The influence of flow and thermal properties on injection pressure and cooling time prediction von Huszar, Marton, Belblidia, Fawzi, Alston, Sue, Wlodarski, Patrick, Arnold, Cris, Bould, David, Sienz, Johann

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On the optimisation of mechanical properties of PP moulded parts von Huszar, Marton, Belblidia, Fawzi, Wlodarski, Patrick, Arnold, Cris, Sienz, Johann, Bould, David

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Genotype‐phenotype correlation and molecular heterogeneity in pyruvate kinase deficiency von Bianchi, Paola, Fermo, Elisa, Lezon‐Geyda, Kimberly, Beers, Eduard J., Morton, Holmes D., Barcellini, Wilma, Glader, Bertil, Chonat, Satheesh, Ravindranath, Yaddanapudi, Newburger, Peter E., Kollmar, Nina, Despotovic, Jenny M., Verhovsek, Madeleine, Sharma, Mukta, Kwiatkowski, Janet L., Kuo, Kevin H. M., Wlodarski, Marcin W., Yaish, Hassan M., Holzhauer, Susanne, Wang, Heng, Kunz, Joachim, Addonizio, Kathryn, Al‐Sayegh, Hasan, London, Wendy B., Andres, Oliver, Wijk, Richard, Gallagher, Patrick G., Grace, Rachael F. F.

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Gain-of-function mutations in RPA1 cause a syndrome with short telomeres and somatic genetic rescue von Sharma, Richa, Sahoo, Sushree S., Honda, Masayoshi, Granger, Sophie L., Goodings, Charnise, Sanchez, Louis, Künstner, Axel, Busch, Hauke, Beier, Fabian, Pruett-Miller, Shondra M., Valentine, Marcus B., Fernandez, Alfonso G., Chang, Ti-Cheng, Géli, Vincent, Churikov, Dmitri, Hirschi, Sandrine, Pastor, Victor B., Boerries, Melanie, Lauten, Melchior, Kelaidi, Charikleia, Cooper, Megan A., Nicholas, Sarah, Rosenfeld, Jill A., Polychronopoulou, Sophia, Kannengiesser, Caroline, Saintomé, Carole, Niemeyer, Charlotte M., Revy, Patrick, Wold, Marc S., Spies, Maria, Erlacher, Miriam, Coulon, Stéphane, Wlodarski, Marcin W.

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Frequency and prognostic impact of mutations in SRSF2, U2AF1, and ZRSR2 in patients with myelodysplastic syndromes von Thol, Felicitas, Kade, Sofia, Schlarmann, Carola, Löffeld, Patrick, Morgan, Michael, Krauter, Jürgen, Wlodarski, Marcin W., Kölking, Britta, Wichmann, Martin, Görlich, Kerstin, Göhring, Gudrun, Bug, Gesine, Ottmann, Oliver, Niemeyer, Charlotte M., Hofmann, Wolf-Karsten, Schlegelberger, Brigitte, Ganser, Arnold, Heuser, Michael

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Clinical spectrum of pyruvate kinase deficiency: data from the Pyruvate Kinase Deficiency Natural History Study von Grace, Rachael F., Bianchi, Paola, van Beers, Eduard J., Eber, Stefan W., Glader, Bertil, Yaish, Hassan M., Despotovic, Jenny M., Rothman, Jennifer A., Sharma, Mukta, McNaull, Melissa M., Fermo, Elisa, Lezon-Geyda, Kimberly, Morton, D. Holmes, Neufeld, Ellis J., Chonat, Satheesh, Kollmar, Nina, Knoll, Christine M., Kuo, Kevin, Kwiatkowski, Janet L., Pospíšilová, Dagmar, Pastore, Yves D., Thompson, Alexis A., Newburger, Peter E., Ravindranath, Yaddanapudi, Wang, Winfred C., Wlodarski, Marcin W., Wang, Heng, Holzhauer, Susanne, Breakey, Vicky R., Kunz, Joachim, Sheth, Sujit, Rose, Melissa J., Bradeen, Heather A., Neu, Nolan, Guo, Dongjing, Al-Sayegh, Hasan, London, Wendy B., Gallagher, Patrick G., Zanella, Alberto, Barcellini, Wilma

