H. Moine

发表

Messenger RNA structure and gene regulation at the translational level in Escherichia coli: the case of threonine:tRNAThr ligase.

M. Grunberg‐Manago, J. Ebel, C. Ehresmann, 1988, Proceedings of the National Academy of Sciences of the United States of America.

A Single Internal Ribosome Entry Site Containing a G Quartet RNA Structure Drives Fibroblast Growth Factor 2 Gene Expression at Four Alternative Translation Initiation Codons*

L. Créancier, A. Prats, S. Bonnal, 2003, Journal of Biological Chemistry.

Fragile X syndrome

Heather Cody Hazlett, Nahum Sonenberg, Ilse Gantois, 2017, Nature Reviews Disease Primers.

A Novel Role for the RNA–Binding Protein FXR1P in Myoblasts Cell-Cycle Progression by Modulating p21/Cdkn1a/Cip1/Waf1 mRNA Stability

L. Davidovic, B. Bardoni, P. Barbry, 2013, PLoS genetics.

Escherichia coli threonyl-tRNA synthetase and tRNA(Thr) modulate the binding of the ribosome to the translational initiation site of the thrS mRNA.

M. Grunberg‐Manago, J. Ebel, C. Ehresmann, 1990, Journal of molecular biology.

Internal Ribosome Entry Site Structural Motifs Conserved among Mammalian Fibroblast Growth Factor 1 Alternatively Spliced mRNAs

A. Prats, H. Prats, O. Danos, 2004, Molecular and Cellular Biology.

AAV‐delivered diacylglycerol kinase DGKk achieves long‐term rescue of fragile X syndrome mouse model

J. Mandel, D. Dembélé, R. Laufer, 2022, EMBO molecular medicine.

Ultrastructural analysis of the functional domains in FMRP using primary hippocampal mouse neurons

D. Nelson, B. Oostra, R. Willemsen, 2009, Neurobiology of Disease.

Structure of 4.5S RNA in the signal recognition particle of Escherichia coli as studied by enzymatic and chemical probing.

W. Wintermeyer, C. Ehresmann, B. Ehresmann, 1996, RNA.

Probing RNA Structure and Function in Solution

C. Ehresmann, P. Romby, B. Ehresmann, 1998 .

Detailed analysis of RNA-protein interactions within the ribosomal protein S8-rRNA complex from the archaeon Methanococcus jannaschii.

C. Ehresmann, P. Dumas, S. Tishchenko, 2001, Journal of molecular biology.

The RNA binding site of S8 ribosomal protein of Escherichia coli: Selex and hydroxyl radical probing studies.

E. Westhof, C. Ehresmann, B. Ehresmann, 1997, RNA.

Large-scale neuroanatomical study uncovers 198 gene associations in mouse brain morphogenesis

Jacqueline K. White, A. Reymond, C. Webber, 2019, Nature Communications.

AAV-delivery of diacylglycerol kinase kappa achieves long-term rescue of Fmr1-KO mouse model deficits of fragile X syndrome

J. Mandel, D. Dembélé, R. Laufer, 2021, bioRxiv.

Phosphatidic Acid: From Pleiotropic Functions to Neuronal Pathology

Emeline Tanguy, Qili Wang, N. Vitale, 2019, Front. Cell. Neurosci..

A Novel Function for Fragile X Mental Retardation Protein in Translational Activation

É. Khandjian, E. Bechara, L. Davidovic, 2009, PLoS biology.

Translational regulation of the Escherichia coli threonyl-tRNA synthetase gene: structural and functional importance of the thrS operator domains.

M. Grunberg‐Manago, C. Ehresmann, P. Romby, 1993, Biochimie.

Domains of the Escherichia coli threonyl-tRNA synthetase translational operator and their relation to threonine tRNA isoacceptors.

M. Grunberg‐Manago, C. Ehresmann, P. Romby, 1992, Journal of Molecular Biology.

Sequestration of DROSHA and DGCR8 by expanded CGG RNA repeats alters microRNA processing in fragile X-associated tremor/ataxia syndrome.

Peter K. Todd, M. Disney, P. Hagerman, 2013, Cell reports.

Internal Ribosome Entry Site Structural Motifs Conserved among Mammalian Fibroblast Growth Factor 1 Alternatively Spliced mRNAs

A. Prats, H. Prats, O. Danos, 2004, Molecular and Cellular Biology.

The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif

C. Ehresmann, J. Mandel, B. Bardoni, 2001, The EMBO journal.

The G-quartet containing FMRP binding site in FMR1 mRNA is a potent exonic splicing enhancer

J. Mandel, M. Subramanian, H. Moine, 2008, Nucleic acids research.

G‐quadruplexes in RNA biology

H. Moine, S. Vagner, S. Millevoi, 2012, Wiley interdisciplinary reviews. RNA.

G–quadruplex RNA structure as a signal for neurite mRNA targeting

J. Mandel, M. Subramanian, H. Moine, 2011, EMBO reports.

Spatial control of nucleoporin condensation by fragile X‐related proteins

I. Sumara, L. Pacini, J. Mandel, 2020, The EMBO journal.

Spatial control of nucleoporin assembly by Fragile X-related proteins

I. Sumara, L. Pacini, J. Mandel, 2019 .

The FMRP/GRK4 mRNA interaction uncovers a new mode of binding of the Fragile X mental retardation protein in cerebellum

E. Bechara, L. Davidovic, Mireille Melko, 2015, Nucleic acids research.

Cells lacking the fragile X mental retardation protein (FMRP) have normal RISC activity but exhibit altered stress granule assembly.

