Human Genome Epidemiology Literature Finder
Records 1 - 29 (of 29 Records) |
Query Trace: TNC[original query] |
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Coding SNP in tenascin-C Fn-III-D domain associates with adult asthma. Human molecular genetics 2005 Oct 14 (19): 2779-86. Matsuda A, Hirota T, Akahoshi M, Shimizu M, Tamari M, Miyatake A, Takahashi A, Nakashima K, Takahashi N, Obara K, Yuyama N, Doi S, Kamogawa Y, Enomoto T, Ohshima K, Tsunoda T, Miyatake S, Fujita K, Kusakabe M, Izuhara K, Nakamura Y, Hopkin J, Shirakawa |
The COL12A1 and COL14A1 genes and Achilles tendon injuries. International journal of sports medicine 2008 Mar 29 (3): 257-63. September A V, Posthumus M, van der Merwe L, Schwellnus M, Noakes T D, Collins |
Lack of association between Tenascin-C gene and spondyloarthritis. Rheumatology (Oxford, England) 2008 Nov 47 (11): 1655-8. Zinovieva E, Lebrun N, Letourneur F, Laurent F-X, Said-Nahal R, Chiocchia G, Breban |
Investigation of the Sp1-binding site polymorphism within the COL1A1 gene in participants with Achilles tendon injuries and controls. Journal of science and medicine in sport / Sports Medicine Australia 2009 Jan 12 (1): 184-9. Posthumus Michael, September Alison V, Schwellnus Martin P, Collins Malco |
Biological and genetic interaction between tenascin C and neuropeptide S receptor 1 in allergic diseases. Human molecular genetics 2008 Jun 17 (11): 1673-82. Orsmark-Pietras Christina, Melén Erik, Vendelin Johanna, Bruce Sara, Laitinen Annika, Laitinen Lauri A, Lauener Roger, Riedler Josef, von Mutius Erika, Doekes Gert, Wickman Magnus, van Hage Marianne, Pershagen Göran, Scheynius Annika, Nyberg Fredrik, Kere Juha, |
Variants within the MMP3 gene are associated with Achilles tendinopathy: possible interaction with the COL5A1 gene. British journal of sports medicine 2009 Jul 43 (7): 514-20. Raleigh S M, van der Merwe L, Ribbans W J, Smith R K W, Schwellnus M P, Collins |
Genome-wide analysis of chromosomal alterations in patients with esophageal squamous cell carcinoma exposed to tobacco and betel quid from high-risk area in India. Mutation research 2010 Feb 696 (2): 130-8. Chattopadhyay Indranil, Singh Avninder, Phukan Rupkumar, Purkayastha Joydeep, Kataki Amal, Mahanta Jagadish, Saxena Sunita, Kapur Suja |
Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease. Human genetics 2011 Jun 129 (6): 641-54. Minear Mollie A, Crosslin David R, Sutton Beth S, Connelly Jessica J, Nelson Sarah C, Gadson-Watson Shera, Wang Tianyuan, Seo David, Vance Jeffrey M, Sketch Michael H, Haynes Carol, Goldschmidt-Clermont Pascal J, Shah Svati H, Kraus William E, Hauser Elizabeth R, Gregory Simon |
Investigation of variants within the COL27A1 and TNC genes and Achilles tendinopathy in two populations. Journal of orthopaedic research : official publication of the Orthopaedic Research Society 2013 Apr 31 (4): 632-7. Saunders Colleen J, van der Merwe Lize, Posthumus Michael, Cook Jill, Handley Christopher J, Collins Malcolm, September Alison |
Polymorphism of ORM1 is associated with the pharmacokinetics of telmisartan. PloS one 2013 8 (8): e70341. Chen Wang-Qing, Shu Yan, Li Qing, Xu Lin-Yong, Roederer Mary W, Fan Lan, Wu Lan-Xiang, He Fa-Zhong, Luo Jian-Quan, Tan Zhi-Rong, He Yi-Jing, Zhou Hong-Hao, Chen Xiang, Zhang W |
