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Items: 20

1.

Whole-genome landscape of Medicago truncatula symbiotic genes.

Pecrix Y, Staton SE, Sallet E, Lelandais-Brière C, Moreau S, Carrère S, Blein T, Jardinaud MF, Latrasse D, Zouine M, Zahm M, Kreplak J, Mayjonade B, Satgé C, Perez M, Cauet S, Marande W, Chantry-Darmon C, Lopez-Roques C, Bouchez O, Bérard A, Debellé F, Muños S, Bendahmane A, Bergès H, Niebel A, Buitink J, Frugier F, Benhamed M, Crespi M, Gouzy J, Gamas P.

Nat Plants. 2018 Dec;4(12):1017-1025. doi: 10.1038/s41477-018-0286-7. Epub 2018 Nov 5.

PMID:
30397259
2.

Laser Capture Micro-Dissection Coupled to RNA Sequencing: A Powerful Approach Applied to the Model Legume Medicago truncatula in Interaction with Sinorhizobium meliloti.

Roux B, Rodde N, Moreau S, Jardinaud MF, Gamas P.

Methods Mol Biol. 2018;1830:191-224. doi: 10.1007/978-1-4939-8657-6_12.

PMID:
30043372
3.

Cytokinins in Symbiotic Nodulation: When, Where, What For?

Gamas P, Brault M, Jardinaud MF, Frugier F.

Trends Plant Sci. 2017 Sep;22(9):792-802. doi: 10.1016/j.tplants.2017.06.012. Epub 2017 Jul 21. Review.

PMID:
28739135
4.

MtNF-YA1, A Central Transcriptional Regulator of Symbiotic Nodule Development, Is Also a Determinant of Medicago truncatula Susceptibility toward a Root Pathogen.

Rey T, Laporte P, Bonhomme M, Jardinaud MF, Huguet S, Balzergue S, Dumas B, Niebel A, Jacquet C.

Front Plant Sci. 2016 Dec 5;7:1837. eCollection 2016.

5.

Reprogramming of DNA methylation is critical for nodule development in Medicago truncatula.

Satgé C, Moreau S, Sallet E, Lefort G, Auriac MC, Remblière C, Cottret L, Gallardo K, Noirot C, Jardinaud MF, Gamas P.

Nat Plants. 2016 Oct 31;2(11):16166. doi: 10.1038/nplants.2016.166.

PMID:
27797357
6.

A Laser Dissection-RNAseq Analysis Highlights the Activation of Cytokinin Pathways by Nod Factors in the Medicago truncatula Root Epidermis.

Jardinaud MF, Boivin S, Rodde N, Catrice O, Kisiala A, Lepage A, Moreau S, Roux B, Cottret L, Sallet E, Brault M, Emery RJ, Gouzy J, Frugier F, Gamas P.

Plant Physiol. 2016 Jul;171(3):2256-76. doi: 10.1104/pp.16.00711. Epub 2016 May 23.

7.

Genomics and transcriptomics of Xanthomonas campestris species challenge the concept of core type III effectome.

Roux B, Bolot S, Guy E, Denancé N, Lautier M, Jardinaud MF, Fischer-Le Saux M, Portier P, Jacques MA, Gagnevin L, Pruvost O, Lauber E, Arlat M, Carrère S, Koebnik R, Noël LD.

BMC Genomics. 2015 Nov 18;16:975. doi: 10.1186/s12864-015-2190-0.

8.

The Decoy Substrate of a Pathogen Effector and a Pseudokinase Specify Pathogen-Induced Modified-Self Recognition and Immunity in Plants.

Wang G, Roux B, Feng F, Guy E, Li L, Li N, Zhang X, Lautier M, Jardinaud MF, Chabannes M, Arlat M, Chen S, He C, Noël LD, Zhou JM.

Cell Host Microbe. 2015 Sep 9;18(3):285-95. doi: 10.1016/j.chom.2015.08.004.

9.

Combined genetic and transcriptomic analysis reveals three major signalling pathways activated by Myc-LCOs in Medicago truncatula.

Camps C, Jardinaud MF, Rengel D, Carrère S, Hervé C, Debellé F, Gamas P, Bensmihen S, Gough C.

New Phytol. 2015 Oct;208(1):224-40. doi: 10.1111/nph.13427. Epub 2015 Apr 28.

10.

Two CCAAT-box-binding transcription factors redundantly regulate early steps of the legume-rhizobia endosymbiosis.

