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