Ribosome Levels Selectively Regulate Translation and Lineage Commitment in Human Hematopoiesis

Analysis of protein-coding genetic variation in 60,706 humans

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CellProfiler: image analysis software for identifying and quantifying cell phenotypes

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Hematopoiesis: An Evolving Paradigm for Stem Cell Biology

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Identification and characterization of essential genes in the human genome

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A unifying model for mTORC1-mediated regulation of mRNA translation

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The translational landscape of mTOR signalling steers cancer initiation and metastasis

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Transcriptional Heterogeneity and Lineage Commitment in Myeloid Progenitors

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Translational control by 5′-untranslated regions of eukaryotic mRNAs

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The Xist lncRNA Exploits Three-Dimensional Genome Architecture to Spread Across the X Chromosome

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Absolute quantification of transcription factors reveals principles of gene regulation in erythropoiesisPreprint

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rDNA Transcription in Developmental Diseases and Stem Cells

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Deficiency of the ribosomal protein uS10 (RPS20) reorganizes human cells translatome according to the abundance, CDS length and GC content of mRNAs

Tian, Y., Babaylova, E. S., Gopanenko, A. V., Tupikin, A. E., Kabilov, M. R., & Malygin, A. A. (2024) · Open Biology · doi:10.1098/rsob.230366 · Cited by 9

Differential impacts of ribosomal protein haploinsufficiency on mitochondrial function

Surya, A., Bolton, B., Rothe, R., Mejia-Trujillo, R., Leonita, A., Zhao, Q., Arya, A., Liu, Y., Rangan, R., Gorusu, Y., et al. (2024) · The Journal of Cell Biology · doi:10.1083/jcb.202404084 · Cited by 12

Multiomic Profiling of Central Nervous System Leukemia Identifies mRNA Translation as a Therapeutic Target

Vanner, R. J., Dobson, S. M., Gan, O. I., McLeod, J. L., Schoof, E. M., Grandal, I., Wintersinger, J. A., García‐Prat, L., Hosseini, M., Xie, S. Z.-J., et al. (2021) · Blood Cancer Discovery · doi:10.1158/2643-3230.bcd-20-0216 · Cited by 12

Concurrent Zrsr2 mutation and Tet2 loss promote myelodysplastic neoplasm in mice

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Unraveling 3′-end RNA uridylation at nucleotide resolution

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Impact of Next-Generation Sequencing on the Diagnosis and Treatment of Congenital Anemias

Steinberg‐Shemer, O., & Tamary, H. (2020) · Molecular Diagnosis & Therapy · doi:10.1007/s40291-020-00478-3 · Cited by 10

Pan-cellular organelles and suborganelles—from common functions to cellular diversity?Preprint

Schieweck, R., & Götz, M. (2024) · Genes & Development · doi:10.1101/gad.351337.123 · Cited by 10

Treatment of refractory/relapsed Diamond–Blackfan anaemia with eltrombopag

Duncan, B. B., Lotter, J., Superata, J., Barranta, M. E., Machado, T. R., Darden, I., Venugopal, S., Wu, C. O., Abkowitz, J. L., Dunbar, C. E., et al. (2024) · British Journal of Haematology · doi:10.1111/bjh.19357 · Cited by 9

Ribosome biogenesis is essential for hemogenic endothelial cells to generate hematopoietic stem cells

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Pediatric myelodysplastic syndrome

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Rfoot‐seq: Transcriptomic RNase Footprinting for Mapping Stable RNA‐Protein Complexes and Rapid Ribosome Profiling

Li, Q., Stroup, E. K., & Ji, Z. (2023) · Current Protocols · doi:10.1002/cpz1.761 · Cited by 9

Neutral sphingomyelinase blockade enhances hematopoietic stem cell fitness through an integrated stress response

Hurwitz, S. N., Jung, S. K., Kobulsky, D. R., Fazelinia, H., Spruce, L. A., Pérez, E. B., Gröen, N., Mesaros, C., & Kurre, P. (2023) · Blood · doi:10.1182/blood.2023022147 · Cited by 9

Protein Synthesis and Translational Control in Neural Stem Cell Development and Neurogenesis

Mohammad, L., Wiseman, J., Erickson, S. E., & Yang, G. (2019) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780190686307.013.21 · Cited by 8

