| scholarly article | Q13442814 |
| P50 | author | Yuanyuan Li | Q59694695 |
| P2093 | author name string | Hui Zhang | |
| Xin-Guang Zhu | |||
| Jiajia Xu | |||
| Noor Ul Haq | |||
| P2860 | cites work | Inhibition of mutation and combating the evolution of antibiotic resistance | Q21146100 |
| Ultrafast and memory-efficient alignment of short DNA sequences to the human genome | Q21183894 | ||
| What have we learned from 15 years of free-air CO2 enrichment (FACE)? A meta-analytic review of the responses of photosynthesis, canopy properties and plant production to rising CO2 | Q22065657 | ||
| Mapping and quantifying mammalian transcriptomes by RNA-Seq | Q22122035 | ||
| Analysis of the genome sequence of the flowering plant Arabidopsis thaliana | Q22122387 | ||
| The transcriptional landscape of the yeast genome defined by RNA sequencing | Q24633693 | ||
| Evolution of leaf-form in land plants linked to atmospheric CO2 decline in the Late Palaeozoic era | Q28206754 | ||
| Genetic manipulation of stomatal density influences stomatal size, plant growth and tolerance to restricted water supply across a growth carbon dioxide gradient | Q28740608 | ||
| Physiological framework for adaptation of stomata to CO2 from glacial to future concentrations | Q28740614 | ||
| GNC and CGA1 modulate chlorophyll biosynthesis and glutamate synthase (GLU1/Fd-GOGAT) expression in Arabidopsis | Q28742938 | ||
| The making of a chloroplast | Q28751580 | ||
| Maximum leaf conductance driven by CO2 effects on stomatal size and density over geologic time | Q28752581 | ||
| Is atmospheric CO2 a selective agent on model C3 annuals? | Q30460762 | ||
| Food for thought: lower-than-expected crop yield stimulation with rising CO2 concentrations | Q31047577 | ||
| AGAMOUS-LIKE 24, a dosage-dependent mediator of the flowering signals | Q33337912 | ||
| The microRNA-regulated SBP-Box transcription factor SPL3 is a direct upstream activator of LEAFY, FRUITFULL, and APETALA1. | Q33347619 | ||
| Functional analysis of the Arabidopsis thaliana SBP-box gene SPL3: a novel gene involved in the floral transition | Q33368257 | ||
| Small chloroplast-targeted DnaJ proteins are involved in optimization of photosynthetic reactions in Arabidopsis thaliana | Q33537475 | ||
| Effects of low atmospheric CO(2) on plants: more than a thing of the past | Q34133509 | ||
| Photorespiration and the evolution of C4 photosynthesis | Q34190007 | ||
| C4 cycles: past, present, and future research on C4 photosynthesis | Q34236863 | ||
| Characteristics of C4 photosynthesis in stems and petioles of C3 flowering plants | Q34520570 | ||
| Supramolecular organization of thylakoid membrane proteins in green plants | Q34553745 | ||
| Temporal regulation of shoot development in Arabidopsis thaliana by miR156 and its target SPL3 | Q34558030 | ||
| GLK transcription factors coordinate expression of the photosynthetic apparatus in Arabidopsis | Q34976560 | ||
| Control of the phosphorylation of phosphoenolpyruvate carboxylase in higher plants | Q35143153 | ||
| Impact of a stress-inducible switch to mutagenic repair of DNA breaks on mutation in Escherichia coli | Q35170976 | ||
| Chloroplast biogenesis: control of plastid development, protein import, division and inheritance | Q35625788 | ||
| RNA binding and RNA remodeling activities of the half-a-tetratricopeptide (HAT) protein HCF107 underlie its effects on gene expression | Q35889283 | ||
| Rising atmospheric carbon dioxide: plants FACE the future | Q35891660 | ||
| Plant responses to low [CO2] of the past | Q37788795 | ||
| The role of proteins in C(3) plants prior to their recruitment into the C(4) pathway | Q37842014 | ||
| What can enzymes of C₄ photosynthesis do for C₃ plants under stress? | Q37855295 | ||
| Functional analysis of an Arabidopsis transcription factor, DREB2A, involved in drought-responsive gene expression | Q39423355 | ||
| Arabidopsis phosphoenolpyruvate carboxylase genes encode immunologically unrelated polypeptides and are differentially expressed in response to drought and salt stress. | Q39503380 | ||
| Effects of low and elevated CO2 on C3 and C4 annuals : I. Growth and biomass allocation. | Q40998193 | ||
| The GATA-type transcription factors GNC and GNL/CGA1 repress gibberellin signaling downstream from DELLA proteins and PHYTOCHROME-INTERACTING FACTORS. | Q42038116 | ||
| Fine-tuning of early events in the jasmonate response | Q42923555 | ||
| Identity and function of a large gene network underlying mutagenic repair of DNA breaks | Q42969505 | ||
| C acid decarboxylases required for C photosynthesis are active in the mid-vein of the C species Arabidopsis thaliana, and are important in sugar and amino acid metabolism | Q43266357 | ||
| Arabidopsis transcriptome reveals control circuits regulating redox homeostasis and the role of an AP2 transcription factor | Q46336150 | ||
