Source:http://linkedlifedata.com/resource/pubmed/id/10969942
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2000-9-14
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pubmed:abstractText |
Medulloblastomas and related primitive neuroectodermal tumors (PNETs) of the central nervous system are malignant, invasive embryonal tumors with predominantly neuronal differentiation that comprise 20% of pediatric brain tumors. Cytogenetic analysis has shown that alterations in chromosome 17, particularly the loss of 17p and the formation of isochromosome 17q, as well as the gain of chromosome 7 are the most common changes among this group of tumors. Comparative genomic hybridization (CGH) studies have largely confirmed these cytogenetic findings and have also identified novel regions of gain, loss, and amplification. The advent of more sophisticated multicolored fluorescence in situ hybridization (FISH) procedures such as spectral karyotyping (SKY) now permits complete recognition of all aberrations including extremely complex rearrangements. The authors report a retrospective analysis of 19 medulloblastoma and five PNET cases studied using combinations of classic banding analysis, FISH, CGH, and SKY to examine comprehensively the chromosomal aberrations present in this tumor group and to attempt to identify common structural rearrangement(s).
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0022-3085
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
93
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
437-48
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:10969942-Brain Neoplasms,
pubmed-meshheading:10969942-Child,
pubmed-meshheading:10969942-Child, Preschool,
pubmed-meshheading:10969942-Chromosomes, Human, Pair 17,
pubmed-meshheading:10969942-Chromosomes, Human, Pair 7,
pubmed-meshheading:10969942-Female,
pubmed-meshheading:10969942-Humans,
pubmed-meshheading:10969942-In Situ Hybridization, Fluorescence,
pubmed-meshheading:10969942-Infant,
pubmed-meshheading:10969942-Karyotyping,
pubmed-meshheading:10969942-Male,
pubmed-meshheading:10969942-Medulloblastoma,
pubmed-meshheading:10969942-Neuroectodermal Tumors, Primitive,
pubmed-meshheading:10969942-Supratentorial Neoplasms
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pubmed:year |
2000
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pubmed:articleTitle |
Molecular cytogenetic analysis of medulloblastomas and supratentorial primitive neuroectodermal tumors by using conventional banding, comparative genomic hybridization, and spectral karyotyping.
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pubmed:affiliation |
University Health Network, Hospital for Sick Children, and Department of Laboratory Medicine and Pathobiology and Medical Biophysics, Faculty of Medicine, University of Toronto, Ontario, Canada.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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