Bibliography about the Prion Protein family (161 articles)
Add article(s) associated with Prion Protein family
- Identification of prion protein gene polymorphisms in goats from Italian scrapie outbreaks.
- Acutis P.L., Bossers A., Priem J. et al
2006, J. Gen. Virol. - Efficient transmission and characterization of creutzfeldt-jakob disease strains in bank voles.
- Nonno R., Di, Bari M.A. et al
2006, PLoS Pathog. (2) 0-0 - Prion protein NMR structures of chickens, turtles, and frogs.
- Calzolai L., Lysek D.A., Perez D.R. et al
2005, Proc. Natl. Acad. Sci. U.S.A. (102) 651-655 - Low frequency of PrP genotype 225SF among free-ranging mule deer (Odocoileus hemionus) with chronic wasting disease.
- Jewell J.E., Conner M.M., Wolfe L.L. et al
2005, J. Gen. Virol. (86) 2127-2134 - Prion protein NMR structures of cats, dogs, pigs, and sheep.
- Lysek D.A., Schorn C., Nivon L.G. et al
2005, Proc. Natl. Acad. Sci. U.S.A. (102) 640-645 - Polymorphisms of the prion protein gene (PRNP) in Chinese domestic sika deer (Cervus nippon hortulorum).
- Meng L.P., Zhao D.M., Liu H.X. et al
2005, Anim. Genet. (36) 266-267 - Comparative analysis of the prion protein open reading frame nucleotide sequences in peacock and parakeet.
- Yang J.M., Zhao D.M., Liu H.X. et al
2005, Virus Genes (30) 193-196 - Prion Protein gene polymorphisms in healthy and scrapie affected sheep in Greece.
- Billinis C., Psychas V., Leontides L. et al
2004, J. Gen. Virol. (85) 547-554 - A processed pseudogene contributes to apparent mule deer prion gene heterogeneity.
- Brayton K.A., O&apos, Rourke K.I. et al
2004, Gene (326) 167-173 - Accelerated evolution of nervous system genes in the origin of Homo sapiens.
- Dorus S., Vallender E.J., Evans P.D. et al
2004, Cell (119) 1027-1040 - Insight into the PrPC-->PrPSc conversion from the structures of antibody-bound ovine prion scrapie-susceptibility variants.
- Eghiaian F., Grosclaude J., Lesceu S. et al
2004, Proc. Natl. Acad. Sci. U.S.A. (101) 10254-10259 - The crystal structure of the globular domain of sheep prion protein.
- Haire L.F., Whyte S.M., Vasisht N. et al
2004, J. Mol. Biol. (336) 1175-1183 - Amino acid sequence of the Felis catus prion protein.
- Lysek D.A., Nivon L.G., Wuethrich K. et al
2004, Gene (341) 249-253 - Prion protein and New World primate phylogeny.
- Schneider I., Schneider H., Schneider M.P.C. et al
2004, Genet. Mol. Biol. - Prion protein gene (PRNP) variants and evidence for strong purifying selection in functionally important regions of bovine exon 3.
- Seabury C.M., Honeycutt R.L., Rooney A.P. et al
2004, Proc. Natl. Acad. Sci. U.S.A. (101) 15142-15147 - Polymorphisms of the PRNP gene in Chinese populations and the identification of a novel insertion mutation.
- Yu S.L., Jin L., Sy M.S. et al
2004, Eur. J. Hum. Genet. (12) 867-870 - PRNP polymorphisms in Chinese ovine, caprine and bovine breeds.
- Zhang L., Li N., Fan B. et al
2004, Anim. Genet. (35) 457-461 - Transmission of transmissible mink encephalopathy (TME) to raccoons (Procyon lotor) by intracerebral inoculation.
- Hamir A.N., Miller J.M., O&apos et al
2003, J. Vet. Diagn. Invest. - Transmission of transmissible mink encephalopathy (TME) to raccoons (Procyon lotor) by intracerebral inoculation.
- Hamir A.N., Miller J.M., O&apos et al
2003, J. Vet. Diagn. Invest. - Prion gene sequence variation within diverse groups of U.S. sheep, beef cattle, and deer.
