Gene ID | At3g01970 |
Gene name | WRKY45 |
Functional description | member of WRKY Transcription Factor; Group I |
Std2 GX | %ile | GSM ID | Assay name | GSE ID | Experiment title | Link to GEO |
---|---|---|---|---|---|---|
73.2 | 99.9 | ArrayExpress | E-ATMX-31-raw-cel-1516948018 | - | - | - |
71.5 | 99.9 | ArrayExpress | E-MEXP-1797-raw-cel-1669768030 | - | - | - |
70.4 | 99.9 | ArrayExpress | E-MEXP-1797-raw-cel-1669767967 | - | - | - |
64.2 | 99.8 | ArrayExpress | E-MEXP-1797-raw-cel-1669767940 | - | - | - |
56.5 | 99.8 | ArrayExpress | E-MEXP-711-raw-cel-1563002902 | - | - | - |
50.8 | 99.8 | GSM128677 | Underwood_1-30_DC3000-10e8-7h_Rep3_ATH1 | GSE5520 | Genome-wide transcriptional analysis of the compatible A. thaliana-P. syringae pv. tomato DC3000 interaction | ![]() |
47.3 | 99.8 | GSM128661 | Underwood_1-14_Cor-5x10e7-10h_Rep2_ATH1 | GSE5520 | Genome-wide transcriptional analysis of the compatible A. thaliana-P. syringae pv. tomato DC3000 interaction | ![]() |
44.6 | 99.8 | GSM143302 | Ts_genomic_hyb_1 | GSE6203 | Rus_etal_High_Na_Arabidopsis_accessions_mapping_HKT1 | ![]() |
43.5 | 99.8 | GSM184551 | Whole roots 2hr KCl control treated then incubated in protoplast-generating solution minus enzymes, biological rep1 | GSE7631 | Cell-specific nitrogen responses in the Arabidopsis root | ![]() |
40.5 | 99.8 | ArrayExpress | E-MEXP-1797-raw-cel-1669768039 | - | - | - |
39.6 | 99.8 | GSM143300 | Ts_genomic_hyb_3 | GSE6203 | Rus_etal_High_Na_Arabidopsis_accessions_mapping_HKT1 | ![]() |
39.5 | 99.8 | GSM253648 | Col-0-1 | GSE10039 | Low_Mo_Arabidopsis_mapping_MOT1 | ![]() |
38.1 | 99.8 | GSM143299 | High_Na_seg_pool_ts_col_F2 | GSE6203 | Rus_etal_High_Na_Arabidopsis_accessions_mapping_HKT1 | ![]() |
37.7 | 99.7 | GSM143301 | Ts_genomic_hyb_2 | GSE6203 | Rus_etal_High_Na_Arabidopsis_accessions_mapping_HKT1 | ![]() |
35.0 | 99.7 | ArrayExpress | E-MEXP-1797-raw-cel-1669768084 | - | - | - |
34.5 | 99.7 | GSM253652 | Ler 2 | GSE10039 | Low_Mo_Arabidopsis_mapping_MOT1 | ![]() |
33.4 | 99.7 | ArrayExpress | E-ATMX-31-raw-cel-1516947984 | - | - | - |
32.5 | 99.7 | GSM253650 | Ler 3 | GSE10039 | Low_Mo_Arabidopsis_mapping_MOT1 | ![]() |
32.4 | 99.7 | GSM133030 | BC482-2 | GSE5684 | AtGenExpress: Pathogen Series: Response to Botrytis cinerea infection | ![]() |
32.4 | 99.7 | GSM133029 | BC482-1 | GSE5684 | AtGenExpress: Pathogen Series: Response to Botrytis cinerea infection | ![]() |
31.2 | 99.7 | GSM253651 | Ler 1 | GSE10039 | Low_Mo_Arabidopsis_mapping_MOT1 | ![]() |
31.1 | 99.7 | GSM143310 | Tsu_genomic_hyb_1 | GSE6203 | Rus_etal_High_Na_Arabidopsis_accessions_mapping_HKT1 | ![]() |
30.7 | 99.7 | GSM142652 | MC002_ATH1_A10.3-dubos-wth | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | ![]() |
30.5 | 99.7 | GSM142650 | MC002_ATH1_A10.1-dubos-wth | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | ![]() |
30.0 | 99.7 | GSM142638 | MC002_ATH1_A6.1-dubos-5kc_repeat | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | ![]() |
29.8 | 99.7 | GSM142640 | MC002_ATH1_A6.3-dubos-5kc | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | ![]() |
