2001
DOI: 10.1001/archderm.137.11.1503
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T-Cell Receptor and Immunoglobulin Gene Rearrangements in Diagnosing Skin Disease

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Cited by 31 publications
(12 citation statements)
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“…Also, this can be a false-negative result, due to poor sampling, i.e. taking the skin sample with small number of malignant T-cells, and there is a possibility that primers used in this study did not cover all possible TCR-g gene rearrangements (5,21,22).…”
Section: Patients With Idiopathic Erythroderma and Clinical Suspicionmentioning
confidence: 99%
“…Also, this can be a false-negative result, due to poor sampling, i.e. taking the skin sample with small number of malignant T-cells, and there is a possibility that primers used in this study did not cover all possible TCR-g gene rearrangements (5,21,22).…”
Section: Patients With Idiopathic Erythroderma and Clinical Suspicionmentioning
confidence: 99%
“…The technique is dependent on the fact that T cells bear a unique antigen receptor on their cell surface that serves as a specific marker for that cell and its clonal progeny. If a cell undergoes neoplastic transformation, its TCR becomes a tumor marker specific to that cell lineage (Wood, 2001). Using PCR and high-resolution electrophoresis, a TCR clone can be demonstrated in up to 90% of skin biopsies in MF cases (Bottaro et al, 1994).…”
Section: Limitationsmentioning
confidence: 99%
“…This loss is replaced by the insertion of N nucleotides at the joins. The result is a unique V/N nucleotide/J structure that serves as a "fingerprint" for that particular T cell and all its clonal progeny (Wood, 2001;Wood et al, 1994).…”
Section: How Is Tcr Gene Rearrangement Analysis Performed?mentioning
confidence: 99%
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