- Heaton M.P., Leymaster K.A., Freking B.A. et al
2003, Mamm. Genome (14) 765-777 - Eight prion protein genotypes in white tailed deer with chronic wasting disease.
- O&apos, Rourke K.I., Spraker T.R. et al
2003, J. Gen. Virol. - Eight prion protein genotypes in white tailed deer with chronic wasting disease.
- O&apos, Rourke K.I., Spraker T.R. et al
2003, J. Gen. Virol. - Identification of a novel ovine PrP polymorphism and scrapie- resistant genotypes for St. Croix White and a related composite breed.
- Seabury C.M., Derr J.N.
2003, Cytogenet. Genome Res. (102) 85-88 - The PrP genotype of sheep of the improved Valachian breed.
- Tkacikova L., Hanusovska E., Novak M. et al
2003, Folia Microbiol. (Praha) (48) 269-276 - The octapeptide repeats in mammalian prion protein constitute a pH- dependent folding and aggregation site.
- Zahn R.
2003, J. Mol. Biol. (334) 477-488 - Molecular evolution of the mammalian prion protein.
- van, Rheede T., Smolenaars M.M. et al
2003, Mol. Biol. Evol. (20) 111-121 - Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.
- Strausberg R.L., Feingold E.A., Grouse L.H. et al
2002, Proc. Natl. Acad. Sci. U.S.A. (99) 16899-16903 - Cloning and sequencing of PrPc mature protein gene of Chinese yellow cattle.
- Wang Z., Wang C., Wu X. et al
2002, Zhongguo Dongwu Jianyi (19) 21-22 - Cloning and sequencing of PrPc mature protein gene of Chinese yellow cattle.
- Wang Z., Wang C., Wu X. et al
2002, Zhongguo Dongwu Jianyi (19) 21-22 - The DNA sequence and comparative analysis of human chromosome 20.
- Deloukas P., Matthews L.H., Ashurst J.L. et al
2001, Nature (414) 865-871 - Complete genomic sequence of the bovine prion gene (PRNP) and polymorphism in its promoter region.
- Hills D., Comincini S., Schlaepfer J. et al
2001, Anim. Genet. (32) 231-232 - A new PRNP mutation (G131V) associated with Gerstmann-Straussler- Scheinker disease.
- Panegyres P.K., Toufexis K., Kakulas B.A. et al
2001, Arch. Neurol. (58) 1899-1902 - Comparative analysis of the prion protein open reading frame nucleotide sequences of two wild ruminants, the moufflon and golden takin.
- Seo S.W., Hara K., Kubosaki A. et al
2001, Intervirology (44) 359-363 - PrP genotype in Sarda breed sheep and its relevance to scrapie.
- Vaccari G., Petraroli R., Agrimi U. et al
2001, Arch. Virol. (146) 2029-2037 - NMR structures of three single-residue variants of the human prion protein.
- Calzolai L., Lysek D.A., Guntert P. et al
2000, Proc. Natl. Acad. Sci. U.S.A. (97) 8340-8345 - High prevalence of pathogenic mutations in patients with early-onset dementia detected by sequence analyses of four different genes.
- Finckh U., Mueller-Thomsen T., Mann U. et al
2000, Am. J. Hum. Genet. (66) 110-117 - Post-translational hydroxylation at the N-terminus of the prion protein reveals presence of PPII structure in vivo.
- Gill A.C., Ritchie M.A., Hunt L.G. et al
2000, EMBO J. (19) 5324-5331 - NMR structure of the bovine prion protein.
- Lopez, Garcia F., Zahn R. et al
2000, Proc. Natl. Acad. Sci. U.S.A. (97) 8334-8339 - Preclinical diagnosis of scrapie by immunohistochemistry of third eyelid lymphoid tissue.
- O&apos, Rourke K.I., Baszler T.V. et al
2000, J. Clin. Microbiol. (38) 3254-3259 - Identification of three novel mutations (E196K, V203I, E211Q) in the prion protein gene (PRNP) in inherited prion diseases with Creutzfeldt-Jakob disease phenotype.
- Peoc&apos, h K., Manivet P. et al
2000, Hum. Mutat. (15) 482-482 - Evidence of a molecular barrier limiting susceptibility of humans, cattle and sheep to chronic wasting disease.
