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very low expression level
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of germinated seeds
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of germinated seeds
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of germinated seeds
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of germinated seeds
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source for mRNA isolation
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of germinated seeds
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NXG1 is exclusively expressed in cotyledons
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XET1 is highly expressed in young epicotyls
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eXET, in epicotyls and other growing regions
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isozyme eXET
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low expression level
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very low expression level
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high expression level of FvXTH6
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high expression level of FvXTH9
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C0IRH4, C0IRH6, C0IRH7, C0IRH8, C0IRH9, C0IRI0, C0IRI1, C0IRI2, C0IRI3, C0IRI4, Q8GTJ0 -
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ripe fruit
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core tissue of ripe kiwifruit
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ripe fruit
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ripe fruit
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ripe fruit
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ripe fruit
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isozyme DkXTH2 reaches maximum expression concomitance with pronounced fruit softening
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isozyme DkXTH3 reaches maximum expression concomitance with pronounced fruit softening
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isozyme expression level during softening for 18-24 d using quantitative real-time PCR analysis. Isozymes DKXTH1 and DKXTH2 in untreated fruit have different expression patterns during fruit softening, in which maximum expression occurs on days 3 and 12 of ripening, respectively. 1-Methylcyclopropene (1-MCP) and gibberellic acid (GA3) treatments delay the softening and ethylene peak of persimmon fruit, as well as suppress the expression of both XTH genes, especially gene DKXTH1
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isozyme expression level during softening for 18-24 d using quantitative realtime PCR analysis. Isozymes DKXTH1 and DKXTH2 in untreated fruit have different expression patterns during fruit softening, in which maximum expression occurs on days 3 and 12 of ripening, respectively. 1-Methylcyclopropene (1-MCP) and gibberellic acid (GA3) treatments delay the softening and ethylene peak of persimmon fruit, as well as suppress the expression of both XTH genes, especially gene DKXTH1
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the expression of isozyme DkXTH1 is very high in immature growing fruit and peaks before the mature stage
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the expression of isozyme DkXTH4 is very high in immature growing fruit and peaks before the mature stage
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the expression of isozyme DkXTH5 is very high in immature growing fruit and peaks before the mature stage
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expression analysis of isozymes DkXTH1-5 during Fuping Jianshi fruit development, expression patterns, overview
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low expression level in young fruits, very low expression level in ripe fruits
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lower expression level in young fruits, moderate to high expression level in ripe fruits
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ripe fruits, mainly
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-
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FvXTH9 is highly expressed in fully developed green fruit, whereas its expression level dropped in later stages
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the expression pattern of FvXTH6 during fruit development shows the highest level in fully developed green fruit and with a clear decline in later stages
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C0IRH4, C0IRH6, C0IRH7, C0IRH8, C0IRH9, C0IRI0, C0IRI1, C0IRI2, C0IRI3, C0IRI4, Q8GTJ0 ripe fruit
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C0IRH4, C0IRH6, C0IRH7, C0IRH8, C0IRH9, C0IRI0, C0IRI1, C0IRI2, C0IRI3, C0IRI4, Q8GTJ0 expression levels of isozymes, overview
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Piper sp.