J. Mandel, M. Subramanian, H. Moine, 2009, Molecular biology of the cell.

The RNA binding protein FMRP: new connections and missing links

C. Ehresmann, B. Ehresmann, H. Moine, 2003, Biology of the cell.

FMRP interferes with the Rac1 pathway and controls actin cytoskeleton dynamics in murine fibroblasts.

J. Mandel, E. Bechara, B. Bardoni, 2005, Human molecular genetics.

The expression of E.coli threonyl‐tRNA synthetase is regulated at the translational level by symmetrical operator‐repressor interactions.

C. Ehresmann, P. Romby, M. Springer, 1996, The EMBO journal.

In Vitro and in Cellulo Evidences for Association of the Survival of Motor Neuron Complex with the Fragile X Mental Retardation Protein*

H. Moine, C. Branlant, F. Rage, 2008, Journal of Biological Chemistry.

Genetic probes of ribosomal RNA function.

K. Lieberman, H. Moine, M. Firpo, 1995, Biochemistry and cell biology = Biochimie et biologie cellulaire.

In vivo selection of functional ribosomes with variations in the rRNA-binding site of Escherichia coli ribosomal protein S8: evolutionary implications.

C. Ehresmann, B. Ehresmann, C. Squires, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Fragile X Mental Retardation Protein (FMRP) controls diacylglycerol kinase activity in neurons

D. Muller, J. Mandel, B. Bardoni, 2016, Proceedings of the National Academy of Sciences.

Translational Feedback Control in E.Coli : The Role of tRNA Thr and tRNA Thr -Like Structures in the Operator of the Gene for Threonyl-tRNA Synthetase

M. Grunberg‐Manago, J. Ebel, C. Ehresmann, 1990 .

In vivo selection of functional variations in essential sites of ribosomal RNA.

C. Ehresmann, B. Ehresmann, H. Moine, 2001, Methods.

The relation between catalytic activity and gene regulation in the case of E coli threonyl-tRNA synthetase.

M. Grunberg‐Manago, J. Ebel, C. Ehresmann, 1990, Biochimie.

Crosslinking of ribosomal protein S18 to 16 S RNA in E. coli ribosomal 30 S subunits by the use of a reversible crosslinking agent: Trans‐diamminedichloroplatinum(II)

J. Ebel, C. Ehresmann, B. Ehresmann, 1988, FEBS letters.

Cross-linking of initiation factor IF3 to Escherichia coli 30S ribosomal subunit by trans-diamminedichloroplatinum(II): characterization of two cross-linking sites in 16S rRNA; a possible way of functioning for IF3.

M. Grunberg‐Manago, J. Ebel, C. Ehresmann, 1986, Nucleic acids research.

Of local translation control and lipid signaling in neurons.

N. Vitale, H. Moine, 2019, Advances in biological regulation.

The translational regulation of threonyl-tRNA synthetase. Functional relationship between the enzyme, the cognate tRNA and the ribosome.

M. Grunberg‐Manago, J. Ebel, C. Ehresmann, 1990, Biochimica et biophysica acta.

Pioglitazone improves deficits of Fmr1-KO mouse model of Fragile X syndrome by interfering with excessive diacylglycerol signaling

Y. Hérault, J. Mandel, A. Duchon, 2020, bioRxiv.

Translational Control of Gene Expression in E. Coli: The Case of Threonyl-tRNA Synthetase

M. Grunberg‐Manago, J. Ebel, C. Ehresmann, 1989 .

Mutations in helix 34 of Escherichia coli 16 S ribosomal RNA have multiple effects on ribosome function and synthesis.

H. Moine, A. E. Dahlberg, 1994, Journal of molecular biology.

Comparative analysis of PDZ-binding motifs in the diacylglycerol kinase family

G. Travé, G. Gógl, L. Negroni, 2023, bioRxiv.

Fragile X syndrome: Are signaling lipids the missing culprits?

N. Vitale, H. Moine, Ricardos Tabet, 2016, Biochimie.

G–quadruplex RNA structure as a signal for neurite mRNA targeting

J. Mandel, M. Subramanian, H. Moine, 2011, EMBO reports.

Cells lacking the fragile X mental retardation protein (FMRP) have normal RISC activity but exhibit altered stress granule assembly.

J. Mandel, M. Subramanian, H. Moine, 2009, Molecular biology of the cell.

Do G Quartets Orchestrate Fragile X Pathology?

J. Mandel, H. Moine, 2001, Science.