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Anne Galinier

Researcher at Paul Sabatier University

Publications -  102
Citations -  5590

Anne Galinier is an academic researcher from Paul Sabatier University. The author has contributed to research in topics: Catabolite repression & Bacillus subtilis. The author has an hindex of 42, co-authored 95 publications receiving 5222 citations. Previous affiliations of Anne Galinier include University of Lyon & Centre national de la recherche scientifique.

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Physiological diversity of mitochondrial oxidative phosphorylation

TL;DR: The study demonstrates that, in tissues, oxidative phosphorylation capacity is highly variable and diverse, as determined by different combinations of 1) the mitochondrial content, 2) the amount of respiratory chain complexes, and 3) their intrinsic activity.
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The Bacillus subtilis crh gene encodes a HPr-like protein involved in carbon catabolite repression

TL;DR: The results suggest that CCR of certain catabolic operons requires, in addition to CcpA, ATP-dependent phosphorylation of Crh, and HPr at Ser-46, as well as the discovery of a new B. subtilis gene encoding a HPr-like protein, Crh (for catabolite repression HPr).
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Adipose tissues as an ancestral immune organ: site-specific change in obesity.

TL;DR: Cytofluorometric analysis reveals the presence of significant levels of lymphocytes in the stroma‐vascular fraction of white adipose tissues, supporting the notion that adipose tissue may elaborate immunological mechanisms to regulate its functions which might be altered in obesity.
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Specific recognition of the Bacillus subtilis gnt cis‐acting catabolite‐responsive element by a protein complex formed between CcpA and seryl‐phosphorylated HPr

TL;DR: A molecular mechanism underlying catabolite repression in B. subtilis mediated by CcpA and P‐ser‐HPr is proposed and specific protection of the gnt CRE against DNase I digestion is confirmed.
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Browning of White Adipose Cells by Intermediate Metabolites:An Adaptive Mechanism to Alleviate Redox Pressure

TL;DR: It is demonstrated that lactate, an important metabolic intermediate, induces browning of murine white adipose cells with expression of functional UCP1, and that the lactate effect on Ucp1 is mediated by intracellular redox modifications as a result of lactate transport through monocarboxylate transporters.