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Select item 79278861.

Integrated analyses of translatome and proteome identify the rules of translation selectivity in RPS14-deficient cells

Ismael Boussaid, Salomé Le Goff, Célia Floquet, Emilie-Fleur Gautier, Anna Raimbault, Pierre-Julien Viailly, Dina Al Dulaimi, Barbara Burroni, Isabelle Dusanter-Fourt, Isabelle Hatin, Patrick Mayeux, Bertrand Cosson, Michaela Fontenay

Haematologica. 2021 Mar 1; 106(3): 746–758. Published online 2020 Apr 23. doi: 10.3324/haematol.2019.239970

PMCID:: PMC7927886

Abstract Article PDF–6.0M

Select item 37905132.

Diminutive somatic deletions in the 5q region lead to a phenotype atypical of classical 5q− syndrome

Adrianna Vlachos, Jason E. Farrar, Eva Atsidaftos, Ellen Muir, Anupama Narla, Thomas C. Markello, Sharon A. Singh, Michael Landowski, Hanna T. Gazda, Lionel Blanc, Johnson M. Liu, Steven R. Ellis, Robert J. Arceci, Benjamin L. Ebert, David M. Bodine, Jeffrey M. Lipton

Blood. 2013 Oct 3; 122(14): 2487–2490. Prepublished online 2013 Aug 13. doi: 10.1182/blood-2013-06-509935

PMCID:: PMC3790513

Abstract Article

Select item 27549643.

Low RPS14 expression is common in myelodysplastic syndromes without 5q- aberration and defines a subgroup of patients with prolonged survival

Akos Czibere, Ingmar Bruns, Bärbel Junge, Raminder Singh, Guido Kobbe, Rainer Haas, Ulrich Germing

Haematologica. 2009 Oct; 94(10): 1453–1455. doi: 10.3324/haematol.2009.008508

PMCID:: PMC2754964

Abstract Article PDF–197K

Select item 3696114.

Fine-structure map of the human ribosomal protein gene RPS14.

J J Diaz, D J Roufa

Mol Cell Biol. 1992 Apr; 12(4): 1680–1686. doi: 10.1128/mcb.12.4.1680

PMCID:: PMC369611

Summary Page Browse PDF–1.6M

Select item 3678445.

Primary structure of human ribosomal protein S14 and the gene that encodes it.

D D Rhoads, A Dixit, D J Roufa

Mol Cell Biol. 1986 Aug; 6(8): 2774–2783. doi: 10.1128/mcb.6.8.2774

PMCID:: PMC367844

Summary Page Browse PDF–2.0M

Select item 62789846.

L-leucine increases translation of RPS14 and LARP1 in erythroblasts from del(5q) myelodysplastic syndrome patients

Erica Bello, Jonathan Kerry, Shalini Singh, Bon Ham Yip, Rajko Kušec, Sally Killick, Sophie Raynaud, Jacqueline Boultwood, Andrea Pellagatti

Haematologica. 2018 Nov; 103(11): e496–e500. doi: 10.3324/haematol.2018.190447

PMCID:: PMC6278984

Article PDF–1.0M

Select item 37718557.

Identification of RPS14 as a 5q- syndrome gene by RNA interference screen

Benjamin L. Ebert, Jennifer Pretz, Jocelyn Bosco, Cindy Y. Chang, Pablo Tamayo, Naomi Galili, Azra Raza, David E. Root, Eyal Attar, Steven R. Ellis, Todd R. Golub

Nature. Author manuscript; available in PMC 2013 Sep 12.

Published in final edited form as: Nature. 2008 Jan 17; 451(7176): 335–339. doi: 10.1038/nature06494

PMCID:: PMC3771855

Abstract Article PDF–469K

Select item 37246368.

Ribosomal Protein S14 Negatively Regulates c-Myc Activity

Xiang Zhou, Qian Hao, Jun-ming Liao, Peng Liao, Hua Lu

J Biol Chem. 2013 Jul 26; 288(30): 21793–21801. Published online 2013 Jun 17. doi: 10.1074/jbc.M112.445122

PMCID:: PMC3724636

Abstract Article PDF–1.4M

Select item 32082829.

Coordinate loss of a microRNA and protein-coding gene cooperate in the pathogenesis of 5q− syndrome

Madhu S. Kumar, Anupama Narla, Atsushi Nonami, Ann Mullally, Nadya Dimitrova, Brian Ball, J. Randall McAuley, Luke Poveromo, Jeffrey L. Kutok, Naomi Galili, Azra Raza, Eyal Attar, D. Gary Gilliland, Tyler Jacks, Benjamin L. Ebert

Blood. 2011 Oct 27; 118(17): 4666–4673. Prepublished online 2011 Aug 26. doi: 10.1182/blood-2010-12-324715

PMCID:: PMC3208282

Abstract Article

Select item 36803310.

A cloned human ribosomal protein gene functions in rodent cells.

D D Rhoads, D J Roufa

Mol Cell Biol. 1987 Oct; 7(10): 3767–3774. doi: 10.1128/mcb.7.10.3767

PMCID:: PMC368033

Summary Page Browse PDF–1.8M

Select item 491906611.

Efficacy and Mechanism of Action of Low Dose Emetine against Human Cytomegalovirus

Rupkatha Mukhopadhyay, Sujayita Roy, Rajkumar Venkatadri, Yu-Pin Su, Wenjuan Ye, Elena Barnaeva, Lesley Mathews Griner, Noel Southall, Xin Hu, Amy Q. Wang, Xin Xu, Andrés E. Dulcey, Juan J. Marugan, Marc Ferrer, Ravit Arav-Boger

PLoS Pathog. 2016 Jun; 12(6): e1005717. Published online 2016 Jun 23. doi: 10.1371/journal.ppat.1005717

PMCID:: PMC4919066

Abstract Article PDF–6.8M

Select item 373683212.

