Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 60 Records) |
Query Trace: LRP6[original query] |
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Strong Association of Lipid Metabolism Related MicroRNA Binding Sites Polymorphisms with the Risk of Late Onset Alzheimer's Disease. Current neurovascular research 2016 Oct . Tan Lin, Zhao Da-Long, Sun Fu-Rong, Tan Meng-Shan, Wan Yu, Tan Chen-Chen, Zhang Wei, Miao Dan, Yu Jin-Tai, Tan L |
Validation of Recently Proposed Colorectal Cancer Susceptibility Gene Variants in an Analysis of Families and Patients-a Systematic Review. Gastroenterology 2016 Oct . Broderick Peter, Dobbins Sara E, Chubb Daniel, Kinnersley Ben, Dunlop Malcolm G, Tomlinson Ian, Houlston Richard |
Novel Mutation of LRP6 Identified in Chinese Han Population Links Canonical WNT Signaling to Neural Tube Defects. Birth defects research 2017 9 110 (1): 63-71. Shi Zhiwen, Yang Xueyan, Li Bin-Bin, Chen Shuxia, Yang Luming, Cheng Liangping, Zhang Ting, Wang Hongyan, Zheng Yufa |
Interaction between LRP5 and periostin gene polymorphisms on serum periostin levels and cortical bone microstructure. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2018 02 29 (2): 339-346. Pepe J, Bonnet N, Herrmann F R, Biver E, Rizzoli R, Chevalley T, Ferrari S |
Gene-gene interactions of the Wnt/?-catenin signaling pathway in knee osteoarthritis. Molecular biology reports 2018 Aug . Fernández-Torres Javier, Zamudio-Cuevas Yessica, López-Reyes Alberto, Garrido-Rodríguez Daniela, Martínez-Flores Karina, Lozada Carlos Alberto, Muñóz-Valle José Francisco, Oregon-Romero Edith, Martínez-Nava Gabriela Angéli |
The association of LRP6 rs2302685 (V1062I) polymorphism with the risk of hyperlipidemia in Iranian children and adolescents. Annals of human genetics 2018 Jul . Montazeri-Najafabady Nima, Dabbaghmanesh Mohammad Hossein, Mohammadian Amiri Raje |
Mutations in the fourth ?-propeller domain of LRP4 are associated with isolated syndactyly with fusion of the third and fourth fingers. Human mutation 2018 3 39 (6): 811-815. Sukenik Halevy Rivka, Chien Huan-Chieh, Heinz Bo, Bamshad Michael J, Nickerson Deborah A, , Kircher Martin, Ahituv Nad |
Genetic variants in the WNT signaling pathway are protectively associated with colorectal cancer in a Saudi population. Saudi journal of biological sciences 2019 Feb 26 (2): 286-293. Parine Narasimha Reddy, Azzam Nahla A, Shaik Jilani, Aljebreen Abdulrahman M, Alharbi Othman, Almadi Majid A, Alanazi Mohammad, Khan Zah |
Risk of Wnt/?-catenin signalling pathway gene polymorphisms in primary Sjögren's syndrome. Rheumatology (Oxford, England) 2019 Jul . Fernández-Torres Javier, Pérez-Hernández Nonanzit, Hernández-Molina Gabriela, Martínez-Nava Gabriela A, Garrido-Rodríguez Daniela, López-Reyes Alberto, Rodríguez-Pérez José |
The LRP6 functional mutation rs2302685 contributes to individual susceptibility to alcoholic liver injury related to the Wnt/?-catenin-TCF1-CYP2E1 signaling pathway. Archives of toxicology 2019 4 93 (6): 1679-1695. Xu Ying, Chen Dan, Lin Xiu-Xian, Zhao Qing, Guo Jing, Chen Li-Jie, Zhang Wei, Xiao Jian, Lian Guang-Hui, Peng Shi-Fang, Guo Dong, Yang Hong, Obianom Obinna, Shu Yan, Chen Y |
