Human Genome Epidemiology Literature Finder
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Records 1 - 9 (of 9 Records) |
| Query Trace: Disease and ACAN[original query] |
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| Association between the CpG island methylator phenotype and its prognostic significance in primary pulmonary adenocarcinoma. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2016 Feb . Koh Young Wha, Chun Sung-Min, Park Young-Soo, Song Joon Seon, Lee Geon Kook, Khang Shin Kwang, Jang Se J |
| Genetic screening confirms heterozygous mutations in ACAN as a major cause of idiopathic short stature. Scientific reports 2017 9 7 (1): 12225. Hauer Nadine N, Sticht Heinrich, Boppudi Sangamitra, Büttner Christian, Kraus Cornelia, Trautmann Udo, Zenker Martin, Zweier Christiane, Wiesener Antje, Jamra Rami Abou, Wieczorek Dagmar, Kelkel Jaqueline, Jung Anna-Maria, Uebe Steffen, Ekici Arif B, Rohrer Tilman, Reis André, Dörr Helmuth-Günther, Thiel Christian |
| The Evaluation of Proteoglycan Levels and the Possible Role of ACAN Gene (c.6423T>C) Variant in Patients with Lumbar Disc Degeneration Disease. In vivo (Athens, Greece) 0 33 (2): 413-417. Yaltirik Cumhur Kaan, Timirci-Kahraman Özlem, Gulec-Yilmaz Seda, Ozdogan Selcuk, Atalay Basar, Isbir Turg |
| A wide range of protective and predisposing variants in aggrecan influence the susceptibility for otosclerosis. Human genetics 2021 Aug . Højland Allan Thomas, Tavernier Lisse J M, Schrauwen Isabelle, Sommen Manou, Topsakal Vedat, Schatteman Isabelle, Dhooge Ingeborg, Huber Alex, Zanetti Diego, Kunst Henricus P M, Hoischen Alexander, Petersen Michael B, Van Camp Guy, Fransen Er |
| Association between vitamin D receptor gene polymorphism (rs731236) and aggrecan gene VNTR polymorphism with the risk of lumbar intervertebral disc degeneration. Caspian journal of internal medicine 2022 13 (2): 418-424. Haddadi Kaveh, Sahebi Mohammad, Mahrooz Abdolkarim, ShayestehAzar Masoud, Hashemi-Soteh Mohammad Bagh |
| Clinical and genetic evaluation of children with short stature of unknown origin. BMC medical genomics 2023 8 16 (1): 194. Qianqian Zhao, Yanying Li, Qian Shao, Chuanpeng Zhang, Shuang Kou, Wanling Yang, Mei Zhang, Bo B |
| Preliminary investigation into the genetic etiology of short stature in children through whole exon sequencing of the core family. Open life sciences 2024 5 19 (1): 20220853. Jinshui He, Shuyun Zhang, Yueya Kang, Yugui Zhang, Zhugui Zheng, Minyi Ru |
| The Genetic Markers of Knee Osteoarthritis in Women from Russia. Biomedicines 2024 4 12 (4): . Anton Tyurin, Karina Akhiiarova, Ildar Minniakhmetov, Natalia Mokrysheva, Rita Khusaino |
| Matrisome and Immune Pathways Contribute to Extreme Vascular Outcomes in Williams-Beuren Syndrome. Journal of the American Heart Association 2024 1 13 (3): e031377. Delong Liu, Charles J Billington, Neelam Raja, Zoe C Wong, Mark D Levin, Wulfgang Resch, Camille Alba, Daniel N Hupalo, Elisa Biamino, Maria Francesca Bedeschi, Maria Cristina Digilio, Gabriella Maria Squeo, Roberta Villa, Pheobe C R Parrish, Russell H Knutsen, Sharon Osgood, Joy A Freeman, Clifton L Dalgard, Giuseppe Merla, Barbara R Pober, Carolyn B Mervis, Amy E Roberts, Colleen A Morris, Lucy R Osborne, Beth A Koz |
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