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Items: 1 to 20 of 100

1.

RNA-Seq analysis discloses early senescence and nucleolar dysfunction triggered by Tdp1α depletion in Medicago truncatula.

Donà M, Confalonieri M, Minio A, Biggiogera M, Buttafava A, Raimondi E, Delledonne M, Ventura L, Sabatini ME, Macovei A, Giraffa G, Carbonera D, Balestrazzi A.

J Exp Bot. 2013 Apr;64(7):1941-51. doi: 10.1093/jxb/ert063. Epub 2013 Mar 6.

2.

The tyrosyl-DNA phosphodiesterase gene family in Medicago truncatula Gaertn.: bioinformatic investigation and expression profiles in response to copper- and PEG-mediated stress.

Macovei A, Balestrazzi A, Confalonieri M, Carbonera D.

Planta. 2010 Jul;232(2):393-407. doi: 10.1007/s00425-010-1179-9. Epub 2010 May 11.

PMID:
20458495
3.

Seed imbibition in Medicago truncatula Gaertn.: Expression profiles of DNA repair genes in relation to PEG-mediated stress.

Balestrazzi A, Confalonieri M, Macovei A, Carbonera D.

J Plant Physiol. 2011 May 1;168(7):706-13. doi: 10.1016/j.jplph.2010.10.008. Epub 2010 Dec 3.

PMID:
21129815
4.

Copper-mediated genotoxic stress is attenuated by the overexpression of the DNA repair gene MtTdp2α (tyrosyl-DNA phosphodiesterase 2) in Medicago truncatula plants.

Faè M, Balestrazzi A, Confalonieri M, Donà M, Macovei A, Valassi A, Giraffa G, Carbonera D.

Plant Cell Rep. 2014 Jul;33(7):1071-80. doi: 10.1007/s00299-014-1595-6. Epub 2014 Mar 18.

PMID:
24638978
5.

Depletion of tyrosyl-DNA phosphodiesterase 1α (MtTdp1α) affects transposon expression in Medicago truncatula.

Sabatini ME, Donà M, Leonetti P, Minio A, Delledonne M, Carboneral D, Confalonieri M, Giraffa G, Balestrazzi A.

J Integr Plant Biol. 2016 Jul;58(7):618-22. doi: 10.1111/jipb.12457. Epub 2016 Feb 24.

PMID:
26699667
6.

In Medicago truncatula, water deficit modulates the transcript accumulation of components of small RNA pathways.

Capitão C, Paiva JA, Santos DM, Fevereiro P.

BMC Plant Biol. 2011 May 10;11:79. doi: 10.1186/1471-2229-11-79.

7.

Transcriptome analysis of Medicago truncatula leaf senescence: similarities and differences in metabolic and transcriptional regulations as compared with Arabidopsis, nodule senescence and nitric oxide signalling.

De Michele R, Formentin E, Todesco M, Toppo S, Carimi F, Zottini M, Barizza E, Ferrarini A, Delledonne M, Fontana P, Lo Schiavo F.

New Phytol. 2009;181(3):563-75. doi: 10.1111/j.1469-8137.2008.02684.x. Epub 2008 Nov 17.

8.

Exploring the nuclear proteome of Medicago truncatula at the switch towards seed filling.

Repetto O, Rogniaux H, Firnhaber C, Zuber H, Küster H, Larré C, Thompson R, Gallardo K.

Plant J. 2008 Nov;56(3):398-410. doi: 10.1111/j.1365-313X.2008.03610.x. Epub 2008 Jul 4.

9.

[Expression of the WOX and PIN Genes in the Course of Somatic and Zygotic Embryogenesis of a Medicago truncatula].

Tvorogova VE, Lebedeva MA, Lutova LA.

Genetika. 2015 Dec;51(12):1376-85. Russian.

PMID:
27055297
10.

Insight into the role of anthocyanin biosynthesis-related genes in Medicago truncatula mutants impaired in pigmentation in leaves.

Carletti G, Lucini L, Busconi M, Marocco A, Bernardi J.

Plant Physiol Biochem. 2013 Sep;70:123-32. doi: 10.1016/j.plaphy.2013.05.030. Epub 2013 May 31.

