Analysis of the function s of nuclear mouse Ovo1 proteins must await a comprehensive analysis of the various mOvo1 isoforms and an exploration into their ability to regulate specific genes or processes involved in terminal differentiation.
Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders. Disruption of neurexin 1 associated with autism spectrum disorder. Finally, Henn and Zhang raised the possibility that the presence of residual Y chromosome sequences in a subset of cells in the brain could explain the greater vulnerability of X m TS females to social dysfunction, but this hypothesis is untestable without access to brain tissue.
As before, three hybridizing bands were detected, although their relative levels were somewhat different from those observed in skin. This may be related to having a short, horizontally oriented eustachian tube which results in poor drainage and ventilation of the middle ear space.
Trends Genet. In situ hybridizations of wild-type mature testis detected movo1 RNAs in primary and secondary spermatocytes, but not in spermatogonia Fig. Moreover, whereas sperm production was greatly diminished, male movo1 mutant mice were not completely sterile.
Drosophila OVO zinc-finger protein regulates ovo and ovarian tumor target promoters. This may be related to having a short, horizontally oriented eustachian tube which results in poor drainage and ventilation of the middle ear space. However, recent comparative transcriptome sequencing  indicated that genes on the single Z in female chicken had equivalent expression levels to orthologous genes in outgroup species, where the Z is autosomal i.
Large-scale population study of human cell lines indicates that dosage compensation is virtually complete. Figure 5. Dev Neuropsychol. Ohno S Sex chromosomes and sex-linked genes. Therefore, TS represents a powerful model for investigating both X chromosome and gonadal steroid effects.