(Q28210578)

2

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Lucía Rodero

3

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Enrique Palacio

4

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José Berciano

5

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Onofre Combarros

Codon 129 prion protein genotype and sporadic Creutzfeldt-Jakob disease

6

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language of work or name

English

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publication date

8 November 2002

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published in

Neuroscience Letters

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volume

332

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issue

3

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page(s)

213-5

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cites work

1 reference

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7 January 2021

Small is not beautiful: antagonizing functions for the prion protein PrP(C) and its homologue Dpl.

1 reference

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7 January 2021

Prion protein gene polymorphism and Alzheimer's disease: one modulatory trait of cognitive decline?

1 reference

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7 January 2021

Polymorphism at codon 129 of the prion protein gene is not associated with sporadic AD

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7 January 2021

Medicine: danger--misfolding proteins.

1 reference

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7 January 2021

The prion gene complex encoding PrP(C) and Doppel: insights from mutational analysis

1 reference

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7 January 2021

Examination of the human prion protein-like gene doppel for genetic susceptibility to sporadic and variant Creutzfeldt-Jakob disease

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7 January 2021

Two different neurodegenerative diseases caused by proteins with similar structures

1 reference

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7 January 2021

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

1 reference

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7 January 2021

First report of polymorphisms in the prion-like protein gene (PRND): implications for human prion diseases

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7 January 2021

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Onset of ataxia and Purkinje cell loss in PrP null mice inversely correlated with Dpl level in brain

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7 January 2021

Polymorphisms within the prion-like protein gene (Prnd) and their implications in human prion diseases, Alzheimer's disease and other neurological disorders

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7 January 2021

Chaperoning brain diseases.

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7 January 2021

Mammalian prion proteins: enigma, variation and vaccination

1 reference

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7 January 2021

Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP gene.

1 reference

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