Polarized cell growth in higher plants.

By P. K. Hepler, L. Vidali, A. Cheung. Annual Review of Cell and Developmental Biology, 2001

781 citations recorded by the source corpus.

Subfields: Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/580f46bd6e608011b8bccce390f8db64d09e7eac

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Citations in the corpus

Report Shape and Dynamics of Tip-Growing Cells (2009, positive): “Far away from the apex, in the cylindrical part of the cell, there is no material addition (g = 0) [3, 17, 18], so that the net flux of cell wall material is a constant J0 (Equation 4; Figure 2).”
REVIEW: PART OF A SPECIAL ISSUE ON SEXUAL PLANT REPRODUCTION Pollen tube growth and guidance: roles of small, secreted proteins (2011, background): “Activated calcium channels trigger calcium influx through the plasma membrane of the growing pollen tube tip (Hepler et al., 2001), which results in a tip-focused intracellular calcium gradient for directional pollen tube growth (Malho et al., 2000).”
Proteome profile and functional classification of proteins in Arabidopsis thaliana (Landsberg erecta) mature pollen (2006, background): “Profilin is a key actin-binding protein involved in pollen tube growth (Hepler et al. 2001) and its presence has also been reported in mature Arabidopsis (Columbia ecotype) (Holmes-Davis et al. 2005; Noir et al. 2005) and rice pollen (Dai et al. 2006).”
CDPKs CPK6 and CPK3 Function in ABA Regulation of Guard Cell S-Type Anion- and Ca2+- Permeable Channels and Stomatal Closure (2006, background): “In summary, the lack of R-type anion channel activity alteration and the residual S-type anion current in cpk3cpk6 mutant guard cells (Figures 2, 3, and 8) correlate with the partial ABA- and Ca2þ-induced stomatal closing responses found here (Figures 6, 7, and 9) and may also reflect a contribution”
Mechanical Principles Governing Pollen Tube Growth (2007, background): “While the principal source of Ca seems to be extracellular, Ca release from internal stores, conceivably from vesicles or ER located in the apical region, is likely to contribute (Kost et al. 1999; Hepler et al. 2001).”
Calcium Signals: The Lead Currency of Plant Information Processing (2010, background): “In pollen tubes, [Ca2+]cyt is highly concentrated at the apex by an extracellular influx (Sanders et al., 1999; Hepler et al., 2001).”
The Physiology of Potassium in Crop Production (2014, background): “Potassium is essential for cell growth, a vital process for adequate plant functioning and development (Marschner, 1995; Hepler et al., 2001).”
Calcium Signaling through Protein Kinases. The Arabidopsis Calcium-Dependent Protein Kinase Gene Family1 (2002, background): “A wide variety of growth and developmental processes in plants are regulated by Ca2 fluxes (Evans et al., 2001; Hepler et al., 2001).”
Infection and Invasion of Roots by Symbiotic, Nitrogen-Fixing Rhizobia during Nodulation of Temperate Legumes (2004, background): “This pattern, most obvious in pollen tubes, is referred to as reverse fountain streaming (75, 83).”
Comprehending crystalline β-carotene accumulation by comparing engineered cell models and the natural carotenoid-rich system of citrus (2011, neutral): “The transcript abundance was normalized against peanut Ubiquitin (Luo et al. , 2005) transcript levels.”
The local cytomechanical properties of growing pollen tubes correspond to the axial distribution of structural cellular elements (2004, background): “Numerous cellular processes, such as ion fluxes and exocytosis, are known to be essential for this process (Hepler et al. 2001; Holdaway-Clarke and Hepler 2003), but the physical constraints that control this particular cellular morphogenesis are still largely unknown.”