Human Genome Epidemiology Literature Finder
Records 1 - 22 (of 22 Records) |
Query Trace: ACTN2[original query] |
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ACTN3 genotype is associated with human elite athletic performance. American journal of human genetics 2003 Sep 73 (3): 627-31. Yang Nan, MacArthur Daniel G, Gulbin Jason P, Hahn Allan G, Beggs Alan H, Easteal Simon, North Kathr |
alpha-actinin-3 and performance. Medicine and sport science 2009 54 88-101. Yang Nan, Garton Fleur, North Kathr |
Nucleotide variation in central nervous system genes among male suicide attempters. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010 Jan 153B (1): 208-13. Baca-Garcia Enrique, Vaquero-Lorenzo Concepción, Perez-Rodriguez M Mercedes, Gratacòs Mònica, Bayés Mònica, Santiago-Mozos Ricardo, Leiva-Murillo Jose Miguel, de Prado-Cumplido Mario, Artes-Rodriguez Antonio, Ceverino Antonio, Diaz-Sastre Carmen, Fernandez-Navarro Pablo, Costas Javier, Fernandez-Piqueras José, Diaz-Hernandez Montserrat, de Leon Jose, Baca-Baldomero Enrique, Saiz-Ruiz Jeronimo, Mann J John, Parsey Ramin V, Carracedo Angel, Estivill Xavier, Oquendo Maria |
Strength, power, fiber types, and mRNA expression in trained men and women with different ACTN3 R577X genotypes. Journal of applied physiology (Bethesda, Md. : 1985) 2009 Mar 106 (3): 959-65. Norman Barbara, Esbjörnsson Mona, Rundqvist Håkan, Osterlund Ted, von Walden Ferdinand, Tesch Per |
Genome-wide association scan for childhood caries implicates novel genes.
Journal of dental research 2011 Dec 90 (12): 1457-62. Shaffer J R, Wang X, Feingold E, Lee M, Begum F, Weeks D E, Cuenco K T, Barmada M M, Wendell S K, Crosslin D R, Laurie C C, Doheny K F, Pugh E W, Zhang Q, Feenstra B, Geller F, Boyd H A, Zhang H, Melbye M, Murray J C, Weyant R J, Crout R, McNeil D W, Levy S M, Slayton R L, Willing M C, Broffitt B, Vieira A R, Marazita M |
Genetic Association of MPPED2 and ACTN2 with Dental Caries. Journal of dental research 2014 May 93 (7): 626-632. Stanley B O C, Feingold E, Cooper M, Vanyukov M M, Maher B S, Slayton R L, Willing M C, Reis S E, McNeil D W, Crout R J, Weyant R J, Levy S M, Vieira A R, Marazita M L, Shaffer J |
ACTN3 R577X genotypes associate with Class II and deepbite malocclusions. American journal of orthodontics and dentofacial orthopedics : official publication of the American Association of Orthodontists, its constituent societies, and the American Board of Orthodontics 2014 Nov 146 (5): 603-11. Zebrick Brian, Teeramongkolgul Teesit, Nicot Romain, Horton Michael J, Raoul Gwenael, Ferri Joel, Vieira Alexandre R, Sciote James |
Association of the ACTN3 R577X polymorphism with glucose tolerance and gene expression of sarcomeric proteins in human skeletal muscle. Physiological reports 2015 Mar 3 (3): . Riedl Isabelle, Osler Megan E, Benziane Boubacar, Chibalin Alexander V, Zierath Juleen |
Analysis of the ACTN3 heterozygous genotype suggests that a-actinin-3 controls sarcomeric composition and muscle function in a dose-dependent fashion. Human molecular genetics 2015 Dec . Hogarth Marshall W, Garton Fleur C, Houweling Peter J, Tukiainen Taru, Lek Monkol, MacArthur Daniel G, Seto Jane T, Quinlan Kate G R, Yang Nan, Head Stewart I, North Kathryn |
Defining the genetic architecture of hypertrophic cardiomyopathy: re-evaluating the role of non-sarcomeric genes. European heart journal 2017 Jan . Walsh Roddy, Buchan Rachel, Wilk Alicja, John Shibu, Felkin Leanne E, Thomson Kate L, Chiaw Tang Hak, Loong Calvin Chin Woon, Pua Chee Jian, Raphael Claire, Prasad Sanjay, Barton Paul J, Funke Birgit, Watkins Hugh, Ware James S, Cook Stuart |
A breast one-patient panel of heterogeneous genomes reveals genetic alterations driving DCIS into invasive lesions. Future oncology (London, England) 2019 Mar . Yang Mei, Xu Zhe, Zhang Qiang-Zu, Wang Kun, Ji Xiao-Yang, Xu Juan, Zhang Jiang-Yu, Niu Ga |
