Helge Kuster
Overview
Explore the profile of Helge Kuster including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
60
Citations
1754
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
11.
Chen H, Osuna D, Colville L, Lorenzo O, Graeber K, Kuster H, et al.
PLoS One
. 2013 Nov;
8(10):e78471.
PMID: 24205239
Understanding of seed ageing, which leads to viability loss during storage, is vital for ex situ plant conservation and agriculture alike. Yet the potential for regulation at the transcriptional level...
12.
Limpens E, Moling S, Hooiveld G, Pereira P, Bisseling T, Becker J, et al.
PLoS One
. 2013 Jun;
8(5):e64377.
PMID: 23734198
Legumes have the unique ability to host nitrogen-fixing Rhizobium bacteria as symbiosomes inside root nodule cells. To get insight into this key process, which forms the heart of the endosymbiosis,...
13.
Hogekamp C, Kuster H
BMC Genomics
. 2013 May;
14:306.
PMID: 23647797
Background: About 80% of today's land plants are able to establish an arbuscular mycorrhizal (AM) symbiosis with Glomeromycota fungi to improve their access to nutrients and water in the soil....
14.
Vorholter F, Wiggerich H, Scheidle H, Sidhu V, Mrozek K, Kuster H, et al.
BMC Microbiol
. 2012 Oct;
12:239.
PMID: 23082751
Background: Efficient perception of attacking pathogens is essential for plants. Plant defense is evoked by molecules termed elicitors. Endogenous elicitors or damage-associated molecular patterns (DAMPs) originate from plant materials upon...
15.
Czaja L, Hogekamp C, Lamm P, Maillet F, Martinez E, Samain E, et al.
Plant Physiol
. 2012 Jun;
159(4):1671-85.
PMID: 22652128
The formation of root nodules and arbuscular mycorrhizal (AM) roots is controlled by a common signaling pathway including the calcium/calmodulin-dependent kinase Doesn't Make Infection3 (DMI3). While nodule initiation by lipochitooligosaccharide...
16.
Ortu G, Balestrini R, Pereira P, Becker J, Kuster H, Bonfante P
Mol Plant
. 2012 Mar;
5(4):951-4.
PMID: 22451647
No abstract available.
17.
Kamphuis L, Williams A, Kuster H, Trengove R, Singh K, Oliver R, et al.
Mol Plant Pathol
. 2012 Jan;
13(6):593-603.
PMID: 22212347
Gene expression changes and metabolite abundances were measured during the interaction of Medicago truncatula with the fungal necrotrophic pathogen Phoma medicaginis in leaf tissue of susceptible and resistant accessions. Over...
18.
Hogekamp C, Arndt D, Pereira P, Becker J, Hohnjec N, Kuster H
Plant Physiol
. 2011 Oct;
157(4):2023-43.
PMID: 22034628
Arbuscular mycorrhizae (AM) are the most widespread symbioses on Earth, promoting nutrient supply of most terrestrial plant species. To unravel gene expression in defined stages of Medicago truncatula root colonization...
19.
Fondevilla S, Kuster H, Krajinski F, Cubero J, Rubiales D
BMC Genomics
. 2011 Jan;
12:28.
PMID: 21226971
Background: Ascochyta blight, caused by Mycosphaerella pinodes is one of the most important pea pathogens. However, little is known about the genes and mechanisms of resistance acting against M. pinodes...
20.
Radchuk R, Conrad U, Saalbach I, Giersberg M, Emery R, Kuster H, et al.
Plant J
. 2010 Nov;
64(5):715-30.
PMID: 21105920
The transition of pea embryos from pre-storage to maturation is partially controlled by abscisic acid (ABA). Immunomodulation in pea embryos specifically reduces free ABA levels during transition stages. Such seeds...