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1 lacking Nanog fail to mature on reaching the genital ridge.
2 y due to the action of WNT4 within the early genital ridge.
3 erm cells begin to migrate to the developing genital ridge.
4 erm cells shortly after their arrival in the genital ridge.
5 initiates just before translocation into the genital ridge.
6 ation, followed by directed migration to the genital ridges.
7 GCs), resulting in fewer PGCs colonizing the genital ridges.
8 approximately 10.5 dpc as the PGCs enter the genital ridges.
9 in which they migrate out of the gut to the genital ridges.
10 al and migration as these cells colonize the genital ridges.
11 ctionally from the dorsal body wall into the genital ridges.
12 exit the gut, but do not migrate towards the genital ridges.
13 the gut mesentery at E10.5 migrate into the genital ridges.
14 e identify a possible PGC niche in the mouse genital ridges.
15 both around the dorsal aorta and in the uro-genital ridges.
16 in the allantois to the time they enter the genital ridges.
17 expressed in cells located centrally in the genital ridge and then later in cells located at the cra
18 find that chicken Dmrt1 is expressed in the genital ridge and Wolffian duct prior to sexual differen
19 romotes mesonephric cell survival within the genital ridges and that these cells support correct deve
20 nitial specification until they colonize the genital ridges, and suggest the existence of a ;spatio-t
22 entifies the most striking difference in the genital ridge at early stages of its development between
23 s within the coelomic epithelium (CE) of the genital ridge, but from cells also able to give rise to
24 reactivation is thought to emanate from the genital ridge, but it is unclear whether it is specific
25 no longer migrate directionally towards the genital ridges, but instead rapidly fragment and disappe
26 to the masculinising environment of the male genital ridge, defining a temporal window during which P
29 s migrate normally, but somatic cells of the genital ridge fail to proliferate and a discrete gonad f
33 uced to minimal levels in the Lhx9-deficient genital ridge, indicating that Lhx9 may lie upstream of
34 C-met expression is not detectable in male genital ridges isolated from embryos at 11.5 days postco
36 t of Wt1 in mice results in apoptosis of the genital ridge, it is unknown whether WT1 is required for
37 cells derived after PGC colonisation of the genital ridge, "late" and embryonic stem (ES) cell lines
39 ac and the para-aortic splanchnopleura/aorta-genital ridges-mesonephros (P-Sp/AGM) region are the mai
42 of Sry in the undifferentiated, bipotential genital ridges of mammalian XY fetuses initiates testis
45 o track through endoderm on their way to the genital ridge, our work raises the possibility that cons
48 as deleted before sex determination and most genital ridge somatic cells differentiated into steroido
50 haracteristics in both sexes at indifferent (genital ridge) stages and that these persist, becoming m
51 stitution of the EGCs or with the sex of the genital ridge (testis versus ovary) from which the PGCs
54 e number of PGCs reaching and populating the genital ridges, the molecular identity of only two of th
55 mitive vasculature is identical in XX and XY genital ridges until 11.5 days postcoitum (dpc), by 12.5
56 the developing hindgut, and traverse to the genital ridge where they cluster and ultimately inhabit
57 e through somatic tissues to the presumptive genital ridges, where they proliferate and differentiate
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