73 related articles for article (PubMed ID: 18070444)
1. [Analysis of 13q14 chromosomal instability in soft tissue tumors by fluorescence in-situ hybridization].
Zhou WX; Zeng X; Liu TH; Wu SF
Zhonghua Bing Li Xue Za Zhi; 2007 Sep; 36(9):582-6. PubMed ID: 18070444
[TBL] [Abstract][Full Text] [Related]
2. Aberrations of chromosome 13q in gastrointestinal stromal tumors: analysis of 91 cases by fluorescence in situ hybridization (FISH).
Zhou W; Zeng X; Liu T
Diagn Mol Pathol; 2009 Jun; 18(2):72-80. PubMed ID: 19430298
[TBL] [Abstract][Full Text] [Related]
3. [Fluorescence in-situ hybrydization detection of 18q21 LOH in human pancreatic ductal carcinoma and chronic pancreatitis].
Wang WZ; Zhou WX; Liang ZY; Zeng X; Gao J; Wu SF; Liu TH
Zhonghua Bing Li Xue Za Zhi; 2008 Nov; 37(11):732-6. PubMed ID: 19094706
[TBL] [Abstract][Full Text] [Related]
4. [Specific loss of heterozygosity of chromosome 3p loci in soft tissue leiomyosarcoma].
Peng H; Yang GH; Bu H; Gou LX
Zhonghua Bing Li Xue Za Zhi; 2003 Apr; 32(2):124-7. PubMed ID: 12839673
[TBL] [Abstract][Full Text] [Related]
5. Consistent patterns of allelic loss in natural killer cell lymphoma.
Siu LL; Chan V; Chan JK; Wong KF; Liang R; Kwong YL
Am J Pathol; 2000 Dec; 157(6):1803-9. PubMed ID: 11106552
[TBL] [Abstract][Full Text] [Related]
6. Diagnostic utility of NCOA2 fluorescence in situ hybridization and Stat6 immunohistochemistry staining for soft tissue angiofibroma and morphologically similar fibrovascular tumors.
Sugita S; Aoyama T; Kondo K; Keira Y; Ogino J; Nakanishi K; Kaya M; Emori M; Tsukahara T; Nakajima H; Takagi M; Hasegawa T
Hum Pathol; 2014 Aug; 45(8):1588-96. PubMed ID: 24856853
[TBL] [Abstract][Full Text] [Related]
7. Improved clonality analysis of multifocal bladder tumors by combination of histopathologic organ mapping, loss of heterozygosity, fluorescence in situ hybridization, and p53 analyses.
Denzinger S; Mohren K; Knuechel R; Wild PJ; Burger M; Wieland WF; Hartmann A; Stoehr R
Hum Pathol; 2006 Feb; 37(2):143-51. PubMed ID: 16426913
[TBL] [Abstract][Full Text] [Related]
8. Comparison of allelic losses in chondroblastoma and primary chondrosarcoma of bone and correlation with fluorescence in situ hybridization analysis.
Papachristou DJ; Goodman MA; Cieply K; Hunt JL; Rao UN
Hum Pathol; 2006 Jul; 37(7):890-8. PubMed ID: 16784990
[TBL] [Abstract][Full Text] [Related]
9. Loss of heterozygosity on chromosomes 10q, 9p, 17p and 13q in malays with malignant glioma.
Zainuddin N; Jaafart H; Isa MN; Abdullah JM
Neurol Res; 2004 Jan; 26(1):88-92. PubMed ID: 14977064
[TBL] [Abstract][Full Text] [Related]
10. The neurofibromatosis type 2 gene is mutated in perineurial cell tumors: a molecular genetic study of eight cases.
Lasota J; Fetsch JF; Wozniak A; Wasag B; Sciot R; Miettinen M
Am J Pathol; 2001 Apr; 158(4):1223-9. PubMed ID: 11290539
[TBL] [Abstract][Full Text] [Related]
