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Results: 1 to 20 of 27

1.

A long QT mutation substitutes cholesterol for phosphatidylinositol-4,5-bisphosphate in KCNQ1 channel regulation.

Coyan FC, Abderemane-Ali F, Amarouch MY, Piron J, Mordel J, Nicolas CS, Steenman M, Mérot J, Marionneau C, Thomas A, Brasseur R, Baró I, Loussouarn G.

PLoS One. 2014 Mar 28;9(3):e93255. doi: 10.1371/journal.pone.0093255. eCollection 2014.

PMID:
24681627
[PubMed - in process]
Free PMC Article
2.

[Arterial heterogeneity].

Gouëffic Y, Davaine JM, Merlini T, Rimbert A, Hérisson F, Heymann MF, Heymann D, Steenman M, Lambert G.

Rev Med Interne. 2013 Jan;34(1):61-5. doi: 10.1016/j.revmed.2012.10.364. Epub 2012 Nov 16. Review. French.

PMID:
23159822
[PubMed - indexed for MEDLINE]
3.

Immune response and mitochondrial metabolism are commonly deregulated in DMD and aging skeletal muscle.

Baron D, Magot A, Ramstein G, Steenman M, Fayet G, Chevalier C, Jourdon P, Houlgatte R, Savagner F, Pereon Y.

PLoS One. 2011;6(11):e26952. doi: 10.1371/journal.pone.0026952. Epub 2011 Nov 9.

PMID:
22096509
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Meta-analysis of muscle transcriptome data using the MADMuscle database reveals biologically relevant gene patterns.

Baron D, Dubois E, Bihouée A, Teusan R, Steenman M, Jourdon P, Magot A, Péréon Y, Veitia R, Savagner F, Ramstein G, Houlgatte R.

BMC Genomics. 2011 Feb 16;12:113. doi: 10.1186/1471-2164-12-113.

PMID:
21324190
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

MADGene: retrieval and processing of gene identifier lists for the analysis of heterogeneous microarray datasets.

Baron D, Bihouée A, Teusan R, Dubois E, Savagner F, Steenman M, Houlgatte R, Ramstein G.

Bioinformatics. 2011 Mar 1;27(5):725-6. doi: 10.1093/bioinformatics/btq710. Epub 2011 Jan 6.

PMID:
21216776
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Molecular signature of mineralocorticoid receptor signaling in cardiomyocytes: from cultured cells to mouse heart.

Latouche C, Sainte-Marie Y, Steenman M, Castro Chaves P, Naray-Fejes-Toth A, Fejes-Toth G, Farman N, Jaisser F.

Endocrinology. 2010 Sep;151(9):4467-76. doi: 10.1210/en.2010-0237. Epub 2010 Jun 30.

PMID:
20591974
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Molecular risk stratification in advanced heart failure patients.

Lamirault G, Meur NL, Roussel JC, Cunff MF, Baron D, Bihouée A, Guisle I, Raharijaona M, Ramstein G, Teusan R, Chevalier C, Gueffet JP, Trochu JN, Léger JJ, Houlgatte R, Steenman M.

J Cell Mol Med. 2010 Jun;14(6B):1443-52. doi: 10.1111/j.1582-4934.2009.00913.x. Epub 2009 Sep 30.

PMID:
19793385
[PubMed - indexed for MEDLINE]
8.

The prokineticin receptor-1 (GPR73) promotes cardiomyocyte survival and angiogenesis.

Urayama K, Guilini C, Messaddeq N, Hu K, Steenman M, Kurose H, Ert G, Nebigil CG.

FASEB J. 2007 Sep;21(11):2980-93. Epub 2007 Apr 18.

PMID:
17442730
[PubMed - indexed for MEDLINE]
Free Article
9.

Gene expression profile associated with chronic atrial fibrillation and underlying valvular heart disease in man.

Lamirault G, Gaborit N, Le Meur N, Chevalier C, Lande G, Demolombe S, Escande D, Nattel S, Léger JJ, Steenman M.

J Mol Cell Cardiol. 2006 Jan;40(1):173-84. Epub 2005 Oct 19.

PMID:
16242148
[PubMed - indexed for MEDLINE]
10.

Gene expression profiling in human cardiovascular disease.

