CiteULike: applebyb's prion_disease [15 articles]

Molecular model of prion transmission to humans.

Emerging infectious diseases, Vol. 15, No. 12. (December 2009), pp. 2013-2016.

by Michael Jones, Darren Wight, Rona Barron, et al.Martin Jeffrey, Jean Manson, Christopher Prowse, James W. Ironside, Mark W. Head

posted to transmission prion_disease molecular_model by applebyb on 2009-12-10 16:05:46 as

Synthesis of Monomeric and Dimeric Acridine Compounds as Potential Therapeutics in Alzheimer and Prion Diseases.

Archiv der Pharmazie (6 November 2009)

by René Csuk, Alexander Barthel, Christian Raschke, et al.Ralph Kluge, Dieter Ströhl, Lothar Trieschmann, Gerald Böhm

posted to therapy prion_disease alzheimers_disease acridine by applebyb on 2009-11-11 13:10:01 as

Changes in Sympathetic Activity in Prion Neuroinvasion.

Neurobiology of disease (2 October 2009)

by Gianpietro Bondiolotti, Giuseppe Rossoni, Maria Puricelli, et al.Elena Formentin, Barbara Lucchini, Giorgio Poli, Wilma Ponti, Silvio R. Bareggi

posted to prion_disease prion pathogenesis by applebyb on 2009-10-09 12:41:14 as

Electroretinograms in three cases of Creutzfeldt-Jakob disease with visual disturbances

Japanese Journal of Ophthalmology, Vol. 53, No. 1. (1 January 2009), pp. 31-34.

by Akira Ishikawa, Atsuhiro Tanikawa, Yoshiaki Shimada, Tatsuro Mutoh, Hiroko Yamamoto, Masayuki Horiguchi

posted to cjd phenotype prion_disease by applebyb on 2009-02-06 19:24:41 as

Familial Creutzfeldt-Jakob disease presenting as epilepsia partialis continua.

Epileptic disorders : international epilepsy journal with videotape, Vol. 10, No. 4. (18 November 2008), pp. 271-275.

by Max R R. Lowden, Kevin Scott, Milind J J. Kothari

posted to cjd diagnosis gcjd genetics phenotype prion_disease by applebyb on 2008-11-21 14:45:47 as read

Fluorine 18-labeled fluorodeoxyglucose positron emission tomography in familial Creutzfeldt-Jakob disease.

Archives of neurology, Vol. 65, No. 10. (October 2008), pp. 1390-1391.

by D. Renard, L. Collombier, G. Castelnovo, A. Remy, J. L. Laplanche, P. Labauge

posted to cjd gcjd neuroimaging pet prion_disease by applebyb on 2008-11-21 14:42:37 as

A novel insertional mutation in the prion protein gene: clinical and bio-molecular findings.

Journal of neurology, neurosurgery, and psychiatry, Vol. 79, No. 12. (December 2008), pp. 1395-1398.

by C. Mauro, G. Giaccone, G. Piscosquito, et al.A. Lavorgna, M. Nigro, G. Di Fede, A. Leonardi, C. Coppola, S. Formisano, F. Tagliavini, R. Cotrufo, G. Puoti

posted to genetics prion_disease prnp by applebyb on 2008-11-21 14:38:55 as read

Heightened incidence of sporadic Creutzfeldt-Jakob disease is associated with a shift in clinicopathological profiles

Journal of Neurology, Vol. 255, No. 10. (1 October 2008), pp. 1464-1472.

by Katharina Stoeck, Klaus Hess, Lorenz Amsler, et al.Tobias Eckert, Dieter Zimmermann, Adriano Aguzzi, Markus Glatzel

posted to cjd phenotype prion_disease scjd by applebyb on 2008-11-21 14:37:22 as read

Infectious nucleic acids in prion disease: halfway there

Trends in Biochemical Sciences (06 November 2008)

by R. Radulescu, B. Brenig

posted to nucleic_acid prion_disease by applebyb on 2008-11-21 14:33:39 as

along with 1 person reyez

An unusually presenting case of sCJD-The VV1 subtype.

Clinical neurology and neurosurgery (6 November 2008)

by Kaloyan S S. Tanev, Mimi Yilma

posted to cjd molecular_subtype phenotype prion_disease scjd vv1 by applebyb on 2008-11-21 14:33:03 as read

Human platelets as a substrate source for the in vitro amplification of the abnormal prion protein (PrP) associated with variant Creutzfeldt-Jakob disease.