Identification of key pathways and genes in PTEN mutation prostate cancer by bioinformatics analysis. BMC medical genetics 2019 12 20 (1): 191. Sun Jian, Li Shugen, Wang Fei, Fan Caibin, Wang Jianqi |
Characterization of clinically relevant copy-number variants from exomes of patients with inherited heart disease and unexplained sudden cardiac death. Genetics in medicine : official journal of the American College of Medical Genetics 2020 9 23 (1): 86-93. Singer Emma S, Ross Samantha B, Skinner Jon R, Weintraub Robert G, Ingles Jodie, Semsarian Christopher, Bagnall Richard |
"Concealed cardiomyopathy" as a cause of previously unexplained sudden cardiac arrest. International journal of cardiology 2020 9 324 96-101. Isbister Julia C, Nowak Natalie, Butters Alexandra, Yeates Laura, Gray Belinda, Sy Raymond W, Ingles Jodie, Bagnall Richard D, Semsarian Christoph |
Differential regulation of Actn2 and Actn3 expression during unfolded protein response in C2C12 myotubes. Journal of muscle research and cell motility 2020 5 41 (2-3): 199-209. Harada Nagakatsu, Gotoda Yuka, Hatakeyama Adzumi, Nakagawa Tadahiko, Miyatake Yumiko, Kuroda Masashi, Masumoto Saeko, Tsutsumi Rie, Nakaya Yutaka, Sakaue Hiros |
ACTN2 (rs6656267) and MPPED2 (rs11031093 and rs536007) polymorphisms in primary dentition caries: A case-control study. International journal of paediatric dentistry 2020 Feb . Katifelis Hector, Sioziou Anna, Gazouli Maria, Emmanouil Dimitr |
Genetic Determinants and Genotype-Phenotype Correlations in Vietnamese Patients With Dilated Cardiomyopathy. Circulation journal : official journal of the Japanese Circulation Society 2021 5 85 (9): 1469-1478. Nguyen Thuy Vy, Tran Vu Minh Thu, Do Thi Nam Phuong, Tran Thi Huynh Nga, Do Thi Hao, Nguyen Thi My Hanh, Tran Huynh Bao Nam, Le Lan Anh, Nguyen Pham Ngoc Thieu, Nguyen Thi Dieu Ai, Nguyen Thi My Nuong, Le Ngoc Hong Phuong, Pham Nguyen Vinh, Ho Huynh Thuy Duo |
Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies. Genetics in medicine : official journal of the American College of Medical Genetics 2021 Jan . Mazzarotto Francesco, Hawley Megan H, Beltrami Matteo, Beekman Leander, de Marvao Antonio, McGurk Kathryn A, Statton Ben, Boschi Beatrice, Girolami Francesca, Roberts Angharad M, Lodder Elisabeth M, Allouba Mona, Romeih Soha, Aguib Yasmine, Baksi A John, Pantazis Antonis, Prasad Sanjay K, Cerbai Elisabetta, Yacoub Magdi H, O'Regan Declan P, Cook Stuart A, Ware James S, Funke Birgit, Olivotto Iacopo, Bezzina Connie R, Barton Paul J R, Walsh Rod |
In-Silico and In-Vitro Analysis of Human SOS1 Protein Causing Noonan Syndrome - A Novel Approach to Explore the Molecular Pathways. Current genomics 2022 4 22 (7): 526-540. Sigamani Vinoth, Rajasingh Sheeja, Gurusamy Narasimman, Panda Arunima, Rajasingh Johns |
Genetic variants in Chinese patients with sporadic dilated cardiomyopathy: a cross-sectional study. Annals of translational medicine 2022 3 10 (3): 129. Shen Cheng, Xu Lei, Sun Xiaoning, Sun Aijun, Ge Jun |
Cells 2022 Sep 11 (17): . Zech Antonia T L, Prondzynski Maksymilian, Singh Sonia R, Pietsch Niels, Orthey Ellen, Alizoti Erda, Busch Josefine, Madsen Alexandra, Behrens Charlotta S, Meyer-Jens Moritz, Mearini Giulia, Lemoine Marc D, Krämer Elisabeth, Mosqueira Diogo, Virdi Sanamjeet, Indenbirken Daniela, Depke Maren, Salazar Manuela Gesell, Völker Uwe, Braren Ingke, Pu William T, Eschenhagen Thomas, Hammer Elke, Schlossarek Saskia, Carrier Luc |
Data mining on identifying diagnosis and prognosis biomarkers in head and neck squamous carcinoma. Scientific reports 2023 6 13 (1): 10020. Guoyuan Ju, Zhangyu Yao, Yanbin Zhao, Xiaotong Zhao, Fangzhou L |
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- Page last updated:Apr 22, 2024
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