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A transgenic insertion causing cryptorchidism in mice.
A novel ubiquitin ligase is deficient in Fanconi anemia.
The mouse juvenile spermatogonial depletion (jsd) phenotype is due to a mutation in the X-derived retrogene, mUtp14b.
A mouse Y chromosome gene encoded by a region essential for spermatogenesis and expression of male-specific minor histocompatibility antigens.
A novel X gene with a widely transcribed Y-linked homologue escapes X-inactivation in mouse and human.
Analysis of mutation rates in the SMCY/SMCX genes shows that mammalian evolution is male driven.
Mouse H-Y encoding Smcy gene and its X chromosomal homolog Smcx.
Evidence for distinguishable transcripts of the putative testis determining gene (ZFY) and mapping of homologous cDNA sequences to chromosomes X,Y and 9.
A murine TSPY.
Homology of a candidate spermatogenic gene from the mouse Y chromosome to the ubiquitin-activating enzyme E1.
The ubiquitin-activating enzyme E1 homologous genes on the mouse Y chromosome (Ube1y) represent one functional gene and six partial pseudogenes.
Sequence Homology, Amino Acid
Sequence Homology, Nucleic Acid