Human Genome Epidemiology Literature Finder
Records 1 - 17 (of 17 Records) |
Query Trace: RPS6KB1[original query] |
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ERBB2, TBX2, RPS6KB1, and MYC alterations in breast tissues of BRCA1 and BRCA2 mutation carriers. Genes, chromosomes & cancer 2004 Sep 41 (1): 1-11. Adem Camilo, Soderberg Cheryl L, Hafner Kari, Reynolds Carol, Slezak Jeffrey M, Sinclair Colleen S, Sellers Thomas A, Schaid Daniel J, Couch Fergus, Hartmann Lynn C, Jenkins Robert |
Genetic variation in RPS6KA1, RPS6KA2, RPS6KB1, RPS6KB2, and PDK1 and risk of colon or rectal cancer. Mutation research 2011 Jan 706 (1-2): 13-20. Slattery Martha L, Lundgreen Abbie, Herrick Jennifer S, Wolff Roger |
Genetic variation in the tau kinases pathway may modify the risk and age at onset of Alzheimer's disease. Journal of Alzheimer's disease : JAD 2011 27 (2): 291-7. Vázquez-Higuera José Luis, Mateo Ignacio, Sánchez-Juan Pascual, Rodríguez-Rodríguez Eloy, Pozueta Ana, Calero Miguel, Dobato José Luis, Frank-García Ana, Valdivieso Fernando, Berciano José, Bullido Maria J, Combarros Onof |
Diet and colorectal cancer: analysis of a candidate pathway using SNPS, haplotypes, and multi-gene assessment. Nutrition and cancer 2011 Nov 63 (8): 1226-34. Slattery Martha L, Lundgreen Abbie, Herrick Jennifer S, Caan Bette J, Potter John D, Wolff Roger |
MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis. Brain : a journal of neurology 2013 Jun 136 (Pt 6): 1778-82. , Lill Christina M, Schjeide Brit-Maren M, Graetz Christine, Ban Maria, Alcina Antonio, Ortiz Miguel A, Pérez Jennifer, Damotte Vincent, Booth David, Lopez de Lapuente Aitzkoa, Broer Linda, Schilling Marcel, Akkad Denis A, Aktas Orhan, Alloza Iraide, Antigüedad Alfredo, Arroyo Rafa, Blaschke Paul, Buttmann Mathias, Chan Andrew, Compston Alastair, Cournu-Rebeix Isabelle, Dörner Thomas, Epplen Joerg T, Fernández Óscar, Gerdes Lisa-Ann, Guillot-Noël Léna, Hartung Hans-Peter, Hoffjan Sabine, Izquierdo Guillermo, Kemppinen Anu, Kroner Antje, Kubisch Christian, Kümpfel Tania, Li Shu-Chen, Lindenberger Ulman, Lohse Peter, Lubetzki Catherine, Luessi Felix, Malhotra Sunny, Mescheriakova Julia, Montalban Xavier, Papeix Caroline, Paredes Lidia F, Rieckmann Peter, Steinhagen-Thiessen Elisabeth, Winkelmann Alexander, Zettl Uwe K, Hintzen Rogier, Vandenbroeck Koen, Stewart Graeme, Fontaine Bertrand, Comabella Manuel, Urcelay Elena, Matesanz Fuencisla, Sawcer Stephen, Bertram Lars, Zipp Frau |
Large multiethnic Candidate Gene Study for C-reactive protein levels: identification of a novel association at CD36 in African Americans. Human genetics 2014 Aug 133 (8): 985-95. Ellis Jaclyn, Lange Ethan M, Li Jin, Dupuis Josee, Baumert Jens, Walston Jeremy D, Keating Brendan J, Durda Peter, Fox Ervin R, Palmer Cameron D, Meng Yan A, Young Taylor, Farlow Deborah N, Schnabel Renate B, Marzi Carola S, Larkin Emma, Martin Lisa W, Bis Joshua C, Auer Paul, Ramachandran Vasan S, Gabriel Stacey B, Willis Monte S, Pankow James S, Papanicolaou George J, Rotter Jerome I, Ballantyne Christie M, Gross Myron D, Lettre Guillaume, Wilson James G, Peters Ulrike, Koenig Wolfgang, Tracy Russell P, Redline Susan, Reiner Alex P, Benjamin Emelia J, Lange Leslie |
