Runx1 Deficiency Decreases Ribosome Biogenesis and Confers Stress Resistance to Hematopoietic Stem and Progenitor Cells von Cai, Xiongwei, Gao, Long, Teng, Li, Ge, Jingping, Oo, Zaw Min, Kumar, Ashish R., Gilliland, D. Gary, Mason, Philip J., Tan, Kai, Speck, Nancy A.

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Identification of ATPases Pontin and Reptin as Telomerase Components Essential for Holoenzyme Assembly von Venteicher, Andrew S., Meng, Zhaojing, Mason, Philip J., Veenstra, Timothy D., Artandi, Steven E.

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G6PD deficiency: the genotype-phenotype association von Mason, Philip J, Bautista, José M, Gilsanz, Florinda

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In-Depth, Label-Free Analysis of the Erythrocyte Cytoplasmic Proteome in Diamond Blackfan Anemia Identifies a Unique Inflammatory Signature von Pesciotta, Esther N, Lam, Ho-Sun, Kossenkov, Andrew, Ge, Jingping, Showe, Louise C, Mason, Philip J, Bessler, Monica, Speicher, David W

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Inherited bone marrow failure syndromes in adolescents and young adults von Wilson, David B., Link, Daniel C., Mason, Philip J., Bessler, Monica

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The role of human ribosomal proteins in the maturation of rRNA and ribosome production von Robledo, Sara, Idol, Rachel A, Crimmins, Dan L, Ladenson, Jack H, Mason, Philip J, Bessler, Monica

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Ribosomal and hematopoietic defects in induced pluripotent stem cells derived from Diamond Blackfan anemia patients von Garçon, Loïc, Ge, Jingping, Manjunath, Shwetha H., Mills, Jason A., Apicella, Marisa, Parikh, Shefali, Sullivan, Lisa M., Podsakoff, Gregory M., Gadue, Paul, French, Deborah L., Mason, Philip J., Bessler, Monica, Weiss, Mitchell J.

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Dysregulation of the Transforming Growth Factor β Pathway in Induced Pluripotent Stem Cells Generated from Patients with Diamond Blackfan Anemia von Ge, Jingping, Apicella, Marisa, Mills, Jason A, Garçon, Loïc, French, Deborah L, Weiss, Mitchell J, Bessler, Monica, Mason, Philip J

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The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita von Vulliamy, Tom, Marrone, Anna, Goldman, Frederick, Dearlove, Andrew, Bessler, Monica, Mason, Philip J., Dokal, Inderjeet

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A Pathogenic Dyskerin Mutation Impairs Proliferation and Activates a DNA Damage Response Independent of Telomere Length in Mice von Gu, Bai-Wei, Bessler, Monica, Mason, Philip J.

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Impaired Telomere Maintenance and Decreased Canonical WNT Signaling but Normal Ribosome Biogenesis in Induced Pluripotent Stem Cells from X-Linked Dyskeratosis Congenita Patients von Gu, Bai-Wei, Apicella, Marisa, Mills, Jason, Fan, Jian-Meng, Reeves, Dara A, French, Deborah, Podsakoff, Gregory M, Bessler, Monica, Mason, Philip J

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Mice with a Mutation in the Mdm2 Gene That Interferes with MDM2/Ribosomal Protein Binding Develop a Defect in Erythropoiesis von Kamio, Takuya, Gu, Bai-wei, Olson, Timothy S, Zhang, Yanping, Mason, Philip J, Bessler, Monica

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Mouse Dyskerin Mutations Affect Accumulation of Telomerase RNA and Small Nucleolar RNA, Telomerase Activity, and Ribosomal RNA Processing von Mochizuki, Yuko, He, Jun, Kulkarni, Shashikant, Bessler, Monica, Mason, Philip J., Steitz, Joan A.

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Heterozygous telomerase RNA mutations found in dyskeratosis congenita and aplastic anemia reduce telomerase activity via haploinsufficiency von Marrone, Anna, Stevens, David, Vulliamy, Tom, Dokal, Inderjeet, Mason, Philip J.

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Clonal evolution and clinical significance of copy number neutral loss of heterozygosity of chromosome arm 6p in acquired aplastic anemia von Betensky, Marisol, Babushok, Daria, Roth, Jacquelyn J, Mason, Philip J, Biegel, Jaclyn A, Busse, Tracy M, Li, Yimei, Lind, Curt, Papazoglou, Anna, Monos, Dimitri, Podsakoff, Gregory, Bessler, Monica, Olson, Timothy S

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Accelerated hematopoietic stem cell aging in a mouse model of dyskeratosis congenita responds to antioxidant treatment von Gu, Bai‐Wei, Fan, Jian‐Meng, Bessler, Monica, Mason, Philip J.

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Dysferlin and other non-red cell proteins accumulate in the red cell membrane of Diamond-Blackfan Anemia patients von Pesciotta, Esther N, Sriswasdi, Sira, Tang, Hsin-Yao, Speicher, David W, Mason, Philip J, Bessler, Monica

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Dyskerin Ablation in Mouse Liver Inhibits rRNA Processing and Cell Division von Ge, Jingping, Rudnick, David A., He, Jun, Crimmins, Dan L., Ladenson, Jack H., Bessler, Monica, Mason, Philip J.

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Single nucleotide polymorphism array analysis of bone marrow failure patients reveals characteristic patterns of genetic changes von Babushok, Daria V., Xie, Hongbo M., Roth, Jacquelyn J., Perdigones, Nieves, Olson, Timothy S., Cockroft, Joshua D., Gai, Xiaowu, Perin, Juan C., Li, Yimei, Paessler, Michele E., Hakonarson, Hakon, Podsakoff, Gregory M., Mason, Philip J., Biegel, Jaclyn A., Bessler, Monica

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The Effect of TERC Haploinsufficiency on the Inheritance of Telomere Length von Goldman, Fred, Rachida Bouarich, Kulkarni, Shashikant, Sara Freeman, Hong-Yan Du, Harrington, Lea, Mason, Philip J., Arturo Londono-Vallejo, Bessler, Monica

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