RPS2 c.261T>C ;(p.P87=)

Variant ID: 16-2014283-A-G

NM_002952.3(RPS2):c.261T>C;(p.P87=)

This variant was identified in 31 publications

View GRCh38 version.




Publications:


A Phase II Trial of Guadecitabine plus Atezolizumab in Metastatic Urothelial Carcinoma Progressing after Initial Immune Checkpoint Inhibitor Therapy.

Clinical Cancer Research : An Official Journal Of The American Association For Cancer Research
Jang, H Josh HJ; Hostetter, Galen G; MacFarlane, Alexander W AW; Madaj, Zachary Z; Ross, Eric A EA; Hinoue, Toshinori T; Kulchycki, Justin R JR; Burgos, Ryan S RS; Tafseer, Mahvish M; Alpaugh, R Katherine RK; Schwebel, Candice L CL; Kokate, Rutika R; Geynisman, Daniel M DM; Zibelman, Matthew R MR; Ghatalia, Pooja P; Nichols, Peter W PW; Chung, Woonbok W; Madzo, Jozef J; Hahn, Noah M NM; Quinn, David I DI; Issa, Jean-Pierre J JJ; Topper, Michael J MJ; Baylin, Stephen B SB; Shen, Hui H; Campbell, Kerry S KS; Jones, Peter A PA; Plimack, Elizabeth R ER
Publication Date: 2023-03-16

Variant appearance in text: RPS2: P87P
PubMed Link: 36928921
Variant Present in the following documents:
  • ccr-22-3642_supplementary_tables_1_suppts1.xlsx, sheet 3
View BVdb publication page



Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem
Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS
Publication Date: 2022-11

Variant appearance in text: RPS2: P87P; rs2286466
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Whole genome DNA and RNA sequencing of whole blood elucidates the genetic architecture of gene expression underlying a wide range of diseases.

Scientific Reports
Liu, Chunyu C; Joehanes, Roby R; Ma, Jiantao J; Wang, Yuxuan Y; Sun, Xianbang X; Keshawarz, Amena A; Sooda, Meera M; Huan, Tianxiao T; Hwang, Shih-Jen SJ; Bui, Helena H; Tejada, Brandon B; Munson, Peter J PJ; Demirkale, Cumhur Y CY; Heard-Costa, Nancy L NL; Pitsillides, Achilleas N AN; Peloso, Gina M GM; Feolo, Michael M; Sharopova, Nataliya N; Vasan, Ramachandran S RS; Levy, Daniel D
Publication Date: 2022-11-23

Variant appearance in text: rs2286466
PubMed Link: 36424512
Variant Present in the following documents:
  • Main text
  • 41598_2022_Article_24611.pdf
View BVdb publication page



Beneficial effects of mifepristone treatment in breast cancer patients selected by the progesterone receptor isoform ratio: Results from the MIPRA trial.

Clinical Cancer Research : An Official Journal Of The American Association For Cancer Research
Elía, Andrés A; Saldain, Leo L; Vanzulli, Silvia I SI; Helguero, Luisa A LA; Lamb, Caroline A CA; Fabris, Victoria V; Pataccini, Gabriela G; Martínez-Vazquez, Paula P; Burruchaga, Javier J; Caillet-Bois, Ines I; Spengler, Eunice E; Acosta Haab, Gabriela G; Liguori, Marcos M; Castets, Alejandra A; Lovisi, Silvia S; Abascal, María F MF; Novaro, Virginia V; Sánchez, Jana J; Muñoz, Javier J; Belizán, Jose M JM; Abba, Martín C MC; Gass, Hugo H; Rojas, Paola P; Lanari, Claudia C
Publication Date: 2022-10-21

Variant appearance in text: rs2286466
PubMed Link: 36269797
Variant Present in the following documents:
  • ccr-22-2060_supplementary_table_s5_suppts5.xlsx, sheet 1
View BVdb publication page



Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports
Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-10-14

Variant appearance in text: RPS2: P87P
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM15_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM8_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM5_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM4_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM10_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM3_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM2_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM9_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM6_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM7_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM11_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM13_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM12_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2
View BVdb publication page



A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts.

