Lufkin T - Search Results

1

The cellular retinoic acid binding protein I is dispensable.

Gorry P, Lufkin T, Dierich A, Rochette-Egly C, Décimo D, Dollé P, Mark M, Durand B, Chambon P. Gorry P, et al. Among authors: lufkin t. Proc Natl Acad Sci U S A. 1994 Sep 13;91(19):9032-6. doi: 10.1073/pnas.91.19.9032. Proc Natl Acad Sci U S A. 1994. PMID: 8090764 Free PMC article.

2

Function of the retinoic acid receptors (RARs) during development (II). Multiple abnormalities at various stages of organogenesis in RAR double mutants.

Mendelsohn C, Lohnes D, Décimo D, Lufkin T, LeMeur M, Chambon P, Mark M. Mendelsohn C, et al. Among authors: lufkin t. Development. 1994 Oct;120(10):2749-71. doi: 10.1242/dev.120.10.2749. Development. 1994. PMID: 7607068

3

Mice deficient in cellular retinoic acid binding protein II (CRABPII) or in both CRABPI and CRABPII are essentially normal.

Lampron C, Rochette-Egly C, Gorry P, Dollé P, Mark M, Lufkin T, LeMeur M, Chambon P. Lampron C, et al. Among authors: lufkin t. Development. 1995 Feb;121(2):539-48. doi: 10.1242/dev.121.2.539. Development. 1995. PMID: 7768191

4

Local alterations of Krox-20 and Hox gene expression in the hindbrain suggest lack of rhombomeres 4 and 5 in homozygote null Hoxa-1 (Hox-1.6) mutant embryos.

Dollé P, Lufkin T, Krumlauf R, Mark M, Duboule D, Chambon P. Dollé P, et al. Among authors: lufkin t. Proc Natl Acad Sci U S A. 1993 Aug 15;90(16):7666-70. doi: 10.1073/pnas.90.16.7666. Proc Natl Acad Sci U S A. 1993. PMID: 8102800 Free PMC article.

5

High postnatal lethality and testis degeneration in retinoic acid receptor alpha mutant mice.

Lufkin T, Lohnes D, Mark M, Dierich A, Gorry P, Gaub MP, LeMeur M, Chambon P. Lufkin T, et al. Proc Natl Acad Sci U S A. 1993 Aug 1;90(15):7225-9. doi: 10.1073/pnas.90.15.7225. Proc Natl Acad Sci U S A. 1993. PMID: 8394014 Free PMC article.

6

Retinoid receptors and binding proteins.

Lohnes D, Dierich A, Ghyselinck N, Kastner P, Lampron C, LeMeur M, Lufkin T, Mendelsohn C, Nakshatri H, Chambon P. Lohnes D, et al. Among authors: lufkin t. J Cell Sci Suppl. 1992;16:69-76. doi: 10.1242/jcs.1992.supplement_16.9. J Cell Sci Suppl. 1992. PMID: 1338435 Review.

7

Homeotic transformation of the occipital bones of the skull by ectopic expression of a homeobox gene.

Lufkin T, Mark M, Hart CP, Dollé P, LeMeur M, Chambon P. Lufkin T, et al. Nature. 1992 Oct 29;359(6398):835-41. doi: 10.1038/359835a0. Nature. 1992. PMID: 1359423

8

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. Cell. 1991 Sep 20;66(6):1105-19. doi: 10.1016/0092-8674(91)90034-v. Cell. 1991. PMID: 1680563

9

Roles of Hox genes: what we have learnt from gain of function and loss of function mutations in the mouse.

Mark M, Lufkin T, Dollé P, Dierich A, LeMeur M, Chambon P. Mark M, et al. Among authors: lufkin t. C R Acad Sci III. 1993 Sep;316(9):995-1008. C R Acad Sci III. 1993. PMID: 7915637 Review. English, French.

10

Two rhombomeres are altered in Hoxa-1 mutant mice.

Mark M, Lufkin T, Vonesch JL, Ruberte E, Olivo JC, Dollé P, Gorry P, Lumsden A, Chambon P. Mark M, et al. Among authors: lufkin t. Development. 1993 Oct;119(2):319-38. doi: 10.1242/dev.119.2.319. Development. 1993. PMID: 8287791

This study provides a detailed description of the anatomical defects in the Hoxa-1-/- mutant mice previously generated in our laboratory (T. Lufkin, A. Dierich, M. LeMeur, M. Mark and P. Chambon, 1991; Cell 66, 1105-1119). ...These morphological data, combined with …

This study provides a detailed description of the anatomical defects in the Hoxa-1-/- mutant mice previously generated in our laboratory ( …

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