Resultados de procura - d’Escamard, Valentina
- Mostrando 1 - 16 Resultados de 16
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Ablation of oncogenic ALK is a viable therapeutic approach for anaplastic large-cell lymphomas por Piva, Roberto, Chiarle, Roberto, Manazza, Andrea D., Taulli, Riccardo, Simmons, William, Ambrogio, Chiara, D'Escamard, Valentina, Pellegrino, Elisa, Ponzetto, Carola, Palestro, Giorgio, Inghirami, Giorgio
Publicado 2006Text -
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FOXO3-mTOR Metabolic Cooperation in the Regulation of Erythroid Cell Maturation and Homeostasis por Zhang, Xin, Campreciós, Genís, Rimmelé, Pauline, Liang, Raymond, Yalcin, Safak, Mungamuri, Sathish Kumar, Barminko, Jeffrey, D’Escamard, Valentina, Baron, Margaret H., Brugnara, Carlo, Papatsenko, Dmitri, Rivella, Stefano, Ghaffari, Saghi
Publicado 2014Text -
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Tissue-Resident PDGFRα(+) Progenitor Cells Contribute to Fibrosis versus Healing in a Context- and Spatiotemporally Dependent Manner por Santini, Maria Paola, Malide, Daniela, Hoffman, Gabriel, Pandey, Gaurav, D’Escamard, Valentina, Nomura-Kitabayashi, Aya, Rovira, Ilsa, Kataoka, Hiroshi, Ochando, Jordi, Harvey, Richard P., Finkel, Toren, Kovacic, Jason C.
Publicado 2020Text -
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Integrative Prioritization of Causal Genes for Coronary Artery Disease por Hao, Ke, Ermel, Raili, Sukhavasi, Katyayani, Cheng, Haoxiang, Ma, Lijiang, Li, Ling, Amadori, Letizia, Koplev, Simon, Franzén, Oscar, d’Escamard, Valentina, Chandel, Nirupama, Wolhuter, Kathryn, Bryce, Nicole S., Venkata, Vamsidhar RM, Miller, Clint L., Ruusalepp, Arno, Schunkert, Heribert, Björkegren, Johan L.M., Kovacic, Jason C.
Publicado 2022Text -
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Matricellular Protein CCN5 Reverses Established Cardiac Fibrosis por Jeong, Dongtak, Lee, Min-Ah, Li, Yan, Yang, Dong Kwon, Kho, Changwon, Oh, Jae Gyun, Hong, Gyeongdeok, Lee, Ahyoung, Song, Min Ho, LaRocca, Thomas J., Chen, Jiqiu, Liang, Lifan, Mitsuyama, Shinichi, D’Escamard, Valentina, Kovacic, Jason C., Kwak, Tae Hwan, Hajjar, Roger J., Park, Woo Jin
Publicado 2016Text -
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CD90 Identifies Adventitial Mesenchymal Progenitor Cells in Adult Human Medium- and Large-Sized Arteries por Michelis, Katherine C., Nomura-Kitabayashi, Aya, Lecce, Laura, Franzén, Oscar, Koplev, Simon, Xu, Yang, Santini, Maria Paola, D'Escamard, Valentina, Lee, Jonathan T.L., Fuster, Valentin, Hajjar, Roger, Reddy, Ramachandra C., Chikwe, Joanna, Stelzer, Paul, Filsoufi, Farzan, Stewart, Allan, Anyanwu, Anelechi, Björkegren, Johan L.M., Kovacic, Jason C.
Publicado 2018Text -
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The HDAC9-associated risk locus promotes coronary artery disease by governing TWIST1 por Ma, Lijiang, Bryce, Nicole S., Turner, Adam W., Di Narzo, Antonio F., Rahman, Karishma, Xu, Yang, Ermel, Raili, Sukhavasi, Katyayani, d’Escamard, Valentina, Chandel, Nirupama, V’Gangula, Bhargavi, Wolhuter, Kathryn, Kadian-Dodov, Daniella, Franzen, Oscar, Ruusalepp, Arno, Hao, Ke, Miller, Clint L., Björkegren, Johan L. M., Kovacic, Jason C.
