CD34+ cells from paroxysmal nocturnal hemoglobinuria (PNH) patients are deficient in surface expression of cellular prion protein (PrPc). (Q53943768)

22 May 2018

title

CD34+ cells from paroxysmal nocturnal hemoglobinuria (PNH) patients are deficient in surface expression of cellular prion protein (PrPc). (English)

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22 May 2018

paroxysmal nocturnal hemoglobinuria

main subject

prion protein family

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2

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22 May 2018

author name string

Antonio M Risitano

1

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22 May 2018

Guibin Chen

3

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22 May 2018

Jan Simak

4

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22 May 2018

Jaroslav G Vostal

5

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22 May 2018

Neal S Young

6

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22 May 2018

Jaroslaw P Maciejewski

7

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22 May 2018

publication date

1 January 2003

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22 May 2018

published in

Experimental Hematology

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22 May 2018

volume

31

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22 May 2018

issue

1

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22 May 2018

page(s)

65-72

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22 May 2018

Molecular biology of prion diseases

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Scrapie prion protein contains a phosphatidylinositol glycolipid

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Distribution of cell-associated prion protein in normal adult blood determined by flow cytometry

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Different levels of prion protein (PrPc) expression on hamster, mouse and human blood cells

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Increased expression of phosphatidylinositol-specific phospholipase C resistant prion proteins on the surface of activated platelets.

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Differential constitutive and activation-dependent expression of prion protein in human peripheral blood leucocytes.

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7 January 2021

Somatic mutations in paroxysmal nocturnal hemoglobinuria: a blessing in disguise?

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Genetic and environmental effects in paroxysmal nocturnal hemoglobinuria: this little PIG-A goes "Why? Why? Why?"

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Natural history of paroxysmal nocturnal hemoglobinuria

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Paroxysmal nocturnal hemoglobinuria cells in patients with bone marrow failure syndromes

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A knock-out model of paroxysmal nocturnal hemoglobinuria: Pig-a(-) hematopoiesis is reconstituted following intercellular transfer of GPI-anchored proteins

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A crucial role for B cells in neuroinvasive scrapie.

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PrP-expressing tissue required for transfer of scrapie infectivity from spleen to brain.

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Scrapie replication in lymphoid tissues depends on prion protein-expressing follicular dendritic cells

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T‐lymphocyte activation and the cellular form of the prion protein

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The expression and potential function of cellular prion protein in human lymphocytes.

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Decreased prion protein expression in human peripheral blood leucocytes from patients with paroxysmal nocturnal haemoglobinuria

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7 January 2021

The failure of Daudi cells to express the cellular prion protein is caused by a lack of glycosyl-phosphatidylinositol anchor formation

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7 January 2021

Wild-type PrP and a mutant associated with prion disease are subject to retrograde transport and proteasome degradation

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Proteasomes and ubiquitin are involved in the turnover of the wild-type prion protein

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7 January 2021

GATA1-Cre mediates Piga gene inactivation in the erythroid/megakaryocytic lineage and leads to circulating red cells with a partial deficiency in glycosyl phosphatidylinositol-linked proteins (paroxysmal nocturnal hemoglobinuria type II cells).

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7 January 2021

10.1016/S0301-472X(02)01011-1

Identifiers

DOI

1 reference

22 May 2018

PubMed ID

12543108

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22 May 2018