Dierich A - Search Results

1

Gastric mucosa abnormalities and tumorigenesis in mice lacking the pS2 trefoil protein.

Lefebvre O, Chenard MP, Masson R, Linares J, Dierich A, LeMeur M, Wendling C, Tomasetto C, Chambon P, Rio MC. Lefebvre O, et al. Among authors: dierich a. Science. 1996 Oct 11;274(5285):259-62. doi: 10.1126/science.274.5285.259. Science. 1996. PMID: 8824193

2

Mice lacking TdT: mature animals with an immature lymphocyte repertoire.

Gilfillan S, Dierich A, Lemeur M, Benoist C, Mathis D. Gilfillan S, et al. Among authors: dierich a. Science. 1993 Aug 27;261(5125):1175-8. doi: 10.1126/science.8356452. Science. 1993. PMID: 8356452

3

Impaired neural tube closure, axial skeleton malformations, and tracheal ring disruption in TRAF4-deficient mice.

Régnier CH, Masson R, Kedinger V, Textoris J, Stoll I, Chenard MP, Dierich A, Tomasetto C, Rio MC. Régnier CH, et al. Among authors: dierich a. Proc Natl Acad Sci U S A. 2002 Apr 16;99(8):5585-90. doi: 10.1073/pnas.052124799. Epub 2002 Apr 9. Proc Natl Acad Sci U S A. 2002. PMID: 11943846 Free PMC article.

4

Enhanced aggressive behavior in mice lacking 5-HT1B receptor.

Saudou F, Amara DA, Dierich A, LeMeur M, Ramboz S, Segu L, Buhot MC, Hen R. Saudou F, et al. Among authors: dierich a. Science. 1994 Sep 23;265(5180):1875-8. doi: 10.1126/science.8091214. Science. 1994. PMID: 8091214

5

In vivo evidence that the stromelysin-3 metalloproteinase contributes in a paracrine manner to epithelial cell malignancy.

Masson R, Lefebvre O, Noël A, Fahime ME, Chenard MP, Wendling C, Kebers F, LeMeur M, Dierich A, Foidart JM, Basset P, Rio MC. Masson R, et al. Among authors: dierich a. J Cell Biol. 1998 Mar 23;140(6):1535-41. doi: 10.1083/jcb.140.6.1535. J Cell Biol. 1998. PMID: 9508784 Free PMC article.

6

A conditional floxed (loxP-flanked) allele for the retinoic acid receptor beta (RARbeta) gene.

Chapellier B, Mark M, Bastien J, Dierich A, LeMeur M, Chambon P, Ghyselinck NB. Chapellier B, et al. Among authors: dierich a. Genesis. 2002 Feb;32(2):91-4. doi: 10.1002/gene.10073. Genesis. 2002. PMID: 11857787 No abstract available.

7

A Hoxa2 mutant conditional allele generated by Flp- and Cre-mediated recombination.

Ren SY, Pasqualetti M, Dierich A, Le Meur M, Rijli FM. Ren SY, et al. Among authors: dierich a. Genesis. 2002 Feb;32(2):105-8. doi: 10.1002/gene.10052. Genesis. 2002. PMID: 11857791 No abstract available.

8

A Hoxa2 knockin allele that expresses EGFP upon conditional Cre-mediated recombination.

Pasqualetti M, Ren SY, Poulet M, LeMeur M, Dierich A, Rijli FM. Pasqualetti M, et al. Among authors: dierich a. Genesis. 2002 Feb;32(2):109-11. Genesis. 2002. PMID: 11857792 No abstract available.

9

Disruption of the Hox-1.6 homeobox gene results in defects in a region corresponding to its rostral domain of expression.

Lufkin T, Dierich A, LeMeur M, Mark M, Chambon P. Lufkin T, et al. Among authors: dierich a. Cell. 1991 Sep 20;66(6):1105-19. doi: 10.1016/0092-8674(91)90034-v. Cell. 1991. PMID: 1680563

10

Mice lacking MHC class II molecules.

Cosgrove D, Gray D, Dierich A, Kaufman J, Lemeur M, Benoist C, Mathis D. Cosgrove D, et al. Among authors: dierich a. Cell. 1991 Sep 6;66(5):1051-66. doi: 10.1016/0092-8674(91)90448-8. Cell. 1991. PMID: 1909605

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