Analysis of loss of heterozygosity on chromosomes 10q, 11, and 16 in medulloblastomas

Journal of Neurosurgery

Volumn 94, Issue 5, 2001, Pages 799-805

  Yin, X L ^a   Pang, J C ^a   Liu, Y H ^a   Chong, E Y ^a   Cheng, Y ^a   Poon, W S ^a   Ng, H K ^a  

^a CHINESE UNIVERSITY OF HONG KONG   (Hong Kong)

Author keywords

Chromosome 11; Chromosome 16; Loss of heterozygosity; Medulloblastoma

Indexed keywords

MICROSATELLITE DNA;

ADOLESCENT; ADULT; AGED; ARTICLE; CANCER GENETICS; CARCINOGENESIS; CHILD; CHROMOSOME 10Q; CHROMOSOME 11; CHROMOSOME 16; CHROMOSOME ANALYSIS; CLINICAL ARTICLE; DNA DETERMINATION; FEMALE; GENE DELETION; HETEROZYGOSITY LOSS; HUMAN; MALE; MEDULLOBLASTOMA; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL;

EID: 0034876027     PISSN: 00223085     EISSN: None     Source Type: Journal    
DOI: 10.3171/jns.2001.94.5.0799     Document Type: Article

References (42)

1. PTEN gene mutations are seen in high-grade but not in low-grade gliomas
2. Microsatellite analysis of loss of heterozygosity on chromosomes 9q, 11p and 17p in medulloblastomas
3. Comparative genomic hybridization detects many recurrent imbalances in central nervous system primitive neuroectodermal tumors in children
4. Three tumor-suppressor regions on chromosome 11p identified by high-resolution deletion mapping in human non-small-cell lung cancer
5. Isochromosome 17q in primitive neuroectodermal tumors of the central nervous system
6. Structural chromosomal abnormalities in human medulloblastoma
7. Chromosomal characteristics of childhood brain tumors
8. Microsatellite analysis of childhood brain tumors
9. Deletion map of chromosome 16q in ductal carcinoma in situ of the breast: Refining a putative tumor suppressor gene region
10. At least two different regions are involved in allelic imbalance on chromosome arm 16q in breast cancer
11. Involvement of multiple chromosome 17p loci in medulloblastoma tumorigenesis
12. The PISSLRE gene: Structure, exon skipping, and exclusion as tumor suppressor in breast cancer
13. Allelic loss and replication errors at microsatellite loci on chromosome 11p in head and neck squamous carcinoma: Association with aggressive biological features
14. Loss of heterozygosity at 16q24.1-q24.2 is significantly associated with metastatic and aggressive behavior of prostate cancer
15. Chromosome 11p15 deletions in human malignant astrocytomas and primitive neuroectodermal tumors
16. Loss of heterozygosity on chromosome 16 in sporadic Wilms' tumor
17. Tumors of the central nervous system
18. Involvement of H-cadherin (CDH13) on 16q in the region of frequent deletion in ovarian cancer
19. Loss of heterozygosity at chromosome 16q in prostate adenocarcinoma: Identification of three independent regions
20. H-cadherin, a novel cadherin with growth inhibitory functions and diminished expression in human breast cancer
21. Molecular genetic studies of chromosome 11 and chromosome 22q DNA sequences in pediatric medulloblastomas
22. Tsg101: A novel tumor susceptibility gene isolated by controlled homozygous functional knockout of allelic loci in mammalian cells
23. The TSG101 tumor susceptibility gene is located in chromosome 11 band p15 and is mutated in human breast cancer
24. Human chromosome 16 suppresses metastasis but not tumorigenesis in rat prostatic tumor cells
25. Exclusion of BBC1 and CMAR as candidate breast tumour-suppressor genes
26. The genomic structure of the DMBT1 gene: Evidence for a region with susceptibility to genomic instability
27. DMBT1, a new member of the SRCR superfamily, on chromosome 10q25.3-26.1 is deleted in malignant brain tumours
28. Chromosome band 16q24 is frequently deleted in human gastric cancer
29. Cytogenetic analysis of 109 pediatric central nervous system tumors
30. Outcome for children with medulloblastoma treated with radiation and cisplatin, CCNU, and vincristine chemotherapy
31. Deletion mapping of chromosome 16q in hepatocellular carcinoma
32. Extensive genomic abnormalities in childhood medulloblastoma by comparative genomic hybridization
33. The H-cadherin (CDH13) gene is inactivated in human lung cancer
34. Identification of a 910-Kb region of common allelic loss in chromosome bands 16q24.1-q24.2 in human lung cancer
35. Infrequent p53 gene mutations in medulloblastomas
36. Molecular analysis of childhood primitive neuroectodermal tumors defines markers associated with poor outcome
37. Mutational profile of the PTEN gene in primary human astrocytic tumors and cultivated xenografts
38. Deletion mapping of chromosome 11 in carcinoma of the bladder
39. Functional and molecular analyses of 10q deletions in human gliomas
40. Loss of heterozygosity on 6q, 16q, and 17p in human central nervous system primitive neuroectodermal tumors
41. Loss of heterozygosity for alleles on chromosome 10 in human brain tumours