ライフサイエンスコーパス: fungal protein

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1 fungal culture, comprises 20 to 40% of total fungal protein.

2 e gene for a human protein homologous to the fungal proteins.

3 rved domains also present in uncharacterized fungal proteins.

4 icity and conservation of calnexin make this fungal protein a promising vaccine target.

5 plant DSPs, share with the above animal and fungal proteins a widespread and ancient carbohydrate-bi

6 Several well-characterized fungal proteins act as prions, proteins capable of multi

7 presumably with preferential assimilation of fungal protein, and autotrophic, mycorrhizal plants are

8 Model animal and fungal proteins are included in the database to facilita

9 The fungal protein CBP (calcium binding protein) is a known

10 e show that inhibition of these enzymes in a fungal protein expression system (Aspergillus niger) lea

11 Yeast and fungal protein expression systems are used for the produ

12 Increased IgG and IgA reactivity to fungal proteins in the BALF of asthmatics may reflect a

13 related to a small group of uncharacterized fungal proteins, including a second S. pombe protein tha

14 est that the unusual attributes of SOD5-like fungal proteins, including the absence of zinc and an op

15 This homology suggests that fungal proteins involved in either disease susceptibilit

16 a member (SC3) of the hydrophobin family of fungal proteins involved in the erection of aerial hypha

17 n but, like the streptomycetes proteins, the fungal protein is a surface active agent.

18 , whereas the N-terminal region is closer to fungal protein kinase A enzymes (PKA, members of the AGC

19 al development include several inhibitors of fungal protein, lipid and cell wall syntheses.

20 milar animal-plant, animal-fungal, and plant-fungal protein pairs.

21 CRO1 and She4p are fungal proteins required for the segregation of other mo

22 t identifies surprisingly many bacterial and fungal protein sequences that play a role in human infec

23 rent models, suggesting that both animal and fungal proteins share one topology.

24 ied the sordarins as selective inhibitors of fungal protein synthesis acting via a specific interacti

25 ic diterpene glycoside, selectively inhibits fungal protein synthesis by impairing the function of eu

26 arin derivatives are selective inhibitors of fungal protein synthesis, which specifically impair elon

27 present a novel class of agents that inhibit fungal protein synthesis.

28 Nep1 is an extracellular fungal protein that causes necrosis when applied to many

29 aracterization revealed that MesA is a novel fungal protein that contains predicted transmembrane dom

30 HET-C2 is a fungal protein that transfers glycosphingolipids between

31 scent of hydrophobins, which are amphiphilic fungal proteins that accumulate at interfaces.

32 Ryp1 is a member of a family of fungal proteins that includes Wor1, a master transcripti

33 ced in response to both the bacterial or the fungal proteins were undifferentiated vegetative hyphae

34 o identifies at least one previously unknown fungal protein with strong affinity to the Myc-Max-Mad n

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