Detailed molecular analysis of 1p36 in neuroblastoma

Medical and Pediatric Oncology

Volumn 36, Issue 1, 2001, Pages 37-41

  White, P S ^a   Thompson, P M ^a   Seifried, B A ^a   Sulman, E P ^a   Jensen, S J ^a   Guo, C ^a   Maris, J M ^a   Hogarty, M D ^a   Allen, C ^a   Biegel, J A ^a   Matise, T C ^a   Gregory, S G ^a   Reynolds, C P ^a   Brodeur, G M ^a  

^a NONE

Author keywords

Chromosome deletion; Chromosome mapping; Chromosomes; Fluorescence; Heterozygote; Human; In situ hybridization; Molecular sequence data; Neuroblastoma; Pair 1

Indexed keywords

CONTIG;

CHROMOSOME 1P; CHROMOSOME DELETION; CHROMOSOME MAP; CONFERENCE PAPER; CYTOGENETICS; GENETIC ANALYSIS; HETEROZYGOSITY LOSS; HUMAN; NEUROBLASTOMA; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE;

EID: 0035165221     PISSN: 00981532     EISSN: None     Source Type: Journal    
DOI: 10.1002/1096-911X(20010101)36:1<37::AID-MPO1010>3.0.CO;2-L     Document Type: Conference Paper

References (30)

1. Biology and genetics of human neuroblastoma
2. A region of consistent deletion in neuroblastoma maps within 1p36.2-.3
3. Significance of chromosome 1p loss of heterozygosity in neuroblastomas
4. Molecular analysis of the region of distal 1p commonly deleted in neuroblastoma
5. Dissociation of suppression of tumorigenicity and differentiation in vitro effected by transfer of single human chromosomes into human neuroblastoma cells
6. Constitutional 1p36 deletion in a child with neuroblastoma
7. Evidence for two turnout suppressor loci on chromosomal bands 1p35-36 involved in neuroblastoma: One probably imprinted, another associated with N-myc amplification
8. Deletion of chromosome 1p loci and microsatellite instability in neuroblastomas analyzed with short-tandem repeat polymorphisms
9. Constitutional translocation t(1;17)(p36.31-p36.13;q11.2-q12.1) in a neuroblastoma patient. Establishment of somatic cell hybrids and identification of PND/A12M2 on chromosome 1 and NF1/SCYA7 on chromosome 17 as breakpoint flanking single copy markers
10. Analysis of 1;17 translocation breakpoints in neuroblastoma: Implications for mapping of neuroblastoma genes
11. Monoallelically expressed gene related to p53 at 1p36, a region frequently deleted in neuroblastoma and other human cancers
12. Human Krüppel-Related 3 (HKR3): A candidate for the 1p36 neuroblastoma tumor suppressor gene?
13. Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplification
14. Alterations in the PITSLRE protein kinase gene complex on chromosome 1p36 in childhood neuroblastoma
15. There may be two tumor suppressor genes on chromosome arm 1p closely associated with biologically distinct subtypes of neuroblastoma
16. 1p36: Every subband a suppressor?
17. A comprehensive human linkage map with centimorgan density
18. A comprehensive genetic map of the human genome based on 5,264 microsatellites
19. An integrated transcript map of human chromosome 1p35-p36
20. A PCR-based linkage map of human chromosome 1
21. ESTablishing a human transcript map
22. GenBank
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24. Report of the Third International Workshop on human chromosome 1 mapping 1997
25. A reciprocal translocation (1;15) (36.2;q24) in a neuroblastoma cell line is accompanied by DNA duplication and may signal the site of a putative tumor suppressor-gene
26. Physical mapping of the retinoblastoma interacting zinc finger gene RIZ to D1S228 on chromosome 1p36
27. Molecular and genetic studies on the region of translocation and duplication in the neuroblastoma cell line NGP at the 1p36.13-p36.32 chromosomal site
28. Mapping of the CA6, ENO1, and SLC2A5 (GLUT5) genes and reassignment of SLC2A5 to 1p36.2
29. Two distinct deleted regions on the short arm of chromosome 1 in neuroblastoma
30. Chromosome 1p36 deletions: The clinical phenotype and molecular characterization of a common newly delineated syndrome