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Publications about 'genetics'
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J L Laplanche,
V Lepage,
K Peoc'h,
N Delasnerie-Laupretre,
and D Charron.
HLA in French patients with variant Creutzfeldt-Jakob disease.
Lancet,
361(9356):531-2,
February 2003.
Keywords:
Alleles,
Creutzfeldt-Jakob Syndrome,
genetics,
France,
Gene Frequency,
HLA-DQ Antigens,
genetics,
Histocompatibility Antigens Class II,
genetics,
Histocompatibility Testing,
Human,
Tumor Necrosis Factor,
genetics.
[bibtex-entry]
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Azra C Ghani,
Christl A Donnelly,
Neil M Ferguson,
and Roy M Anderson.
The transmission dynamics of BSE and vCJD.
C R Acad Sci III,
325(1):37-47,
January 2002.
Keywords:
Age Factors,
Animal,
Cattle,
Creutzfeldt-Jakob Syndrome,
epidemiology,
Encephalopathy Bovine Spongiform,
epidemiology,
Europe,
epidemiology,
Great Britain,
epidemiology,
Human,
Meat,
Northern Ireland,
epidemiology,
Prions,
genetics,
Support Non-U.S. Gov't.
[Abstract] [bibtex-entry]
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Kurt Krapfenbauer,
Byong Chul Yoo,
Michael Fountoulakis,
Eva Mitrova,
and Gert Lubec.
Expression patterns of antioxidant proteins in brains of patients with sporadic Creutzfeldt-Jacob disease.
Electrophoresis,
23(15):2541-7,
August 2002.
Keywords:
Aged,
Antioxidants,
isolation & purification,
Blotting Western,
Case-Control Studies,
Creutzfeldt-Jakob Syndrome,
genetics,
Electrophoresis Gel Two-Dimensional,
methods,
Female,
Gene Expression,
Human,
Male,
Middle Age,
Nerve Tissue Proteins,
genetics,
Peroxidases,
genetics,
Spectrometry Mass Matrix-Assisted Laser Desorption-Ionization,
Support Non-U.S. Gov't.
[Abstract] [bibtex-entry]
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Sylvain Lehmann.
[The prion protein].
J Soc Biol,
196(4):309-12,
2002.
Keywords:
Animal,
Cattle,
English Abstract,
Glycosylphosphatidylinositols,
Human,
Mice,
Mice Transgenic,
Neurons,
metabolism,
Nuclear Magnetic Resonance Biomolecular,
PrPC Proteins,
chemistry,
PrPSc Proteins,
metabolism,
Prion Diseases,
genetics,
Protein Conformation,
Protein Structure Tertiary,
Scrapie,
genetics,
Sheep,
Signal Transduction,
Structure-Activity Relationship.
[Abstract] [bibtex-entry]
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A J Thompson,
K J Barnham,
R S Norton,
and C J Barrow.
The Val-210-Ile pathogenic Creutzfeldt-Jakob disease mutation increases both the helical and aggregation propensities of a sequence corresponding to helix-3 of PrP(C).
Biochim Biophys Acta,
1544(1-2):242-54,
January 2001.
Keywords:
Amino Acid Sequence,
Circular Dichroism,
Creutzfeldt-Jakob Syndrome,
genetics,
Isoleucine,
genetics,
Molecular Sequence Data,
Mutation,
Nuclear Magnetic Resonance Biomolecular,
Phosphoprotein Phosphatase,
chemistry,
Protein Structure Secondary,
Support Non-U.S. Gov't,
Valine,
genetics.
[Abstract] [bibtex-entry]
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Last modified: Fri Jun 6 11:58:11 2003
Author: mlingura.
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