Artikel mit Open-Access-Mandaten - Olivier POCHWeitere Informationen
Nicht verfügbar: 2
Heterogeneous biological data integration with declarative query language
H Nguyen, L Michel, JD Thompson, O Poch
IBM Journal of Research and Development 58 (2/3), 15: 1-15: 12, 2014
Mandate: US National Institutes of Health, National Institute of Health and Medical …
Reflectance study of ice and Mars soil simulant associations—II. CO2 and H2O ice
Z Yoldi, A Pommerol, O Poch, N Thomas
Icarus 386, 115116, 2022
Mandate: Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
Verfügbar: 94
Reflection, emission, and polarization properties of surfaces made of hyperfine grains, and implications for the nature of primitive small bodies
R Sultana, O Poch, P Beck, B Schmitt, E Quirico, S Spadaccia, L Patty, ...
Icarus 395, 115492, 2023
Mandate: Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung …
Seven new loci associated with age-related macular degeneration
Nature genetics 45 (4), 433-439, 2013
Mandate: US National Institutes of Health, UK Medical Research Council, Wellcome Trust
EGFR and EphA2 are host factors for hepatitis C virus entry and possible targets for antiviral therapy
J Lupberger, MB Zeisel, F Xiao, C Thumann, I Fofana, L Zona, C Davis, ...
Nature medicine 17 (5), 589-595, 2011
Mandate: US National Institutes of Health, Howard Hughes Medical Institute, National …
ADCK3, an ancestral kinase, is mutated in a form of recessive ataxia associated with coenzyme Q10 deficiency
C Lagier-Tourenne, M Tazir, LC López, CM Quinzii, M Assoum, N Drouot, ...
The American Journal of Human Genetics 82 (3), 661-672, 2008
Mandate: National Institute of Health and Medical Research, France
A comprehensive benchmark study of multiple sequence alignment methods: current challenges and future perspectives
JD Thompson, B Linard, O Lecompte, O Poch
PloS one 6 (3), e18093, 2011
Mandate: National Institute of Health and Medical Research, France
Characterization of accessory genes in coronavirus genomes
CJ Michel, C Mayer, O Poch, JD Thompson
Virology journal 17, 1-13, 2020
Mandate: European Commission, Agence Nationale de la Recherche
Cell-specific interaction of retinoic acid receptors with target genes in mouse embryonic fibroblasts and embryonic stem cells
L Delacroix, E Moutier, G Altobelli, S Legras, O Poch, MA Choukrallah, ...
Molecular and cellular biology 30 (1), 231-244, 2010
Mandate: National Institute of Health and Medical Research, France
Exome sequencing of Bardet–Biedl syndrome patient identifies a null mutation in the BBSome subunit BBIP1 (BBS18)
S Scheidecker, C Etard, NW Pierce, V Geoffroy, E Schaefer, J Muller, ...
Journal of medical genetics 51 (2), 132-136, 2014
Mandate: US National Institutes of Health, National Institute of Health and Medical …
Identification of 28 novel mutations in the Bardet–Biedl syndrome genes: the burden of private mutations in an extensively heterogeneous disease
J Muller, C Stoetzel, MC Vincent, CC Leitch, V Laurier, JM Danse, S Hellé, ...
Human genetics 127, 583-593, 2010
Mandate: US National Institutes of Health, National Institute of Health and Medical …
Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness
C Zeitz, SG Jacobson, CP Hamel, K Bujakowska, M Neuillé, E Orhan, ...
The American Journal of Human Genetics 92 (1), 67-75, 2013
Mandate: National Institute of Health and Medical Research, France
Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness
I Audo, K Bujakowska, E Orhan, CM Poloschek, S Defoort-Dhellemmes, ...
The American Journal of Human Genetics 90 (2), 321-330, 2012
Mandate: US National Institutes of Health
Ortho-proteogenomics: multiple proteomes investigation through orthology and a new MS-based protocol
S Gallien, E Perrodou, C Carapito, C Deshayes, JM Reyrat, ...
Genome research 19 (1), 128-135, 2009
Mandate: National Institute of Health and Medical Research, France
Homozygosity mapping and candidate prioritization identify mutations, missed by whole-exome sequencing, in SMOC2, causing major dental developmental defects
A Bloch-Zupan, X Jamet, C Etard, V Laugel, J Muller, V Geoffroy, ...
The American Journal of Human Genetics 89 (6), 773-781, 2011
Mandate: National Institute of Health and Medical Research, France
Genome-wide in silico identification of new conserved and functional retinoic acid receptor response elements (direct repeats separated by 5 bp)
S Lalevée, YN Anno, A Chatagnon, E Samarut, O Poch, V Laudet, ...
Journal of Biological Chemistry 286 (38), 33322-33334, 2011
Mandate: National Institute of Health and Medical Research, France
TBP2 is essential for germ cell development by regulating transcription and chromatin condensation in the oocyte
E Gazdag, A Santenard, C Ziegler-Birling, G Altobelli, O Poch, L Tora, ...
Genes & development 23 (18), 2210-2223, 2009
Mandate: National Institute of Health and Medical Research, France
Issues in bioinformatics benchmarking: the case study of multiple sequence alignment
MR Aniba, O Poch, JD Thompson
Nucleic acids research 38 (21), 7353-7363, 2010
Mandate: National Institute of Health and Medical Research, France
A benchmark study of ab initio gene prediction methods in diverse eukaryotic organisms
N Scalzitti, A Jeannin-Girardon, P Collet, O Poch, JD Thompson
BMC genomics 21, 1-20, 2020
Mandate: Agence Nationale de la Recherche
The disruption of the rod-derived cone viability gene leads to photoreceptor dysfunction and susceptibility to oxidative stress
T Cronin, W Raffelsberger, I Lee-Rivera, C Jaillard, ML Niepon, B Kinzel, ...
Cell Death & Differentiation 17 (7), 1199-1210, 2010
Mandate: National Institute of Health and Medical Research, France
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