Translational efficiency in patients with Diamond-Blackfan anemia.
about
The human Shwachman-Diamond syndrome protein, SBDS, associates with ribosomal RNAAbnormalities of the large ribosomal subunit protein, Rpl35a, in Diamond-Blackfan anemiaRibosomopathies: Global process, tissue specific defectsRibosomopathies: how a common root can cause a tree of pathologiesProgress towards mechanism-based treatment for Diamond-Blackfan anemiaMolecular basis of Diamond Blackfan anemia: structure and function analysis of RPS19Fibroblasts from patients with Diamond-Blackfan anaemia show abnormal expression of genes involved in protein synthesis, amino acid metabolism and cancer.Ribosome biogenesis in skeletal development and the pathogenesis of skeletal disordersRibosomopathies: human disorders of ribosome dysfunction.Altered translation of GATA1 in Diamond-Blackfan anemia.Diamond Blackfan anemia 2008-2009: broadening the scope of ribosome biogenesis disorders.Defects of protein production in erythroid cells revealed in a zebrafish Diamond-Blackfan anemia model for mutation in RPS19.Drosophila ribosomal protein mutants control tissue growth non-autonomously via effects on the prothoracic gland and ecdysoneMarrow failure: a window into ribosome biologyRibosomopathies: mechanisms of disease.Diamond Blackfan anemia treatment: past, present, and future.L-Leucine improves the anemia and developmental defects associated with Diamond-Blackfan anemia and del(5q) MDS by activating the mTOR pathway.Important genes in the pathogenesis of 5q- syndrome and their connection with ribosomal stress and the innate immune system pathway.Diamond-Blackfan anemia, ribosome and erythropoiesis.Ribosomal and hematopoietic defects in induced pluripotent stem cells derived from Diamond Blackfan anemia patients.Posttranscriptional down-regulation of small ribosomal subunit proteins correlates with reduction of 18S rRNA in RPS19 deficiency.Ribosomal protein S19 and S24 insufficiency cause distinct cell cycle defects in Diamond-Blackfan anemia.GATA1 and PU.1 Bind to Ribosomal Protein Genes in Erythroid Cells: Implications for Ribosomopathies.Ribosomal protein L11 mutation in zebrafish leads to haematopoietic and metabolic defects.Bmi1 promotes erythroid development through regulating ribosome biogenesisInnate immune system activation in zebrafish and cellular models of Diamond Blackfan Anemia.
P2860
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P2860
Translational efficiency in patients with Diamond-Blackfan anemia.
description
2006 nî lūn-bûn
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2006年の論文
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2006年学术文章
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2006年学术文章
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2006年学术文章
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2006年学术文章
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2006年学术文章
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2006年學術文章
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name
Translational efficiency in patients with Diamond-Blackfan anemia.
@en
Translational efficiency in patients with Diamond-Blackfan anemia.
@nl
type
label
Translational efficiency in patients with Diamond-Blackfan anemia.
@en
Translational efficiency in patients with Diamond-Blackfan anemia.
@nl
prefLabel
Translational efficiency in patients with Diamond-Blackfan anemia.
@en
Translational efficiency in patients with Diamond-Blackfan anemia.
@nl
P2093
P1433
P1476
Translational efficiency in patients with Diamond-Blackfan anemia.
@en
P2093
Dagmar Pospisilova
Jana Cmejlova
Jiri Petrak
Kvetoslava Petrtylova
Ludmila Dolezalova
Radek Cmejla
P304
P577
2006-11-01T00:00:00Z