- Raymond G.J., Bossers A., Raymond L.D. et al
2000, EMBO J. (19) 4425-4430 - cDNA cloning of turtle prion protein.
- Simonic T., Duga S., Strumbo B. et al
2000, FEBS Lett. (469) 33-38 - NMR solution structure of the human prion protein.
- Zahn R., Liu A., Luhrs T. et al
2000, Proc. Natl. Acad. Sci. U.S.A. (97) 145-150 - Solution structure of the E200K variant of human prion protein. Implications for the mechanism of pathogenesis in familial prion diseases.
- Zhang Y., Swietnicki W., Zagorski M.G. et al
2000, J. Biol. Chem. (275) 33650-33654 - Novel PRNP sequence variant associated with familial encephalopathy.
- Cervenakova L., Buetefisch C., Lee H.S. et al
1999, Am. J. Med. Genet. (88) 653-656 - PrP (prion) gene expression in sheep may be modulated by alternative polyadenylation of its messenger RNA.
- Goldmann W., O&apos, Neill G. et al
1999, J. Gen. Virol. (80) 2275-2283 - Ataxia in prion protein (PrP)-deficient mice is associated with upregulation of the novel PrP-like protein doppel.
- Moore R.C., Lee I.Y., Silverman G.L. et al
1999, J. Mol. Biol. (292) 797-817 - PrP genotypes of captive and free-ranging Rocky Mountain elk (Cervus elaphus nelsoni) with chronic wasting disease.
- O&apos, Rourke K.I., Besser T.E. et al
1999, J. Gen. Virol. (80) 2765-2769 - PrP genotypes of captive and free-ranging Rocky Mountain elk (Cervus elaphus nelsoni) with chronic wasting disease.
- O&apos, Rourke K.I., Besser T.E. et al
1999, J. Gen. Virol. (80) 2765-2769 - Immune surveillance and antigen conformation determines humoral immune response to the prion protein immunogen.
- Rubenstein R., Kascsak R.J., Papini M. et al
1999, J. Neurovirol. (5) 401-413 - Molecular genetics of human prion diseases in Germany.
- Windl O., Giese A., Schulz-Schaeffer W. et al
1999, Hum. Genet. (105) 244-252 - Analysis of 27 mammalian and 9 avian PrPs reveals high conservation of flexible regions of the prion protein.
- Wopfner F., Weidenhofer G., Schneider R. et al
1999, J. Mol. Biol. (289) 1163-1178 - Complete genomic sequence and analysis of the prion protein gene region from three mammalian species.
- Lee I.Y., Westaway D., Smit A.F.A. et al
1998, Genome Res. (8) 1022-1037 - Monoclonal antibody F89/160.1.5 defines a conserved epitope on the ruminant prion protein.
- O&apos, Rourke K.I., Baszler T.V. et al
1998, J. Clin. Microbiol. (36) 1750-1755 - Phenotypic variability of Gerstmann-Straussler-Scheinker disease is associated with prion protein heterogeneity.
- Piccardo P., Dlouhy S.R., Lievens P.M. et al
1998, J. Neuropathol. Exp. Neurol. (57) 979-988 - High sequence homology of the PrP gene in mule deer and Rocky Mountain elk.
- Cervenakova L., Rohwer R., Williams S. et al
1997, Lancet (350) 219-220 - Structure of the recombinant full-length hamster prion protein PrP(29-231): the N terminus is highly flexible.
- Donne D.G., Viles J.H., Groth D. et al
1997, Proc. Natl. Acad. Sci. U.S.A. (94) 13452-13457 - Solution structure of a 142-residue recombinant prion protein corresponding to the infectious fragment of the scrapie isoform.
- James T.L., Liu H., Ulyanov N.B. et al
1997, Proc. Natl. Acad. Sci. U.S.A. (94) 10086-10091 - Sequencing analysis of prion genes from red deer and camel.
- Kaluz S., Kaluzova M., Flint A.P.F. et al
1997, Gene (199) 283-286 - Characterization of a prion protein (PrP) gene from rabbit; a species with apparent resistance to infection by prions.
- Loftus B., Rogers M.
1997, Gene (184) 215-219 - Familial spongiform encephalopathy associated with a novel prion protein gene mutation.
