90 Detection of chromosomal aberrations in interphase nuclei from human primary breast tumors using in situ hybridization with chromosome-specific repetitive DNA-probes

1989 ◽  
Vol 38 (2) ◽  
pp. 186
Author(s):  
P. Devilee ◽  
R.F. Thierry ◽  
T. Kievits ◽  
R. Kolluri ◽  
A.H.N. Hopman ◽  
...  
Mutagenesis ◽  
1989 ◽  
Vol 4 (3) ◽  
pp. 165-169 ◽  
Author(s):  
E. Raimondi ◽  
S. Scariolo ◽  
A. De Sario ◽  
L. De Carli

Genome ◽  
2014 ◽  
Vol 57 (11/12) ◽  
pp. 601-607 ◽  
Author(s):  
Edina Türkösi ◽  
András Farkas ◽  
Nikolett Réka Aranyi ◽  
Borbála Hoffmann ◽  
Viola Tóth ◽  
...  

The 3HS.3BL spontaneous Robertsonian translocation obtained from the progenies of wheat–barley (Chinese Spring × Betzes) hybrids backcrossed with wheat line Mv9kr1 was transferred into the modern Martonvásár wheat cultivar Mv Bodri. The translocation was identified with molecular cytogenetic methods. The inheritance of the translocation was traced using genomic in situ hybridization. Fluorescence in situ hybridization using barley subtelomeric (HvT01) and centromere-specific [(AGGGAG)4] repetitive DNA probes confirmed that the complete barley chromosome arm was involved in the Robertsonian translocation. The wheat-specific repetitive DNA probes identified the presence of the whole wheat genome, except the short arm of the 3B chromosome. Genotypes homozygous for the centric fusion were selected, after which morphological analysis was performed on the plants and the yield components were measured in the field during two consecutive vegetative seasons. The introgression of the 3HS.3BL translocation into the modern wheat cultivar Mv Bodri significantly reduced the plant height due to the incorporation of the dwarfing allele RhtD1b. The presence of the 3HS.3BL translocation in the Mv9kr1 and Mv Bodri wheat background improved tillering and seeds per plant productivity in field experiments carried out in Martonvásár and Keszthely, Hungary.


Cytometry ◽  
1994 ◽  
Vol 17 (1) ◽  
pp. 13-25 ◽  
Author(s):  
Dino Celeda ◽  
Klaus Aldinger ◽  
Frank-Martin Haar ◽  
Michael Hausmann ◽  
Markus Durm ◽  
...  

1991 ◽  
Vol 56 (1) ◽  
pp. 94
Author(s):  
Heinz-Ulrich Weier ◽  
Horst Zitzelsberger ◽  
Mayumi Matsuta ◽  
Morimasa Matsuta ◽  
Joe W. Gray

1992 ◽  
Vol 47 (9-10) ◽  
pp. 739-747 ◽  
Author(s):  
Dino Celeda ◽  
Ulrich Bettag ◽  
Christoph Cremer

Fluorescence in situ hybridization (FISH) has found widespread applications in cytogenetics. So far the standard protocols for probe amplification (and simultaneous labeling) by PCR, nick translation and in situ hybridization involve different buffer systems leading to a number of time consuming washing steps even before hybridization. In this manuscript we show a fast technique of a close combination of DNA probe preparation and in situ hybridization (ISH). This method was applied to metaphase chromosomes from human lymphocytes fixed on slides. Two specific repetitive DNA probes, the pUC 1.77 DNA probe and the DYZ 1 repetitive DNA fraction were used, amplified and labeled in different ways. Additional experiments with total genomic male human DNA as the DNA probe suggest that this method may be extended to a large variety of other probes. Moreover the ISH technique described does not require toxic denaturing agents, such as formamide.


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