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Q40144, Q43527, Q43528, Q6RHX7, Q6RHX8, Q6RHX9, Q6RHY0, Q6RHY1, Q9FR51, Q9FZ05, Q9SLN9 -
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tXET-B1 is most abundant in pink fruit pericarp
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etiolated
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LeEXT gene is expressed in outer cell layers of the hypocotyl, after auxin treatment overlapping spatial distribution in the epidermis and outer cortical cell layers
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internodes I, II, III and V, numbered from the cotyledonary node
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highest expression of Ac(MD2)2XTH13
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bases
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very low expression level
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high expression level in young leaves, very high in older leaves
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very high expression level in young leaves, low in older leaves
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highest in green immature leaves as compared to maature leaves and brown, over-wintered leaves
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FvXTH6 is expressed at a relatively high level in young leaf tissue but at a low level in old leaf tissue
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Lactuca sativa ssp. capitata
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C0IRH4, C0IRH6, C0IRH7, C0IRH8, C0IRH9, C0IRI0, C0IRI1, C0IRI2, C0IRI3, C0IRI4, Q8GTJ0 -
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source leaf, levels of NtXET-1 mRNA decreases in midribs with increasing age of leaves
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leaves from 5-day seedlings
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highest level of transcripts of PtrXTH1 is detected in young, intensively growing leaves
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PttXET16A is expressed transiently in developing leaves
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XET1 is expressed in young and mature leaves at lower levels than in young epicotyls and roots, 7fold higher expression in young leaves than in mature ones
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DcXTH2 transcript is detected in large quantities in petals as compared with other tissues
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DcXTH3 transcript is detected in large quantities in petals as compared with other tissues
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DcXTH3 transcript is detected in large quantities in petals as compared with other tissues
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DcXTH2 transcript is detected in large quantities in petals as compared with other tissues
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Apium sp.
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activity is very pronounced in the vicinity of the vascular bundles
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Apium sp.
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young petioles, high activity in thick-walled collenchyma cells
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XET activity in xylem and phloem fibers at the stage of secondary wall formation, PttXET16A
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Adiantum capillus-veneri
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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Aloe sp.
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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highest expression of Ac(MD2)XTH18
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Anthurium upalaense
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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XET activity in the initiating root hairs
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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XET activity in the root cell elongation zone
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isozymes XTH14 and XTH26 are predominantly root-specific
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five predominantly root-expressed Arabidopsis thaliana XTHs belong to subgroup I/II, AtXTH12 is trichoblast-enriched
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five predominantly root-expressed Arabidopsis thaliana XTHs belong to subgroup I/II, AtXTH13 is trichoblast-enriched
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five predominantly root-expressed Arabidopsis thaliana XTHs belong to subgroup I/II, AtXTH17 is expressed in all cell types in the elongating and differentiating regions of the root
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five predominantly root-expressed Arabidopsis thaliana XTHs belong to subgroup I/II, AtXTH18 is expressed in all cell types in the elongating and differentiating regions of the root
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five predominantly root-expressed Arabidopsis thaliana XTHs belong to subgroup I/II, AtXTH19 is expressed in nearly all cell types in the root
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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Azolla sp.
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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Chamaecyparis sp.
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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Commelina nilagirica
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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C0IRH4, C0IRH6, C0IRH7, C0IRH8, C0IRH9, C0IRI0, C0IRI1, C0IRI2, C0IRI3, C0IRI4, Q8GTJ0 -
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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XET activity in the root cell elongation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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Pitcairnia imbricata
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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PttXET16A expression in young roots and root tips
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Pothomorphe petalta
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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Selaginella sp.
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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Tragopodon pratensis
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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XET1 is highly expressed in young roots
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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high XET activity in the epidermis cell wall of the elongation zone and in trichoblasts in the differentation zone
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elongation zone of the maize root
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comparisons of mRNA populations of Arabidopsis root hair cells and cells of an Arabidopsis root hair mutant show AtXTH12 to be 4fold upregulated in root hair cells
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cotyledons of germinated seeds
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cotyledons of germinated seeds
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cotyledons of germinated seeds
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accumulation of XET/H transcripts during seed germination, increased expression of PhXET influences seed germination in Podophyllum, expression analysis, overview
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cotyledons of germinated seeds
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germinated
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cotyledons of germinated seeds
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sXET, expressed during germination
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expression of isozyme sXET during germination
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7-8-day etiolated seedlings
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Sinapis sp.
