195 related articles for article (PubMed ID: 34919720)
41. SNF1-RELATED KINASE 1 and TARGET OF RAPAMYCIN control light-responsive splicing events and developmental characteristics in etiolated Arabidopsis seedlings.
Saile J; Wießner-Kroh T; Erbstein K; Obermüller DM; Pfeiffer A; Janocha D; Lohmann J; Wachter A
Plant Cell; 2023 Sep; 35(9):3413-3428. PubMed ID: 37338062
[TBL] [Abstract][Full Text] [Related]
42. Glucan, water dikinase activity stimulates breakdown of starch granules by plastidial beta-amylases.
Edner C; Li J; Albrecht T; Mahlow S; Hejazi M; Hussain H; Kaplan F; Guy C; Smith SM; Steup M; Ritte G
Plant Physiol; 2007 Sep; 145(1):17-28. PubMed ID: 17631522
[TBL] [Abstract][Full Text] [Related]
43. Target of rapamycin signaling regulates metabolism, growth, and life span in Arabidopsis.
Ren M; Venglat P; Qiu S; Feng L; Cao Y; Wang E; Xiang D; Wang J; Alexander D; Chalivendra S; Logan D; Mattoo A; Selvaraj G; Datla R
Plant Cell; 2012 Dec; 24(12):4850-74. PubMed ID: 23275579
[TBL] [Abstract][Full Text] [Related]
44. Starch biosynthesis in guard cells has features of both autotrophic and heterotrophic tissues.
Flütsch S; Horrer D; Santelia D
Plant Physiol; 2022 Jun; 189(2):541-556. PubMed ID: 35238373
[TBL] [Abstract][Full Text] [Related]
45. Exogenous Application of Low-Concentration Sugar Enhances Brassinosteroid Signaling for Skotomorphogenesis by Promoting BIN2 Degradation.
Sheng H; Zhang S; Wei Y; Chen S
Int J Mol Sci; 2021 Dec; 22(24):. PubMed ID: 34948385
[TBL] [Abstract][Full Text] [Related]
46. Sulfur availability regulates plant growth via glucose-TOR signaling.
Dong Y; Silbermann M; Speiser A; Forieri I; Linster E; Poschet G; Allboje Samami A; Wanatabe M; Sticht C; Teleman AA; Deragon JM; Saito K; Hell R; Wirtz M
Nat Commun; 2017 Oct; 8(1):1174. PubMed ID: 29079776
[TBL] [Abstract][Full Text] [Related]
47. Shaping plant development through the SnRK1-TOR metabolic regulators.
Baena-González E; Hanson J
Curr Opin Plant Biol; 2017 Feb; 35():152-157. PubMed ID: 28027512
[TBL] [Abstract][Full Text] [Related]
48. Differential TOR activation and cell proliferation in
Li X; Cai W; Liu Y; Li H; Fu L; Liu Z; Xu L; Liu H; Xu T; Xiong Y
Proc Natl Acad Sci U S A; 2017 Mar; 114(10):2765-2770. PubMed ID: 28223530
[TBL] [Abstract][Full Text] [Related]
49. A negative feedback loop of TOR signaling balances growth and stress-response trade-offs in plants.
Jamsheer K M; Jindal S; Sharma M; Awasthi P; S S; Sharma M; Mannully CT; Laxmi A
Cell Rep; 2022 Apr; 39(1):110631. PubMed ID: 35385724
[TBL] [Abstract][Full Text] [Related]
50. TOR is a negative regulator of autophagy in Arabidopsis thaliana.
Liu Y; Bassham DC
PLoS One; 2010 Jul; 5(7):e11883. PubMed ID: 20686696
[TBL] [Abstract][Full Text] [Related]
51. Saccharomyces cerevisiae FKBP12 binds Arabidopsis thaliana TOR and its expression in plants leads to rapamycin susceptibility.
Sormani R; Yao L; Menand B; Ennar N; Lecampion C; Meyer C; Robaglia C
BMC Plant Biol; 2007 Jun; 7():26. PubMed ID: 17543119
[TBL] [Abstract][Full Text] [Related]
52. Mutations in the Arabidopsis homolog of LST8/GβL, a partner of the target of Rapamycin kinase, impair plant growth, flowering, and metabolic adaptation to long days.
Moreau M; Azzopardi M; Clément G; Dobrenel T; Marchive C; Renne C; Martin-Magniette ML; Taconnat L; Renou JP; Robaglia C; Meyer C
Plant Cell; 2012 Feb; 24(2):463-81. PubMed ID: 22307851
[TBL] [Abstract][Full Text] [Related]
53. BAM 1 and RECEPTOR-LIKE PROTEIN KINASE 2 constitute a signaling pathway and modulate CLE peptide-triggered growth inhibition in Arabidopsis root.
Shimizu N; Ishida T; Yamada M; Shigenobu S; Tabata R; Kinoshita A; Yamaguchi K; Hasebe M; Mitsumasu K; Sawa S
New Phytol; 2015 Dec; 208(4):1104-13. PubMed ID: 26083273
[TBL] [Abstract][Full Text] [Related]
54. Adjustment of diurnal starch turnover to short days: depletion of sugar during the night leads to a temporary inhibition of carbohydrate utilization, accumulation of sugars and post-translational activation of ADP-glucose pyrophosphorylase in the following light period.
Gibon Y; Bläsing OE; Palacios-Rojas N; Pankovic D; Hendriks JH; Fisahn J; Höhne M; Günther M; Stitt M
Plant J; 2004 Sep; 39(6):847-62. PubMed ID: 15341628
[TBL] [Abstract][Full Text] [Related]
55. Characterization of Maf1 in Arabidopsis: function under stress conditions and regulation by the TOR signaling pathway.
Ahn CS; Lee DH; Pai HS
Planta; 2019 Feb; 249(2):527-542. PubMed ID: 30293201
[TBL] [Abstract][Full Text] [Related]
56. TOR dynamically regulates plant cell-cell transport.
Brunkard JO; Xu M; Scarpin MR; Chatterjee S; Shemyakina EA; Goodman HM; Zambryski P
Proc Natl Acad Sci U S A; 2020 Mar; 117(9):5049-5058. PubMed ID: 32051250
[TBL] [Abstract][Full Text] [Related]
57. SIZ1-Dependent Post-Translational Modification by SUMO Modulates Sugar Signaling and Metabolism in Arabidopsis thaliana.
Castro PH; Verde N; Lourenço T; Magalhães AP; Tavares RM; Bejarano ER; Azevedo H
Plant Cell Physiol; 2015 Dec; 56(12):2297-311. PubMed ID: 26468507
[TBL] [Abstract][Full Text] [Related]
58. Starch and the clock: the dark side of plant productivity.
Graf A; Smith AM
Trends Plant Sci; 2011 Mar; 16(3):169-75. PubMed ID: 21216654
[TBL] [Abstract][Full Text] [Related]
59. Young seedlings adapt to stress by retaining starch and retarding growth through ABA-Dependent and -independent pathways in Arabidopsis.
Liu K; Zou W; Gao X; Wang X; Yu Q; Ge L
Biochem Biophys Res Commun; 2019 Aug; 515(4):699-705. PubMed ID: 31186142
[TBL] [Abstract][Full Text] [Related]
60. Gene Regulation and Survival under Hypoxia Requires Starch Availability and Metabolism.
Loreti E; Valeri MC; Novi G; Perata P
Plant Physiol; 2018 Feb; 176(2):1286-1298. PubMed ID: 29084901
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]