Cellulose biosynthesis and deposition in higher plants

NG Taylor - New phytologist, 2008 - Wiley Online Library
The plant cell wall is central to plant development. Cellulose is a major component of plant
cell walls, and is the world's most abundant biopolymer. Cellulose contains apparently …

The many functions of ERECTA

M van Zanten, LB Snoek, MCG Proveniers… - Trends in plant …, 2009 - cell.com
The Arabidopsis thaliana accession Landsberg erecta contains an induced mutation in the
leucine-rich repeat receptor-like Ser/Thr kinase gene ERECTA. Landsberg erecta is …

Natural allelic variation at seed size loci in relation to other life history traits of Arabidopsis thaliana

C Alonso-Blanco… - Proceedings of the …, 1999 - National Acad Sciences
We have analyzed two Arabidopsis strains differing in the mean seed size and seed number
they produced. The accession Cape Verde Islands (Cvi) yielded on average about 40 …

Dominant-negative receptor uncovers redundancy in the Arabidopsis ERECTA leucine-rich repeat receptor–like kinase signaling pathway that regulates organ shape

ED Shpak, MB Lakeman, KU Torii - The Plant Cell, 2003 - academic.oup.com
Arabidopsis ERECTA, a Leu-rich repeat receptor-like Ser/Thr kinase (LRR-RLK), regulates
organ shape and inflorescence architecture. Here, we show that a truncated ERECTA …

Interaction of auxin and ERECTA in elaborating Arabidopsis inflorescence architecture revealed by the activation tagging of a new member of the YUCCA family …

C Woodward, SM Bemis, EJ Hill, S Sawa… - Plant …, 2005 - academic.oup.com
The aboveground body of higher plants has a modular structure of repeating units, or
phytomers. As such, the position, size, and shape of the individual phytomer dictate the plant …

Genome-wide association mapping of growth dynamics detects time-specific and general quantitative trait loci

JA Bac-Molenaar, D Vreugdenhil… - Journal of …, 2015 - academic.oup.com
Growth is a complex trait determined by the interplay between many genes, some of which
play a role at a specific moment during development whereas others play a more general …

Inflorescence and bunch architecture development in Vitis vinifera L.

YN Shavrukov, IB Dry… - Australian journal of grape …, 2004 - Wiley Online Library
Inflorescence development from budburst to harvest was analysed in four cultivars of
grapevine. Two cultivars with tight or compact bunches (Riesling, Chardonnay) and two with …

CRM1/BIG-mediated auxin action regulates Arabidopsis inflorescence development

N Yamaguchi, M Suzuki, H Fukaki… - Plant and cell …, 2007 - academic.oup.com
The shape of the inflorescence in Arabidopsis thaliana ecotype Columbia is a raceme with
individual flowers developing acropetally. The ecotype Landsberg harboring the erecta (er) …

LEAFY controls Arabidopsis pedicel length and orientation by affecting adaxial–abaxial cell fate

N Yamaguchi, A Yamaguchi, M Abe… - The Plant …, 2012 - Wiley Online Library
Pedicel length and orientation (angle) contribute to the diversity of inflorescence
architecture, and are important for optimal positioning of the flowers. However, relatively little …

The role of CORYMBOSA1/BIG and auxin in the growth of Arabidopsis pedicel and internode

N Yamaguchi, Y Komeda - Plant Science, 2013 - Elsevier
The developmental regulation of pedicel and internode ensures that plants of the same
species have similar inflorescence architecture. In Arabidopsis, the elongation of pedicels …