Elastase inhibitors as potential therapies for ELANE‐associated neutropenia von Makaryan, Vahagn, Kelley, Merideth L., Fletcher, Breanna, Bolyard, Audrey Anna, Aprikyan, A. Andrew, Dale, David C.

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Kostmann syndrome: severe congenital neutropenia associated with defective expression of Bcl-2, constitutive mitochondrial release of cytochrome c, and excessive apoptosis of myelo... von Carlsson, Göran, Aprikyan, Andrew A.G., Tehranchi, Ramin, Dale, David C., Porwit, Anna, Hellström-Lindberg, Eva, Palmblad, Jan, Henter, Jan-Inge, Fadeel, Bengt

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Prevalence of mutations in ELANE, GFI1, HAX1, SBDS, WAS and G6PC3 in patients with severe congenital neutropenia von Xia, Jun, Bolyard, Audrey A., Rodger, Elin, Stein, Steve, Aprikyan, Andrew A., Dale, David C., Link, Daniel C.

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Neutrophil elastase and granulocyte colony-stimulating factor receptor mutation analyses and leukemia evolution in severe congenital neutropenia patients belonging to the original... von Carlsson, G, Aprikyan, AA, Ericson, KG, Stein, S, Makaryan, V, Dale, DC, Nordenskjold, M, Fadeel, B, Palmblad, J, Hentera, JI

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The cellular and molecular mechanisms for neutropenia in Barth syndrome von Makaryan, Vahagn, Kulik, Willem, Vaz, Frederic M., Allen, Christopher, Dror, Yigal, Dale, David C., Aprikyan, Andrew A.

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Cyclic neutropenia and severe congenital neutropenia in patients with a shared ELANE mutation and paternal haplotype: Evidence for phenotype determination by modifying genes von Newburger, Peter E., Pindyck, Talia N., Zhu, Zhiqing, Bolyard, Audrey Anna, Aprikyan, Andrew A.G., Dale, David C., Smith, Gary D., Boxer, Laurence A.

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Neutrophil elastase mutations and risk of leukaemia in severe congenital neutropenia von Rosenberg, Philip S., Alter, Blanche P., Link, Daniel C., Stein, Steven, Rodger, Elin, Bolyard, Audrey A., Aprikyan, Andrew A., Bonilla, Mary A., Dror, Yigal, Kannourakis, George, Newburger, Peter E., Boxer, Laurence A., Dale, David C.

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Impaired survival of bone marrow hematopoietic progenitor cells in cyclic neutropenia von Aprikyan, Andrew A.G., Liles, W. Conrad, Rodger, Elin, Jonas, Mechthild, Chi, Emil Y., Dale, David C.

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Functional interaction between mutations in the granulocyte colony‐stimulating factor receptor in severe congenital neutropenia von Ward, Alister C., Gits, Judith, Majeed, Fidel, Aprikyan, Andrew A., Lewis, Rowena S., O’Sullivan, Lynda A., Freedman, Melvin, Shigdar, Sarah, Touw, Ivo P., Dale, David C., Dror, Yigal

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Mosaic tetraploidy and transient GFI1 mutation in a patient with severe chronic neutropenia von Hochberg, Jessica C., Miron, Patricia M., Hay, Beverly N., Woda, Bruce A., Wang, Sa A., Richert-Przygonska, Monika, Aprikyan, Andrew A.G., Newburger, Peter E.

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Mutant elastase in pathogenesis of cyclic and Severe congenital neutropenia von APRIKYAN, Andrew A. G, LILES, W. Conrad, BOXER, Laurence A, DALE, David C

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Loss of Tafazzin (TAZ) Function and Accelerated Apoptosis of Human Bone Marrow Stem and Myeloid Progenitors in Barth Syndrome von Makaryan, Vahagn, Dror, Yigal, Aprikyan, Andrew A

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The Cellular and Molecular Mechanisms of Neutropenia in Barth Syndrome von Aprikyan, Andrew A, Makaryan, Vahagn, Kulik, Willem, Vaz, Frederic, Allen, Christopher, Dror, Yigal, Dale, David C.

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Mutant CXCR4-Induced Aberrant Retention and Apoptosis of Hematopoietic Cells in Myelokathexis and Normalization of Cell Survival and Mobilization with Specific Inhibitors von Makaryan, Vahagn, Penate, Oscar, Dale, David C., Aprikyan, Andrew A

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Small Molecule Inhibitor of Neutrophil Elastase Normalizes Myeloid Differentiation and Improves Impaired Cell Survival Triggered by Elastase Mutations In Patients with Severe Conge... von Aprikyan, Andrew A., Makaryan, Vahagn, Totrov, Maxim, Abagyan, Ruben, Dale, David C.

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Knock-Down of TAZ Gene Expression: A Model of Barth Syndrome with Accelerated Apoptosis of Myeloid Progenitor Cells Improved upon Treatment with Caspase-Specific Inhibitor von Makaryan, Vahagn, Dale, David C., Aprikyan, Andrew A

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Small Molecule Inhibitor of Neutrophil Elastase and Severe Congenital Neutropenia von Aprikyan, Andrew A, Makaryan, Vahagn, Totrov, Maxim, Abagyan, Ruben, Dale, David C.

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Molecular Studies of Neutropenia in Barth Syndrome von Aprikyan, Andrew A., Makaryan, Vahagn, Dale, David C.

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Cellular and molecular abnormalities in severe congenital neutropenia predisposing to leukemia von Aprikyan, Andrew A.G, Kutyavin, Tatyana, Stein, Steven, Aprikian, Pavel, Rodger, Elin, Liles, W.Conrad, Boxer, Laurence A, Dale, David C

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ELANE Mutations in Cyclic and Congenital Neutropenia: Genotype-Phenotype Relationships von Dale, David C., Makaryan, Vahagn, Bolyard, Audrey Anna, Rodger, Elin R., Kelley, Merideth L., Marrero, Tracy M., Phan, Lan, Aprikyan, Andrew A, Bonilla, Mary Ann, Newburger, Peter E., Boxer, Laurence A., Link, Daniel

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