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dc.contributor.authorKumar, Shant
dc.contributor.authorCarr, T
dc.contributor.authorMarsden, Henry B
dc.contributor.authorMorris-Jones, P H
dc.date.accessioned2010-11-09T15:57:00Z
dc.date.available2010-11-09T15:57:00Z
dc.date.issued1986-07
dc.identifier.citationStudy of childhood renal tumours using peroxidase conjugated lectins. 1986, 39 (7):736-41 J Clin Patholen
dc.identifier.issn0021-9746
dc.identifier.pmid3016034
dc.identifier.doi10.1136/jcp.39.7.736
dc.identifier.urihttp://hdl.handle.net/10541/115158
dc.description.abstractSix peroxidase conjugated lectins were used to compare their ability to bind to formalin fixed paraffin embedded tissue sections of childhood renal tumours (Wilms' tumour, mesoblastic nephroma, renal carcinoma, rhabdoid renal tumour, and bone metastasising renal tumour of childhood (BMRTC) with fetal and normal children's kidney. Lectins were found to be helpful in the differential diagnosis of renal tumours. Another important finding was that the mesenchyme of renal tumours showed differences in its reactivity among various types of kidney tumours. The results of lectin binding were not helpful in establishing the origin of kidney tumours.
dc.language.isoenen
dc.subjectKidney Canceren
dc.subjectWilms Tumouren
dc.subject.meshChild
dc.subject.meshHumans
dc.subject.meshImmunoenzyme Techniques
dc.subject.meshKidney
dc.subject.meshKidney Neoplasms
dc.subject.meshLectins
dc.subject.meshPlant Lectins
dc.subject.meshWilms Tumor
dc.titleStudy of childhood renal tumours using peroxidase conjugated lectins.en
dc.typeArticleen
dc.identifier.eissn1472-4146
dc.contributor.departmentThe Christie hospital and Holt Radium Institute, Manchester M20 9BX, UKen
dc.identifier.journalJournal of Clinical Pathologyen
html.description.abstractSix peroxidase conjugated lectins were used to compare their ability to bind to formalin fixed paraffin embedded tissue sections of childhood renal tumours (Wilms' tumour, mesoblastic nephroma, renal carcinoma, rhabdoid renal tumour, and bone metastasising renal tumour of childhood (BMRTC) with fetal and normal children's kidney. Lectins were found to be helpful in the differential diagnosis of renal tumours. Another important finding was that the mesenchyme of renal tumours showed differences in its reactivity among various types of kidney tumours. The results of lectin binding were not helpful in establishing the origin of kidney tumours.


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