V. Hindié

发表

Structure and allosteric effects of low-molecular-weight activators on the protein kinase PDK1.

D. Hirschberg, P. Alzari, R. Biondi, 2009, Nature chemical biology.

Allosteric activation of the protein kinase PDK1 with low molecular weight compounds

Stefan Zeuzem, Albrecht Piiper, R. Hartmann, 2006, The EMBO journal.

Structural insights into the functional versatility of an FHA domain protein in mycobacterial signaling

P. Alzari, B. Raynal, H. O’Hare, 2019, Science Signaling.

GmZPR3d Interacts with GmHD-ZIP III Proteins and Regulates Soybean Root and Nodule Vascular Development

Juan Xie, Q. Ma, V. Hindié, 2019, International journal of molecular sciences.

Chr21 protein–protein interactions: enrichment in proteins involved in intellectual disability, autism, and late-onset Alzheimer’s disease

Y. Hérault, R. Huganir, J. Rain, 2022, Life Science Alliance.

Supplemental Information Bidirectional Allosteric Communication between the ATP-Binding Site and the Regulatory PIF Pocket in PDK 1 Protein Kinase

F. Gervasio, G. Saladino, P. Alzari, 2016 .

HENA, heterogeneous network-based data set for Alzheimer’s disease

Hedi Peterson, Henning Hermjakob, Tal Pupko, 2019, Scientific Data.

3,5-Diphenylpent-2-enoic acids as allosteric activators of the protein kinase PDK1: structure-activity relationships and thermodynamic characterization of binding as paradigms for PIF-binding pocket-targeting compounds.

R. Hartmann, R. Biondi, V. Hindié, 2009, Journal of medicinal chemistry.

Tissue‐specific and inducible Cre‐mediated recombination in the gut epithelium

Daniel Metzger, Pierre Chambon, P. Chambon, 2004, Genesis.

Discovery of a putative blood-based protein signature associated with response to ALK tyrosine kinase inhibition

Yannick-André Breton, C. Couture, G. Batist, 2020, Clinical Proteomics.

Chr21 protein-protein interactions: enrichment in products involved in intellectual disabilities, autism and Late Onset Alzheimer Disease

Y. Hérault, R. Huganir, J. Rain, 2019, bioRxiv.

Use of a fluorescent ATP analog to probe the allosteric conformational change in the active site of the protein kinase PDK1.

R. Biondi, V. Hindié, Laura A. Lopez-Garcia, 2012, Methods in molecular biology.

Allosteric regulation of protein kinase PKCζ by the N-terminal C1 domain and small compounds to the PIF-pocket.

P. Alzari, R. Biondi, S. Zeuzem, 2011, Chemistry & biology.

Plasma DYRK1A as a novel risk factor for Alzheimer's disease

B. Dubois, J. Rain, M. Sarazin, 2014, Translational Psychiatry.

HENA, heterogeneous network-based data set for Alzheimer’s disease

Y. Hérault, J. Vilo, I. Xenarios, 2019, Scientific Data.

LPS-Induced Inflammation Abolishes the Effect of DYRK1A on IkB Stability in the Brain of Mice

J. Rain, J. Delabar, N. Janel, 2018, Molecular Neurobiology.

BIN1 genetic risk factor for Alzheimer is sufficient to induce early structural tract alterations in entorhinal cortex-dentate gyrus pathway and related hippocampal multi-scale impairments

Y. Hérault, P. Dutar, D. Le Bihan, 2018, bioRxiv.

Discovery of a putative blood-based protein signature associated with response to ALK tyrosine kinase inhibition

Yannick-André Breton, C. Couture, G. Batist, 2020, Clinical Proteomics.

Plasma DYRK 1 A as a novel risk factor for Alzheimer ’ s disease

B. Dubois, J. Rain, M. Sarazin, 2018 .

Bidirectional Allosteric Communication between the ATP-Binding Site and the Regulatory PIF Pocket in PDK1 Protein Kinase.

F. Gervasio, G. Saladino, P. Alzari, 2016, Cell chemical biology.

LPS-Induced Inflammation Abolishes the Effect of DYRK1A on IkB Stability in the Brain of Mice

J. Rain, J. Delabar, N. Janel, 2018, Molecular Neurobiology.