A new murine Rpl5 ( uL18 ) mutation provides a unique model of variably penetrant Diamond-Blackfan anemia

Yu, L., Lemay, P., Ludlow, A. V., Guyot, M., Jones, M., Mohamed, F. F., Saroya, G.-A., Panaretos, C., Schneider, E., Wang, Y., et al. (2021) · Blood Advances · doi:10.1182/bloodadvances.2021004658 · Cited by 9

Deficiency of the Ribosomal Protein uL5 Leads to Significant Rearrangements of the Transcriptional and Translational Landscapes in Mammalian Cells

Babaylova, E. S., Gopanenko, A. V., Tupikin, A. E., Kabilov, M. R., Malygin, A. A., & Karpova, G. G. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222413485 · Cited by 9

Single-cell multi-omics defines the cell-type specific impact of splicing aberrations in human hematopoietic clonal outgrowthsPreprint

Gaiti, F., Chamely, P., Hawkins, A. G., Cortés-López, M., Swett, A. D., Ganesan, S., Mouhieddine, T. H., Dai, X., Kluegel, L., Chen, C. Y., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.06.08.495292 · Cited by 9

The Diverse Genomic Landscape of Diamond–Blackfan Anemia: Two Novel Variants and a Mini-Review

Pelagiadis, I., Kyriakidis, I., Katzilakis, N., Kosmeri, C., Veltra, D., Sofocleous, C., Glentis, S., Kattamis, A., Makis, A. C., & Stiakaki, E. (2023) · Children · doi:10.3390/children10111812 · Cited by 8

Stem cell transcriptional profiles from mouse subspecies reveal cis-regulatory evolution at translation genes

Simon, N. M., Kim, Y., Gribnau, J. H., Bautista, D. M., Dutton, J. R., & Brem, R. B. (2024) · Heredity · doi:10.1038/s41437-024-00715-z · Cited by 12

The role of glucocorticoids in erythropoiesis

Hanssen, L. L. P., & Iskander, D. (2025) · Frontiers in Hematology · doi:10.3389/frhem.2025.1540152 · Cited by 8

Ribosome biogenesis controls cranial suture MSC fate via the complement pathway in mouse and human iPSC models

Jariyasakulroj, S., Zhang, W., Bai, J., Zhang, M., Lu, Z., & Chen, J.-F. (2023) · Stem Cell Reports · doi:10.1016/j.stemcr.2023.10.015 · Cited by 8

Disruption of mitochondrial energy metabolism is a putative pathogenesis of Diamond-Blackfan anemia

Xiao, R., Zhang, L., Xin, Z., Zhu, J., Zhang, Q., Zheng, G., Chu, S., Wu, J., Zhang, L., Wan, Y., et al. (2024) · iScience · doi:10.1016/j.isci.2024.109172 · Cited by 8

Proteomic/transcriptomic analysis of erythropoiesis

Brand, M., & Ranish, J. A. (2021) · Current Opinion in Hematology · doi:10.1097/moh.0000000000000647 · Cited by 7

Downregulation of SATB1 by miRNAs reduces megakaryocyte/erythroid progenitor expansion in preclinical models of Diamond–Blackfan anemia

Wilkes, M. C., Scanlon, V. M., Shibuya, A., Cepika, A., Eskin, A., Chen, Z., Narla, A., Glader, B. E., Roncarolo, M. G., Nelson, S. F., et al. (2022) · Experimental Hematology · doi:10.1016/j.exphem.2022.04.005 · Cited by 8

Erythroid Cell Research: 3D Chromatin, Transcription Factors and Beyond

Andrieu‐Soler, C., & Soler, É. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23116149 · Cited by 8

Stemness‐related genes revealed by single‐cell profiling of naïve and stimulated human CD34 + cells from CB and mPB

Dong, G., Xu, X., Li, Y., Ouyang, W., Zhao, W., Gu, Y., Li, J., Liu, T., Zeng, X., Zou, H., et al. (2023) · Clinical and Translational Medicine · doi:10.1002/ctm2.1175 · Cited by 8

Engineered human Diamond-Blackfan anemia disease model confirms therapeutic effects of clinically applicable lentiviral vector at single-cell resolution

