Chromosome Preparation for Cytogenetic Analyses in Arabidopsis

2016 ◽  
Vol 1 (1) ◽  
pp. 43-51 ◽  
Author(s):  
Terezie Mandáková ◽  
Martin A. Lysak

Placenta ◽  
1997 ◽  
Vol 18 (7) ◽  
pp. 611 ◽  
Author(s):  
D.K. Kalousek


1994 ◽  
Vol 80 (2) ◽  
pp. 151-156
Author(s):  
Elvira D'Alessandro ◽  
Maria Luisa Lo Re ◽  
Roberto Crisci ◽  
Claudio Ligas ◽  
Giorgio Furio Coloni

Non-small cell lung cancer (NSCLC) shows a complex cytogenetic heterogeneity and up to now no particular chromosomal aberration seems to characterize its malignant evolution. We therefore performed cytogenetic analyses of 20 primary NSCLC, 8 adenocarcinomas and 12 squamous cell carcinomas on direct preparations or short-term cultures. Only 1 case was analyzed after long-term culture. Results were obtained from 11 samples and clonal rearrangements were found in 3 cases, a diploid and a near-triploid clone with several aberrations such as i (9q), rob (14; 15) and rob (21; 21) in 1 case, a near-triploid clone in 1 case, and Y chromosome loss in 1 case. Other aberrations found were sporadic, but + 7 aneuploidy and translocations involving 1p were detected in 2 and 3 samples respectively. Although to date it has been very difficult to recognize primary changes in NSCLC, nevertheless a literature review and our results indicate that i(9q) and robertsonian translocations are relevant findings.



2006 ◽  
Vol 27 (5) ◽  
pp. 1784-1794 ◽  
Author(s):  
Sudha Sharma ◽  
Deborah J. Stumpo ◽  
Adayabalam S. Balajee ◽  
Cheryl B. Bock ◽  
Peter M. Lansdorp ◽  
...  

ABSTRACT The mouse gene Recql is a member of the RecQ subfamily of DEx-H-containing DNA helicases. Five members of this family have been identified in both humans and mice, and mutations in three of these, BLM, WRN, and RECQL4, are associated with human diseases and a cellular phenotype that includes genomic instability. To date, no human disease has been associated with mutations in RECQL and no cellular phenotype has been associated with its deficiency. To gain insight into the physiological function of RECQL, we disrupted Recql in mice. RECQL-deficient mice did not exhibit any apparent phenotypic differences compared to wild-type mice. Cytogenetic analyses of embryonic fibroblasts from the RECQL-deficient mice revealed aneuploidy, spontaneous chromosomal breakage, and frequent translocation events. In addition, the RECQL-deficient cells were hypersensitive to ionizing radiation, exhibited an increased load of DNA damage, and displayed elevated spontaneous sister chromatid exchanges. These results provide evidence that RECQL has a unique cellular role in the DNA repair processes required for genomic integrity. Genetic background, functional redundancy, and perhaps other factors may protect the unstressed mouse from the types of abnormalities that might be expected from the severe chromosomal aberrations detected at the cellular level.



Copeia ◽  
1984 ◽  
Vol 1984 (1) ◽  
pp. 232 ◽  
Author(s):  
Chris T. Amemiya ◽  
John W. Bickham ◽  
John R. Gold


1999 ◽  
Vol 36 (6) ◽  
pp. 892-895 ◽  
Author(s):  
A. Jitpakdi ◽  
W. Choochote ◽  
D. Insun ◽  
P. Tippawangkosol ◽  
P. Keha ◽  
...  


Zootaxa ◽  
2021 ◽  
Vol 4958 (1) ◽  
pp. 345-358
Author(s):  
JADER OLIVEIRA ◽  
KAIO CESAR CHABOLI ALEVI ◽  
HÉLCIO R. GIL-SANTANA ◽  
CLEBER GALVÃO

Based on specimens of Zelurus ochripennis (Stål, 1854) collected in the entrance zone of a small terrestrial cave, some biological, ecological, morphological and cytogenetic data, as well, as the general morphology of their nymphs are presented for the first time. A short taxonomic summary of the species is also provided. 



2001 ◽  
Vol 155 (3) ◽  
pp. 417-423 ◽  
Author(s):  
S. Cigarrán ◽  
J. F. Barquinero ◽  
L. Barrios ◽  
M. Ribas ◽  
J. Egozcue ◽  
...  


1995 ◽  
Vol 341 (3) ◽  
pp. 199-206 ◽  
Author(s):  
A.D. Kligerman ◽  
K. Mottus ◽  
G.L. Erexson


Crop Science ◽  
2018 ◽  
Vol 58 (5) ◽  
pp. 1919-1931 ◽  
Author(s):  
Cong Liu ◽  
Narong Shi ◽  
Huiyu Wu ◽  
Xuyao An ◽  
Jinjuan Zheng ◽  
...  


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