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Journal of Pediatric Hematology/Oncology|July 11, 2006
Low frequency of telomerase RNA mutations among children with aplastic anemia or myelodysplastic syndromeJoshua J Field, Philip J Mason, Ping An, et al.
British Journal of Haematology|March 5, 2003
High-dose cyclophosphamide does not eradicate paroxysmal nocturnal haemoglobinuria haematopoiesis in mice carrying a Piga gene mutationAnne Schaefer, Marek Jasinski, Monica Bessler
BMC Blood Disorders|June 24, 2004
A mutation in a functional Sp1 binding site of the telomerase RNA gene (hTERC) promoter in a patient with Paroxysmal Nocturnal HaemoglobinuriaW Nicol Keith, Tom Vulliamy, Jiangqin Zhao, et al.
Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology|January 23, 2003
Stem cells, telomerase and dyskeratosis congenitaPhilip J Mason
Leukemia & Lymphoma|December 24, 2015
Genetic predisposition to myelodysplastic syndrome and acute myeloid leukemia in children and young adultsDaria V Babushok, Monica Bessler, Timothy S Olson
F1000Research|February 28, 2015
Case Report: Paroxysmal nocturnal hemoglobinuria in a woman heterozygous for G6PD A-Nieves Perdigones, Mariela Morales, Philip Mason, et al.
Pediatric Clinics of North America|November 19, 2013
Acquired aplastic anemia in childrenHelge D Hartung, Timothy S Olson, Monica Bessler
Cancer Genetics|December 26, 2015
Clonal evolution and clinical significance of copy number neutral loss of heterozygosity of chromosome arm 6p in acquired aplastic anemiaMarisol Betensky, Daria Babushok, Jacquelyn J Roth, et al.
Molecular Immunology|January 17, 2004
ScFv-mediated in vivo targeting of DAF to erythrocytes inhibits lysis by complementDirk Spitzer, Jacqueline Unsinger, Monica Bessler, et al.
British Journal of Haematology|November 20, 2002
Bone marrow failure in Shwachman-Diamond syndrome does not select for clonal haematopoiesis of the paroxysmal nocturnal haemoglobinuria phenotypePeter Keller, Michael R Debaun, Robert J Rothbaum, et al.
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