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Stem-cell and Brain Research Institute
 
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Conference by Adrien Meguerditchian

Published on March 28, 2017



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Nathalie Doerflinger

Position: Research Engineer

Company: Inserm u846


Mailing Address:
18 avenue du Doyen Jean LÚpine

69675 - Bron Cedex - France
External Link: www.sbri.fr
E-mail: Nathalie.Doerflinger@inserm.fr
Phone: 04.72.91.34.86
Fax: 04.72.91.34.61


Group(s):
Stem cells and cortical development - Teams
-

Research interest

Molecular biology : cloning, PCR and qPCR (on DNA, RT or single cell cytoplasm), LCM, RNA microarray, RNAi (siRNA and shRNA), ISH, IHC,...

Publications
Arcila ML, Betizeau M, Cambronne L, Guzman E, Doerflinger N, Bouhallier F, Zhou H, Wu B, Borello U, Huissoud C, Goodman R, Dehay C, Kosik KS (2014) Novel primate miRNAs co-evolved with ancient target genes in germinal zone specific expression patterns Neuron 81 (6): 1255-1262
Christophe E, Doerflinger N, Lavery DJ, Molnar Z, Charpak S, Audinat E (2005) Two populations of Layer V Pyramidal Cells of the mouse Neocortex : Development and sensitivity to Anesthetics J Neurophysiol 94(5):3357-67 download
Schnutgen F, Doerflinger N, Calleja C, Wendling O, Chambon P, Ghyselinck NB (2003) A directional strategy for monitoring Cre-mediated recombination at the cellular level in the mouse. Nat Biotechnol 21 (5):562-5 download
Doerflinger NH, Mackling WB, Popko B (2003) Inducible Site Specific Recombination in Myelinating Cells Genesis 35(1):63-72 download
Doerflinger NH, Miclea JM, Lopez J, Chomienne C, Bougneres P, Aubourg P, Cartier N (1998) Retroviral Transfer and Long-Term Expression of the Adrenoleukodystrophy Gene in Human CD34+ Cells Hum Gene Ther 9(7):1025-36 download
Troffer-Charlier N, Doerflinger N, Metzger E, Fouquet F, Mandel JL, Aubourg P (1998) Mirror expression of adrenoleukodystrophy and adrenoleukodystrophy related genes in mouse tissues and human cell lines. Eur J Cell Biol 75(3):254-64.
Doerfling N and Al (1995) Ataxia vitamin E deficiency: Refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 families. Am J Hum Genet 56:1116-24 download
Hamida CB, Doerflinger N, Belal S, Linder C, Reutenauer L, Dib C, Gyapay G, Vignal A, Lepaslier D, Cohen D, Pandolfo M, Mokini V, Novelli G, Hentati F, Benhamida M, Mandel JL, Koenig M (1993) Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping. Nature Genetics 5(2): 195-200 download



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