ライフサイエンスコーパス: EER

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1 four mouse EER-associated genes contained an EER in the orthologous human gene, although nucleotide s

2 functional analyses of two motifs, RXLR and EER, present in translocated oomycete effectors.

3 here-derived MBF-EER was noted with A . beta-EER (r=0.88, P<0.01).

4 The correlation with beta-EER was better (r=0.69, P<0.01).

5 Among these conserved EER-associated genes were several TNF alpha-signaling ge

6 el of obesity, and to compare TEE to the DRI EER.

7 During EER, individuals alternatively viewed and upregulated an

8 orroborates the use of the DRI equations for EER.

9 ults with GSP (EER n = 19; TAC n = 18), GAD (EER n = 17; TAC n = 17), GSP/GAD (EER n = 17; TAC n = 15

10 18), GAD (EER n = 17; TAC n = 17), GSP/GAD (EER n = 17; TAC n = 15), and no psychopathology (EER n =

11 Medication-free adults with GSP (EER n = 19; TAC n = 18), GAD (EER n = 17; TAC n = 17), G

12 on with radiolabeled microsphere-derived MBF-EER was noted with A . beta-EER (r=0.88, P<0.01).

13 lume was observed during reversal of the MBF-EER.

14 Seventy-four mouse EER-associated genes contained an EER in the orthologous

15 Here we compare the neural correlates of EER and TAC in GSP, GAD, and GSP/GAD.

16 n = 17; TAC n = 15), and no psychopathology (EER n = 18; TAC n = 18) participated.

17 ved MBF and A-endocardial/epicardial ratios (EER) (r=0.46).

18 cortex in both explicit emotion regulation (EER) and top-down attentional control (TAC).

19 e exceeded the estimated energy requirement (EER) for ideal body weight in 1995 by 62% for males and

20 TER-CF was the estimated energy requirement (EER) formula at the active level (EERact).

21 Intake (DRI) estimated energy requirements (EER) noted that DLW studies in adults aged 40 to 60 y we

22 ectors in oomycete pathogens possess an RXLR-EER motif in their amino acid sequence that is necessary

23 However, following replacement of Avr3a RXLR-EER motifs with alanine residues, singly or in combinati

24 cribe recent progress in characterizing RXLR-EER effectors and discuss why so many of these rapidly e

25 We use the Phytophthora infestans RXLR-EER-containing protein Avr3a as a reporter for transloca

26 s 425 potential genes encoding secreted RXLR-EER class proteins in the P. infestans genome.

27 We show that RXLR-EER-encoding genes are transcriptionally upregulated dur

28 r for translocation because it triggers RXLR-EER-independent hypersensitive cell death following reco

29 We show that Avr3a, with or without RXLR-EER motifs, is secreted from P. infestans biotrophic str

30 caloric intake still remained >19% above the EER in both groups.

31 d 39% for females and decreased by 3% of the EER per year in males (P = 0.02) and by 2% in females (P

32 om DLW was highly correlated (r = 0.93) with EER from the DRI equations.

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