Human Genome Variation
Irum, Bushra B; Kabir, Firoz F; Shoshany, Nadav N; Khan, Shahid Y SY; Rauf, Bushra B; Naeem, Muhammad Asif MA; Qaiser, Tanveer A TA; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-09-08

Variant appearance in text: RPS2: P87P; rs2286466
PubMed Link: 36075891
Variant Present in the following documents:
  • 41439_2022_208_MOESM4_ESM.xlsx, sheet 2
View BVdb publication page



Whole Genome DNA and RNA Sequencing of Whole Blood Elucidates the Genetic Architecture of Gene Expression Underlying a Wide Range of Diseases.

Research Square
Liu, Chunyu C; Joehanes, Roby R; Ma, Jiantao J; Wang, Yuxuan Y; Sun, Xianbang X; Keshawarz, Amena A; Sooda, Meera M; Huan, Tianxiao T; Hwang, Shih-Jen SJ; Bui, Helena H; Tejada, Brandon B; Munson, Peter J PJ; Cumhur, Demirkale D; Heard-Costa, Nancy L NL; Pitsillides, Achilleas N AN; Peloso, Gina M GM; Feolo, Michael M; Sharopova, Nataliya N; Vasan, Ramachandran S RS; Levy, Daniel D
Publication Date: 2022-05-31

Variant appearance in text: rs2286466
PubMed Link: 35664994
Variant Present in the following documents:
  • nihpp-rs1598646v1.pdf
View BVdb publication page



Case Report: A Variant Non-ketotic Hyperglycinemia With GLRX5 Mutations: Manifestation of Deficiency of Activities of the Respiratory Chain Enzymes.

Frontiers In Genetics
Feng, Wei-Xing WX; Zhuo, Xiu-Wei XW; Liu, Zhi-Mei ZM; Li, Jiu-Wei JW; Zhang, Wei-Hua WH; Wu, Yun Y; Han, Tong-Li TL; Fang, Fang F
Publication Date: 2021

Variant appearance in text: N/A
PubMed Link: 34054912
Variant Present in the following documents:
View BVdb publication page



Disseminated Talaromyces marneffei Infection in a Non-HIV Infant With a Homozygous Private Variant of RELB.

Frontiers In Cellular And Infection Microbiology
Ding, Xiaofang X; Huang, Han H; Zhong, Lili L; Chen, Min M; Peng, Fang F; Zhang, Bing B; Cui, Xinyu X; Yang, Xiu-An XA
Publication Date: 2021

Variant appearance in text: RPS2: Pro87Pro; rs2286466
PubMed Link: 33791233
Variant Present in the following documents:
  • Table_2.xlsx, sheet 1
View BVdb publication page



Integrated genetic and metabolic landscapes predict vulnerabilities of temozolomide resistant glioblastoma cells.

Npj Systems Biology And Applications
Immanuel, Selva Rupa Christinal SRC; Ghanate, Avinash D AD; Parmar, Dharmeshkumar S DS; Yadav, Ritu R; Uthup, Riya R; Panchagnula, Venkateswarlu V; Raghunathan, Anu A
Publication Date: 2021-01-08

Variant appearance in text: N/A
PubMed Link: 33420045
Variant Present in the following documents:
View BVdb publication page



Genetics of Atrial Fibrillation in 2020: GWAS, Genome Sequencing, Polygenic Risk, and Beyond.

Circulation Research
Roselli, Carolina C; Rienstra, Michiel M; Ellinor, Patrick T PT
Publication Date: 2020-06-19

Variant appearance in text: rs2286466
PubMed Link: 32716721
Variant Present in the following documents:
  • Main text
View BVdb publication page



Identification of a nonsense mutation in TNNI3K associated with cardiac conduction disease.

Journal Of Clinical Laboratory Analysis
Liu, Jiang J; Liu, Da D; Li, Muzheng M; Wu, Keke K; Liu, Na N; Zhao, Chenyu C; Shi, Xiaoliu X; Liu, Qiming Q
Publication Date: 2020-09

Variant appearance in text: RPS2: P87P; rs2286466
PubMed Link: 32529721
Variant Present in the following documents:
  • JCLA-34-e23418-s003.xls, sheet 1
View BVdb publication page



Loss of heterozygosity of essential genes represents a widespread class of potential cancer vulnerabilities.

