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1 stasis, whereas excess RA is well known as a teratogen.
2 transition metal cadmium is an environmental teratogen.
3 require treatment with isotretinoin, a known teratogen.
4    Marginal biotin deficiency may be a human teratogen.
5 n the early 1960s after it was found to be a teratogen.
6 result from exposure to this important human teratogen.
7  belief that cocaine is a uniquely dangerous teratogen.
8 odium valproate and carbamazepine, are human teratogens.
9 oxification of environmental carcinogens and teratogens.
10  "proximate zone" of most likely exposure to teratogens.
11 Moreover, astrogliosis may be common to both teratogens.
12 tiologies include the local formation of the teratogen acetaldehyde or oxygen radicals by fetal ethan
13 s well as the causal involvement of specific teratogens acting at the earliest stages of neurulation.
14 ilbestrol (DES), a known human developmental teratogen and carcinogen.
15 lysis indicated that the interaction between teratogen and genotype was highly significant (P < or =
16 Although hyperthermia is a recognized animal teratogen and maternal fever has been associated with bi
17 d suggest apoptosis as a potential target of teratogens and genetic defects that are associated with
18 ren (5000+) worldwide exposed to this potent teratogen, and the many informative cases in which the e
19                             New uses for old teratogens as well as novel chemical modulators of devel
20 sy and bipolar disorder and is also a potent teratogen, but its mechanisms of action in any of these
21 een studied for more than 30 years as potent teratogens capable of inducing cyclopia and other birth
22                          RA is also a potent teratogen, causing multi-organ birth defects in humans.
23                                              Teratogens could disrupt the two cellular processes to a
24          Here we show that the plant-derived teratogen cyclopamine, which inhibits the Hh response, i
25 xamine craniofacial defects by a known human teratogen, cyclopamine.
26 served when cocultures were treated with the teratogen cyclophosphamide.
27                                        These teratogens did not prevent the sterol modification of Sh
28             Although alcohol is a recognized teratogen, evidence is limited on alcohol intake and ora
29 ant exposure were compared with those of non-teratogen-exposed controls.
30                          Results showed that teratogen exposure was followed by decreased levels of R
31 into the approximate timing of the causative teratogen exposure.
32  screening platform to mitigate the risks of teratogen exposures in human.
33 apeutic interventions to mitigate effects of teratogen exposures.
34      We propose that increased deposition of teratogens/fetotoxicants to the embryonic compartment is
35  Maternal diabetes, genetic factors and some teratogens have been shown to be associated with its pat
36                            Ethanol acts as a teratogen in developing fetuses causing abnormalities of
37 mentally ubiquitous contaminant, is a potent teratogen in mice.
38  only TCAA appeared to be a specific cardiac teratogen in the fetus when imbibed by the maternal rat.
39 zopanib, vandetanib, and everolimus are also teratogens in these models.
40 The fetal brain is sensitive to a variety of teratogens, including ethanol.
41 f teratogens to achieve this; testing single teratogens independently and not examining combinatorial
42 ome-wide search for susceptibility genes for teratogen-induced clefting in the AXB and BXA set of rec
43 an harm neurons subjected to excitotoxic and teratogen-induced injury.
44 omal regions for both forms of clefting when teratogen-induced.
45                             We conclude that teratogen induction of p53-dependent apoptosis in the de
46 h both multiple genetic loci and exposure to teratogens influencing susceptibility.
47 gesting that the mechanism of action of this teratogen involves a pathway(s) requiring Paraxis activi
48                        Isotretinoin, a known teratogen, is strictly regulated through the iPLEDGE pro
49                We investigated mechanisms of teratogen-mediated blockade of maternofetal transport by
50 xification of and protection from cadmium, a teratogen, mutagen and potentially lethal heavy metal.
51 posed rat embryos to valproic acid, a second teratogen newly linked to autism.
52  basis underlying HPE is not known, although teratogens, non-random chromosomal anomalies and familia
53 e analysed the effects of several classes of teratogens on cartilage formation using 200 independent
54                 Retinoic acid (RA), a potent teratogen, produces a characteristic set of embryonic ca
55                                 In addition, teratogens such as jervine, which inhibit the response o
56               Despite its history as a human teratogen, thalidomide is emerging as a treatment for ca
57 myeloma and inflammatory diseases, is also a teratogen that causes birth defects, such as limb trunca
58                                 Alcohol is a teratogen that induces a variety of abnormalities includ
59 , an effective anti-acne therapy, is a known teratogen that is strictly regulated through the iPLEDGE
60 um could be a target of genetic mutations or teratogens that cause human conotruncal heart defects.
61 ryonic exposure to ethanol or retinoic acid, teratogens that cause increased cell death.
62 nd epilepsy but it requires a combination of teratogens to achieve this; testing single teratogens in
63 s as epigenetic intermediaries, which permit teratogens to shape complex, divergent developmental pro
64 gate the mechanism of action of a well-known teratogen, valproic acid (VPA).
65 A during pregnancy also use alcohol, a known teratogen, we examined whether local brain volumes diffe
66  embryos treated with valproic acid, a known teratogen which affects somite segmentation, showed pert
67  genetic or genomic variation to exposure to teratogens, which elicit diverse cell and molecular resp
68 DM (classes A1 and A2) is not an established teratogen yet.

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