1 - 25 of 52 results for author:"Poch O." in Literature citations
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| Nxnl2 splicing results in dual functions in neuronal cell survival and maintenance of cell integrity. Jaillard C., Mouret A., Niepon M.L., Clerin E., Yang Y., Lee-Rivera I., Ait-Ali N., Millet-Puel G., Cronin T., Sedmak T. et al. Hum. Mol. Genet. 21:2298-2311(2012) · Mapped (1) |
| Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness. Audo I., Bujakowska K., Orhan E., Poloschek C.M., Defoort-Dhellemmes S., Drumare I., Kohl S., Luu T.D., Lecompte O., Zrenner E. et al. Am. J. Hum. Genet. 90:321-330(2012) · UniProtKB (1) |
| Homozygosity mapping and candidate prioritization identify mutations, missed by whole-exome sequencing, in SMOC2, causing major dental developmental defects. Bloch-Zupan A., Jamet X., Etard C., Laugel V., Muller J., Geoffroy V., Strauss J.P., Pelletier V., Marion V., Poch O. et al. Am. J. Hum. Genet. 89:773-781(2011) · UniProtKB (2) · Mapped (5) |
| EGFR and EphA2 are host factors for hepatitis C virus entry and possible targets for antiviral therapy. Lupberger J., Zeisel M.B., Xiao F., Thumann C., Fofana I., Zona L., Davis C., Mee C.J., Turek M., Gorke S. et al. Nat. Med. 17:589-595(2011) · Mapped (24) |
| Genome-wide evidence for an essential role of the human Staf/ZNF143 transcription factor in bidirectional transcription. Anno Y.N., Myslinski E., Ngondo-Mbongo R.P., Krol A., Poch O., Lecompte O., Carbon P. Nucleic Acids Res. 39:3116-3127(2011) · Mapped (3) |
| An unusual retinal phenotype associated with a novel mutation in RHO. Audo I., Friedrich A., Mohand-Said S., Lancelot M.E., Antonio A., Moskova-Doumanova V., Poch O., Bhattacharya S., Sahel J.A., Zeitz C. Arch. Ophthalmol. 128:1036-1045(2010) · Mapped (1) |
| Spectrum of rhodopsin mutations in French autosomal dominant rod-cone dystrophy patients. Audo I., Manes G., Mohand-Said S., Friedrich A., Lancelot M.E., Antonio A., Moskova-Doumanova V., Poch O., Zanlonghi X., Hamel C.P. et al. Invest. Ophthalmol. Vis. Sci. 51:3687-3700(2010) · Mapped (1) |
| The disruption of the rod-derived cone viability gene leads to photoreceptor dysfunction and susceptibility to oxidative stress. Cronin T., Raffelsberger W., Lee-Rivera I., Jaillard C., Niepon M.L., Kinzel B., Clerin E., Petrosian A., Picaud S., Poch O. et al. Cell Death Differ. 17:1199-1210(2010) · Mapped (1) |
| Cell-specific interaction of retinoic acid receptors with target genes in mouse embryonic fibroblasts and embryonic stem cells. Delacroix L., Moutier E., Altobelli G., Legras S., Poch O., Choukrallah M.A., Bertin I., Jost B., Davidson I. Mol. Cell. Biol. 30:231-244(2010) · Mapped (7) |
| The homeobox gene CHX10/VSX2 regulates RdCVF promoter activity in the inner retina. Reichman S., Kalathur R.K., Lambard S., Ait-Ali N., Yang Y., Lardenois A., Ripp R., Poch O., Zack D.J., Sahel J.A. et al. Hum. Mol. Genet. 19:250-261(2010) · Mapped (2) |
| TBP2 is essential for germ cell development by regulating transcription and chromatin condensation in the oocyte. Gazdag E., Santenard A., Ziegler-Birling C., Altobelli G., Poch O., Tora L., Torres-Padilla M.E. Genes Dev. 23:2210-2223(2009) · Mapped (2) |
| The thioredoxin-like protein rod-derived cone viability factor (RdCVFL) interacts with TAU and inhibits its phosphorylation in the retina. Fridlich R., Delalande F., Jaillard C., Lu J., Poidevin L., Cronin T., Perrocheau L., Millet-Puel G., Niepon M.L., Poch O. et al. Mol. Cell Proteomics 8:1206-1218(2009) · Mapped (6) |