PMID:
23774374
11.

Medicago truncatula (E)-beta-ocimene synthase is induced by insect herbivory with corresponding increases in emission of volatile ocimene.

Navia-Giné WG, Yuan JS, Mauromoustakos A, Murphy JB, Chen F, Korth KL.

Plant Physiol Biochem. 2009 May;47(5):416-25. doi: 10.1016/j.plaphy.2009.01.008. Epub 2009 Feb 8.

PMID:
19249223
12.

A CDPK isoform participates in the regulation of nodule number in Medicago truncatula.

Gargantini PR, Gonzalez-Rizzo S, Chinchilla D, Raices M, Giammaria V, Ulloa RM, Frugier F, Crespi MD.

Plant J. 2006 Dec;48(6):843-56. Epub 2006 Nov 21.

13.

Identification and expression analysis of multiple FRO gene copies in Medicago truncatula.

Del C Orozco-Mosqueda M, Santoyo G, Farías-Rodríguez R, Macías-Rodríguez L, Valencia-Cantero E.

Genet Mol Res. 2012 Dec 17;11(4):4402-10. doi: 10.4238/2012.October.9.7.

14.

Dual involvement of a Medicago truncatula NAC transcription factor in root abiotic stress response and symbiotic nodule senescence.

de Zélicourt A, Diet A, Marion J, Laffont C, Ariel F, Moison M, Zahaf O, Crespi M, Gruber V, Frugier F.

Plant J. 2012 Apr;70(2):220-30. doi: 10.1111/j.1365-313X.2011.04859.x. Epub 2012 Jan 10.

15.

Silencing of the Rac1 GTPase MtROP9 in Medicago truncatula stimulates early mycorrhizal and oomycete root colonizations but negatively affects rhizobial infection.

Kiirika LM, Bergmann HF, Schikowsky C, Wimmer D, Korte J, Schmitz U, Niehaus K, Colditz F.

Plant Physiol. 2012 May;159(1):501-16. doi: 10.1104/pp.112.193706. Epub 2012 Mar 7.

16.

From model to crop: functional analysis of a STAY-GREEN gene in the model legume Medicago truncatula and effective use of the gene for alfalfa improvement.

Zhou C, Han L, Pislariu C, Nakashima J, Fu C, Jiang Q, Quan L, Blancaflor EB, Tang Y, Bouton JH, Udvardi M, Xia G, Wang ZY.

Plant Physiol. 2011 Nov;157(3):1483-96. doi: 10.1104/pp.111.185140. Epub 2011 Sep 28.

17.

The TFIIS and TFIIS-like genes from Medicago truncatula are involved in oxidative stress response.

Macovei A, Balestrazzi A, Confalonieri M, Buttafava A, Carbonera D.

Gene. 2011 Jan 1;470(1-2):20-30. doi: 10.1016/j.gene.2010.09.004. Epub 2010 Sep 19.

PMID:
20858537
18.

Analysis of B function in legumes: PISTILLATA proteins do not require the PI motif for floral organ development in Medicago truncatula.

Benlloch R, Roque E, Ferrándiz C, Cosson V, Caballero T, Penmetsa RV, Beltrán JP, Cañas LA, Ratet P, Madueño F.

Plant J. 2009 Oct;60(1):102-11. doi: 10.1111/j.1365-313X.2009.03939.x. Epub 2009 May 28.

19.

New insights on the barrel medic MtOGG1 and MtFPG functions in relation to oxidative stress response in planta and during seed imbibition.

Macovei A, Balestrazzi A, Confalonieri M, Faé M, Carbonera D.

Plant Physiol Biochem. 2011 Sep;49(9):1040-50. doi: 10.1016/j.plaphy.2011.05.007. Epub 2011 May 23.

PMID:
21696973
20.

Large-scale phosphoprotein analysis in Medicago truncatula roots provides insight into in vivo kinase activity in legumes.

Grimsrud PA, den Os D, Wenger CD, Swaney DL, Schwartz D, Sussman MR, Ané JM, Coon JJ.

Plant Physiol. 2010 Jan;152(1):19-28. doi: 10.1104/pp.109.149625. Epub 2009 Nov 18.

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