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Items: 1 to 20 of 232

1.

Transcription reprogramming during root nodule development in Medicago truncatula.

Moreau S, Verdenaud M, Ott T, Letort S, de Billy F, Niebel A, Gouzy J, de Carvalho-Niebel F, Gamas P.

PLoS One. 2011 Jan 27;6(1):e16463. doi: 10.1371/journal.pone.0016463.

2.

Rhizobial infection is associated with the development of peripheral vasculature in nodules of Medicago truncatula.

Guan D, Stacey N, Liu C, Wen J, Mysore KS, Torres-Jerez I, Vernié T, Tadege M, Zhou C, Wang ZY, Udvardi MK, Oldroyd GE, Murray JD.

Plant Physiol. 2013 May;162(1):107-15. doi: 10.1104/pp.113.215111. Epub 2013 Mar 27.

3.

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.

4.

Transcriptomic Analysis of Sinorhizobium meliloti and Medicago truncatula Symbiosis Using Nitrogen Fixation-Deficient Nodules.

Lang C, Long SR.

Mol Plant Microbe Interact. 2015 Aug;28(8):856-68. doi: 10.1094/MPMI-12-14-0407-R. Epub 2015 Jul 16.

5.

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.

6.

MtZR1, a PRAF protein, is involved in the development of roots and symbiotic root nodules in Medicago truncatula.

Hopkins J, Pierre O, Kazmierczak T, Gruber V, Frugier F, Clement M, Frendo P, Herouart D, Boncompagni E.

Plant Cell Environ. 2014 Mar;37(3):658-69. doi: 10.1111/pce.12185. Epub 2013 Sep 17.

7.

RNA-seq transcriptome profiling reveals that Medicago truncatula nodules acclimate N₂ fixation before emerging P deficiency reaches the nodules.

Cabeza RA, Liese R, Lingner A, von Stieglitz I, Neumann J, Salinas-Riester G, Pommerenke C, Dittert K, Schulze J.

J Exp Bot. 2014 Nov;65(20):6035-48. doi: 10.1093/jxb/eru341. Epub 2014 Aug 23.

8.

The C2H2 transcription factor regulator of symbiosome differentiation represses transcription of the secretory pathway gene VAMP721a and promotes symbiosome development in Medicago truncatula.

Sinharoy S, Torres-Jerez I, Bandyopadhyay K, Kereszt A, Pislariu CI, Nakashima J, Benedito VA, Kondorosi E, Udvardi MK.

Plant Cell. 2013 Sep;25(9):3584-601. doi: 10.1105/tpc.113.114017. Epub 2013 Sep 30.

9.

Differentiation of symbiotic cells and endosymbionts in Medicago truncatula nodulation are coupled to two transcriptome-switches.

Maunoury N, Redondo-Nieto M, Bourcy M, Van de Velde W, Alunni B, Laporte P, Durand P, Agier N, Marisa L, Vaubert D, Delacroix H, Duc G, Ratet P, Aggerbeck L, Kondorosi E, Mergaert P.

PLoS One. 2010 Mar 4;5(3):e9519. doi: 10.1371/journal.pone.0009519.

10.

Different cytokinin histidine kinase receptors regulate nodule initiation as well as later nodule developmental stages in Medicago truncatula.

Boivin S, Kazmierczak T, Brault M, Wen J, Gamas P, Mysore KS, Frugier F.

Plant Cell Environ. 2016 Oct;39(10):2198-209. doi: 10.1111/pce.12779. Epub 2016 Jul 28.

PMID:
27341695
11.

A Medicago truncatula NADPH oxidase is involved in symbiotic nodule functioning.

Marino D, Andrio E, Danchin EG, Oger E, Gucciardo S, Lambert A, Puppo A, Pauly N.

New Phytol. 2011 Jan;189(2):580-92. doi: 10.1111/j.1469-8137.2010.03509.x. Epub 2010 Dec 13.

12.

The peptide-encoding CEP1 gene modulates lateral root and nodule numbers in Medicago truncatula.

Imin N, Mohd-Radzman NA, Ogilvie HA, Djordjevic MA.

J Exp Bot. 2013 Dec;64(17):5395-409. doi: 10.1093/jxb/ert369.

PMID:
24259455
13.

Two direct targets of cytokinin signaling regulate symbiotic nodulation in Medicago truncatula.

Ariel F, Brault-Hernandez M, Laffont C, Huault E, Brault M, Plet J, Moison M, Blanchet S, Ichanté JL, Chabaud M, Carrere S, Crespi M, Chan RL, Frugier F.

Plant Cell. 2012 Sep;24(9):3838-52. doi: 10.1105/tpc.112.103267. Epub 2012 Sep 28.

14.

The identification of novel loci required for appropriate nodule development in Medicago truncatula.

Domonkos A, Horvath B, Marsh JF, Halasz G, Ayaydin F, Oldroyd GE, Kalo P.

BMC Plant Biol. 2013 Oct 11;13:157. doi: 10.1186/1471-2229-13-157.

15.

Nitric oxide is required for an optimal establishment of the Medicago truncatula-Sinorhizobium meliloti symbiosis.

del Giudice J, Cam Y, Damiani I, Fung-Chat F, Meilhoc E, Bruand C, Brouquisse R, Puppo A, Boscari A.

New Phytol. 2011 Jul;191(2):405-17. doi: 10.1111/j.1469-8137.2011.03693.x. Epub 2011 Apr 1.

16.

Transcription of ENOD8 in Medicago truncatula nodules directs ENOD8 esterase to developing and mature symbiosomes.

Coque L, Neogi P, Pislariu C, Wilson KA, Catalano C, Avadhani M, Sherrier DJ, Dickstein R.

Mol Plant Microbe Interact. 2008 Apr;21(4):404-10. doi: 10.1094/MPMI-21-4-0404.

17.

NODULE ROOT and COCHLEATA maintain nodule development and are legume orthologs of Arabidopsis BLADE-ON-PETIOLE genes.

Couzigou JM, Zhukov V, Mondy S, Abu el Heba G, Cosson V, Ellis TH, Ambrose M, Wen J, Tadege M, Tikhonovich I, Mysore KS, Putterill J, Hofer J, Borisov AY, Ratet P.

Plant Cell. 2012 Nov;24(11):4498-510. doi: 10.1105/tpc.112.103747. Epub 2012 Nov 6.

18.

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.

19.

nip, a symbiotic Medicago truncatula mutant that forms root nodules with aberrant infection threads and plant defense-like response.

Veereshlingam H, Haynes JG, Penmetsa RV, Cook DR, Sherrier DJ, Dickstein R.

Plant Physiol. 2004 Nov;136(3):3692-702. Epub 2004 Oct 29.

20.

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.

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