Laloum T, Baudin M, Frances L, Lepage A, Billault-Penneteau B, Cerri MR, Ariel F, Jardinaud MF, Gamas P, de Carvalho-Niebel F, Niebel A.

Plant J. 2014 Sep;79(5):757-68. doi: 10.1111/tpj.12587. Epub 2014 Jul 28.

11.

An integrated analysis of plant and bacterial gene expression in symbiotic root nodules using laser-capture microdissection coupled to RNA sequencing.

Roux B, Rodde N, Jardinaud MF, Timmers T, Sauviac L, Cottret L, Carrère S, Sallet E, Courcelle E, Moreau S, Debellé F, Capela D, de Carvalho-Niebel F, Gouzy J, Bruand C, Gamas P.

Plant J. 2014 Mar;77(6):817-37. doi: 10.1111/tpj.12442. Epub 2014 Feb 24.

12.

The symbiotic transcription factor MtEFD and cytokinins are positively acting in the Medicago truncatula and Ralstonia solanacearum pathogenic interaction.

Moreau S, Fromentin J, Vailleau F, Vernié T, Huguet S, Balzergue S, Frugier F, Gamas P, Jardinaud MF.

New Phytol. 2014 Mar;201(4):1343-57. doi: 10.1111/nph.12636. Epub 2013 Dec 11.

13.

The CCAAT box-binding transcription factor NF-YA1 controls rhizobial infection.

Laporte P, Lepage A, Fournier J, Catrice O, Moreau S, Jardinaud MF, Mun JH, Larrainzar E, Cook DR, Gamas P, Niebel A.

J Exp Bot. 2014 Feb;65(2):481-94. doi: 10.1093/jxb/ert392. Epub 2013 Dec 6.

14.

MtQRRS1, an R-locus required for Medicago truncatula quantitative resistance to Ralstonia solanacearum.

Ben C, Debellé F, Berges H, Bellec A, Jardinaud MF, Anson P, Huguet T, Gentzbittel L, Vailleau F.

New Phytol. 2013 Aug;199(3):758-72. doi: 10.1111/nph.12299. Epub 2013 May 2.

15.

Next-generation annotation of prokaryotic genomes with EuGene-P: application to Sinorhizobium meliloti 2011.

Sallet E, Roux B, Sauviac L, Jardinaud MF, Carrère S, Faraut T, de Carvalho-Niebel F, Gouzy J, Gamas P, Capela D, Bruand C, Schiex T.

DNA Res. 2013 Aug;20(4):339-54. doi: 10.1093/dnares/dst014. Epub 2013 Apr 18.

16.

NFP, a LysM protein controlling Nod factor perception, also intervenes in Medicago truncatula resistance to pathogens.

Rey T, Nars A, Bonhomme M, Bottin A, Huguet S, Balzergue S, Jardinaud MF, Bono JJ, Cullimore J, Dumas B, Gough C, Jacquet C.

New Phytol. 2013 May;198(3):875-86. doi: 10.1111/nph.12198. Epub 2013 Feb 25.

17.

Dissection of bacterial Wilt on Medicago truncatula revealed two type III secretion system effectors acting on root infection process and disease development.

Turner M, Jauneau A, Genin S, Tavella MJ, Vailleau F, Gentzbittel L, Jardinaud MF.

Plant Physiol. 2009 Aug;150(4):1713-22. doi: 10.1104/pp.109.141523. Epub 2009 Jun 3.

18.

Characterization of the interaction between the bacterial wilt pathogen Ralstonia solanacearum and the model legume plant Medicago truncatula.

Vailleau F, Sartorel E, Jardinaud MF, Chardon F, Genin S, Huguet T, Gentzbittel L, Petitprez M.

Mol Plant Microbe Interact. 2007 Feb;20(2):159-67.

19.

Comparative analysis of early embryonic sunflower cDNA libraries.

Ben C, Hewezi T, Jardinaud MF, Bena F, Ladouce N, Moretti S, Tamborindeguy C, Liboz T, Petitprez M, Gentzbittel L.

Plant Mol Biol. 2005 Jan;57(2):255-70.

PMID:
15821881
20.

Optimisation of DNA transfer and transientβ-glucuronidase expression in electroporated maize (Zea mays L.) microspores.

Jardinaud MF, Souvré A, Beckert M, Alibert G.

Plant Cell Rep. 1995 Jan;15(1-2):55-8. doi: 10.1007/BF01690253.

PMID:
24185654

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