Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: MATN3[original query] |
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Mutations in the known genes are not the major cause of MED; distinctive phenotypic entities among patients with no identified mutations. European journal of human genetics : EJHG 2005 Mar 13 (3): 292-301. Jakkula Eveliina, Mäkitie Outi, Czarny-Ratajczak Malwina, Czarny-Ratacjzak Malwina, Jackson Gail C, Damignani Rita, Susic Miki, Briggs Michael D, Cole William G, Ala-Kokko Lee |
Association of matrilin-3 polymorphisms with spinal disc degeneration and osteoarthritis of the first carpometacarpal joint of the hand. Annals of the rheumatic diseases 2006 Aug 65 (8): 1060-6. Min J L, Meulenbelt I, Riyazi N, Kloppenburg M, Houwing-Duistermaat J J, Seymour A B, van Duijn C M, Slagboom P |
Identification of genes for bone mineral density variation by computational disease gene identification strategy. Journal of bone and mineral metabolism 2011 Nov 29 (6): 709-16. Li Gloria H Y, Deng Hong-Wen, Kung Annie W C, Huang Qing-Ya |
Revisit of multiple epiphyseal dysplasia: ethnic difference in genotypes and comparison of radiographic features linked to the COMP and MATN3 genes. American journal of medical genetics. Part A 2011 Nov 155A (11): 2669-80. Kim Ok-Hwa, Park Hyunwoong, Seong Moon-Woo, Cho Tae-Joon, Nishimura Gen, Superti-Furga Andrea, Unger Sheila, Ikegawa Shiro, Choi In Ho, Song Hae-Ryong, Kim Hyun Woo, Yoo Won Joon, Shim Jong Sup, Chung Chin Youb, Oh Chang-Wug, Jeong Changhoon, Song Kwang Soon, Seo Sang Gyo, Cho Sung Im, Yeo Im Kyung, Kim So Yeon, Park Seungman, Park Sung S |
MATN3 gene polymorphism is associated with osteoarthritis in Chinese Han population: a community-based case-control study. TheScientificWorldJournal 2012 2012 656084. Gu Jiaao, Rong Jiesheng, Guan Fulin, Jiang Liying, Tao Shuqing, Guan Guofa, Tao Tianz |
A haplotype of MATN3 is associated with vertebral fracture in Chinese postmenopausal women: Peking Vertebral Fracture (PK-VF) study. Bone 2012 Apr 50 (4): 917-24. Zhao Jing, Xia Weibo, Nie Min, Zheng Xin, Wang Qiuping, Wang Xiran, Wang Wenbo, Ning Zhiwei, Huang Wei, Jiang Yan, Li Mei, Wang Ou, Xing Xiaoping, Sun Yue, Luo Lianmei, He Shuli, Yu Wei, Lin Qiang, Pei Yu, Zhang Fan, Han Youxia, Tong Yanmin, Che Ying, Shen Ruixin, Hu Yingying, Zhou Xueying, Chen Qian, Xu Li |
Genetic, clinical and radiographic signs in knee osteoarthritis susceptibility. Arthritis research & therapy 2014 16 (2): R91. Minafra Luigi, Bravatà Valentina, Saporito Michele, Cammarata Francesco P, Forte Giusi I, Caldarella Salvatore, D'Arienzo Michele, Gilardi Maria C, Messa Cristina, Boniforti Filip |
Comparison of orthopaedic manifestations of multiple epiphyseal dysplasia caused by MATN3 versus COMP mutations: a case control study. BMC musculoskeletal disorders 2014 15 (1): 84. Seo Sang Gyo, Song Hae-Ryong, Kim Hyun Woo, Yoo Won Joon, Shim Jong Sup, Chung Chin Youb, Park Moon Seok, Oh Chang-Wug, Jeong Changhoon, Song Kwang Soon, Kim Ok-Hwa, Park Sung Sup, Choi In Ho, Cho Tae-Jo |
A pilot study of gene testing of genetic bone dysplasia using targeted next-generation sequencing. Journal of human genetics 2015 Sep . Zhang Huiwen, Yang Rui, Wang Yu, Ye Jun, Han Lianshu, Qiu Wenjuan, Gu Xuef |
Association of Matrilin-3 Gene Polymorphism with Temporomandibular Joint Internal Derangement. Genetic testing and molecular biomarkers 2016 Oct 20 (10): 563-568. Yilmaz Ayça Dilara, Yazicio?lu Duygu, Tuzuner Oncul Mine Aysegul, Ere? Gülden, Sayan Nejat Bo |
Genome and epigenome wide studies of neurological protein biomarkers in the Lothian Birth Cohort 1936.
Nature communications 2019 Jul 10 (1): 3160. Hillary Robert F, McCartney Daniel L, Harris Sarah E, Stevenson Anna J, Seeboth Anne, Zhang Qian, Liewald David C, Evans Kathryn L, Ritchie Craig W, Tucker-Drob Elliot M, Wray Naomi R, McRae Allan F, Visscher Peter M, Deary Ian J, Marioni Riccardo |
Exome sequencing reveals a novel COL2A1 mutation implicated in multiple epiphyseal dysplasia. American journal of medical genetics. Part A 2019 2 179 (4): 534-541. Dasa Vinod, Eastwood James R B, Podgorski Michal, Park Heewon, Blackstock Christopher, Antoshchenko Tetyana, Rogala Piotr, Bieganski Tadeusz, Jazwinski S Michal, Czarny-Ratajczak Malwi |
The Somatic Mutation Landscape and RNA Prognostic Markers in Stomach Adenocarcinoma. OncoTargets and therapy 2020 8 13 7735-7746. Zhang Xiulei, Zheng Peiming, Li Zhen, Gao Shanjun, Liu Guangz |
Analysis of Polymorphisms in the MATN3 and DOT1L Genes and CTX-II Urinary Levels in Patients with Knee Osteoarthritis in a Northeast Mexican-Mestizo Population. Genetic testing and molecular biomarkers 2020 1 24 (2): 105-111. García-Alvarado Francisco J, Delgado-Aguirre Héctor A, Rosales-González Manuel, González-Martínez Marisela Del R, Ruiz-Flores Pablo, González-Galarza Faviel F, Arellano Perez Vertti Ruben Dani |
Next-generation sequencing-based mutational analysis of idiopathic short stature and isolated growth hormone deficiency in Korean pediatric patients. Molecular and cellular endocrinology 2021 10 544 111489. Ahn Jungmin, Oh Jiyoung, Suh Junghwan, Song Kyungchul, Kwon Ahreum, Chae Hyun Wook, Oh Jun Suk, Lee Hae In, Lee Myeong Seob, Kim Ho-Seo |
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- Page last updated:Apr 29, 2024
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