de Verneuil H - Search Results

1

Endotoxin-induced tissue factor messenger RNA in human monocytes is negatively regulated by a cyclic AMP-dependent mechanism.

Ollivier V, Houssaye S, Ternisien C, Léon A, de Verneuil H, Elbim C, Mackman N, Edgington TS, de Prost D. Ollivier V, et al. Among authors: de verneuil h, de prost d. Blood. 1993 Feb 15;81(4):973-9. Blood. 1993. PMID: 7679011 Free article.

2

Increased plasma transferrin, altered body iron distribution, and microcytic hypochromic anemia in ferrochelatase-deficient mice.

Lyoumi S, Abitbol M, Andrieu V, Henin D, Robert E, Schmitt C, Gouya L, de Verneuil H, Deybach JC, Montagutelli X, Beaumont C, Puy H. Lyoumi S, et al. Among authors: de verneuil h. Blood. 2007 Jan 15;109(2):811-8. doi: 10.1182/blood-2006-04-014142. Epub 2006 Sep 26. Blood. 2007. PMID: 17003376 Free article.

3

Metabolic correction of congenital erythropoietic porphyria by retrovirus-mediated gene transfer into Epstein-Barr virus-transformed B-cell lines.

Moreau-Gaudry F, Mazurier F, Bensidhoum M, Ged C, de Verneuil H. Moreau-Gaudry F, et al. Among authors: de verneuil h. Blood. 1995 Mar 15;85(6):1449-53. Blood. 1995. PMID: 7888667 Free article.

4

Correction of uroporphyrinogen decarboxylase deficiency (hepatoerythropoietic porphyria) in Epstein-Barr virus-transformed B-cell lines by retrovirus-mediated gene transfer: fluorescence-based selection of transduced cells.

Fontanellas A, Mazurier F, Moreau-Gaudry F, Belloc F, Ged C, de Verneuil H. Fontanellas A, et al. Among authors: de verneuil h. Blood. 1999 Jul 15;94(2):465-74. Blood. 1999. PMID: 10397714 Free article.

5

Point mutations in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyria (Günther's disease).

Deybach JC, de Verneuil H, Boulechfar S, Grandchamp B, Nordmann Y. Deybach JC, et al. Among authors: de verneuil h. Blood. 1990 May 1;75(9):1763-5. Blood. 1990. PMID: 2331520 Free article.

6

Ferrochelatase structural mutant (Fechm1Pas) in the house mouse.

Boulechfar S, Lamoril J, Montagutelli X, Guenet JL, Deybach JC, Nordmann Y, Dailey H, Grandchamp B, de Verneuil H. Boulechfar S, et al. Among authors: de verneuil h. Genomics. 1993 Jun;16(3):645-8. doi: 10.1006/geno.1993.1242. Genomics. 1993. PMID: 8325637

7

Heterogeneity of mutations in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyria.

Boulechfar S, Da Silva V, Deybach JC, Nordmann Y, Grandchamp B, de Verneuil H. Boulechfar S, et al. Among authors: de verneuil h. Hum Genet. 1992 Jan;88(3):320-4. doi: 10.1007/BF00197267. Hum Genet. 1992. PMID: 1733834

8

Molecular cloning, sequencing, and functional expression of a cDNA encoding human coproporphyrinogen oxidase.

Martasek P, Camadro JM, Delfau-Larue MH, Dumas JB, Montagne JJ, de Verneuil H, Labbe P, Grandchamp B. Martasek P, et al. Among authors: de verneuil h. Proc Natl Acad Sci U S A. 1994 Apr 12;91(8):3024-8. doi: 10.1073/pnas.91.8.3024. Proc Natl Acad Sci U S A. 1994. PMID: 8159699 Free PMC article.

9

Characterization of hypersensitive sites, protein-binding motifs, and regulatory elements in both promoters of the mouse porphobilinogen deaminase gene.

Porcher C, Pitiot G, Plumb M, Lowe S, de Verneuil H, Grandchamp B. Porcher C, et al. Among authors: de verneuil h. J Biol Chem. 1991 Jun 5;266(16):10562-9. J Biol Chem. 1991. PMID: 2037597 Free article.

10

The hematopoietic stem cell compartment of JAK2V617F-positive myeloproliferative disorders is a reflection of disease heterogeneity.

James C, Mazurier F, Dupont S, Chaligne R, Lamrissi-Garcia I, Tulliez M, Lippert E, Mahon FX, Pasquet JM, Etienne G, Delhommeau F, Giraudier S, Vainchenker W, de Verneuil H. James C, et al. Among authors: de verneuil h. Blood. 2008 Sep 15;112(6):2429-38. doi: 10.1182/blood-2008-02-137877. Epub 2008 Jul 8. Blood. 2008. PMID: 18612101 Free article.

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