11. Genetic alterations in 'normal' luminal and myoepithelial cells of the breast.
Lakhani SR; Chaggar R; Davies S; Jones C; Collins N; Odel C; Stratton MR; O'Hare MJ
J Pathol; 1999 Dec; 189(4):496-503. PubMed ID: 10629549
[TBL] [Abstract][Full Text] [Related]
12. Loss of heterozygosity and tumor suppressor gene mutations in chondrosarcomas.
Yamaguchi T; Toguchida J; Wadayama B; Kanoe H; Nakayama T; Ishizaki K; Ikenaga M; Kotoura Y; Sasaki MS
Anticancer Res; 1996; 16(4A):2009-15. PubMed ID: 8712735
[TBL] [Abstract][Full Text] [Related]
13. Comprehensive loss of heterozygosity analysis and identification of a novel hotspot at 3p21 in salivary gland neoplasms.
Honjo N; Gunduz M; Fukushima K; Cengiz B; Beder LB; Gunduz E; Nagatsuka H; Xiao J; Shimizu K; Nishizaki K
Otolaryngol Head Neck Surg; 2007 Jul; 137(1):119-25. PubMed ID: 17599578
[TBL] [Abstract][Full Text] [Related]
14. Analysis of chromosome 1p abnormalities in renal oncocytomas by loss of heterozygosity studies: correlation with conventional cytogenetics and fluorescence in situ hybridization.
Picken MM; Chyna B; Flanigan RC; Lee JM
Am J Clin Pathol; 2008 Mar; 129(3):377-82. PubMed ID: 18285259
[TBL] [Abstract][Full Text] [Related]
15. MUC4 is a sensitive and extremely useful marker for sclerosing epithelioid fibrosarcoma: association with FUS gene rearrangement.
Doyle LA; Wang WL; Dal Cin P; Lopez-Terrada D; Mertens F; Lazar AJ; Fletcher CD; Hornick JL
Am J Surg Pathol; 2012 Oct; 36(10):1444-51. PubMed ID: 22982887
[TBL] [Abstract][Full Text] [Related]
16. Correlations of telomere length, P53 mutation, and chromosomal translocation in soft tissue sarcomas.
Liu C; Li B; Li L; Zhang H; Chen Y; Cui X; Hu J; Jiang J; Qi Y; Li F
Int J Clin Exp Pathol; 2015; 8(5):5666-73. PubMed ID: 26191279
[TBL] [Abstract][Full Text] [Related]
17. [Loss of heterozygosity on chromosome 13 in squamous cell carcinomas of the larynx].
Bai S; Zhang X; Wang J
Zhonghua Zhong Liu Za Zhi; 1997 Jan; 19(1):35-7. PubMed ID: 10743052
[TBL] [Abstract][Full Text] [Related]
18. High frequency loss of heterozygosity on the long arms of chromosomes 13 and 14 in nasopharyngeal carcinoma in Southern China.
Shao J; Li Y; Wu Q; Liang X; Yu X; Huang L; Hou J; Huang X; Ernberg I; Hu LF; Zeng Y
Chin Med J (Engl); 2002 Apr; 115(4):571-5. PubMed ID: 12133301
[TBL] [Abstract][Full Text] [Related]
19. Diverse p53 gene aberration in hepatocellular carcinoma detected by dual-color fluorescence in situ hybridization.
Kondo M; Marusawa H; Ueda Y; Katsurada A; Kawasome C; Takami S; Kinoshita M; Ikai I; Yamaoka Y; Chiba T
J Gastroenterol Hepatol; 2004 Sep; 19(9):1066-73. PubMed ID: 15304126
[TBL] [Abstract][Full Text] [Related]
20. Molecular studies of loss of heterozygosity in Chinese sporadic retinoblastoma patients.
Zhang XL; Fu WL; Zhao HX; Zhou LX; Huang JF; Wang JH
Clin Chim Acta; 2005 Aug; 358(1-2):75-80. PubMed ID: 15921673
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]