<style face="normal" font="default" size="100%">The Cd(II)-binding abilities of recombinant Quercus suber metallothionein: bridging the gap between phytochelatins and metallothioneins.</style>

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<style face="normal" font="default" size="100%">The Cd(II)-binding abilities of recombinant Quercus suber metallothionein: bridging the gap between phytochelatins and metallothioneins.</style>

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17

<style face="normal" font="default" size="100%">The Cd(II)-binding abilities of recombinant Quercus suber metallothionein: bridging the gap between phytochelatins and metallothioneins.</style>

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17

<style face="normal" font="default" size="100%">Plant metallothionein domains: functional insight into physiological metal binding and protein folding</style>

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<style face="normal" font="default" size="100%">Plant metallothionein domains: functional insight into physiological metal binding and protein folding</style>

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<style face="normal" font="default" size="100%">Influence of weather on cork-ring width</style>

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<style face="normal" font="default" size="100%">Influence of weather on cork-ring width</style>

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<style face="normal" font="default" size="100%">Developmental anatomy and apical organization of the primary root of cork oak (Quercus auber L.</style>

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<style face="normal" font="default" size="100%">Stress proteins co-expressed in suberized and lignified cells and in apical meristems</style>

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<style face="normal" font="default" size="100%">Development and ultrastructure of the endodermis in the primary root of cork oak (Quercus suber)</style>