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A metabolic interplay coordinated by HLX regulates myeloid differentiation and AML through partly overlapping pathways von Piragyte, Indre, Clapes, Thomas, Polyzou, Aikaterini, Klein Geltink, Ramon I., Lefkopoulos, Stylianos, Yin, Na, Cauchy, Pierre, Curtis, Jonathan D., Klaeylé, Lhéanna, Langa, Xavier, Beckmann, Cora C. A., Wlodarski, Marcin W., Müller, Patrick, Van Essen, Dominic, Rambold, Angelika, Kapp, Friedrich G., Mione, Marina, Buescher, Joerg M., Pearce, Erika L., Polyzos, Alexander, Trompouki, Eirini

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Synonymous GATA2 mutations result in selective loss of mutated RNA and are common in patients with GATA2 deficiency von Kozyra, Emilia J., Pastor, Victor B., Lefkopoulos, Stylianos, Sahoo, Sushree S., Busch, Hauke, Voss, Rebecca K., Erlacher, Miriam, Lebrecht, Dirk, Szvetnik, Enikoe A., Hirabayashi, Shinsuke, Pasaulienė, Ramunė, Pedace, Lucia, Tartaglia, Marco, Klemann, Christian, Metzger, Patrick, Boerries, Melanie, Catala, Albert, Hasle, Henrik, de Haas, Valerie, Kállay, Krisztián, Masetti, Riccardo, De Moerloose, Barbara, Dworzak, Michael, Schmugge, Markus, Smith, Owen, Starý, Jan, Mejstrikova, Ester, Ussowicz, Marek, Morris, Emma, Singh, Preeti, Collin, Matthew, Derecka, Marta, Göhring, Gudrun, Flotho, Christian, Strahm, Brigitte, Locatelli, Franco, Niemeyer, Charlotte M., Trompouki, Eirini, Wlodarski, Marcin W.

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Biallelic inactivation of the NF1 tumour suppressor gene in juvenile myelomonocytic leukaemia: Genetic evidence of driver function and implications for diagnostic workup von Ramamoorthy, Senthilkumar, Lebrecht, Dirk, Schanze, Denny, Schanze, Ina, Wieland, Ilse, Andrieux, Geoffroy, Metzger, Patrick, Hess, Maria, Albert, Michael H., Borkhardt, Arndt, Bresters, Dorine, Buechner, Jochen, Catala, Albert, De Haas, Valerie, Dworzak, Michael, Erlacher, Miriam, Hasle, Henrik, Jahnukainen, Kirsi, Locatelli, Franco, Masetti, Riccardo, Stary, Jan, Turkiewicz, Dominik, Vinci, Luca, Wlodarski, Marcin W., Yoshimi, Ayami, Boerries, Melanie, Niemeyer, Charlotte M., Zenker, Martin, Flotho, Christian

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Phenotypic differences between healthy effector CTL and leukemic LGL cells support the notion of antigen-triggered clonal transformation in T-LGL leukemia von Wlodarski, Marcin W., Nearman, Zachary, Jankowska, Anna, Babel, Nina, Powers, Jennifer, Leahy, Patrick, Volk, Hans‐Dieter, Maciejewski, Jaroslaw P.

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Gain-of-function mutations in RPA1 cause a syndrome with short telomeres and somatic genetic rescue von Sharma, Richa, Sahoo, Sushree, Honda, Masayoshi, Granger, Sophie, Goodings, Charnise, Sanchez, Louis, Künstner, Axel, Busch, Hauke, Beier, Fabian, Pruett-Miller, Shondra, Valentine, Marcus, Fernandez, Alfonso, Chang, Ti-Cheng, Géli, Vincent, Churikov, Dmitri, Hirschi, Sandrine, Pastor, Victor, Boerries, Melanie, Lauten, Melchior, Kelaidi, Charikleia, Cooper, Megan, Nicholas, Sarah, Rosenfeld, Jill, Polychronopoulou, Sophia, Kannengiesser, Caroline, Saintomé, Carole, Niemeyer, Charlotte, Revy, Patrick, Wold, Marc, Spies, Maria, Erlacher, Miriam, Coulon, Stephane, Wlodarski, Marcin

