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1. LIKE EARLY STARVATION 1 interacts with amylopectin during starch biosynthesis.

2. Abscisic acid modulates neighbor proximity-induced leaf hyponasty in Arabidopsis.

3. Rising rates of starch degradation during daytime and trehalose 6-phosphate optimize carbon availability.

4. ACA pumps maintain leaf excitability during herbivore onslaught.

5. Coalescence and directed anisotropic growth of starch granule initials in subdomains of Arabidopsis thaliana chloroplasts.

6. Ectopic maltase alleviates dwarf phenotype and improves plant frost tolerance of maltose transporter mutants.

7. STARCH SYNTHASE5, a Noncanonical Starch Synthase-Like Protein, Promotes Starch Granule Initiation in Arabidopsis.

8. Starch: A Flexible, Adaptable Carbon Store Coupled to Plant Growth.

9. Two Plastidial Coiled-Coil Proteins Are Essential for Normal Starch Granule Initiation in Arabidopsis.

10. Distinct Functions of STARCH SYNTHASE 4 Domains in Starch Granule Formation.

11. OCTOPUS-LIKE 2, a novel player in Arabidopsis root and vascular development, reveals a key role for OCTOPUS family genes in root metaphloem sieve tube differentiation.

12. Homologs of PROTEIN TARGETING TO STARCH Control Starch Granule Initiation in Arabidopsis Leaves.

13. Regulation of Leaf Starch Degradation by Abscisic Acid Is Important for Osmotic Stress Tolerance in Plants.

14. The Starch Granule-Associated Protein EARLY STARVATION1 Is Required for the Control of Starch Degradation in Arabidopsis thaliana Leaves.

15. PROTEIN TARGETING TO STARCH is required for localising GRANULE-BOUND STARCH SYNTHASE to starch granules and for normal amylose synthesis in Arabidopsis.

16. Replacement of the endogenous starch debranching enzymes ISA1 and ISA2 of Arabidopsis with the rice orthologs reveals a degree of functional conservation during starch synthesis.

17. Arabidopsis thaliana AMY3 is a unique redox-regulated chloroplastic α-amylase.

18. The simultaneous abolition of three starch hydrolases blocks transient starch breakdown in Arabidopsis.

19. Comprehensive survey of redox sensitive starch metabolising enzymes in Arabidopsis thaliana.

20. Mutagenesis of cysteine 81 prevents dimerization of the APS1 subunit of ADP-glucose pyrophosphorylase and alters diurnal starch turnover in Arabidopsis thaliana leaves.

21. The phosphoglucan phosphatase like sex Four2 dephosphorylates starch at the C3-position in Arabidopsis.

22. β-amylase-like proteins function as transcription factors in Arabidopsis, controlling shoot growth and development.

23. Callose synthase GSL7 is necessary for normal phloem transport and inflorescence growth in Arabidopsis.

24. The Laforin-like dual-specificity phosphatase SEX4 from Arabidopsis hydrolyzes both C6- and C3-phosphate esters introduced by starch-related dikinases and thereby affects phase transition of alpha-glucans.

25. A putative phosphatase, LSF1, is required for normal starch turnover in Arabidopsis leaves.

26. STARCH-EXCESS4 is a laforin-like Phosphoglucan phosphatase required for starch degradation in Arabidopsis thaliana.

27. Similar protein phosphatases control starch metabolism in plants and glycogen metabolism in mammals.

28. A previously unknown maltose transporter essential for starch degradation in leaves.

29. Distinct Functions of STARCH SYNTHASE 4 Domains in Starch Granule Formation1[OPEN]

30. Replacement of the endogenous starch debranching enzymes ISA1 and ISA2 of Arabidopsis with the rice orthologs reveals a degree of functional conservation during starch synthesis

31. Starch Granule-Associated Protein EARLY STARVATION1 Is Required for the Control of Starch Degradation in Arabidopsis thaliana Leaves.

32. Abscisic Acid Modulates Neighbor Proximity-Induced Leaf Hyponasty in Arabidopsis

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