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Items: 4

1.

Tomato floral induction and flower development are orchestrated by the interplay between gibberellin and two unrelated microRNA-controlled modules.

Silva GFF, Silva EM, Correa JPO, Vicente MH, Jiang N, Notini MM, Junior AC, De Jesus FA, Castilho P, Carrera E, López-Díaz I, Grotewold E, Peres LEP, Nogueira FTS.

New Phytol. 2018 Sep 20. doi: 10.1111/nph.15492. [Epub ahead of print]

PMID:
30238569
2.

SELF-PRUNING Acts Synergistically with DIAGEOTROPICA to Guide Auxin Responses and Proper Growth Form.

Silva WB, Vicente MH, Robledo JM, Reartes DS, Ferrari RC, Bianchetti R, Araújo WL, Freschi L, Peres LEP, Zsögön A.

Plant Physiol. 2018 Apr;176(4):2904-2916. doi: 10.1104/pp.18.00038. Epub 2018 Mar 2.

PMID:
29500181
3.

NO, hydrogen sulfide does not come first during tomato response to high salinity.

da-Silva CJ, Mollica DCF, Vicente MH, Peres LEP, Modolo LV.

Nitric Oxide. 2018 Jun 1;76:164-173. doi: 10.1016/j.niox.2017.09.008. Epub 2017 Sep 28.

PMID:
28963074
4.

Semi-determinate growth habit adjusts the vegetative-to-reproductive balance and increases productivity and water-use efficiency in tomato (Solanum lycopersicum).

Vicente MH, Zsögön A, de Sá AFL, Ribeiro RV, Peres LEP.

J Plant Physiol. 2015 Apr 1;177:11-19. doi: 10.1016/j.jplph.2015.01.003. Epub 2015 Jan 13.

PMID:
25659332

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