Localization of the gene for the vitamin B12 binding protein, transcobalamin II, near the centromere on mouse chromosome 11, linked with the hemoglobin alpha-chain locus

1985 ◽  
Vol 23 (1-2) ◽  
pp. 139-153 ◽  
Author(s):  
M. Fr�ter-Schr�der ◽  
M. Prochazka ◽  
O. Haller ◽  
F. Arwert ◽  
H. J. Porck ◽  
...  
1989 ◽  
Vol 82 (3) ◽  
pp. 234-238 ◽  
Author(s):  
Adelina A. Davies ◽  
Stephen E. Moss ◽  
Mark R. Crompton ◽  
Tania A. Jones ◽  
Nigel K. Spurr ◽  
...  

1994 ◽  
Vol 6 (1) ◽  
pp. 33-40 ◽  
Author(s):  
Y. Hayashizaki ◽  
H. Shibata ◽  
S. Hirotsune ◽  
H. Sugino ◽  
Y. Okazaki ◽  
...  

1994 ◽  
Vol 5 (12) ◽  
pp. 805-806 ◽  
Author(s):  
E. H. Birkenmeier ◽  
L. B. Rowe ◽  
M. W. Crossman ◽  
J. I. Gordon

Genomics ◽  
1993 ◽  
Vol 18 (2) ◽  
pp. 407-409 ◽  
Author(s):  
Stephanie L. Simek ◽  
Christine A. Kozak ◽  
Dolores Winterstein ◽  
Glenn Hegamyer ◽  
Nancy H. Colburn

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.


1996 ◽  
Vol 7 (2) ◽  
pp. 163-163
Author(s):  
G. C. Voss ◽  
H. Jockusch

Sign in / Sign up

Export Citation Format

Share Document