Hakutulokset - Nicolas Lévy
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XRCC1 is phosphorylated by DNA-dependent protein kinase in response to DNA damage Tekijä Nicolas Lévy
Julkaistu 2006Artigo -
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Molecular bases of progeroid syndromes Tekijä Claire Navarro, Pierre Cau, Nicolas Lévy
Julkaistu 2006Revisão -
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Evidence of SARS-CoV-2 re-infection with a different genotype Tekijä Philippe Colson, M Finaud, Nicolas Lévy, Jean‐Christophe Lagier, Didier Raoult
Julkaistu 2020Carta -
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Prognostic significance of the Ki-67-associated proliferative antigen in aggressive non-Hodgkin's lymphomas: a prospective Southwest Oncology Group trial Tekijä TP Miller, TM Grogan, Steve Dahlberg, CM Spier, RM Braziel, PM Banks, Kathryn Foucar, CR Kjeldsberg, Nicolas Lévy, BN Nathwani
Julkaistu 1994Artigo -
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UMD‐Predictor: A High‐Throughput Sequencing Compliant System for Pathogenicity Prediction of any Human cDNA Substitution Tekijä David Salgado, Jean-Pierre Desvignes, Ghadi Raï, Arnaud Blanchard, Morgane Miltgen, Amélie Pinard, Nicolas Lévy, Gwenaëlle Collod‐Béroud, Christophe Béroud
Julkaistu 2016Artigo -
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Prognostic significance of the Ki-67-associated proliferative antigen in aggressive non-Hodgkin's lymphomas: a prospective Southwest Oncology Group trial Tekijä TP Miller, TM Grogan, Steve Dahlberg, CM Spier, RM Braziel, PM Banks, Kathryn Foucar, CR Kjeldsberg, Nicolas Lévy, BN Nathwani
Julkaistu 1994Artigo -
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Brief research communication: serotonin transporter (5-HTT) gene polymorphisms are not associated with susceptibility to mood disorders Tekijä Margret R. Hoehe, Birgit Wendel, Ingrid Grunewald, Pierre Chiaroni, Nicolas Lévy, Deborah Morris‐Rosendahl, Jean-Paul Macher, Thomas Sander, Marc‐Antoine Crocq
Julkaistu 1998Artigo -
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AP1S2 is mutated in X-linked Dandy–Walker malformation with intellectual disability, basal ganglia disease and seizures (Pettigrew syndrome) Tekijä Pierre Cacciagli, Jean-Pierre Desvignes, Nadine Girard, Marc Delépine, Diana Zélénika, Mark Lathrop, Nicolas Lévy, David H. Ledbetter, William B. Dobyns, Laurent Villard
Julkaistu 2013Artigo -
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Unique Preservation of Neural Cells in Hutchinson- Gilford Progeria Syndrome Is Due to the Expression of the Neural-Specific miR-9 MicroRNA Tekijä Xavier Nissan, Sophie Blondel, Claire Navarro, Yves Maury, Cécile V. Denis, Mathilde Girard, Cécile Martinat, Annachiara De Sandre‐Giovannoli, Nicolas Lévy, Marc Peschanski
Julkaistu 2012Artigo
Työkalut:
Liittyvät aiheet
Biology
Gene
Genetics
Medicine
Mutation
Cell biology
Internal medicine
Cancer research
Pathology
Phenotype
Lamin
Progeria
LMNA
Biochemistry
Transcription factor
Exon
Muscular dystrophy
Premature aging
Lymphoma
Bioinformatics
Exome sequencing
Missense mutation
Molecular biology
Allele
Computational biology
Computer science
Disease
Dysferlin
Endocrinology
Enzyme