Impaired motor coordination in mice lacking prion protein (Q28292921)

Europe PubMed Central

title

Impaired motor coordination in mice lacking prion protein (English)

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S Katamine

1

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N Nishida

2

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T Sugimoto

3

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T Noda

4

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S Sakaguchi

5

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K Shigematsu

6

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Y Kataoka

7

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A Nakatani

8

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S Hasegawa

9

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R Moriuchi

10

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T Miyamoto

Cellular and Molecular Neurobiology

11

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language of work or name

English

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publication date

December 1998

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published in

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volume

18

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page(s)

731-42

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issue

6

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cites work

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Mice devoid of PrP are resistant to scrapie

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Excitation-contraction uncoupling and muscular degeneration in mice lacking functional skeletal muscle ryanodine-receptor gene

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Kinetics of infectivity are dissociated from PrP accumulation in salivary glands of Creutzfeldt-Jakob disease agent-inoculated mice

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

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Placental defect and embryonic lethality in mice lacking hepatocyte growth factor/scatter factor

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Genomic structure of the human prion protein gene

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Conservation of the cellular gene encoding the scrapie prion protein

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Changes in the localization of brain prion proteins during scrapie infection

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Transmission of chronic spongiform encephalopathy with kuru plaques from humans to small rodents

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Evidence that the Transmission of One Source of Scrapie Agent to Hamsters Involves Separation of Agent Strains from a Mixture

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Inactivation of MyoD in mice leads to up-regulation of the myogenic HLH gene Myf-5 and results in apparently normal muscle development.

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Molecular cloning and complete sequence of prion protein cDNA from mouse brain infected with the scrapie agent

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Different forms of the bovine PrP gene have five or six copies of a short, G-C-rich element within the protein-coding exon.

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Rescue of neurophysiological phenotype seen in PrP null mice by transgene encoding human prion protein

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Creutzfeldt-Jakob Disease (Spongiform Encephalopathy): Transmission to the Chimpanzee

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Neurotoxicity of a prion protein fragment.

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Altered microtubule organization in small-calibre axons of mice lacking tau protein

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The glutamate receptor subtype mediating parallel fibre-Purkinje cell transmission in rabbit cerebellar cortex.

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Purification and structural studies of a major scrapie prion protein.

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Amphotericin B treatment dissociates in vivo replication of the scrapie agent from PrP accumulation

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Prion protein is necessary for normal synaptic function.

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Experimental transmission of a Kuru-like syndrome to chimpanzees

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A prion-like protein from chicken brain copurifies with an acetylcholine receptor-inducing activity

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Biology and genetics of prion diseases

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Gene targeting approaches to complex genetic diseases: atherosclerosis and essential hypertension

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Identification of a protein that purifies with the scrapie prion.

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Ablation of the prion protein (PrP) gene in mice prevents scrapie and facilitates production of anti-PrP antibodies

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Biological evidence that scrapie agent has an independent genome.

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PrP gene dosage determines the timing but not the final intensity or distribution of lesions in scrapie pathology.

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The prion protein gene: a role in mouse embryogenesis?

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Spontaneous neurodegeneration in transgenic mice with mutant prion protein

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Scrapie agent reflication without the prion protein?

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High prion and PrPSc levels but delayed onset of disease in scrapie-inoculated mice heterozygous for a disrupted PrP gene

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Immunoreactivity of a synthetic pentadecapeptide corresponding to the N-terminal region of the scrapie prion protein.

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Encephalopathy in mice produced by inoculation with scrapie brain material.

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beta-Amyloid precursor protein metabolites and loss of neuronal Ca2+ homeostasis in Alzheimer's disease.

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The Wnt-1 (int-1) proto-oncogene is required for development of a large region of the mouse brain

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Transmission of Creutzfeldt-Jakob disease to Syrian hamster

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Calcium is an intracellular mediator of the climbing fiber in induction of cerebellar long-term depression

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Cell-free formation of protease-resistant prion protein.

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A protease-resistant protein is a structural component of the scrapie prion.

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No propagation of prions in mice devoid of PrP.

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Targeted mutation of the DNA methyltransferase gene results in embryonic lethality

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Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted disease.

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129/Ola mice carrying a null mutation in PrP that abolishes mRNA production are developmentally normal.

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Novel proteinaceous infectious particles cause scrapie

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Loss of cerebellar Purkinje cells in aged mice homozygous for a disrupted PrP gene.

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Prion dementia without characteristic pathology

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Lethal thalassemia after insertional disruption of the mouse major adult beta-globin gene

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Scrapie prion protein contains a phosphatidylinositol glycolipid.

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12 December 2020

Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene

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12 December 2020

Accumulation of proteinase K-resistant prion protein (PrP) is restricted by the expression level of normal PrP in mice inoculated with a mouse-adapted strain of the Creutzfeldt-Jakob disease agent

1 reference

12 December 2020

Antigenic changes similar to those seen in neurofibrillary tangles are elicited by glutamate and Ca2+ influx in cultured hippocampal neurons

1 reference

12 December 2020

A cellular gene encodes scrapie PrP 27-30 protein

1 reference

12 December 2020