Liu, Y., Schmiderer, L., Hjort, M., Lang, S., Bremborg, T., Rydström, A., Schambach, A., Larsson, J., & Karlsson, S. (2023) · Haematologica · doi:10.3324/haematol.2022.282068 · Cited by 8

Comprehensive Genome-Wide Approaches to Activity-Dependent Translational Control in Neurons

Choe, H. K., & Cho, J. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21051592 · Cited by 11

Serotonergic neuron ribosomal proteins regulate the neuroendocrine control of Drosophila development

Deliu, L. P., Turingan, M. J., Jadir, D., Lee, B., Ghosh, A., & Grewal, S. (2022) · PLoS Genetics · doi:10.1371/journal.pgen.1010371 · Cited by 8

Bloody Mysteries of Ribosomes

Sulima, S. O., & Keersmaecker, K. D. (2018) · HemaSphere · doi:10.1097/hs9.0000000000000095 · Cited by 8

RNA binding protein‐directed control of leukemic stem cell evolution and function

Joshi, P., Chahi, A. K., Liu, L., Moreira, S., Vujovic, A., & Hope, K. J. (2024) · HemaSphere · doi:10.1002/hem3.116 · Cited by 9

Cell type–specific purifying selection of synonymous mitochondrial DNA variation

Lareau, C. A., Maschmeyer, P., Yin, Y., Gutierrez, J. C., Dhindsa, R. S., Gribling-Burrer, A.-S., Zielinski, S., Hsieh, Y.-H., Nitsch, L., Dimitrova, V., et al. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2505704122 · Cited by 6

Monosomes buffer translational stress to allow for active ribosome elongation

Schieweck, R., Ciccopiedi, G., Klau, K., & Popper, B. (2023) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2023.1158043 · Cited by 7

Functionally impaired RPL8 variants associated with Diamond–Blackfan anemia and a Diamond–Blackfan anemia‐like phenotype

Lebaron, S., O’Donohue, M.-F., Smith, S. C., Engleman, K. L., Juusola, J., Safina, N. P., Thiffault, I., Saunders, C., & Gleizes, P. (2021) · Human Mutation · doi:10.1002/humu.24323 · Cited by 7

Invariable Ribosome Stoichiometry During Murine Erythroid Differentiation: Implications for Understanding Ribosomopathies

Papagiannopoulos, C. I., Kyritsis, K., Psatha, K., Mavridou, D., Chatzopoulou, F. M., Orfanoudaki, G., Aivaliotis, M., & Vizirianakis, I. S. (2022) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2022.805541 · Cited by 7

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

Comerford, S. A., Hinnant, E. A., Chen, Y., & Hammer, R. E. (2023) · PLoS Genetics · doi:10.1371/journal.pgen.1010595 · Cited by 7

Comparative Transcriptome Analysis Reveals the Role of Ribosome Reduction in Impeding Oogenesis in Female Triploid Crassostrea Gigas

Yang, Q., Yu, H., & Li, Q. (2024) · Marine Biotechnology · doi:10.1007/s10126-024-10283-2 · Cited by 7

The Beak of Eukaryotic Ribosomes: Life, Work and Miracles

Martín‐Villanueva, S., Galmozzi, C. V., Ruger-Herreros, C., Kressler, D., & de la Cruz, J. (2024) · Biomolecules · doi:10.3390/biom14070882 · Cited by 7

Discriminative feature of cells characterizes cell populations of interest by a small subset of genes

Fujii, T., Maehara, K., Fujita, M., & Ohkawa, Y. (2021) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1009579 · Cited by 6

Impaired phase separation and nucleolar functions in hiPSC models of SNORD118-related ribosomopathies

Zhang, W., Zhang, M., Ma, L., Jariyasakulroj, S., Chang, Q., Lin, Z., Lu, Z., & Chen, J. (2024) · iScience · doi:10.1016/j.isci.2024.110430 · Cited by 6

Proteostasis disruption in inherited bone marrow failure syndromes

Yu, H., & Signer, R. A. J. (2025) · Blood · doi:10.1182/blood.2024024956 · Cited by 6

Loss of coordinated expression between ribosomal and mitochondrial genes revealed by comprehensive characterization of a large family with a rare Mendelian disorder

Panici, B., Nakajima, H., Carlston, C. M., Özadam, H., Cenik, C., & Cenik, E. S. (2021) · Genomics · doi:10.1016/j.ygeno.2021.04.020 · Cited by 5