- Nitrini R., Rosemberg S., Passos-Bueno M.R. et al
1997, Ann. Neurol. (42) 138-146 - NMR characterization of the full-length recombinant murine prion protein, mPrP(23-231).
- Riek R., Hornemann S., Wider G. et al
1997, FEBS Lett. (413) 282-288 - A prion-linked psychiatric disorder.
- Samaia H.B., Mari J.J., Vallada H.P. et al
1997, Nature (390) 241-241 - Is codon 129 of prion protein polymorphic in human beings but not in animals?
- Schatzl H.M., Wopfner F., Gilch S. et al
1997, Lancet (349) 1603-1604 - Polymorphism at codon 129 or codon 219 of PRNP and clinical heterogeneity in a previously unreported family with Gerstmann- Straussler-Scheinker disease (PrP-P102L mutation).
- Barbanti P., Fabbrini G., Salvatore M. et al
1996, Neurology (47) 734-741 - PrP genotype contributes to determining survival times of sheep with natural scrapie.
- Bossers A., Schreuder B.E.C., Muileman I.H. et al
1996, J. Gen. Virol. (77) 2669-2673 - Novel polymorphisms in the caprine PrP gene: a codon 142 mutation associated with scrapie incubation period.
- Goldmann W., Martin T., Foster J. et al
1996, J. Gen. Virol. (77) 2885-2891 - Mutation of the prion protein gene at codon 208 in familial Creutzfeldt-Jakob disease.
- Mastrianni J.A., Iannicola C., Myers R.M. et al
1996, Neurology (47) 1305-1312 - NMR structure of the mouse prion protein domain PrP(121-321).
- Riek R., Hornemann S., Wider G. et al
1996, Nature (382) 180-182 - Three-exon structure of the gene encoding the rat prion protein and its expression in tissues.
- Saeki K., Matsumoto Y., Hirota Y. et al
1996, Virus Genes (12) 15-20 - Identification of five allelic variants of the sheep PrP gene and their association with natural scrapie.
- Belt P.B.G.M., Muileman I.H., Schreuder B.E.C. et al
1995, J. Gen. Virol. (76) 509-517 - Direct sequencing of PCR amplified pig PrP genes.
- Martin T., Hughes S., Hughes K. et al
1995, Biochim. Biophys. Acta (1270) 211-214 - Spongiform central nervous system myelinopathy in African dwarf goats.
- Obermaier G., Kretzschmar H.A., Hafner A. et al
1995, J. Comp. Pathol. (113) 357-372 - SSCP analysis and sequencing of the human prion protein gene (PRNP) detects two different 24 bp deletions in an atypical Alzheimer's disease family.
- Perry R.T., Go R.C., Harrell L.E. et al
1995, Am. J. Med. Genet. (60) 12-18 - Prion protein gene variation among primates.
- Schaetzl H.M., Da, Costa M. et al
1995, J. Mol. Biol. (245) 362-374 - A candidate marsupial PrP gene reveals two domains conserved in mammalian PrP proteins.
- Windl O., Dempster M., Estibeiro P. et al
1995, Gene (159) 181-186 - Gerstmann-Straussler-Scheinker disease with mutation at codon 102 and methionine at codon 129 of PRNP in previously unreported patients.
- Young K., Jones C.K., Piccardo P. et al
1995, Neurology (45) 1127-1134 - Transmissible mink encephalopathy species barrier effect between ferret and mink: PrP gene and protein analysis.
- Bartz J.C., McKenzie D.I., Bessen R.A. et al
1994, J. Gen. Virol. (75) 2947-2953 - Infectious amyloid precursor gene sequences in primates used for experimental transmission of human spongiform encephalopathy.
- Cervenakova L., Brown P., Goldfarb L.G. et al
1994, Proc. Natl. Acad. Sci. U.S.A. (91) 12159-12162 - Mutation in codon 200 and polymorphism in codon 129 of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease.
- Gabizon R., Rosenman H., Meiner Z. et al
1994, Philos. Trans. R. Soc. Lond., B, Biol. Sci. (343) 385-390 - Prion protein (PrP) is not involved in the pathogenesis of spongiform encephalopathy in zitter rats.
