Erythroid precursors in congenital hypoplastic (Diamond-Blackfan) anemia
about
Human RPS19, the gene mutated in Diamond-Blackfan anemia, encodes a ribosomal protein required for the maturation of 40S ribosomal subunitsDiamond-Blackfan anaemia in a girl with a de novo balanced reciprocal X;19 translocationProgress towards mechanism-based treatment for Diamond-Blackfan anemiaThe inherited bone marrow failure syndromesPathology-important advances in clinical medicine: assessing fetal lung maturity.Altered translation of GATA1 in Diamond-Blackfan anemia.Diamond-Blackfan anemia: diagnosis, treatment, and molecular pathogenesis.Congenital bone marrow failure syndromes.Pure red cell aplasia.Marrow failure: a window into ribosome biologyRibosomopathies: mechanisms of disease.Influence of cell cycle phase-specific agents on simian fetal hemoglobin synthesis.Isolation and transcriptome analyses of human erythroid progenitors: BFU-E and CFU-EDiamond Blackfan anemia treatment: past, present, and future.Red cell aplasia in children.Purification of human erythroid colony-forming units and demonstration of specific binding of erythropoietin.PPAR-α and glucocorticoid receptor synergize to promote erythroid progenitor self-renewalEstablishing Rps6 hemizygous mice as a model for studying how ribosomal protein haploinsufficiency impairs erythropoiesis.Defective ribosomal protein gene expression alters transcription, translation, apoptosis, and oncogenic pathways in Diamond-Blackfan anemia.Mature bone marrow erythroid burst-forming units do not require T cells for induction of erythropoietin-dependent differentiation.Advances in understanding erythropoiesis: evolving perspectivesControl of the simian fetal hemoglobin switch at the progenitor cell levelNeutropenia in three patients with rheumatic disorders. Suppression of granulopoiesis by control-sensitive thymus-dependent lymphocytes.Glucocorticoids improve erythroid progenitor maintenance and dampen Trp53 response in a mouse model of Diamond-Blackfan anaemia.Dysferlin and other non-red cell proteins accumulate in the red cell membrane of Diamond-Blackfan Anemia patients.Erythropoietin receptor. Subunit structure and activation.Molecular mechanisms of pathology and treatment in Diamond Blackfan Anaemia.Diamond Blackfan anemia: a model for the translational approach to understanding human disease.GATA1 and PU.1 Bind to Ribosomal Protein Genes in Erythroid Cells: Implications for Ribosomopathies.Molecular convergence in ex vivo models of Diamond-Blackfan anemia.Drug discovery for Diamond-Blackfan anemia using reprogrammed hematopoietic progenitorsPathogenesis of the erythroid failure in Diamond Blackfan anaemia.Ribosome Levels Selectively Regulate Translation and Lineage Commitment in Human Hematopoiesis.
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Erythroid precursors in congenital hypoplastic (Diamond-Blackfan) anemia
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on February 1978
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Erythroid precursors in congenital hypoplastic (Diamond-Blackfan) anemia
@en
Erythroid precursors in congenital hypoplastic
@nl
type
label
Erythroid precursors in congenital hypoplastic (Diamond-Blackfan) anemia
@en
Erythroid precursors in congenital hypoplastic
@nl
prefLabel
Erythroid precursors in congenital hypoplastic (Diamond-Blackfan) anemia
@en
Erythroid precursors in congenital hypoplastic
@nl
P2093
P2860
P356
P1476
Erythroid precursors in congenital hypoplastic (Diamond-Blackfan) anemia
@en
P2093
P2860
P304
P356
10.1172/JCI108960
P407
P577
1978-02-01T00:00:00Z