(Q28272985)

1

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L Ianzano

2

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C Lunardi

3

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G De Sandre

4

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M Carotenuto

5

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P Musto

6

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L Zelante

[Erythrocytic acetylcholinesterase. II. Relations to hemolytic diseases]

7

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language of work or name

English

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publication date

January 1996

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published in

Human Genetics

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volume

97

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issue

1

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page(s)

45-8

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cites work

1 reference

12 December 2020

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

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12 December 2020

An enzymic disorder in the erythrocytes of paroxysmal nocturnal haemoglobinuria: a deficiency in acetylcholinesterase activity

1 reference

12 December 2020

Membrane proteins in paroxysmal nocturnal haemoglobinuria

1 reference

12 December 2020

Characterization of genomic PIG-A gene: a gene for glycosylphosphatidylinositol-anchor biosynthesis and paroxysmal nocturnal hemoglobinuria

1 reference

12 December 2020

Paroxysmal nocturnal haemoglobinuria (PNH) is caused by somatic mutations in the PIG-A gene

1 reference

12 December 2020

Abnormalities of PIG-A transcripts in granulocytes from patients with paroxysmal nocturnal hemoglobinuria

1 reference

12 December 2020

Development of RNA-SSCP protocols for the identification and screening of CFTR mutations: identification of two new mutations

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12 December 2020

Paroxysmal nocturnal haemoglobinuria

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12 December 2020

The cloning of PIG-A, a component in the early step of GPI-anchor biosynthesis

1 reference

12 December 2020

Somatic mutations and cellular selection in paroxysmal nocturnal haemoglobinuria

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12 December 2020

Screening for mutations by RNA single-strand conformation polymorphism (rSSCP): comparison with DNA-SSCP

1 reference

12 December 2020

Paroxysmal nocturnal hemoglobinuria: evidence for monoclonal origin of abnormal red cells

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12 December 2020

Mutations within the Piga gene in patients with paroxysmal nocturnal hemoglobinuria

1 reference

12 December 2020

Identification of defects in glycosylphosphatidylinositol anchor biosynthesis in the Thy-1 expression mutants

1 reference

12 December 2020

Comparison of RNase A, a chemical cleavage and GC-clamped denaturing gradient gel electrophoresis for the detection of mutations in exon 9 of the human acid beta-glucosidase gene

1 reference

12 December 2020

Genomic organization of the X-linked gene (PIG-A) that is mutated in paroxysmal nocturnal haemoglobinuria and of a related autosomal pseudogene mapped to 12q21

1 reference

12 December 2020

Paroxysmal nocturnal hemoglobinuria: the biochemical defects and the clinical syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Attachment of a 40-base-pair G + C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction results in improved detection of single-base changes

1 reference

12 December 2020

Defective glycosyl phosphatidylinositol biosynthesis in extracts of three Thy-1 negative lymphoma cell mutants

1 reference

12 December 2020

Reactivity of cytosine and thymine in single-base-pair mismatches with hydroxylamine and osmium tetroxide and its application to the study of mutations

1 reference

12 December 2020

Phosphatidylinositol-linked proteins and paroxysmal nocturnal hemoglobinuria

1 reference

12 December 2020