| The nuclear gene HCF107 encodes a membrane-associated R-TPR (RNA tetratricopeptide repeat)-containing protein involved in expression of the plastidial psbH gene in Arabidopsis | Q46512125 | ||
| Genetic analysis of Arabidopsis GATA transcription factor gene family reveals a nitrate-inducible member important for chlorophyll synthesis and glucose sensitivity | Q46785653 | ||
| Sugars and circadian regulation make major contributions to the global regulation of diurnal gene expression in Arabidopsis | Q46813402 | ||
| Functional characterization of the GATA transcription factors GNC and CGA1 reveals their key role in chloroplast development, growth, and division in Arabidopsis | Q47368781 | ||
| The N-terminal domain of chlorophyllide a oxygenase confers protein instability in response to chlorophyll B accumulation in Arabidopsis. | Q50773087 | ||
| Evolution of C4 photosynthesis in the genus Flaveria: how many and which genes does it take to make C4? | Q51863039 | ||
| Two GATA transcription factors are downstream effectors of floral homeotic gene action in Arabidopsis. | Q51959354 | ||
| GLK gene pairs regulate chloroplast development in diverse plant species. | Q52115023 | ||
| An mRNA blueprint for C4 photosynthesis derived from comparative transcriptomics of closely related C3 and C4 species | Q57251605 | ||
| Characterization of a Unique GATA Family Gene That Responds to Both Light and Cytokinin inArabidopsis thaliana | Q57782691 | ||
| Signals from mature to new leaves | Q58071153 | ||
| Stomatal numbers are sensitive to increases in CO2 from pre-industrial levels | Q59064682 | ||
| Acclimation of Arabidopsis thaliana to the light environment: the existence of separate low light and high light responses | Q60323594 | ||
| Independent and Parallel Recruitment of Preexisting Mechanisms Underlying C4 Photosynthesis | Q63440033 | ||
| The nucleus-encoded HCF107 gene of Arabidopsis provides a link between intercistronic RNA processing and the accumulation of translation-competent psbH transcripts in chloroplasts | Q74494369 | ||
| The structure and function of the chloroplast photosynthetic membrane - a model for the domain organization | Q86885134 | ||
| Variations among races of Arabidopsis thaliana (L.) heynh for survival in limited carbon dioxide | Q86898244 | ||
| The zinc-finger protein Zat12 plays a central role in reactive oxygen and abiotic stress signaling in Arabidopsis | Q94460114 | ||
| P433 | issue | 13 | |
| P304 | page(s) | 3657-3667 | |
| P577 | publication date | 2014-05-22 | |
| P1433 | published in | Journal of Experimental Botany | Q6295179 |
| P1476 | title | Was low CO2 a driving force of C4 evolution: Arabidopsis responses to long-term low CO2 stress | |
| P478 | volume | 65 |
| Q48268224 | Aberrant regulation of autophagy in mammalian diseases. |
| Q57070702 | Accelerating Soybean Breeding in a CO2-Supplemented Growth Chamber |
| Q62488061 | C anatomy can evolve via a single developmental change |
| Q42318018 | Characterization of Leaf Transcriptome in Banksia hookeriana |
| Q35553720 | Developmental genetic mechanisms of C4 syndrome based on transcriptome analysis of C3 cotyledons and C4 assimilating shoots in Haloxylon ammodendron. |
| Q50080966 | Highly Expressed Genes Are Preferentially Co-Opted for C4 Photosynthesis |
| Q38778611 | Inorganic nitrogen form: a major player in wheat and Arabidopsis responses to elevated CO2. |
| Q90613943 | Involvement of abscisic acid, ABI5, and PPC2 in plant acclimation to low CO2 |
| Q61815777 | Low CO2 induces urea cycle intermediate accumulation in Arabidopsis thaliana |
| Q50100706 | Mechanisms of glacial-to-future atmospheric CO2 effects on plant immunity. |
| Q47560485 | Molecular mechanisms underlying stress response and adaptation |
| Q28601376 | Multi-Year Leaf-Level Response to Sub-Ambient and Elevated Experimental CO2 in Betula nana |
| Q40902077 | Multi-scale modeling of Arabidopsis thaliana response to different CO2 conditions: From gene expression to metabolic flux |
| Q64116423 | Phylostratigraphic analysis of gene co-expression network reveals the evolution of functional modules for ovarian cancer |
| Q52668317 | Physiological and Molecular Processes Associated with Long Duration of ABA Treatment. |
| Q38916722 | T-DNA insertion in aquaporin gene AtPIP1;2 generates transcription profiles reminiscent of a low CO2 response |
| Q88153240 | The intracellular distribution of inorganic carbon fixing enzymes does not support the presence of a C4 pathway in the diatom Phaeodactylum tricornutum |
| Q57473219 | Therapeutic targeting of cellular stress responses in cancer |
| Q40411830 | Transcriptome analysis of the aquaporin AtPIP1;2 deficient line in Arabidopsis thaliana |
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