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1 The Finsen Laboratory, Rigshospitalet, Faculty of Health Sciences, University of Copenhagen, Denmark 2 Biotech Research and Innovation Centre (BRIC), University of Copenhagen, Copenhagen, Denmark 4 Novo Nordisk Foundation Center for Stem Cell Biology, DanStem, Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark
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Division of Genome Sciences and Cancer, The John Curtin School of Medical Research, The Australian National University, Canberra
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Institut Cochin, INSERM U1016, CNRS UMR8104, Paris Descartes University
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The Francis Crick Institute, London NW1 1AT, UK
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Weill Institute for Cell and Molecular Biology and Section of Plant Biology, School of Integrative Plant Science, Cornell University, Ithaca, NY 14853, USA
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xref:PubMed:35115551
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Potentials of ribosomopathy gene as pharmaceutical targets for cancer treatment.
Not available
S-EPMC11010632
|
biostudies-literature
Cite
Diphthamide-deficiency syndrome: a novel human developmental disorder and ribosomopathy.
Not available
S-EPMC7575589
|
biostudies-literature
Cite
Convergent somatic evolution commences in utero in a germline ribosomopathy.
Not available
S-EPMC10444798
|
biostudies-literature
Cite
CblX disease is both an inborn error of cobalamin metabolism and a ribosomopathy
CblX disease is both an inborn error of cobalamin metabolism and a ribosomopathy
PRJNA679313
|
ENA
Cite
Expression of ribosomopathy genes during Xenopus tropicalis embryogenesis.
Not available
S-EPMC5081970
|
biostudies-literature
Cite
A Ribosomopathy Reveals Decoding Defective Ribosomes Driving Human Dysmorphism.
Not available
S-EPMC5339345
|
biostudies-literature
Cite
Ribosomopathy-like properties of murine and human cancers.
Not available
S-EPMC5562309
|
biostudies-literature
Cite
Recapitulating and reversing human brain ribosomopathy defects via the maladaptive integrated stress response.
Not available
S-EPMC10836730
|
biostudies-literature
Cite
Ribosomopathy-associated mutations cause proteotoxic stress that is alleviated by TOR inhibition.
Not available
S-EPMC7116740
|
biostudies-literature
Cite
Hepatic ribosomal protein S6 (Rps6) insufficiency results in failed bile duct development and loss of hepatocyte viability; a ribosomopathy-like phenotype that is partially p53-dependent.
Not available
S-EPMC9888725
|
biostudies-literature
Cite
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