Pages that link to "Q24629546"
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The following pages link to Assignment of the human and mouse prion protein genes to homologous chromosomes (Q24629546):
Displaying 50 items.
- Chromosomal localization of genes encoding guanine nucleotide-binding protein subunits in mouse and human (Q24293764) (← links)
- Prions (Q24633319) (← links)
- α-Cleavage of cellular prion protein (Q26863324) (← links)
- Cellular aspects of prion replication in vitro (Q27014940) (← links)
- Alzheimer's disease and prion protein (Q28250275) (← links)
- Alternate centromere inactivation in a pseudodicentric (15;20)(pter;pter) associated with a progressive neurological disorder (Q28273014) (← links)
- Host genes and infectious diseases. HIV, other pathogens, and a public health perspective. (Q30322079) (← links)
- Creutzfeldt-Jakob disease segregating in a three generation Danish family (Q32153658) (← links)
- Genomic structure of the human prion protein gene (Q33247141) (← links)
- Sporadic Creutzfeldt-Jakob disease--a review (Q33513272) (← links)
- Neurodegeneration in humans caused by prions (Q33582070) (← links)
- Dysregulation of gene expression in mouse trisomy 16, an animal model of Down syndrome (Q33937409) (← links)
- Mad cow and other maladies: update on emerging infectious diseases (Q33945003) (← links)
- Creutzfeldt-Jakob disease and the eye. I. Background and patient management (Q34057654) (← links)
- The prion gene complex encoding PrP(C) and Doppel: insights from mutational analysis (Q34382758) (← links)
- Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease (Q34389352) (← links)
- Is prnt a pseudogene? Identification of ram Prt in testis and ejaculated spermatozoa. (Q34398905) (← links)
- Molecular biology of prion diseases (Q34534878) (← links)
- Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles (Q34539307) (← links)
- Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene (Q34569015) (← links)
- Factor VIII and transmissible spongiform encephalopathy: the case for safety (Q34600710) (← links)
- Purified prion proteins and scrapie infectivity copartition into liposomes (Q34630806) (← links)
- Copper-dependent functions for the prion protein (Q34982956) (← links)
- Fundamentals of prion biology and diseases (Q35035428) (← links)
- Biochemical insight into the prion protein family (Q35072161) (← links)
- Perspectives on prion biology, prion disease pathogenesis, and pharmacologic approaches to treatment (Q35122315) (← links)
- Mutation and polymorphism of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease (CJD). (Q35194938) (← links)
- Comparative map for mice and humans (Q35364327) (← links)
- Mouse chromosome 2. (Q35675740) (← links)
- Etiology and pathogenesis of prion diseases. (Q35795039) (← links)
- A hypothalamic neuronal cell line persistently infected with scrapie prions exhibits apoptosis. (Q35899061) (← links)
- Molecular biology and genetics of neurodegenerative diseases caused by prions (Q36063397) (← links)
- The risk of transmission of variant Creutzfeldt-Jakob disease via contact lenses and ophthalmic devices (Q36319802) (← links)
- Molecular biology and pathology of scrapie and the prion diseases of humans (Q36477026) (← links)
- Molecular biology and transgenetics of prion diseases (Q36538997) (← links)
- Genetics of Prion Diversity and Host Susceptibility (Q36549304) (← links)
- Novel Properties and Biology of Scrapie Prions (Q36549325) (← links)
- The Scrapie Fibril Protein and Its Cellular Isoform (Q36549334) (← links)
- Novel aspects of prions, their receptor molecules, and innovative approaches for TSE therapy (Q36676179) (← links)
- Three hamster species with different scrapie incubation times and neuropathological features encode distinct prion proteins (Q36721451) (← links)
- Genetics and polymorphism of the mouse prion gene complex: control of scrapie incubation time (Q36851207) (← links)
- Prions: Beyond a Single Protein (Q37162363) (← links)
- Prion protein scrapie and the normal cellular prion protein (Q37167885) (← links)
- SIRPα polymorphisms, but not the prion protein, control phagocytosis of apoptotic cells (Q37322155) (← links)
- Prion liposomes (Q37581303) (← links)
- Roles of the cellular prion protein in the regulation of cell-cell junctions and barrier function (Q38199102) (← links)
- Implications of peptide assemblies in amyloid diseases (Q39431937) (← links)
- Novel mechanisms of degeneration of the central nervous system--prion structure and biology. (Q39469619) (← links)
- Genetic control of prion incubation period in mice. (Q39469625) (← links)
- The map of chromosome 20. (Q39568169) (← links)