cDNA cloning of turtle prion protein

[1]  J. Sambrook,et al.  Molecular Cloning: A Laboratory Manual , 2001 .

[2]  Inyoul Y. Lee,et al.  Ataxia in prion protein (PrP)-deficient mice is associated with upregulation of the novel PrP-like protein doppel. , 1999, Journal of molecular biology.

[3]  B. Dijkstra,et al.  Binding of calcium in the EF‐hand of Escherichia coli lytic transglycosylase Slt35 is important for stability , 1999, FEBS letters.

[4]  G. Forloni,et al.  Molecular determinants of the physicochemical properties of a critical prion protein region comprising residues 106-126. , 1999, The Biochemical journal.

[5]  T. Werner,et al.  Analysis of 27 mammalian and 9 avian PrPs reveals high conservation of flexible regions of the prion protein. , 1999, Journal of molecular biology.

[6]  F. Cohen,et al.  Solution structure of Syrian hamster prion protein rPrP(90-231). , 1999, Biochemistry.

[7]  D Eisenberg,et al.  Chicken prion tandem repeats form a stable, protease-resistant domain. , 1999, Biochemistry.

[8]  J. Feeney,et al.  Cooperative cyclic interactions involved in metal binding to pairs of sites in EF‐hand proteins , 1998, FEBS letters.

[9]  Inyoul Y. Lee,et al.  Complete genomic sequence and analysis of the prion protein gene region from three mammalian species. , 1998, Genome research.

[10]  F. Cohen,et al.  Prion protein selectively binds copper(II) ions. , 1998, Biochemistry.

[11]  Christian von Mering,et al.  Expression of Amino-Terminally Truncated PrP in the Mouse Leading to Ataxia and Specific Cerebellar Lesions , 1998, Cell.

[12]  D. Westaway,et al.  The cellular prion protein binds copper in vivo , 1997, Nature.

[13]  P E Wright,et al.  Structure of the recombinant full-length hamster prion protein PrP(29-231): the N terminus is highly flexible. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[14]  S. Prusiner,et al.  Prion diseases and the BSE crisis. , 1997, Science.

[15]  K Wüthrich,et al.  NMR characterization of the full‐length recombinant murine prion protein, mPrP(23–231) , 1997, FEBS letters.

[16]  S. Duga,et al.  cDNA cloning and expression of the flavoprotein D-aspartate oxidase from bovine kidney cortex. , 1997, The Biochemical journal.

[17]  F. Cohen,et al.  Recombinant scrapie-like prion protein of 106 amino acids is soluble. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[18]  R. Timpl,et al.  The C-terminal portion of BM-40 (SPARC/osteonectin) is an autonomously folding and crystallisable domain that binds calcium and collagen IV. , 1995, Journal of molecular biology.

[19]  R. Timpl,et al.  Changes in calcium and collagen IV binding caused by mutations in the EF hand and other domains of extracellular matrix protein BM-40 (SPARC, osteonectin). , 1994, Journal of molecular biology.

[20]  S. Prusiner,et al.  Molecular cloning of a candidate chicken prion protein. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[21]  T. Tanaka,et al.  cDNA cloning of a novel heterogeneous nuclear ribonucleoprotein gene homologue in Caenorhabditis elegans using hamster prion protein cDNA as a hybridization probe. , 1992, Nucleic Acids Research.

[22]  J. Mallet,et al.  Oligodeoxyribonucleotide ligation to single-stranded cDNAs: a new tool for cloning 5' ends of mRNAs and for constructing cDNA libraries by in vitro amplification. , 1991, Nucleic acids research.

[23]  G. Fischbach,et al.  A prion-like protein from chicken brain copurifies with an acetylcholine receptor-inducing activity. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[24]  S. Prusiner,et al.  Molecular biology of prion diseases , 1991, Science.

[25]  F. Collins,et al.  Construction of T-vectors, a rapid and general system for direct cloning of unmodified PCR products. , 1991, Nucleic acids research.

[26]  S. Prusiner,et al.  Differential release of cellular and scrapie prion proteins from cellular membranes by phosphatidylinositol-specific phospholipase C. , 1990, Biochemistry.

[27]  D. Lipman,et al.  Improved tools for biological sequence comparison. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[28]  C. Locht,et al.  Molecular cloning and complete sequence of prion protein cDNA from mouse brain infected with the scrapie agent. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[29]  R. Lebo,et al.  Human prion protein cDNA: molecular cloning, chromosomal mapping, and biological implications. , 1986, Science.

[30]  S. Prusiner,et al.  Conservation of the cellular gene encoding the scrapie prion protein. , 1986, Nucleic acids research.

[31]  Ruedi Aebersold,et al.  A cellular gene encodes scrapie PrP 27-30 protein , 1985, Cell.

[32]  S. Prusiner Novel proteinaceous infectious particles cause scrapie. , 1982, Science.

[33]  N. Guex,et al.  SWISS‐MODEL and the Swiss‐Pdb Viewer: An environment for comparative protein modeling , 1997, Electrophoresis.