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1.

Condensate functionalization with microtubule motors directs their nucleation in space and allows manipulating RNA localization.

Cochard, Audrey; Safieddine, Adham; Combe, Pauline; Benassy, Marie-Noëlle; Weil, Dominique; Gueroui, Zoher.

EMBO J ; 42(20): e114106, 2023 10 16.

Artículo en Inglés | MEDLINE | ID: mdl-37724036

2.

Re-viewing the 3D Organization of mRNPs.

Pierron, Gérard; Weil, Dominique.

Mol Cell ; 72(4): 603-605, 2018 11 15.

Artículo en Inglés | MEDLINE | ID: mdl-30444995

3.

P-Body Purification Reveals the Condensation of Repressed mRNA Regulons.

Hubstenberger, Arnaud; Courel, Maïté; Bénard, Marianne; Souquere, Sylvie; Ernoult-Lange, Michèle; Chouaib, Racha; Yi, Zhou; Morlot, Jean-Baptiste; Munier, Annie; Fradet, Magali; Daunesse, Maëlle; Bertrand, Edouard; Pierron, Gérard; Mozziconacci, Julien; Kress, Michel; Weil, Dominique.

Mol Cell ; 68(1): 144-157.e5, 2017 Oct 05.

Artículo en Inglés | MEDLINE | ID: mdl-28965817

4.

Evolution is not Uniform Along Coding Sequences.

Bricout, Raphaël; Weil, Dominique; Stroebel, David; Genovesio, Auguste; Roest Crollius, Hugues.

Mol Biol Evol ; 40(3)2023 03 04.

Artículo en Inglés | MEDLINE | ID: mdl-36857092

5.

Inherited deficiency of stress granule ZNFX1 in patients with monocytosis and mycobacterial disease.

Le Voyer, Tom; Neehus, Anna-Lena; Yang, Rui; Ogishi, Masato; Rosain, Jérémie; Alroqi, Fayhan; Alshalan, Maha; Blumental, Sophie; Al Ali, Fatima; Khan, Taushif; Ata, Manar; Rozen, Laurence; Demulder, Anne; Bastard, Paul; Gruber, Conor; Roynard, Manon; Seeleuthener, Yoann; Rapaport, Franck; Bigio, Benedetta; Chrabieh, Maya; Sng, Danielle; Berteloot, Laureline; Boddaert, Nathalie; Rozenberg, Flore; Al-Muhsen, Saleh; Bertoli-Avella, Aida; Abel, Laurent; Bogunovic, Dusan; Marr, Nico; Mansouri, Davood; Al Mutairi, Fuad; Béziat, Vivien; Weil, Dominique; Mahdaviani, Seyed Alireza; Ferster, Alina; Zhang, Shen-Ying; Reversade, Bruno; Boisson-Dupuis, Stéphanie; Casanova, Jean-Laurent; Bustamante, Jacinta.

Proc Natl Acad Sci U S A ; 118(15)2021 04 13.

Artículo en Inglés | MEDLINE | ID: mdl-33876776

6.

RNA at the surface of phase-separated condensates impacts their size and number.

Cochard, Audrey; Garcia-Jove Navarro, Marina; Piroska, Leonard; Kashida, Shunnichi; Kress, Michel; Weil, Dominique; Gueroui, Zoher.

Biophys J ; 121(9): 1675-1690, 2022 05 03.

Artículo en Inglés | MEDLINE | ID: mdl-35364105

7.

Rare De Novo Missense Variants in RNA Helicase DDX6 Cause Intellectual Disability and Dysmorphic Features and Lead to P-Body Defects and RNA Dysregulation.

Balak, Chris; Benard, Marianne; Schaefer, Elise; Iqbal, Sumaiya; Ramsey, Keri; Ernoult-Lange, Michèle; Mattioli, Francesca; Llaci, Lorida; Geoffroy, Véronique; Courel, Maité; Naymik, Marcus; Bachman, Kristine K; Pfundt, Rolph; Rump, Patrick; Ter Beest, Johanna; Wentzensen, Ingrid M; Monaghan, Kristin G; McWalter, Kirsty; Richholt, Ryan; Le Béchec, Antony; Jepsen, Wayne; De Both, Matt; Belnap, Newell; Boland, Anne; Piras, Ignazio S; Deleuze, Jean-François; Szelinger, Szabolcs; Dollfus, Hélène; Chelly, Jamel; Muller, Jean; Campbell, Arthur; Lal, Dennis; Rangasamy, Sampathkumar; Mandel, Jean-Louis; Narayanan, Vinodh; Huentelman, Matt; Weil, Dominique; Piton, Amélie.

Am J Hum Genet ; 105(3): 509-525, 2019 09 05.

Artículo en Inglés | MEDLINE | ID: mdl-31422817

8.

P-Bodies: Cytosolic Droplets for Coordinated mRNA Storage.

Standart, Nancy; Weil, Dominique.

Trends Genet ; 34(8): 612-626, 2018 08.

Artículo en Inglés | MEDLINE | ID: mdl-29908710

9.

Mutations in genes encoding regulators of mRNA decapping and translation initiation: links to intellectual disability.

Weil, Dominique; Piton, Amélie; Lessel, Davor; Standart, Nancy.

Biochem Soc Trans ; 48(3): 1199-1211, 2020 06 30.

Artículo en Inglés | MEDLINE | ID: mdl-32412080

10.

The DDX6-4E-T interaction mediates translational repression and P-body assembly.

