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Gabriel García Caballero

Researcher at Ludwig Maximilian University of Munich

Publications -  23
Citations -  549

Gabriel García Caballero is an academic researcher from Ludwig Maximilian University of Munich. The author has contributed to research in topics: Galectin & Glycan. The author has an hindex of 12, co-authored 21 publications receiving 459 citations.

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Galectins: their network and roles in immunity/tumor growth control

TL;DR: To delineate the factors that underlie the specificity of a galectin for its counterreceptor(s) in the cellular context and the details of structure–activity relationships by comparatively analyzing natural and rationally engineered proteins is the main challenge for ongoing research.
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Lectins: a primer for histochemists and cell biologists.

TL;DR: The functional pairing with physiological counterreceptors is involved in a wide range of cellular activities from cell adhesion, glycoconjugate trafficking to growth regulation and lets lectins act as sensors/effectors in host defense.
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From glycophenotyping by (plant) lectin histochemistry to defining functionality of glycans by pairing with endogenous lectins

TL;DR: The detection of mammalian (tissue) lectins and the emerging evidence for intimate molecular recognition between this class of receptors and their (glycoconjugate) counterreceptors substantiate that understanding the rules of the sugar code is presently a major challenge.
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How galectins have become multifunctional proteins.

TL;DR: The generation of a network of (GA)lectins by evolutionary diversification affords the opportunity for additive/synergistic or antagonistic interplay in situ, an emerging aspect of (ga)lectin functionality that warrants close scrutiny.
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Network analysis of adhesion/growth-regulatory galectins and their binding sites in adult chicken retina and choroid

TL;DR: The highly ordered multilayered organization of the adult chicken retina is a suitable test model for examining zonal distribution of the members of a bioeffector family and the results underline the requirement for network analysis for these proteins that can functionally interact in additive or antagonistic modes.