Pathophysiology of Myelodysplastic Syndromes

Fontenay, M., Farhat, B., & Boussaid, I. (2021) · Hemato · doi:10.3390/hemato2030030 · Cited by 6

Translation defects in ribosomopathies

Boussaid, I., & Fontenay, M. (2022) · Current Opinion in Hematology · doi:10.1097/moh.0000000000000705 · Cited by 7

Regulation of Ribosome Function by RNA Modifications in Hematopoietic Development and Leukemia: It Is Not Only a Matter of m6A

Fazi, F., & Fatica, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22094755 · Cited by 7

Activation of nemo-like kinase in diamond blackfan anemia suppresses early erythropoiesis by preventing mitochondrial biogenesis

Wilkes, M., Shibuya, A., Liu, Y., Mark, K., Mercado, J., Saxena, M., Sathianathen, R. S., Kim, H., Glader, B., Kenny, P., et al. (2024) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2024.107542 · Cited by 7

Translational control of leukemic metabolism and disease progression

Mercier, F., Gife, V., Aloyz, R. S., & Hulea, L. (2025) · Trends in Cell Biology · doi:10.1016/j.tcb.2025.04.006 · Cited by 6

Harnessing Single-Cell Technologies in the Search for New Therapies for Diamond–Blackfan Anemia Syndrome

Iskander, D., Karadimitris, A., & Roberts, I. A. G. (2024) · Experimental Hematology · doi:10.1016/j.exphem.2024.104235 · Cited by 5

Essential genes encoded by the mating-type locus of the human fungal pathogen Cryptococcus neoformans

Bian, Z., Xu, Z. Z., Peer, A., Choi, Y., Priest, S. J., Akritidou, K., Dasgupta, A., Dahlmann, T. A., Kück, U., Nowrousian, M., et al. (2025) · mBio · doi:10.1128/mbio.00223-25 · Cited by 5

Nucleolar control by a non‐apoptotic p53‐caspases‐deubiquitinylase axis promotes resistance to bacterial infection

Chen, P., Chen, Y., Chu, T., Ma, T., Wu, M.-H., Lin, H., Chang, Y., Tan, B. C., & Lo, S. J. (2019) · The FASEB Journal · doi:10.1096/fj.201901959r · Cited by 5

Computational Studies of the Structural Basis of Human RPS19 Mutations Associated With Diamond-Blackfan Anemia

An, K., Zhou, J., Xiong, Y., Han, W., Wang, T., Ye, Z., & Wu, Y. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2021.650897 · Cited by 5

Decreased expression of RPL15 and RPL18 exacerbated the calcification of valve interstitial cells during aortic valve calcification

Wang, G., Qin, M., Zhang, B., Yan, Y., Yang, F., Chen, Q., Liu, Y., Qiao, F., & Ni, Y. (2023) · Cell Biology International · doi:10.1002/cbin.12070 · Cited by 5

A unique poly(A) tail profile uncovers the stability and translational activation of TOP transcripts during neuronal differentiation

Baptissart, M., Papas, B. N., Chi, A., Li, Y., Lee, D., Puviindran, B. J., & Morgan, M. (2023) · iScience · doi:10.1016/j.isci.2023.107511 · Cited by 5

Transcriptomic evidence of erythropoietic adaptation from the International Space Station and from an Earth-based space analog

Trudel, G., Stratis, D., Rocheleau, L., Pelchat, M., & Laneuville, O. (2024) · npj Microgravity · doi:10.1038/s41526-024-00400-9 · Cited by 5

Absence of SMARCB1 in rhabdoid tumor cells increases sensitivity to translation inhibition and alters translation efficiency of specific mRNAs

Nguyen, L. T., Hains, A. E., Aziz‐Zanjani, M. O., Dalsass, M., Farooqee, S. B. U. D., Lu, Y., Jackson, P. K., & Rechem, C. V. (2024) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2024.107988 · Cited by 5

Ribosomal protein control of hematopoietic stem cell transformation through regulation of metabolism

Harris, B. D., Singh, D. K., Truong, B., Rhodes, M. R., Price, R., Shinton, S. A., Verma, M., Aylward, B. A., Fahl, S. P., Sprinkle, S. R., et al. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116688 · Cited by 7

