ライフサイエンスコーパス: Northern hybridization

1 ffs, and alpha-tmRNA) was next confirmed by Northern hybridization.

2 appeared to be full length, as determined by Northern hybridization.

3 and hyphal forms of C. albicans as judged by Northern hybridization.

4 nohistochemistry, in situ hybridization, and Northern hybridization.

5 th Moa1 isoforms were detected in the eye by Northern hybridization.

6 -9 expression by semiquantitative RT-PCR and Northern hybridization.

7 was subjected to semiquantitative RT-PCR and Northern hybridization.

8 e and infected tissue culture cells by using Northern hybridization.

9 stry and a 3-kb transcript was identified by Northern hybridization.

10 ental stages and in various adult tissues by Northern hybridization.

11 electrophoretic mobility shift analysis and Northern hybridization.

12 solateral Na(+)-K(+)-ATPase were measured by Northern hybridization.

13 ion of GAP-43 expression was corroborated by Northern hybridization.

14 he tissue distribution of gene expression by Northern hybridization.

15 d transfected-cell cultures was confirmed by Northern hybridization.

16 own to be a single copy gene by Southern and Northern hybridization.

17 own to be a single copy gene by Southern and Northern hybridizations.

18 By Northern hybridization, a factor XI mRNA transcript of a

19 Northern hybridization analyses demonstrated that e subu

20 Using Northern hybridization analyses of RNA isolated from tra

21 that of tad secretion complex genes, we used Northern hybridization analysis and a lacZ reporter assa

22 Northern hybridization analysis demonstrated that Pt4CL1

23 transcription polymerase chain reaction and Northern hybridization analysis did not show significant

24 Northern hybridization analysis indicated that AtPRP1 an

25 Northern hybridization analysis indicated that overexpre

26 Northern hybridization analysis of 460 surveillance samp

27 Northern hybridization analysis of HUVECs revealed that

28 Northern hybridization analysis of mRNA levels and enzym

29 Northern hybridization analysis of the cbl locus identif

30 Northern hybridization analysis revealed that an intact

31 Northern hybridization analysis revealed that arp1 is de

32 Northern hybridization analysis revealed that in fetal t

33 Northern hybridization analysis reveals a peak of TIP60

34 Northern hybridization analysis showed high level arfoph

35 expression is restricted to embryogenesis, a Northern hybridization analysis showed low-level express

36 Northern hybridization analysis showed strong expression

37 Northern hybridization analysis showed that high level e

38 Northern hybridization analysis suggested that hisCl1 an

39 iption-polymerase chain reaction (RT-PCR) or Northern hybridization analysis to quantify TTase mRNA.

40 procollagen messenger RNA were evaluated by Northern hybridization analysis, and the transcriptional

41 ntation, gene replacement, DNA sequence, and Northern hybridization analysis.

42 ted sid2 transcript of 11 kb was detected by Northern hybridization analysis.

43 induction in WEHI7.2 cells, detected by both Northern hybridization and a grp78 promoter-luciferase r

44 ved a single mRNA ( approximately 7.5 kb) by Northern hybridization and a major approximately 130 kDa

45 Using Northern hybridization and beta-galactosidase assays of

46 Northern hybridization and immunoblotting of tissue extr

47 Northern hybridization and immunoblotting studies indica

48 Northern hybridization and in situ hybridization indicat

49 transcription in WEHI7.2 cells, measured by Northern hybridization and nuclear run-on assays, even i

50 Northern hybridization and primer extension experiments

51 nd other putative promoters was performed by Northern hybridization and primer extension experiments.

52 Analysis of HRV-5 expression by Northern hybridization and reverse transcriptase PCR ind

53 Intriguingly, Northern hybridization and reverse transcriptase-polymer

54 Northern hybridization and reverse transcription-PCR ana

55 Now, using Northern hybridization and RNase protection assay, we pr

56 Northern hybridization and RT-PCR demonstrated that the

57 a1 RNA was detected in both skin and eyes by Northern hybridization and was not affected by the absen

58 Northern hybridization and Western blot analysis demonst

59 The results of Northern hybridization and/or real-time reverse transcri

60 Northern hybridizations and RT-PCR indicate that d4-662

61 ) collagens and fibronectin were assessed by Northern hybridization, and the transcription of the alp

62 mRNA levels, and stability were assessed by Northern hybridizations, and COL1A1 transcription by in