Single nucleotide polymorphisms associated with non-contact soft tissue injuries in elite professional soccer players: influence on degree of injury and recovery time. BMC musculoskeletal disorders 2013 14 221. Pruna Ricard, Artells Rosa, Ribas Jordi, Montoro Bruno, Cos Francesc, Muñoz Carme, Rodas Gil, Maffulli Nico |
Association of variants of ABCB11 with transient neonatal cholestasis. Pediatrics international : official journal of the Japan Pediatric Society 2013 Jan . Liu LY, Wang XH, Lu Y, Zhu QR, Wang JS |
Rare variants in tenascin genes in a cohort of children with primary vesicoureteric reflux. Pediatric nephrology (Berlin, Germany) 2015 Sep . Elahi Shan, Homstad Alison, Vaidya Himani, Stout Jennifer, Hall Gentzon, Wu Guanghong, Conlon Peter, Routh Jonathan C, Wiener John S, Ross Sherry S, Nagaraj Shashi, Wigfall Delbert, Foreman John, Adeyemo Adebowale, Gupta Indra R, Brophy Patrick D, Rabinovich C Egla, Gbadegesin Rasheed |
Candidate gene approach identifies six SNPs in tenascin-C (TNC) associated with degenerative rotator cuff tears. Journal of orthopaedic research : official publication of the Orthopaedic Research Society 2016 Jun . Kluger Rainer, Burgstaller Joerg, Vogl Claus, Brem Gottfried, Skultety Michal, Mueller Simo |
Genome-Wide Association Study Identifies African-Specific Susceptibility Loci in African Americans With Inflammatory Bowel Disease. Gastroenterology 2016 Sep . Brant Steven R, Okou David T, Simpson Claire L, Cutler David J, Haritunians Talin, Bradfield Jonathan P, Chopra Pankaj, Prince Jarod, Begum Ferdouse, Kumar Archana, Huang Chengrui, Venkateswaran Suresh, Datta Lisa W, Wei Zhi, Thomas Kelly, Herrinton Lisa J, Klapproth Jan-Micheal A, Quiros Antonio J, Seminerio Jenifer, Liu Zhenqiu, Alexander Jonathan S, Baldassano Robert N, Dudley-Brown Sharon, Cross Raymond K, Dassopoulos Themistocles, Denson Lee A, Dhere Tanvi A, Dryden Gerald W, Hanson John S, Hou Jason K, Hussain Sunny Z, Hyams Jeffrey S, Isaacs Kim L, Kader Howard, Kappelman Michael D, Katz Jeffry, Kellermayer Richard, Kirschner Barbara S, Kuemmerle John F, Kwon John H, Lazarev Mark, Li Ellen, Mack David, Mannon Peter, Moulton Dedrick E, Newberry Rodney D, Osuntokun Bankole O, Patel Ashish S, Saeed Shehzad A, Targan Stephan R, Valentine John F, Wang Ming-Hsi, Zonca Martin, Rioux John D, Duerr Richard H, Silverberg Mark S, Cho Judy H, Hakonarson Hakon, Zwick Michael E, McGovern Dermot P B, Kugathasan Sub |
Novel Tenascin-C Haplotype Modifies the Risk for a Failure to Heal After Rotator Cuff Repair. The American journal of sports medicine 2017 Sep 363546517729810. Kluger Rainer, Huber Klaus R, Seely Philipp G, Berger Christian E, Frommlet Flori |
Investigating the mechanisms of papillary thyroid carcinoma using transcriptome analysis. Molecular medicine reports 2017 Aug . Qiu Jie, Zhang Wenwei, Xia Qingsheng, Liu Fuxue, Zhao Shuwei, Zhang Kailing, Chen Min, Zang Chuanshan, Ge Ruifeng, Liang Dapeng, Sun Y |
Dermal fibroblast transcriptome indicates contribution of WNT signaling pathways in the pathogenesis of Apert syndrome. The Turkish journal of pediatrics 2018 7 59 (6): 619-624. Çetinkaya Arda, Ta?k?ran Ekim, Soyer Tutku, ?im?ek-Kiper Pelin Özlem, Utine Gülen Eda, Tunçbilek Gökhan, Boduro?lu Koray, Alika?ifo?lu Mehm |
