scholarly journals Non-random chromosome positioning in mammalian sperm nuclei, with migration of the sex chromosomes during late spermatogenesis

2005 ◽  
Vol 118 (9) ◽  
pp. 1811-1820 ◽  
Author(s):  
H. A. Foster
1988 ◽  
Vol 39 (1) ◽  
pp. 157-167 ◽  
Author(s):  
Sally D. Perreault ◽  
Randy R. Barbee ◽  
Kenneth H. Elstein ◽  
Robert M. Zucker ◽  
Carol L. Keefer

Chromosoma ◽  
1990 ◽  
Vol 100 (1) ◽  
pp. 32-36 ◽  
Author(s):  
Douglas K. Palmer ◽  
Kathleen O'Day ◽  
Robert L. Margolis
Keyword(s):  

1997 ◽  
Vol 99 (4) ◽  
pp. 474-477 ◽  
Author(s):  
M. Guttenbach ◽  
H. W. Michelmann ◽  
B. Hinney ◽  
W. Engel ◽  
M. Schmid

Author(s):  
G. Bench ◽  
M.H. Corzett ◽  
C.E. Kramer ◽  
P.G. Grant ◽  
R. Balhorn

1979 ◽  
Vol 27 (1) ◽  
pp. 353-358 ◽  
Author(s):  
D Pinkel ◽  
P Dean ◽  
S Lake ◽  
D Peters ◽  
M Mendelsohn ◽  
...  

Variability in DNA content and head shape of mammalian sperm are potentially useful markers for flow cytometric monitoring of genetic damage in spermatogenic cells. The high refractive index and extreme flatness of the sperm heads produce an optical effect which interferes with DNA measurements in flow cytometers which have dye excitation and fluorescence light collection normal to the axis of flow. Orientation of sperm in flow controls this effect and results in coefficients of variation of 2.5% and 4.2%, respectively, for DNA measurements of mouse and human sperm. Alternatively, the optical effect can be used to generate shape-related information. Measurements on randomly oriented sperm from three mammalian species using a pair of fluorescence detectors indicate that large shape differences are detectable. Acriflavine-Feulgen stained sperm nuclei are significantly bleached during flow cytometric measurements at power levels routinely used in many flow cytometers. Dual beam studies of this phenomenon indicate it may be useful in detecting abnormally shaped sperm.


1997 ◽  
Vol 99 (3) ◽  
pp. 407-412 ◽  
Author(s):  
E. Chevret ◽  
S. Rousseaux ◽  
M. Monteil ◽  
Y. Usson ◽  
J. Cozzi ◽  
...  

1994 ◽  
Vol 41 (1) ◽  
pp. 318
Author(s):  
V. Tok ◽  
S.C. Ng ◽  
M. Montag ◽  
S.L. Liow ◽  
A. Bongso ◽  
...  

2003 ◽  
Vol 83 (3) ◽  
pp. 375-384 ◽  
Author(s):  
D. L. Garner ◽  
G. E. Seidel Jr.

Development of flow cytometry for sorting mammalian sperm according to their sex chromosomes began in the late 1970s and early 1980s. This technology, which has recently been commercialized for bovine sperm, is based on the differences in DNA content between X- and Y-chromosome-bearing sperm. Under ideal conditions, 5000 live bovine sperm of each sex can be sorted per second at 90% accuracy. Pregnancy rates of 50% have been achieved routinely in well-managed heifers with sex-sorted, cryopreserved bovine sperm compared to 60–80% with unsexed control sperm. About 90% of offspring have been of the selected sex. Sorting sperm according to sex chromosome content is similarly successful in many other mammals including exotic species, but sorting efficiencies are somewhat less for sperm from some species. Key words: Mammals, sex chromosomes, flow cytometer, cell sorter, DNA content, X and Y sperm, Hoechst 33342


1975 ◽  
Vol 47 (2) ◽  
pp. 349-365 ◽  
Author(s):  
Anthony R. Bellvé ◽  
Everett Anderson ◽  
Linda Hanley-Bowdoin

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