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Items: 9

1.

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. 2014 Mar 19;81(6):1255-1262. doi: 10.1016/j.neuron.2014.01.017. Epub 2014 Feb 27.

2.

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. 2009 Dec 22;106(51):21924-9. doi: 10.1073/pnas.0909894106. Epub 2009 Dec 3.

3.

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. 2005 Nov;94(5):3357-67. Epub 2005 Jul 6.

4.

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 May;21(5):562-5. Epub 2003 Mar 31.

PMID:
12665802
5.

Inducible site-specific recombination in myelinating cells.

Doerflinger NH, Macklin WB, Popko B.

Genesis. 2003 Jan;35(1):63-72.

PMID:
12481300
6.

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 May 1;9(7):1025-36.

PMID:
9607414
7.

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. 1998 Mar;75(3):254-64.

PMID:
9587057
8.

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. 1995 May;56(5):1116-24.

9.

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. 1993 Oct;5(2):195-200.

PMID:
8252047

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