ライフサイエンスコーパス: intranuclear localization

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1 and immunoelectron microscopy confirmed the intranuclear localization.

2 tionary related holoenzymes may share common intranuclear localization and assembly pathways to coord

3 with binding to p130 or pRb but rather with intranuclear localization and modest induction of bindin

4 V (rAAV) to establish a relationship between intranuclear localization and rAAV transduction.

5 These results highlight the importance of intranuclear localization and suggest that Rep interacti

6 endocytic sorting, transcriptional control, intranuclear localization, and retroviral virion budding

7 Both of these observed intranuclear localizations have relevance to the potenti

8 with 480-1 virus (up to 96 h p.i.), and its intranuclear localization is not detected until 96 h p.i

9 asmic and nuclear membranes, suggesting that intranuclear localization is not essential for oncogenes

10 of up-regulated LT synthesis associated with intranuclear localization of 5-LO observed in PMN and ot

11 hibition of poly(ADP-ribosylation) prevented intranuclear localization of apoptosis-inducing factor a

12 Analysis of the intranuclear localization of fluorescently labeled RNAs

13 es ICP0-mediated transactivation, alters the intranuclear localization of ICP0, and significantly inc

14 rtments, small compartments, and no specific intranuclear localization of ICP8.

15 The lack of SUMOylation did not affect the intranuclear localization of IE1-72 kDa, including its a

16 The precise intranuclear localization of latent p53 protein in non-s

17 ered that mutant Nna1 dramatically increases intranuclear localization of lysyl oxidase propeptide, w

18 on of oxidative stress markers, and enhanced intranuclear localization of pancreatic and duodenal hom

19 ic evidence demonstrates the requirement for intranuclear localization of regulatory complexes that f

20 RXR alpha C terminus may play a role in the intranuclear localization of RXR alpha.

21 Because the intranuclear localization of the UL9 protein, along with

22 we show an explicit relationship between the intranuclear localization of various chromosome segments

23 an aberrant Ad E2 DNA-binding protein (DBP) intranuclear localization pattern and an apparent failur

24 We have examined the intranuclear localization pattern of both the IE1 and IE

25 This intranuclear localization remains throughout adulthood a

26 It controls the intranuclear localization, stability, and DNA repair fun

27 shown in cells by coimmunoprecipitation, and intranuclear localization studies using confocal microsc

28 cient p53 mutant showed a similar pattern of intranuclear localization, suggesting that SUMO-1 does n

29 ingle amino acid substitution that abrogates intranuclear localization was introduced in the AML1 sub

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