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Items: 12


Phostine 3.1a as a pharmacological compound with antiangiogenic properties against diseases with excess vascularization.

Bousseau S, Marchand M, Soleti R, Vergori L, Hilairet G, Recoquillon S, Le Mao M, Gueguen N, Khiati S, Clarion L, Bakalara N, Martinez MC, Germain S, Lenaers G, Andriantsitohaina R.

FASEB J. 2019 May;33(5):5864-5875. doi: 10.1096/fj.201801450RRR. Epub 2019 Feb 28.


Lysyl oxidase-like 2 (LOXL2)-mediated cross-linking of tropoelastin.

Schmelzer CEH, Heinz A, Troilo H, Lockhart-Cairns MP, Jowitt TA, Marchand MF, Bidault L, Bignon M, Hedtke T, Barret A, McConnell JC, Sherratt MJ, Germain S, Hulmes DJS, Baldock C, Muller L.

FASEB J. 2019 Apr;33(4):5468-5481. doi: 10.1096/fj.201801860RR. Epub 2019 Jan 24.


Extracellular matrix scaffolding in angiogenesis and capillary homeostasis.

Marchand M, Monnot C, Muller L, Germain S.

Semin Cell Dev Biol. 2019 May;89:147-156. doi: 10.1016/j.semcdb.2018.08.007. Epub 2018 Sep 5. Review.


The Space Weather and Ultraviolet Solar Variability (SWUSV) Microsatellite Mission.

Damé L; SWUSV Team.

J Adv Res. 2013 May;4(3):235-51. doi: 10.1016/j.jare.2013.03.002. Epub 2013 Mar 20. Review.


Loss-of-function mutations in MC4R are very rare in the Greek severely obese adult population.

Rouskas K, Meyre D, Stutzmann F, Paletas K, Papazoglou D, Vatin V, Marchand M, Kouvatsi A, Froguel P.

Obesity (Silver Spring). 2012 Nov;20(11):2278-82. doi: 10.1038/oby.2012.77. Epub 2012 Mar 26.


TCF7L2 splice variants have distinct effects on beta-cell turnover and function.

Le Bacquer O, Shu L, Marchand M, Neve B, Paroni F, Kerr Conte J, Pattou F, Froguel P, Maedler K.

Hum Mol Genet. 2011 May 15;20(10):1906-15. doi: 10.1093/hmg/ddr072. Epub 2011 Feb 28.


Genetic and functional assessment of the role of the rs13431652-A and rs573225-A alleles in the G6PC2 promoter that are strongly associated with elevated fasting glucose levels.

Bouatia-Naji N, Bonnefond A, Baerenwald DA, Marchand M, Bugliani M, Marchetti P, Pattou F, Printz RL, Flemming BP, Umunakwe OC, Conley NL, Vaxillaire M, Lantieri O, Balkau B, Marre M, Lévy-Marchal C, Elliott P, Jarvelin MR, Meyre D, Dina C, Oeser JK, Froguel P, O'Brien RM.

Diabetes. 2010 Oct;59(10):2662-71. doi: 10.2337/db10-0389. Epub 2010 Jul 9.


G-allele of intronic rs10830963 in MTNR1B confers increased risk of impaired fasting glycemia and type 2 diabetes through an impaired glucose-stimulated insulin release: studies involving 19,605 Europeans.

Sparsø T, Bonnefond A, Andersson E, Bouatia-Naji N, Holmkvist J, Wegner L, Grarup N, Gjesing AP, Banasik K, Cavalcanti-Proença C, Marchand M, Vaxillaire M, Charpentier G, Jarvelin MR, Tichet J, Balkau B, Marre M, Lévy-Marchal C, Faerch K, Borch-Johnsen K, Jørgensen T, Madsbad S, Poulsen P, Vaag A, Dina C, Hansen T, Pedersen O, Froguel P.

Diabetes. 2009 Jun;58(6):1450-6. doi: 10.2337/db08-1660. Epub 2009 Mar 26.


Smallness for gestational age interacts with high mobility group A2 gene genetic variation to modulate height.

Bouatia-Naji N, Marchand M, Cavalcanti-Proença C, Daghmoun S, Durand E, Tichet J, Marre M, Balkau B, Froguel P, Lévy-Marchal C.

Eur J Endocrinol. 2009 Apr;160(4):557-60. doi: 10.1530/EJE-08-0794. Epub 2009 Jan 12.


A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk.

Bouatia-Naji N, Bonnefond A, Cavalcanti-Proença C, Sparsø T, Holmkvist J, Marchand M, Delplanque J, Lobbens S, Rocheleau G, Durand E, De Graeve F, Chèvre JC, Borch-Johnsen K, Hartikainen AL, Ruokonen A, Tichet J, Marre M, Weill J, Heude B, Tauber M, Lemaire K, Schuit F, Elliott P, Jørgensen T, Charpentier G, Hadjadj S, Cauchi S, Vaxillaire M, Sladek R, Visvikis-Siest S, Balkau B, Lévy-Marchal C, Pattou F, Meyre D, Blakemore AI, Jarvelin MR, Walley AJ, Hansen T, Dina C, Pedersen O, Froguel P.

Nat Genet. 2009 Jan;41(1):89-94. doi: 10.1038/ng.277. Epub 2008 Dec 7.


Neonatal diabetes mellitus because of pancreatic agenesis with dysmorphic features and recurrent bacterial infections.

Taha D, Bardise J, Hegab A, Bonnefond A, Marchand M, Drunat S, Vaxillaire M, Polak M.

Pediatr Diabetes. 2008 Jun;9(3 Pt 1):240-4. doi: 10.1111/j.1399-5448.2007.00365.x.


A polymorphism within the G6PC2 gene is associated with fasting plasma glucose levels.

Bouatia-Naji N, Rocheleau G, Van Lommel L, Lemaire K, Schuit F, Cavalcanti-Proença C, Marchand M, Hartikainen AL, Sovio U, De Graeve F, Rung J, Vaxillaire M, Tichet J, Marre M, Balkau B, Weill J, Elliott P, Jarvelin MR, Meyre D, Polychronakos C, Dina C, Sladek R, Froguel P.

Science. 2008 May 23;320(5879):1085-8. doi: 10.1126/science.1156849. Epub 2008 May 1.

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