A citation-based method for searching scientific literature

Jason E Farrar, Michelle Nater, Emi Caywood, Michael A McDevitt, Jeanne Kowalski, Clifford M Takemoto, C Conover Talbot, Paul Meltzer, Diane Esposito, Alan H Beggs, Hal E Schneider, Agnieszka Grabowska, Sarah E Ball, Edyta Niewiadomska, Colin A Sieff, Adrianna Vlachos, Eva Atsidaftos, Steven R Ellis, Jeffrey M Lipton, Hanna T Gazda, Robert J Arceci. Blood 2008
Times Cited: 174







List of co-cited articles
1121 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Ribosomal protein L23 activates p53 by inhibiting MDM2 function in response to ribosomal perturbation but not to translation inhibition.
Mu-Shui Dai, Shelya X Zeng, Yetao Jin, Xiao-Xin Sun, Larry David, Hua Lu. Mol Cell Biol 2004
384
13

Erythropoiesis failure due to RPS19 deficiency is independent of an activated Tp53 response in a zebrafish model of Diamond-Blackfan anaemia.
Hidetsugu Torihara, Tamayo Uechi, Anirban Chakraborty, Minori Shinya, Noriyoshi Sakai, Naoya Kenmochi. Br J Haematol 2011
47
27

The role of human ribosomal proteins in the maturation of rRNA and ribosome production.
Sara Robledo, Rachel A Idol, Dan L Crimmins, Jack H Ladenson, Philip J Mason, Monica Bessler. RNA 2008
165
13

Diamond Blackfan anaemia in the UK: clinical and genetic heterogeneity.
Karen A Orfali, Yaw Ohene-Abuakwa, Sarah E Ball. Br J Haematol 2004
83
15


Uncoupling of GTP hydrolysis from eIF6 release on the ribosome causes Shwachman-Diamond syndrome.
Andrew J Finch, Christine Hilcenko, Nicolas Basse, Lesley F Drynan, Beatriz Goyenechea, Tobias F Menne, Africa González Fernández, Paul Simpson, Clive S D'Santos, Mark J Arends,[...]. Genes Dev 2011
185
13

How common are extraribosomal functions of ribosomal proteins?
Jonathan R Warner, Kerri B McIntosh. Mol Cell 2009
472
13

L-Leucine improves the anemia and developmental defects associated with Diamond-Blackfan anemia and del(5q) MDS by activating the mTOR pathway.
Elspeth M Payne, Maria Virgilio, Anupama Narla, Hong Sun, Michelle Levine, Barry H Paw, Nancy Berliner, A Thomas Look, Benjamin L Ebert, Arati Khanna-Gupta. Blood 2012
106
13

Primary hematopoietic cells from DBA patients with mutations in RPL11 and RPS19 genes exhibit distinct erythroid phenotype in vitro.
H Moniz, M Gastou, T Leblanc, C Hurtaud, A Crétien, Y Lécluse, H Raslova, J Larghero, L Croisille, M Faubladier,[...]. Cell Death Dis 2012
49
26

Ribosomal protein L11 negatively regulates oncoprotein MDM2 and mediates a p53-dependent ribosomal-stress checkpoint pathway.
Yanping Zhang, Gabrielle White Wolf, Krishna Bhat, Aiwen Jin, Theresa Allio, William A Burkhart, Yue Xiong. Mol Cell Biol 2003
425
12

Successful treatment of a Diamond-Blackfan anemia patient with amino acid leucine.
D Pospisilova, J Cmejlova, J Hak, T Adam, R Cmejla. Haematologica 2007
60
20

Diamond-Blackfan anaemia in the U.K.: analysis of 80 cases from a 20-year birth cohort.
S E Ball, C P McGuckin, G Jenkins, E C Gordon-Smith. Br J Haematol 1996
113
12

Loss of p53 synthesis in zebrafish tumors with ribosomal protein gene mutations.
Alyson W MacInnes, Adam Amsterdam, Charles A Whittaker, Nancy Hopkins, Jacqueline A Lees. Proc Natl Acad Sci U S A 2008
106
12

Suppression of Myc oncogenic activity by ribosomal protein haploinsufficiency.
Maria Barna, Aya Pusic, Ornella Zollo, Maria Costa, Nadya Kondrashov, Eduardo Rego, Pulivarthi H Rao, Davide Ruggero. Nature 2008
292
11

Prevention of the neurocristopathy Treacher Collins syndrome through inhibition of p53 function.
Natalie C Jones, Megan L Lynn, Karin Gaudenz, Daisuke Sakai, Kazushi Aoto, Jean-Phillipe Rey, Earl F Glynn, Lacey Ellington, Chunying Du, Jill Dixon,[...]. Nat Med 2008
300
11

Ribosomal protein L11 mutation in zebrafish leads to haematopoietic and metabolic defects.
Nadia Danilova, Kathleen M Sakamoto, Shuo Lin. Br J Haematol 2011
70
15