29.5 | 99.7 | ArrayExpress | E-MEXP-711-raw-cel-1563002768 | - | - | - |
29.0 | 99.7 | GSM253649 | Col-0-2 | GSE10039 | Low_Mo_Arabidopsis_mapping_MOT1 | ![]() |
28.9 | 99.7 | GSM142639 | MC002_ATH1_A6.2-dubos-5kc | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | ![]() |
28.6 | 99.7 | GSM143308 | Tsu_genomic_hyb_3 | GSE6203 | Rus_etal_High_Na_Arabidopsis_accessions_mapping_HKT1 | ![]() |
28.1 | 99.7 | GSM142828 | PJ002_ATH1_A9-jarvis-B1798 | GSE6175 | Clarification of the genetic basis of the iae1 and iae2 phenotypes | ![]() |
27.8 | 99.7 | ArrayExpress | E-ATMX-31-raw-cel-1516948001 | - | - | - |
27.8 | 99.7 | GSM143306 | High_Na_seg_pool_tsu_col_F2 | GSE6203 | Rus_etal_High_Na_Arabidopsis_accessions_mapping_HKT1 | ![]() |
27.4 | 99.7 | GSM142653 | MC002_ATH1_A11.1-dubos-mxh | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | ![]() |
27.1 | 99.7 | GSM253645 | High_Mo_seg_pool_Ler_col_F2 | GSE10039 | Low_Mo_Arabidopsis_mapping_MOT1 | ![]() |
27.1 | 99.7 | ArrayExpress | E-ATMX-13-raw-cel-1556149743 | - | - | - |
27.1 | 99.7 | ArrayExpress | E-MEXP-1094-raw-cel-1379507313 | - | - | - |
27.0 | 99.7 | GSM128676 | Underwood_1-29_DC3000-10e8-7h_Rep2_ATH1 | GSE5520 | Genome-wide transcriptional analysis of the compatible A. thaliana-P. syringae pv. tomato DC3000 interaction | ![]() |
26.2 | 99.7 | GSM253647 | Col-0 3 | GSE10039 | Low_Mo_Arabidopsis_mapping_MOT1 | ![]() |
26.2 | 99.7 | GSM142827 | PJ002_ATH1_A8-jarvis-B1798 | GSE6175 | Clarification of the genetic basis of the iae1 and iae2 phenotypes | ![]() |
25.7 | 99.7 | GSM143307 | Low_Na_seg_pool_tsu_col_F2 | GSE6203 | Rus_etal_High_Na_Arabidopsis_accessions_mapping_HKT1 | ![]() |
25.1 | 99.6 | GSM143298 | Low_Na_seg_pool_ts_col_F2 | GSE6203 | Rus_etal_High_Na_Arabidopsis_accessions_mapping_HKT1 | ![]() |
24.9 | 99.6 | GSM133721 | Deeken_A-1-Deeke-Tum_SLD_REP2 | GSE5725 | Agrobacterium tumefaciens-induced tumour development of Arabidopsis thaliana | ![]() |
24.2 | 99.6 | GSM128654 | Underwood_1-7_DC3000-10e6-24h_Rep1_ATH1 | GSE5520 | Genome-wide transcriptional analysis of the compatible A. thaliana-P. syringae pv. tomato DC3000 interaction | ![]() |
24.2 | 99.6 | GSM142628 | MC002_ATH1_A2.3-dubos-wtc | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | ![]() |
24.1 | 99.6 | GSM143309 | Tsu_genomic_hyb_2 | GSE6203 | Rus_etal_High_Na_Arabidopsis_accessions_mapping_HKT1 | ![]() |
24.0 | 99.6 | GSM134208 | Murray_3-4_D7-GROWTH_Rep1_ATH1 | GSE5750 | Growth of suspension-cultured cells | ![]() |
23.9 | 99.6 | GSM142824 | PJ002_ATH1_A5-jarvis-iae2 | GSE6175 | Clarification of the genetic basis of the iae1 and iae2 phenotypes | ![]() |
23.8 | 99.6 | GSM142646 | MC002_ATH1_A8.3-dubos-aih | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | ![]() |
23.0 | 99.6 | GSM142626 | MC002_ATH1_A2.1-dubos-wtc | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | ![]() |
23.0 | 99.6 | GSM142654 | MC002_ATH1_A11.2-dubos-mxh | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | ![]() |
22.8 | 99.6 | GSM226552 | Slice10JW | GSE8934 | A high resolution organ expression map reveals novel expression patterns and predicts cellular function | ![]() |