Sequence variation, common tissue expression patterns and learning models: a genome-wide survey of vertebrate ribosomal proteins

Kyritsis, K., Ouzounis, C., Angelis, L., & Vizirianakis, I. S. (2020) · NAR Genomics and Bioinformatics · doi:10.1093/nargab/lqaa088 · Cited by 6

The Use of B-Cell Polysome Profiling to Validate Novel RPL5 (uL18) and RPL26 (uL24) Variants in Diamond-Blackfan Anemia

Ludlow, A. V., George, N. B., Glassford, M. R., Udenberg, K., Hannibal, M., Schwalm, C. M., Scott, K., Rothstein, T. L., & Singh, S. A. (2020) · Journal of Pediatric Hematology/Oncology · doi:10.1097/mph.0000000000001980 · Cited by 5

Tissue-Specific Ribosome Profiling in Drosophila

Chen, X., & Dickman, D. K. (2021) · Methods in molecular biology · doi:10.1007/978-1-0716-1150-0_7 · Cited by 5

Comprehensive transcriptome analysis of erythroid differentiation potential of olive leaf in haematopoietic stem cells

Kondo, S., Ferdousi, F., Yamauchi, K., Suidasari, S., Yokozawa, M., Harrabi, M. M., Tominaga, K., & Isoda, H. (2021) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.16752 · Cited by 5

Reprogrammed mRNA translation drives resistance to therapeutic targeting of ribosome biogenesisPreprint

Kusnadi, E. P., Trigos, A., Cullinane, C. M., Goode, D. L., Larsson, O. S., Devlin, J. R., Chan, K. T., Souza, D. P. D., McConville, M. J., McArthur, G. A., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/847723 · Cited by 5

Codon affinity in mitochondrial DNA shapes evolutionary and somatic fitnessPreprint

Lareau, C. A., Yin, Y., Gutierrez, J. C., Dhindsa, R. S., Gribling-Burrer, A.-S., Hsieh, Y.-H., Nitsch, L., Buquicchio, F. A., Abay, T., Zielinski, S., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.04.23.537997 · Cited by 4

Innate immune mechanisms hijacked by leukemia-initiating stem cells for selective advantage and immune evasion in Ptpn11-associated JMML

Zheng, H., Zhao, P., Tan, Z., Yu, W., Werner, J., Stieglitz, E., Porter, C. C., Chandrakasan, S., Wechsler, D. S., Méndez‐Ferrer, S., et al. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116087 · Cited by 4

The intrinsic properties of mRNAs define their translation efficiency at ribosome shortage

Babaylova, E. S., Gopanenko, A. V., Tupikin, A. E., Kabilov, M. R., & Malygin, A. A. (2025) · Nucleic Acids Research · doi:10.1093/nar/gkaf1013 · Cited by 4

An atypical form of 60S ribosomal subunit in Diamond-Blackfan anemia linked to RPL17 variants

Fellmann, F., Saunders, C., O’Donohue, M.-F., Reid, D. W., McFadden, K., Montel-Lehry, N., Yu, C., Fang, M., Zhang, J., Royer‐Bertrand, B., et al. (2024) · JCI Insight · doi:10.1172/jci.insight.172475 · Cited by 7

Is mitochondrial function at the heart of ribosome-related diseases?

Zhao, Q., & Cenik, E. S. (2025) · Trends in Cell Biology · doi:10.1016/j.tcb.2025.07.007 · Cited by 4

Reversing lysosome-ribosome circuit dysregulation mitigates C9FTD/ALS neurodegeneration and behaviors

Ma, L., Chen, L., Wang, J., Chang, Q., Wang, Y., Zhang, W., Du, Y., Sadan, J., & Chen, J. (2022) · Human Molecular Genetics · doi:10.1093/hmg/ddac271 · Cited by 4

A De Novo Frameshift Mutation in RPL5 with Classical Phenotype Abnormalities and Worsening Anemia Diagnosed in a Young Adult—A Case Report and Review of the Literature

Dorenkamp, M., Porret, N. A., Diepold, M., & Rovó, A. (2023) · Medicina · doi:10.3390/medicina59111953 · Cited by 4

Rpl5-Inducible Mouse Model for Studying Diamond-Blackfan Anemia

Kazerounian, S., Yuan, D., Alexander, M. S., Beggs, A. H., & Gazda, H. T. (2019) · Discoveries · doi:10.15190/d.2019.9 · Cited by 4