Mutations in the ribosomal protein genes in Japanese patients with Diamond-Blackfan anemia.
Yuki Konno, Tsutomu Toki, Satoru Tandai, Gang Xu, Runan Wang, Kiminori Terui, Shouichi Ohga, Toshiro Hara, Asahito Hama, Seiji Kojima,[...]. Haematologica 2010
31
35

X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions.
N S Heiss, S W Knight, T J Vulliamy, S M Klauck, S Wiemann, P J Mason, A Poustka, I Dokal. Nat Genet 1998
653
11

Missense mutations associated with Diamond-Blackfan anemia affect the assembly of ribosomal protein S19 into the ribosome.
Mara Angelini, Stefano Cannata, Valentina Mercaldo, Luisa Gibello, Claudio Santoro, Irma Dianzani, Fabrizio Loreni. Hum Mol Genet 2007
49
22


Dietary L-leucine improves the anemia in a mouse model for Diamond-Blackfan anemia.
Pekka Jaako, Shubhranshu Debnath, Karin Olsson, David Bryder, Johan Flygare, Stefan Karlsson. Blood 2012
58
18

Ribosomal protein SA haploinsufficiency in humans with isolated congenital asplenia.
Alexandre Bolze, Nizar Mahlaoui, Minji Byun, Bridget Turner, Nikolaus Trede, Steven R Ellis, Avinash Abhyankar, Yuval Itan, Etienne Patin, Samuel Brebner,[...]. Science 2013
124
11

Inactivation of ribosomal protein L22 promotes transformation by induction of the stemness factor, Lin28B.
Shuyun Rao, Sang-Yun Lee, Alejandro Gutierrez, Jacqueline Perrigoue, Roshan J Thapa, Zhigang Tu, John R Jeffers, Michele Rhodes, Stephen Anderson, Tamas Oravecz,[...]. Blood 2012
103
11

Exome sequencing identifies mutation in CNOT3 and ribosomal genes RPL5 and RPL10 in T-cell acute lymphoblastic leukemia.
Kim De Keersmaecker, Zeynep Kalender Atak, Ning Li, Carmen Vicente, Stephanie Patchett, Tiziana Girardi, Valentina Gianfelici, Ellen Geerdens, Emmanuelle Clappier, Michaël Porcu,[...]. Nat Genet 2013
277
11

Exome sequencing identified RPS15A as a novel causative gene for Diamond-Blackfan anemia.
Fumika Ikeda, Kenichi Yoshida, Tsutomu Toki, Tamayo Uechi, Shiori Ishida, Yukari Nakajima, Yoji Sasahara, Yusuke Okuno, Rika Kanezaki, Kiminori Terui,[...]. Haematologica 2017
23
47

Regulation of HDM2 activity by the ribosomal protein L11.
Marion A E Lohrum, Robert L Ludwig, Michael H G Kubbutat, Mary Hanlon, Karen H Vousden. Cancer Cell 2003
504
10

Regulation of p53 translation and induction after DNA damage by ribosomal protein L26 and nucleolin.
Masatoshi Takagi, Michael J Absalon, Kevin G McLure, Michael B Kastan. Cell 2005
468
10

The p53 tumor suppressor causes congenital malformations in Rpl24-deficient mice and promotes their survival.
Martina Barkić, Sladana Crnomarković, Kristina Grabusić, Ivana Bogetić, Linda Panić, Sanda Tamarut, Maja Cokarić, Ines Jerić, Sandra Vidak, Sinisa Volarević. Mol Cell Biol 2009
80
12


RPS19 mutations in patients with Diamond-Blackfan anemia.
Maria Francesca Campagnoli, Ugo Ramenghi, Marta Armiraglio, Paola Quarello, Emanuela Garelli, Adriana Carando, Federica Avondo, Elisa Pavesi, Sébastien Fribourg, Pierre-Emmanuel Gleizes,[...]. Hum Mutat 2008
78
12

Erythrocyte adenosine deaminase: diagnostic value for Diamond-Blackfan anaemia.
John H Fargo, Christian P Kratz, Neelam Giri, Sharon A Savage, Carolyn Wong, Karen Backer, Blanche P Alter, Bertil Glader. Br J Haematol 2013
48
20

Loss of GATA-1 full length as a cause of Diamond-Blackfan anemia phenotype.
Sara Parrella, Anna Aspesi, Paola Quarello, Emanuela Garelli, Elisa Pavesi, Adriana Carando, Margherita Nardi, Steven R Ellis, Ugo Ramenghi, Irma Dianzani. Pediatr Blood Cancer 2014
54
18

Ribosome Levels Selectively Regulate Translation and Lineage Commitment in Human Hematopoiesis.
Rajiv K Khajuria, Mathias Munschauer, Jacob C Ulirsch, Claudia Fiorini, Leif S Ludwig, Sean K McFarland, Nour J Abdulhay, Harrison Specht, Hasmik Keshishian, D R Mani,[...]. Cell 2018
174
10

