ライフサイエンスコーパス: nuclear pore complex protein

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1 nce that specifies the need for a particular nuclear pore complex protein.

2 anism and involves a direct interaction with nuclear pore complex proteins.

3 entry by binding to carbohydrate moieties on nuclear pore complex proteins.

4 cterized a proteolytic cleavage in conserved nuclear pore complex proteins.

5 at are a characteristic of a number of other nuclear pore complex proteins.

6 iphery and localizes in a pattern similar to nuclear pore complex proteins.

7 ions between cytosolic transport factors and nuclear pore complex proteins.

8 removing FG repeat domains from a subset of nuclear pore complex proteins.

9 Nup160 encodes a nuclear pore complex protein and shows evidence of adapt

10 NTF2 has been shown to bind nuclear pore complex proteins and the GDP form of Ran in

11 We also provide evidence that specific nuclear pore complex proteins contribute to this process

12 Kee et al. now propose that nuclear pore complex proteins form a fundamental part of

13 biochemical and genetic approaches, several nuclear pore complex proteins from yeast and vertebrates

14 nsistent with its purification as a putative nuclear pore complex protein, gp40 was localized to the

15 cells has shown that human (h)RAE1 binds the nuclear pore complex protein hNUP98 via a short NUP98 mo

16 ional allele of NUP82, encoding an essential nuclear pore complex protein in Saccharomyces cerevisiae

17 ed to be essential for the biogenesis of two nuclear pore complex proteins in mammals (Nup98 and Nup9

18 and cytoplasm requires interactions between nuclear pore complex proteins (nucleoporins) and soluble

19 Here, one SLAP is identified as the nuclear pore complex protein Nup153, one member of the F

20 The nuclear pore complex protein NUP88 is frequently elevate

21 that the Arabidopsis (Arabidopsis thaliana) nuclear pore complex protein Nup88/MOS7 is essential for

22 a region at the amino terminus of the human nuclear pore complex protein Nup96 interacts with the WD

23 d mutagenesis, we demonstrate that the human nuclear pore complex protein Nup98 specifically cleaves

24 s the interaction of N-terminal htt with the nuclear pore complex protein Tpr.

25 the Sad1p, UNC-84 domain protein Klaroid and nuclear pore complex proteins were mislocalized to the c

26 proteins (hnRNPs), zinc finger proteins, and nuclear pore complex proteins were sumoylated.

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