Functional characterisation of Arabidopsis SPL7 conserved protein domains suggests novel regulatory mechanisms in the Cu deficiency response

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1471-2229

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Functional characterisation of Arabidopsis SPL7 conserved protein domains suggests novel regulatory mechanisms in the Cu deficiency response ; volume:14 ; number:1 ; day:30 ; month:8 ; year:2014 ; pages:1-14 ; date:12.2014
BMC plant biology ; 14, Heft 1 (30.8.2014), 1-14, 12.2014

Creator: Garcia-Molina, Antoni

Contributor: Xing, Shuping
Huijser, Peter
SpringerLink (Online service)

DOI: 10.1186/s12870-014-0231-5

URN: urn:nbn:de:1111-2016041427505

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:53 AM CEST

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Garcia-Molina, Antoni
Xing, Shuping
Huijser, Peter
SpringerLink (Online service)

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Functional characterisation of Arabidopsis SPL7 conserved protein domains suggests novel regulatory mechanisms in the Cu deficiency response

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Other Objects (12)

NovelFam3000 – Uncharacterized human protein domains conserved across model organisms

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Multiple conserved regulatory domains promote Fezf2 expression in the developing cerebral cortex

Ancient conserved domains shared by animal soluble guanylyl cyclases and bacterial signaling proteins

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Molecular characterisation of dominant repressors of the cytokinin deficiency syndrome

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Single-cell sequencing suggests a conserved function of Hedgehog-signalling in spider eye development

Neurolysosomal pathology in human prosaposin deficiency suggests essential neurotrophic function of prosaposin

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Ancient conserved domains shared by animal soluble guanylyl cyclases and bacterial signaling proteins

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Molecular characterisation of dominant repressors of the cytokinin deficiency syndrome

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Exploratory visual analysis of conserved domains on multiple sequence alignments

Single-cell sequencing suggests a conserved function of Hedgehog-signalling in spider eye development

Neurolysosomal pathology in human prosaposin deficiency suggests essential neurotrophic function of prosaposin

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Evolutionary stability of topologically associating domains is associated with conserved gene regulation

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