63 DNA microarrays, Northern hybridizations, and RNA slot blot analyses were

64 The results of Northern hybridization confirmed that SOWgp expression i

65 Northern hybridization confirmed the production of HaCHI

66 Northern hybridization confirms that the expression of N

67 Southern and northern hybridization data indicate that A. thaliana ex

68 Analysis of RNA by Northern hybridization demonstrated that the emml, hasA

69 Northern hybridizations demonstrated that in the outer m

70 Northern hybridizations demonstrated that the E1-b varia

71 Northern hybridizations demonstrated that TSP-1 expressi

72 Northern hybridization detects the expression of three s

73 9, TIMP-1, TIMP-2, and uPA was determined by Northern hybridization, ELISA, and Western blotting, res

74 nctivochalasis fibroblasts was determined by Northern hybridization, enzyme-linked immunosorbent assa

75 nctivochalasis fibroblasts was determined by Northern hybridization, enzyme-linked immunosorbent assa

76 Further, Northern hybridization experiments defined the tissue di

77 The analysis of total RNA by Northern hybridization experiments reveals the presence

78 Northern hybridization experiments with several differen

79 A cDNA was obtained which, in Northern hybridization experiments, revealed a character

80 examined the expression of human Id mRNAs by Northern hybridization in 11 human myeloid cell lines, s

81 ifferential display pattern was confirmed by Northern hybridization in both prostate tissue and cell

82 UT-A3b mRNA was easily detected by Northern hybridization in the inner medulla.

83 ecrosis factor-alpha mRNA levels, assayed by Northern hybridization, increased in the order +/+ < fa/

84 Northern hybridization indicated that pepO is transcribe

85 Mapping of these transcripts by Northern hybridization indicated that the 1.4- and 2.0-k

86 Based on Northern hybridization, mRNA for GC-G was predominantly

87 Northern hybridization of RNA isolated from transfected

88 Northern hybridization of the transcript expression of t

89 Northern hybridization of tissue RNA indicated that epil

90 Northern hybridizations of mutant leaf, root, tassel, en

91 DNA fragments were used as probes to perform Northern hybridization on RNA from P. carinii-infected a

92 ther monitor one gene at a time, for example northern hybridization or RT-PCR methods, or are designe

93 decreases in levels of Thy-1 mRNA assayed by Northern hybridization or T2 nuclease protection.

94 Northern hybridization, quantitative RT-PCR, and splinte

95 Northern hybridization revealed that gamma-FBG mRNA incr

96 Northern hybridization revealed that mRNA levels for the

97 Northern hybridization revealed that the expression of R

98 Semiquantitative RT-PCR and Northern hybridization revealed that the mRNAs of MMP-1,

99 Northern hybridization revealed that vimentin was expres

100 Northern hybridizations revealed that the cellulosomal c

101 Northern hybridizations revealed that the engO gene is t

102 Northern hybridizations revealed that xynB is transcribe

103 Northern hybridization reveals that the dFKBP59 mRNA is

104 As assessed by northern hybridization, RNase protection assay, and reve

105 only 1 of 34 tested clones showed a band in Northern hybridization, RT-PCR demonstrated that at leas

106 Northern hybridization showed differential distribution

107 immunoblot, indirect immunofluorescence, and Northern hybridization showed dramatically reduced expre

108 Northern hybridization studies revealed that mibp1 is ex

109 Northern-hybridization studies performed on developing s

110 In Northern hybridizations, the C mu 4 probe detected two t

111 rveillance samples were analyzed by dot-blot Northern hybridization to detect RotaTeq vaccine-derived

112 nce of bisabolene synthase mRNA was shown by Northern hybridization to lag behind that of mRNAs respo

113 measurement of [3H]ouabain binding and (ii) Northern hybridization to measure expression of alpha-1

114 -oncogene in adult Syrian hamster tissues by northern hybridization using cph-specific genomic probes

115 normal lymphoid cells were characterized by Northern hybridization using DNA probes from various reg

116 However, by Northern hybridization using either the entire cap8 gene

117 By Northern hybridization using the entire gene cluster as

118 Northern hybridization was performed on 15 of the most a

119 Northern hybridization was used to show that clusterin i

120 ot hybridization, and for gene expression by Northern hybridization, Western immunoblot, or immunohis

121 d during TAM treatment, and was confirmed by Northern hybridization, which showed a 2.7-kb band in bo

122 epitope-specific anti-keratin 12 antibodies, Northern hybridization with 32P-labeled keratin 12 cDNA,

123 Primer extension analysis and Northern hybridization with 5'-untranslated region probe

124 Northern hybridization with the maize cDNA clone shows a