Characterization of the A673 cell line (Ewing tumor) by molecular cytogenetic techniques

2003 ◽  
Vol 141 (2) ◽  
pp. 138-142 ◽  
Author(s):  
A Martı́nez-Ramı́rez ◽  
S Rodrı́guez-Perales ◽  
B Meléndez ◽  
B Martı́nez-Delgado ◽  
M Urioste ◽  
...  
Keyword(s):  
Cell Line ◽  
Molecular Cytogenetic ◽  
Molecular Cytogenetic Techniques ◽  
Ewing Tumor

scholarly journals Conventional and Molecular Cytogenetic Characterization of a New Human Cell Line, GIST-T1, Established from Gastrointestinal Stromal Tumor

2002 ◽  
Vol 82 (5) ◽  
pp. 663-665 ◽  
Author(s):  
Takahiro Taguchi ◽  
Hiroshi Sonobe ◽  
Shin-ichi Toyonaga ◽  
Ichiro Yamasaki ◽  
Taro Shuin ◽  
...  
Keyword(s):  
Gastrointestinal Stromal Tumor ◽  
Cell Line ◽  
Human Cell ◽  
Human Cell Line ◽  
Stromal Tumor ◽  
Molecular Cytogenetic ◽  
Cytogenetic Characterization

Characterization of trisomy 8 in pediatric undifferentiated sarcomas using advanced molecular cytogenetic techniques

2007 ◽  
Vol 174 (1) ◽  
pp. 35-41 ◽  
Author(s):  
Shamini Selvarajah ◽  
Maisa Yoshimoto ◽  
Mona Prasad ◽  
Mary Shago ◽  
Jeremy A. Squire ◽  
...  
Keyword(s):  
Trisomy 8 ◽  
Molecular Cytogenetic ◽  
Molecular Cytogenetic Techniques

Molecular cytogenetic characterization of human papillomavirus16-transformed foreskin keratinocyte cell line 16-MT

2006 ◽  
Vol 168 (1) ◽  
pp. 36-43 ◽  
Author(s):  
Eva M. McGhee ◽  
Philip D. Cotter ◽  
Jingly F. Weier ◽  
Jennifer W. Berline ◽  
Mary A. Turner ◽  
...  
Keyword(s):  
Cell Line ◽  
Molecular Cytogenetic ◽  
Keratinocyte Cell ◽  
Cytogenetic Characterization

scholarly journals Genotype-Phenotype Characterization of Wolf-Hirschhorn Syndrome Confirmed by FISH: Case Reports

2012 ◽  
Vol 2012 ◽  
pp. 1-5 ◽  
Author(s):  
F. Sheth ◽  
O. R. Akinde ◽  
C. Datar ◽  
O. V. Adeteye ◽  
J. Sheth
Keyword(s):  
Cytogenetic Study ◽  
Case Reports ◽  
Normal Karyotype ◽  
Comparative Genomic ◽  
Molecular Cytogenetic ◽  
Contiguous Gene ◽  
Multiple Malformation ◽  
Molecular Cytogenetic Techniques

The Wolf-Hirschhorn syndrome (WHS) is a multiple malformation and contiguous gene syndrome resulting from the deletion encompassing a 4p16.3 region. A microscopically visible terminal deletion on chromosome 4p (4p16→pter) was detected in Case 1 with full blown features of WHS. The second case which had an interstitial microdeletion encompassingWHSC 1andWHSC 2genes at 4p16.3 presented with less striking clinical features of WHS and had an apparently “normal” karyotype. The severity of the clinical presentation was as a result of haploinsufficiency and interaction with surrounding genes as well as mutations in modifier genes located outside the WHSCR regions. The study emphasized that an individual with a strong clinical suspicion of chromosomal abnormality and a normal conventional cytogenetic study should be further investigated using molecular cytogenetic techniques such as fluorescencein situhybridization (FISH) or array-comparative genomic hybridization (a-CGH).

Cytogenetic and molecular cytogenetic characterization of the stable ovarian carcinoma cell line (OvBH-1)

2006 ◽  
Vol 164 (1) ◽  
pp. 10-15 ◽  
Author(s):  
Kamila Schlade-Bartusiak ◽  
Maria M. Sasiadek ◽  
Julia K. Bar ◽  
Steffi Urbschat ◽  
Nikolaus Blin ◽  
...  
Keyword(s):  
Ovarian Carcinoma ◽  
Cell Line ◽  
Carcinoma Cell ◽  
Carcinoma Cell Line ◽  
Ovarian Carcinoma Cell Line ◽  
Molecular Cytogenetic ◽  
Cytogenetic Characterization
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