- Gomi H., Ikeda T., Kunieda T. et al
1994, Neurosci. Lett. (166) 171-174 - Japanese family with Creutzfeldt-Jakob disease with codon 200 point mutation of the prion protein gene.
- Inoue I., Kitamoto T., Doh-Ura K. et al
1994, Neurology (44) 299-301 - A variant of Gerstmann-Straussler-Scheinker disease carrying codon 105 mutation with codon 129 polymorphism of the prion protein gene: a clinicopathological study.
- Itoh Y., Yamada M., Hayakawa M. et al
1994, J. Neurol. Sci. (127) 77-86 - Homozygosity for prion protein alleles encoding glutamine-171 renders sheep susceptible to natural scrapie.
- Westaway D., Zuliani V., Cooper C.M. et al
1994, Genes Dev. (8) 959-969 - Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Straussler syndrome.
- Kitamoto T., Ohta M., Doh-Ura K. et al
1993, Biochem. Biophys. Res. Commun. (191) 709-714 - PrP polymorphisms associated with natural scrapie discovered by denaturing gradient gel electrophoresis.
- Laplanche J.L., Chatelain J., Westaway D. et al
1993, Genomics (15) 30-37 - Mutations and polymorphisms in the prion protein gene.
- Palmer M.S., Collinge J.
1993, Hum. Mutat. (2) 168-173 - A new point mutation of the prion protein gene in Creutzfeldt-Jakob disease.
- Pocchiari M., Salvatore M., Cutruzzola F. et al
1993, Ann. Neurol. (34) 802-807 - Genetic and infectious prion diseases.
- Prusiner S.B.
1993, Arch. Neurol. (50) 1129-1153 - Immunologic and molecular biologic studies of prion proteins in bovine spongiform encephalopathy.
- Prusiner S.B., Fuzi M., Scott M. et al
1993, J. Infect. Dis. (167) 602-613 - A missense mutation at codon 105 with codon 129 polymorphism of the prion protein gene in a new variant of Gerstmann-Straussler-Scheinker disease.
- Yamada M., Itoh Y., Fujigasaki H. et al
1993, Neurology (43) 2723-2724 - Deletion in the prion protein gene in a demented patient.
- Diedrich J.F., Knopman D.S., List J.F. et al
1992, Hum. Mol. Genet. (1) 443-444 - Molecular cloning of a candidate chicken prion protein.
- Gabriel J.M., Oesch B., Kretzschmar H. et al
1992, Proc. Natl. Acad. Sci. U.S.A. (89) 9097-9101 - Mutant prion proteins in Gerstmann-Straussler-Scheinker disease with neurofibrillary tangles.
- Hsiao K., Dlouhy S.R., Farlow M.R. et al
1992, Nat. Genet. (1) 68-71 - Molecular cloning of a mink prion protein gene.
- Kretzschmar H.A., Neumann M., Riethmueller G. et al
1992, J. Gen. Virol. (73) 2757-2761 - Fatal familial insomnia: a second kindred with mutation of prion protein gene at codon 178.
- Medori R., Montagna P., Tritschler H.J. et al
1992, Neurology (42) 669-670 - Comparative sequence analysis and expression of bovine PrP gene in mouse L-929 cells.
- Yoshimoto J., Iinuma T., Ishiguro N. et al
1992, Virus Genes (6) 343-356 - Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene.
- Goldfarb L.G., Brown P., McCombie W.R. et al
1991, Proc. Natl. Acad. Sci. U.S.A. (88) 10926-10930 - New mutation in scrapie amyloid precursor gene (at codon 178) in Finnish Creutzfeldt-Jakob kindred.
- Goldfarb L.G., Haltia M., Brown P. et al
1991, Lancet (337) 425-425 - Different scrapie-associated fibril proteins (PrP) are encoded by lines of sheep selected for different alleles of the Sip gene.
- Goldmann W., Hunter N., Benson G. et al
1991, J. Gen. Virol. (72) 2411-2417 - Different forms of the bovine PrP gene have five or six copies of a short, G-C-rich element within the protein-coding exon.
- Goldmann W., Hunter N., Martin T. et al
1991, J. Gen. Virol. (72) 201-204 - A prion-like protein from chicken brain copurifies with an acetylcholine receptor-inducing activity.
