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

Cytogenetic abnormalities in PHA-stimulated lymphocytes from patients with Langerhans cell histiocytosis

1 Oct 2000

Abstract excerpt

The aetiopathogenesis of Langerhans cell histiocytosis (LCH) is still undefined. Constitutional abnormalities in LCH have rarely been reported. One study showed chromosomal instability in lesional cells from three patients. No chromosomal studies are available on peripheral blood lymphocytes. Peripheral blood lymphocytes were analysed for the presence of chromatid and/or chromosomal breaks and structural...

Read the complete abstract on PubMed

Topics

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

Share to Histiocytic Disorders and Treatments
Share to Parvovirus B19 Infection Studies
Share to Viral-associated cancers and disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 11091209
DOI: 10.1046/j.1365-2141.2000.02313.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Cytogenetic abnormalities in PHA-stimulated lymphocytes from patients with Langerhans cell histiocytosisPMID 11091209Read ↗

Cytogenetic abnormalities in Langerhans cell histiocytosisSemantic proximity Read ↗

No genomic aberrations in Langerhans cell histiocytosis as assessed by diverse molecular technologies.Semantic proximity Read ↗

Dyskeratosis Congenita Is a Chromosomal Instability DisorderSemantic proximity Read ↗

Multicolor fluorescence in situ hybridization (SKY) in mycosis fungoides and Sézary syndrome: Search for recurrent chromosome abnormalitiesSemantic proximity Read ↗

Recurring Structural Chromosome Abnormalities in Peripheral Blood Lymphocytes of Patients With Mycosis Fungoides/Sezary SyndromeSemantic proximity Read ↗

Increased DNA damage sensitivity of Cornelia de Lange syndrome cells: evidence for impaired recombinational repairSemantic proximity Read ↗

Centromere defects, chromosome instability, and cGAS-STING activation in systemic sclerosisSemantic proximity Read ↗

Fine mapping of an apparently targeted latent human herpesvirus type 6 integration site in chromosome band 17p13.3Semantic proximity Read ↗

Chromosome aberrations in Raynaud's phenomenon.Semantic proximity Read ↗

The spontaneous frequency of chromosomal aberrations and sister-chromatid exchanges in cultured peripheral lymphocytes of a single blood donor sampled more than 200 times.Semantic proximity Read ↗

Expression of Cell Cycle–Related Gene Products in Langerhans Cell HistiocytosisSemantic proximity Read ↗

Activation of pericentromeric and telomeric heterochromatin in cultured lymphocytes from old individuals.Semantic proximity Read ↗

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