22.7 | 99.6 | GSM142655 | MC002_ATH1_A11.3-dubos-mxh | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | ![]() |
22.5 | 99.6 | GSM142645 | MC002_ATH1_A8.2-dubos-aih | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | ![]() |
22.3 | 99.6 | GSM142647 | MC002_ATH1_A9.1-dubos-aah | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | ![]() |
22.3 | 99.6 | GSM253646 | Low_Mo_seg_pool_Ler_col_F2 | GSE10039 | Low_Mo_Arabidopsis_mapping_MOT1 | ![]() |
22.2 | 99.6 | GSM128719 | Pieterse_1-5_avrPstDC3000-12h_Rep1_ATH1 | GSE5525 | Transcriptome changes of Arabidopsis during pathogen and insect attack | ![]() |
21.9 | 99.6 | GSM142826 | PJ002_ATH1_A7-jarvis-B1798 | GSE6175 | Clarification of the genetic basis of the iae1 and iae2 phenotypes | ![]() |
21.7 | 99.6 | ArrayExpress | E-MEXP-1797-raw-cel-1669768021 | - | - | - |
21.5 | 99.6 | GSM142821 | PJ002_ATH1_A2-jarvis-iae1 | GSE6175 | Clarification of the genetic basis of the iae1 and iae2 phenotypes | ![]() |
20.9 | 99.6 | ArrayExpress | E-ATMX-31-raw-cel-1516947916 | - | - | - |
20.7 | 99.6 | ArrayExpress | E-ATMX-13-raw-cel-1556149759 | - | - | - |
20.6 | 99.6 | ArrayExpress | E-NASC-76-raw-cel-1359878976 | - | - | - |
20.6 | 99.6 | ArrayExpress | E-MEXP-1797-raw-cel-1669768003 | - | - | - |
20.5 | 99.6 | ArrayExpress | E-MEXP-1797-raw-cel-1669767976 | - | - | - |
20.3 | 99.6 | GSM142651 | MC002_ATH1_A10.2-dubos-wth | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | ![]() |
20.2 | 99.6 | ArrayExpress | E-MEXP-1138-raw-cel-1432773322 | - | - | - |
20.2 | 99.6 | GSM133025 | BC181-1 | GSE5684 | AtGenExpress: Pathogen Series: Response to Botrytis cinerea infection | ![]() |
20.0 | 99.6 | ArrayExpress | E-MEXP-1797-raw-cel-1669767949 | - | - | - |
19.8 | 99.6 | GSM205185 | protoplast_KIN10_rep2 | GSE8257 | Identification of KIN10-target genes in Arabidopsis mesophyll cells | ![]() |
19.8 | 99.6 | GSM133294 | NO.31 | GSE5698 | AtGenExpress: Cytokinin treatment of seedlings | ![]() |
19.7 | 99.6 | ArrayExpress | E-MEXP-807-raw-cel-1173273032 | - | - | - |
19.3 | 99.6 | ArrayExpress | E-NASC-76-raw-cel-1359879158 | - | - | - |
19.2 | 99.6 | ArrayExpress | E-MEXP-1094-raw-cel-1379507273 | - | - | - |
18.7 | 99.5 | GSM142825 | PJ002_ATH1_A6-jarvis-iae2 | GSE6175 | Clarification of the genetic basis of the iae1 and iae2 phenotypes | ![]() |
18.3 | 99.5 | GSM142627 | MC002_ATH1_A2.2-dubos-wtc | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | ![]() |
18.0 | 99.5 | GSM142822 | PJ002_ATH1_A3-jarvis-iae1 | GSE6175 | Clarification of the genetic basis of the iae1 and iae2 phenotypes | ![]() |
17.6 | 99.5 | GSM142623 | MC002_ATH1_A1.1-dubos-wtx | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | ![]() |
17.4 | 99.5 | ArrayExpress | E-NASC-76-raw-cel-1359878900 | - | - | - |
17.3 | 99.5 | ArrayExpress | E-MEXP-1797-raw-cel-1669768075 | - | - | - |
17.1 | 99.5 | ArrayExpress | E-MEXP-711-raw-cel-1563002803 | - | - | - |
17.1 | 99.5 | GSM133296 | NO.33 | GSE5698 | AtGenExpress: Cytokinin treatment of seedlings | ![]() |
16.8 | 99.5 | GSM133295 | NO.32 | GSE5698 | AtGenExpress: Cytokinin treatment of seedlings | ![]() |
