Nathalie Doerflinger

Pilaz LJ, Patti D, Marcy G, Ollier E, Pfister S, Douglas RJ, Betizeau M, Gautier E, Cortay V, Doerflinger N, Kennedy H, Dehay C (2009) Forced G1-phase reduction alters mode of division, neuron number, and laminar phenotype in the cerebral cortex PNAS vol 106(51): 21924-21929 download

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