METHOD FOR THE EXPANSION AND DIFFERENTIATION OF T LYMPHOCYTES AND NK CELLS IN ADOPTIVE TRANSFER THERAPIES
LEON MONZON KALET, ORTIZ MIRANDA YAQUELIN, IRVING MELITA, CRIBIOLI ELISABETTA, CORRIA OSORIO ANGEL DE JESUS, MONTALVO BEREAU GALIA MAGELA, COUKOS GEORGE
Year of Publication 10.12.2021
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Year of Publication 10.12.2021
Patent
MÉTODO PARA LA EXPANSIÓN Y DIFERENCIACIÓN DE LINFOCITOS T Y CÉLULAS NK EN TERAPIAS DE TRANSFERENCIA ADOPTIVA
CORRIA OSORIO, NGELA DE JESS, CRIBIOLI, ELISABETTA, COUKOS, GEORGE, ORTIZ MIRANDA, YAQUELN, LEN MONZN, KALET, MONTALVO BEREAU, MAGELA, IRVING, MELITA
Year of Publication 29.09.2021
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Year of Publication 29.09.2021
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Method for T lymphocytes and NK cells expansion and differentiation for adoptive cell therapies
LEON MONZON, KALET, CRIBIOLI, ELISABETTA, ORTIZ MIRANDA, YAQUELIN, COUKOS, GEORGE, CORRIA OSORIO, ANGEL DE JESUS, MONTALVO BEREAU, MAGELA, IRVING, MELITA
Year of Publication 16.01.2021
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Year of Publication 16.01.2021
Patent
MÉTODO PARA LA EXPANSIÓN Y DIFERENCIACIÓN DE LINFOCITOS T Y CÉLULAS NK EN TERAPIAS DE TRANSFERENCIA ADOPTIVA
Montalvo Bereau, Galia Magela, León Monzón, Kalet, Ortiz Miranda, Yaquelin, Corria Osorio, Ángel de Jesús, Coukos, George, Cribioli, Elisabetta, Irving, Melita
Year of Publication 20.10.2020
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Year of Publication 20.10.2020
Patent
Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation
Fitzgerald, Tomas W, Kaplanis, Joanna, Aitken, Stuart, Jones, Philip, Singh, Tarjinder, Banka, Siddharth, Baralle, Diana, Barnicoat, Angela, Berg, Jonathan, Blair, Edward, Bohanna, David, Bourdon, Louise, Bourn, David, Bradley, Lisa, Brewer, Carole, Bunyan, David J, Chatzimichali, Elena, Clasper, Susan, Cole, Trevor, Colgiu, Irina, Collins, Amanda, Davidson, Rosemarie, Donaldson, Alan, Donnelly, Carina, Douglas, Angela, Douzgou, Sofia, Ellard, Sian, Ellis, Ian, Evans, Karenza, Everest, Sarah, Gardiner, Carol, Ghali, Neeti, Gibbons, Richard, Gill, Harinder, Goodship, Judith, Gray, Emma, Greene, Philip, Liu, He, Hellens, Stephen, Hildyard, Lucy, Holder, Muriel, Hutton, Ben, Ingram, Stuart, Irving, Melita, Josifova, Dragana, Joss, Shelagh, Kazembe, Sandra, Kerr, Bronwyn, Kingston, Helen, Kirby, Gail, Kirk, Claire, Kumar, Dhavendra, Vk Ajith Kumar, Lachlan, Katherine, Magee, Alex, Male, Alison, Mcconnell, Vivienne, Mckay, Kirsten, Mcmullan, Dominic J, Mcnerlan, Susan, Middleton, Anna, Miedzybrodzka, Zosia, Mohammed, Shehla, Morgan, Sian, Nemeth, Andrea, Parker, Michael J, Paterson, Joan, Perrett, Daniel, Pottinger, Caroline, Price, Sue, Ragge, Nicola, Rankin, Julia, Rice, Debbie, Samant, Shalaka, Schweiger, Susann, Scott, Richard, Selby, Ann, Seller, Anneke, Shears, Debbie, Sheridan, Eamonn, Smithson, Sarah, Splitt, Miranda, Squires, Miranda, Stewart, Fiona, Straub, Volker, Suri, Mohnish, Sutton, Vivienne, Thomson, Jenny, Tysoe, Carolyn, Wakeling, Emma, Whiteford, Margo, Widaa, Sara, Wilcox, Sarah, Wilkinson, Emily, Williams, Nicola, Yates, Laura, Firth, Helen V, Wright, Caroline F, Barrett, Jeffrey C, Hurles, Matthew E
Published in bioRxiv (16.06.2016)
Published in bioRxiv (16.06.2016)
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Possible association between complex congenital heart defects and 11p15 hypomethylation in three patients with severe Silver-Russell syndrome
Ghanim, Mustafa, Rossignol, Sylvie, Delobel, Bruno, Irving, Melita, Miller, Owen, Devisme, Louise, Plennevaux, Jean-Louis, Lucidarme-Rossi, Sophie, Manouvrier, Sylvie, Salah, Azzi, Chivu, Olimpia, Netchine, Irène, Vincent-Delorme, Catherine
Published in American Journal of Medical Genetics Part A (01.03.2013)
Published in American Journal of Medical Genetics Part A (01.03.2013)
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