Inhibition of HDM2 and activation of p53 by ribosomal protein L23.
Aiwen Jin, Koji Itahana, Kevin O'Keefe, Yanping Zhang. Mol Cell Biol 2004
288
9

MYC as a regulator of ribosome biogenesis and protein synthesis.
Jan van Riggelen, Alper Yetil, Dean W Felsher. Nat Rev Cancer 2010
540
9

Analysis of nucleolar protein dynamics reveals the nuclear degradation of ribosomal proteins.
Yun Wah Lam, Angus I Lamond, Matthias Mann, Jens S Andersen. Curr Biol 2007
258
9

Specific Role for Yeast Homologs of the Diamond Blackfan Anemia-associated Rps19 Protein in Ribosome Synthesis.
Isabelle Léger-Silvestre, Jacqueline Marie Caffrey, Rosy Dawaliby, Diana Alehandrovna Alvarez-Arias, Nicole Gas, Salvatore J Bertolone, Pierre-Emmanuel Gleizes, Steven Robert Ellis. J Biol Chem 2005
102
9

Roles of eukaryotic ribosomal proteins in maturation and transport of pre-18S rRNA and ribosome function.
Sébastien Ferreira-Cerca, Gisela Pöll, Pierre-Emmanuel Gleizes, Herbert Tschochner, Philipp Milkereit. Mol Cell 2005
221
9

Translational efficiency in patients with Diamond-Blackfan anemia.
Jana Cmejlova, Ludmila Dolezalova, Dagmar Pospisilova, Kvetoslava Petrtylova, Jiri Petrak, Radek Cmejla. Haematologica 2006
59
15


Gene transfer improves erythroid development in ribosomal protein S19-deficient Diamond-Blackfan anemia.
Isao Hamaguchi, Andreas Ooka, Ann Brun, Johan Richter, Niklas Dahl, Stefan Karlsson. Blood 2002
68
13

Hematopoietic defects in rps29 mutant zebrafish depend upon p53 activation.
Alison M Taylor, Jessica M Humphries, Richard M White, Ryan D Murphey, Caroline E Burns, Leonard I Zon. Exp Hematol 2012
52
17

Hematopoietic stem cell transplantation for Diamond Blackfan anemia: a report from the Diamond Blackfan Anemia Registry.
A Vlachos, N Federman, C Reyes-Haley, J Abramson, J M Lipton. Bone Marrow Transplant 2001
63
14


A new database for ribosomal protein genes which are mutated in Diamond-Blackfan Anemia.
Ilenia Boria, Paola Quarello, Federica Avondo, Emanuela Garelli, Anna Aspesi, Adriana Carando, Maria Francesca Campagnoli, Irma Dianzani, Ugo Ramenghi. Hum Mutat 2008
33
27

Mutual protection of ribosomal proteins L5 and L11 from degradation is essential for p53 activation upon ribosomal biogenesis stress.
Sladana Bursać, Maja Cokarić Brdovčak, Martin Pfannkuchen, Ines Orsolić, Lior Golomb, Yan Zhu, Chen Katz, Lilyn Daftuar, Kristina Grabušić, Iva Vukelić,[...]. Proc Natl Acad Sci U S A 2012
135
9

Inhibition of RNA polymerase I as a therapeutic strategy to promote cancer-specific activation of p53.
Megan J Bywater, Gretchen Poortinga, Elaine Sanij, Nadine Hein, Abigail Peck, Carleen Cullinane, Meaghan Wall, Leonie Cluse, Denis Drygin, Kenna Anderes,[...]. Cancer Cell 2012
369
9

Ribosomal protein mutations induce autophagy through S6 kinase inhibition of the insulin pathway.
Harry F Heijnen, Richard van Wijk, Tamara C Pereboom, Yvonne J Goos, Cor W Seinen, Brigitte A van Oirschot, Rowie van Dooren, Marc Gastou, Rachel H Giles, Wouter van Solinge,[...]. PLoS Genet 2014
42
21

A Ribosomopathy Reveals Decoding Defective Ribosomes Driving Human Dysmorphism.
Nahuel A Paolini, Martin Attwood, Samuel B Sondalle, Carolina Marques Dos Santos Vieira, Anita M van Adrichem, Franca M di Summa, Marie-Françoise O'Donohue, Pierre-Emmanuel Gleizes, Swaksha Rachuri, Joseph W Briggs,[...]. Am J Hum Genet 2017
48
18

Impaired control of IRES-mediated translation in X-linked dyskeratosis congenita.
Andrew Yoon, Guang Peng, Yves Brandenburger, Ornella Zollo, Wei Xu, Eduardo Rego, Davide Ruggero. Science 2006
301
8


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.