Results 211 to 220 of about 57,548 (261)

Double gene overexpression of ZNF746 and cellular prion protein in rat adipose-derived mesenchymal stromal cell therapy protects the liver against ischemia‒reperfusion injury. [PDF]

Cell Transplant
Ko SF, Huang CR, Chiang JY, Chen YL, Yip HK.   +4 more
europepmc   +1 more source

Wnt, glucocorticoid and cellular prion protein cooperate to drive a mesenchymal phenotype with poor prognosis in colon cancer. [PDF]

J Transl Med
Mouillet-Richard S, Gougelet A, Passet B, Brochard C, Le Corre D, Pitasi CL, Joubel C, Sroussi M, Gallois C, Lavergne J, Castille J, Vilotte M, Daniel-Carlier N, Pilati C, de Reyniès A, Djouadi F, Colnot S, André T, Taieb J, Vilotte JL, Romagnolo B, Laurent-Puig P.   +21 more
europepmc   +1 more source

The role of cellular prion protein in lipid metabolism in the liver. [PDF]

Prion, 2020
Arora AS, Zafar S, Latif U, Llorens F, Sabine M, Kumar P, Tahir W, Thüne K, Shafiq M, Schmitz M, Zerr I.   +10 more
europepmc   +1 more source

Lack of cellular prion protein causes Amyloid β accumulation, increased extracellular vesicle abundance, and changes to exosome biogenesis proteins. [PDF]

Mol Cell Biochem
Johansson L, Reyes JF, Ali T, Schätzl H, Gilch S, Hallbeck M.   +5 more
europepmc   +1 more source

Impact of cellular prion protein expression on disease progression and pathology in two mouse models of Alzheimer’s disease

, 2022
Purro SA, Farmer M, Noble E, Sarell CJ, Powell M, Yip DC, Giggins L, Zakka L, Thomas DX, Farrow MA, Nicoll AJ, Walsh D, Collinge J.   +12 more
europepmc   +1 more source

The 37kDa/67kDa Laminin Receptor LRP/LR as a molecular target in neurodegenerative diseases [PDF]

, 2009
Pflanz, Heike
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Preventing Prion Pathogenicity by Targeting the Cellular Prion Protein

Infectious Disorders - Drug Targets, 2009
Prions are unique in that the infectious particles contain no detectable nucleic acid and appear to consist of aggregated forms of misfolded cellular prion protein. Prions form distinct strains and can transmit disease between species. Whilst the molecular basis of prion diseases is beginning to be unravelled, much remains unknown including the atomic ...
Andrew J, Nicoll, John, Collinge
openaire   +2 more sources

Cellular prion protein neuroprotective function: implications in prion diseases

Journal of Molecular Medicine, 2004
Prion protein can display two conformations: a normal cellular conformation (PrP) and a pathological conformation associated with prion diseases (PrP(Sc)). Three complementary strategies are used by researchers investigating how PrP is involved in the pathogenesis of prion diseases: elucidation of the normal function of PrP, determination of how PrP(Sc)
Xavier, Roucou, Andréa C, LeBlanc
openaire   +2 more sources