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Gain-of-Function Mutations in RPA1 Cause a Syndrome with Short Telomeres and Somatic Genetic Rescue von Sharma, Richa, Sahoo, Sushree, Honda, Masayoshi, Granger, Sophie, Goodings, Charnise, Sanchez, Louis, Künstner, Axel, Busch, Hauke, Beier, Fabian, Pruett-Miller, Shondra, Valentine, Marcus, Fernandez, Alfonso Gonzalez, Chang, Ti-Cheng, Géli, Vincent, Churikov, Dmitri, Hirschi, Sandrine, Pastor, Victor, Boerries, Melanie, Lauten, Melchior, Kelaidi, Charikleia, Wlodarski, Marcin, Cooper, Megan Anne, Nicholas, Sarah, Rosenfeld, Jill, Polychronopoulou, Sophia, Kannengiesser, Caroline, Saintome, Carole, Niemeyer, Charlotte, Revy, Patrick, Wold, Marc, Spies, Maria, Erlacher, Miriam, Coulon, Stéphane

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Molecular Characterization of 140 Patients in the Pyruvate Kinase Deficiency (PKD) Natural History Study (NHS): Report of 20 New Variants von Bianchi, Paola, Fermo, Elisa, Lezon-Geyda, Kimberly, Gallagher, Patrick G., Morton, D Holmes, Barcellini, Wilma, Glader, Bertil, Eber, Stefan W., Despotovic, Jenny M., Knoll, Christine M., Yaish, Hassan M., Newburger, Peter E., Rothman, Jennifer, Thompson, Alexis A., Ravindranath, Yaddanapudi, Nottage, Kerri A, Wang, Heng, van Beers, Eduard J., Kunz, Joachim, Wlodarski, Marcin W, Sharma, Mukta, Rose, Melissa J., Pastore, Yves D., Giardina, Patricia J., Rhodes, Melissa, Kuo, Kevin, Guo, Dongjing, London, Wendy B., Grace, Rachael F.

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Synonymous GATA2 mutations result in selective loss of mutated RNA and are common in patients with GATA2 deficiency von Kozyra, Emilia J, Pastor, Victor B, Lefkopoulos, Stylianos, Sahoo, Sushree S, Busch, Hauke, Voss, Rebecca K, Erlacher, Miriam, Lebrecht, Dirk, Szvetnik, Enikoe A, Hirabayashi, Shinsuke, Pasauliene, Ramunè, Pedace, Lucia, Tartaglia, Marco, Klemann, Christian, Metzger, Patrick, Boerries, Melanie, Catala, Albert, Hasle, Henrik, de Haas, Valerie, Kallay, Krisztian, Masetti, Riccardo, De Moerloose, Barbara, Dworzak, Michael, Schmugge, Markus, Smith, Owen, Stary, Jan, Mejstrikova, Ester, Ussowicz, Marek, Morris, Emma, Singh, Preeti, Collin, Matthew, Derecka, Marta, Göhring, Gudrun, Flotho, Christian, Strahm, Brigitte, Locatelli, Franco, Niemeyer, Charlotte M, Trompouki, Eirini, Wlodarski, Marcin W

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Genotype-Phenotype Correlation and Molecular Heterogeneity in Pyruvate Kinase Deficiency: Data from the PKD Natural History Study von Bianchi, Paola, Fermo, Elisa, Lezon-Geyda, Kimberly, Gallagher, Patrick G., van Wijk, Richard, Van Beers, Eduard J., Yaish, Hassan M., Kwiatkowski, Janet L., Newburger, Peter E., Ravindranath, Yaddanapudi, Andres, Oliver, Barcellini, Wilma, Morton, D. Holmes, Glader, Bertil, Eber, Stefan W., Chonat, Satheesh, Kollmar, Nina, Despotovic, Jenny M., Knoll, Christine M., Kuo, Kevin H.M., Pospisilova, Dagmar, Pastore, Yves D., Thompson, Alexis A, Wang, Winfred, Wlodarski, Marcin W., Rothman, Jennifer A., Wang, Heng, Holzhauer, Suzanne, Breakey, Vicky R., Kunz, Joachim B., Sheth, Sujit, Sharma, Mukta, Rose, Melissa J., Bradeen, Heather A., McNaull, Melissa N., Ooyama, Gabrielle P., Neu, Nolan, Al-Sayegh, Hasan, London, Wendy B., Grace, Rachael F.

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Cytokine Proteome of Terminally Differentiated Effector T Cells and Their Malignant Counterparts in T-LGL. Distinct Changes Consistent with Response to a Viral Pathogen von Wlodarski, Marcin W., Powers, Jennifer, Leahy, Patrick, Maciejewski, Jaroslaw P.

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