ライフサイエンスコーパス: embryonic age

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1 proliferation varies by location rather than embryonic age.

2 Galpha(i2) promoter activity independent of embryonic age.

3 an dorsal forebrain stem cells from the same embryonic age.

4 uctive interactions changes as a function of embryonic age.

5 ursors from neural tissue derived from early embryonic ages.

6 ction system in the MA-Ao region starting at embryonic age 11.5.

7 f LHRH neurons from rhesus monkey embryos at embryonic ages 35-37 were dissected out and cultured on

8 opment examined, at Carnegie stage 15 or 16 (embryonic age 5-6 weeks).

9 d in vivo function-blocking of GDNF at early embryonic ages almost entirely suppresses ciliary axon o

10 At all embryonic ages analyzed, the distribution of SPNs and PP

11 ences in permeability among RPE of different embryonic age and culture conditions.

12 ing chick long bones changes with increasing embryonic age and that syndecan-3 gene expression change

13 lls (iPSCs) resets their identity back to an embryonic age and, thus, presents a significant hurdle f

14 gal (TCF optimal promoter) reporter mouse at embryonic ages and compared to Axin2 mRNA expression, an

15 se transcription factors emerges at distinct embryonic ages and only in postmitotic cells.

16 auditory system, initial connections form at embryonic ages, but the functional characteristics of th

17 ptors and ephrins in the VIIIth nerve during embryonic ages corresponding to the initial innervation

18 We have found that, during early embryonic ages (E12-E16), both glutamic acid decarboxyla

19 At later embryonic ages EphA4 expression is symmetric around NL,

20 At the three embryonic ages examined, E70, E90, and E120, alpha 2A re

21 promoted an increase in neuron number at all embryonic ages examined, there was a developmental shift

22 use embryonic SC, this activity starts at an embryonic age of approximately 12 d and is characterized

23 ncephalic morphology was abnormal at all the embryonic ages studied (days 10.5, 12.5 and 14.5).

24 The incidence of each subunit declined with embryonic age, suggesting a role in early development.

25 At young embryonic ages there was significant overlap in sensitiv

26 visual cortex of cats and ferrets from late embryonic ages to adulthood.

27 tiated thymidine ([(3)H]dT, or TdR) at early embryonic ages were killed at different intervals postin

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