Transfusion (29 October 2008)

by Michael Jones, Alexander H H. Peden, Helen Yull, et al.Darren Wight, Matthew T T. Bishop, Chris V V. Prowse, Marc L L. Turner, James W W. Ironside, Ian R R. Macgregor, Mark W W. Head

posted to cjd platelets prion prion_disease by applebyb on 2008-11-21 14:26:20 as

Creutzfeldt-Jakob disease presenting with visual manifestations.

Canadian journal of ophthalmology. Journal canadien d'ophtalmologie, Vol. 43, No. 5. (October 2008), pp. 591-595.

by A. A. Proulx, M. J. Strong, D. A. Nicolle

posted to cjd heidenhain phenotype prion_disease by applebyb on 2008-11-21 14:25:47 as read

Effects of human PrPSc type and PRNP genotype in an in-vitro conversion assay.

Neuroreport (24 October 2008)

by Michael Jones, Alexander H. Peden, Darren Wight, et al.Christopher Prowse, Ian Macgregor, Jean Manson, Marc Turner, James W. Ironside, Mark W. Head

posted to phenotype prion_disease prnp protein prpsc by applebyb on 2008-11-21 14:16:55 as

Detection of infectious prions in urine.

FEBS letters (12 August 2008)

by Dennisse Gonzalez-Romero, Marcelo A A. Barria, Patricia Leon, Rodrigo Morales, Claudio Soto

posted to prion_disease urine by applebyb on 2008-08-26 02:26:04 as read

Lactoferrin induces cell surface retention of prion protein and inhibits prion accumulation.

Journal of neurochemistry (20 August 2008)

by Yoshifumi Iwamaru, Yoshihisa Shimizu, Morikazu Imamura, et al.Yuichi Murayama, Ryo Endo, Yuichi Tagawa, Yuko Ushiki-Kaku, Takato Takenouchi, Hiroshi Kitani, Shirou Mohri, Takashi Yokoyama, Hiroyuki Okada

posted to lactoferrin prion_disease therapy by applebyb on 2008-08-26 02:13:13 as

