1 - 25 of 68 results for author:"Weil D." in Literature citations
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| Multiple binding of repressed mRNAs by the P-body protein Rck/p54. Ernoult-Lange M., Baconnais S., Harper M., Minshall N., Souquere S., Boudier T., Benard M., Andrey P., Pierron G., Kress M. et al. RNA 18:1702-1715(2012) · Mapped (3) |
| Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafness. Delmaghani S., Aghaie A., Michalski N., Bonnet C., Weil D., Petit C. Hum. Mol. Genet. 21:3835-3844(2012) · UniProtKB (2) · Mapped (2) |
| RNA-related nuclear functions of human Pat1b, the P-body mRNA decay factor. Marnef A., Weil D., Standart N. Mol. Biol. Cell 23:213-224(2012) · UniProtKB (2) · Mapped (2) |
| CPEB1, a novel gene silenced in gastric cancer: a Drosophila approach. Caldeira J., Simoes-Correia J., Paredes J., Pinto M.T., Sousa S., Corso G., Marrelli D., Roviello F., Pereira P.S., Weil D. et al. Gut 61:1115-1123(2012) · Mapped (18) |
| Usher type 1G protein sans is a critical component of the tip-link complex, a structure controlling actin polymerization in stereocilia. Caberlotto E., Michel V., Foucher I., Bahloul A., Goodyear R.J., Pepermans E., Michalski N., Perfettini I., Alegria-Prevot O., Chardenoux S. et al. Proc. Natl. Acad. Sci. U.S.A. 108:5825-5830(2011) · UniProtKB (2) · Mapped (64) |
| Stereocilin connects outer hair cell stereocilia to one another and to the tectorial membrane. Verpy E., Leibovici M., Michalski N., Goodyear R.J., Houdon C., Weil D., Richardson G.P., Petit C. J. Comp. Neurol. 519:194-210(2011) · UniProtKB (1) · Mapped (67) |
| Distinct functions of maternal and somatic Pat1 protein paralogs. Marnef A., Maldonado M., Bugaut A., Balasubramanian S., Kress M., Weil D., Standart N. |
| Screening mutations of OTOF gene in Chinese patients with auditory neuropathy, including a familial case of temperature-sensitive auditory neuropathy. Wang D.Y., Wang Y.C., Weil D., Zhao Y.L., Rao S.Q., Zong L., Ji Y.B., Liu Q., Li J.Q., Yang H.M. et al. BMC Med. Genet. 11:79-79(2010) · Mapped (3) |
| Cochlear outer hair cells undergo an apical circumference remodeling constrained by the hair bundle shape. Etournay R., Lepelletier L., Boutet de Monvel J., Michel V., Cayet N., Leibovici M., Weil D., Foucher I., Hardelin J.P., Petit C. Development 137:1373-1383(2010) · Mapped (31) |
| Vezatin, an integral membrane protein of adherens junctions, is required for the sound resilience of cochlear hair cells. Bahloul A., Simmler M.C., Michel V., Leibovici M., Perfettini I., Roux I., Weil D., Nouaille S., Zuo J., Zadro C. et al. EMBO Mol Med 1:125-138(2009) · Mapped (6) |
| Harmonin-b, an actin-binding scaffold protein, is involved in the adaptation of mechanoelectrical transduction by sensory hair cells. Michalski N., Michel V., Caberlotto E., Lefevre G.M., van Aken A.F., Tinevez J.Y., Bizard E., Houbron C., Weil D., Hardelin J.P. et al. Pflugers Arch. 459:115-130(2009) · Mapped (4) |
| Role of p54 RNA helicase activity and its C-terminal domain in translational repression, P-body localization and assembly. Minshall N., Kress M., Weil D., Standart N. Mol. Biol. Cell 20:2464-2472(2009) · Mapped (3) |
| Nucleocytoplasmic traffic of CPEB1 and accumulation in Crm1 nucleolar bodies. Ernoult-Lange M., Wilczynska A., Harper M., Aigueperse C., Dautry F., Kress M., Weil D. Mol. Biol. Cell 20:176-187(2009) · Mapped (3) |
| Stereocilin-deficient mice reveal the origin of cochlear waveform distortions. Verpy E., Weil D., Leibovici M., Goodyear R.J., Hamard G., Houdon C., Lefevre G.M., Hardelin J.P., Richardson G.P., Avan P. et al. Nature 456:255-258(2008) · Mapped (12) |
| Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11. Hilgert N., Alasti F., Dieltjens N., Pawlik B., Wollnik B., Uyguner O., Delmaghani S., Weil D., Petit C., Danis E. et al. Clin. Genet. 74:223-232(2008) · Mapped (5) |
| A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth. Lefevre G., Michel V., Weil D., Lepelletier L., Bizard E., Wolfrum U., Hardelin J.P., Petit C. Development 135:1427-1437(2008) · Mapped (91) |
| CPEB interacts with an ovary-specific eIF4E and 4E-T in early Xenopus oocytes. Minshall N., Reiter M.H., Weil D., Standart N. J. Biol. Chem. 282:37389-37401(2007) · UniProtKB (6) |
| Molecular characterization of the ankle-link complex in cochlear hair cells and its role in the hair bundle functioning. Michalski N., Michel V., Bahloul A., Lefevre G., Barral J., Yagi H., Chardenoux S., Weil D., Martin P., Hardelin J.P. et al. J. Neurosci. 27:6478-6488(2007) · Mapped (72) |
| Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndrome. Hoskins B.E., Cramer C.H., Silvius D., Zou D., Raymond R.M., Orten D.J., Kimberling W.J., Smith R.J.H., Weil D., Petit C. et al. Am. J. Hum. Genet. 80:800-804(2007) · UniProtKB (1) |
| Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy. Delmaghani S., Del Castillo F.J., Michel V., Leibovici M., Aghaie A., Ron U., Van Laer L., Ben-Tal N., Van Camp G., Weil D. et al. |
| CDC2L5, a Cdk-like kinase with RS domain, interacts with the ASF/SF2-associated protein p32 and affects splicing in vivo. Even Y., Durieux S., Escande M.L., Lozano J.C., Peaucellier G., Weil D., Geneviere A.M. J. Cell. Biochem. 99:890-904(2006) · UniProtKB (2) · Mapped (7) |
| Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells. Adato A., Lefevre G., Delprat B., Michel V., Michalski N., Chardenoux S., Weil D., El-Amraoui A., Petit C. Hum. Mol. Genet. 14:3921-3932(2005) · UniProtKB (4) · Mapped (15) |
| Autosomal recessive and sporadic deafness in Morocco: high frequency of the 35delG GJB2 mutation and absence of the 342-kb GJB6 variant. Gazzaz B., Weil D., Rais L., Akhyat O., Azeddoug H., Nadifi S. Hear. Res. 210:80-84(2005) · Mapped (3) |
| A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment. del Castillo F.J., Rodriguez-Ballesteros M., Alvarez A., Hutchin T., Leonardi E., de Oliveira C.A., Azaiez H., Brownstein Z., Avenarius M.R., Marlin S. et al. J. Med. Genet. 42:588-594(2005) · UniProtKB (2) |
| Cadherin 23 is a component of the transient lateral links in the developing hair bundles of cochlear sensory cells. Michel V., Goodyear R.J., Weil D., Marcotti W., Perfettini I., Wolfrum U., Kros C.J., Richardson G.P., Petit C. Dev. Biol. 280:281-294(2005) · Mapped (13) |