ライフサイエンスコーパス: hybridization analyses

1 mouse brain development we have used in situ hybridization analyses.

2 1p22 by karyotypic and fluorescence in situ hybridization analyses.

3 conserved among strains of GAS, as shown by hybridization analyses.

4 histologic, immunohistochemical, and in situ hybridization analyses.

5 iption-polymerase chain reaction and in situ hybridization analyses.

6 acids, 16S rRNA gene sequencing, and DNA-DNA hybridization analyses.

7 chain reaction and mRNA fluorescence in situ hybridization analyses.

8 re verified by gene fusion and Northern blot hybridization analyses.

9 ET(A) and ET(B) by Northern blot and in situ hybridization analyses.

10 fied two INK4 genes using degenerate PCR and hybridization analyses.

11 nd used in Northern and fluorescence in situ hybridization analyses.

12 r in rat CNS using blotting and mRNA in situ hybridization analyses.

13 rosatellite markers and fluorescence in situ hybridization analyses.

14 s was evaluated by Northern blot and in situ hybridization analyses.

15 ining was combined with fluorescence in situ hybridization analyses.

16 RNA) were evaluated by Northern and dot-blot hybridization analyses.

17 leotide sequence, Northern blot, and in situ hybridization analyses.

18 by radiation hybrid and fluorescent in situ hybridization analyses.

19 Based on GUS fusion and in situ hybridization analyses, ALS3 is primarily expressed in l

20 In situ hybridization analyses and immunohistochemistry of embry

21 Northern blot hybridization analyses and reverse transcription-PCR dem

22 stitutively as demonstrated by northern-blot hybridization analyses and the presence of feedback-inse

23 l multiplexed sandwich immunoassays, DNA/RNA hybridization analyses, and enzyme linked immunosorbent

24 ern blot and interphase fluorescence in situ hybridization analyses, and the results of real-time RT-

25 ice and suggest that multiparametric in situ hybridization analyses can be used to identify the metas

26 Further statistical and fluorescence in situ hybridization analyses confirmed that the 9q LOH was a r

27 Real-time quantitative PCR and in situ hybridization analyses confirmed the findings.

28 In this study, in situ hybridization analyses demonstrate that BMP-specific typ

29 In situ hybridization analyses demonstrate that GFRalpha-3 is lo

30 Both Northern blot and in situ hybridization analyses demonstrated increased EGR-1, but

31 Pulsed-field gel electrophoresis and hybridization analyses demonstrated that all isolates th

32 In situ hybridization analyses demonstrated that cdk10 is expres

33 Northern hybridization analyses demonstrated that e subunit mRNA

34 In situ hybridization analyses demonstrated that expression of N

35 In situ hybridization analyses demonstrated that there were temp

36 Southern hybridization analyses determined that the iraAB locus w

37 Here, in situ hybridization analyses for FoxP1 and FoxP2 in a songbird

38 We confirmed the results of these in situ hybridization analyses for the CysLT1 receptor, and prod

39 scence in situ hybridization and in situ RNA hybridization analyses for this gene have demonstrated a

40 In situ hybridization analyses further indicated that ovarian PR

41 In situ hybridization analyses have further revealed that AE2 tr

42 In situ hybridization analyses have revealed the joint-associate

43 allelic loss in MM, our comparative genomic hybridization analyses identified a new recurrent site o

44 In fluorescent in situ hybridization analyses, IFI16 colocalized with multiple

45 ss of heterozygosity and comparative genomic hybridization analyses in human prostate cancer, suggest

46 Northern blot and mRNA in situ hybridization analyses indicate that RASAL, in contrast

47 Subsequent RT-PCR and section-based in situ hybridization analyses indicate that SOX7 mRNA is locali

48 nd DNA methylation) and fluorescence in situ hybridization analyses indicate that the transgene-induc

49 Southern blot hybridization analyses indicate that there are multiple

50 Hybridization analyses indicate the clones represent ENO

51 Array-based comparative genomic hybridization analyses indicated that double, but not si

52 In situ hybridization analyses indicated that expression of PhK-

53 Northern blotting, RT-PCR, and in situ hybridization analyses indicated that the protein was ab

54 Fluorescence in situ hybridization analyses localized the mouse RAD50 gene to

55 In situ hybridization analyses localized v-ATPase subunit transc

56 rspecific backcross and fluorescence in situ hybridization analyses map the transgene insertion, and

57 equencing and multiplex fluorescence in situ hybridization analyses mapped the emergence of extra-chr

58 Immunohistochemical and in situ hybridization analyses of 30 primary glioblastoma tissue

59 Comparative genomic hybridization analyses of 41 strains indicate that subst

60 Tissue in situ hybridization analyses of a mouse homolog of the DSCAM g

61 RT-PCR and in situ hybridization analyses of a time course of juvenile test

62 In situ hybridization analyses of all 30 genes identified four g

63 immunohistochemistry or fluorescence in-situ hybridization analyses of biopsied tissue.

64 Northern and in situ hybridization analyses of E8 chicken embryo tissues indi

65 Fluorescence in situ hybridization analyses of each of these cell lines showe

66 In situ hybridization analyses of ETS1 and ETS2 expression durin

67 immunohistochemistry and fluorescent in situ hybridization analyses of gastric tissue sections.

