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1 X. tropicalis is a close relative of X. laevis that shar
5 similar metamorphic changes in X. laevis and X. tropicalis, making it possible to use the large amoun
6 cytoplasm ("MPF activity") into G2-arrested X. tropicalis oocytes induces entry into meiosis I even
10 nce that tsg acts as a BMP antagonist during X. tropicalis gastrulation since the tsg depletion pheno
20 Indeed, TPX2 was threefold more abundant in X. tropicalis extracts, and elevated TPX2 levels in X. l
24 ex-determining gene, DM-W, does not exist in X. tropicalis, and the sex chromosomes in the two specie
26 tanin-dependent MT severing was increased in X. tropicalis, which, unlike X. laevis, lacks an inhibit
27 nsgenesis in X. laevis and gene knockdown in X. tropicalis, we demonstrate that endogenous Dot1L is c
29 he first positional cloning of a mutation in X. tropicalis, we show that non-contractile hearts in mu
30 al for embryogenesis and premetamorphosis in X. tropicalis On the other hand, knocking out EVI and MD
32 aled that microtubules polymerized slower in X. tropicalis extracts compared to X. laevis, but that t
33 derstanding the sex-determination systems in X. tropicalis is critical for developing this flexible a
34 LOGY/PRINCIPAL FINDINGS: We observed that in X. tropicalis, the premetamorphic intestine was made of
37 quence information and genetic advantages of X. tropicalis to dissect the pathways governing adult in
41 Like that of other tetrapods, the genome of X. tropicalis contains gene deserts enriched for conserv
42 dies of X. laevis oocytes holds for those of X. tropicalis, and suggest that X. tropicalis oocytes of
43 and cell biological experiments, the use of X. tropicalis provides novel insight into the complex me
45 for those of X. tropicalis, and suggest that X. tropicalis oocytes offer a good experimental system f
47 es representation of a minimum of 66% of the X. tropicalis genome, incorporating 758 of the approxima
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