Nature Communications
Nichols, Caitlin A CA; Gibson, William J WJ; Brown, Meredith S MS; Kosmicki, Jack A JA; Busanovich, John P JP; Wei, Hope H; Urbanski, Laura M LM; Curimjee, Naomi N; Berger, Ashton C AC; Gao, Galen F GF; Cherniack, Andrew D AD; Dhe-Paganon, Sirano S; Paolella, Brenton R BR; Beroukhim, Rameen R
Publication Date: 2020-05-20

Variant appearance in text: RPS2: 261T>C; rs2286466
PubMed Link: 32433464
Variant Present in the following documents:
  • 41467_2020_16399_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page



Multi-level evidence of an allelic hierarchy of USH2A variants in hearing, auditory processing and speech/language outcomes.

Communications Biology
Perrino, Peter A PA; Talbot, Lidiya L; Kirkland, Rose R; Hill, Amanda A; Rendall, Amanda R AR; Mountford, Hayley S HS; Taylor, Jenny J; , ; Buscarello, Alexzandrea N AN; Lahiri, Nayana N; Saggar, Anand A; Fitch, R Holly RH; Newbury, Dianne F DF
Publication Date: 2020-04-20

Variant appearance in text: rs2286466
PubMed Link: 32313182
Variant Present in the following documents:
  • 42003_2020_885_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Identification of atrial fibrillation associated genes and functional non-coding variants.

Nature Communications
van Ouwerkerk, Antoinette F AF; Bosada, Fernanda M FM; van Duijvenboden, Karel K; Hill, Matthew C MC; Montefiori, Lindsey E LE; Scholman, Koen T KT; Liu, Jia J; de Vries, Antoine A F AAF; Boukens, Bastiaan J BJ; Ellinor, Patrick T PT; Goumans, Marie José T H MJTH; Efimov, Igor R IR; Nobrega, Marcelo A MA; Barnett, Phil P; Martin, James F JF; Christoffels, Vincent M VM
Publication Date: 2019-10-18

Variant appearance in text: rs2286466
PubMed Link: 31628324
Variant Present in the following documents:
  • 41467_2019_12721_MOESM2_ESM.pdf
View BVdb publication page



Distinctive mutational spectrum and karyotype disruption in long-term cisplatin-treated urothelial carcinoma cell lines.

Scientific Reports
Skowron, Margaretha A MA; Petzsch, Patrick P; Hardt, Karin K; Wagner, Nicholas N; Beier, Manfred M; Stepanow, Stefanie S; Drechsler, Matthias M; Rieder, Harald H; Köhrer, Karl K; Niegisch, Günter G; Hoffmann, Michèle J MJ; Schulz, Wolfgang A WA
Publication Date: 2019-10-09

Variant appearance in text: RPS2: P87P; rs2286466
PubMed Link: 31597922
Variant Present in the following documents:
  • 41598_2019_50891_MOESM6_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM9_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM2_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM3_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM7_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM5_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM8_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM4_ESM.xlsx, sheet 1
View BVdb publication page



Dissecting TSC2-mutated renal and hepatic angiomyolipomas in an individual with ARID1B-associated intellectual disability.

Bmc Cancer
Popp, Bernt B; Agaimy, Abbas A; Kraus, Cornelia C; Knaup, Karl X KX; Ekici, Arif B AB; Uebe, Steffen S; Reis, André A; Wiesener, Michael M; Zweier, Christiane C
Publication Date: 2019-05-10

Variant appearance in text: N/A
PubMed Link: 31077186
Variant Present in the following documents:
View BVdb publication page



Multiple genetic mutations caused by NKX6.3 depletion contribute to gastric tumorigenesis.

Scientific Reports
Yoon, Jung Hwan JH; Kim, Olga O; Eun, Jung Woo JW; Choi, Sung Sook SS; Ashktorab, Hassan H; Smoot, Duane T DT; Nam, Suk Woo SW; Park, Won Sang WS
Publication Date: 2018-12-04

Variant appearance in text: rs2286466
PubMed Link: 30514953
Variant Present in the following documents:
  • 41598_2018_35733_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: RPS2: 261T>C; rs2286466
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_5.xlsx, sheet 1
  • Table_6.xlsx, sheet 1
  • Table_7.xlsx, sheet 1
View BVdb publication page



Multi-ethnic genome-wide association study for atrial fibrillation.

