Literature DB >> 1373228

Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein.

H Büeler1, M Fischer, Y Lang, H Bluethmann, H P Lipp, S J DeArmond, S B Prusiner, M Aguet, C Weissmann.   

Abstract

PrPC is a host protein anchored to the outer surface of neurons and to a lesser extent of lymphocytes and other cells. The transmissible agent (prion) responsible for scrapie is believed to be a modified form of PrPC. Mice homozygous for disrupted PrP genes have been generated. Surprisingly, they develop and behave normally for at least seven months, and no immunological defects are apparent. It is now feasible to determine whether mice devoid of PrPC can propagate prions and are susceptible to scrapie pathogenesis.

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Year:  1992        PMID: 1373228     DOI: 10.1038/356577a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  507 in total

1.  Mimicking dominant negative inhibition of prion replication through structure-based drug design.

Authors:  V Perrier; A C Wallace; K Kaneko; J Safar; S B Prusiner; F E Cohen
Journal:  Proc Natl Acad Sci U S A       Date:  2000-05-23       Impact factor: 11.205

2.  Normal prion protein has an activity like that of superoxide dismutase.

Authors:  D R Brown; B S Wong; F Hafiz; C Clive; S J Haswell; I M Jones
Journal:  Biochem J       Date:  1999-11-15       Impact factor: 3.857

3.  Adenoviral and adeno-associated viral transfer of genes to the peripheral nervous system.

Authors:  M Glatzel; E Flechsig; B Navarro; M A Klein; J C Paterna; H Büeler; A Aguzzi
Journal:  Proc Natl Acad Sci U S A       Date:  2000-01-04       Impact factor: 11.205

4.  Copper binding to the PrP isoforms: a putative marker of their conformation and function.

Authors:  Y Shaked; H Rosenmann; N Hijazi; M Halimi; R Gabizon
Journal:  J Virol       Date:  2001-09       Impact factor: 5.103

Review 5.  Tissue-specific targeting of the insulin receptor gene.

Authors:  Rohit N Kulkarni; Terumasa Okada
Journal:  Endocrine       Date:  2002-12       Impact factor: 3.633

6.  Expression and knockdown of cellular prion protein (PrPC) in differentiating mouse embryonic stem cells.

Authors:  Oscar A Peralta; William R Huckle; Willard H Eyestone
Journal:  Differentiation       Date:  2011-01       Impact factor: 3.880

7.  Identification of a novel gene encoding a PrP-like protein expressed as chimeric transcripts fused to PrP exon 1/2 in ataxic mouse line with a disrupted PrP gene.

Authors:  A Li; S Sakaguchi; R Atarashi; B C Roy; R Nakaoke; K Arima; N Okimura; J Kopacek; K Shigematsu
Journal:  Cell Mol Neurobiol       Date:  2000-10       Impact factor: 5.046

Review 8.  Cellular prion protein: implications in seizures and epilepsy.

Authors:  Roger Walz; Rosa Maria R P S Castro; Tonicarlo R Velasco; Carlos G Carlotti; Américo C Sakamoto; Ricardo R Brentani; Vilma R Martins
Journal:  Cell Mol Neurobiol       Date:  2002-06       Impact factor: 5.046

Review 9.  Getting a grip on prions: oligomers, amyloids, and pathological membrane interactions.

Authors:  Byron Caughey; Gerald S Baron; Bruce Chesebro; Martin Jeffrey
Journal:  Annu Rev Biochem       Date:  2009       Impact factor: 23.643

Review 10.  Insights into Mechanisms of Transmission and Pathogenesis from Transgenic Mouse Models of Prion Diseases.

Authors:  Julie A Moreno; Glenn C Telling
Journal:  Methods Mol Biol       Date:  2017
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