Publicado 2022Text -
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Endothelial to mesenchymal transition is common in atherosclerotic lesions and is associated with plaque instability por Evrard, Solene M., Lecce, Laura, Michelis, Katherine C., Nomura-Kitabayashi, Aya, Pandey, Gaurav, Purushothaman, K-Raman, d'Escamard, Valentina, Li, Jennifer R., Hadri, Lahouaria, Fujitani, Kenji, Moreno, Pedro R., Benard, Ludovic, Rimmele, Pauline, Cohain, Ariella, Mecham, Brigham, Randolph, Gwendalyn J., Nabel, Elizabeth G., Hajjar, Roger, Fuster, Valentin, Boehm, Manfred, Kovacic, Jason C.
Publicado 2016Text -
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Corrigendum: Endothelial to mesenchymal transition is common in atherosclerotic lesions and is associated with plaque instability por Evrard, Solene M., Lecce, Laura, Michelis, Katherine C., Nomura-Kitabayashi, Aya, Pandey, Gaurav, Purushothaman, K-Raman, d'Escamard, Valentina, Li, Jennifer R., Hadri, Lahouaria, Fujitani, Kenji, Moreno, Pedro R., Benard, Ludovic, Rimmele, Pauline, Cohain, Ariella, Mecham, Brigham, Randolph, Gwendalyn J., Nabel, Elizabeth G., Hajjar, Roger, Fuster, Valentin, Boehm, Manfred, Kovacic, Jason C.
Publicado 2017Text -
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A plasma proteogenomic signature for fibromuscular dysplasia por Olin, Jeffrey W, Di Narzo, Antonio F, d’Escamard, Valentina, Kadian-Dodov, Daniella, Cheng, Haoxiang, Georges, Adrien, King, Annette, Thomas, Allison, Barwari, Temo, Michelis, Katherine C, Bouchareb, Rihab, Bander, Emir, Anyanwu, Anelechi, Stelzer, Paul, Filsoufi, Farzan, Florman, Sander, Civelek, Mete, Debette, Stephanie, Jeunemaitre, Xavier, Björkegren, Johan L M, Mayr, Manuel, Bouatia-Naji, Nabila, Hao, Ke, Kovacic, Jason C
Publicado 2020Text -
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Histone deacetylase 9 promotes endothelial-mesenchymal transition and an unfavorable atherosclerotic plaque phenotype por Lecce, Laura, Xu, Yang, V’Gangula, Bhargavi, Chandel, Nirupama, Pothula, Venu, Caudrillier, Axelle, Santini, Maria Paola, d’Escamard, Valentina, Ceholski, Delaine K., Gorski, Przemek A., Ma, Lijiang, Koplev, Simon, Bjørklund, Martin Mæng, Björkegren, Johan L.M., Boehm, Manfred, Bentzon, Jacob Fog, Fuster, Valentin, Kim, Ha Won, Weintraub, Neal L., Baker, Andrew H., Bernstein, Emily, Kovacic, Jason C.
Publicado 2021Text -
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PHACTR1 Is a Genetic Susceptibility Locus for Fibromuscular Dysplasia Supporting Its Complex Genetic Pattern of Inheritance por Kiando, Soto Romuald, Tucker, Nathan R., Castro-Vega, Luis-Jaime, Katz, Alexander, D’Escamard, Valentina, Tréard, Cyrielle, Fraher, Daniel, Albuisson, Juliette, Kadian-Dodov, Daniella, Ye, Zi, Austin, Erin, Yang, Min-Lee, Hunker, Kristina, Barlassina, Cristina, Cusi, Daniele, Galan, Pilar, Empana, Jean-Philippe, Jouven, Xavier, Gimenez-Roqueplo, Anne-Paule, Bruneval, Patrick, Hyun Kim, Esther Soo, Olin, Jeffrey W., Gornik, Heather L., Azizi, Michel, Plouin, Pierre-François, Ellinor, Patrick T., Kullo, Iftikhar J., Milan, David J., Ganesh, Santhi K., Boutouyrie, Pierre, Kovacic, Jason C., Jeunemaitre, Xavier, Bouatia-Naji, Nabila
