Evolution by fusion and amplification: the murine Sp100-rs gene cluster

1998 ◽  
Vol 80 (1-4) ◽  
pp. 226-231 ◽  
Author(s):  
D. Weichenhan ◽  
B. Kunze ◽  
W. Traut ◽  
H. Winking
Keyword(s):  
Author(s):  
H. Fryssira ◽  
P. Makrythanasis ◽  
A. Kattamis ◽  
K. Stokidis ◽  
B. Menten ◽  
...  

2001 ◽  
Vol 7 (5) ◽  
pp. 349-358 ◽  
Author(s):  
N. Misawa ◽  
K. Kawashima ◽  
F. Kondo ◽  
B.M. Allos ◽  
M.J. Blaser

2009 ◽  
Vol 2 (3) ◽  
pp. 119-128 ◽  
Author(s):  
Eva Lattka ◽  
Thomas Illig ◽  
Joachim Heinrich ◽  
Berthold Koletzko

Genome ◽  
1989 ◽  
Vol 32 (3) ◽  
pp. 365-372 ◽  
Author(s):  
T. Starr ◽  
A. M. Howell ◽  
J. McDowall ◽  
K. Peters ◽  
A. M. Rose

We have isolated probes for DNA polymorphisms across the linkage group I gene cluster in Caenorhabditis elegans, using Tc1-linkage selection. The probes detect strain polymorphism between the wild-type strains of var. Bristol and var. Bergerac. As a result of mapping the sites hP4, hP5, hP6, hP7, hP9, and sP1, more than 1000 kilobases (kb) of cloned cosmid DNA has been positioned on the genetic map. We found there is more DNA per map unit in the center of the gene cluster than expected on the basis of the genomic average. Furthermore, the amount is not constant across the entire region but reaches a peak in the hP9 unc-13 interval. To find the coding regions, we examined DNA cross-homology between two species, Caenorhabditis elegans and Caenorhabditis briggsae. Approximately one-third of the DNA in the hP5 hP9 interval was examined for coding regions and 21 sequences were identified within 318 kb of DNA.Key words: Caenorhabditis elegans, physical map, DNA polymorphisms, genetic mapping, Caenorhabditis briggsae.


2006 ◽  
Vol 61 (2) ◽  
pp. 87-96 ◽  
Author(s):  
Sara C. Hamon ◽  
Sharon L.R. Kardia ◽  
Eric Boerwinkle ◽  
Kiang Liu ◽  
Kathy L.E. Klos ◽  
...  
Keyword(s):  

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