Lentivirus-mediated gene therapy for Fabry disease von Khan, Aneal, Barber, Dwayne L., Huang, Ju, Rupar, C. Anthony, Rip, Jack W., Auray-Blais, Christiane, Boutin, Michel, O’Hoski, Pamela, Gargulak, Kristy, McKillop, William M., Fraser, Graeme, Wasim, Syed, LeMoine, Kaye, Jelinski, Shelly, Chaudhry, Ahsan, Prokopishyn, Nicole, Morel, Chantal F., Couban, Stephen, Duggan, Peter R., Fowler, Daniel H., Keating, Armand, West, Michael L., Foley, Ronan, Medin, Jeffrey A.

Volltext

IDH1(R132H) mutation increases murine haematopoietic progenitors and alters epigenetics von Sasaki, Masato, Knobbe, Christiane B., Munger, Joshua C., Lind, Evan F., Brenner, Dirk, Brüstle, Anne, Harris, Isaac S., Holmes, Roxanne, Wakeham, Andrew, Haight, Jillian, You-Ten, Annick, Li, Wanda Y., Schalm, Stefanie, Su, Shinsan M., Virtanen, Carl, Reifenberger, Guido, Ohashi, Pamela S., Barber, Dwayne L., Figueroa, Maria E., Melnick, Ari, Zúñiga-Pflücker, Juan-Carlos, Mak, Tak W.

Volltext

Turning cells red: signal transduction mediated by erythropoietin von Richmond, Terri D., Chohan, Manprit, Barber, Dwayne L.

Volltext

CBL Linker Region and RING Finger Mutations Lead to Enhanced Granulocyte-Macrophage Colony-stimulating Factor (GM-CSF) Signaling via Elevated Levels of JAK2 and LYN von Javadi, Mojib, Richmond, Terri D., Huang, Kai, Barber, Dwayne L.

Volltext

Myelodysplastic syndromes: the complexity of stem-cell diseases von Corey, Seth J., Minden, Mark D., Barber, Dwayne L., Kantarjian, Hagop, Wang, Jean C. Y., Schimmer, Aaron D.

Volltext

Chopped and diced: Dicer1 deletion generates myeloid dysplasia von Barber, Dwayne L.

Volltext

Random mutagenesis reveals residues of JAK2 critical in evading inhibition by a tyrosine kinase inhibitor von Marit, Michael R, Chohan, Manprit, Matthew, Natasha, Huang, Kai, Kuntz, Douglas A, Rose, David R, Barber, Dwayne L

Volltext

GRPling with PTEN von Barber, Dwayne L.

Volltext

Loss of JAK2 regulation via a heterodimeric VHL-SOCS1 E3 ubiquitin ligase underlies Chuvash polycythemia von Russell, Ryan C, Sufan, Roxana I, Zhou, Bing, Heir, Pardeep, Bunda, Severa, Sybingco, Stephanie S, Greer, Samantha N, Roche, Olga, Heathcote, Samuel A, Chow, Vinca W K, Boba, Lukasz M, Richmond, Terri D, Hickey, Michele M, Barber, Dwayne L, Cheresh, David A, Simon, M Celeste, Irwin, Meredith S, Kim, William Y, Ohh, Michael

Volltext

Persistent hematopoietic polyclonality after lentivirus-mediated gene therapy for Fabry disease von Saleh, Amr H., Rothe, Michael, Barber, Dwayne L., McKillop, William M., Fraser, Graeme, Morel, Chantal F., Schambach, Axel, Auray-Blais, Christiane, West, Michael L., Khan, Aneal, Fowler, Daniel H., Rupar, C. Anthony, Foley, Ronan, Medin, Jeffrey A., Keating, Armand

Volltext

Lentivirus‐mediated gene therapy for Fabry disease: 5‐year End‐of‐Study results from the Canadian FACTs trial von Khan, Aneal, Barber, Dwayne L., McKillop, William M., Rupar, C. Anthony, Auray‐Blais, Christiane, Fraser, Graeme, Fowler, Daniel H., Berger, Alexandra, Foley, Ronan, Keating, Armand, West, Michael L., Medin, Jeffrey A.

Volltext

The inositol phosphatase SHIP-1 is negatively regulated by Fli-1 and its loss accelerates leukemogenesis von Lakhanpal, Gurpreet K., Vecchiarelli-Federico, Laura M., Li, You-Jun, Cui, Jiu-Wei, Bailey, Monica L., Spaner, David E., Dumont, Daniel J., Barber, Dwayne L., Ben-David, Yaacov

Volltext

Lentivector Iterations and Pre-Clinical Scale-Up/Toxicity Testing: Targeting Mobilized CD34 + Cells for Correction of Fabry Disease von Huang, Ju, Khan, Aneal, Au, Bryan C, Barber, Dwayne L, López-Vásquez, Lucía, Prokopishyn, Nicole L, Boutin, Michel, Rothe, Michael, Rip, Jack W, Abaoui, Mona, Nagree, Murtaza S, Dworski, Shaalee, Schambach, Axel, Keating, Armand, West, Michael L, Klassen, John, Turner, Patricia V, Sirrs, Sandra, Rupar, C Anthony, Auray-Blais, Christiane, Foley, Ronan, Medin, Jeffrey A

Volltext

STAT1 promotes megakaryopoiesis downstream of GATA-1 in mice von Huang, Zan, Richmond, Terri D, Muntean, Andrew G, Barber, Dwayne L, Weiss, Mitchell J, Crispino, John D

Volltext

The T Cell Protein Tyrosine Phosphatase Is a Negative Regulator of Janus Family Kinases 1 and 3 von Simoncic, Paul D., Lee-Loy, Ailsa, Barber, Dwayne L., Tremblay, Michel L., McGlade, C.Jane

Volltext

Src homology 2 domain–containing inositol 5-phosphatase 1 deficiency leads to a spontaneous allergic inflammation in the murine lung von Oh, Sun-Young, PhD, Zheng, Tao, MD, Bailey, Monica L., BS, Barber, Dwayne L., PhD, Schroeder, John T., PhD, Kim, Yoon-Keun, MD, PhD, Zhu, Zhou, MD, PhD

Volltext

Tyrosine kinase chromosomal translocations mediate distinct and overlapping gene regulation events von Kim, Hani, Gillis, Lisa C, Jarvis, Jordan D, Yang, Stuart, Huang, Kai, Der, Sandy, Barber, Dwayne L

Volltext

The SH2B1 Adaptor Protein Associates with a Proximal Region of the Erythropoietin Receptor von Javadi, Mojib, Hofstätter, Edda, Stickle, Natalie, Beattie, Bryan K., Jaster, Robert, Carter-Su, Christin, Barber, Dwayne L.

Volltext

Truth or dare: role of Liar in EPO-dependent signaling von Barber, Dwayne L.

Volltext

Ibrutinib synergizes with poly(ADP-ribose) glycohydrolase inhibitors to induce cell death in AML cells via a BTK-independent mechanism von Rotin, Lianne E, Gronda, Marcela, MacLean, Neil, Hurren, Rose, Wang, XiaoMing, Lin, Feng-Hsu, Wrana, Jeff, Datti, Alessandro, Barber, Dwayne L, Minden, Mark D, Slassi, Malik, Schimmer, Aaron D

Volltext