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Georg J. Arnold

Researcher at Ludwig Maximilian University of Munich

Publications -  94
Citations -  3820

Georg J. Arnold is an academic researcher from Ludwig Maximilian University of Munich. The author has contributed to research in topics: Proteome & Rainbow trout. The author has an hindex of 30, co-authored 93 publications receiving 3294 citations.

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The ecoresponsive genome of Daphnia pulex

John K. Colbourne, +85 more
- 04 Feb 2011 - 
TL;DR: The Daphnia genome reveals a multitude of genes and shows adaptation through gene family expansions, and the coexpansion of gene families interacting within metabolic pathways suggests that the maintenance of duplicated genes is not random.
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Human CLP36, a PDZ-domain and LIM-domain protein, binds to α-actinin-1 and associates with actin filaments and stress fibers in activated platelets and endothelial cells

TL;DR: The study shows that CLP36 associates with actin filaments and stress fibers that are formed during shape change and spreading of platelets and during migration and contraction of endothelial cells, and suggests that this association might modulate the function of alpha-actinin-1.
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Dual specificities of the glyoxysomal/peroxisomal processing protease Deg15 in higher plants.

TL;DR: A knockout mutation in the DEG15 gene of Arabidopsis prevents processing of the glyoxysomal malate dehydrogenase precursor to the mature form, and the GPP/Deg15 possesses specific characteristics and is therefore a new subgroup within the Deg proteases.
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Assessing quantitative post-mortem changes in the gray matter of the human frontal cortex proteome by 2-D DIGE.

TL;DR: Proteins vulnerable to PMI were analyzed by the 2‐D DIGE analysis of cortex samples from three donors, and were derived from a variety of functional groups, including metabolic, structural, stress response, antioxidants, synaptosomal, and neuronal proteins.
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Invasion of tumorigenic HT1080 cells is impeded by blocking or downregulating the 37-kDa/67-kDa laminin receptor.

TL;DR: In vitro data suggest that reagents directed against LRP/LR or LRP mRNA such as antibodies, polysulfated glycans, or small interfering RNAs, previously shown to encompass an anti-prion activity by blocking or downregulating the prion receptor L RP/LR, might also be potential cancer therapeutics blocking metastasis by interfering with the LRP-laminin interaction in neoplastic tissues.