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PIGA wt Allele

Known as: GPI3, PIG-A, Paroxysmal Nocturnal Hemoglobinuria Gene 
Human PIGA wild-type allele is located in the vicinity of Xp22.1 and is approximately 16 kb in length. This allele, which encodes… 
National Institutes of Health

Related topics

Related topics

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Broader (1)

PIGA gene
Phosphatidylinositol N-Acetylglucosaminyltransferase Subunit AProtein GlycosylationXp22.1glycosylation

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Monitoring genotoxicity in patients receiving chemotherapy for cancer: application of the PIG-A assay.
2011
2011
Relevance of PIG-A mutation in aplastic anemia and myelodysplastic syndromes.
6596 Background: Aplastic anemia (AA), paroxysmal nocturnal hemoglobinuria (PNH), and myelodysplastic syndromes (MDS) are… 
2006
2006
High frequency of several PIG-A mutations in patients with aplastic anemia and myelodysplastic syndrome
To clarify some characteristics of phosphatidylinositol glycan-class A gene (PIG-A) mutations in aplastic anemia (AA) and… 
2005
2005
T cells from paroxysmal nocturnal haemoglobinuria (PNH) patients show an altered CD40‐dependent pathway
Paroxysmal nocturnal haemoglobinuria (PNH) is a haematopoiesis disorder characterized by the expansion of a stem cell bearing a… 
Review
1996
Review
1996
Role of phosphatidylinositol-linked proteins in paroxysmal nocturnal hemoglobinuria pathogenesis.
Patients with paroxysmal nocturnal hemoglobinuria have one or more mutant hematopoietic stem cell clones deficient in… 
1996
1996
Identification and characterization of an inherited mutation of PIG‐A in a patient with paroxysmal nocturnal haemoglobinuria
Analysis of the X‐linked gene PIG‐A from haemopoietic cells of a female PNH patient showed a homozygous C‐55‐T substitution that… 
Review
1996
Review
1996
Molecular Basis of Paroxysmal Nocturnal Hemoglobinuria
The purpose of this review is to summarize recent studies that have led to a more complete understanding of the molecular basis… 
1995
1995
PIG-A gene abnormalities in Thai patients with paroxysmal nocturnal hemoglobinuria.
Deficient biosynthesis of the glycosyl phosphatidyl inositol (GPI)-anchor in blood cells is implicated in the pathogenesis of… 
1995
1995
Somatic mutations of PIG-A in Thai patients with paroxysmal nocturnal hemoglobinuria.
Paroxysmal nocturnal hemoglobinuria (PNH) is a hematopoietic stem cell disorder characterized by clonal blood cells that are… 
1989
1989
Erythrocyte enzyme polymorphisms in the Kamboh caste of Patiala, Punjab.
Data are presented on six erythrocyte enzyme polymorphisms (ADA, GLO I, EsD, AK, AP, GPI) in the Kamboh, a scheduled caste… 
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