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PLoS ONE, ISSN 1932-6203, 09/2014, Volume 9, Issue 9, p. e108578
Background: Pre-term birth (PTB) remains the leading cause of infant mortality and morbidity. Its etiology is multifactorial, with a strong genetic component.... 
ETHNIC-DIFFERENCES | INTERLEUKIN-6 IL-6 | PREMATURE RUPTURE | TUMOR-NECROSIS-FACTOR | INCREASED RISK | MULTIDISCIPLINARY SCIENCES | RACIAL DISPARITY | FACTOR-ALPHA GENE | FAMILIAL PATTERNS | FETAL MEMBRANES | TNF-ALPHA | Genetic Predisposition to Disease | Premature Birth - genetics | Receptors, Estrogen - genetics | Infant Mortality | Humans | Autoimmunity - genetics | Infant | Fetal Membranes, Premature Rupture - epidemiology | Premature Birth - epidemiology | STAT1 Transcription Factor - genetics | Interferon Regulatory Factor-3 - genetics | Polymorphism, Genetic | Pregnancy | Fetal Membranes, Premature Rupture - genetics | NF-kappa B - genetics | Pregnancy Complications - genetics | Receptors, Glucocorticoid - genetics | Female | Infant, Newborn | Pregnancy Complications - epidemiology | PPAR gamma - genetics | Membranes | Regulators | Transcription factors | Racial differences | Glucocorticoids | Identification methods | Pathogenesis | Genes | Premature birth | Genomics | Estrogens | Childrens health | Inflammatory response | Genomes | Single-nucleotide polymorphism | Birth | Pathways | Etiology | Genetic factors | Stat1 protein | Cytokines | Infant mortality | Inflammation | Metabolism | Morbidity | Children & youth | Medicine | Studies | Interferon regulatory factor 3 | Womens health | Collagen | Interferon | Peroxisome proliferator-activated receptors
Journal Article
Journal of Molecular Neuroscience, ISSN 0895-8696, 9/2018, Volume 66, Issue 1, pp. 135 - 145
Journal Article
Journal Article
Cardiovascular research, ISSN 0008-6363, 2009, Volume 84, Issue 2, pp. 273 - 282
Our objective was to study the effect of the genetic background on the wound healing process after myocardial infarction (MI) in mice. MI was induced in five... 
Heart failure | Myocardial infarction | Genetic background | Infarct rupture | Inflammatory cells | CARDIAC & CARDIOVASCULAR SYSTEMS | PHENOTYPE | ISCHEMIA | MODEL | FAILURE | RANDOMIZED TRIAL | INHIBITION | GRANULATION-TISSUE | PREVENTS CARDIAC RUPTURE | MICE | TARGETED DELETION | Inflammation - pathology | Myocardial Infarction - genetics | Antihypertensive Agents - pharmacology | Matrix Metalloproteinases - genetics | Species Specificity | Blood Pressure - genetics | Ventricular Function, Left - genetics | Male | RNA, Messenger - metabolism | Time Factors | Atrial Natriuretic Factor - genetics | Myocardial Infarction - pathology | Polymerase Chain Reaction | Myocardial Infarction - physiopathology | Heart Rupture, Post-Infarction - prevention & control | Wound Healing - genetics | Disease Models, Animal | Natriuretic Peptide, Brain - genetics | Echocardiography | Ventricular Pressure - genetics | Mice, Inbred C57BL | Myocardium - pathology | Stroke Volume - genetics | Gene Expression Regulation, Enzymologic | Myocardium - enzymology | Animals | Myocardial Infarction - drug therapy | Inflammation - genetics | Heart Rupture, Post-Infarction - genetics | Mice | Mice, Inbred BALB C | Matrix Metalloproteinases - metabolism | Heart Rupture, Post-Infarction - pathology | Heart Rupture, Post-Infarction - physiopathology | Inflammation - physiopathology
Journal Article
Journal Article
