Autoren-Indexdatei meiner TSE-Literatur-Datenbank

File of the authors index for my TSE-Literature-Collection

Bosque,P.

AWVW - Anderson,C.A.; Bosque,P.; Filley,C.M.; Arciniegas,D.B.; Kleinschmidt-DeMasters,B.K.; Pape,W.J.; Tyler,K.L. - Colorado surveillance program for chronic wasting disease transmission to humans: lessons from 2 highly suspicious but negative cases. - Archives of Neurology 2007 Mar; 64(3): 439-41

Bosque,P.J.

ATZF - Bosque,P.J. - Molecular types of Creutzfeldt-Jakob disease: the strange diversity of prions. - Neurology 2005 Nov 22; 65(10): 1520-1

ABNJ - Bosque,P.J. - Bovine spongiform encephalopathy, chronic wasting disease, scrapie, and the threat to humans from prion disease epizootics - Current Neurology and Neuroscience Reports 2002 Nov; 2(6): 488-95

ABNK - Bosque,P.J.; Ryou,C.; Telling,G.; Peretz,D.; Legname,G.; DeArmond,S.J.; Prusiner,S.B. - Prions in skeletal muscle - Proceedings of the National Academy of Sciences of the United States of America 2002 Mar 19; 99(6): 3812-7

ABNL - Bosque,P.J.; Prusiner,S.B. - Cultured cell sublines highly susceptible to prion infection - Journal of Virology 2000 May; 74(9): 4377-86

AODW - Bosque,P.J.; Telling,G.C.; Cayetano-Canlas,J.; DeArmond,S.J.; Prusiner,S.B. - Evidence for prion replication in skeletal-muscle - Annals of Neurology 1997; 42(N6): 1

ANZZ - Bosque,P.J.; Telling,G.C.; Westaway,D.; Cayetano-Canlas,J.; DeArmond,S.J.; Prusiner,S.B. - Prion protein overexpression exclusively in skeletal-muscle causes spontaneous myopathy - Neurology 1996; 46(N2): S73.006

AOAA - Bosque,P.J.; Telling,G.; Hanahan,D.; Prusiner,S.B. - Ectopic expression of the prion protein directed by the insulin gene promoter to the pancreas of transgenic mice - Neurology 1995; 45(N4): A 308

ABNM - Bosque,P.J.; Vnencak-Jones,C.L.; Johnson,M.D.; Whitlock,J.A.; McLean,M.J. - A PrP gene codon 178 base substitution and a 24-bp interstitial deletion in familial Creutzfeldt-Jakob disease - Neurology 1992 Oct; 42(10): 1864-70

AUAN - Hall,D.A.; Leehey,M.A.; Filley,C.M.; Steinbart,E.; Montine,T.; Schellenberg,G.D.; Bosque,P.J.; Nixon,R.; Bird,T.D. - PRNP H187R mutation associated with neuropsychiatric disorders in childhood and dementia - Neurology 2005 Apr 12; 64(7): 1304-6

AIAK - Mastrianni,J.A.; Capellari,S.; Telling,G.C.; Han,D.; Bosque,P.J.; Prusiner,S.B.; DeArmond,S.J. - Inherited prion disease caused by the V210I mutation: transmission to transgenic mice. - Neurology 2001 Dec 26; 57(12): 2198-205

AVXO - MaWhinney,S.; Pape,W.J.; Forster,J.E.; Anderson,C.A.; Bosque,P.J.; Miller,M.W. - Human prion disease and relative risk associated with chronic wasting disease - Emerging Infectious Diseases 2006 Oct; 12(10): 1527-35

AKNS - Schmitt-Ulms,G.; Legname,G.; Baldwin,M.A.; Ball,H.L.; Bradon,N.; Bosque,P.J.; Crossin,K.L.; Edelman,G.M.; DeArmond,S.J.; Cohen,F.E.; Prusiner,S.B. - Binding of neural cell adhesion molecules (N-CAMs) to the cellular prion protein - Journal of Molecular Biology 2001 Dec 14; 314(5): 1209-25

ALGW - Supattapone,S.; Bosque,P.J.; Muramoto,T.; Wille,H.; Aagaard,C.; Peretz,D.; Nguyen,H.O.B.; Heinrich,C.; Torchia,M.; Safar,J.G.; Cohen,F.E.; DeArmond,S.J.; Prusiner,S.B.; Scott,M.R.D. - Prion protein of 106 residues creates an artifical transmission barrier for prion replication in transgenic mice - Cell 1999 Mar 19; 96(6): 869-78

AWOP - Tamgüney,G.; Giles,K.; Bosque,P.J.; Miller,M.W.; Safar,J.G.; DeArmond,S.J.; Prusiner,S.B. - Transmission of CWD to transgenic mice - International Conference - Prion 2006: Strategies, advances and trends towards protection of society - 3.10.-6.10.2006, Torino, Italy, Lingotto Conference Centre - Poster sessions PR-32

AVGQ - Tamgüney,G.; Giles,K.; Bouzamondo-Bernstein,E.; Bosque,P.J.; Miller,M.W.; Safar,J.G.; DeArmond,S.J.; Prusiner,S.B. - Transmission of elk and deer prions to transgenic mice - Journal of Virology 2006 Sep; 80(18): 9104-14

ALVV - Ulm,J.E.; Vnencak-Jones,C.L.; Bosque,P.J. - Research on familial Creutzfeldt-Jakob disease (FCJD) resulting in presymptomatic testing: implications for the Human Genome Project. - Journal of Genetic Counseling 1993 Mar; 2(1): 9-15

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