CD74 is expressed in a subset of pediatric acute myeloid leukemia patients and is a promising target for therapy: a report from the Children's Oncology Group
Menssen, Andrew J, Hudson, Chad A, Alonzo, Todd, Gerbing, Robert, Pardo, Laura, Leonti, Amanda, Cook, Jacqueline A, Hsu, Fan-Chi, Lott, Loren L, Dai, Fangyan, Fearing, Collette, Ghirardelli, Keely, Hylkema, Tiffany, Tarlock, Katherine, Loeb, Keith R, Kolb, Edward A, Cooper, Todd, Pollard, Jessica, Wells, Denise A, Loken, Michael R, Aplenc, Richard, Meshinchi, Soheil, Brodersen, Lisa Eidenschink
Published in Haematologica (Roma) (01.02.2024)
Published in Haematologica (Roma) (01.02.2024)
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Addressing a Pre-Clinical Pipeline Gap: Development of the Pediatric Acute Myeloid Leukemia Patient-Derived Xenograft Program at Texas Children's Hospital at Baylor College of Medicine
Stevens, Alexandra M, Terrell, Maci, Rashid, Raushan, Fisher, Kevin E, Marcogliese, Andrea N, Gaikwad, Amos, Rao, Pulivarthi, Vrana, Chelsea, Krueger, Michael, Loken, Michael, Menssen, Andrew J, Cook, Jacqueline A, Keogh, Noah, Alozie, Michelle, Oviedo, Hailey, Gonzalez, Alan K, Ilangovan, Tamilini, Kim, Julia, Sandhu, Sohani, Redell, Michele S
Published in Biomedicines (01.02.2024)
Published in Biomedicines (01.02.2024)
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Fusion-harboring mast cells can explain molecular positivity in flow cytometric MRD-negative core-binding factor AML
Cook, Jacqueline A., Lott, Loren, Perry, Jenna, Eckel, Ashley M., Xu, Dongbin, Hudson, Chad A., Wells, Denise A., Loken, Michael R., Menssen, Andrew J.
Published in Blood (01.08.2024)
Published in Blood (01.08.2024)
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Residual Mast Cells Can Explain Persistent Molecular Positivity in Difference from Normal Flow Cytometric-Defined MRD Negative Core Binding Factor AML
Cook, Jacqueline A., Lott, Loren, Perry, Jenna, Nalla, Arun, Xu, Dongbin, Hudson, Chad A., Wells, Denise A., Loken, Michael R., Menssen, Andrew J.
Published in Blood (02.11.2023)
Published in Blood (02.11.2023)
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Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism
Ansari, Morad, Poke, Gemma, Ferry, Quentin, Williamson, Kathleen, Aldridge, Roland, Meynert, Alison M, Bengani, Hemant, Chan, Cheng Yee, Kayserili, Hülya, Avci, Şahin, Hennekam, Raoul C M, Lampe, Anne K, Redeker, Egbert, Homfray, Tessa, Ross, Alison, Falkenberg Smeland, Marie, Mansour, Sahar, Parker, Michael J, Cook, Jacqueline A, Splitt, Miranda, Fisher, Richard B, Fryer, Alan, Magee, Alex C, Wilkie, Andrew, Barnicoat, Angela, Brady, Angela F, Cooper, Nicola S, Mercer, Catherine, Deshpande, Charu, Bennett, Christopher P, Pilz, Daniela T, Ruddy, Deborah, Cilliers, Deirdre, Johnson, Diana S, Josifova, Dragana, Rosser, Elisabeth, Thompson, Elizabeth M, Wakeling, Emma, Kinning, Esther, Stewart, Fiona, Flinter, Frances, Girisha, Katta M, Cox, Helen, Firth, Helen V, Kingston, Helen, Wee, Jamie S, Hurst, Jane A, Clayton-Smith, Jill, Tolmie, John, Vogt, Julie, Tatton–Brown, Katrina, Chandler, Kate, Prescott, Katrina, Wilson, Louise, Behnam, Mahdiyeh, McEntagart, Meriel, Davidson, Rosemarie, Lynch, Sally-Ann, Sisodiya, Sanjay, Mehta, Sarju G, McKee, Shane A, Mohammed, Shehla, Holden, Simon, Park, Soo-Mi, Holder, Susan E, Harrison, Victoria, McConnell, Vivienne, Lam, Wayne K, Green, Andrew J, Donnai, Dian, Bitner-Glindzicz, Maria, Donnelly, Deirdre E, Nellåker, Christoffer, Taylor, Martin S, FitzPatrick, David R
Published in Journal of medical genetics (01.10.2014)
Published in Journal of medical genetics (01.10.2014)
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