1929
DOI: 10.1007/bf02110964
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Über die Determination der larvalen Organe und der Imaginalanlage bei Seeigeln

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Cited by 48 publications
(14 citation statements)
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“…Animal hemispheres (presumptive ectoderm) (12) and animal mesomere pairs isolated from 16-cell embryos (13) that are cultured in the presence of LiCl form spicules and guts, structures normally derived only from vegetal cells. Increasing LiCl concentration induces correspondingly increased levels of expression of vegetal molecular markers, which mimics the effect of transplantation of vegetal cells to the animal pole of cleaving embryos.…”
mentioning
confidence: 99%
“…Animal hemispheres (presumptive ectoderm) (12) and animal mesomere pairs isolated from 16-cell embryos (13) that are cultured in the presence of LiCl form spicules and guts, structures normally derived only from vegetal cells. Increasing LiCl concentration induces correspondingly increased levels of expression of vegetal molecular markers, which mimics the effect of transplantation of vegetal cells to the animal pole of cleaving embryos.…”
mentioning
confidence: 99%
“…Such embryos are said to be "vegetalized" (4). Von Ubisch (5) reported in 1929 that treatment of the separated animal hemisphere with LiCl resulted in the subsequent formation of guts and spicules by these blastomeres. This result suggests that the capability to form vegetal structures also resides in the animal blastomeres, but in a suppressed or inactive form, and that LiCl may somehow allow vegetal structures to form in blastomeres that have an otherwise quite different determination and fate.…”
mentioning
confidence: 99%
“…Furthermore, it has been shown that embryos derived only from animal cap mesomeres that once received appropriate induction from the micromeres developed into juveniles (Minokawa & Amemiya 1999). Animal caps treated with LiCl also had the potential to develop into pluteus‐like larvae (von Ubisch 1929). However, the potential of the pluteus‐like larvae derived from the LiCl‐treated animal caps to metamorphose into juveniles is yet to be examined.…”
Section: Discussionmentioning
confidence: 99%
“…After various intervals, the embryos were rinsed with JSW and then cultured in plastic Petri dishes filled with JSW. Isolated animal caps were treated with LiCl at an appropriate concentration immediately after isolation for 2 h as reported for indirect developers (von Ubisch 1929) and then rinsed with JSW. Occasionally, unfertilized eggs were treated with LiCl for 2 h, rinsed with JSW and fertilized.…”
Section: Treatment Of Embryos With Liclmentioning
confidence: 99%
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