Nature Genetics
Roselli, Carolina C; Chaffin, Mark D MD; Weng, Lu-Chen LC; Aeschbacher, Stefanie S; Ahlberg, Gustav G; Albert, Christine M CM; Almgren, Peter P; Alonso, Alvaro A; Anderson, Christopher D CD; Aragam, Krishna G KG; Arking, Dan E DE; Barnard, John J; Bartz, Traci M TM; Benjamin, Emelia J EJ; Bihlmeyer, Nathan A NA; Bis, Joshua C JC; Bloom, Heather L HL; Boerwinkle, Eric E; Bottinger, Erwin B EB; Brody, Jennifer A JA; Calkins, Hugh H; Campbell, Archie A; Cappola, Thomas P TP; Carlquist, John J; Chasman, Daniel I DI; Chen, Lin Y LY; Chen, Yii-Der Ida YI; Choi, Eue-Keun EK; Choi, Seung Hoan SH; Christophersen, Ingrid E IE; Chung, Mina K MK; Cole, John W JW; Conen, David D; Cook, James J; Crijns, Harry J HJ; Cutler, Michael J MJ; Damrauer, Scott M SM; Daniels, Brian R BR; Darbar, Dawood D; Delgado, Graciela G; Denny, Joshua C JC; Dichgans, Martin M; Dörr, Marcus M; Dudink, Elton A EA; Dudley, Samuel C SC; Esa, Nada N; Esko, Tonu T; Eskola, Markku M; Fatkin, Diane D; Felix, Stephan B SB; Ford, Ian I; Franco, Oscar H OH; Geelhoed, Bastiaan B; Grewal, Raji P RP; Gudnason, Vilmundur V; Guo, Xiuqing X; Gupta, Namrata N; Gustafsson, Stefan S; Gutmann, Rebecca R; Hamsten, Anders A; Harris, Tamara B TB; Hayward, Caroline C; Heckbert, Susan R SR; Hernesniemi, Jussi J; Hocking, Lynne J LJ; Hofman, Albert A; Horimoto, Andrea R V R ARVR; Huang, Jie J; Huang, Paul L PL; Huffman, Jennifer J; Ingelsson, Erik E; Ipek, Esra Gucuk EG; Ito, Kaoru K; Jimenez-Conde, Jordi J; Johnson, Renee R; Jukema, J Wouter JW; Kääb, Stefan S; Kähönen, Mika M; Kamatani, Yoichiro Y; Kane, John P JP; Kastrati, Adnan A; Kathiresan, Sekar S; Katschnig-Winter, Petra P; Kavousi, Maryam M; Kessler, Thorsten T; Kietselaer, Bas L BL; Kirchhof, Paulus P; Kleber, Marcus E ME; Knight, Stacey S; Krieger, Jose E JE; Kubo, Michiaki M; Launer, Lenore J LJ; Laurikka, Jari J; Lehtimäki, Terho T; Leineweber, Kirsten K; Lemaitre, Rozenn N RN; Li, Man M; Lim, Hong Euy HE; Lin, Henry J HJ; Lin, Honghuang H; Lind, Lars L; Lindgren, Cecilia M CM; Lokki, Marja-Liisa ML; London, Barry B; Loos, Ruth J F RJF; Low, Siew-Kee SK; Lu, Yingchang Y; Lyytikäinen, Leo-Pekka LP; Macfarlane, Peter W PW; Magnusson, Patrik K PK; Mahajan, Anubha A; Malik, Rainer R; Mansur, Alfredo J AJ; Marcus, Gregory M GM; Margolin, Lauren L; Margulies, Kenneth B KB; März, Winfried W; McManus, David D DD; Melander, Olle O; Mohanty, Sanghamitra S; Montgomery, Jay A JA; Morley, Michael P MP; Morris, Andrew P AP; Müller-Nurasyid, Martina M; Natale, Andrea A; Nazarian, Saman S; Neumann, Benjamin B; Newton-Cheh, Christopher C; Niemeijer, Maartje N MN; Nikus, Kjell K; Nilsson, Peter P; Noordam, Raymond R; Oellers, Heidi H; Olesen, Morten S MS; Orho-Melander, Marju M; Padmanabhan, Sandosh S; Pak, Hui-Nam HN; Paré, Guillaume G; Pedersen, Nancy L NL; Pera, Joanna J; Pereira, Alexandre A; Porteous, David D; Psaty, Bruce M BM; Pulit, Sara L SL; Pullinger, Clive R CR; Rader, Daniel J DJ; Refsgaard, Lena L; Ribasés, Marta M; Ridker, Paul M PM; Rienstra, Michiel M; Risch, Lorenz L; Roden, Dan M DM; Rosand, Jonathan J; Rosenberg, Michael A MA; Rost, Natalia N; Rotter, Jerome I JI; Saba, Samir S; Sandhu, Roopinder K RK; Schnabel, Renate B RB; Schramm, Katharina K; Schunkert, Heribert H; Schurman, Claudia C; Scott, Stuart A SA; Seppälä, Ilkka I; Shaffer, Christian C; Shah, Svati S; Shalaby, Alaa A AA; Shim, Jaemin J; Shoemaker, M Benjamin MB; Siland, Joylene E JE; Sinisalo, Juha J; Sinner, Moritz F MF; Slowik, Agnieszka A; Smith, Albert V AV; Smith, Blair H BH; Smith, J Gustav JG; Smith, Jonathan D JD; Smith, Nicholas L NL; Soliman, Elsayed Z EZ; Sotoodehnia, Nona N; Stricker, Bruno H BH; Sun, Albert A; Sun, Han H; Svendsen, Jesper H JH; Tanaka, Toshihiro T; Tanriverdi, Kahraman K; Taylor, Kent D KD; Teder-Laving, Maris M; Teumer, Alexander A; Thériault, Sébastien S; Trompet, Stella S; Tucker, Nathan R NR; Tveit, Arnljot A; Uitterlinden, Andre G AG; Van Der Harst, Pim P; Van Gelder, Isabelle C IC; Van Wagoner, David R DR; Verweij, Niek N; Vlachopoulou, Efthymia E; Völker, Uwe U; Wang, Biqi B; Weeke, Peter E PE; Weijs, Bob B; Weiss, Raul R; Weiss, Stefan S; Wells, Quinn S QS; Wiggins, Kerri L KL; Wong, Jorge A JA; Woo, Daniel D; Worrall, Bradford B BB; Yang, Pil-Sung PS; Yao, Jie J; Yoneda, Zachary T ZT; Zeller, Tanja T; Zeng, Lingyao L; Lubitz, Steven A SA; Lunetta, Kathryn L KL; Ellinor, Patrick T PT
Publication Date: 2018-06-11