Gene-gene interaction and association of Wnt/Β-catenin signalling pathway gene polymorphisms with ankylosing spondylitis susceptibility in the Chinese Han population. Autoimmunity 2019 Oct 1-8. Liu Rui, Zhang Xu, Jiang Guangming, Ma Yubo, Yang Jiajia, Wu Meng, Han Renfang, Chen Mengya, Yuan Yaping, Hu Xingxing, Pan Meijuan, Xu Shengqian, Xu Jianhua, Shuai Zongwen, Zou Yanfeng, Pan Guixia, Pan Fami |
Exome sequencing in patients with microphthalmia, anophthalmia, and coloboma (MAC) from a consanguineous population. Clinical genetics 2020 8 98 (5): 499-506. Islam Farrah, Htun Stephanie, Lai Li-Wen, Krall Max, Poranki Menitha, Martin Pierre-Marie, Sobreira Nara, Wohler Elizabeth S, Yu Jingwei, Moore Anthony T, Slavotinek Anne |
The rs2302685 polymorphism in the LRP6 gene is associated with bone mineral density and body composition in Iranian children. The journal of gene medicine 2020 6 22 (11): e3245. Montazeri-Najafabady Nima, Dabbaghmanesh Mohammad Hossein, Mohammadian Amiri Raje |
Candidate genes for hereditary colorectal cancer: Mutational screening and systematic review. Human mutation 2020 May . Belhadj Sami, Terradas Mariona, Munoz-Torres Pau M, Aiza Gemma, Navarro Matilde, Capellá Gabriel, Valle Lau |
Targeted next generation sequencing of nine osteoporosis-related genes in the Wnt signaling pathway among Chinese postmenopausal women. Endocrine 2020 Mar . Li Can, Huang Qin, Yang Rui, Guo Xiaodong, Dai Yu, Zeng Junchao, Zeng Yun, Tao Lailin, Li Xiaolong, Zhou Haolong, Wang |
Gastrointestinal symptoms in patients with isolated oligodontia and a Wnt gene mutation. Oral diseases 2021 7 29 (1): 300-307. Ross Jamila N, Ruigrok Lisanne C, Fennis Willem M M, Cune Marco S, Rosenberg Antoine J W P, van Nunen Annick B, Créton Marijn A, Ploos van Amstel Hans-Kristian, van den Boogaard Marie-José J |
Genetic determinants of multiple myeloma risk within the Wnt/beta-catenin signaling pathway. Cancer epidemiology 2021 Jun 73 101972. Belachew Alem A, Wu Xifeng, Callender Rashida, Waller Rosalie, Orlowski Robert Z, Vachon Celine M, Camp Nicola J, Ziv Elad, Hildebrandt Michelle A |
WNT3A rs752107(C > T) Polymorphism Is Associated With an Increased Risk of Essential Hypertension and Related Cardiovascular Diseases. Frontiers in cardiovascular medicine 2021 7 8 675222. Ren Huan, Luo Jian-Quan, Ouyang Fan, Cheng Li, Chen Xiao-Ping, Zhou Hong-Hao, Huang Wei-Hua, Zhang W |
Identification of Novel Variants in Cleft Palate-Associated Genes in Brazilian Patients With Non-syndromic Cleft Palate Only. Frontiers in cell and developmental biology 2021 9 638522. Machado Renato Assis, Martelli-Junior Hercílio, Reis Silvia Regina de Almeida, Küchler Erika Calvano, Scariot Rafaela, das Neves Lucimara Teixeira, Coletta Ricardo |
Targeted next-generation sequencing (NGS) analysis of mutations in nonsyndromic tooth agenesis candidate genes : Analysis of a Turkish cohort. Journal of orofacial orthopedics = Fortschritte der Kieferorthopadie : Organ/official journal Deutsche Gesellschaft fur Kieferorthopadie 2021 3 83 (Suppl 1): 65-74. Keskin Gül, Karaer Kadri, Uçar Gündo?ar Zübey |
Synergistic Mutations of LRP6 and WNT10A in Familial Tooth Agenesis. Journal of personalized medicine 2021 11 11 (11): . Chu Kuan-Yu, Wang Yin-Lin, Chou Yu-Ren, Chen Jung-Tsu, Wang Yi-Ping, Simmer James P, Hu Jan C-C, Wang Shih-K |