by Bourcier, Romain and Le Scouarnec, Solena and Bonnaud, Stéphanie and Karakachoff, Matilde and Bourcereau, Emmanuelle and Heurtebise-Chrétien, Sandrine and Menguy, Céline and Dina, Christian and Simonet, Floriane and Moles, Alexis and Lenoble, Cédric and Lindenbaum, Pierre and Chatel, Stéphanie and Isidor, Bertrand and Génin, Emmanuelle and Deleuze, Jean-François and Schott, Jean-Jacques and Le Marec, Hervé and Desal, Hubert and Daumas-Duport, Benjamin and Connault, Jérôme and Lebranchu, Pierre and Le Tourneau, Thierry and Viarouge, Marie Pierre and Papagiannaki, Chrisanthi and Piotin, Michel and Redjem, Hocine and Mazighi, Mikael and Desilles, Jean Philippe and Naggara, Olivier and Trystram, Denis and Edjlali-Goujon, Myriam and Rodriguez, Christine and Ben Hassen, Waghi and Saleme, Suzanna and Mounayer, Charbel and Levrier, Olivier and Aguettaz, Pierre and Combaz, Xavier and Pasco, Anne and Berthier, Emeline and Bintner, Marc and Molho, Marc and Gauthier, Pascale and Chivot, Cyril and Costalat, Vincent and Darganzil, Cyril and Bonafé, Alain and Januel, Anne Christine and Michelozzi, Caterina and Cognard, Christophe and Bonneville, Fabrice and Tall, Philippe and Darcourt, Jean and Biondi, Alessandra and Iosif, Cristina and Pomero, Elisa and Ferre, Jean Christophe and Gauvrit, Jean Yves and Eugene, François and Raoult, Hélène and Gentric, Jean Christophe and Ognard, Julien and Anxionnat, René and Bracard, Serge and Derelle, Anne Laure and Tonnelet, Romain and Spelle, Laurent and Ikka, Léon and Fahed, Robert and Rouchaud, Aymeric and Ozanne, Augustin and Caroff, Jildaz and Ben Achour, Nidal and Moret, Jacques and Chabert, Emmanuel and Berge, Jérôme and Marnat, Gaultier and Barreau, Xavier and Gariel, Florent and Clarencon, Frédéric and Aggour, Mohammed and Ricolfi, Frédéric and Chavent, Adrien and Thouant, Pierre and Lebidinsky, Pablo and Lemogne, Brivael and Herbreteau, Denis and Bibi, Richard and Pierot, Laurent and Soize, Sébastien and Labeyrie, Marc Antoine and Vandendries, Christophe and Houdart, Emmanuel and Kazemi, Appoline and Leclerc, Xavier and Pruvo, Jean Pierre and Gallas, Sophie and Velasco, Stéphane and Loirand, Gervaise and ... and ICAN Study Grp and ICAN Study Group
The American Journal of Human Genetics, ISSN 0002-9297, 01/2018, Volume 102, Issue 1, pp. 133 - 141
Journal Article
American Journal of Obstetrics and Gynecology, ISSN 0002-9378, 2010, Volume 203, Issue 4, pp. 361.e1 - 361.e30
Objective We sought to determine whether maternal/fetal single-nucleotide polymorphisms (SNPs) in candidate genes are associated with preterm prelabor rupture... 
Obstetrics and Gynecology | DNA variants | haplotype | high dimensional biology | prematurity | preterm prelabor rupture of membranes | chorioamnionitis | parturition | genetic association study | genotype | genomics | matrix metalloproteinase | single-nucleotide polymorphism | extracellular matrix | INTERLEUKIN-1 RECEPTOR ANTAGONIST | FACTOR-ALPHA GENE | THAN-G POLYMORPHISM | MIDTRIMESTER AMNIOTIC-FLUID | OBSTETRICS & GYNECOLOGY | FALSE DISCOVERY RATE | TUMOR-NECROSIS-FACTOR | PREMATURE-RUPTURE | SINGLE NUCLEOTIDE POLYMORPHISM | HUMAN UTERINE CERVIX | EHLERS-DANLOS-SYNDROME | Haplotypes | Humans | Receptors, Corticotropin-Releasing Hormone - genetics | Male | Autoantigens - genetics | Mothers | Receptors, Prostaglandin E - genetics | Case-Control Studies | Tissue Inhibitor of Metalloproteinase-2 - genetics | alpha-Defensins - genetics | Fetal Membranes, Premature Rupture - genetics | Adult | Female | Fetus | Collagen - genetics | Infant, Newborn | Procollagen | Genetic Association Studies | Endothelin-1 - genetics | Gene Frequency | Collagen Type I | Genotype | Sequence Analysis, DNA | Pregnancy | Chorioamnionitis - pathology | Protein Isoforms | Collagen Type IV - genetics | Models, Genetic | Polymorphism, Single Nucleotide | Receptors, Prostaglandin E, EP1 Subtype | Genetic research | Physiological aspects | Genomics | DNA | Public health | Chorioamnionitis | MMP | SNP | pPROM
Journal Article
BONE & JOINT JOURNAL, ISSN 2049-4394, 03/2013, Volume 95B, Issue 3, pp. 305 - 313
Journal Article