Variant appearance in text: rs2286466
PubMed Link: 29892015
Variant Present in the following documents:
  • Main text
View BVdb publication page



Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.

Oncotarget
Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH
Publication Date: 2017-11-10

Variant appearance in text: RPS2: P87P; rs2286466
PubMed Link: 29221171
Variant Present in the following documents:
  • oncotarget-08-95841-s002.xlsx, sheet 1
  • oncotarget-08-95841-s002.xlsx, sheet 4
View BVdb publication page



Whole-exome sequencing analysis of Waardenburg syndrome in a Chinese family.

Human Genome Variation
Chen, Dezhong D; Zhao, Na N; Wang, Jing J; Li, Zhuoyu Z; Wu, Changxin C; Fu, Jie J; Xiao, Han H
Publication Date: 2017

Variant appearance in text: rs2286466
PubMed Link: 28690861
Variant Present in the following documents:
  • hgv201727-s1.xls, sheet 1
View BVdb publication page



Identification of EML4-ALK as an alternative fusion gene in epithelioid inflammatory myofibroblastic sarcoma.

Orphanet Journal Of Rare Diseases
Jiang, Quan Q; Tong, Han-Xing HX; Hou, Ying-Yong YY; Zhang, Yong Y; Li, Jing-Lei JL; Zhou, Yu-Hong YH; Xu, Jing J; Wang, Jiong-Yuan JY; Lu, Wei-Qi WQ
Publication Date: 2017-05-23

Variant appearance in text: RPS2: P87P; rs2286466
PubMed Link: 28535796
Variant Present in the following documents:
  • 13023_2017_647_MOESM1_ESM.xlsx, sheet 4
View BVdb publication page



Generation of a High Number of Healthy Erythroid Cells from Gene-Edited Pyruvate Kinase Deficiency Patient-Specific Induced Pluripotent Stem Cells.