- Harris D.A., Falls D.L., Johnson F.A. et al
1991, Proc. Natl. Acad. Sci. U.S.A. (88) 7664-7668 - Genomic structure of the human prion protein gene.
- Puckett C., Concannon P., Casey C. et al
1991, Am. J. Hum. Genet. (49) 320-329 - Amyloid protein of Gerstmann-Straussler-Scheinker disease (Indiana kindred) is an 11 kd fragment of prion protein with an N-terminal glycine at codon 58.
- Tagliavini F., Prelli F., Ghiso J. et al
1991, EMBO J. (10) 513-519 - Mr 42,000 ARIA: a protein that may regulate the accumulation of acetylcholine receptors at developing chick neuromuscular junctions.
- Falls D.L., Harris D.A., Johnson F.A. et al
1990, Cold Spring Harb. Symp. Quant. Biol. (55) 397-406 - Mutation in codon 200 of scrapie amyloid protein gene in two clusters of Creutzfeldt-Jakob disease in Slovakia.
- Goldfarb L., Mitrova E., Brown P. et al
1990, Lancet (336) 514-515 - Two alleles of a neural protein gene linked to scrapie in sheep.
- Goldmann W., Hunter N., Foster J.D. et al
1990, Proc. Natl. Acad. Sci. U.S.A. (87) 2476-2480 - Three hamster species with different scrapie incubation times and neuropathological features encode distinct prion proteins.
- Lowenstein D.H., Butler D.A., Westaway D. et al
1990, Mol. Cell. Biol. (10) 1153-1163 - Intracellular accumulation of the cellular prion protein after mutagenesis of its Asn-linked glycosylation sites.
- Rogers M., Taraboulos A., Scott M. et al
1990, Glycobiology (1) 101-109 - Identification of glycoinositol phospholipid linked and truncated forms of the scrapie prion protein.
- Stahl N., Baldwin M.A., Burlingame A.L. et al
1990, Biochemistry (29) 8879-8884 - Pro-->Leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Straussler syndrome.
- Doh-Ura K., Tateishi J., Sasaki H. et al
1989, Biochem. Biophys. Res. Commun. (163) 974-979 - Linkage of a prion protein missense variant to Gerstmann-Straussler syndrome.
- Hsiao K., Baker H.F., Crow T.J. et al
1989, Nature (338) 342-345 - Molecular pathology of scrapie-associated fibril protein (PrP) in mouse brain affected by the ME7 strain of scrapie.
- Hope J., Multhaup G., Reekie L.J.D. et al
1988, Eur. J. Biochem. (172) 271-277 - Fibrils from brains of cows with new cattle disease contain scrapie- associated protein.
- Hope J., Reekie L.J.D., Hunter N. et al
1988, Nature (336) 390-392 - Purification and properties of the cellular and scrapie hamster prion proteins.
- Turk E., Teplow D.B., Hood L.E. et al
1988, Eur. J. Biochem. (176) 21-30 - Cloning of rat 'prion-related protein' cDNA.
- Liao Y.-C., Tokes Z., Lim E. et al
1987, Lab. Invest. (57) 370-374 - Scrapie prion protein contains a phosphatidylinositol glycolipid.
- Stahl N., Borchelt D.R., Hasiao K. et al
1987, Cell (51) 229-240 - Distinct prion proteins in short and long scrapie incubation period mice.
- Westaway D., Goodman P.A., Mirenda C.A. et al
1987, Cell (51) 651-662 - Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene.
- Basler K., Oesch B., Scott M. et al
1986, Cell (46) 417-428 - Molecular cloning of a human prion protein cDNA.
- Kretzschmar H.A., Stowring L.E., Westaway D. et al
1986, DNA (5) 315-324 - Human prion protein cDNA: molecular cloning, chromosomal mapping, and biological implications.
- Liao Y.-C.J., Lebo R.V., Clawson G.A. et al
1986, Science (233) 364-367 - Molecular cloning and complete sequence of prion protein cDNA from mouse brain infected with the scrapie agent.
- Locht C., Chesebro B., Race R. et al
1986, Proc. Natl. Acad. Sci. U.S.A. (83) 6372-6376 - Biology and structure of scrapie prions.
- McKinley M.P., Prusiner S.B.