Cell autonomous and non-autonomous consequences of deviations in translation machinery on organism growth and the connecting signalling pathways

Surya, A., & Cenik, E. S. (2022) · Open Biology · doi:10.1098/rsob.210308 · Cited by 9

Contributions of transcriptional noise to leukaemia evolution: KAT2A as a case-study

Pina, C. (2024) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2023.0052 · Cited by 6

MOTS-c is a mitochondrial-encoded interferon-linked host defense peptide

Rice, M. C., Imun, M., Jung, S., Park, C., Kim, J., Lai, R., Barr, C. R., Son, J., Tor, K., Kim, E., et al. (2023) · eLife · doi:10.1101/2023.03.02.530691 · Cited by 5

Ribosomal protein deficiencies linked to Diamond-Blackfan anemia induce distinctive alterations of ATF4 expression

Lorenzo‐Martín, L. F., Robles‐Valero, J., Cota, R. R., Gaspar, S. G., Fuentes, P. J. B., Gentilella, A., Bustelo, X. R., & Dosil, M. (2025) · iScience · doi:10.1016/j.isci.2025.112138 · Cited by 3

Restricting glycine uptake with bitopertin improves erythropoiesis in preclinical models of Diamond-Blackfan anemia

Doty, R. T., Munday, A. D., Cottnair, H., Funk, S. E., Young, D. J., Dunbar, C. E., Wu, M., & Abkowitz, J. L. (2025) · Blood Red Cells & Iron · doi:10.1016/j.brci.2025.100010 · Cited by 3

Diabetes is causally associated with increased breast cancer mortality by inducing FIBCD1 to activate MCM5-mediated cell cycle arrest via modulating H3K27ac

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Nucleolus as a cornerstone linking proliferation and metabolism to cellular responses to stress: involvement of transcription factors MYC and p53

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Eukaryote initiation factor 6 modulates small-cell lung carcinoma plasticity via the integrin-FAK signaling axis

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A deep dive into functional ribosome specialization

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Heterogeneity of Neural Stem Cells in the Ventricular–Subventricular Zone

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DNA-repair enzyme turns to translation

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Targeting elevated heme levels to treat a mouse model for Diamond-Blackfan Anemia

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Glucocorticoids Induce the Expansion of an Immature Human CFU-E PopulationPreprint

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A translation control module coordinates germline stem cell differentiation with ribosome biogenesis during Drosophila oogenesisPreprint

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DRMY1 promotes robust morphogenesis by sustaining the translation of cytokinin signaling inhibitor proteinsPreprint

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LARP1 senses free ribosomes to coordinate supply and demand of ribosomal proteinsPreprint

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An inappropriate decline in ribosome levels drives a diverse set of neurodevelopmental disordersPreprint

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Dbp1 is a low performance paralog of RNA helicase Ded1 that drives impaired translation and heat stress responsePreprint

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KDM2B is required for ribosome biogenesis and its depletion unequally affects mRNA translationPreprint

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GDF15 Ameliorates Deoxynivalenol‐Induced Anemia by Resolving Ribosomal Stress–Mediated Erythropoietic Arrest

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Ribosome collisions and ZAKα activation: explores the therapeutic potential of metabolic diseases

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Beyond Hematologic Malignancies: Colorectal Cancer as a Solid Tumor Manifestation of Inherited Bone Marrow Failure Syndromes

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Decoding immune-metabolic crosstalk in ARDS: a transcriptomic exploration of biomarkers, cellular dynamics, and therapeutic pathways

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TORC1-dependent translation drives chromatin remodeling during the germ-cell-to-maternal transition in Drosophila

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RPS19 and RPL5 haploinsufficient models reveal divergent ribosomal subunit controls of fetal hematopoiesis

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TP53 -mutant AML with ribosomal gene loss exhibits impaired protein translation and sensitivity to HSP90 inhibition

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Ribosomal Proteins in Cell Biology and Cancer

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Consequences of ribosomal perturbations in human hematopoiesis

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Ribosomal deficiencies in Diamond-Blackfan anemia impair translation of transcripts essential for differentiation of murine and human erythroblasts

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mRNA translation regulation in Diamond Blackfan Anaemia

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