Stem Cell Reports
Garate, Zita Z; Quintana-Bustamante, Oscar O; Crane, Ana M AM; Olivier, Emmanuel E; Poirot, Laurent L; Galetto, Roman R; Kosinski, Penelope P; Hill, Collin C; Kung, Charles C; Agirre, Xabi X; Orman, Israel I; Cerrato, Laura L; Alberquilla, Omaira O; Rodriguez-Fornes, Fatima F; Fusaki, Noemi N; Garcia-Sanchez, Felix F; Maia, Tabita M TM; Ribeiro, Maria L ML; Sevilla, Julian J; Prosper, Felipe F; Jin, Shengfang S; Mountford, Joanne J; Guenechea, Guillermo G; Gouble, Agnes A; Bueren, Juan A JA; Davis, Brian R BR; Segovia, Jose C JC
Publication Date: 2015-12-08

Variant appearance in text: RPS2: P87P; rs2286466
PubMed Link: 26549847
Variant Present in the following documents:
  • mmc3.xlsx, sheet 2
  • mmc3.xlsx, sheet 1
View BVdb publication page



Proteogenomic analysis reveals exosomes are more oncogenic than ectosomes.

Oncotarget
Keerthikumar, Shivakumar S; Gangoda, Lahiru L; Liem, Michael M; Fonseka, Pamali P; Atukorala, Ishara I; Ozcitti, Cemil C; Mechler, Adam A; Adda, Christopher G CG; Ang, Ching-Seng CS; Mathivanan, Suresh S
Publication Date: 2015-06-20

Variant appearance in text: RPS2: P87P; rs2286466
PubMed Link: 25944692
Variant Present in the following documents:
  • oncotarget-06-15375-s005.xlsx, sheet 2
View BVdb publication page



Whole-genome sequencing of the world's oldest people.

Plos One
Gierman, Hinco J HJ; Fortney, Kristen K; Roach, Jared C JC; Coles, Natalie S NS; Li, Hong H; Glusman, Gustavo G; Markov, Glenn J GJ; Smith, Justin D JD; Hood, Leroy L; Coles, L Stephen LS; Kim, Stuart K SK
Publication Date: 2014

Variant appearance in text: RPS2: P87P; rs2286466
PubMed Link: 25390934
Variant Present in the following documents:
  • pone.0112430.s004.xlsx, sheet 1
View BVdb publication page



Exome sequencing is an efficient tool for variant late-infantile neuronal ceroid lipofuscinosis molecular diagnosis.

Plos One
Patiño, Liliana Catherine LC; Battu, Rajani R; Ortega-Recalde, Oscar O; Nallathambi, Jeyabalan J; Anandula, Venkata Ramana VR; Renukaradhya, Umashankar U; Laissue, Paul P
Publication Date: 2014

Variant appearance in text: RPS2: P87P
PubMed Link: 25333361
Variant Present in the following documents:
  • pone.0109576.s002.xls, sheet 3
  • pone.0109576.s001.xls, sheet 3
View BVdb publication page



Integrated mRNA and microRNA transcriptome sequencing characterizes sequence variants and mRNA-microRNA regulatory network in nasopharyngeal carcinoma model systems.

Febs Open Bio
Szeto, Carol Ying-Ying CY; Lin, Chi Ho CH; Choi, Siu Chung SC; Yip, Timothy T C TT; Ngan, Roger Kai-Cheong RK; Tsao, George Sai-Wah GS; Li Lung, Maria M
Publication Date: 2014

Variant appearance in text: RPS2: P87P; rs2286466
PubMed Link: 24490137
Variant Present in the following documents:
  • mmc5.xlsx, sheet 2
View BVdb publication page



Effect of a poly(ADP-ribose) polymerase-1 inhibitor against esophageal squamous cell carcinoma cell lines.

Cancer Science
Nasuno, Tomomitsu T; Mimaki, Sachiyo S; Okamoto, Makito M; Esumi, Hiroyasu H; Tsuchihara, Katsuya K
Publication Date: 2014-02

Variant appearance in text: RPS2: P87P; rs2286466
PubMed Link: 24219164
Variant Present in the following documents:
  • cas0105-0202-SD2.xlsx, sheet 1
  • cas0105-0202-SD3.xlsx, sheet 1
View BVdb publication page



Identification of novel SNPs in glioblastoma using targeted resequencing.

Plos One
Keller, Andreas A; Harz, Christian C; Matzas, Mark M; Meder, Benjamin B; Katus, Hugo A HA; Ludwig, Nicole N; Fischer, Ulrike U; Meese, Eckart E
Publication Date: 2011

Variant appearance in text: rs2286466
PubMed Link: 21695249
Variant Present in the following documents:
  • pone.0018158.s001.xls, sheet 5
  • pone.0018158.s001.xls, sheet 4
View BVdb publication page