ライフサイエンスコーパス: hybridization analyses

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

2 by radiation hybrid and fluorescent in situ hybridization analyses.

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

4 1p22 by karyotypic and fluorescence in situ hybridization analyses.

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

6 ining was combined with fluorescence in situ hybridization analyses.

7 histologic, immunohistochemical, and in situ hybridization analyses.

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

9 ase chain reaction, and fluorescence in situ hybridization analyses.

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

11 chain reaction and mRNA fluorescence in situ hybridization analyses.

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

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

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

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

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

17 rosatellite markers and fluorescence in situ hybridization analyses.

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

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

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

21 In situ hybridization analyses and immunohistochemistry of embry

22 Northern blot hybridization analyses and reverse transcription-PCR dem

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

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

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

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

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

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

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

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

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

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

33 In situ hybridization analyses demonstrated that cdk10 is expres

34 Northern hybridization analyses demonstrated that e subunit mRNA

35 In situ hybridization analyses demonstrated that expression of N

36 In situ hybridization analyses demonstrated that there were temp

37 Southern hybridization analyses determined that the iraAB locus w

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

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

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

41 In situ hybridization analyses further indicated that ovarian PR

42 In situ hybridization analyses have further revealed that AE2 tr

43 In situ hybridization analyses have revealed the joint-associate

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

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

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

47 ories, and then validated them using in situ hybridization analyses in the developing mouse spinal co

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

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

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

51 Southern blot hybridization analyses indicate that there are multiple

52 Hybridization analyses indicate the clones represent ENO

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

54 In situ hybridization analyses indicated that expression of PhK-

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

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

57 In situ hybridization analyses localized v-ATPase subunit transc

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

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

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

61 Comparative genomic hybridization analyses of 41 strains indicate that subst

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

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

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

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

66 were verified by histopathology and in situ hybridization analyses of both male and recipient female

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

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

69 In situ hybridization analyses of ETS1 and ETS2 expression durin

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

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

72 In situ hybridization analyses of mouse embryos show that Cnot1

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

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

75 Using Northern hybridization analyses of RNA isolated from transiently

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

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

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

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

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

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

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

83 In situ hybridization analyses of transcript distribution in mou

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

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

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

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

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

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

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

91 In situ hybridization analyses revealed expression in rat cardio

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

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

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

95 Northern blot hybridization analyses revealed that katB was transcribe

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

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

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

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

100 Hybridization analyses revealed that the upstream sequen

101 Hybridization analyses revealed that these additional ba

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

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

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

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

106 In situ hybridization analyses show that trapped genes are expre

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

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

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

110 In situ hybridization analyses showed that gonadotropin-releasin

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

112 Hybridization analyses showed that simultaneous inoculat

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

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

115 In situ hybridization analyses suggest that Cxcl10 mRNA is mainl

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

117 In situ hybridization analyses suggested that cardiomyocytes wer

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

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

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

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

122 idization chain reaction fluorescent in situ hybridization analyses to discern the distinct cellular

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

124 (sc)RNA sequencing, and whole-mount in situ hybridization analyses to study pCharme cardiac expressi

125 sequencing, flow cytometry, and RNA in situ hybridization analyses to validate key findings.

126 In situ hybridization analyses uncovered donor-dependent changes

127 By Southern hybridization analyses under high-stringency conditions,

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

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

130 In situ hybridization analyses using P1 clones as probes identif

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

132 Through in situ hybridization analyses, we demonstrate that expression o

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

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

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

136 icroscopy-, immunofluorescence-, and in situ hybridization analyses, we investigated the initial step

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

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

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

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

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

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

143 Microarray hybridization analyses were then performed to survey the

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

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

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

147 Southern blot hybridization analyses with genomic DNA from different a

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

149 Further hybridization analyses with single- and double-restricti

150 Hybridization analyses with specific gene probes reveale