1986, Int. Rev. Neurobiol. (28) 1-57 - Isolation of a cDNA clone encoding the leader peptide of prion protein and expression of the homologous gene in various tissues.
- Robakis N.K., Sawh P.R., Wolfe G.C. et al
1986, Proc. Natl. Acad. Sci. U.S.A. (83) 6377-6381 - Identification of scrapie prion protein-specific mRNA in scrapie- infected and uninfected brain.
- Chesebro B., Race R., Wehrly K. et al
1985, Nature (315) 331-333 - A cellular gene encodes scrapie PrP 27-30 protein.
- Oesch B., Westaway D., Walchli M. et al
1985, Cell (40) 735-746 - PrP allelic variants associated with natural scrapie.
- Bossers A.
Submitted AUG-1997 to the EMBL GenBank DDBJ databases - Analysis of the Sequence and Polymorphism of Human PrPc Mature Protein Gene.
- Cui X., Wang Z., Chen J. et al
Submitted MAR-2004 to the EMBL GenBank DDBJ databases - Cloning, Prokaryotic Expression and Antigenic Analysis of Resistant Core of Human PrP in E. coli.
- Cui X., Wang Z., Chen J. et al
Submitted MAR-2004 to the EMBL GenBank DDBJ databases - Prion genotypes in feral herds of Alaska caribou.
- Happ G.M., Huson H.J., Beckmen K.J. et al
Submitted AUG-2005 to the EMBL GenBank DDBJ databases - A set of genotyping controls for 15 haplotype combinations of ovine PRNP codons 136, 154, and 171.
- Heaton M.P., Leymaster K.A., Clawson M.L. et al
Submitted JAN-2005 to the EMBL GenBank DDBJ databases - A set of genotyping controls for 15 haplotype combinations of ovine PRNP codons 136, 154, and 171.
- Heaton M.P., Leymaster K.A., Clawson M.L. et al
Submitted JAN-2005 to the EMBL GenBank DDBJ databases - A set of genotyping controls for 17 haplotype combinations of ovine PRNP codons 136, 154, and 171.
- Heaton M.P., Leymaster K.A., Clawson M.L. et al
Submitted DEC-2005 to the EMBL GenBank DDBJ databases - A set of genotyping controls for 17 haplotype combinations of ovine PRNP codons 136, 154, and 171.
- Heaton M.P., Leymaster K.A., Clawson M.L. et al
Submitted JAN-2005 to the EMBL GenBank DDBJ databases - Cloning of human prostate prion protein cDNA.
- Hryb D.J., Reynolds T.A., Nakhla A.M. et al
Submitted SEP-2000 to the EMBL GenBank DDBJ databases - Polymorphisms of the prion protein gene in Korea.
- Jeong B.H., Lee Y.J., Lee K.H. et al
Submitted JAN-2003 to the EMBL GenBank DDBJ databases - Prion protein (PrP) gene of Sika deer.
- Jeong H.-J., Kim B.-S., Lee J.-B. et al
Submitted JAN-2006 to the EMBL GenBank DDBJ databases - Low Chronic Wasting Disease Prevalence Among Free-Ranging Mule Deer (Odocoileus hemionus) with PrP Genotype 225SF.
- Jewell J.E., Conner M.M., Wolfe L.L. et al
Submitted OCT-2004 to the EMBL GenBank DDBJ databases - Low chronic wasting disease prevalence among free-ranging mule deer (Odocoileus hemionus) with PrP genotype 225SF.
- Jewell J.E., Conner M.M., Wolfe L.L. et al
Submitted OCT-2004 to the EMBL GenBank DDBJ databases - Prion protein (PrP) gene of Rocky Mountain elk (Cervus elaphus nelsoni), and partial intron 2 sequence.
- Jewell J.E., Williams E.S.
Submitted FEB-2003 to the EMBL GenBank DDBJ databases - Prion protein (PrP) gene of white-tailed deer (Odocoileus virginianus), coding region and intron 2 sequence.
- Jewell J.E., Wolfe L.L., Williams E.S. et al
Submitted APR-2003 to the EMBL GenBank DDBJ databases - Prion protein (PrP) gene of white-tailed deer (Odocoileus virginianus), coding region and intron 2 sequence.
