Genetic mapping of the homeobox-containing gene Otxl gene on mouse Chromosome 11

1996 ◽  
Vol 7 (3) ◽  
pp. 241-241 ◽  
Author(s):  
L. De Gregorio ◽  
G. Manenti ◽  
A. Simeone ◽  
T. A. Dragani
1995 ◽  
Vol 6 (8) ◽  
pp. 559-559
Author(s):  
C. A. Kozak ◽  
C. E. Buckler ◽  
M. Srivastava

Genomics ◽  
1997 ◽  
Vol 40 (1) ◽  
pp. 114-122 ◽  
Author(s):  
Dawn E. Watkins-Chow ◽  
Marion S. Buckwalter ◽  
Matthew M. Newhouse ◽  
Amy C. Lossie ◽  
Michelle L. Brinkmeier ◽  
...  

Genomics ◽  
1995 ◽  
Vol 29 (3) ◽  
pp. 576-581 ◽  
Author(s):  
MICHELLE L. BENNETT ◽  
ASTRID HAUGEN-STRANO ◽  
CHARLES COCHRAN ◽  
HEATHER A. BROWNLEE ◽  
FRED T. FIEDOREK, JR. ◽  
...  

1996 ◽  
Vol 7 (3) ◽  
pp. 242-242 ◽  
Author(s):  
L. De Gregorio ◽  
K. Harshman ◽  
J. Rosenthal ◽  
T. A. Dragani ◽  
M. A. Pierotti

Genetics ◽  
2002 ◽  
Vol 161 (4) ◽  
pp. 1651-1659 ◽  
Author(s):  
Elena de la Casa-Esperón ◽  
J Concepción Loredo-Osti ◽  
Fernando Pardo-Manuel de Villena ◽  
Tammi L Briscoe ◽  
Jan Michel Malette ◽  
...  

AbstractWe observed that maternal meiotic drive favoring the inheritance of DDK alleles at the Om locus on mouse chromosome 11 was correlated with the X chromosome inactivation phenotype of (C57BL/ 6-Pgk1a × DDK)F1 mothers. The basis for this unexpected observation appears to lie in the well-documented effect of recombination on meiotic drive that results from nonrandom segregation of chromosomes. Our analysis of genome-wide levels of meiotic recombination in females that vary in their X-inactivation phenotype indicates that an allelic difference at an X-linked locus is responsible for modulating levels of recombination in oocytes.


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