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sprouting seedlings, more abundant in the growing tissues of the hypocotyls and leaves than in the cotyledons
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26 days old
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MXE, EC 2.4.1., and XET, actions are both detectable in living Equisetum fluviatile shoots, the MXE:XET ratio increasing with age
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etiolated shoots
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first year stem
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peduncle
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very low expression level
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lower expression level
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mature
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etiolated stem, activity is positively correlated with growth rate in different zones of pea stem
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etiolated 7-day stems
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tXET-B1 is detected in stems
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peduncle
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XET1 is expressed at lower levels in stems than in young epicotyls and roots
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XET activity in xylem and phloem fibers at the stage of secondary wall formation, PttXET16A
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developing, at least 16 Populus XTH genes are expressed in developing wood. Five genes are highly and ubiquitously expressed, whereas PtxtXET16-34 is expressed more weakly but specifically in developing wood
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primary- and secondary-walled xylem tissues
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additional information
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Ac(MD2)XTH15 shows the highest relative expression level in the green leaf tip, sequentially in the root, and finally in the white leaf base
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additional information
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XETs accumulates in expanding cells, at the sites of intercellular airspace, formation, and at the bases of leaves, cotyledons and hypocotyls, detailed localization
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additional information
isozyme XTH15 is predominantly expressed in early-stage organs
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additional information
isozyme XTH15 is predominantly expressed in early-stage organs
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additional information
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isozyme XTH15 is predominantly expressed in early-stage organs
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additional information
isozyme XTH31 is predominantly expressed in early-stage organs
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additional information
isozyme XTH31 is predominantly expressed in early-stage organs
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additional information
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isozyme XTH31 is predominantly expressed in early-stage organs
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additional information
enzyme XTH15 is strongly expressed in young, rapidly growing organs, but particularly in 24-h imbibed seeds, the seedling hypocotyl and root, and early-stage flowers (especially in the carpels)
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additional information
enzyme XTH15 is strongly expressed in young, rapidly growing organs, but particularly in 24-h imbibed seeds, the seedling hypocotyl and root, and early-stage flowers (especially in the carpels)
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additional information
enzyme XTH31 is strongly expressed in young, rapidly growing organs
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additional information
enzyme XTH31 is strongly expressed in young, rapidly growing organs
brenda
additional information
XTH30 is highly expressed in the root, flower, stem, and etiolated hypocotyl. XTH30 accumulates at high levels in root, stem, and flower but at low levels in rosette leaves and cauline leaves, real-time PCR enzyme expression analysis, expression pattern, overview
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additional information
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XTH30 is highly expressed in the root, flower, stem, and etiolated hypocotyl. XTH30 accumulates at high levels in root, stem, and flower but at low levels in rosette leaves and cauline leaves, real-time PCR enzyme expression analysis, expression pattern, overview
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additional information
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XTH30 is highly expressed in the root, flower, stem, and etiolated hypocotyl. XTH30 accumulates at high levels in root, stem, and flower but at low levels in rosette leaves and cauline leaves, real-time PCR enzyme expression analysis, expression pattern, overview
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additional information
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the level of xyloglucan endotransglucosylation (XET) activity peaks at the penetrating stage of Cuscuta reflexa on its host Pelargonium zonale
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additional information
transcript levels of XTH genes are regulaated in floral and vegetative tissues of carnation plants with opening flowers, quantitative tissse expression analysis by real-time RT-PCR
