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Figure 1 shows the effect of P. tuber-regium treatment on testes of animals administered CCl4 for 13 weeks.
The present study was designed to investigate the effect of MSG on testes of young male Wistar rats (n = 30).
Persistent effects on testes of developmental exposure to similar levels of EE2 in zebrafish were not reported by Weber et al. (2003), but duct morphology was not examined.
To study the correlation of Pol II binding with gene expression in spermatogenesis, we performed two Pol II ChIP-Seq experiments, on testes of 10 and 16dpp mice, and used a third, published dataset for adult testis [ 46].
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Fig. 1 Effect of P. tuber-regium on relative weight of testes of animals treated with CCl4 for 13 weeks (n = 10).
M. coronatus has much smaller reproductive organs during breeding (Fig. 1a, b): their testes are on average 10% of the size of testes of other Malurus (range: 6 – 18%; Fig. 1b) and cloacal protuberances (CP; the site of sperm storage) in breeding males (57.4 ± 3.6 mm, n = 40) are on average about half of the CP size of other fairy-wrens (28 – 87%; Fig. 1a).
Lice previously marked on the ears of one host were most frequently recaptured on the testes of that same host or other hosts, rather than the ears.
The majority of the marked recovered lice (80.3%) were found on the testes of new hosts.
The hybridization experiments were repeated on dissected testes of D. melanogaster and D. virilis.
Interestingly, vitellogenin mRNA is also expressed by follicle cells on the testes of both the primary bud and the zooid.
Because of the known effects on fetal testes of MEHP, the nonbrominated analog of TBMEHP, we evaluated testes from fetuses of exposed dams for induction of MNGs (a manifestation of altered seminiferous cords) and testosterone production.
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