart, G.E.3
-
15
-
-
0034173484
-
The new variant of Creutzfeldt-Jakob disease
-
M Zeidler JW Ironside 2000 The new variant of Creutzfeldt-Jakob disease Rev Sci Tech 19 98 120
-
(2000)
Rev Sci Tech
, vol.19
, pp. 98-120
-
-
Zeidler, M.1
Ironside, J.W.2
-
16
-
-
0028131841
-
Molecular genetics of prion diseases in France. French Research Group on Epidemiology of Human Spongiform Encephalopathies
-
JL Laplanche N Delasnerie-Laupretre JP Brandel 1994 Molecular genetics of prion diseases in France. French Research Group on Epidemiology of Human Spongiform Encephalopathies Neurology 44 2347 2351
-
(1994)
Neurology
, vol.44
, pp. 2347-2351
-
-
Laplanche, J.L.1
Delasnerie-Laupretre, N.2
Brandel, J.P.3
-
19
-
-
0033845154
-
Polymorphism at codon 129 of the prion protein gene is not associated with sporadic AD
-
O Combarros M Sanchez-Guerra J Llorca 2000 Polymorphism at codon 129 of the prion protein gene is not associated with sporadic AD Neurology 55 593 595
-
(2000)
Neurology
, vol.55
, pp. 593-595
-
-
Combarros, O.1
Sanchez-Guerra, M.2
Llorca, J.3
-
20
-
-
0034911096
-
Increased incidence of sporadic Creutzfeldt-Jakob disease on the island of Crete associated with a high rate of PRNP 129-methionine homozygosity in the local population
-
A Plaitakis AK Viskadouraki M Tzagournissakis 2001 Increased incidence of sporadic Creutzfeldt-Jakob disease on the island of Crete associated with a high rate of PRNP 129-methionine homozygosity in the local population Ann Neurol 50 227 233
-
(2001)
Ann Neurol
, vol.50
, pp. 227-233
-
-
Plaitakis, A.1
Viskadouraki, A.K.2
Tzagournissakis, M.3
-
21
-
-
0035544643
-
Distribution of the M129V polymorphism of the prion protein gene in a Turkish population suggests a high risk for Creutzfeldt-Jakob disease
-
N Erginel-Unaltuna K Peoc'h E Komurcu TT Acuner H Issever JL Laplanche 2001 Distribution of the M129V polymorphism of the prion protein gene in a Turkish population suggests a high risk for Creutzfeldt-Jakob disease Eur J Hum Genet 9 965 968
-
(2001)
Eur J Hum Genet
, vol.9
, pp. 965-968
-
-
Erginel-Unaltuna, N.1
Peoc'H, K.2
Komurcu, E.3
Acuner, T.T.4
Issever, H.5
Laplanche, J.L.6
-
22
-
-
10744219606
-
The normal population distribution of PRNP codon 129 polymorphism
-
Nurmi MH, Bishop M, Strain L, et al. The normal population distribution of PRNP codon 129 polymorphism. Acta Neurol Scand 2003;: 374-378.
-
(2003)
Acta Neurol Scand
, pp. 374-378
-
-
Nurmi, M.H.1
Bishop, M.2
Strain, L.3
-
23
-
-
0242684410
-
Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemics
-
S Mead MP Stumpf J Whitfield 2003 Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemics Science 300 640 643
-
(2003)
Science
, vol.300
, pp. 640-643
-
-
Mead, S.1
Stumpf, M.P.2
Whitfield, J.3
-
24
-
-
0023112595
-
A PvuII RFLP detected in the human prion protein (PrP) gene
-
Y Wu WT Brown NK Robakis 1987 A PvuII RFLP detected in the human prion protein (PrP) gene Nucleic Acids Res 15 3191
-
(1987)
Nucleic Acids Res
, vol.15
, pp. 3191
-
-
Wu, Y.1
Brown, W.T.2
Robakis, N.K.3
-
27
-
-
0032843132
-
Molecular genetics of human prion diseases in Germany
-
O Windl A Giese W Schulz-Schaeffer 1999 Molecular genetics of human prion diseases in Germany Hum Genet 105 244 252
-
(1999)
Hum Genet
, vol.105
, pp. 244-252
-
-
Windl, O.1
Giese, A.2
Schulz-Schaeffer, W.3
-
28
-
-
65749320253
-
The theory of cline
-
J.B.S Haldane 1948 The theory of cline J. Genet 48 277 284
-
(1948)
J. Genet
, vol.48
, pp. 277-284
-
-
Haldane, B.S.1
-
29
-
-
0016614695
-
Conditions for the existence of clines
-
T Nagylaki 1975 Conditions for the existence of clines Genetics 3 595 615
-
(1975)
Genetics
, vol.3
, pp. 595-615
-
-
Nagylaki, T.1
-
30
-
-
0027831931
-
Human genomic diversity in Europe:a summary of recent research and prospects for the future
-
1
-
LL Cavalli-Sforza A Piazza 1993 Human genomic diversity in Europe:a summary of recent research and prospects for the future Eur J Genet. 1 1 3 18
-
(1993)
Eur J Genet.
, vol.1
, pp. 3-18
-
-
Cavalli-Sforza, L.L.1
Piazza, A.2
-
32
-
-
0032891297
-
Autosomal, mitochondrial and Y chromosome DNA variation in Finland: Evidence for a male-specific bottleneck
-
RA Kittles AW Bergen M Urbanek 1999 Autosomal, mitochondrial and Y chromosome DNA variation in Finland: evidence for a male-specific bottleneck Am J Phys Anthropol. 108 381 399
-
(1999)
Am J Phys Anthropol.
, vol.108
, pp. 381-399
-
-
Kittles, R.A.1
Bergen, A.W.2
Urbanek, M.3
|