Doerflinger Nathalie
Doerflinger Nathalie / IR - INSERM
Research interests
Molecular biology : cloning, PCR and qPCR (on DNA, RT or single cell cytoplasm), LCM, RNA microarray, RNAi (siRNA and shRNA), ISH, IHC,...
Member of SBRI Teams
Selected Publications of Doerflinger Nathalie
Year |
Reference | Title | Authors | Journal | PUB MED | ||
|---|---|---|---|---|---|---|---|
| 2014 | 81(6):1255-62 | Novel primate miRNAs coevolved with ancient target genes in germinal zone-specific expression patterns | Arcila ML, Betizeau M, Cambronne XA, Guzman E, Doerflinger N, Bouhallier F, Zhou H, Wu B, Rani N, Bassett DS, Borello U, Huissoud C, Goodman RH, Dehay C, Kosik KS | Neuron | - | ||
| 2009 | 106(51):21924-9 | Forced G1-phase reduction alters mode of division, neuron number, and laminar phenotype in the cerebral cortex | Pilaz LJ, Patti D, Marcy G, Ollier E, Pfister S, Douglas RJ, Betizeau M, Gautier E, Cortay V, Doerflinger N, Kennedy H, Dehay C | Proc Natl Acad Sci U S A | |||
| 2005 | 94(5):3357-67 | Two populations of layer v pyramidal cells of the mouse neocortex: development and sensitivity to anesthetics | Christophe E, Doerflinger N, Lavery DJ, Molnár Z, Charpak S, Audinat E | J Neurophysiol | |||
| 2003 | 21(5):562-5 | A directional strategy for monitoring Cre-mediated recombination at the cellular level in the mouse | Schnütgen F, Doerflinger N, Calléja C, Wendling O, Chambon P, Ghyselinck NB | Nat Biotechnol | |||
| 2003 | 35(1):63-72 | Inducible site-specific recombination in myelinating cells | Doerflinger NH, Macklin WB, Popko B | Genesis | |||
| 1998 | 9(7):1025-36 | Retroviral transfer and long-term expression of the adrenoleukodystrophy gene in human CD34+ cells | Doerflinger N, Miclea JM, Lopez J, Chomienne C, Bougnères P, Aubourg P, Cartier N | Hum Gene Ther | |||
| 1998 | 75(3):254-64 | Mirror expression of adrenoleukodystrophy and adrenoleukodystrophy related genes in mouse tissues and human cell lines | Troffer-Charlier N, Doerflinger N, Metzger E, Fouquet F, Mandel JL, Aubourg P | Eur J Cell Biol | - | ||
| 1995 | 56(5):1116-24 | Ataxia with vitamin E deficiency: refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 families | Doerflinger N, Linder C, Ouahchi K, Gyapay G, Weissenbach J, Le Paslier D, Rigault P, Belal S, Ben Hamida C, Hentati F, et al | Am J Hum Genet | |||
| 1993 | 5(2):195-200 | Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping | Ben Hamida C, Doerflinger N, Belal S, Linder C, Reutenauer L, Dib C, Gyapay G, Vignal A, Le Paslier D, Cohen D, et al | Nat Genet | - | ||