Are TNC gene variants associated with anterior cruciate ligament rupture susceptibility? Journal of science and medicine in sport 2018 Oct . Luli?ska-Kuklik Ewelina, Laguette Mary-Jessica Nancy, Moska Waldemar, Weber-Rajek Magdalena, Ficek Krzysztof, Puchala Ryszard, Ci?szczyk Pawe?, Sawczuk Marek, September Alison Victoria, Maciejewska-Skrendo Agniesz |
Defining the molecular signatures of Achilles tendinopathy and anterior cruciate ligament ruptures: A whole-exome sequencing approach. PloS one 2018 10 13 (10): e0205860. Gibbon Andrea, Saunders Colleen J, Collins Malcolm, Gamieldien Junaid, September Alison |
Genetic basis of rotator cuff injury: a systematic review. BMC medical genetics 2019 9 20 (1): 149. Longo Umile Giuseppe, Candela Vincenzo, Berton Alessandra, Salvatore Giuseppe, Guarnieri Andrea, DeAngelis Joseph, Nazarian Ara, Denaro Vincen |
In trans variant calling reveals enrichment for compound heterozygous variants in genes involved in neuronal development and growth. Genetics research 2019 6 101 e8. Cox Allison J, Grady Fillan, Velez Gabriel, Mahajan Vinit B, Ferguson Polly J, Kitchen Andrew, Darbro Benjamin W, Bassuk Alexander |
Cellular Aspects of Muscle Specialization Demonstrate Genotype - Phenotype Interaction Effects in Athletes. Frontiers in physiology 2019 5 10 526. Flück Martin, Kramer Manuel, Fitze Daniel P, Kasper Stephanie, Franchi Martino V, Valdivieso Pao |
Genetic variants associated with rotator cuff tearing utilizing multiple population-based genetic resources.
Journal of shoulder and elbow surgery 2020 Jul . Tashjian Robert Z, Kim Stuart K, Roche Megan D, Jones Kevin B, Teerlink Craig |
Impact of STAT1 polymorphisms on crizotinib-induced hepatotoxicity in ALK-positive non-small cell lung cancer patients. Journal of cancer research and clinical oncology 2021 1 147 (3): 725-737. Xin Shuang, Fang Wenfeng, Li Jianwen, Li Delan, Wang Changzheng, Huang Quanfei, Huang Min, Zhuang Wei, Wang Xueding, Chen Lik |
The Neoantigen Landscape of the Coding and Noncoding Cancer Genome Space. The Journal of molecular diagnostics : JMD 2022 4 24 (6): 609-618. Lau Tammy T Y, Sefid Dashti Zahra J, Titmuss Emma, Pender Alexandra, Topham James T, Bridgers Joshua, Loree Jonathan M, Feng Xiaolan, Pleasance Erin D, Renouf Daniel J, Schrader Kasmintan A, Sun Sophie, Ho Cheryl, Marra Marco A, Laskin Janessa, Karsan A |
Genome-Wide Association Analysis to Search for New Loci Associated with Lifelong Premature Ejaculation Risk in Chinese Male Han Population.
The world journal of men's health 2022 1 40 (2): 330-339. Wang Fei, Luo Defan, Chen Jianxiang, Pan Cuiqing, Wang Zhongyao, Fu Housheng, Xu Jianbing, Yang Meng, Mo Shaowei, Zhuang Liying, Ye Liefu, Wang Wei |
Association of Gene Variants with Seasonal Variation in Muscle Strength and Aerobic Capacity in Elite Skiers. Genes 2023 6 14 (6): . Benedikt Gasser, Walter O Frey, Paola Valdivieso, Johannes Scherr, Jörg Spörri, Martin Flü |
The role of rare genetic variants enrichment in epilepsies of presumed genetic etiology. medRxiv : the preprint server for health sciences 2023 3 . Bundalian Linnaeus, Su Yin-Yuan, Chen Siwei, Velluva Akhil, Kirstein Anna Sophia, Garten Antje, Biskup Saskia, Battke Florian, Lal Dennis, Heyne Henrike O, Platzer Konrad, Lin Chen-Ching, Lemke Johannes R, Le Duc Diana, |
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