Glycosyl phosphatidylinositol-linked blood group antigens and paroxysmal nocturnal hemoglobinuria (Q40935136)

25 September 2017

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title

Glycosyl phosphatidylinositol-linked blood group antigens and paroxysmal nocturnal hemoglobinuria (English)

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25 September 2017

Telen MJ

1

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25 September 2017

publication date

1 January 1995

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Transfusion Clinique et Biologique

25 September 2017

published in

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25 September 2017

volume

2

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25 September 2017

issue

4

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25 September 2017

page(s)

277-290

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Glycolipid anchoring of plasma membrane proteins

25 September 2017

cites work

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Glycosyl-phosphatidylinositol moiety that anchors Trypanosoma brucei variant surface glycoprotein to the membrane

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Complete structure of the glycosyl phosphatidylinositol membrane anchor of rat brain Thy-1 glycoprotein

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Signal for attachment of a phospholipid membrane anchor in decay accelerating factor

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7 January 2021

Signal peptide for protein secretion directing glycophospholipid membrane anchor attachment

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Analysis of the signal for attachment of a glycophospholipid membrane anchor

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Immune lysis of normal human and paroxysmal nocturnal hemoglobinuria (PNH) red blood cells. I. The sensitivity of PNH red cells to lysis by complement and specific antibody

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7 January 2021

Paroxysmal Nocturnal Hemoglobinuria (PNH) as a Clonal Disorder

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The erythrocytes in paroxysmal nocturnal haemoglobinuria of intermediate sensitivity to complement lysis

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Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria

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7 January 2021

Deficiency of the complement regulatory protein, "decay-accelerating factor," on membranes of granulocytes, monocytes, and platelets in paroxysmal nocturnal hemoglobinuria

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Inhibition of complement activation on the surface of cells after incorporation of decay-accelerating factor (DAF) into their membranes

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Relationship between the membrane inhibitor of reactive lysis and the erythrocyte phenotypes of paroxysmal nocturnal hemoglobinuria

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7 January 2021

Identification of the complement decay-accelerating factor (DAF) on epithelium and glandular cells and in body fluids

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7 January 2021

Cloning of decay-accelerating factor suggests novel use of splicing to generate two proteins

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Decay-accelerating factor. Genetic polymorphism and linkage to the RCA (regulator of complement activation) gene cluster in humans

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7 January 2021

A possible null phenotype in the Cromer blood group complex

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A 'new' Cromer-related high frequency antigen probably antithetical to WES

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7 January 2021

UMC, another Cromer-related blood group antigen

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7 January 2021

Use of the MAIEA technique to confirm the relationship between the Cromer antigens and decay-accelerating factor and to assign provisionally antigens to the short-consensus repeats

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7 January 2021

Analysis of PI (phosphatidylinositol)-anchoring antigens in a patient of paroxysmal nocturnal hemoglobinuria (PNH) reveals deficiency of 1F5 antigen (CD59), a new complement-regulatory factor

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7 January 2021

Inherited complete deficiency of 20-kilodalton homologous restriction factor (CD59) as a cause of paroxysmal nocturnal hemoglobinuria

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7 January 2021

Absorption and elution of anti-Hy from one of four Gy(a-) human red blood cell samples

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7 January 2021

Evidence That the Human Blood Group Antigens Gyaand Hy Are Carried on a Novel Glycosylphosphatidylinositol-Linked Erythrocyte Membrane Glycoprotein

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7 January 2021

Investigations using a novel monoclonal antibody to the glycosylphosphatidylinositol-anchored protein that carries Gregory, Holley, and Dombrock blood group antigens

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https://api.crossref.org/works/10.1016%2FS1246-7820%2805%2980094-1

7 January 2021

A monoclonal antibody to the high frequency red cell antigen JMH

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https://api.crossref.org/works/10.1016%2FS1246-7820%2805%2980094-1

7 January 2021

Further analysis of the monoclonal antibody H8 demonstrating a JMH-related specificity

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7 January 2021

10.1016/S1246-7820(05)80094-1

Identifiers

DOI

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25 September 2017

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