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additional information
transcript levels of XTH genes are regulaated in floral and vegetative tissues of carnation plants with opening flowers, quantitative tissse expression analysis by real-time RT-PCR
brenda
additional information
transcript levels of XTH genes are regulaated in floral and vegetative tissues of carnation plants with opening flowers, quantitative tissse expression analysis by real-time RT-PCR
brenda
additional information
transcript levels of XTH genes are regulaated in floral and vegetative tissues of carnation plants with opening flowers, quantitative tissse expression analysis by real-time RT-PCR
brenda
additional information
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transcript levels of XTH genes are regulaated in floral and vegetative tissues of carnation plants with opening flowers, quantitative tissse expression analysis by real-time RT-PCR
brenda
additional information
transcript levels of XTH genes are regulated in floral and vegetative tissues of carnation plants with opening flowers, quantitative tissse expression analysis by real-time RT-PCR
brenda
additional information
transcript levels of XTH genes are regulated in floral and vegetative tissues of carnation plants with opening flowers, quantitative tissse expression analysis by real-time RT-PCR
brenda
additional information
transcript levels of XTH genes are regulated in floral and vegetative tissues of carnation plants with opening flowers, quantitative tissse expression analysis by real-time RT-PCR
brenda
additional information
transcript levels of XTH genes are regulated in floral and vegetative tissues of carnation plants with opening flowers, quantitative tissse expression analysis by real-time RT-PCR
brenda
additional information
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transcript levels of XTH genes are regulated in floral and vegetative tissues of carnation plants with opening flowers, quantitative tissse expression analysis by real-time RT-PCR
brenda
additional information
transcript levels of XTH genes are regulated in floral and vegetative tissues of carnation plants with opening flowers, quantitative tissue expression analysis by real-time RT-PCR
brenda
additional information
transcript levels of XTH genes are regulated in floral and vegetative tissues of carnation plants with opening flowers, quantitative tissue expression analysis by real-time RT-PCR
brenda
additional information
transcript levels of XTH genes are regulated in floral and vegetative tissues of carnation plants with opening flowers, quantitative tissue expression analysis by real-time RT-PCR
brenda
additional information
transcript levels of XTH genes are regulated in floral and vegetative tissues of carnation plants with opening flowers, quantitative tissue expression analysis by real-time RT-PCR
brenda
additional information
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transcript levels of XTH genes are regulated in floral and vegetative tissues of carnation plants with opening flowers, quantitative tissue expression analysis by real-time RT-PCR
brenda
additional information
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transcript levels of XTH genes are regulaated in floral and vegetative tissues of carnation plants with opening flowers, quantitative tissse expression analysis by real-time RT-PCR
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brenda
additional information
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transcript levels of XTH genes are regulated in floral and vegetative tissues of carnation plants with opening flowers, quantitative tissse expression analysis by real-time RT-PCR
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brenda
additional information
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transcript levels of XTH genes are regulated in floral and vegetative tissues of carnation plants with opening flowers, quantitative tissue expression analysis by real-time RT-PCR
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brenda
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isozymes DkXTH1, DkXTH4, and DkXTH5 peak in immature expanding fruit, and their higher expression is observed along with higher fruit firmness in cold-treated fruit or firmer cultivar fruit during storage, while isozymes DkXTH2 and DkXTH3, which reach maxima concomitance with pronounced fruit softening, quantitative real-time PCR expression analysis, overview
brenda
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isozymes DkXTH1, DkXTH4, and DkXTH5 peak in immature expanding fruit, and their higher expression is observed along with higher fruit firmness in cold-treated fruit or firmer cultivar fruit during storage, while isozymes DkXTH2 and DkXTH3, which reach maxima concomitance with pronounced fruit softening, quantitative real-time PCR expression analysis, overview
brenda
additional information
isozymes DkXTH1, DkXTH4, and DkXTH5 peak in immature expanding fruit, and their higher expression is observed along with higher fruit firmness in cold-treated fruit or firmer cultivar fruit during storage, while isozymes DkXTH2 and DkXTH3, which reach maxima concomitance with pronounced fruit softening, quantitative real-time PCR expression analysis, overview
brenda
additional information
isozymes DkXTH1, DkXTH4, and DkXTH5 peak in immature expanding fruit, and their higher expression is observed along with higher fruit firmness in cold-treated fruit or firmer cultivar fruit during storage, while isozymes DkXTH2 and DkXTH3, which reach maxima concomitance with pronounced fruit softening, quantitative real-time PCR expression analysis, overview