16.8 | 99.5 | GSM158702 | HY213-ESTRADIOL-REP1 | GSE6954 | Identification of AGL24 downstream genes by using XVE inducible system | ![]() |
16.8 | 99.5 | GSM156792 | control rep2 | GSE6788 | Expression data of an albino mutant DS 13-2198-1 | ![]() |
16.7 | 99.5 | GSM142820 | PJ002_ATH1_A1-jarvis-iae1 | GSE6175 | Clarification of the genetic basis of the iae1 and iae2 phenotypes | ![]() |
16.6 | 99.5 | GSM142658 | MC002_ATH1_A12.3-dubos-arh | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | ![]() |
16.5 | 99.5 | GSM142823 | PJ002_ATH1_A4-jarvis-iae2 | GSE6175 | Clarification of the genetic basis of the iae1 and iae2 phenotypes | ![]() |
16.4 | 99.5 | GSM142904 | WW002_ATH1_A1-willa-CON-REP2 | GSE6181 | Assembly of the cell wall pectic matrix. | ![]() |
16.3 | 99.5 | GSM142728 | CH001_ATH1_A007-Hampt-c4b | GSE6161 | Differential gene expression patterns in Arabidopsis mutants lacking the K+ channels, akt1, cngc1 and cngc4. | ![]() |
16.3 | 99.5 | GSM142846 | MG001_ATH1_A27-Torres-9N1 | GSE6176 | Impact of Type III effectors on plant defense responses | ![]() |
15.9 | 99.5 | ArrayExpress | E-MEXP-807-raw-cel-1173272921 | - | - | - |
15.4 | 99.5 | GSM142648 | MC002_ATH1_A9.2-dubos-aah | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | ![]() |
15.2 | 99.4 | GSM39200 | Col_C2 | GSE2169 | rre1 and rre2 mutants | ![]() |
15.0 | 99.4 | GSM88049 | csn4-1_mutant replicate 1 | GSE3865 | CSN4-1 mutant analysis | ![]() |
15.0 | 99.4 | GSM142656 | MC002_ATH1_A12.1-dubos-arh | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | ![]() |
14.7 | 99.4 | ArrayExpress | E-MEXP-1797-raw-cel-1669768066 | - | - | - |
14.4 | 99.4 | GSM39214 | RRE2_Chitin4 | GSE2169 | rre1 and rre2 mutants | ![]() |
14.4 | 99.4 | ArrayExpress | E-MEXP-1797-raw-cel-1669767958 | - | - | - |
14.1 | 99.4 | ArrayExpress | E-ATMX-13-raw-cel-1556149791 | - | - | - |
14.1 | 99.4 | GSM142642 | MC002_ATH1_A7.2-dubos-wLh | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | ![]() |
14.0 | 99.4 | GSM39209 | RRE2_C3 | GSE2169 | rre1 and rre2 mutants | ![]() |
13.9 | 99.4 | GSM128686 | Underwood_1-39_E.coli-TUV86-2-fliC-10e8-7h_Rep2_ATH1 | GSE5520 | Genome-wide transcriptional analysis of the compatible A. thaliana-P. syringae pv. tomato DC3000 interaction | ![]() |
13.9 | 99.4 | GSM205160 | protoplast_controlDNA_rep2 | GSE8257 | Identification of KIN10-target genes in Arabidopsis mesophyll cells | ![]() |
13.9 | 99.4 | ArrayExpress | E-MEXP-711-raw-cel-1563002839 | - | - | - |
13.8 | 99.4 | GSM142649 | MC002_ATH1_A9.3-dubos-aah | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | ![]() |
13.7 | 99.4 | ArrayExpress | E-ATMX-31-raw-cel-1516947899 | - | - | - |
13.7 | 99.4 | GSM156790 | control rep1 | GSE6788 | Expression data of an albino mutant DS 13-2198-1 | ![]() |
13.6 | 99.4 | ArrayExpress | E-MEXP-1138-raw-cel-1432773290 | - | - | - |
13.5 | 99.4 | GSM142657 | MC002_ATH1_A12.2-dubos-arh | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | ![]() |
13.5 | 99.4 | ArrayExpress | E-MEXP-1797-raw-cel-1669767985 | - | - | - |
