What are the germ cell phenotypes from infertile men telling us about spermatogenesis

Histology and Histopathology

Volumn 14, Issue 3, 1999, Pages 959-971

  Escalier, D ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

Meiosis; Mutants; Sperm; Spermatogenesis; Testis; Transgenic

Indexed keywords

DROSOPHILA; GENE ISOLATION; GENETIC ENGINEERING; GENOTYPE; GERM CELL; MALE INFERTILITY; MEIOSIS; METAPHASE; MITOSIS INHIBITION; PHENOTYPE; PLEIOTROPY; POLYPLOIDY; POLYTENE CHROMOSOME; REVIEW; SEQUENCE HOMOLOGY; SPERMATOGENESIS;

ANIMALS; GENOTYPE; HUMANS; INFERTILITY, MALE; MALE; PHENOTYPE; SPERMATOGENESIS; SPERMATOZOA;

EID: 0033064737     PISSN: 02133911     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (3)

1. Alexandre C., Bisson J.P. and David G. (1975). Asthénospermie totale avec anomalie ultrastructurale du flagelle chez deux frères stériles. J. Gyn. Obst. Biol. Reprod. 7, 31-38.
2. Aumuller G., Fuhrmann W. and Krause W. (1987). Spermatogenetic arrest with inhibition of acrosome and sperm tail development. Andrologia 19, 9-17.
3. Baker S.M., Bronner C.E., Zhang L., Plug A.W., Elliot E.A., Yu J., Ashley T., Arnheim N., Flavell R.A. and Liskay R.M. (1995). Male defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis. Cell 82, 309-319.