Kamenska, Anastasiia; Simpson, Clare; Vindry, Caroline; Broomhead, Helen; Bénard, Marianne; Ernoult-Lange, Michèle; Lee, Benjamin P; Harries, Lorna W; Weil, Dominique; Standart, Nancy.

Nucleic Acids Res ; 44(13): 6318-34, 2016 07 27.

Artículo en Inglés | MEDLINE | ID: mdl-27342281

11.

Estimation of Recent and Ancient Inbreeding in a Small Endogamous Tunisian Community Through Genomic Runs of Homozygosity.

Ben Halim, Nizar; Nagara, Majdi; Regnault, Béatrice; Hsouna, Sana; Lasram, Khaled; Kefi, Rym; Azaiez, Hela; Khemira, Laroussi; Saidane, Rachid; Ammar, Slim Ben; Besbes, Ghazi; Weil, Dominique; Petit, Christine; Abdelhak, Sonia; Romdhane, Lilia.

Ann Hum Genet ; 79(6): 402-17, 2015 Nov.

Artículo en Inglés | MEDLINE | ID: mdl-26420437

12.

Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy.

Delmaghani, Sedigheh; del Castillo, Francisco J; Michel, Vincent; Leibovici, Michel; Aghaie, Asadollah; Ron, Uri; Van Laer, Lut; Ben-Tal, Nir; Van Camp, Guy; Weil, Dominique; Langa, Francina; Lathrop, Mark; Avan, Paul; Petit, Christine.

Nat Genet ; 38(7): 770-8, 2006 Jul.

Artículo en Inglés | MEDLINE | ID: mdl-16804542

13.

Cytoplasmic organelles on the road to mRNA decay.

Weil, Dominique; Hollien, Julie.

Biochim Biophys Acta ; 1829(6-7): 725-31, 2013.

Artículo en Inglés | MEDLINE | ID: mdl-23337852

14.

Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafness.

Delmaghani, Sedigheh; Aghaie, Asadollah; Michalski, Nicolas; Bonnet, Crystel; Weil, Dominique; Petit, Christine.

Hum Mol Genet ; 21(17): 3835-44, 2012 Sep 01.

Artículo en Inglés | MEDLINE | ID: mdl-22678063

15.

Multiple binding of repressed mRNAs by the P-body protein Rck/p54.

Ernoult-Lange, Michèle; Baconnais, Sonia; Harper, Maryannick; Minshall, Nicola; Souquere, Sylvie; Boudier, Thomas; Bénard, Marianne; Andrey, Philippe; Pierron, Gérard; Kress, Michel; Standart, Nancy; le Cam, Eric; Weil, Dominique.

RNA ; 18(9): 1702-15, 2012 Sep.

Artículo en Inglés | MEDLINE | ID: mdl-22836354

16.

Stereocilin-deficient mice reveal the origin of cochlear waveform distortions.

Verpy, Elisabeth; Weil, Dominique; Leibovici, Michel; Goodyear, Richard J; Hamard, Ghislaine; Houdon, Carine; Lefèvre, Gaelle M; Hardelin, Jean-Pierre; Richardson, Guy P; Avan, Paul; Petit, Christine.

Nature ; 456(7219): 255-8, 2008 Nov 13.

Artículo en Inglés | MEDLINE | ID: mdl-18849963

17.

Association between altered placental human chorionic gonadotrophin (hCG) production and the occurrence of cryptorchidism: a retrospective study.

Chedane, Carole; Puissant, Hugues; Weil, Dominique; Rouleau, Stéphanie; Coutant, Régis.

BMC Pediatr ; 14: 191, 2014 Jul 26.

Artículo en Inglés | MEDLINE | ID: mdl-25064170

18.

Usher type 1G protein sans is a critical component of the tip-link complex, a structure controlling actin polymerization in stereocilia.

Caberlotto, Elisa; Michel, Vincent; Foucher, Isabelle; Bahloul, Amel; Goodyear, Richard J; Pepermans, Elise; Michalski, Nicolas; Perfettini, Isabelle; Alegria-Prévot, Olinda; Chardenoux, Sébastien; Do Cruzeiro, Marcio; Hardelin, Jean-Pierre; Richardson, Guy P; Avan, Paul; Weil, Dominique; Petit, Christine.

Proc Natl Acad Sci U S A ; 108(14): 5825-30, 2011 Apr 05.

Artículo en Inglés | MEDLINE | ID: mdl-21436032

19.

Cochlear outer hair cells undergo an apical circumference remodeling constrained by the hair bundle shape.

Etournay, Raphaël; Lepelletier, Léa; Boutet de Monvel, Jacques; Michel, Vincent; Cayet, Nadège; Leibovici, Michel; Weil, Dominique; Foucher, Isabelle; Hardelin, Jean-Pierre; Petit, Christine.

Development ; 137(8): 1373-83, 2010 Apr.

Artículo en Inglés | MEDLINE | ID: mdl-20332152

20.

Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31.

Mburu, Philomena; Mustapha, Mirna; Varela, Anabel; Weil, Dominique; El-Amraoui, Aziz; Holme, Ralph H; Rump, Andreas; Hardisty, Rachel E; Blanchard, Stéphane; Coimbra, Roney S; Perfettini, Isabelle; Parkinson, Nick; Mallon, Ann-Marie; Glenister, Pete; Rogers, Mike J; Paige, Adam J; Moir, Lee; Clay, Jo; Rosenthal, Andre; Liu, Xue Zhong; Blanco, Gonzalo; Steel, Karen P; Petit, Christine; Brown, Steve D M.

Nat Genet ; 34(4): 421-8, 2003 Aug.

Artículo en Inglés | MEDLINE | ID: mdl-12833159

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