- Jewell J.E., Wolfe L.L., Williams E.S. et al
Submitted APR-2003 to the EMBL GenBank DDBJ databases - PrP gene sequence for big horn sheep (Ovis canadensis).
- O&apos, Rourke K.I., Spraker T.R. et al
Submitted JUL-1999 to the EMBL GenBank DDBJ databases - Analysis of the Prion Protein of Big Game Cervids in Sweden Indicate Susceptibility to Chronic Wasting Disease.
- Simonsson M., Klingeborn M., Linne T. et al
Submitted MAY-2004 to the EMBL GenBank DDBJ databases - Analysis of the Prion Protein of Big Game Cervids in Sweden Indicate Susceptibility to Chronic Wasting Disease.
- Simonsson M., Klingeborn M., Linne T. et al
Submitted MAY-2004 to the EMBL GenBank DDBJ databases - PRNP gene of bottle-nosed dolphin clone and sequence analysis.
- Sun Y., Zhao D., Meng L. et al
Submitted JUL-2005 to the EMBL GenBank DDBJ databases - PRNP gene of bottle-nosed dolphin clone and sequence analysis.
- Sun Y.M., Zhao D.M., Meng L.P. et al
Submitted MAR-2005 to the EMBL GenBank DDBJ databases - Evolutionary Genetics of Neutral and immune related loci in North American Thinhorn sheep (Ovis dalli spp).
- Worley K.
Submitted MAY-2005 to the EMBL GenBank DDBJ databases - Amino acid sequence of the Pekingese prion protein.
- Wu C.-D., Zhao D.-M., Pang W.-Y. et al
Submitted MAR-2006 to the EMBL GenBank DDBJ databases - Cloning and sequence analysis of prion protein (PrPC) genes from bactrian camel and musk deer.
- Wu R., Xie Q.G., Liu X.T. et al
Submitted AUG-2004 to the EMBL GenBank DDBJ databases - Cloning and sequence analysis of prion protein (PrPC) genes from sheep and goat.
- Wu R., Xie Q.G., Liu X.T. et al
Submitted AUG-2004 to the EMBL GenBank DDBJ databases - Cloning and sequence analysis of prion protein (PrPC) genes from bactrian camel and musk deer.
- Wu R., Xie Q.G., Liu X.T. et al
Submitted AUG-2004 to the EMBL GenBank DDBJ databases - Cloning and sequence analysis of prion protein (PrPC) genes from sheep and goat.
- Wu R., Xie Q.G., Liu X.T. et al
Submitted AUG-2004 to the EMBL GenBank DDBJ databases - Prion protein gene amplification and sequences analysis of two local domestic animals.
- Xiangmei Z., Deming Z., Jianmin Y. et al
Submitted NOV-2004 to the EMBL GenBank DDBJ databases - Molecular cloning of prion genes in giant panda.
- Yang J., Zhao D., Li N. et al
Submitted JUN-2003 to the EMBL GenBank DDBJ databases - Nucleotide sequence of PrP cDNA in Korean cattle.
- Yoo H.S., Kang S.G., Choi I.S. et al
Submitted JUN-2002 to the EMBL GenBank DDBJ databases - Molecular cloning of prion gene of Dezhou donkey.
- Zhang T.-X., Zhao D.-M., Ning Z.-Y. et al
Submitted MAR-2005 to the EMBL GenBank DDBJ databases - Evidence for an increased substitution rate of the hominoid prion protein gene during the period of brain expansion.
- van, der, Kuyl A.C. et al
Submitted NOV-1996 to the EMBL GenBank DDBJ databases - Evidence for an increased substitution rate of the hominoid prion protein gene during the period of brain expansion.
- van, der, Kuyl A.C. et al
Submitted OCT-1996 to the EMBL GenBank DDBJ databases - Evidence for an increased substitution rate of the hominoid prion protein gene during the period of brain expansion.
- van, der, Kuyl A.C. et al
Submitted NOV-1996 to the EMBL GenBank DDBJ databases - Evidence for an increased substitution rate of the hominoid prion protein gene during the period of brain expansion.
- van, der, Kuyl A.C. et al
Submitted OCT-1996 to the EMBL GenBank DDBJ databases