1 - 25 of 449 results for uniprot:P04156 in Computationally mapped citations
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| Polymorphism at codon 129 of the prion protein gene is not associated with sporadic AD. Combarros O., Sanchez-Guerra M., Llorca J., Alvarez-Arcaya A., Berciano J., Pena N., Fernandez-Viadero C. Neurology 55:593-595(2000) GAD 133180 · Mapped (19) |
| Does PRNP gene control the clinical and pathological phenotype of human spongiform transmissible encephalopathies? Masullo C., Macchi G. Clin. Neuropathol. 20:19-25(2001) GAD 133203 GeneRIF 5621 · Mapped (19) |
| Lack of evidence to support the association of the human prion gene with schizophrenia. Tsai M.T., Su Y.C., Chen Y.H., Chen C.H. Mol. Psychiatry 6:74-78(2001) GAD 133204 GAD 133174 GeneRIF 5621 · Mapped (19) |
| Influence of the prion protein and the apolipoprotein E genotype on the Creutzfeldt-Jakob Disease phenotype. Van Everbroeck B., Croes E.A., Pals P., Dermaut B., Jansen G., van Duijn C.M., Cruts M., Van Broeckhoven C., Martin J.J., Cras P. Neurosci. Lett. 313:69-72(2001) GAD 133214 GeneRIF 5621 · Mapped (24) |
| Sporadic--but not variant--Creutzfeldt-Jakob disease is associated with polymorphisms upstream of PRNP exon 1. Mead S., Mahal S.P., Beck J., Campbell T., Farrall M., Fisher E., Collinge J. Am. J. Hum. Genet. 69:1225-1235(2001) GAD 133181 GeneRIF 5621 · Mapped (19) |
| Methionine homozygosity at codon 129 in the prion protein is associated with white matter reduction and enlargement of CSF compartments in healthy volunteers and schizophrenic patients. Rujescu D., Meisenzahl E.M., Giegling I., Kirner A., Leinsinger G., Hegerl U., Hahn K., Moller H.J. Neuroimage 15:200-206(2002) GAD 133179 · Mapped (19) |
| Polymorphism at codon 174 of the prion-like protein gene is not associated with sporadic Alzheimer's disease. Infante J., Llorca J., Rodero L., Palacio E., Berciano J., Combarros O. Neurosci. Lett. 332:213-215(2002) GAD 133182 GAD 133194 GeneRIF 5621 · Mapped (19) |
| Creutzfeldt-Jakob disease associated with a deletion of two repeats in the prion protein gene. Capellari S., Parchi P., Wolff B.D., Campbell J., Atkinson R., Posey D.M., Petersen R.B., Gambetti P. Neurology 59:1628-1630(2002) GAD 133177 · Mapped (19) |
| Early cognitive decline is associated with prion protein codon 129 polymorphism. Croes E.A., Dermaut B., Houwing-Duistermaat J.J., Van den Broeck M., Cruts M., Breteler M.M., Hofman A., van Broeckhoven C., van Duijn C.M. Ann. Neurol. 54:275-276(2003) GAD 133187 · Mapped (19) |
| Polymorphisms of the prion protein gene (PRNP) in a Korean population. Jeong B.H., Nam J.H., Lee Y.J., Lee K.H., Jang M.K., Carp R.I., Lee H.D., Ju Y.R., Ahn Jo S., Park K.Y. et al. J. Hum. Genet. 49:319-324(2004) GAD 133197 GeneRIF 5621 · UniProtKB (2) · Mapped (17) |
| Cognitive performance of patients with mesial temporal lobe epilepsy is not associated with human prion protein gene variant allele at codons 129 and 171. Coimbra E.R., Rezek K., Escorsi-Rosset S., Landemberger M.C., Castro R.M., Valadao M.N., Guarnieri R., Velasco T.R., Terra-Bustamante V.C., Bianchin M.M. et al. Epilepsy Behav 8:635-642(2006) GAD 152845 GeneRIF 5621 · Mapped (19) |
