100 related articles for article (PubMed ID: 15110790)
1. Ectopic expression of the maize chromosomal HMGB1 protein causes defects in root development of tobacco seedlings.
Lichota J; Ritt C; Grasser KD
Biochem Biophys Res Commun; 2004 May; 318(1):317-22. PubMed ID: 15110790
[TBL] [Abstract][Full Text] [Related]
2. The expression level of the chromatin-associated HMGB1 protein influences growth, stress tolerance, and transcriptome in Arabidopsis.
Lildballe DL; Pedersen DS; Kalamajka R; Emmersen J; Houben A; Grasser KD
J Mol Biol; 2008 Dec; 384(1):9-21. PubMed ID: 18822296
[TBL] [Abstract][Full Text] [Related]
3. Expression of BjMT2, a metallothionein 2 from Brassica juncea, increases copper and cadmium tolerance in Escherichia coli and Arabidopsis thaliana, but inhibits root elongation in Arabidopsis thaliana seedlings.
Zhigang A; Cuijie L; Yuangang Z; Yejie D; Wachter A; Gromes R; Rausch T
J Exp Bot; 2006; 57(14):3575-82. PubMed ID: 16957018
[TBL] [Abstract][Full Text] [Related]
4. A cell wall extract from the endophytic fungus Piriformospora indica promotes growth of Arabidopsis seedlings and induces intracellular calcium elevation in roots.
Vadassery J; Ranf S; Drzewiecki C; Mithöfer A; Mazars C; Scheel D; Lee J; Oelmüller R
Plant J; 2009 Jul; 59(2):193-206. PubMed ID: 19392691
[TBL] [Abstract][Full Text] [Related]
5. Phosphorylation of maize and Arabidopsis HMGB proteins by protein kinase CK2alpha.
Stemmer C; Leeming DJ; Franssen L; Grimm R; Grasser KD
Biochemistry; 2003 Apr; 42(12):3503-8. PubMed ID: 12653554
[TBL] [Abstract][Full Text] [Related]
6. Interactions of the basic N-terminal and the acidic C-terminal domains of the maize chromosomal HMGB1 protein.
Thomsen MS; Franssen L; Launholt D; Fojan P; Grasser KD
Biochemistry; 2004 Jun; 43(25):8029-37. PubMed ID: 15209498
[TBL] [Abstract][Full Text] [Related]
7. Chromosomal high mobility group (HMG) proteins of the HMGB-type occurring in the moss Physcomitrella patens.
Kiilerich B; Stemmer C; Merkle T; Launholt D; Gorr G; Grasser KD
Gene; 2008 Jan; 407(1-2):86-97. PubMed ID: 17980517
[TBL] [Abstract][Full Text] [Related]
8. Arabidopsis chromatin-associated HMGA and HMGB use different nuclear targeting signals and display highly dynamic localization within the nucleus.
Launholt D; Merkle T; Houben A; Schulz A; Grasser KD
Plant Cell; 2006 Nov; 18(11):2904-18. PubMed ID: 17114349
[TBL] [Abstract][Full Text] [Related]
9. The accumulation of alpha-zein in transgenic tobacco endosperm is stabilized by co-expression of beta-zein.
Coleman CE; Yoho PR; Escobar S; Ogawa M
Plant Cell Physiol; 2004 Jul; 45(7):864-71. PubMed ID: 15295069
[TBL] [Abstract][Full Text] [Related]
10. Bacterial thermostable beta-glucanases as a tool for plant functional genomics.
Abdeev RM; Abdeeva IA; Bruskin SS; Musiychuk KA; Goldenkova-Pavlova IV; Piruzian ES
Gene; 2009 May; 436(1-2):81-9. PubMed ID: 19393166
[TBL] [Abstract][Full Text] [Related]
11. Arabidopsis and tobacco plants ectopically expressing the soybean antiquitin-like ALDH7 gene display enhanced tolerance to drought, salinity, and oxidative stress.
Rodrigues SM; Andrade MO; Gomes AP; Damatta FM; Baracat-Pereira MC; Fontes EP
J Exp Bot; 2006; 57(9):1909-18. PubMed ID: 16595581
[TBL] [Abstract][Full Text] [Related]
12. Phytodegradation of organophosphorus compounds by transgenic plants expressing a bacterial organophosphorus hydrolase.
Wang X; Wu N; Guo J; Chu X; Tian J; Yao B; Fan Y
Biochem Biophys Res Commun; 2008 Jan; 365(3):453-8. PubMed ID: 17996731
[TBL] [Abstract][Full Text] [Related]
13. Root-selective expression of AtCAX4 and AtCAX2 results in reduced lamina cadmium in field-grown Nicotiana tabacum L.
Korenkov V; King B; Hirschi K; Wagner GJ
Plant Biotechnol J; 2009 Apr; 7(3):219-26. PubMed ID: 19175521
[TBL] [Abstract][Full Text] [Related]
14. Development of transgenic tobacco plants overexpressing maize glutathione S-transferase I for chloroacetanilide herbicides phytoremediation.
Karavangeli M; Labrou NE; Clonis YD; Tsaftaris A
Biomol Eng; 2005 Oct; 22(4):121-8. PubMed ID: 16085457
[TBL] [Abstract][Full Text] [Related]
15. Rootless with undetectable meristem 1 encodes a monocot-specific AUX/IAA protein that controls embryonic seminal and post-embryonic lateral root initiation in maize.
von Behrens I; Komatsu M; Zhang Y; Berendzen KW; Niu X; Sakai H; Taramino G; Hochholdinger F
Plant J; 2011 Apr; 66(2):341-53. PubMed ID: 21219511
[TBL] [Abstract][Full Text] [Related]
16. Cytokinin-binding protein (70 kDa): localization in tissues and cells of etiolated maize seedlings and its putative function.
Brovko FA; Vasil'eva VS; Shepelyakovskaya AO; Selivankina SY; Kudoyarova GR; Nosov AV; Moshkov DA; Laman AG; Boziev KM; Kusnetsov VV; Kulaeva ON
J Exp Bot; 2007; 58(10):2479-90. PubMed ID: 17584953
[TBL] [Abstract][Full Text] [Related]
17. Positive role of a wheat HvABI5 ortholog in abiotic stress response of seedlings.
Kobayashi F; Maeta E; Terashima A; Takumi S
Physiol Plant; 2008 Sep; 134(1):74-86. PubMed ID: 18433415
[TBL] [Abstract][Full Text] [Related]
18. Basic and acidic regions flanking the HMG-box domain of maize HMGB1 and HMGB5 modulate the stimulatory effect on the DNA binding of transcription factor Dof2.
Grasser M; Christensen JM; Peterhänsel C; Grasser KD
Biochemistry; 2007 May; 46(21):6375-82. PubMed ID: 17487980
[TBL] [Abstract][Full Text] [Related]
19. Enhanced resistance to Helicoverpa zea in tobacco expressing an activated form of maize ribosome- inactivating protein.
Dowd PF; Zuo WN; Gillikin JW; Johnson ET; Boston RS
J Agric Food Chem; 2003 Jun; 51(12):3568-74. PubMed ID: 12769526
[TBL] [Abstract][Full Text] [Related]
20. Growth, nitrogen uptake and flow in maize plants affected by root growth restriction.
Xu L; Niu J; Li C; Zhang F
J Integr Plant Biol; 2009 Jul; 51(7):689-97. PubMed ID: 19566647
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]