| Structure of the archaeal pab87 peptidase reveals a novel self-compartmentalizing protease family. Delfosse V., Girard E., Birck C., Delmarcelle M., Delarue M., Poch O., Schultz P., Mayer C. PLoS ONE 4:e4712-e4712(2009) · UniProtKB (1) |
| Ortho-proteogenomics: multiple proteomes investigation through orthology and a new MS-based protocol. Gallien S., Perrodou E., Carapito C., Deshayes C., Reyrat J.-M., Van Dorsselaer A., Poch O., Schaeffer C., Lecompte O. Genome Res. 19:128-135(2009) · UniProtKB (6,583) |
| PtdIns5P regulation through evolution: roles in membrane trafficking? Lecompte O., Poch O., Laporte J. Trends Biochem. Sci. 33:453-460(2008) · Mapped (15) |
| Gene expression is altered in the lateral hypothalamus upon activation of the mu opioid receptor. Befort K., Filliol D., Darcq E., Ghate A., Matifas A., Lardenois A., Muller J., Thibault C., Dembele D., Poch O. et al. Ann. N. Y. Acad. Sci. 1129:175-184(2008) · Mapped (22) |
| ADCK3, an ancestral kinase, is mutated in a form of recessive ataxia associated with coenzyme Q10 deficiency. Lagier-Tourenne C., Tazir M., Lopez L.C., Quinzii C.M., Assoum M., Drouot N., Busso C., Makri S., Ali-Pacha L., Benhassine T. et al. Am. J. Hum. Genet. 82:661-672(2008) · UniProtKB (1) · Mapped (6) |
| Interrupted coding sequences in Mycobacterium smegmatis: authentic mutations or sequencing errors? Deshayes C., Perrodou E., Gallien S., Euphrasie D., Schaeffer C., Van-Dorsselaer A., Poch O., Lecompte O., Reyrat J.-M. Genome Biol. 8:R20.1-R20.9(2007) · UniProtKB (6,588) |
| Identification of a novel BBS gene (BBS12) highlights the major role of a vertebrate-specific branch of chaperonin-related proteins in Bardet-Biedl syndrome. Stoetzel C., Muller J., Laurier V., Davis E.E., Zaghloul N.A., Vicaire S., Jacquelin C., Plewniak F., Leitch C.C., Sarda P. et al. Am. J. Hum. Genet. 80:1-11(2007) · UniProtKB (1) · Mapped (8) |
| [Bardet-Biedl syndrome: a unique family for a major gene (BBS10)]. Dollfus H., Muller J., Stoetzel C., Laurier V., Bonneau D., Megarbane A., Poch O., Mandel J.L. Med Sci (Paris) 22:901-904(2006) · Mapped (2) |
| BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locus. Stoetzel C., Laurier V., Davis E.E., Muller J., Rix S., Badano J.L., Leitch C.C., Salem N., Chouery E., Corbani S. et al. |
| Cloning, purification and crystallization of a Walker-type Pyrococcus abyssi ATPase family member. Uhring M., Bey G., Lecompte O., Cavarelli J., Moras D., Poch O. Acta Crystallogr. Sect. F Struct. Biol. Cryst. Commun. 61:925-927(2005) · Mapped (1) |
| The evolutionary origin of peroxisomes: an ER-peroxisome connection. Schluter A., Fourcade S., Ripp R., Mandel J.L., Poch O., Pujol A. Mol. Biol. Evol. 23:838-845(2006) · Mapped (10) |
| ICDS database: interrupted CoDing sequences in prokaryotic genomes. Perrodou E., Deshayes C., Muller J., Schaeffer C., Van Dorsselaer A., Ripp R., Poch O., Reyrat J.M., Lecompte O. Nucleic Acids Res. 34:D338-D343(2006) · UniProtKB (3,984) |
| Head and neck squamous cell carcinoma transcriptome analysis by comprehensive validated differential display. Carles A., Millon R., Cromer A., Ganguli G., Lemaire F., Young J., Wasylyk C., Muller D., Schultz I., Rabouel Y. et al. Oncogene 25:1821-1831(2006) · UniProtKB (2) |