Dye efflux studies suggest that hematopoietic stem cells expressing low or undetectable levels of CD34 antigen exist in multiple species

MA Goodell, M Rosenzweig, H Kim, DF Marks… - Nature medicine, 1997 - nature.com
We previously described a method for isolating murine hematopoietic stem cells capable of
reconstituting lethally irradiated recipients, which depends solely on dual-wavelength flow …

[PDF][PDF] Ribosomal protein L5 and L11 mutations are associated with cleft palate and abnormal thumbs in Diamond-Blackfan anemia patients

HT Gazda, MR Sheen, A Vlachos, V Choesmel… - The American Journal of …, 2008 - cell.com
Diamond-Blackfan anemia (DBA), a congenital bone-marrow-failure syndrome, is
characterized by red blood cell aplasia, macrocytic anemia, clinical heterogeneity, and …

Gene dose-dependent control of hematopoiesis and hematologic tumor suppression by CBP

AL Kung, VI Rebel, RT Bronson, LE Ch'ng… - Genes & …, 2000 - genesdev.cshlp.org
Mice with monoallelic inactivation of the CBP gene develop highly penetrant, multilineage
defects in hematopoietic differentiation and, with advancing age, an increased incidence of …

[HTML][HTML] Exome sequencing identifies GATA1 mutations resulting in Diamond-Blackfan anemia

VG Sankaran, R Ghazvinian, R Do… - The Journal of …, 2012 - Am Soc Clin Investig
Mutations in numerous genes encoding ribosomal proteins (RPs) occur in 50%–70% of
individuals with Diamond-Blackfan anemia (DBA), establishing the disease as a …

[PDF][PDF] Ribosomal protein S24 gene is mutated in Diamond-Blackfan anemia

HT Gazda, A Grabowska, LB Merida-Long… - The American Journal of …, 2006 - cell.com
Diamond-Blackfan anemia (DBA) is a rare congenital red-cell aplasia characterized by
anemia, bone-marrow erythroblastopenia, and congenital anomalies and is associated with …

Altered translation of GATA1 in Diamond-Blackfan anemia

LS Ludwig, HT Gazda, JC Eng, SW Eichhorn, P Thiru… - Nature medicine, 2014 - nature.com
Ribosomal protein haploinsufficiency occurs in diverse human diseases including Diamond-
Blackfan anemia (DBA),, congenital asplenia and T cell leukemia. Yet, how mutations in …

Abnormalities of the large ribosomal subunit protein, Rpl35a, in Diamond-Blackfan anemia

JE Farrar, M Nater, E Caywood… - Blood, The Journal …, 2008 - ashpublications.org
Diamond-Blackfan anemia (DBA) is an inherited bone marrow failure syndrome
characterized by anemia, congenital abnormalities, and cancer predisposition. Small …

[PDF][PDF] Ribosomal protein genes RPS10 and RPS26 are commonly mutated in Diamond-Blackfan anemia

L Doherty, MR Sheen, A Vlachos, V Choesmel… - The American Journal of …, 2010 - cell.com
Diamond-Blackfan anemia (DBA), an inherited bone marrow failure syndrome characterized
by anemia that usually presents before the first birthday or in early childhood, is associated …

[PDF][PDF] The genetic landscape of Diamond-Blackfan anemia

JC Ulirsch, JM Verboon, S Kazerounian… - The American Journal of …, 2018 - cell.com
Diamond-Blackfan anemia (DBA) is a rare bone marrow failure disorder that affects 7 out of
1,000,000 live births and has been associated with mutations in components of the …

[PDF][PDF] Hematopoietic growth factors.

CA Sieff - The Journal of clinical investigation, 1987 - Am Soc Clin Investig
The process of blood cell formation, by which a small number of self-renewing stem cells
give rise to lineage committed pro-genitor cells that subsequently proliferateand differentiate …