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Highly derived eutherian mammals from the earliest Cretaceous of southern Britain.
2
Double cones were present, a feature not found in eutherian mammals or marsupials.
3
These properties are again analogous to those observed for eutherian IGFBPs.
4
A Jurassic eutherian mammal and the divergence of marsupials and placentals.
5
The origins of eutherian mammals is one such problematic case.
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The exact origins of eutherian mammals is among them.
7
As a consequence of random decay and chromosome rearrangements over evolutionary time, Y chromosome gene repertoires differ between eutherian lineages.
8
Galectins are glycan-binding proteins that regulate innate and adaptive immune responses, and some confer maternal-fetal immune tolerance in eutherian mammals.
9
The sperm DNA of the marsupial species studied were significantly more sensitive to oxidative stress than the spermatozoa of eutherian species.
10
N- and C-terminal regions of possum alpha-lactalbumin were also sequenced and have been compared with wallaby alpha-lactalbumin and several eutherian alpha-lactalbumins.
11
We discuss the possibility that these additional somatosensory areas (SC and SR) are homologous to somatosensory areas in eutherian mammals.
12
Our results indicate the domestic cat Y chromosome has retained most X-degenerate genes that were present on the ancestral eutherian Y chromosome.
13
Upon the emergence of eutherian mammals, one of them was lost, whereas, the other acquired a novel genomic environment owing to translocation.
14
X-chromosome inactivation (XCI) is the epigenetic transcriptional silencing of an X-chromosome during the early stages of embryonic development in female eutherian mammals.
15
Comparative mapping of the X chromosome in eutherian mammals has revealed distinct regions of conservation as well as evolutionary rearrangements between human and mouse.
16
Unlike other eutherians, but similar to other marsupials investigated, only 40% of the neurons were orientation selective.