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	Molecular model of prion transmission to humans. [My Copy] Emerging infectious diseases, Vol. 15, No. 12. (December 2009), pp. 2013-2016. by Michael Jones, Darren Wight, Rona Barron, et al.Martin Jeffrey, Jean Manson, Christopher Prowse, James W. Ironside, Mark W. Head posted to transmission prion_disease molecular_model by applebyb on 2009-12-10 16:05:46 as
	Synthesis of Monomeric and Dimeric Acridine Compounds as Potential Therapeutics in Alzheimer and Prion Diseases. [My Copy] Archiv der Pharmazie (6 November 2009) by René Csuk, Alexander Barthel, Christian Raschke, et al.Ralph Kluge, Dieter Ströhl, Lothar Trieschmann, Gerald Böhm posted to therapy prion_disease alzheimers_disease acridine by applebyb on 2009-11-11 13:10:01 as
	Changes in Sympathetic Activity in Prion Neuroinvasion. [My Copy] Neurobiology of disease (2 October 2009) by Gianpietro Bondiolotti, Giuseppe Rossoni, Maria Puricelli, et al.Elena Formentin, Barbara Lucchini, Giorgio Poli, Wilma Ponti, Silvio R. Bareggi posted to prion_disease prion pathogenesis by applebyb on 2009-10-09 12:41:14 as
	Electroretinograms in three cases of Creutzfeldt-Jakob disease with visual disturbances [My Copy] Japanese Journal of Ophthalmology, Vol. 53, No. 1. (1 January 2009), pp. 31-34. by Akira Ishikawa, Atsuhiro Tanikawa, Yoshiaki Shimada, Tatsuro Mutoh, Hiroko Yamamoto, Masayuki Horiguchi posted to cjd phenotype prion_disease by applebyb on 2009-02-06 19:24:41 as
	Familial Creutzfeldt-Jakob disease presenting as epilepsia partialis continua. [My Copy] Epileptic disorders : international epilepsy journal with videotape, Vol. 10, No. 4. (18 November 2008), pp. 271-275. by Max R R. Lowden, Kevin Scott, Milind J J. Kothari posted to cjd diagnosis gcjd genetics phenotype prion_disease by applebyb on 2008-11-21 14:45:47 as
	Fluorine 18-labeled fluorodeoxyglucose positron emission tomography in familial Creutzfeldt-Jakob disease. [My Copy] Archives of neurology, Vol. 65, No. 10. (October 2008), pp. 1390-1391. by D. Renard, L. Collombier, G. Castelnovo, A. Remy, J. L. Laplanche, P. Labauge posted to cjd gcjd neuroimaging pet prion_disease by applebyb on 2008-11-21 14:42:37 as
	A novel insertional mutation in the prion protein gene: clinical and bio-molecular findings. [My Copy] Journal of neurology, neurosurgery, and psychiatry, Vol. 79, No. 12. (December 2008), pp. 1395-1398. by C. Mauro, G. Giaccone, G. Piscosquito, et al.A. Lavorgna, M. Nigro, G. Di Fede, A. Leonardi, C. Coppola, S. Formisano, F. Tagliavini, R. Cotrufo, G. Puoti posted to genetics prion_disease prnp by applebyb on 2008-11-21 14:38:55 as
	Heightened incidence of sporadic Creutzfeldt-Jakob disease is associated with a shift in clinicopathological profiles [My Copy] Journal of Neurology, Vol. 255, No. 10. (1 October 2008), pp. 1464-1472. by Katharina Stoeck, Klaus Hess, Lorenz Amsler, et al.Tobias Eckert, Dieter Zimmermann, Adriano Aguzzi, Markus Glatzel posted to cjd phenotype prion_disease scjd by applebyb on 2008-11-21 14:37:22 as
	Infectious nucleic acids in prion disease: halfway there [My Copy] Trends in Biochemical Sciences (06 November 2008) by R. Radulescu, B. Brenig posted to nucleic_acid prion_disease by applebyb on 2008-11-21 14:33:39 as along with 1 person reyez
	An unusually presenting case of sCJD-The VV1 subtype. [My Copy] Clinical neurology and neurosurgery (6 November 2008) by Kaloyan S S. Tanev, Mimi Yilma posted to cjd molecular_subtype phenotype prion_disease scjd vv1 by applebyb on 2008-11-21 14:33:03 as
	Human platelets as a substrate source for the in vitro amplification of the abnormal prion protein (PrP) associated with variant Creutzfeldt-Jakob disease. [My Copy] Transfusion (29 October 2008) by Michael Jones, Alexander H H. Peden, Helen Yull, et al.Darren Wight, Matthew T T. Bishop, Chris V V. Prowse, Marc L L. Turner, James W W. Ironside, Ian R R. Macgregor, Mark W W. Head posted to cjd platelets prion prion_disease by applebyb on 2008-11-21 14:26:20 as
	Creutzfeldt-Jakob disease presenting with visual manifestations. [My Copy] Canadian journal of ophthalmology. Journal canadien d'ophtalmologie, Vol. 43, No. 5. (October 2008), pp. 591-595. by A. A. Proulx, M. J. Strong, D. A. Nicolle posted to cjd heidenhain phenotype prion_disease by applebyb on 2008-11-21 14:25:47 as
	Effects of human PrPSc type and PRNP genotype in an in-vitro conversion assay. [My Copy] Neuroreport (24 October 2008) by Michael Jones, Alexander H. Peden, Darren Wight, et al.Christopher Prowse, Ian Macgregor, Jean Manson, Marc Turner, James W. Ironside, Mark W. Head posted to phenotype prion_disease prnp protein prpsc by applebyb on 2008-11-21 14:16:55 as
	Detection of infectious prions in urine. [My Copy] FEBS letters (12 August 2008) by Dennisse Gonzalez-Romero, Marcelo A A. Barria, Patricia Leon, Rodrigo Morales, Claudio Soto posted to prion_disease urine by applebyb on 2008-08-26 02:26:04 as
	Lactoferrin induces cell surface retention of prion protein and inhibits prion accumulation. [My Copy] Journal of neurochemistry (20 August 2008) by Yoshifumi Iwamaru, Yoshihisa Shimizu, Morikazu Imamura, et al.Yuichi Murayama, Ryo Endo, Yuichi Tagawa, Yuko Ushiki-Kaku, Takato Takenouchi, Hiroshi Kitani, Shirou Mohri, Takashi Yokoyama, Hiroyuki Okada posted to lactoferrin prion_disease therapy by applebyb on 2008-08-26 02:13:13 as

applebyb's prion_disease [15 articles] Export Sort

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prion	276
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