Lrp6 Genotype affects Individual Susceptibility to Nonalcoholic Fatty Liver Disease and Silibinin Therapeutic Response via Wnt/?-catenin-Cyp2e1 Signaling. International journal of biological sciences 2021 10 17 (14): 3936-3953. Chen Li-Jie, Lin Xiu-Xian, Guo Jing, Xu Ying, Zhang Song-Xia, Chen Dan, Zhao Qing, Xiao Jian, Lian Guang-Hui, Peng Shi-Fang, Guo Dong, Yang Hong, Shu Yan, Zhou Hong-Hao, Zhang Wei, Chen Y |
Analyses of oligodontia phenotypes and genetic etiologies. International journal of oral science 2021 10 13 (1): 32. Zhou Mengqi, Zhang Hong, Camhi Heather, Seymen Figen, Koruyucu Mine, Kasimoglu Yelda, Kim Jung-Wook, Kim-Berman Hera, Yuson Ninna M R, Benke Paul J, Wu Yiqun, Wang Feng, Zhu Yaqin, Simmer James P, Hu Jan C |
An LRP6 mutation (Arg360His) associated with low bone mineral density but not cardiovascular events in a Caucasian family. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2022 7 33 (11): 2445-2448. Puente Nuria, Vega Ana I, Hernandez José L, Fernandez-Luna Jose L, Riancho Jose |
Whole Exome/Genome Sequencing Joint Analysis of a Family with Oligogenic Familial Hypercholesterolemia. Metabolites 2022 3 12 (3): . Ghaleb Youmna, Elbitar Sandy, Philippi Anne, El Khoury Petra, Azar Yara, Andrianirina Miangaly, Loste Alexia, Abou-Khalil Yara, Nicolas Gaël, Le Borgne Marie, Moulin Philippe, Di-Filippo Mathilde, Charrière Sybil, Farnier Michel, Yelnick Cécile, Carreau Valérie, Ferrières Jean, Lecerf Jean-Michel, Derksen Alexa, Bernard Geneviève, Gauthier Marie-Soleil, Coulombe Benoit, Lütjohann Dieter, Fin Bertrand, Boland Anne, Olaso Robert, Deleuze Jean-François, Rabès Jean-Pierre, Boileau Catherine, Abifadel Marianne, Varret Mathil |
LRP6 Polymorphisms Is Associated With Sudden Cardiac Death in Patients With Chronic Heart Failure in the Chinese Han Population. Frontiers in cardiovascular medicine 2022 2 8 815595. Guo Qi, Lai Yiwei, Chu Jianmin, Chen Xuhua, Gao Mingyang, Sang Caihua, Dong Jianzeng, Pu Jielin, Ma Changshe |
Clinical relevance of genetic polymorphisms in WNT signaling pathway (SFRP1, WNT3A, CTNNB1, WIF-1, DKK-1, LRP5, LRP6) on pulmonary tuberculosis in a Chinese population. Frontiers in immunology 2022 12 13 1011700. Huang Qian, Wang Chao-Cai, Liu Yun-Guang, Zhao Chang-Ming, Zhang Tian-Ping, Liu Yan, Wang H |
LRP5-/6 gene polymorphisms and its association with risk of abnormal bone mass in postmenopausal women. Journal of orthopaedic surgery and research 2023 5 18 (1): 369. Jun Li, Zebing Liu, Yanxia Ren, Han Shao, Siyuan |
The Relationship between LRP6 and Wnt/?-Catenin Pathway in Colorectal and Esophageal Cancer. Life (Basel, Switzerland) 2023 3 13 (3): . Shishido Akemi, Miyo Masaaki, Oishi Kazuki, Nishiyama Natsumi, Wu Meiqiao, Yamamoto Hiroyuki, Kouda Shihori, Wu Xin, Shibata Satoshi, Yokoyama Yuhki, Yamamoto Hirofu |
Identification of Novel Risk Variants of Non-Syndromic Cleft Palate by Targeted Gene Panel Sequencing. Journal of clinical medicine 2023 3 12 (5): . D?browska Justyna, Biedziak Barbara, Bogdanowicz Agnieszka, Mostowska Adrian |
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- Page last updated:Mar 25, 2024
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