ライフサイエンスコーパス: mRNA differential display

1 prepared from the intestine and analyzed by mRNA differential display.

2 legume Lotus japonicus were identified using mRNA differential display; 110 differentially displayed

3 ematically investigate such changes, we used mRNA differential display and cDNA microarrays to screen

4 ement-binding proteins (SREBPs), we utilized mRNA differential display and mutant cells that express

5 Using mRNA differential display and screening of the cDNA libr

6 e of Petunia inflata, we had previously used mRNA differential display and subtractive hybridization

7 or suppressor gene, rCop-1 was identified by mRNA differential display as a gene whose expression bec

8 An mRNA differential display comparison of mouse JB6 promot

9 We used mRNA differential display (DD) to detect global differen

10 This work validates the application of mRNA differential display for the discovery of new micro

11 on and apoptosis in v-Rel-transformed cells, mRNA differential display has been used.

12 mRNA differential display identified TFF1 as a gastrin-r

13 d as a putative ethanol-regulated gene using mRNA differential display in mice genetically selected f

14 eceptor fusion gene (DeltaRaf-1:ER) and used mRNA differential display in search of messages induced

15 This work shows that mRNA differential display is an important tool for the i

16 ystematic identification of these genes, the mRNA differential display method circumvents this proble

17 We have used a mRNA differential display method to identify FGF-1-induc

18 Using the mRNA differential display method, we have identified the

19 that of its thin littermate (ob/+) using the mRNA differential display method.

20 ell-activating agents, was isolated using an mRNA differential display method.

21 In an effort to make mRNA differential display more amenable as a molecular s

22 (msg1) related gene], was identified through mRNA differential display of interleukin (IL) 9-stimulat

23 tive genes were identified by messenger RNA (mRNA) differential display of the gastric fundus from ga

24 s in the neurons was also investigated using mRNA differential display PCR in an attempt to elucidate

25 derstanding of its cold tolerance mechanism, mRNA differential display reverse transcriptase polymera

26 during initial interactions, as revealed by mRNA differential display reverse transcription-PCR and

27 mRNA differential display RT-PCR has been extensively us

28 e activities in the two limbs, we employed a mRNA differential display screen for the detection of ca

29 regulated gene from L. bicolor employing the mRNA differential display technique (DDRT-PCR).

30 By using a mRNA differential display technique to search for salicy

31 es accumulate excess lipids, we employed the mRNA differential display technique using RNA isolated f

32 nd/or carcinogenicity of nickel compounds, a mRNA differential display technique was used to identify

33 Using the mRNA differential display technique, seven cDNAs have be

34 Using an mRNA differential display technique, we have isolated a

35 By using mRNA differential display technique, we show, herein, th

36 finger proteins was used in conjunction with mRNA differential display to amplify related mRNAs from

37 We now report the use of mRNA differential display to examine the extent to which

38 d, and parental DC-3F cells were compared by mRNA differential display to identify genetic changes oc

39 in prostate cancer differentiation, we used mRNA differential display to identify the gene(s) induce

40 aracterize shared molecular defects, we used mRNA differential display to isolate genes that have alt

41 mRNA differential display was used in conjunction with a

42 The technique of mRNA differential display was used to identify simultane

43 mRNA differential display was used to screen for novel g

44 sing the reverse transcriptase-PCR method of mRNA differential display, we compared intestinal mRNA f

45 Using mRNA differential display, we identified 42 different cD

46 Using mRNA differential display, we isolated a rat homologue t

47 stis, Sertoli cell-germ cell co-cultures and mRNA differential display were used.