Developmental expression of PrP in the post-implantation embryo.
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The Cellular Prion Protein: A Player in Immunological QuiescenceNCAM1 Polysialylation: The Prion Protein's Elusive Reason for Being?Brain transcriptional stability upon prion protein-encoding gene invalidation in zygotic or adult mouseThe biological function of the cellular prion protein: an updateSignal sequence insufficiency contributes to neurodegeneration caused by transmembrane prion protein.Pathogenesis of chronic wasting disease in cervidized transgenic mice.Transcriptomic analysis brings new insight into the biological role of the prion protein during mouse embryogenesisPrion protein and Shadoo are involved in overlapping embryonic pathways and trophoblastic developmentExpression and knockdown of cellular prion protein (PrPC) in differentiating mouse embryonic stem cells.The prion protein family: a view from the placentaTo develop with or without the prion protein.Conditional transgenic mouse models: from the basics to genome-wide sets of knockouts and current studies of tissue regeneration.Developmental expression of the cellular prion protein (PrP(C) ) in bovine embryos.ATP-binding cassette transporter A7 (ABCA7) loss of function alters Alzheimer amyloid processing.The cellular form of the prion protein guides the differentiation of human embryonic stem cells into neuron-, oligodendrocyte-, and astrocyte-committed lineagesPrion protein localizes at the ciliary base during neural and cardiovascular development, and its depletion affects α-tubulin post-translational modificationsThe cellular form of the prion protein is involved in controlling cell cycle dynamics, self-renewal, and the fate of human embryonic stem cell differentiation.The prion protein family: looking outside the central nervous system.Motor neuron rescue in spinal muscular atrophy mice demonstrates that sensory-motor defects are a consequence, not a cause, of motor neuron dysfunctionPhysiological Functions of the Cellular Prion Protein.Prion potency in stem cells biology.Gene expression resulting from PrPC ablation and PrPC overexpression in murine and cellular models.PrP(C) from stem cells to cancer.The Cellular Prion Protein Controls Notch Signaling in Neural Stem/Progenitor Cells.Dual role of cellular prion protein in normal host and Alzheimer's disease.Developmental influence of the cellular prion protein on the gene expression profile in mouse hippocampus.A novel Gerstmann-Sträussler-Scheinker disease mutation defines a precursor for amyloidogenic 8 kDa PrP fragments and reveals N-terminal structural changes shared by other GSS alleles.Stress Resilience of Spermatozoa and Blood Mononuclear Cells without Prion Protein.iPS Cell Cultures from a Gerstmann-Sträussler-Scheinker Patient with the Y218N PRNP Mutation Recapitulate tau Pathology.Enhanced neural progenitor/stem cells self-renewal via the interaction of stress-inducible protein 1 with the prion protein.Identification of a putative transcriptome signature common to neuroblastoma and neural crest cells.Prion protein is essential for the RE1 silencing transcription factor (REST)-dependent developmental switch in synaptic NMDA receptors.
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Developmental expression of PrP in the post-implantation embryo.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on 23 December 2006
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Developmental expression of PrP in the post-implantation embryo.
@en
Developmental expression of PrP in the post-implantation embryo.
@nl
type
label
Developmental expression of PrP in the post-implantation embryo.
@en
Developmental expression of PrP in the post-implantation embryo.
@nl
prefLabel
Developmental expression of PrP in the post-implantation embryo.
@en
Developmental expression of PrP in the post-implantation embryo.
@nl
P2093
P2860
P1433
P1476
Developmental expression of PrP in the post-implantation embryo.
@en
P2093
Cornelia Heinrich
Essia Bouzamondo-Bernstein
Patrick Tremblay
P2860
P356
10.1016/J.BRAINRES.2006.12.055
P407
P577
2006-12-23T00:00:00Z