Polymorphisms in MicroRNA Binding Sites Predict Colorectal Cancer Survival. International journal of medical sciences 2017 14 (1): 53-57. Yang Ying-Pi, Ting Wen-Chien, Chen Lu-Min, Lu Te-Ling, Bao Bo-Yi |
Identification of single nucleotide polymorphisms of the PI3K-AKT-mTOR pathway as a risk factor of central nervous system metastasis in metastatic breast cancer. European journal of cancer (Oxford, England : 1990) 2017 11 87 189-198. Le Rhun Emilie, Bertrand Nicolas, Dumont Aurélie, Tresch Emmanuelle, Le Deley Marie-Cécile, Mailliez Audrey, Preusser Matthias, Weller Michael, Revillion Françoise, Bonneterre Jacqu |
Polymorphisms of RPS6KB1 and CD86 associates with susceptibility to multiple sclerosis in Iranian population. Neurological research 2017 Jan 1-6. Abdollah Zadeh Rasoul, Jalilian Nazanin, Sahraian Mohammad Ali, Kasraian Zeinab, Noori-Daloii Mohammad Re |
MTOR Pathway-Based Discovery of Genetic Susceptibility to L-DOPA-Induced Dyskinesia in Parkinson's Disease Patients. Molecular neurobiology 2018 Jul . Martín-Flores Núria, Fernández-Santiago Rubén, Antonelli Francesa, Cerquera Catalina, Moreno Verónica, Martí Maria Josep, Ezquerra Mario, Malagelada Cristi |
Ribosomal protein S6 kinase beta-1 gene variants cause hypertrophic cardiomyopathy. Journal of medical genetics 2021 12 59 (10): 984-992. Jain Pratul Kumar, Jayappa Shashank, Sairam Thiagarajan, Mittal Anupam, Paul Sayan, Rao Vinay J, Chittora Harshil, Kashyap Deepak K, Palakodeti Dasaradhi, Thangaraj Kumarasamy, Shenthar Jayaprakash, Koranchery Rakesh, Rajendran Ranjith, Alireza Haghighi, Mohanan Kurukkanparampil Sreedharan, Rathinavel Andiappan, Dhandapany Perundurai |
Functional variants of RPS6KB1 and PIK3R1 in the autophagy pathway genes and risk of bladder cancer. Archives of toxicology 2021 Oct . Ma Lan, Zhang Dongjian, Huang Zhengkai, Zheng Rui, Du Mulong, Lv Qiang, Qin Chao, Chu Haiyan, Yuan Lin, Zhang Zhengdo |
Multilocus evaluation of genetic predictors of multiple sclerosis. Gene 2021 10 809 146008. Timasheva Yanina, Nasibullin Timur R, Tuktarova Ilsiyar A, Erdman Vera V, Galiullin Timur R, Zaplakhova Oksana V, Bakhtiiarova Klara |
Molecular profiling of Asian patients with advanced melanoma receiving check-point inhibitor treatment. ESMO open 2021 1 6 (1): 100002. Byeon S, Cho H J, Jang K-T, Kwon M, Lee J, Lee J, Kim S |
Clinical Impact of Genomic and Pathway Alterations in Stage I EGFR-Mutant Lung Adenocarcinoma. Cancer research and treatment 2023 7 . Jae Seok Lee, Eun Kyung Kim, Kyung A Kim, Hyo Sup Sh |
PPM1H is down-regulated by ATF6 and dephosphorylates p-RPS6KB1 to inhibit progression of hepatocellular carcinoma. Molecular therapy. Nucleic acids 2023 7 33 164-179. Xiaoshuang Yang, Jianting Guo, Wei Li, Chunrui Li, Xilin Zhu, Ying Liu, Xiaopan |
A Genome-Wide Association Study of Metabolic Syndrome in the Taiwanese Population. Nutrients 2024 1 16 (1): . Chih-Yi Ho, Jia-In Lee, Shu-Pin Huang, Szu-Chia Chen, Jiun-Hung Ge |
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