| Inherited Creutzfeldt-Jakob disease in a British family associated with a novel 144 base pair insertion of the prion protein gene. Nicholl D., Windl O., de Silva R., Sawcer S., Dempster M., Ironside J.W., Estibeiro J.P., Yuill G.M., Lathe R., Will R.G. J. Neurol. Neurosurg. Psychiatr. 58:65-69(1995) GAD 133178 · Mapped (19) |
| Deletions in the prion protein gene are not associated with CJD. Palmer M.S., Mahal S.P., Campbell T.A., Hill A.F., Sidle K.C., Laplanche J.L., Collinge J. Hum. Mol. Genet. 2:541-544(1993) GAD 133176 · Mapped (19) |
| The D178N (cis-129M) "fatal familial insomnia" mutation associated with diverse clinicopathologic phenotypes in an Australian kindred. McLean C.A., Storey E., Gardner R.J., Tannenberg A.E., Cervenakova L., Brown P. Neurology 49:552-558(1997) GAD 133191 · Mapped (19) |
| Increased susceptibility to Kuru of carriers of the PRNP 129 methionine/methionine genotype. Lee H.S., Brown P., Cervenakova L., Garruto R.M., Alpers M.P., Gajdusek D.C., Goldfarb L.G. J. Infect. Dis. 183:192-196(2001) GeneRIF 5621 · Mapped (19) |
| All or none fibrillogenesis of a prion peptide. Zou W.Q., Yang D.S., Fraser P.E., Cashman N.R., Chakrabartty A. Eur. J. Biochem. 268:4885-4891(2001) GeneRIF 5621 · Mapped (19) |
| Codon 129 polymorphism of the PRNP gene in normal Polish population and in Creutzfeldt-Jakob disease, and the search for new mutations in PRNP gene. Bratosiewicz J., Liberski P.P., Kulczycki J., Kordek R. Acta Neurobiol Exp (Wars) 61:151-156(2001) GeneRIF 5621 · Mapped (19) |
| Huntington disease phenocopy is a familial prion disease. Moore R.C., Xiang F., Monaghan J., Han D., Zhang Z., Edstrom L., Anvret M., Prusiner S.B. Am. J. Hum. Genet. 69:1385-1388(2001) GeneRIF 5621 · Mapped (19) |
| Cellular phenotyping of secretory and nuclear prion proteins associated with inherited prion diseases. Lorenz H., Windl O., Kretzschmar H.A. J. Biol. Chem. 277:8508-8516(2002) GeneRIF 5621 · Mapped (25) |
| Molecular dynamics simulations of wild-type and point mutation human prion protein at normal and elevated temperature. el-Bastawissy E., Knaggs M.H., Gilbert I.H. J. Mol. Graph. Model. 20:145-154(2001) GeneRIF 5621 · Mapped (19) |
| The cellular prion protein: a new partner of the lectin CBP70 in the nucleus of NB4 human promyelocytic leukemia cells. Rybner C., Finel-Szermanski S., Felin M., Sahraoui T., Rousseau C., Fournier J.G., Seve A.P., Botti J. J. Cell. Biochem. 84:408-419(2002) GeneRIF 5621 · Mapped (19) |
| Rapid typing of the codon 129 polymorphism of the human prion protein gene by combined real-time PCR and melting curve analysis. Schalasta G., Roth B., Enders G. Clin. Lab. 48:25-30(2002) GeneRIF 5621 · Mapped (19) |
| Distribution of the M129V polymorphism of the prion protein gene in a Turkish population suggests a high risk for Creutzfeldt-Jakob disease. Erginel-Unaltuna N., Peoc'h K., Komurcu E., Acuner T.T., Issever H., Laplanche J.L. Eur. J. Hum. Genet. 9:965-968(2001) GeneRIF 5621 · Mapped (19) |
| Cellular prion protein is expressed on endothelial cells and is released during apoptosis on membrane microparticles found in human plasma. Simak J., Holada K., D'Agnillo F., Janota J., Vostal J.G. Transfusion 42:334-342(2002) GeneRIF 5621 · Mapped (19) |
| All-trans retinoic acid down-regulates prion protein expression independently of granulocyte maturation. Rybner C., Hillion J., Sahraoui T., Lanotte M., Botti J. Leukemia 16:940-948(2002) GeneRIF 5621 · Mapped (19) |