Ribosomal Protein S14 Unties the MDM2-p53 Loop Upon Ribosomal Stress

Xiang Zhou, Qian Hao, Jun-ming Liao, Qi Zhang, Hua Lu

Oncogene. Author manuscript; available in PMC 2013 Aug 7.

Published in final edited form as: Oncogene. 2013 Jan 17; 32(3): 388–396. Published online 2012 Mar 5. doi: 10.1038/onc.2012.63

PMCID:: PMC3736832

Abstract Article PDF–3.3M

Select item 306235113.

Haploinsufficiency for ribosomal protein genes causes selective activation of p53 in human erythroid progenitor cells

Shilpee Dutt, Anupama Narla, Katherine Lin, Ann Mullally, Nirmalee Abayasekara, Christine Megerdichian, Frederick H. Wilson, Treeve Currie, Arati Khanna-Gupta, Nancy Berliner, Jeffery L. Kutok, Benjamin L. Ebert

Blood. 2011 Mar 3; 117(9): 2567–2576. Prepublished online 2010 Nov 10. doi: 10.1182/blood-2010-07-295238

PMCID:: PMC3062351

Abstract Article

Select item 38661914.

Homologous ribosomal proteins in bacteria, yeast, and humans.

I T Chen, A Dixit, D D Rhoads, D J Roufa

Proc Natl Acad Sci U S A. 1986 Sep; 83(18): 6907–6911. doi: 10.1073/pnas.83.18.6907

PMCID:: PMC386619

Summary Page Browse PDF–1.1M

Select item 36992115.

Selective linkage disruption in human-Chinese hamster cell hybrids: deletion mapping of the leuS, hexB, emtB, and chr genes on human chromosome 5.

S Dana, J J Wasmuth

Mol Cell Biol. 1982 Oct; 2(10): 1220–1228. doi: 10.1128/mcb.2.10.1220

PMCID:: PMC369921

Summary Page Browse PDF–1.8M

Select item 375139716.

Lenalidomide Promotes p53 Degradation by Inhibiting MDM2 Auto-ubiquitination in Myelodysplastic Syndrome with Chromosome 5q Deletion

Sheng Wei, Xianghong Chen, Kathy McGraw, Ling Zhang, Rami Komrokji, Justine Clark, Gisela Caceres, Debbie Billingsley, Lubomir Sokol, Jeffrey Lancet, Nicole Fortenbery, Junmin Zhou, Erika A. Eksioglu, David Sallman, Huaquan Wang, Pearlie K. Epling-Burnette, Julie Djeu, Jaroslaw P. Maciejewski, Mikkael Sekeres, Alan List

Oncogene. Author manuscript; available in PMC 2013 Aug 23.

Published in final edited form as: Oncogene. 2013 Feb 28; 32(9): 1110–1120. Published online 2012 Apr 23. doi: 10.1038/onc.2012.139

PMCID:: PMC3751397

Abstract Article PDF–3.4M

Select item 408714617.

Discovery of novel interacting partners of PSMD9, a proteasomal chaperone: Role of an Atypical and versatile PDZ-domain motif interaction and identification of putative functional modules

Nikhil Sangith, Kannan Srinivasaraghavan, Indrajit Sahu, Ankita Desai, Spandana Medipally, Arun Kumar Somavarappu, Chandra Verma, Prasanna Venkatraman

FEBS Open Bio. 2014; 4: 571–583. Published online 2014 Jun 6. doi: 10.1016/j.fob.2014.05.005

Correction in:: FEBS Open Bio. 2015; 5: 731–732.

PMCID:: PMC4087146

Abstract Article PDF–2.3M

Select item 564712418.

Identification of XBP1-u as a novel regulator of the MDM2/p53 axis using an shRNA library

Can Huang, Shourong Wu, Hong Ji, Xuesong Yan, Yudan Xie, Saomi Murai, Hezhao Zhao, Makoto Miyagishi, Vivi Kasim

Sci Adv. 2017 Oct; 3(10): e1701383. Published online 2017 Oct 18. doi: 10.1126/sciadv.1701383

PMCID:: PMC5647124

Abstract Article PDF–1.8M

Select item 281702219.

Diamond-Blackfan anemia: genotype-phenotype correlations in Italian patients with RPL5 and RPL11 mutations

Paola Quarello, Emanuela Garelli, Adriana Carando, Alfredo Brusco, Roberto Calabrese, Carlo Dufour, Daniela Longoni, Aldo Misuraca, Luciana Vinti, Anna Aspesi, Laura Biondini, Fabrizio Loreni, Irma Dianzani, Ugo Ramenghi

Haematologica. 2010 Feb; 95(2): 206–213. Published online 2009 Sep 22. doi: 10.3324/haematol.2009.011783

PMCID:: PMC2817022

Abstract Article PDF–233K

Select item 439207320.

Ribosomal proteins L11 and L5 activate TAp73 by overcoming MDM2 inhibition

X Zhou, Q Hao, Q Zhang, J-m Liao, J-w Ke, P Liao, B Cao, H Lu

Cell Death Differ. 2015 Apr; 22(5): 755–766. Published online 2014 Oct 10. doi: 10.1038/cdd.2014.167

PMCID:: PMC4392073

Abstract Article PDF–3.4M

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