Defining a common region of DNA amplification at 22q11.2-12 in head and neck squamous cell carcinomas by quantitative FISH analysis

Genes Chromosomes and Cancer

Volumn 29, Issue 3, 2000, Pages 207-212

  Matsumura, Kouji ^a,b   Iritani, Akio ^a   Enomoto, Shoji ^a   Torikata, Chikao ^b   Matsuyama, Shigeo ^b   Kurita, Akira ^b   Kurahashi, Hiroki ^c   Tsuchida, Nobuo ^a  

^a TOKYO MEDICAL AND DENTAL UNIVERSITY   (Japan)

^b NATIONAL DEFENSE MEDICAL COLLEGE   (Japan)

^c OSAKA UNIVERSITY MEDICAL SCHOOL   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ARTICLE; CHROMOSOME 22Q; COMPARATIVE GENOMIC HYBRIDIZATION; COSMID; DNA SEQUENCE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE AMPLIFICATION; GENE MAPPING; HEAD AND NECK CARCINOMA; HUMAN; HUMAN CELL; ONCOGENE; PRIORITY JOURNAL; SQUAMOUS CELL CARCINOMA;

EID: 0033800546     PISSN: 10452257     EISSN: None     Source Type: Journal    
DOI: 10.1002/1098-2264(2000)9999:9999<::AID-GCC1032>3.0.CO;2-U     Document Type: Article

References (32)

1. Distinct patterns of chromosomal alterations in high- and low-grade head and neck squamous cell carcinomas
2. Frequent novel DNA copy number increase in squamous cell head and neck tumors
3. Characterization of nonrandom chromosomal gains and losses in multiple myeloma by comparative genomic hybridization
4. A high-density YAC contig map of human chromosome 22
5. The DNA sequence of human chromosome 22
6. Pattern of genomic imbalances in oral squamous cell carcinomas with and without an increased copy number of 11q13
7. Activation of mitogen-activated protein kinase associated with prostate cancer progression
8. Heterogeneous expression of four MAP kinase isoforms in human tissues
9. Constitutive activation of the 41-/43-kDa mitogen-activated protein kinase signaling pathway in human tumors
10. Mapping of chromosomal gains and losses in prostate cancer by comparative genomic hybridization
11. Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors
12. Chromosome arm 20q gains and other genomic alterations in colorectal cancer metastatic to liver, as analyzed by comparative genomic hybridization and fluorescence in situ hybridization
13. Isolation and mapping of cosmid markers on human chromosome 22, including one within the submicroscopically deleted region of DiGeorge syndrome
14. High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones
15. Detection of DNA amplifications and deletions in oral squamous cell carcinoma cell lines by comparative genomic hybridization (CGH)
16. Deletion of chromosome 17p loci in breast cancer cells detected by fluorescence in situ hybridization
17. Overexpression of the ERK/MAP kinases in oral squamous cell carcinoma
18. Parameters of the human genome
19. Molecular cytogenetic fingerprinting of esophageal squamous cell carcinoma by comparative genomic hybridization reveals a consistent pattern of chromosomal alterations
20. Chromosomal and gene amplification in diffuse large B-cell lymphoma
21. Gene amplification and overexpression of epidermal growth factor receptor in squamous cell carcinoma of the head and neck
22. Most human squamous cell carcinomas in the oral cavity contain mutated p53 tumor-suppressor genes
23. Comparative genomic hybridization of human malignant gliomas reveals multiple amplification sites and nonrandom chromosomal gains and losses
24. Amplification of cellular oncogenes: A predictor of clinical outcome in human cancer
25. Comparative genomic hybridization of squamous cell carcinoma of the esophagus: The possible involvement of the DPI gene in the 13q34 amplicon
26. Hyperexpression of mitogen-activated protein kinase in human breast cancer
27. Comparative genomic hybridization detects novel deletions and amplifications in head and neck squamous cell carcinomas
28. Recent progress in understanding mechanisms of mammalian DNA amplification
29. Increased copy number at 20q13 in breast cancer: Defining the critical region and exclusion of candidate genes
30. Detection of chromosomal imbalances in transitional cell carcinoma of the bladder by comparative genomic hybridization
31. Recurrent chromosomal imbalances detected in biopsy material from oral premalignant and malignant lesions by combined tissue microdissection, universal DNA amplification, and comparative genomic hybridization
32. Gene amplification and gene dosage in cell lines derived from squamous cell carcinoma of the head and neck