Boisseau P - Search Results

1

Protease-activated receptor genes are clustered on 5q13.

Guyonnet Dupérat V, Jacquelin B, Boisseau P, Arveiler B, Nurden AT. Guyonnet Dupérat V, et al. Among authors: boisseau p. Blood. 1998 Jul 1;92(1):25-31. Blood. 1998. PMID: 9639495 Free article.

2

Glucanex: a cost-effective yeast lytic enzyme.

Petit J, Boisseau P, Arveiler B. Petit J, et al. Among authors: boisseau p. Trends Genet. 1994 Jan;10(1):4-5. doi: 10.1016/0168-9525(94)90004-3. Trends Genet. 1994. PMID: 8146913 No abstract available.

3

Seeding of YACs over regions 1q41-q42.3 and 11q14.3-q23 with microdissection clones.

Petit J, Boisseau P, Evans K, Christie S, Gosden C, Muir W, St Clair D, Porteous D, Arveiler B. Petit J, et al. Among authors: boisseau p. Eur J Hum Genet. 1995;3(6):351-6. doi: 10.1159/000472324. Eur J Hum Genet. 1995. PMID: 8825577

4

Refined localisation of the voltage-gated chloride channel, CLCN3, to 4q33.

Taine L, Coupry I, Boisseau P, Saura R, Lacombe D, Arveiler B. Taine L, et al. Among authors: boisseau p. Hum Genet. 1998 Feb;102(2):178-81. doi: 10.1007/s004390050673. Hum Genet. 1998. PMID: 9521585

5

A YAC contig encompassing the 11q14.3 breakpoint of a translocation associated with schizophrenia, and including the tyrosinase gene.

Petit J, Boisseau P, Taine L, Gauthier B, Arveiler B. Petit J, et al. Among authors: boisseau p. Mamm Genome. 1999 Jun;10(6):649-52. doi: 10.1007/s003359901064. Mamm Genome. 1999. PMID: 10341105 No abstract available.

6

Unexpected frequency of Upshaw-Schulman syndrome in pregnancy-onset thrombotic thrombocytopenic purpura.

Moatti-Cohen M, Garrec C, Wolf M, Boisseau P, Galicier L, Azoulay E, Stepanian A, Delmas Y, Rondeau E, Bezieau S, Coppo P, Veyradier A; French Reference Center for Thrombotic Microangiopathies. Moatti-Cohen M, et al. Among authors: boisseau p. Blood. 2012 Jun 14;119(24):5888-97. doi: 10.1182/blood-2012-02-408914. Epub 2012 Apr 30. Blood. 2012. PMID: 22547583 Free article.

7

Mutations in the A3 domain of von Willebrand factor inducing combined qualitative and quantitative defects in the protein.

Legendre P, Navarrete AM, Rayes J, Casari C, Boisseau P, Ternisien C, Caron C, Fressinaud E, Goudemand J, Veyradier A, Denis CV, Lenting PJ, Christophe OD. Legendre P, et al. Among authors: boisseau p. Blood. 2013 Mar 14;121(11):2135-43. doi: 10.1182/blood-2012-09-456038. Epub 2013 Jan 18. Blood. 2013. PMID: 23335371 Free article.

8

Molecular misdiagnosis in type 2B von Willebrand disease.

Schmitt S, Trossaert M, Airaud F, Landeau-Trottier G, Talarmain P, Boisseau P, Fressinaud E, Bezieau S. Schmitt S, et al. Among authors: boisseau p. Am J Hematol. 2006 Oct;81(10):805-6. doi: 10.1002/ajh.20661. Am J Hematol. 2006. PMID: 16783788 Free article. No abstract available.

9

Mild hemophilia A with factor VIII assay discrepancy: using thrombin generation assay to assess the bleeding phenotype.

Trossaërt M, Regnault V, Sigaud M, Boisseau P, Fressinaud E, Lecompte T. Trossaërt M, et al. Among authors: boisseau p. J Thromb Haemost. 2008 Mar;6(3):486-93. doi: 10.1111/j.1538-7836.2007.02861.x. Epub 2007 Nov 28. J Thromb Haemost. 2008. PMID: 18047548 Free article.

10

Complex constitutional subtelomeric 1p36.3 deletion/duplication in a mentally retarded child with neonatal neuroblastoma.

Isidor B, Le Cunff M, Boceno M, Boisseau P, Thomas C, Rival JM, David A, Le Caignec C. Isidor B, et al. Among authors: boisseau p. Eur J Med Genet. 2008 Nov-Dec;51(6):679-84. doi: 10.1016/j.ejmg.2008.06.004. Epub 2008 Jul 11. Eur J Med Genet. 2008. PMID: 18672103

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