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「"Espenes A"[Author]」の検索結果

47件中 1件~20件表示    検索結果をPubMedで見る PubMedで見る

Cell and context-dependent sorting of neuropathy-associated protein NDRG1 - insights from canine tissues and primary Schwann cell cultures.

Neuronal ceroid lipofuscinosis in Salukis is caused by a single base pair insertion in CLN8.

Stress Resilience of Spermatozoa and Blood Mononuclear Cells without Prion Protein.

Goats without Prion Protein Display Enhanced Proinflammatory Pulmonary Signaling and Extracellular Matrix Remodeling upon Systemic Lipopolysaccharide Challenge.

Loss of prion protein induces a primed state of type I interferon-responsive genes.

LPS-induced systemic inflammation reveals an immunomodulatory role for the prion protein at the blood-brain interface.

Re-emergence of hereditary polyneuropathy in Scandinavian Alaskan malamute dogs-old enemy or new entity? A case series.

Activation of innate immune genes in caprine blood leukocytes after systemic endotoxin challenge.

NCR1+ cells appear early in GALT development of the ovine foetus and acquire a c-kit+ phenotype towards the end of gestation.

The Cellular Prion Protein: A Player in Immunological Quiescence.

Hematological shift in goat kids naturally devoid of prion protein.

The early intestinal immune response in experimental neonatal ovine cryptosporidiosis is characterized by an increased frequency of perforin expressing NCR1(+) NK cells and by NCR1(-) CD8(+) cell recruitment.

Glomerular Collagen V Codeposition and Hepatic Perisinusoidal Collagen III Accumulation in Canine Collagen Type III Glomerulopathy.

Yessotoxin triggers ribotoxic stress.

Characterization of NCR1+ cells residing in lymphoid tissues in the gut of lambs indicates that the majority are NK cells.

Cytotoxic responses in BC3H1 myoblast cell lines exposed to 1-desulfoyessotoxin.

A Gly98Val Mutation in the N-Myc Downstream Regulated Gene 1 (NDRG1) in Alaskan Malamutes with Polyneuropathy.

Healthy goats naturally devoid of prion protein.

Study of possible combined toxic effects of azaspiracid-1 and okadaic acid in mice via the oral route.

Phenotypic characterization of cells participating in transport of prion protein aggregates across the intestinal mucosa of sheep.

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