68 In addition, hybridization analyses of microarrays made with ATMS/dia

69 siological, immunohistochemical, and in situ hybridization analyses of pob retinas showed a selective

70 Northern blot and in situ hybridization analyses of PtCesA gene transcripts in var

71 Using Northern hybridization analyses of RNA isolated from transiently

72 Fluorescence in situ hybridization analyses of selected class II PAC clones c

73 In situ hybridization analyses of the adult rat brain, spleen, a

74 Interphase fluorescent in situ hybridization analyses of the family members indicated t

75 study, we carried out microarray and in situ hybridization analyses of the mouse Neural retina leucin

76 eatment, was confirmed by Comparative Genome Hybridization analyses of the same DNA samples.

77 In situ hybridization analyses of tissues from LXR agonist-treat

78 n reading frames were also detected by array hybridization analyses of total RNA prepared from the is

79 In situ hybridization analyses of transcript distribution in mou

80 synthesize antisense RNA probes for in situ hybridization analyses of zebrafish embryos.

81 number is estimated by either Southern blot hybridization analyses or quantitative polymerase chain

82 somatic cell hybrid and fluorescence in situ hybridization analyses place the XLIS region within a 1

83 Ribonuclease protection assay and in situ hybridization analyses post-BMT showed that the lung was

84 In situ hybridization analyses reveal that CHO1/MKLP1 is express

85 DNA fiber-based fluorescence in situ hybridization analyses reveal that the mtDNA insert is 6

86 Microarray and in situ hybridization analyses revealed a complex program underl

87 In situ hybridization analyses revealed expression in rat cardio

88 nomic hybridization and fluorescence in situ hybridization analyses revealed genomic amplification at

89 Northern blot and in situ hybridization analyses revealed overlapping as well as d

90 Whole-mount in situ hybridization analyses revealed that ET(A) was ubiquitou

91 Northern blot hybridization analyses revealed that katB was transcribe

92 Northern blot and in situ hybridization analyses revealed that MGL mRNA is heterog

93 In situ RNA hybridization analyses revealed that RET-RGS-d is expres

94 Hybridization analyses revealed that the 56-1 mRNA is ex

95 nsional pulsed-field gel electrophoresis and hybridization analyses revealed that the B. hermsii gene

96 Hybridization analyses revealed that the upstream sequen

97 Hybridization analyses revealed that these additional ba

98 Northern and in situ hybridization analyses show that MsNOS and the MsGCs are

99 Southern blot and fluorescence in situ hybridization analyses show that NTT is a single-copy ge

100 Northern blot and in situ hybridization analyses show that the AM mRNA begins to b

101 PCR and Southern blot hybridization analyses show that these three transcripts

102 In situ hybridization analyses show that trapped genes are expre

103 Immunohistochemical and in situ hybridization analyses show, for the first time, the pre

104 RT-PCR and in situ hybridization analyses showed that bHLH142 is specifical

105 In addition, Southern hybridization analyses showed that cap8H, cap8I, cap8J,

106 In situ hybridization analyses showed that gonadotropin-releasin

107 Fluorescence in situ hybridization analyses showed that P. denitrificans was

108 Hybridization analyses showed that simultaneous inoculat

109 Southern hybridization analyses showed that the mVL30-1 cDNA inte

110 In addition, hybridization analyses suggest that an SUPT4H-related ge

111 In situ hybridization analyses suggest that Cxcl10 mRNA is mainl

112 Subsequent in-situ hybridization analyses suggest that the down-regulation

113 In situ hybridization analyses suggested that cardiomyocytes wer

114 homogeneous electric field gel and Southern hybridization analyses suggested that the bee locus is l

115 These observations, along with mRNA in situ hybridization analyses, suggested a defect in the anteri

116 for immunohistochemistry and for RNA in situ hybridization analyses, this method allows optimal evalu

117 tial for export of heat shock mRNAs, in situ hybridization analyses to detect mRNA and pulse-labeling

118 alactosidase, and have undertaken microarray hybridization analyses to identify genes whose expressio

119 In situ hybridization analyses uncovered donor-dependent changes

120 By Southern hybridization analyses under high-stringency conditions,

121 In situ hybridization analyses using GCT from Catnb(flox(ex3)/+)

122 d for genome comparisons and high-resolution hybridization analyses using megabase stretches of known

123 In situ hybridization analyses using P1 clones as probes identif

124 Using RNA-seq and in situ hybridization analyses, we also show that Ptf1a induces

125 Through Southern hybridization analyses, we demonstrate that repA (or a c

126 Based on bioinformatic and in situ hybridization analyses, we demonstrated the exclusive ex

127 Through sequence and hybridization analyses, we examined regions from Arabido

128 By performing microarray hybridization analyses, we show that constitutive expres

129 tional fusions and Northern and Western blot hybridization analyses, we show that RNAIII does, indeed

130 In this study, in situ hybridization analyses were performed to characterize th

131 Polymerase chain reaction and DNA-DNA hybridization analyses were performed to detect the pres

132 eaction, immunoblot, and comparative genomic hybridization analyses were performed using normal and t

133 s located near chromosomal termini, Southern hybridization analyses were performed.

134 Microarray hybridization analyses were then performed to survey the

135 ltiple Adh gene family members, and Southern hybridization analyses were used to document variation i

136 d genetically, including fluorescent in situ hybridization analyses with commercially available MALT1

137 to the genes they carried, as determined by hybridization analyses with DNA fragments from several h

138 Southern blot hybridization analyses with genomic DNA from different a

139 However, Southern hybridization analyses with ORF 1, 2, and 4 probes detec

140 Further hybridization analyses with single- and double-restricti

141 Hybridization analyses with specific gene probes reveale