Human Genome Epidemiology Literature Finder
Records 1 - 14 (of 14 Records) |
Query Trace: RPL5[original query] |
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Replication of KIAA0350, IL2RA, RPL5 and CD58 as multiple sclerosis susceptibility genes in Australians. Genes and immunity 2008 Oct 9 (7): 624-30. Rubio J P, Stankovich J, Field J, Tubridy N, Marriott M, Chapman C, Bahlo M, Perera D, Johnson L J, Tait B D, Varney M D, Speed T P, Taylor B V, Foote S J, Butzkueven H, Kilpatrick T |
Diamond-Blackfan anemia: genotype-phenotype correlations in Italian patients with RPL5 and RPL11 mutations. Haematologica 2010 Feb 95 (2): 206-13. Quarello Paola, Garelli Emanuela, Carando Adriana, Brusco Alfredo, Calabrese Roberto, Dufour Carlo, Longoni Daniela, Misuraca Aldo, Vinti Luciana, Aspesi Anna, Biondini Laura, Loreni Fabrizio, Dianzani Irma, Ramenghi U |
Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20.
Nature genetics 2009 Jul 41 (7): 824-8. Authors are not available |
Fine mapping of multiple sclerosis susceptibility genes provides evidence of allelic heterogeneity at the IL2RA locus. Journal of neuroimmunology 2009 Jun 211 (1-2): 105-9. Perera Devindri, Stankovich Jim, Butzkueven Helmut, Taylor Bruce V, Foote Simon J, Kilpatrick Trevor J, Rubio Justin |
Multiple sclerosis susceptibility-associated SNPs do not influence disease severity measures in a cohort of Australian MS patients. PloS one 2010 5 (4): e10003. Jensen Cathy J, Stankovich Jim, Van der Walt Anneke, Bahlo Melanie, Taylor Bruce V, van der Mei Ingrid A F, Foote Simon J, Kilpatrick Trevor J, Johnson Laura J, Wilkins Ella, Field Judith, Danoy Patrick, Brown Matthew A, , Rubio Justin P, Butzkueven Helm |
Mutations in the ribosomal protein genes in Japanese patients with Diamond-Blackfan anemia. Haematologica 2010 Apr . Konno Y, Toki T, Tandai S, Xu G, Wang R, Terui K, Ohga S, Hara T, Hama A, Kojima S, Hasegawa D, Kosaka Y, Yanagisawa R, Koike K, Kanai R, Imai T, Hongo T, Park MJ, Sugita K, Ito E |
Tag-SNP analysis of the GFI1-EVI5-RPL5-FAM69 risk locus for multiple sclerosis. European journal of human genetics : EJHG 2010 Jul 18 (7): 827-31. Alcina Antonio, Fernández Oscar, Gonzalez Juan Ramón, Catalá-Rabasa Antonio, Fedetz María, Ndagire Dorothy, Leyva Laura, Guerrero Miguel, Arnal Carmen, Delgado Concepción, Lucas Miguel, Izquierdo Guillermo, Matesanz Fuencis |
The ribosomal protein gene RPL5 is a haploinsufficient tumor suppressor in multiple cancer types. Oncotarget 2017 Jan . Fancello Laura, Kampen Kim R, Hofman Isabel Jf, Verbeeck Jelle, De Keersmaecker K |
Molecular analysis and genotype-phenotype correlation of Diamond-Blackfan anemia. Clinical genetics 2017 10 93 (2): 320-328. Arbiv O A, Cuvelier G, Klaassen R J, Fernandez C V, Robitaille N, Steele M, Breakey V, Abish S, Wu J, Sinha R, Silva M, Goodyear L, Jardine L, Lipton J H, Corriveau-Bourque C, Brossard J, Michon B, Ghemlas I, Waespe N, Zlateska B, Sung L, Cada M, Dror |
Germline Duplication of SNORA18L5 Increases Risk for HBV-related Hepatocellular Carcinoma by Altering Localization of Ribosomal Proteins and Decreasing Levels of p53. Gastroenterology 2018 4 155 (2): 542-556. Cao Pengbo, Yang Aiqing, Wang Rui, Xia Xia, Zhai Yun, Li Yuanfeng, Yang Fei, Cui Ying, Xie Weimin, Liu Ying, Liu Taotao, Jia Weihua, Jiang Zhengwen, Li Zhuo, Han Yuqing, Gao Chengming, Song Qingfeng, Xie Bobo, Zhang Luo, Zhang Hongxing, Zhang Jinxu, Shen Xizhong, Yuan Yunfei, Yu Feng, Wang Ying, Xu Jing, Ma Yilong, Mo Zengnan, Yu Wuzhong, He Fuchu, Zhou Gangqi |
Reanalysing genomic data by normalized coverage values uncovers CNVs in bone marrow failure gene panels. NPJ genomic medicine 2019 4 30. Lauhasurayotin Supanun, Cuvelier Geoff D, Klaassen Robert J, Fernandez Conrad V, Pastore Yves D, Abish Sharon, Rayar Meera, Steele MacGregor, Jardine Lawrence, Breakey Vicky R, Brossard Josee, Sinha Roona, Silva Mariana, Goodyear Lisa, Lipton Jeffrey H, Michon Bruno, Corriveau-Bourque Catherine, Sung Lillian, Shabanova Iren, Li Hongbing, Zlateska Bozana, Dhanraj Santhosh, Cada Michaela, Scherer Stephen W, Dror Yig |
Pediatric bone marrow failure: Clinical, hematological and targeted next generation sequencing data. Blood cells, molecules & diseases 2020 11 87 102510. Chhabra Prashant, Bhatia Prateek, Singh Minu, Bansal Deepak, Jain Richa, Varma Neelam, Trehan Ami |
Identification of RPL5 gene variants and the risk of hepatic vein thrombosis in Saudi patients. Saudi medical journal 2021 9 42 (9): 969-974. Hassan Fathelrahman M, Alsultan Afnan A, Alzahrani Faisal, Albuali Waleed H, Bubshait Dalal K, Abass Elfadil M, Elbasheer Mudathir A, Alkhanbashi Abdulmohsen |
Integrated exome sequencing and microarray analyses detected genetic defects and underlying pathways of hepatocellular carcinoma. Cancer genetics 2023 7 276-277 30-35. Mei Ling Chong, James Knight, Gang Peng, Weizhen Ji, Hongyan Chai, Yufei Lu, Shengming Wu, Peining Li, Qiping |
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- Page last updated:Apr 22, 2024
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