brenda
additional information
isozymes DkXTH1, DkXTH4, and DkXTH5 peak in immature expanding fruit, and their higher expression is observed along with higher fruit firmness in cold-treated fruit or firmer cultivar fruit during storage, while isozymes DkXTH2 and DkXTH3, which reach maxima concomitance with pronounced fruit softening, quantitative real-time PCR expression analysis, overview
brenda
additional information
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isozymes DkXTH1, DkXTH4, and DkXTH5 peak in immature expanding fruit, and their higher expression is observed along with higher fruit firmness in cold-treated fruit or firmer cultivar fruit during storage, while isozymes DkXTH2 and DkXTH3, which reach maxima concomitance with pronounced fruit softening, quantitative real-time PCR expression analysis, overview
brenda
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transcriptional profiling reveals that DkXTH8 peaks during dramatic fruit softening. Very lo expression levels in flowers, calyces, leaves and stems, respectively
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total extracts of Equisetum arvense organs exhibit XET activity, but vegetative lateral shoot extracts of contain somewhat less XET activity
brenda
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enzyme FcXTH2 shows a high expression level in vegetative tissues and a relatively low but constant expression level in developing fruit
brenda
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enzyme FcXTH2 shows a high expression level in vegetative tissues and a relatively low but constant expression level in developing fruit
brenda
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to confirm the transcriptome data, the expression pattern of FvXTH6 is examined by quantitative real-time PCR in fruit at different ripening stages as well as in leaf and flower tissues. The expression pattern of FvXTH6 during fruit development shows the highest level in fully developed green fruit and with a clear decline in later stages. The absolute expression level of FvXTH6 in fruit is much lower than that of FvXTH9. FvXTH6 is also highly expressed in flowers. FvXTH6 is expressed at relatively high level in young leaf tissue but at low level in old leaf tissue
brenda
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to confirm the transcriptome data, the expression pattern of FvXTH9 is examined by quantitative real-time PCR in fruit at different ripening stages as well as in leaf and flower tissues. FvXTH9 is highly expressed in fully developed green fruit, whereas its expression level dropped in later stages. A high expression level of FvXTH9 is also determined in flowers, whereas its mRNA abundance is very low in all other tissues investigated. The expression pattern of FvXTH6 during fruit development resembled that of FvXTH9. FvXTH9 shows the highest expression level in green receptacles
brenda
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the three GhXTH genes are expressed differently with GhXTH1 predominantly expressed in elongating cotton fibers, overview. Almost no XTH expression in roots
brenda
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the three GhXTH genes are expressed differently with GhXTH1 predominantly expressed in elongating cotton fibers, overview. Almost no XTH expression in roots
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brenda
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expression profiles based on the barley genome database show that HvXTH family members display different expression patterns in different tissues and at different stages. Transcript levels of HvXTH isozymes in different tissues, overview
brenda
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tissue-specific NtXET-1 expression pattern, highest mRNA levels in organs highly enriched in vascular tissues
brenda
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tissue-specific NtXET-1 expression pattern, highest mRNA levels in organs highly enriched in vascular tissues
brenda
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tissue-specific and growth stage-dependent isozyme expression patterns, negligible expression in shoot, overview
brenda
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tissue-specific and growth stage-dependent isozyme expression patterns, negligible expression in shoot, overview
brenda
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Q5Z6H1
tissue-specific and growth stage-dependent isozyme expression patterns, negligible expression in shoot, overview
brenda
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tissue-specific and growth stage-dependent isozyme expression patterns, negligible expression in shoot, overview
brenda
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Q6ZAN9
tissue-specific and growth stage-dependent isozyme expression patterns, negligible expression in shoot, overview
brenda
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tissue-specific and growth stage-dependent isozyme expression patterns, negligible expression in shoot, overview
brenda
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tissue-specific and growth stage-dependent isozyme expression patterns, negligible expression in shoot, overview
brenda
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detailed localization of XET in poplar stems, PttXET16A expression pattern, expression in secondary vascular tissues
brenda
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XET1 is not expressed in cotyledons
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isozyme eXET also occurs in other growing regions
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