Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

X-linked chronic granulomatous disease in an adult woman. Evidence for a cell selection favoring neutrophils expressing the mutant allele.

Haematologica - 1 Jan 2000

Cazzola M, Sacchi F, Pagani A, Marconi M, Ciriello M M, Fietta A, Clivio A, Ascari E

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Genetic Linkage
Share to Granulomatous Disease, Chronic
Share to Heterozygote
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Neutrophils

Share to Pedigree

Share to X Chromosome

Source

Identifiers

PMID: 3935525

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

X-linked chronic granulomatous disease in an adult woman. Evidence for a cell selection favoring neutrophils expressing the mutant allele.PMID 3935525Read ↗

Hematologically important mutations: X-linked chronic granulomatous disease--an update.Semantic proximity Read ↗

Hematologically important mutations: X-linked chronic granulomatous disease (second update).Semantic proximity Read ↗

Mutations in the X-linked and autosomal recessive forms of chronic granulomatous disease.Semantic proximity Read ↗

Male X-chromosome mosaicism leading to carrier phenotype and inheritance of chronic granulomatous disease.Semantic proximity Read ↗

Severe phenotype of chronic granulomatous disease presenting in a female with a de novo mutation in gp91-phox and a non familial, extremely skewed X chromosome inactivationSemantic proximity Read ↗

Somatic mosaicism in two unrelated patients with X-linked chronic granulomatous disease characterized by the presence of a small population of normal cells.Semantic proximity Read ↗

Increased susceptibility of a carrier of X-linked chronic granulomatous disease (CGD) to Aspergillus fumigatus infection associated with age-related skewing of lyonization.Semantic proximity Read ↗

Unusual late presentation of X-linked chronic granulomatous disease in an adult female with a somatic mosaic for a novel mutation in CYBB.Semantic proximity Read ↗

Generation of functional neutrophils from a mouse model of X-linked chronic granulomatous disorder using induced pluripotent stem cells.Semantic proximity Read ↗

Origin of mutations in two families with X-linked chronic granulomatous disease.Semantic proximity Read ↗

Unusual late onset of X-linked chronic granulomatous disease in an adult woman after unsuspicious childhood.Semantic proximity Read ↗

An assessment of the effects of ectopic gp91phox expression in XCGD iPSC-derived neutrophilsSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.