13.5 | 99.4 | ArrayExpress | E-MEXP-1797-raw-cel-1669768057 | - | - | - |
13.4 | 99.4 | ArrayExpress | E-MEXP-1797-raw-cel-1669768012 | - | - | - |
13.3 | 99.4 | GSM204026 | protoplast_control_rep1 | GSE8248 | Identification of hypoxia-inducible genes in Arabidopsis mesophyll cells | ![]() |
12.8 | 99.3 | ArrayExpress | E-ATMX-13-raw-cel-1556149871 | - | - | - |
12.7 | 99.3 | ArrayExpress | E-ATMX-31-raw-cel-1516947882 | - | - | - |
12.6 | 99.3 | GSM226551 | Slice9JW | GSE8934 | A high resolution organ expression map reveals novel expression patterns and predicts cellular function | ![]() |
12.3 | 99.3 | GSM133302 | NO.27 | GSE5699 | AtGenExpress: ARR21C overexpression | ![]() |
12.1 | 99.3 | GSM158701 | HY213-MOCK-REP1 | GSE6954 | Identification of AGL24 downstream genes by using XVE inducible system | ![]() |
12.0 | 99.3 | ArrayExpress | E-MEXP-1797-raw-cel-1669767994 | - | - | - |
11.9 | 99.3 | GSM39213 | RRE2_Chitin3 | GSE2169 | rre1 and rre2 mutants | ![]() |
11.8 | 99.3 | ArrayExpress | E-NASC-76-raw-cel-1359879210 | - | - | - |
11.5 | 99.3 | GSM39191 | RRE1_C1 | GSE2169 | rre1 and rre2 mutants | ![]() |
11.4 | 99.3 | GSM270866 | Arabidopsis cell culture, 4 h_response to phytoprostane A1_rep1 | GSE10719 | Response of Arabidopsis cell culture to phytoprostane A1 | ![]() |
11.3 | 99.3 | ArrayExpress | E-MEXP-1138-raw-cel-1432773034 | - | - | - |
11.3 | 99.3 | GSM156793 | albino rep2 | GSE6788 | Expression data of an albino mutant DS 13-2198-1 | ![]() |
11.1 | 99.2 | GSM133301 | NO.26 | GSE5699 | AtGenExpress: ARR21C overexpression | ![]() |
11.1 | 99.2 | GSM142643 | MC002_ATH1_A7.3-dubos-wLh | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | ![]() |
11.1 | 99.2 | GSM39210 | RRE2_C4 | GSE2169 | rre1 and rre2 mutants | ![]() |
10.8 | 99.2 | GSM39198 | RRE1_Chitin4 | GSE2169 | rre1 and rre2 mutants | ![]() |
10.8 | 99.2 | GSM142644 | MC002_ATH1_A8.1-dubos-aih | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | ![]() |
10.7 | 99.2 | GSM39208 | RRE2_C2 | GSE2169 | rre1 and rre2 mutants | ![]() |
10.7 | 99.2 | GSM39201 | Col_C3 | GSE2169 | rre1 and rre2 mutants | ![]() |
10.5 | 99.2 | GSM128655 | Underwood_1-8_DC3000-10e6-24h_Rep2_ATH1 | GSE5520 | Genome-wide transcriptional analysis of the compatible A. thaliana-P. syringae pv. tomato DC3000 interaction | ![]() |
10.5 | 99.2 | GSM158703 | WT-ESTRADIOL-REP1 | GSE6954 | Identification of AGL24 downstream genes by using XVE inducible system | ![]() |
10.4 | 99.2 | GSM133965 | Fukuda_1-10_8B_Rep2_ATH1 | GSE5748 | In vitro tracheary element transdifferentiation of Col-0 suspension cells. | ![]() |
10.3 | 99.2 | GSM133300 | NO.25 | GSE5699 | AtGenExpress: ARR21C overexpression | ![]() |
10.2 | 99.2 | GSM142902 | WW001_ATH1_A1-WILLA-CON | GSE6181 | Assembly of the cell wall pectic matrix. | ![]() |
10.1 | 99.2 | GSM131603 | ATGE_41_A | GSE5632 | AtGenExpress: Developmental series (flowers and pollen) | ![]() |
10.1 | 99.2 | GSM142636 | MC002_ATH1_A5.2-dubos-5kx | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | ![]() |
10.1 | 99.2 | GSM131604 | ATGE_41_B | GSE5632 | AtGenExpress: Developmental series (flowers and pollen) | ![]() |