Steenman M, Lamirault G, Le Meur N, Léger JJ.

Clin Chem Lab Med. 2005;43(7):696-701. Review.

PMID:
16207127
[PubMed - indexed for MEDLINE]
11.

Human atrial ion channel and transporter subunit gene-expression remodeling associated with valvular heart disease and atrial fibrillation.

Gaborit N, Steenman M, Lamirault G, Le Meur N, Le Bouter S, Lande G, Léger J, Charpentier F, Christ T, Dobrev D, Escande D, Nattel S, Demolombe S.

Circulation. 2005 Jul 26;112(4):471-81. Epub 2005 Jul 18.

PMID:
16027256
[PubMed - indexed for MEDLINE]
Free Article
12.

Mouse model of SCN5A-linked hereditary Lenègre's disease: age-related conduction slowing and myocardial fibrosis.

Royer A, van Veen TA, Le Bouter S, Marionneau C, Griol-Charhbili V, Léoni AL, Steenman M, van Rijen HV, Demolombe S, Goddard CA, Richer C, Escoubet B, Jarry-Guichard T, Colledge WH, Gros D, de Bakker JM, Grace AA, Escande D, Charpentier F.

Circulation. 2005 Apr 12;111(14):1738-46. Epub 2005 Apr 4.

PMID:
15809371
[PubMed - indexed for MEDLINE]
Free Article
13.

Distinct molecular portraits of human failing hearts identified by dedicated cDNA microarrays.

Steenman M, Lamirault G, Le Meur N, Le Cunff M, Escande D, Léger JJ.

Eur J Heart Fail. 2005 Mar 2;7(2):157-65.

PMID:
15701461
[PubMed - indexed for MEDLINE]
14.

DNA chip technology in cardiovascular research.

Lamirault G, Steenman M, Le Meur N, Demolombe S, Trochu JN, Léger JJ.

Arch Mal Coeur Vaiss. 2004 Dec;97(12):1251-5. Review.

PMID:
15669368
[PubMed - indexed for MEDLINE]
15.

A dynamic, web-accessible resource to process raw microarray scan data into consolidated gene expression values: importance of replication.

Le Meur N, Lamirault G, Bihouée A, Steenman M, Bédrine-Ferran H, Teusan R, Ramstein G, Léger JJ.

Nucleic Acids Res. 2004 Oct 8;32(18):5349-58. Print 2004.

PMID:
15475389
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Transcriptomal analysis of failing and nonfailing human hearts.

Steenman M, Chen YW, Le Cunff M, Lamirault G, Varró A, Hoffman E, Léger JJ.

Physiol Genomics. 2003 Jan 15;12(2):97-112. Erratum in: Physiol Genomics. 2004 Jun 17;1(1):128.

PMID:
12429867
[PubMed - indexed for MEDLINE]
17.

Global/temporal gene expression in diaphragm and hindlimb muscles of dystrophin-deficient (mdx) mice.

Rouger K, Le Cunff M, Steenman M, Potier MC, Gibelin N, Dechesne CA, Leger JJ.

Am J Physiol Cell Physiol. 2002 Sep;283(3):C773-84.

PMID:
12176734
[PubMed - indexed for MEDLINE]
Free Article
18.

Delineation and physical separation of novel translocation breakpoints on chromosome 1p in two genetically closely associated childhood tumors.

Steenman MJ, Zijlstra N, Kruitbosch DL, Wiesmeijer C, Larizza L, Voûte PA, Westerveld A, Mannens MM.

Cytogenet Cell Genet. 2000;88(3-4):289-95.

PMID:
10828613
[PubMed - indexed for MEDLINE]
19.

Genetics of Beckwith-Wiedemann syndrome-associated tumors: common genetic pathways.

Steenman M, Westerveld A, Mannens M.

Genes Chromosomes Cancer. 2000 May;28(1):1-13. Review.

PMID:
10738297
[PubMed - indexed for MEDLINE]
20.

Comparative genomic hybridization analysis of hepatoblastomas: additional evidence for a genetic link with Wilms tumor and rhabdomyosarcoma.

Steenman M, Tomlinson G, Westerveld A, Mannens M.

Cytogenet Cell Genet. 1999;86(2):157-61.

PMID:
10545709
[PubMed - indexed for MEDLINE]

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