Screening of minimalist noncanonical sites in duplex DNA and RNA reveals context and motif‐selective binding by fluorogenic base probes

Author(s):  
Yufeng Liang ◽  
Shiqin Miao ◽  
Jie Mao ◽  
Shekaraiah Devari ◽  
Maricarmen Gonzalez ◽  
...  
1995 ◽  
Vol 23 (19) ◽  
pp. 3916-3921 ◽  
Author(s):  
Parag V. Sahasrabudhe ◽  
Richard T. Pon ◽  
William H. Gmeiner
Keyword(s):  

1998 ◽  
Vol 120 (46) ◽  
pp. 12165-12166 ◽  
Author(s):  
Lauren E. Heystek ◽  
Hui-qiang Zhou ◽  
Prasad Dande ◽  
Barry Gold

1995 ◽  
Vol 33 (6) ◽  
pp. 449-452 ◽  
Author(s):  
William H. Gmeiner ◽  
Parag Sahasrabudhe ◽  
Richard T. Pon

Biopolymers ◽  
2014 ◽  
Vol 101 (4) ◽  
pp. 418-427 ◽  
Author(s):  
Mahmut Kara ◽  
Martin Zacharias

Author(s):  
B.A. Hamkalo ◽  
S. Narayanswami ◽  
A.P. Kausch

The availability of nonradioactive methods to label nucleic acids an the resultant rapid and greater sensitivity of detection has catapulted the technique of in situ hybridization to become the method of choice to locate of specific DNA and RNA sequences on chromosomes and in whole cells in cytological preparations in many areas of biology. It is being applied to problems of fundamental interest to basic cell and molecular biologists such as the organization of the interphase nucleus in the context of putative functional domains; it is making major contributions to genome mapping efforts; and it is being applied to the analysis of clinical specimens. Although fluorescence detection of nucleic acid hybrids is routinely used, certain questions require greater resolution. For example, very closely linked sequences may not be separable using fluorescence; the precise location of sequences with respect to chromosome structures may be below the resolution of light microscopy(LM); and the relative positions of sequences on very small chromosomes may not be feasible.


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