9.9 | 99.1 | GSM39199 | Col_C1 | GSE2169 | rre1 and rre2 mutants | ![]() |
9.9 | 99.1 | ArrayExpress | E-MEXP-1797-raw-cel-1669768048 | - | - | - |
9.9 | 99.1 | GSM133967 | Fukuda_1-12_10B_Rep2_ATH1 | GSE5748 | In vitro tracheary element transdifferentiation of Col-0 suspension cells. | ![]() |
9.9 | 99.1 | GSM142624 | MC002_ATH1_A1.2-dubos-wtx | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | ![]() |
9.8 | 99.1 | ArrayExpress | E-MEXP-1138-raw-cel-1432773066 | - | - | - |
9.7 | 99.1 | GSM142634 | MC002_ATH1_A4.3-dubos-6kc | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | ![]() |
9.6 | 99.1 | ArrayExpress | E-ATMX-13-raw-cel-1556149807 | - | - | - |
9.6 | 99.1 | GSM142633 | MC002_ATH1_A4.2-dubos-6kc | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | ![]() |
9.5 | 99.1 | GSM133733 | Buchanan-Wollaston_A-5-bwoll-NG1_SLD | GSE5727 | The effects of mutants in stress response pathways on gene expression during senescence | ![]() |
9.5 | 99.1 | GSM134206 | Murray_3-3_D5-GROWTH_Rep1_ATH1 | GSE5750 | Growth of suspension-cultured cells | ![]() |
9.5 | 99.1 | GSM133966 | Fukuda_1-11_10A_Rep1_ATH1 | GSE5748 | In vitro tracheary element transdifferentiation of Col-0 suspension cells. | ![]() |
9.4 | 99.1 | ArrayExpress | E-MEXP-1138-raw-cel-1432773258 | - | - | - |
9.4 | 99.1 | GSM157362 | Ulker_2-5_WRKY-KO-40-Pst-DC3000_Rep1_ATH1 | GSE6829 | Group II-A WRKY transcription factors and early leaf senescence | ![]() |
9.3 | 99.1 | GSM142837 | MG001_ATH1_A16-Torres-6N1 | GSE6176 | Impact of Type III effectors on plant defense responses | ![]() |
9.3 | 99.1 | GSM39192 | RRE1_C2 | GSE2169 | rre1 and rre2 mutants | ![]() |
9.2 | 99.1 | ArrayExpress | E-NASC-76-raw-cel-1359879056 | - | - | - |
9.2 | 99.1 | ArrayExpress | E-NASC-76-raw-cel-1359878850 | - | - | - |
9.2 | 99.1 | GSM39202 | Col_C4 | GSE2169 | rre1 and rre2 mutants | ![]() |
9.1 | 99.1 | GSM133964 | Fukuda_1-9_8A_Rep1_ATH1 | GSE5748 | In vitro tracheary element transdifferentiation of Col-0 suspension cells. | ![]() |
8.9 | 99.0 | GSM133957 | Fukuda_1-2_0B_Rep2_ATH1 | GSE5748 | In vitro tracheary element transdifferentiation of Col-0 suspension cells. | ![]() |
8.9 | 99.0 | GSM142641 | MC002_ATH1_A7.1-dubos-wLh | GSE6151 | The mechanisms involved in the interplay between dormancy and secondary growth in Arabidopsis | ![]() |
8.8 | 99.0 | GSM39194 | RRE1_C4 | GSE2169 | rre1 and rre2 mutants | ![]() |
8.7 | 99.0 | GSM226553 | Slice11JW | GSE8934 | A high resolution organ expression map reveals novel expression patterns and predicts cellular function | ![]() |
8.7 | 99.0 | GSM133734 | Buchanan-Wollaston_A-6-bwoll-NG2_SLD | GSE5727 | The effects of mutants in stress response pathways on gene expression during senescence | ![]() |
8.6 | 99.0 | GSM142594 | DB001_ATH1_A4-Brown-cal | GSE6148 | The trans-differentiation of cultured Arabidopsis cells | ![]() |
8.6 | 99.0 | GSM131605 | ATGE_41_C | GSE5632 | AtGenExpress: Developmental series (flowers and pollen) | ![]() |
8.6 | 99.0 | ArrayExpress | E-MEXP-807-raw-cel-1173272948 | - | - | - |
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