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1 sitional cloning and found to encode a novel MADS domain protein.
2 ons affect DNA binding specificity of floral MADS domain proteins.
3 olbox consisting of phylogenetically related MADS domain proteins.
4 nd several higher order complexes with other MADS domain proteins.
5 ription factors, yet the mechanisms by which MADS-domain proteins activate or repress the expression
10 data are consistent with the FRUITFULL (FUL) MADS-domain protein and Auxin Response Factors (ARFs) di
11 strongly supports a mechanistic link between MADS-domain proteins and chromatin remodeling factors.
12 d SOC1 repression by several floral homeotic MADS domain proteins, and we show that, mechanistically,
14 spectrometry that five major floral homeotic MADS-domain proteins (AP1, AP3, PI, AG, and SEP3) intera
19 model was proposed that describes how these MADS domain proteins assemble into higher order complexe
25 studies confirmed a flexible composition of MADS-domain protein complexes depending on relative prot
28 tic studies clearly indicate that many plant MADS domain proteins have different regulatory functions
30 DNA sequencing (SELEX-seq) on several floral MADS domain protein homo- and heterodimers to measure th
33 cent complementation assays demonstrate that MADS-domain proteins interact during meristematic stages
34 teomics approach we were able to establish a MADS-domain protein interactome that strongly supports a
35 Therefore, HUA1 are another example of non-MADS domain proteins involved in organ identity specific
36 in vivo DNA binding data show that homeotic MADS domain proteins recognize partly distinct genomic r
40 identified as interaction partners of floral MADS-domain proteins suggesting various specific combina
43 and AGL2 (for AGAMOUS-like), two Arabidopsis MADS domain proteins that are preferentially expressed i
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