Publicado 2016Text -
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Rare loss-of-function mutations of PTGIR are enriched in fibromuscular dysplasia por Georges, Adrien, Albuisson, Juliette, Berrandou, Takiy, Dupré, Délia, Lorthioir, Aurélien, D’Escamard, Valentina, Di Narzo, Antonio F, Kadian-Dodov, Daniella, Olin, Jeffrey W, Warchol-Celinska, Ewa, Prejbisz, Aleksander, Januszewicz, Andrzej, Bruneval, Patrick, Baranowska, Anna A, Webb, Tom R, Hamby, Stephen E, Samani, Nilesh J, Adlam, David, Fendrikova-Mahlay, Natalia, Hazen, Stanley, Wang, Yu, Yang, Min-Lee, Hunker, Kristina, Combaret, Nicolas, Motreff, Pascal, Chédid, Antoine, Fiquet, Béatrice, Plouin, Pierre-François, Mousseaux, Elie, Azarine, Arshid, Amar, Laurence, Azizi, Michel, Gornik, Heather L, Ganesh, Santhi K, Kovacic, Jason C, Jeunemaitre, Xavier, Bouatia-Naji, Nabila
Publicado 2020Text -
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Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases por Georges, Adrien, Yang, Min-Lee, Berrandou, Takiy-Eddine, Bakker, Mark K., Dikilitas, Ozan, Kiando, Soto Romuald, Ma, Lijiang, Satterfield, Benjamin A., Sengupta, Sebanti, Yu, Mengyao, Deleuze, Jean-François, Dupré, Delia, Hunker, Kristina L., Kyryachenko, Sergiy, Liu, Lu, Sayoud-Sadeg, Ines, Amar, Laurence, Brummett, Chad M., Coleman, Dawn M., d’Escamard, Valentina, de Leeuw, Peter, Fendrikova-Mahlay, Natalia, Kadian-Dodov, Daniella, Li, Jun Z., Lorthioir, Aurélien, Pappaccogli, Marco, Prejbisz, Aleksander, Smigielski, Witold, Stanley, James C., Zawistowski, Matthew, Zhou, Xiang, Zöllner, Sebastian, Amouyel, Philippe, De Buyzere, Marc L., Debette, Stéphanie, Dobrowolski, Piotr, Drygas, Wojciech, Gornik, Heather L., Olin, Jeffrey W., Piwonski, Jerzy, Rietzschel, Ernst R., Ruigrok, Ynte M., Vikkula, Miikka, Warchol Celinska, Ewa, Januszewicz, Andrzej, Kullo, Iftikhar J., Azizi, Michel, Jeunemaitre, Xavier, Persu, Alexandre, Kovacic, Jason C., Ganesh, Santhi K., Bouatia-Naji, Nabila
Publicado 2021Text -
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Author Correction: Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases por Georges, Adrien, Yang, Min-Lee, Berrandou, Takiy-Eddine, Bakker, Mark K., Dikilitas, Ozan, Kiando, Soto Romuald, Ma, Lijiang, Satterfield, Benjamin A., Sengupta, Sebanti, Yu, Mengyao, Deleuze, Jean-François, Dupré, Delia, Hunker, Kristina L., Kyryachenko, Sergiy, Liu, Lu, Sayoud-Sadeg, Ines, Amar, Laurence, Brummett, Chad M., Coleman, Dawn M., d’Escamard, Valentina, de Leeuw, Peter, Fendrikova-Mahlay, Natalia, Kadian-Dodov, Daniella, Li, Jun Z., Lorthioir, Aurélien, Pappaccogli, Marco, Prejbisz, Aleksander, Smigielski, Witold, Stanley, James C., Zawistowski, Matthew, Zhou, Xiang, Zöllner, Sebastian, Amouyel, Philippe, De Buyzere, Marc L., Debette, Stéphanie, Dobrowolski, Piotr, Drygas, Wojciech, Gornik, Heather L., Olin, Jeffrey W., Piwonski, Jerzy, Rietzschel, Ernst R., Ruigrok, Ynte M., Vikkula, Miikka, Warchol Celinska, Ewa, Januszewicz, Andrzej, Kullo, Iftikhar J., Azizi, Michel, Jeunemaitre, Xavier, Persu, Alexandre, Kovacic, Jason C., Ganesh, Santhi K., Bouatia-Naji, Nabila
Publicado 2022Text