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Guido Kroemer

Researcher at Institut Gustave Roussy

Publications -  1546
Citations -  294816

Guido Kroemer is an academic researcher from Institut Gustave Roussy. The author has contributed to research in topics: Programmed cell death & Apoptosis. The author has an hindex of 236, co-authored 1404 publications receiving 246571 citations. Previous affiliations of Guido Kroemer include Karolinska Institutet & Spanish National Research Council.

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Nervous yeast: modeling neurotoxic cell death

TL;DR: Yeast models for several major classes of neurodegeneration, namely alpha-synucleinopathy, polyglutamine disorders, beta-amyloid diseases, tauopathies, and TDP-43 proteinopathies have been established, pointing to ways in which yeast might advance the mechanistic dissection of cell death pathways relevant for human neurodegenersation.
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ATG4B/autophagin-1 regulates intestinal homeostasis and protects mice from experimental colitis.

TL;DR: It is proposed that atg4b-null mice are a suitable model for in vivo studies aimed at testing new therapeutic strategies for intestinal diseases associated with autophagy deficiency and described ATG4B as a novel protective protein in inflammatory colitis.
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Acyl-CoA-Binding Protein Is a Lipogenic Factor that Triggers Food Intake and Obesity.

TL;DR: neutralization of ACBP enhanced autophagy, stimulated fatty acid oxidation, inhibited appetite, reduced weight gain in the context of a high-fat diet or leptin deficiency, and accelerated weight loss in response to dietary changes.
Book ChapterDOI

Molecular and Cellular Mechanisms of T Lymphocyte Apoptosis

TL;DR: This chapter focuses on the genetic and molecular mechanisms of T lymphocyte apoptosis and also deals with the various phases of apoptosis initiation, execution, and degradation of lymphocytes.
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Immunohistochemical detection of cytoplasmic LC3 puncta in human cancer specimens

TL;DR: A validated immunohistochemical protocol for the detection of LC3 puncta in human formalin-fixed, paraffin-embedded cancer specimens that can also be applied to mouse tissues is described and it is surmised that this technique can be employed for retrospective or prospective studies involving large series of human tumor samples.